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Published in final edited form as: Pediatr Res. 2023 Dec 6;95(2):496–507. doi: 10.1038/s41390-023-02929-z

The impact of anthropogenic climate change on pediatric viral diseases

Smit D Chitre 1,7, Cecilia M Crews 2,7, Mesfin Teklu Tessema 2,3, Indrė Plėštytė-Būtienė 4, Megan Coffee 2,3,5,8, Eugene T Richardson 1,6,8
PMCID: PMC10872406  NIHMSID: NIHMS1957664  PMID: 38057578

Abstract

The adverse effects of climate change on human health are unfolding in real time. Environmental fragmentation is amplifying spillover of viruses from wildlife to humans. Increasing temperatures are expanding mosquito and tick habitats, introducing vector-borne viruses into immunologically susceptible populations. More frequent flooding is spreading water-borne viral pathogens, while prolonged droughts reduce regional capacity to prevent and respond to disease outbreaks with adequate water, sanitation, and hygiene resources. Worsening air quality and altered transmission seasons due to an increasingly volatile climate may exacerbate the impacts of respiratory viruses. Furthermore, both extreme weather events and long-term climate variation are causing the destruction of health systems and large-scale migrations, reshaping health care delivery in the face of an evolving global burden of viral disease. Because of their immunological immaturity, differences in physiology (e.g., size), dependence on caregivers, and behavioral traits, children are particularly vulnerable to climate change. This investigation into the unique pediatric viral threats posed by an increasingly inhospitable world elucidates potential avenues of targeted programming and uncovers future research questions to effect equitable, actionable change.

INTRODUCTION

Climate change—A primer

Climate change refers to the effects of accumulated greenhouse gases (GHGs) in the atmosphere on long-term weather patterns. GHG emissions from anthropogenic fossil fuel consumption over the past 150 years have elevated Earth’s mean surface temperature by 1.1 °C in this timespan1—a rate of warming unprecedented in the last 50 million years (Fig. 1).2 Higher mean global temperatures lead to drought, heat waves, and wildfires in dry regions of the world while driving extreme precipitation and flooding in wetter regions. Warming ocean temperatures and melting polar ice caps fuel more severe storms and compromise the habitability of island states such as Tuvalu and Kiribati.3

Fig. 1. Projected Emissions and Global Temperatures.

Fig. 1

The extent of planetary warming under drastic and minimal carbon emission reduction scenarios. Source: Katharine Hayhoe, 2017.4

Climate change is also a key driver of resource scarcity, environmental degradation, precarious migration, violent conflict, and disease. Nearly 60% of all known infectious diseases have been aggravated thus far by climate change.3,4 Here, we specifically explore the impacts of climate change on viral diseases in children, building on a body of literature that explores climate change effects on a range of pathogenic diseases, including malaria and bacterial infections.5,6 Through a virus-specific lens, we examine the intersections of viral transmission with unequal socio-economic conditions, secondary effects of climate change on healthcare access, and the proliferation of non-viral comorbidities. Climate change may see viruses ranging from dengue fever to Hepatitis A, typically restricted to low and middle-income countries (LMICs), occur more frequently in Europe and North America, posing novel pathogenic threats. However, the heaviest burden of viral disease will disproportionately affect LMICs, who have contributed negligibly to GHG emissions, and have the fewest resources for climate change adaptation.7,8 The general scientific consensus is that warming temperatures, changes in humidity and precipitation patterns, and more frequent extreme weather events are altering the burden, spread, and severity of myriad viral diseases.

Children and climate change

Nearly 90% of the disease burden of climate change will be felt by children <5 years of age.9 Children are disproportionately vulnerable to infection, morbidity, and mortality from viral diseases because of their unique physiological, metabolic, and immunological immaturities, as well as their size and behavior.10,11 Globally, the leading causes of death in children remain largely due to infections: pneumonia, diarrhea, malaria, and pre-term birth complications, often precipitated by viral maternal infections (see Appendix 1 for an illustrative list of clinical syndromes discussed within the paper).12

Narrower airways mean that irritation caused by air pollutants may result in more significant airway obstruction in children than in adults, increasing their vulnerability to infections.13,14 The disease experience of acute respiratory infections is more severe in children, as their underdeveloped accessory respiratory muscles struggle to clear phlegm.15,16 Children’s increased diarrheal mortality risk is also driven by their physiological and metabolic vulnerabilities.17 Children have increased water losses due to faster respiratory rates and higher metabolic rates and may not be able to rehydrate because they cannot verbally communicate their need to do so.18-20 A less developed thermoregulatory system and a greater body surface area-to-mass ratio engender higher vulnerability to heat extremes in children.21-23

Critical gaps in children’s underdeveloped immune systems make the early years of life particularly dangerous. Mothers confer maternal antibodies to fetuses transplacentally, wherein fetuses benefit from maternal immunization and previous exposure to disease. However, vulnerabilities remain for novel diseases that mothers experience over the course of pregnancy, as early IgM antibodies will not cross the placenta.24-26 Breastmilk provides another route for young infants to receive maternal antibodies and protect against viral disease.27,28 Nevertheless, infants enter a critical vulnerability period as maternal antibodies from birth and breastfeeding wane, and they lack the adaptive immunity to respond to environmental pathogens.29-31 Though vaccination can bolster these immunological gaps, some vaccines are reserved for older children who can mount an appropriate immune response.32-34 Therefore, infants and young children constitute an immunologically naïve population to infectious diseases against which adults have acquired immunity.

Children’s behavior often puts them in closer contact with environmental risks. School-aged children spend much of their daily lives in congregate classroom settings, increasing their mean contact rate for respiratory illnesses in poorly ventilated indoor spaces.35 Per unit of body weight, they consume more drinking water, eat more food, and ingest more soil than adults, all of which are potential water-borne and soil-borne transmission.36 Young children, owing to crawling habits and their size, are physically closer to the ground, making them especially prone to zoonotic exposures as well as tick bites.37

Children are a heterogenous class, and the impact of viral infections may be vary at different ages. For example, mortality rates of H5N1 differ widely by age group: from 1997-2010, case fatality rate (CFR) was 80% for adolescents between 12–17 years old, compared with 27% in children under 5.38 Climate-related exposure risk similarly fluctuates by age: children under 1 are most affected by heat waves due to their metabolic immaturity and reliance on caregivers, but children aged 5-14 spend more time outside and are therefore exposed to excess heat and disease vectors.37

As climate change increases food insecurity worldwide, children will bear the largest brunt of morbidity and mortality.39 Undernutrition has contributed to 45% of all deaths in children under 5.40 Acute malnutrition, which affected 45.4 million children in 2020, can lead to dramatic reversals in children’s health over a short period of time, while chronic malnutrition, which impacted an additional 149.2 million children in 2020, is associated with poor mental and physical development.41-43 Undernutrition leads to reduced caloric input and loss of critical micronutrients, weakening children’s immune systems and thereby increasing infection severity and duration.44-46 Concurrently, infections contribute to worsened malnutrition outcomes, as illnesses like recurrent diarrhea disrupt the absorptive capacity of the gastrointestinal tract and require high caloric intake for adequate immune response.47,48 Maternal undernutrition, low birth weight, and suboptimal breastfeeding are all risk factors for developing childhood malnutrition.40 This negative causal loop will only accelerate as child food insecurity and pediatric illness incidence increase as a result of climate change.

The vast majority of children and adolescents live in LMICs, where they make up almost 50% of the populations, meaning that the effects of an increasing pediatric viral burden will be felt most acutely in countries with significant resource constraints.49 Thus, mitigation and adaptation strategies designed to reduce viral transmission must employ an equitable framework, ensuring that solutions are effective in a myriad of socio-political contexts.

VIRAL DISEASE THREATS

Zoonotic (non-arbovirus) diseases

As climate variation causes systemic shifts in animal habitats, wildlife will come into increasing contact with human populations, introducing more potential for zoonotic disease spillover (i.e., animal pathogens which make the evolutionary leap to human hosts). Environmental fragmentation will provoke an estimated 15,000 or more novel viral sharing events by 2070, many of which will involve human hosts in tropical hotspots with high population density.50 Of similar concern, novel cross-species transmission from animal to animal can lead to the unanticipated selection of different genetic mutations that can increase the transmissibility and pathogenicity of certain viruses, as has been hypothesized in interactions between wild migratory birds and domestic fowl that increase the pandemic potential of H5N1.51-54

Bats are expected to drive the majority of novel zoonotic spillover into human populations due to the phylogenic relatedness of human and bat viruses.55 Fruit bats, the apparent animal reservoir of Ebola virus disease (EVD), are anticipated to expand beyond their current range, as warming temperatures create suitable conditions in new countries in West and Central Africa, leading to a 1.63-fold higher epidemic likelihood over the next 50 years.56-59 As a likely zoonotic reservoir of several coronavirus (CoV) outbreaks in human populations, including Middle East respiratory syndrome (MERS)60,61 and SARS-CoV-1,62 bats will continue to play a large role in future zoonotic outbreaks of CoV as climate change-affected migratory patterns promote genetic mixing between bat populations.63,64 These epidemiological changes complicate the landscape of our current preventative measures, as unexpected phylogenic and host shifts introduce new channels of infection into human populations.50,65

Extreme weather events will drive animals into closer proximity with human populations, increasing interactions and potential spillover events. Climate-driven food shortages cause fruit bats to feed more often in domestic horse paddocks and swine farms, in which horses and pigs become mediating hosts that facilitate spillover into humans, as is the case for increasing Hendra virus spillover events in Australia66-68 and outbreaks of Nipah virus in Malaysia.69 Excess rainfall and subsequent crop damage can push rodents into human habitations for shelter and food, causing outbreaks of rodent-borne diseases such as hantavirus cardiopulmonary syndrome in the Southwestern US70,71 and Lassa fever in West Africa.72,73

Due to the high lethality and virulence of certain avian flu strains, their endemic presence in Asia, their increasingly large host reservoir, the climate-driven changes in host migration patterns, and the significant rate of viral mutation, highly pathogenic avian influenza (HPAI) is one of the world’s greatest pandemic threats.74-77 Inadequate identification of emerging pandemic threats can be particularly hazardous when early treatment initiation increases child survival, as is the case of H5N1 avian influenza being commonly mistaken for seasonal flu in children, causing increased fatality rates for each day of delayed treatment.38,78

Driven in part by climate-induced contraction of natural resources, the proliferation of high-density, large-scale livestock operations can intensify the speed and spread of infections among animal hosts, while also increasing the rate of genetic mutation.79-82 There have been numerous examples of livestock as intermediary or amplifying reservoirs for viral pathogens, from pig farms driving the 1998-1999 Malaysian Nipah virus outbreak83 to the emergence of avian influenza H5N1 and H7N9 in China as a result of the rapidly intensifying poultry sector.84 A One Health approach is needed to address increasing food insecurity while safely managing agricultural systems to reduce zoonotic spread.85

Time spent playing outdoors puts children at a high risk of interacting with wildlife and domestic livestock, as seen in select Nipah outbreaks and the majority of rabies cases, and in the increased potential for future avian flu spillover.51,86-88 Ultimately, children’s behavior, immunological immaturity, and unique physiology put them at greater risk for morbidity and mortality in an increasingly dangerous, climate-mediated future of expanded zoonotic transmission.

Vector-borne diseases

Much research on climate impacts on global infectious disease is centered on vector-borne diseases, i.e. pathologies transmitted between animals via blood-feeding arthropods. Because arthropods are dependent on ambient temperature to maintain homeostasis, the general scientific consensus is that most disease vectors will do better in a warmer world, by becoming more abundant and expanding their range (Fig. 2).89-93 Ticks and mosquitos, the primary vectors of arthropod-borne viruses (arboviruses), are inhabiting higher latitudes and altitudes, which could expose previously unaffected populations to tick and mosquito-borne diseases.2,94-99 Warmer temperatures tend to accelerate viral replication rates and enhance vector competence, leading to further viral spread.89,100-102 Therefore, almost all vector-borne viral diseases will see a larger portion of the globe become suitable for transmission in upcoming decades.3

Fig. 2. Projected Range of Aedes species Mosquitos.

Fig. 2

Projected expansion of range of Ae. aegypti and Ae. albopictus under drastic and minimal carbon emission reduction scenarios. Source: Ryan, S.J. et al. 2019.310

Dengue

Caused by the dengue virus (DENV), dengue is the most common arbovirus, with 400 million cases and 40,000 deaths reported each year.93,103 Though most children infected with dengue will be asymptomatic or minimally symptomatic, children are more likely than adults to face severe and long-lasting symptoms and die of the virus.104-106 The primary vector of dengue transmission, the Aedes aegypti mosquito, prefers tropical and subtropical urban environments, where breeding habitats and blood meals are abundant.91,107,108 Over the past half-century, DENV has drastically expanded its range, likely due to globalization, widespread urbanization, and insufficient vector control.107 In the wake of extreme precipitation and flooding in Pakistan in June 2022, pools of stagnant water and limited potable water created abundant breeding sites and feeding opportunities for mosquitos, driving surges in malaria and dengue.109,110 Catastrophic flooding also causes widespread malnutrition, outbreaks of gastrointestinal disease, and impediments to accessing medical care, which compromise children’s ability to withstand dengue.110,111 Dengue incidence is skyrocketing in endemic areas such as India112,113 and Southeast Asia;114-119 and is projected to reach new regions such as northern China,120,121 south-central Africa,91,99,122,123 mountainous regions in south Asia,121 the Americas,104,124 and the Mediterranean and Adriatic coasts of Europe.121,125,126

Chikungunya

Like dengue, chikungunya (CHIKV) is transmitted by Aedes-species mosquitos, which have proliferated globally in recent decades.124,127,128 In Brazil, a CHIKV variant has been the principal driver of over three million chikungunya cases since the introduction of the virus in 2013.129,130 In March 2023, neighboring Paraguay experienced an outbreak of over 13,000 chikungunya cases in which over 400 people, mainly children, were hospitalized.124 Climate change is expected to push chikungunya to higher latitudes in the Americas.99,128 In the Eastern Hemisphere, chikungunya epidemic potential is predicted to increase in southern and south-central Africa122,131 and continental Europe.2,126,128,132,133 Due to globalization and climate change, chikungunya’s rapid worldwide spread over the course of two decades is increasingly likely to repeat itself with presently under-explored arboviruses, which have not yet crossed paths with widely distributed mosquito species. If a novel arbovirus is picked up by a ubiquitous mosquito it could quickly become endemic across continents.

Zika

Zika virus (ZIKV) is a flavivirus transmitted by Aedes-species mosquitos that can cause severe neurological birth defects via transplacental infection.134 While most people infected with ZIKV will experience little to no symptoms, the virus can compromise the placental lining in pregnant individuals, subsequently crossing the placenta and damaging fetal brain tissue.135,136 Particularly during the first and second trimesters of pregnancy, maternal infection can lead to a 5–13% risk of the fetus developing severe brain damage, namely microcephaly.137-140 Brain damage due to ZIKV infection, labeled Congenital Zika Syndrome (CZS), is difficult to detect prenatally, and 10% of infants born with CZS will die within the first few months of life.141 Longer warm seasons in tropical and subtropical areas could create ideal conditions for ZIKV spread,136,142,143 and temperate regions may also become susceptible to seasonal epidemics when summer temperatures reach the 30°C range.144 Up to 1.3 billion additional people may be exposed to Zika by 2050 under circumstances of unmitigated global warming.145

Other mosquito-borne viruses

West Nile Virus (WNV) is the most widely distributed known arbovirus in the world, transmitted primarily by Culex-species mosquitos. Historically, major WNV outbreaks have been preceded by heat waves, which will become more frequent in upcoming decades.109,146,147 Planetary warming is driving WNV endemization across much of Europe, western Asia, Australia, and North America.2,89,95,101,126,148 Substantive epidemiological evidence exists to support the predicted expansion of Rift Valley Fever Virus (RFVF) to higher altitudes in East-Central Africa94,106,122 and Ross River Virus (RRV) and Barmah Forest Virus (BFV) in Australia.149-153 In Latin America, Oropouche (OROV) and Mayaro virus (MAYV) harbor epidemic potential as disease vectors expand their range to encompass immunologically naïve human populations, in which children occupy a particularly vulnerable niche.154-157 A climate-mediated increase in emerging infectious febrile viruses, like Mayaro virus, may lead to increased antibiotic treatments for novel viruses with low access to diagnostic facilities.158-160 Antimicrobial resistance is a growing concern of global pediatric health;losing therapeutic options to resistance could bring us back to a pre-antibiotic era when simple infections had fatal consequences.161

Tick-borne viruses

Climate change has affected the distribution and behavior of ticks, as well as the viral diseases they carry, through multiple pathways.162-164 In central and eastern Europe, the Ixodes ricinus tick, which carries the tick-borne encephalitis virus (TBEV) has been inhabiting higher altitudes in mountainous regions,97,165,166 and becoming more plentiful in the areas they currently inhabit.94,167,168 In conjunction with the expansion of I. ricinus due to climate change, the risk of TBEV is increasing as well.162,167,169-171 This is partially behavioral: ticks spend more time questing—that is, primed to latch onto a host—when temperatures are warmer.169,170,172 Incidence of Crimean Congo Hemorrhagic Fever (CCHF), transmitted by Hyalomma-species ticks, is also associated with temperature, and is predicted to become more prevalent as global mean temperatures increase.163,172-179 Warmer weather will most likely push humans, particularly children, outdoors more often, increasing their contact with questing ticks in grassy settings.

Vertical Transmission

Preterm birth is the leading cause of neonatal morbidity and mortality, responsible for approximately 900,000 neonatal deaths in 2019, the highest proportion of which were found in LMICs.12 Increasingly inhospitable climate conditions will affect mothers and neonates alike, as extreme maternal heat exposure has been positively correlated with pre-term birth, low birth weight, and risk of stillbirth.180 In resource-constrained settings, premature birth is often a death sentence for neonates within the first month of life.181 Preterm birth has a number of other causes, but maternal infection during the course of pregnancy often plays a significant role.25,182,183 Maternal influenza and SARS-CoV2 infections, as well as viral hemorrhagic fevers like Lassa, Ebola, Marburg, and Rift Valley fever virus have particularly deleterious effects on premature birth rates and neonatal mortality.184-187 As these diseases often lead to the death of the mother, there is serious concern for neonatal survival given the loss of primary caregiver.188

Of similar concern are the congenital abnormalities that result from vertical transmission through the placental barrier, causing chronic health issues in neonates that last a lifetime, often leading to an early death. Zika, chikungunya, and dengue fever have all been associated with developmental abnormalities and congenital defects, like the much publicized microencephaly in children born to mothers infected with Zika.134,189-191 Viral in-utero infections, including cytomegalovirus, HIV, herpes simplex virus, are also common causes of neonatal morbidity, mortality, and congenital abnormalities, most significantly affecting neonates in LMICs.192,193 As climate change increases the spread of viral vector-borne threats and shifts the seasonality of such respiratory diseases as influenza, preventative measures like vaccination for pregnant women will have positive downstream effects on pediatric health.194,195

Water-borne and fecal-oral diseases

Climate change is expected to increase overall precipitation across much of the globe, but also augment the likelihood and severity of drought in dry regions such as the American Southwest, Sahel, Eastern Horn of Africa, and much of Australia.196 The 2022 IPCC report demonstrates high confidence that warming temperatures and heavy precipitation are associated with increased incidence of water-borne diseases. Extreme rainfall can lead to flooding, which can introduce pathogens into the drinking water supply.197-199 Drought also heightens the risk of water-borne disease, forcing people to turn to alternate unsafe water sources for hydration, share limited existing water resources, which can concentrate pathogens, and compromise hygiene and sanitation practices.199,200

There is significant overlap between water-borne and fecal-oral diseases, which are transmitted when fecal material passes into the mouth. Water is the principal medium for ingestion of fecal matter: nearly 25% of the global population is consuming fecally-contaminated water, and this figure is expected to rise as climate disasters continue.201 Diarrheal diseases, the second-leading cause of death in children under five years of age, are primarily caused by viruses spread via water-borne and fecal-oral routes.2,197,198,202-205 Associations between temperature and/or rainfall and all-cause diarrhea have been extensively documented across the globe.199,206-209 Many diarrhea-causing viruses are nameless and do not cause major epidemics, but their cumulative impact on children cannot be understated. Increasingly, scientists are identifying and researching these emerging pathological agents, which tend to fall into the rotavirus, adenovirus, astrovirus, and norovirus families.201,210-215 For example, Sapovirus—a norovirus-adjacent genus in the calicivirus family—is recently being recognized as a leading cause of diarrheal disease, accounting for up to 17% of diarrheal episodes worldwide.214

Poliomyelitis

Spread through food-borne, waterborne, and fecal-oral routes, poliomyelitis (polio) predominantly affects children under five years of age;one out of every 200 infections can lead to irreversible paralysis, which can beget respiratory failure and death.216 Though preventable through vaccination, polio has experienced a resurgence in recent years, and as the WHO notes, “as long as a single child remains infected, children in all countries are at risk of contracting polio.”217 Worryingly, droughts are known to stymie polio vaccination campaigns.218 Though the effects of climate change on polio transmission dynamics are not fully understood, polio is considered a climate-vulnerable disease.219

Hand-foot-and-mouth

Hand-foot-and-mouth disease (HFMD) is a fecal-oral and contact viral illness that predominantly affects children under five years of age, who are also at highest risk of developing severe symptoms including meningitis, encephalitis, respiratory failure, and cardiac failure.220 There is robust scientific data supporting the role of climate change, namely warming temperatures and higher relative humidity, in driving the rise in HMFD cases across Pacific Asia, where the virus has become a pressing public health threat.221-229 The relationship between HMFD infections and temperature are often non-linear, with one to two temperature peaks for optimal transmission, as children spend more time outside in warm weather, yet retreat inside during extreme heat.220,222,223,227 Additionally, enterovirus survival and infectiousness is enhanced in warmer weather as well as humid conditions, because enteroviruses can attach to airborne water droplets, which subsequently stick to frequently-touched surfaces including children’s toys.220,224,226 Climate change, then, is expected to make more months out of the year conducive to HMFD transmission.220

Respiratory diseases

Climate change has a complex influence on the transmission of viral respiratory diseases. The distribution of acute respiratory infections (ARIs) varies by region, but ARIs continue to be one of the most significant causes of hospitalization and mortality among children globally.230-234 As the global distribution of ARIs is affected by climate change in the coming years, respiratory illness hospitalizations and related mortality will continue to be a pressing pediatric concern worldwide.235-239

Humidity and temperature have a significant but inconsistent effect on the regional incidence of viral respiratory infections, as each virus has a different “u-shape” curve of ideal transmission conditions, affected to varying degrees by a constellation of environmental and host factors.240-251 For example, while warmer winters are associated with fewer infections of influenza A and B, they have been shown to precipitate severe annual influenza seasons with earlier onset in the following year, as there is a larger immunologically susceptible population to attack.252 Conversely, warmer winters shorten the RSV season, creating a protective effect for an immunologically naïve child population.237,253 More climate prediction complexity is introduced on a particle level, where higher temperature and humidity are associated with a shorter virus half-life.254,255 Hotter temperatures and frequent storms could drive people indoors, creating optimal environments for increased circulation of respiratory pathogens in enclosed spaces for more days out of the year.256-259 In settings of water scarcity, hygiene and sanitation may be curtailed, enhancing the spread of viral pathogens through droplets.260,261

Ambient air pollution, a result of fossil fuel combustion through wildfires and human activity, is expected to increase over the coming years.262,263 Increases in air pollution have been directly linked to increased hospitalization rates of ARIs in children, such as pneumonia.264-268 Increased time spent indoors, caused by excess heat or precipitation, exposes children to household air pollution from the combustion of solid fuels for cooking and heating indoors.269-271 Large-scale global and local reductions of fossil fuel emissions are necessary to mitigate these primary and secondary threats to pediatric respiratory health.

SECONDARY CLIMATE-MEDIATED THREATS TO PEDIATRIC BURDEN OF VIRAL DISEASE

Climate-induced migration

Natural disasters, desertification, and rising sea levels are making large swaths of the world uninhabitable, prompting migration that will fundamentally alter the distribution of people across continents.8,272-274 In 2020, close to 10 million children were displaced in the aftermath of weather-related shocks.275 Displacement has myriad impacts on viral disease.

The most common viruses in displaced persons camps are diarrheal diseases and respiratory infections, which significantly impact children’s health.276-279 Crowded living conditions are conducive for the rapid outbreak of respiratory illness, such as measles, varicella, influenza, and other acute respiratory infections, and viruses spread through skin-to-skin contact, such as molluscum and human papillomaviruses.280-283 Isolated outbreaks of poliovirus have been reported in refugee camps, likely due to displacement-related gaps in routine immunization activities and inadequate water, sanitation, and hygiene (WASH) infrastructure.284,285 Other water-borne pathogens, such as Hepatitis A and E, can spread quickly in resettlement camps with over-crowding and poor sanitation, especially those built in areas vulnerable to persistent flooding during rainy seasons.286-288 Poorly planned waste management systems increase the amount of refuse, such as water bottles, old tires, and cans, near human dwellings, which creates more breeding grounds for mosquitos and attracts rodents, leading to outbreaks of dengue, West Nile virus, and Lassa fever.289-291

As families migrate, it is exceedingly difficult to maintain routine immunization schedules for their children.292,293 Migration and infectious disease transmission work bidirectionally, wherein migrants are exposed to new pathogens in host communities to which they have no acquired immunity, and diseases also travel with migratory populations, introducing new pathogens into an immunologically naïve host country.294,295 Chikungunya was likely introduced into Singapore, a population with no natural immunity prior to 2008, as migrant workers moved from the Indian subcontinent in search of work, yet due to their poor living conditions and barriers to healthcare access, migrants themselves were most affected by the local outbreak clusters.279,296 As migrant populations resettle in new regions, they may transport livestock with them, potentially introducing zoonotic hosts and associated vectors into novel geographic niches, as was the case of increased prevalence of tick-borne CCHF from infected livestock following the relocation of Afghan refugees to Pakistan.297 Climate change will continue to provoke complex migratory patterns due to natural disasters, long-term environmental shifts, and lost livelihoods, and the interchange of viral pathogens into new susceptible populations will proliferate.298,299 Migrant-sensitive health systems in host countries are critical to address these vulnerabilities.300,301

Compromised health systems and barriers to treatment

Extreme weather events are becoming more frequent due to climate change: many of the strongest storms in recorded history have occurred in the past few years. Tropical cyclone Freddy broke global and regional records across Madagascar, Mozambique, and Malawi.302 The subsequent mudslides and flooding destroyed over 300 health facilities and disconnected numerous villages from health services, like life-saving antiretroviral treatments.303-305 Severe weather can also compromise electrification, patient records, and vaccine supplies, all of which exacerbate the burden of viral disease.306

While patients face physical barriers to treatment and health centers suffer destruction of medical supplies and infrastructure, storms are likely to result in injuries that make access to care all the more urgent and necessary.307 This worsens resource constraints and makes it more challenging for individuals with viral illnesses to receive appropriate diagnoses and treatment. In these situations, children are most vulnerable, particularly when their viral illnesses require advanced care: due to the specialized nature of the equipment and personnel required, pediatric emergency and intensive care units are even more susceptible to devastating supply shortages.308

CONCLUSION

In a warming world, the mounting threat of viral disease—which must be situated within a broader context of food insecurity, displacement, conflict, and other impacts of climate change—requires sweeping interventions. It mandates that health professionals extend their commitment to human health into the sociopolitical realm, becoming advocates for drastic cutbacks in global GHG emissions. Without these cutbacks, models forecast increases in average global temperatures by 2–5 °C (with localized extremes), which would prove devastating for much of the world’s population, particularly for children.4 Health professionals are on the front lines of this developing crisis;they must recruit their evidence-based understandings of the impacts of climate change on human health to highlight the necessity of political action.307

Finally, to protect the well-being of children worldwide, the vast majority of whom reside in LMICs, health professionals must grapple with the dynamics that impoverish these countries in the first place. These are the very dynamics that engineer the disproportionate vulnerability of LMICs to climate change, putting billions of children at risk of viral disease, among a host of other pathologies. For example, high-interest loans disbursed by global financial institutions to LMICs trap these countries in vicious cycles of debt, whereas unconditional economic support to the Global South would allow for the development of climate-resilient infrastructure, robust universal health care, vaccination campaigns, and research to combat infectious pathologies. By pursuing equitable solutions to systemic racism, legacies of colonialism, predatory neo-colonial extraction, and widespread human rights failings, the world can better mitigate the looming health threats posed by climate change.309

Supplementary Material

Supplemental table

IMPACT:

  • A review of the effects of climate change on viral threats to pediatric health, including zoonotic, vector-borne, water-borne, and respiratory viruses, as well as distal threats related to climate-induced migration and health systems.

  • A unique focus on viruses offers a more in-depth look at the effect of climate change on vector competence, viral particle survival, co-morbidities, and host behavior.

  • An examination of children as a particularly vulnerable population provokes programming tailored to their unique set of vulnerabilities and encourages reflection on equitable climate adaptation frameworks.

FUNDING

Dr. Eugene T. Richardson is funded by a NIAID K08 AI139361 grant and a Harvard Center for African Studies Motsepe Presidential Research Accelerator grant; Smit Chitre is funded by a Weatherhead Center for International Affairs Medium Faculty Grant.

Footnotes

COMPETING INTERESTS

The authors declare no competing interests.

CONSENT STATEMENT

No patient consent was required.

Supplementary information The online version contains supplementary material available at https://doi.org/10.1038/s41390-023-02929-z.

DATA AVAILABILITY

Data sharing is not applicable to this article as no datasets were generated or analyzed during the current study.

REFERENCES

  • 1.NASA Goddard Institute for Space Studies. GISS Surface Temperature Analysis (GISTEMP). National Aeronautics and Space Administration https://data.giss.nasa.gov/gistemp/ (2023).
  • 2.Bernstein AS Climate Change and Infectious Disease. in Harrison’s Principles of Internal Medicine (eds. Loscalzo J et al.) (McGraw-Hill Education, 2022). [Google Scholar]
  • 3.Mora C. et al. Over half of known human pathogenic diseases can be aggravated by climate change. Nat. Clim. Change 12, 869–875 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Hayhoe K. Greater Emissions Lead to Significantly More Warming. (2017). [Google Scholar]
  • 5.Martens WJ, Niessen LW, Rotmans J, Jetten TH & McMichael AJ Potential impact of global climate change on malaria risk. Environ. Health Perspect 103, 458–464 (1995). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Gona PN & More AF Bacterial pathogens and climate change. Lancet 400, 2161–2163 (2022). [DOI] [PubMed] [Google Scholar]
  • 7.Global Climate Change and Human Health: From Science to Practice, 2nd Edition. (Jossey-Bass, 2021). [Google Scholar]
  • 8.IPCC. Climate change 2022: impacts, adaptation and vulnerability. https://www.ipcc.ch/report/ar6/wg2/ (2022).
  • 9.UNICEF. The Climate Crisis is a Child Rights Crisis: Introducing the Children’s Climate Risk Index. https://www.unicef.org/media/105376/file/UNICEF-climate-crisis-child-rights-crisis.pdf (2021).
  • 10.Ahdoot S. et al. Global climate change and children’s health. Pediatrics 136, e1468–e1484 (2015). [DOI] [PubMed] [Google Scholar]
  • 11.Di Cicco ME et al. Climate change and childhood respiratory health: a call to action for paediatricians. Int. J. Environ. Res. Public. Health 17, 5344 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Perin J. et al. Global, regional, and national causes of under-5 mortality in 2000–19: an updated systematic analysis with implications for the sustainable development goals. Lancet Child Adolesc. Health 6, 106–115 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Moya J, Bearer CF & Etzel RA Children’s behavior and physiology and how it affects exposure to environmental contaminants. Pediatrics 113, 996–1006 (2004). [PubMed] [Google Scholar]
  • 14.Kim J. Ambient air pollution: health hazards to children. Pediatrics 114, 1699–1707 (2004). [DOI] [PubMed] [Google Scholar]
  • 15.DeVincenzo JP Factors predicting childhood respiratory syncytial virus severity: what they indicate about pathogenesis. Pediatr. Infect. Dis. J 24, S177 (2005). [DOI] [PubMed] [Google Scholar]
  • 16.Javouhey E, Pouyau R & Massenavette B Pathophysiology of acute respiratory failure in children with bronchiolitis and effect of CPAP. Noninvasive Vent. High-Risk Infect. Mass Casualty Events 233–249, 10.1007/978-3-7091-1496-4_27 (2013). [DOI] [Google Scholar]
  • 17.Hartman RM et al. Risk factors for mortality among children younger than age 5 years with severe diarrhea in low- and middle-income countries: findings from the World Health Organization-coordinated Global Rotavirus and Pediatric Diarrhea Surveillance Networks. Clin. Infect. Dis 76, e1047–e1053 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Landigran P & Garg A Children are not little adults. In Children’s health and the environment (World Health Organization, 2004). [Google Scholar]
  • 19.Bado AR, Susuman AS & Nebie EI Trends and risk factors for childhood diarrhea in sub-Saharan countries (1990–2013): assessing the neighborhood inequalities. Glob. Health Action 9, 10.3402/gha.v9.30166 (2016). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Acácio S. et al. Risk factors for death among children 0–59 months of age with moderate-to-severe diarrhea in Manhiça district, southern Mozambique. BMC Infect. Dis 19, 322 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Bennett CM & Friel S Impacts of climate change on inequities in child health. Children 1, 461–473 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Gao J, Sun Y, Lu Y & Li L Impact of ambient humidity on child health: a systematic review. PLOS ONE 9, e112508 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Xu Z. et al. The impact of heat waves on children’s health: a systematic review. Int. J. Biometeorol 58, 239–247 (2014). [DOI] [PubMed] [Google Scholar]
  • 24.Lindsey B, Kampmann B & Jones C Maternal immunization as a strategy to decrease susceptibility to infection in newborn infants. Curr. Opin. Infect. Dis 26, 248–253 (2013). [DOI] [PubMed] [Google Scholar]
  • 25.Silasi M. et al. Viral infections during pregnancy. Am. J. Reprod. Immunol 73, 199–213 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Carsetti R. et al. The immune system of children: the key to understanding SARS-CoV-2 susceptibility? Lancet Child Adolesc. Health 4, 414–416 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Hanson LA & Söderström T Human milk: Defense against infection. Prog. Clin. Biol. Res 61, 147–159 (1981). [PubMed] [Google Scholar]
  • 28.Hanson LA Breastfeeding provides passive and likely long-lasting active immunity. Ann. Allergy Asthma Immunol 81, 523–534 (1998). [DOI] [PubMed] [Google Scholar]
  • 29.Sato H, Albrecht P, Reynolds DW, Stagno S & Ennis FA Transfer of measles, mumps, and rubella antibodies from mother to infant. Its effect on measles, mumps, and rubella immunization. Am. J. Dis. Child 1960 133, 1240–1243 (1979). [DOI] [PubMed] [Google Scholar]
  • 30.Rijkers GT, Sanders EAM, Breukels MA & Zegers BJM Responsiveness of infants to capsular polysaccharides: implications for vaccine development. Res. Med. Microbiol 7, 3 (1996). [Google Scholar]
  • 31.Simon AK, Hollander GA & McMichael A Evolution of the immune system in humans from infancy to old age. Proc. R. Soc. B Biol. Sci 282, 20143085 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Bridy-Pappas AE, Margolis MB, Center KJ & Isaacman DJ Streptococcus pneumoniae: Description of the pathogen, disease epidemiology, treatment, and prevention. Pharmacother. J. Hum. Pharmacol. Drug Ther 25, 1193–1212 (2005). [DOI] [PubMed] [Google Scholar]
  • 33.Daniels CC, Rogers PD & Shelton CM A review of pneumococcal vaccines: current polysaccharide vaccine recommendations and future protein antigens. J. Pediatr. Pharmacol. Ther. JPPT 21, 27–35 (2016). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Albrecht M & Arck PC Vertically transferred immunity in neonates: mothers, mechanisms and mediators. Front. Immunol 11, 555 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Heymann A, Chodick G, Reichman B, Kokia E & Laufer J Influence of school closure on the incidence of viral respiratory diseases among children and on health care utilization. Pediatr. Infect. Dis. J 23, 675 (2004). [DOI] [PubMed] [Google Scholar]
  • 36.Sheffield PE & Landrigan PJ Global climate change and children’s health: threats and strategies for prevention. Environ. Health Perspect 119, 291–298 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Xu Z. et al. Climate change and children’s health—a call for research on what works to protect children. Int. J. Environ. Res. Public. Health 9, 3298–3316 (2012). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Oner AF et al. H5N1 Avian Influenza in children. Clin. Infect. Dis 55, 26–32 (2012). [DOI] [PubMed] [Google Scholar]
  • 39.WFP. A generation at risk: nearly half of global food crisis hungry are children, say WFP, African Union Development Agency NEPAD, The Education Commission and education partners ∣ World Food Programme. https://www.wfp.org/news/generation-risk-nearly-half-global-food-crisis-hungry-are-children-say-wfp-african-union (2022). [Google Scholar]
  • 40.Black RE et al. Maternal and child undernutrition and overweight in low-income and middle-income countries. Lancet 382, 427–451 (2013). [DOI] [PubMed] [Google Scholar]
  • 41.Victora CG et al. Maternal and child undernutrition: consequences for adult health and human capital. Lancet 371, 340–357 (2008). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Dipasquale V, Cucinotta U & Romano C Acute malnutrition in children: pathophysiology, clinical effects and treatment. Nutrients 12, 2413 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.UNICEF, The World Bank & WHO. Levels and trends in child malnutrition. (2021).
  • 44.Guerrant RL, Schorling JB, McAuliffe JF & Souza MAD Diarrhea as a cause and an effect of malnutrition: diarrhea prevents catch-up growth and malnutrition increases diarrhea frequency and duration. Am. J. Trop. Med. Hyg 47, 28–35 (1992). [DOI] [PubMed] [Google Scholar]
  • 45.Brundtland GH Nutrition and infection: Malnutrition and mortality in public health. Nutr. Rev 58, S1–S4 (2000). ; discussion S63-73. [DOI] [PubMed] [Google Scholar]
  • 46.Bhaskaram P. Micronutrient malnutrition, infection, and immunity: an overview. Nutr. Rev 60, S40–S45 (2002). [DOI] [PubMed] [Google Scholar]
  • 47.Molla A, Molla AM, Sarker SA, Khatoon M & Mujibur Rahaman M Effects of acute diarrhea on absorption of macronutrients during disease and after recorvery. In Diarrhea and Malnutrition 143–155 (Plenum Publishing Corporation, 1983). [Google Scholar]
  • 48.Martorell R & Yarbrough C The energy cost of diarrheal diseases and other common illnesses in children. in Diarrhea and Malnutrition 125–143 (Plenum Publishing Corporation, 1983). [Google Scholar]
  • 49.United Nations, Department of Economic and Social Affairs, Population Division. World Population Prospects: The 2010 Revision. https://www.un.org/en/development/desa/publications/world-population-prospects-the-2010-revision.html (2011).
  • 50.Carlson CJ et al. Climate change increases cross-species viral transmission risk. Nature 607, 555–562 (2022). [DOI] [PubMed] [Google Scholar]
  • 51.Curseu D, Popa M, Sirbu D & Stoian I Potential Impact of Climate Change on Pandemic Influenza Risk. Glob. Warm 643–657, 10.1007/978-1-4419-1017-2_45 (2009). [DOI] [Google Scholar]
  • 52.Morin CW et al. Avian influenza virus ecology and evolution through a climatic lens. Environ. Int 119, 241–249 (2018). [DOI] [PubMed] [Google Scholar]
  • 53.Escudero-Pérez B, Lalande A, Mathieu C & Lawrence P Host–pathogen interactions influencing zoonotic spillover potential and transmission in humans. Viruses 15, 599 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.van Gils JA & et al. Hampered foraging and migratory performance in swans infected with low-pathogenic avian influenza a virus. PLOS ONE 2, e184 (2007). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Olival KJ et al. Host and viral traits predict zoonotic spillover from mammals. Nature 546, 646–650 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Leroy EM et al. Fruit bats as reservoirs of Ebola virus. Nature 438, 575–576 (2005). [DOI] [PubMed] [Google Scholar]
  • 57.Leendertz SAJ, Gogarten JF, Düx A, Calvignac-Spencer S & Leendertz FH Assessing the evidence supporting fruit bats as the primary reservoirs for Ebola viruses. EcoHealth 13, 18–25 (2016). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Redding DW et al. Impacts of environmental and socio-economic factors on emergence and epidemic potential of Ebola in Africa. Nat. Commun 10, 4531 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Kupferschmidt K. This bat species may be the source of the Ebola epidemic that killed more than 11,000 people in West Africa. Science https://www.science.org/content/article/bat-species-may-be-source-ebola-epidemic-killed-more-11000-people-west-africa (2019). [Google Scholar]
  • 60.Memish ZA et al. Middle East Respiratory Syndrome Coronavirus in Bats, Saudi Arabia. Emerg. Infect. Dis 19, 1819–1823 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Anthony SJ et al. Further Evidence for bats as the evolutionary source of Middle East Respiratory Syndrome Coronavirus. mBio 8, e00373–17 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Li W. et al. Bats are natural reservoirs of SARS-like Coronaviruses. Science 310, 676–679 (2005). [DOI] [PubMed] [Google Scholar]
  • 63.Cui J, Li F & Shi Z-L Origin and evolution of pathogenic coronaviruses. Nat. Rev. Microbiol 17, 181–192 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.Beyer RM, Manica A & Mora C Shifts in global bat diversity suggest a possible role of climate change in the emergence of SARS-CoV-1 and SARS-CoV-2. Sci. Total Environ 767, 145413 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 65.Horta MA, Ledesma LA, Moura WC & Lemos ERS From dogs to bats: Concerns regarding vampire bat-borne rabies in Brazil. PLoS Negl. Trop. Dis 16, e0010160 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Martin G. et al. Climate change could increase the geographic extent of Hendra Virus spillover risk. EcoHealth 15, 509–525 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Yuen KY et al. Hendra virus: Epidemiology dynamics in relation to climate change, diagnostic tests and control measures. One Health 12, 100207 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68.Eby P. et al. Pathogen spillover driven by rapid changes in bat ecology. Nature 613, 340–344 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 69.Daszak P. et al. Interdisciplinary approaches to understanding disease emergence: The past, present, and future drivers of Nipah virus emergence. Proc. Natl Acad. Sci 110, 3681–3688 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70.Hjelle B & Glass GE Outbreak of Hantavirus Infection in the Four Corners Region of the United States in the Wake of the 1997–1998 El Nino—Southern Oscillation. J. Infect. Dis 181, 1569–1573 (2000). [DOI] [PubMed] [Google Scholar]
  • 71.Patz JA, Epstein PR, Burke TA & Balbus JM Global climate change and emerging infectious diseases. JAMA 275, 217–223 (1996). [PubMed] [Google Scholar]
  • 72.Bonwitt J. et al. At home with Mastomys and Rattus: Human-rodent interactions and potential for primary transmission of Lassa Virus in domestic spaces. Am. J. Trop. Med. Hyg 96, 935–943 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 73.Redding DW et al. Geographical drivers and climate-linked dynamics of Lassa fever in Nigeria. Nat. Commun 12, 5759 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 74.Zhou J. et al. Biological features of novel avian influenza A (H7N9) virus. Nature 499, 500–503 (2013). [DOI] [PubMed] [Google Scholar]
  • 75.Tian H. et al. Climate change suggests a shift of H5N1 risk in migratory birds. Ecol. Model 306, 6–15 (2015). [Google Scholar]
  • 76.Yang R. et al. Human infection of avian influenza A H3N8 virus and the viral origins: a descriptive study. Lancet Microbe 3, e824–e834 (2022). [DOI] [PubMed] [Google Scholar]
  • 77.CDC. Human Infection with Avian Influenza A(H3N8) Virus Reported by China. Centers for Disease Control and Prevention https://www.cdc.gov/flu/avianflu/spotlights/2022-2023/avian-influenza-h3n8-china.htm (2023). [Google Scholar]
  • 78.Nyamwaya DK, Thumbi SM, Bejon P, Warimwe GM & Mokaya J The global burden of Chikungunya fever among children: A systematic literature review and meta-analysis. PLOS Glob. PLOS Glob. Public Health 2, e0000914 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79.Jones BA et al. Zoonosis emergence linked to agricultural intensification and environmental change. Proc. Natl Acad. Sci 110, 8399–8404 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 80.Herrero M. et al. Livestock and the environment: what have we learned in the past decade? Annu. Rev. Environ. Resour 40, 177–202 (2015). [Google Scholar]
  • 81.Graham JP et al. The animal-human interface and infectious disease in industrial food animal production: rethinking biosecurity and biocontainment. Public Health Rep. Wash. DC 1974 123, 282–299 (2008). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 82.Drew TW The emergence and evolution of swine viral diseases: to what extent have husbandry systems and global trade contributed to their distribution and diversity? Rev. Sci. Tech. Int. Epizoot 30, 95–106 (2011). [DOI] [PubMed] [Google Scholar]
  • 83.Looi L-M & Chua K-B Lessons from the Nipah virus outbreak in Malaysia. Malays. J. Pathol 29, 63–67 (2007). [PubMed] [Google Scholar]
  • 84.Gilbert M, Xiao X & Robinson TP Intensifying poultry production systems and the emergence of avian influenza in China: a ‘One Health/Ecohealth’ epitome. Arch. Public Health 75, 48 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 85.Gibb R, Franklinos LHV, Redding DW & Jones KE Ecosystem perspectives are needed to manage zoonotic risks in a changing climate. BMJ m3389 (2020) 10.1136/bmj.m3389. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 86.Montgomery JM et al. Risk factors for Nipah Virus Encephalitis in Bangladesh. Emerg. Infect. Dis 14, 1526–1532 (2008). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 87.Warrell MJ Emerging aspects of rabies infection: with a special emphasis on children. Curr. Opin. Infect. Dis 21, 251 (2008). [DOI] [PubMed] [Google Scholar]
  • 88.Lunney M. et al. Knowledge, attitudes and practices of rabies prevention and dog bite injuries in urban and peri-urban provinces in Cambodia, 2009. Int. Health 4, 4–9 (2012). [DOI] [PubMed] [Google Scholar]
  • 89.Morin CW, Comrie AC & Ernst K Climate and Dengue transmission: evidence and implications. Environ. Health Perspect 121, 1264–1272 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 90.Kraemer MUG et al. Past and future spread of the arbovirus vectors Aedes aegypti and Aedes albopictus. Nat. Microbiol 4, 854–863 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 91.Messina JP et al. The current and future global distribution and population at risk of dengue. Nat. Microbiol 4, 1508–1515 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 92.Greer A, Ng V & Fisman D Public health: Climate change and infectious diseases in North America: the road ahead. CMAJ Can. Med. Assoc. J 178, 715 (2008). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 93.Rocklöv J & Dubrow R Climate change: an enduring challenge for vector-borne disease prevention and control. Nat. Immunol 21, 479–483 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 94.Gage KL, Burkot TR, Eisen RJ & Hayes EB Clim. Vectorborne Dis. Am. J. Prev. Med 35, 436–450 (2008). [DOI] [PubMed] [Google Scholar]
  • 95.El-Sayed A & Kamel M Climatic changes and their role in emergence and re-emergence of diseases. Environ. Sci. Pollut. Res. Int 27, 22336–22352 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 96.Daniel M, Danielova, Kriz B, Jirsa A & Nozicka J Shift of the tick Ixodes ricinus and tick-borne encephalitis to higher altitudes in Central Europe. Eur. J. Clin. Microbiol. Infect. Dis 22, 327–328 (2003). [DOI] [PubMed] [Google Scholar]
  • 97.Daniel M, Danielová V, Kříž B & Kott I An attempt to elucidate the increased incidence of tick-borne encephalitis and its spread to higher altitudes in the Czech Republic. Int. J. Med. Microbiol 293, 55–62 (2004). [DOI] [PubMed] [Google Scholar]
  • 98.Taylor D. et al. Environmental change and Rift Valley fever in eastern Africa: projecting beyond HEALTHY FUTURES. Geospatial Health 11, 115–128 (2016). [DOI] [PubMed] [Google Scholar]
  • 99.Campbell LP et al. Climate change influences on global distributions of dengue and chikungunya virus vectors. Philos. Trans. R. Soc. B Biol. Sci 370, 1–9 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 100.Ebi KL & Paulson JA Climate change and child health in the United States. Curr. Probl. Pediatr. Adolesc. Health Care 40, 2–18 (2010). [DOI] [PubMed] [Google Scholar]
  • 101.Paz S. Climate change impacts on West Nile virus transmission in a global context. Philos. Trans. R. Soc. Lond. B. Biol. Sci 370, 20130561 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 102.Liu-Helmersson J, Stenlund H, Wilder-Smith A & Rocklöv J Vectorial Capacity of Aedes aegypti: Effects of temperature and implications for global Dengue Epidemic Potential. PLOS ONE 9, e89783 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 103.Tran B-L, Tseng W-C, Chen C-C & Liao S-Y Estimating the threshold effects of climate on Dengue: A case study of Taiwan. Int. J. Environ. Res. Public. Health 17, 1392 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 104.Colón-González FJ, Fezzi C, Lake IR & Hunter PR The effects of weather and climate change on Dengue. PLoS Negl. Trop. Dis 7, e2503 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 105.McMichael C, Barnett J & McMichael AJ An Ill Wind? Climate change, migration, and health. Environ. Health Perspect 120, 646–654 (2012). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 106.Watts N. et al. The 2019 report of The Lancet Countdown on health and climate change: ensuring that the health of a child born today is not defined by a changing climate. Lancet 394, 1836–1878 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 107.Gubler DJ Dengue, urbanization and globalization: the unholy trinity of the 21st Century. Trop. Med. Health 39, S3–S11 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 108.Lowe R. et al. Combined effects of hydrometeorological hazards and urbanisation on dengue risk in Brazil: a spatiotemporal modelling study. Lancet Planet. Health 5, e209–e219 (2021). [DOI] [PubMed] [Google Scholar]
  • 109.Thomson MC & Stanberry LR Climate change and vectorborne diseases. N. Engl. J. Med 387, 1969–1978 (2022). [DOI] [PubMed] [Google Scholar]
  • 110.WHO. Pakistan Floods Situation Report. https://cdn.who.int/media/docs/default-source/documents/emergencies/sitrep-flood-situation-14th-oct-2022-ml-aa.pdf?sfvrsn=9f42ba18_1&download=true (2022).
  • 111.UNICEF. Devastating floods in Pakistan. United Nations Childrens Fund https://www.unicef.org/emergencies/devastating-floods-pakistan-2022 (2022). [Google Scholar]
  • 112.Mondal N. The resurgence of dengue epidemic and climate change in India. Lancet 401, 727–728 (2023). [DOI] [PubMed] [Google Scholar]
  • 113.Khan J, Khan I, Ghaffar A & Khalid B Epidemiological trends and risk factors associated with dengue disease in Pakistan (1980–2014): a systematic literature search and analysis. BMC Public Health 18, 745 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 114.Xuan LTT, Van Hau P, Thu DT & Toan DTT Estimates of meteorological variability in association with dengue cases in a coastal city in northern Vietnam: an ecological study. Glob. Health Action 7, 52–58 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 115.Phung D. et al. Identification of the prediction model for dengue incidence in Can Tho city, a Mekong Delta area in Vietnam. Acta Trop. 141, 88–96 (2015). [DOI] [PubMed] [Google Scholar]
  • 116.Mala S & Jat MK Implications of meteorological and physiographical parameters on dengue fever occurrences in Delhi. Sci. Total Environ 650, 2267–2283 (2019). [DOI] [PubMed] [Google Scholar]
  • 117.Carvajal TM et al. Machine learning methods reveal the temporal pattern of dengue incidence using meteorological factors in metropolitan Manila, Philippines. BMC Infect. Dis 18, 183 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 118.Alkhaldy I. Modelling the association of dengue fever cases with temperature and relative humidity in Jeddah, Saudi Arabia—A generalised linear model with break-point analysis. Acta Trop. 168, 9–15 (2017). [DOI] [PubMed] [Google Scholar]
  • 119.Almeida APG et al. Bioecology and vectorial capacity of Aedes albopictus (Diptera: Culicidae) in Macao, China, in relation to Dengue Virus Transmission. J. Med. Entomol 42, 419–428 (2005). [DOI] [PubMed] [Google Scholar]
  • 120.Bai L, Morton LC & Liu Q Climate change and mosquito-borne diseases in China: a review. Glob. Health 9, 10 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 121.Kulkarni MA, Duguay C & Ost K Charting the evidence for climate change impacts on the global spread of malaria and dengue and adaptive responses: a scoping review of reviews. Glob. Health 18, 1 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 122.Giesen C. et al. The impact of climate change on mosquito-borne diseases in Africa. Pathog. Glob. Health 114, 287–301 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 123.Watts N. et al. The 2020 report of The Lancet Countdown on health and climate change: responding to converging crises. Lancet 397, 129–170 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 124.Taylor L. Dengue and chikungunya cases surge as climate change spreads arboviral diseases to new regions. BMJ Online 380, 717–717 (2023). [DOI] [PubMed] [Google Scholar]
  • 125.Proestos Y. et al. Present and future projections of habitat suitability of the Asian tiger mosquito, a vector of viral pathogens, from global climate simulation. Philos. Trans. R. Soc. B Biol. Sci 370, 1–16 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 126.Baylis M. Potential impact of climate change on emerging vector-borne and other infections in the UK. Environ. Health 16, 112 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 127.Zeller H, Van Bortel W & Sudre B Chikungunya: Its history in Africa and Asia and its spread to new regions in 2013–2014. J. Infect. Dis 214, S436–S440 (2016). [DOI] [PubMed] [Google Scholar]
  • 128.Tjaden NB et al. Modelling the effects of global climate change on Chikungunya transmission in the 21st century. Sci. Rep 7, 3813 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 129.Oliveira E. Cde et al. Short report: Introduction of chikungunya virus ECSA genotype into the Brazilian Midwest and its dispersion through the Americas. PLoS Negl. Trop. Dis 15, e0009290 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 130.Souza de WM & et al. Spatiotemporal dynamics and recurrence of chikungunya virus in Brazil: an epidemiological study. Lancet Microbe 4, e319–e329 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 131.Rezza G. Dengue and chikungunya: long-distance spread and outbreaks in naïve areas. Pathog. Glob. Health 108, 349–355 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 132.Tjaden NB, Cheng Y, Beierkuhnlein C & Thomas SM Chikungunya beyond the tropics: where and when do we expect disease transmission in Europe? Viruses 13, 1024 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 133.Fischer D. et al. Climate change effects on Chikungunya transmission in Europe: geospatial analysis of vector’s climatic suitability and virus’ temperature requirements. Int. J. Health Geogr 12, 51–51 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 134.WHO. Zika virus. https://www.who.int/news-room/fact-sheets/detail/zika-virus.
  • 135.Wen Z, Song H & Ming G How does Zika virus cause microcephaly? Genes Dev. 31, 849–861 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 136.Tesla B. et al. Temperature drives Zika virus transmission: evidence from empirical and mathematical models. Proc. R. Soc. B Biol. Sci 285, 20180795 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 137.Antoniou E. et al. Zika Virus and the risk of developing microcephaly in infants: a systematic review. Int. J. Environ. Res. Public. Health 17, 3806 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 138.Adams Waldorf KM, Olson EM, Nelson BR, Little M-TE & Rajagopal L The aftermath of Zika: Need for long-term monitoring of exposed children. Trends Microbiol 26, 729–732 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 139.Shapiro-Mendoza CK et al. Pregnancy outcomes after maternal Zika Virus infection during pregnancy–U.S. Territories, January 1, 2016–April 25, 2017. MMWR Morb. Mortal. Wkly. Rep 66, 615–621 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 140.Hoen B. et al. Pregnancy outcomes after ZIKV infection in French territories in the Americas. N. Engl. J. Med 378, 985–994 (2018). [DOI] [PubMed] [Google Scholar]
  • 141.Costa MC et al. Case fatality rate related to microcephaly congenital Zika Syndrome and associated factors: a nationwide retrospective study in Brazil. Viruses 12, 1228 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 142.Ali S. et al. Environmental and social change drive the explosive emergence of Zika Virus in the Americas. PLoS Negl. Trop. Dis 11, e0005135 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 143.Sadeghieh T. et al. Zika virus outbreak in Brazil under current and future climate. Epidemics 37, 100491 (2021). [DOI] [PubMed] [Google Scholar]
  • 144.Ngonghala CN et al. Effects of changes in temperature on Zika dynamics and control. J. R. Soc. Interface 18, 20210165 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 145.Ryan SJ et al. Warming temperatures could expose more than 1.3 billion new people to Zika virus risk by 2050. Glob. Change Biol 27, 84–93 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 146.Paz S. The west nile virus outbreak in Israel (2000) from a new perspective: The regional impact of climate change. Int. J. Environ. Health Res 16, 1–13 (2006). [DOI] [PubMed] [Google Scholar]
  • 147.Pradier S, Lecollinet S & Leblond A West Nile virus epidemiology and factors triggering change in its distribution in Europe. Rev. Sci. Tech. Int. Epizoot 31, 829–844 (2012). [DOI] [PubMed] [Google Scholar]
  • 148.Farooq Z. et al. European projections of West Nile virus transmission under climate change scenarios. One Health 16, 100509 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 149.Hu W. et al. Development of a predictive model for Ross River Virus Disease in Brisbane, Australia. Am. J. Trop. Med. Hyg 71, 129–137 (2004). [PubMed] [Google Scholar]
  • 150.Tong S, Hu W & McMichael AJ Climate variability and Ross River virus transmission in Townsville Region, Australia, 1985–1996. Trop. Med. Int. Health 9, 298–304 (2004). [DOI] [PubMed] [Google Scholar]
  • 151.Werner AK et al. Environmental drivers of Ross River virus in southeastern Tasmania, Australia: towards strengthening public health interventions. Epidemiol. Infect 140, 359–371 (2012). [DOI] [PubMed] [Google Scholar]
  • 152.Naish S. et al. Socio-environmental predictors of Barmah forest virus transmission in coastal areas, Queensland, Australia. Trop. Med. Int. Health 14, 247–256 (2009). [DOI] [PubMed] [Google Scholar]
  • 153.Naish S, Mengersen K, Hu W & Tong S Forecasting the future risk of Barmah Forest Virus disease under climate change scenarios in Queensland, Australia. PloS One 8, e62843–e62843 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 154.Sakkas H, Bozidis P, Franks A, Papadopoulou C & Oropouche Fever: A review. Viruses 10, 175 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 155.Files MA et al. Baseline mapping of Oropouche virology, epidemiology, therapeutics, and vaccine research and development. Npj Vaccines 7, 1–10 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 156.Diagne CT et al. Mayaro Virus Pathogenesis and transmission mechanisms. Pathogens 9, 738 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 157.Alomar AA & Alto BW Temperature-mediated effects on Mayaro Virus Vector competency of Florida Aedes aegypti Mosquito Vectors. Viruses 14, 880 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 158.Semret M, Ndao M, Jacobs J & Yansouni CP Point-of-care and point-of-‘can’: leveraging reference-laboratory capacity for integrated diagnosis of fever syndromes in the tropics. Clin. Microbiol. Infect 24, 836–844 (2018). [DOI] [PubMed] [Google Scholar]
  • 159.Romero-Alvarez D & Escobar LE Oropouche fever, an emergent disease from the Americas. Microbes Infect. 20, 135–146 (2018). [DOI] [PubMed] [Google Scholar]
  • 160.Caicedo E-Y et al. The epidemiology of Mayaro virus in the Americas: A systematic review and key parameter estimates for outbreak modelling. PLoS Negl. Trop. Dis 15, e0009418 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 161.Romandini A. et al. Antibiotic resistance in pediatric infections: global emerging threats, predicting the near future. Antibiotics 10, 393 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 162.Jaenson TG, Hjertqvist M, Bergström T & Lundkvist Å Why is tick-borne encephalitis increasing? A review of the key factors causing the increasing incidence of human TBE in Sweden. Parasit. Vectors 5, 184 (2012). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 163.Blair PW et al. An emerging biothreat: Crimean-Congo Hemorrhagic Fever Virus in Southern and Western Asia. Am. J. Trop. Med. Hyg 100, 16–23 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 164.Gilbert L. The impacts of climate change on ticks and tick-borne disease risk. Annu. Rev. Entomol 66, 373–388 (2021). [DOI] [PubMed] [Google Scholar]
  • 165.Danielová V, Kliegrová S, Daniel M & Benes C Influence of climate warming on tickborne encephalitis expansion to higher altitudes over the last decade (1997-2006) in the Highland Region (Czech Republic). Cent. Eur. J. Public Health 16, 4–11 (2008). [DOI] [PubMed] [Google Scholar]
  • 166.Lukan M, Bullova E & Petko B Climate warming and Tick-borne Encephalitis, Slovakia. Emerg. Infect. Dis 16, 524–526 (2010). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 167.Nuttall PA Climate change impacts on ticks and tick-borne infections. Biologia 77, 1503–1512 (2022). [Google Scholar]
  • 168.Ogden NH, Ben Beard C, Ginsberg HS & Tsao JI Possible effects of climate change on ixodid ticks and the pathogens they transmit. Predictions Observations. J. Med. Entomol 58, 1536–1545 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 169.Daniel M. et al. Increased relative risk of tick-borne Encephalitis in warmer weather. Front. Cell. Infect. Microbiol 8, 1012–1025 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 170.Nah K, Bede-Fazekas Á, Trájer AJ & Wu J The potential impact of climate change on the transmission risk of tick-borne encephalitis in Hungary. BMC Infect. Dis 20, 34 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 171.Tokarevich NK et al. The impact of climate change on the expansion of Ixodes persulcatus habitat and the incidence of tick-borne encephalitis in the north of European Russia. Glob. Health Action 4, 8448 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 172.Nili S, Khanjani N, Jahani Y & Bakhtiari B The effect of climate variables on the incidence of Crimean Congo Hemorrhagic Fever (CCHF) in Zahedan, Iran. BMC Public Health 20, 1893 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 173.Ansari H. et al. Crimean-Congo hemorrhagic fever and its relationship with climate factors in southeast Iran: A 13-year experience. J. Infect. Dev. Ctries 8, 749–757 (2014). [DOI] [PubMed] [Google Scholar]
  • 174.Mostafavi E, Chinikar S, Bokaei S & Haghdoost A Temporal modeling of Crimean-Congo hemorrhagic fever in eastern Iran. Int. J. Infect. Dis 17, e524–e528 (2013). [DOI] [PubMed] [Google Scholar]
  • 175.Papa A. et al. Crimean-Congo Hemorrhagic Fever Virus, Greece. Emerg. Infect. Dis 20, 288–290 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 176.Stavropoulou E & Troillet N Crimean-Congo hemorrhagic fever: an emerging viral hemorrhagic fever in Europe. Rev. Médicale Suisse 14, 1786–1789 (2018). [PubMed] [Google Scholar]
  • 177.Bernard C. et al. Systematic Review on Crimean–Congo Hemorrhagic Fever Enzootic Cycle and Factors Favoring Virus Transmission: Special Focus on France, an Apparently Free-Disease Area in Europe. Front. Vet. Sci 9, 932304 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 178.Kuehnert PA, Stefan CP, Badger CV & Ricks KM Crimean-Congo Hemorrhagic Fever Virus (CCHFV): A silent but widespread threat. Curr. Trop. Med. Rep 8, 141–147 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 179.Dreshaj S. et al. Current situation of Crimean-Congo hemorrhagic fever in Southeastern Europe and neighboring countries: a public health risk for the European Union? Travel Med. Infect. Dis 14, 81–91 (2016). [DOI] [PubMed] [Google Scholar]
  • 180.Kuehn L & McCormick S Heat exposure and maternal health in the face of climate change. Int. J. Environ. Res. Public. Health 14, 853 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 181.Lawn J, Kerber K, Enweronu-Laryea C & Massee Bateman O Newborn survival in low resource settings—are we delivering? BJOG Int. J. Obstet. Gynaecol 116, 49–59 (2009). [DOI] [PubMed] [Google Scholar]
  • 182.Cappelletti M, Della Bella S, Ferrazzi E, Mavilio D & Divanovic S Inflammation and preterm birth. J. Leukoc. Biol 99, 67–78 (2016). [DOI] [PubMed] [Google Scholar]
  • 183.Nadeau HCG, Subramaniam A & Andrews WW Infection and preterm birth. Semin. Fetal Neonatal Med 21, 100–105 (2016). [DOI] [PubMed] [Google Scholar]
  • 184.Olsen SJ et al. The effect of influenza vaccination on birth outcomes in a cohort of pregnant women in Lao PDR, 2014–2015. Clin. Infect. Dis 63, 487–494 (2016). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 185.Bobei T-I et al. The impact of SARS-CoV-2 infection on premature birth—our experience as COVID Center. Medicina 58, 587 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 186.Kayem ND et al. Lassa fever in pregnancy: a systematic review and meta-analysis. Trans. R. Soc. Trop. Med. Hyg 114, 385–396 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 187.Coler B. et al. Common pathways targeted by viral hemorrhagic fever viruses to infect the placenta and increase the risk of stillbirth. Placenta 10.1016/j.placenta.2022.10.002 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 188.Moucheraud C et al. Consequences of maternal mortality on infant and child survival: a 25-year longitudinal analysis in Butajira Ethiopia (1987-2011). Reprod. Health 12, S4 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 189.Paixão ES, Teixeira MG, Costa M, da CN, Barreto ML & Rodrigues LC Symptomatic Dengue during Pregnancy and Congenital Neurologic Malformations. Emerg. Infect. Dis 24, 1748–1750 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 190.Satterfield-Nash A. Health and Development at Age 19–24 months of 19 children who were born with microcephaly and laboratory evidence of congenital Zika Virus Infection During the 2015 Zika Virus Outbreak—Brazil, 2017. MMWR Morb. Mortal. Wkly. Rep 66, 1347–1351 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 191.Contopoulos-Ioannidis D, Newman-Lindsay S, Chow C & LaBeaud AD Mother-to-child transmission of Chikungunya virus: A systematic review and meta-analysis. PLoS Negl. Trop. Dis 12, e0006510 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 192.Neu N, Duchon J & Zachariah P TORCH Infections. Clin. Perinatol 42, 77–103 (2015). [DOI] [PubMed] [Google Scholar]
  • 193.Pesch MH, Kuboushek K, McKee MM, Thorne MC & Weinberg JB Congenital cytomegalovirus infection. BMJ 373, n1212 (2021). [DOI] [PubMed] [Google Scholar]
  • 194.Beigi RH et al. The need for inclusion of pregnant women in COVID-19 vaccine trials. Vaccine 39, 868–870 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 195.Dad N, Buhmaid S & Mulik V Vaccination in pregnancy – The when, what and how? Eur. J. Obstet. Gynecol. Reprod. Biol 265, 1–6 (2021). [DOI] [PubMed] [Google Scholar]
  • 196.Burrell AL, Evans JP & De Kauwe MG Anthropogenic climate change has driven over 5 million km2 of drylands towards desertification. Nat. Commun 11, 3853 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 197.Carlton EJ, Woster AP, DeWitt P, Goldstein RS & Levy K A systematic review and meta-analysis of ambient temperature and diarrhoeal diseases. Int. J. Epidemiol 45, 117–130 (2016). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 198.Levy K, Smith SM & Carlton EJ Climate change impacts on waterborne diseases: Moving toward designing interventions. Curr. Environ. Health Rep 5, 272–282 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 199.Thiam S. et al. Association between childhood diarrhoeal incidence and climatic factors in urban and rural settings in the Health District of Mbour, Senegal. Int. J. Environ. Res. Public. Health 14, 1049 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 200.Dimitrova A, Gershunov A, Levy MC & Benmarhnia T Uncovering social and environmental factors that increase the burden of climate-sensitive diarrheal infections on children. Proc. Natl Acad. Sci 120, e2119409120 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 201.Gall AM, Mariñas BJ, Lu Y, Shisler JL & Waterborne Viruses: A barrier to safe drinking water. PLoS Pathog. 11, e1004867 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 202.Herrador BG et al. Association between heavy precipitation events and waterborne outbreaks in four Nordic countries, 1992-2012. J. Water Health 14, 1019–1027 (2016). [DOI] [PubMed] [Google Scholar]
  • 203.Levy K, Woster AP, Goldstein RS & Carlton EJ Untangling the impacts of climate change on waterborne diseases: a systematic review of relationships between diarrheal diseases and temperature, rainfall, flooding, and drought. Environ. Sci. Technol 50, 4905–4922 (2016). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 204.Semenza JC & Paz S Climate change and infectious disease in Europe: Impact, projection and adaptation. Lancet Reg. Health Eur 9, 100230–100230 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 205.Tavakol-Davani H. et al. How does climate change affect combined sewer overflow in a system benefiting from rainwater harvesting systems? Sustain. Cities Soc 27, 430–438 (2016). [Google Scholar]
  • 206.Azage M, Kumie A, Worku A & Bagtzoglou AC Childhood diarrhea exhibits spatiotemporal variation in Northwest Ethiopia: A SaTScan spatial statistical analysis. PloS One 10, e0144690–e0144690 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 207.McIver LJ et al. Review of climate change and water-related diseases in Cambodia and findings from stakeholder knowledge assessments. Asia. Pac. J. Public Health 28, 49S–58S (2016). [DOI] [PubMed] [Google Scholar]
  • 208.Horn LM et al. Association between precipitation and diarrheal disease in Mozambique. Int. J. Environ. Res. Public. Health 15, 709 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 209.Liu Z. et al. Association between floods and infectious diarrhea and their effect modifiers in Hunan province, China: A two-stage model. Sci. Total Environ 626, 630–637 (2018). [DOI] [PubMed] [Google Scholar]
  • 210.Sharma S, Sachdeva P & Virdi JS Emerging water-borne pathogens. Appl. Microbiol. Biotechnol 61, 424–428 (2003). [DOI] [PubMed] [Google Scholar]
  • 211.Zhao H. et al. Detection of a Bocavirus circular genome in fecal specimens from children with acute Diarrhea in Beijing, China. PLoS ONE 7, e48980 (2012). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 212.Lee C. Porcine epidemic diarrhea virus: An emerging and re-emerging epizootic swine virus. Virol. J 12, 193 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 213.Ahmed K. et al. An outbreak of gastroenteritis by emerging norovirus GII.2[P16] in a kindergarten in Kota Kinabalu, Malaysian Borneo. Sci. Rep 10, 7137 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 214.Becker-Dreps S, González F & Bucardo F Sapovirus: an emerging cause of childhood diarrhea. Curr. Opin. Infect. Dis 33, 388–397 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 215.Kumazaki M & Usuku S Influence of herd immunity on norovirus: a long-term field study of repeated viral gastroenteritis outbreaks at the same facilities. BMC Infect. Dis 23, 265 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 216.WHO. Statement of the thirty-fourth Polio IHR Emergency Committee. World Health Organization; https://www.who.int/news/item/02-02-2023-statement-of-the-thirty-fourth-polio-ihr-emergency-committee (2023). [Google Scholar]
  • 217.WHO. Poliomyelitis. World Health Organization; https://www.who.int/news-room/fact-sheets/detail/poliomyelitis (2022). [Google Scholar]
  • 218.Nagata JM, Epstein A, Ganson KT, Benmarhnia T & Weiser SD Drought and child vaccination coverage in 22 countries in sub-Saharan Africa: A retrospective analysis of national survey data from 2011 to 2019. PLoS Med 18, e1003678 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 219.Mahmud AS, Martinez PP, He J & Baker RE The impact of climate change on vaccine-preventable diseases: insights from current research and new directions. Curr. Environ. Health Rep 7, 384–391 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 220.Coates SJ, Davis MDP & Andersen LK Temperature and humidity affect the incidence of hand, foot, and mouth disease: a systematic review of the literature–a report from the International Society of Dermatology Climate Change Committee. Int. J. Dermatol 58, 388–399 (2019). [DOI] [PubMed] [Google Scholar]
  • 221.Yi L. et al. The impact of climate variability on infectious disease transmission in China: Current knowledge and further directions. Environ. Res 173, 255–261 (2019). [DOI] [PubMed] [Google Scholar]
  • 222.Qi H. et al. Impact of meteorological factors on the incidence of childhood hand, foot, and mouth disease (HFMD) analyzed by DLNMs-based time series approach. Infect. Dis. Poverty 7, 7 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 223.Xu M. et al. Non-linear association between exposure to ambient temperature and children’s hand-foot-and-mouth disease in Beijing, China. PLOS ONE 10, e0126171 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 224.Jiang FC et al. Meteorological factors affect the hand, foot, and mouth disease epidemic in Qingdao, China, 2007–2014. Epidemiol. Infect 144, 2354–2362 (2016). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 225.Du Z. et al. Weather effects on hand, foot, and mouth disease at individual level: a case-crossover study. BMC Infect. Dis 19, 1029 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 226.Wu H, Wang H, Wang Q, Xin Q & Lin H The effect of meteorological factors on adolescent hand, foot, and mouth disease and associated effect modifiers. Glob. Health Action 7, 24664 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 227.Hao J. et al. Impact of ambient temperature and relative humidity on the incidence of hand-foot-mouth disease in Wuhan, China. Int. J. Environ. Res. Public. Health 17, 428 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 228.Onozuka D & Hashizume M Effect of weather variability on the incidence of mumps in children: a time-series analysis. Epidemiol. Infect 139, 1692–1700 (2011). [DOI] [PubMed] [Google Scholar]
  • 229.Nhat PD, Phu VL, Chính ÐV, Tam DTM &Thanh MT Impact of weather factors on hospital admission of hand, foot and mouth disease under climate change scenarios in Ho Chi Minh City. IOP Conf. Ser. Earth Environ. Sci 964, 012016 (2022). [Google Scholar]
  • 230.Hanna J, Brauer PR, Morse E, Berson E & Mehra S Epidemiological analysis of croup in the emergency department using two national datasets. Int. J. Pediatr. Otorhinolaryngol 126, 109641 (2019). [DOI] [PubMed] [Google Scholar]
  • 231.Dalziel SR et al. Bronchiolitis. Lancet 400, 392–406 (2022). [DOI] [PubMed] [Google Scholar]
  • 232.Marangu D & Zar HJ Childhood pneumonia in low-and-middle-income countries: An update. Paediatr. Respir. Rev 32, 3–9 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 233.Simoes EAF et al. Acute respiratory infections in children. in Disease Control Priorities in Developing Countries (eds. Jamison DT et al.) (The International Bank for Reconstruction and Development/The World Bank, 2006). [PubMed] [Google Scholar]
  • 234.Caballero MT & Polack FP Respiratory syncytial virus is an “opportunistic” killer. Pediatr. Pulmonol 53, 664–667 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 235.Al-Toum R, Bdour S & Ayyash H Epidemiology and clinical characteristics of respiratory syncytial virus infections in Jordan. J. Trop. Pediatr 52, 282–287 (2006). [DOI] [PubMed] [Google Scholar]
  • 236.Viegas M, Barrero PR, Maffey AF & Mistchenko AS Respiratory viruses seasonality in children under five years of age in Buenos Aires, ArgentinaA five-year analysis. J. Infect 49, 222–228 (2004). [DOI] [PubMed] [Google Scholar]
  • 237.Nenna R. et al. Respiratory syncytial virus bronchiolitis, weather conditions and air pollution in an Italian urban area: An observational study. Environ. Res 158, 188–193 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 238.Tchidjou HK et al. Seasonal pattern of hospitalization from acute respiratory infections in Yaoundé, Cameroon. J. Trop. Pediatr 56, 317–320 (2010). [DOI] [PubMed] [Google Scholar]
  • 239.Nascimento-Carvalho CM et al. Seasonal patterns of viral and bacterial infections among children hospitalized with community-acquired pneumonia in a tropical region. Scand. J. Infect. Dis 42, 839–844 (2010). [DOI] [PubMed] [Google Scholar]
  • 240.Dowell SF & Ho MS Seasonality of infectious diseases and severe acute respiratory syndrome–what we don’t know can hurt us. Lancet Infect. Dis 4, 704–708 (2004). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 241.He D, Chiu APY, Lin Q & Cowling BJ Differences in the seasonality of Middle East respiratory syndrome coronavirus and influenza in the Middle East. Int. J. Infect. Dis 40, 15–16 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 242.Darling ND et al. Retrospective, epidemiological cluster analysis of the Middle East respiratory syndrome coronavirus (MERS-CoV) epidemic using open source data. Epidemiol. Infect 145, 3106–3114 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 243.Tuncer N & Martcheva M Modeling seasonality in Avian Influenza H5N1. J. Biol. Syst 21, 1340004 (2013). [Google Scholar]
  • 244.Davis RE, Dougherty E, McArthur C, Huang QS & Baker MG Cold, dry air is associated with influenza and pneumonia mortality in Auckland, New Zealand. Influenza Other Respir. Viruses 10, 310–313 (2016). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 245.Marr LC, Tang JW, Van Mullekom J & Lakdawala SS Mechanistic insights into the effect of humidity on airborne influenza virus survival, transmission and incidence. J. R. Soc. Interface 16, 20180298 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 246.Lam EKS, Morris DH, Hurt AC, Barr IG & Russell CA The impact of climate and antigenic evolution on seasonal influenza virus epidemics in Australia. Nat. Commun 11, 2741 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 247.Leung NHL Transmissibility and transmission of respiratory viruses. Nat. Rev. Microbiol 19, 528–545 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 248.Miyayo SF, Owili PO, Muga MA & Lin T-H Analysis of Pneumonia occurrence in relation to climate change in Tanga, Tanzania. Int. J. Environ. Res. Public. Health 18, 4731 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 249.Sajadi MM et al. Temperature, humidity, and latitude analysis to estimate potential spread and seasonality of Coronavirus Disease 2019 (COVID-19). JAMA Netw. Open 3, e2011834 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 250.Liu X. et al. The role of seasonality in the spread of COVID-19 pandemic. Environ. Res 195, 110874 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 251.D’Amico F. et al. COVID-19 seasonality in temperate countries. Environ. Res 206, 112614 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 252.Towers S. et al. Climate change and influenza: the likelihood of early and severe influenza seasons following warmer than average winters. PLoS Curr. 5, ecurrents.flu.3679b56a3a5313dc7c043fb944c6f138 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 253.Mirsaeidi M. et al. Climate change and respiratory infections. Ann. Am. Thorac. Soc 13, 1223–1230 (2016). [DOI] [PubMed] [Google Scholar]
  • 254.Irwin CK et al. Using the systematic review methodology to evaluate factors that influence the persistence of influenza virus in environmental matrices. Appl. Environ. Microbiol 77, 1049–1060 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 255.Dombrovsky L. et al. Modeling evaporation of water droplets as applied to survival of airborne viruses. Atmosphere 11, 965 (2020). [Google Scholar]
  • 256.Takaro TK, Knowlton K & Balmes JR Climate change and respiratory health: current evidence and knowledge gaps. Expert Rev. Respir. Med 7, 349–361 (2013). [DOI] [PubMed] [Google Scholar]
  • 257.Evans GW Projected behavioral impacts of global climate change. Annu. Rev. Psychol 70, 449–474 (2019). [DOI] [PubMed] [Google Scholar]
  • 258.Nardell E, Lederer P, Mishra H, Nathavitharana R & Theron G Cool but dangerous: How climate change is increasing the risk of airborne infections. Indoor Air 30, 195–197 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 259.Zhao Q. et al. Global climate change and human health: Pathways and possible solutions. Eco-Environ. Health 1, 53–62 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 260.Staddon C. et al. Water insecurity compounds the global coronavirus crisis. Water Int 45, 416–422 (2020). [Google Scholar]
  • 261.Haddout S, Priya KL, Hoguane AM & Ljubenkov I Water scarcity: A big challenge to slums in Africa to fight against COVID-19. Sci. Technol. Libr 39, 281–288 (2020). [Google Scholar]
  • 262.Xu R. et al. Wildfires, global climate change, and human health. N. Engl. J. Med 383, 2173–2181 (2020). [DOI] [PubMed] [Google Scholar]
  • 263.Romanello M. et al. The 2022 report of the Lancet Countdown on health and climate change: health at the mercy of fossil fuels. Lancet 400, 1619–1654 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 264.Neuzil KM, Wright PF, Mitchel EF & Griffin MR The burden of influenza illness in children with asthma and other chronic medical conditions. J. Pediatr 137, 856–864 (2000). [DOI] [PubMed] [Google Scholar]
  • 265.Wu P & Hartert TV Evidence for a causal relationship between respiratory syncytial virus infection and asthma. Expert Rev. Anti Infect. Ther 9, 731–745 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 266.Guarnieri M & Balmes JR Outdoor air pollution and asthma. Lancet 383, 1581–1592 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 267.Victora CG et al. Countdown to 2015: a decade of tracking progress for maternal, newborn, and child survival. Lancet Lond. Engl 387, 2049–2059 (2016). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 268.Odo DB et al. Ambient air pollution and acute respiratory infection in children aged under 5 years living in 35 developing countries. Environ. Int 159, 107019 (2022). [DOI] [PubMed] [Google Scholar]
  • 269.Kodgule R & Salvi S Exposure to biomass smoke as a cause for airway disease in women and children. Curr. Opin. Allergy Clin. Immunol 12, 82–90 (2012). [DOI] [PubMed] [Google Scholar]
  • 270.World Health Organization. Air pollution and child health: prescribing clean air. Summary https://www.who.int/publications/i/item/WHO-CED-PHE-18-01 (2018).
  • 271.Larson PS et al. Long-term PM2.5 exposure is associated with symptoms of acute respiratory infections among children under five years of age in Kenya, 2014. Int. J. Environ. Res. Public. Health 19, 2525 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 272.Werz M & Hoffman M Europe’s twenty-first century challenge: climate change, migration and security. Eur. View 15, 145–154 (2016). [Google Scholar]
  • 273.Kaczan DJ & Orgill-Meyer J The impact of climate change on migration: a synthesis of recent empirical insights. Clim. Change 158, 281–300 (2020). [Google Scholar]
  • 274.Hoffmann R, Dimitrova A, Muttarak R, Crespo Cuaresma J & Peisker J A meta-analysis of country-level studies on environmental change and migration. Nat. Clim. Change 10, 904–912 (2020). [Google Scholar]
  • 275.UNICEF. New guidelines provide first global policy framework on protecting children on the move in face of climate change. https://www.unicef.org/press-releases/new-guidelines-provide-first-global-policy-framework-protect-children-move-displaced-face (2022).
  • 276.De Bruijn B. The living conditions and well-being of refugees. Hum. Dev. Res. Pap 25, (2009). [Google Scholar]
  • 277.Sverdlik A. Ill-health and poverty: a literature review on health in informal settlements. Environ. Urban 23, 123–155 (2011). [Google Scholar]
  • 278.Hunter LM et al. Scales and sensitivities in climate vulnerability, displacement, and health. Popul. Environ 43, 61–81 (2021). [Google Scholar]
  • 279.Altare C. et al. Infectious disease epidemics in refugee camps: a retrospective analysis of UNHCR data (2009-2017). J. Glob. Health Rep 3, e2019064 (2019). [Google Scholar]
  • 280.Shimakawa Y, Camélique O & Ariyoshi K Outbreak of chickenpox in a refugee camp of northern Thailand. Confl. Health 4, 4 (2010). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 281.Hsan K, Naher S, Gozal D, Griffiths MD & Furkan Siddique Md. R. Varicella outbreak among the Rohingya refugees in Bangladesh: Lessons learned and potential prevention strategies. Travel Med. Infect. Dis 31, 101465 (2019). [DOI] [PubMed] [Google Scholar]
  • 282.Ahmed JA et al. Epidemiology of respiratory viral infections in two long-term refugee camps in Kenya, 2007-2010. BMC Infect. Dis 12, 7 (2012). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 283.Mohamed GA et al. Etiology and incidence of viral acute respiratory infections among refugees aged 5 years and older in Hagadera Camp, Dadaab, Kenya. Am. J. Trop. Med. Hyg 93, 1371–1376 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 284.WHO & CDC. Outbreak of Poliomyelitis—Somalia and Kenya, May 2013. Morb. Mortal. Wkly. Rep 62, 484 (2013). [PMC free article] [PubMed] [Google Scholar]
  • 285.Harvey B. et al. Planning and implementing a targeted polio vaccination campaign for Somali mobile populations in Northeastern Kenya based on migration and settlement patterns. Ethn. Health 27, 817–832 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 286.Kaic B, Borcic B, Ljubicic M, Brkic I & Mihaljevic I Hepatitis A control in a refugee camp by active immunization. Vaccine 19, 3615–3619 (2001). [DOI] [PubMed] [Google Scholar]
  • 287.Hakim MS et al. The global burden of hepatitis E outbreaks: a systematic review. Liver Int 37, 19–31 (2017). [DOI] [PubMed] [Google Scholar]
  • 288.Bagulo H, Majekodunmi AO & Welburn SC Hepatitis E in Sub Saharan Africa – A significant emerging disease. One Health 11, 100186 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 289.Ahmed A, Elduma A, Magboul B, Higazi T & Ali Y The first outbreak of dengue fever in Greater Darfur, Western Sudan. Trop. Med. Infect. Dis 4, 43 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 290.Bonner PC et al. Poor housing quality increases risk of rodent infestation and Lassa Fever in Refugee Camps of Sierra Leone. Am. J. Trop. Med. Hyg 77, 169–175 (2007). [PubMed] [Google Scholar]
  • 291.Kouadio IK, Aljunid S, Kamigaki T, Hammad K & Oshitani H Infectious diseases following natural disasters: prevention and control measures. Expert Rev. Anti Infect. Ther 10, 95–104 (2012). [DOI] [PubMed] [Google Scholar]
  • 292.Mipatrini D, Stefanelli P, Severoni S & Rezza G Vaccinations in migrants and refugees: a challenge for European health systems. A systematic review of current scientific evidence. Pathog. Glob. Health 111, 59–68 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 293.Kusuma YS, Kumari R, Pandav CS & Gupta SK Migration and immunization: determinants of childhood immunization uptake among socioeconomically disadvantaged migrants in Delhi, India. Trop. Med. Int. Health 15, 1326–1332 (2010). [DOI] [PubMed] [Google Scholar]
  • 294.McMichael C. Climate change-related migration and infectious disease. Virulence 6, 548–553 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 295.Wasserman S, Tambyah PA & Lim PL Yellow fever cases in Asia: primed for an epidemic - ClinicalKey. Int. J. Infect. Dis 48, 98–103 (2016). [DOI] [PubMed] [Google Scholar]
  • 296.Sadarangani SP, Lim PL & Vasoo S Infectious diseases and migrant worker health in Singapore: a receiving country’s perspective. J. Travel Med 24, 1–9 (2017). [DOI] [PubMed] [Google Scholar]
  • 297.Atif M, Saqib A, Ikram R, Sarwar MR & Scahill S The reasons why Pakistan might be at high risk of Crimean Congo haemorrhagic fever epidemic; a scoping review of the literature. Virol. J 14, 63 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 298.Zimmerman C, Kiss L & Hossain M Migration and Health: a framework for 21st-century policy-making. PLOS Med 8, e1001034 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 299.Wesolowski A et al. Impact of human mobility on the emergence of dengue epidemics in Pakistan. Proc. Natl Acad. Sci 112, 11887–11892 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 300.Dhesi S, Isakjee A & Davies T Public health in the Calais refugee camp: environment, health and exclusion. Crit. Public Health 28, 140–152 (2018). [Google Scholar]
  • 301.Pottie K. et al. Access to healthcare for the most vulnerable migrants: a humanitarian crisis. Confl. Health 9, 16 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 302.NOAA. Tropical Cyclone Freddy Breaks Records before Lashing Madagascar. National Environmental Satellite, Data, and information Service; https://www.nesdis.noaa.gov/news/tropical-cyclone-freddy-breaks-records-lashing-madagascar (2023). [Google Scholar]
  • 303.WHO Africa. Cyclone Freddy deepens health risks in worst-hit countries. WHO Regional Office for Africa; https://www.afro.who.int/news/cyclone-freddy-deepens-health-risks-worst-hit-countries (2023). [Google Scholar]
  • 304.Africa Research Bulletin. Cyclone Freddy: Malawi and Mozambique. Afr. Res. Bull. Econ. Financ. Tech. Ser 60, 24231 (2023). [Google Scholar]
  • 305.Chinele J. Cyclone Freddy Collapses Malawi’s Health System, Washing Away Medicines And Patient Records - Health Policy Watch. Health Policy Watch https://healthpolicy-watch.news/cyclone-freddy-collapses-malawis-health-system-washing-away-medicines-and-patient-records/ (2023). [Google Scholar]
  • 306.Wong JC Hospitals face critical shortage of IV bags due to Puerto Rico hurricane. The Guardian https://www.theguardian.com/us-news/2018/jan/10/hurricane-maria-puerto-rico-iv-bag-shortage-hospitals (2018). [Google Scholar]
  • 307.Richardson ET, Burkett M & Farmer P Health Effects of Climate Change. In Harrison’s Principles of Internal Medicine (eds. Loscalzo J et al.) (McGraw-Hill Education, 2022). [Google Scholar]
  • 308.Bendix A. Surge of viruses leaves children’s hospitals scrambling to free up beds and find room for patients. NBC News https://www.nbcnews.com/health/health-news/virus-surge-childrens-hospitals-scrambling-rcna53891 (2022). [Google Scholar]
  • 309.Walter and Patricia Rodney Commission on Reparations. https://www.rodneycommission.org/ (2024). [Google Scholar]
  • 310.Ryan SJ, Carlson CJ, Mordecai EA & Johnson LR Global expansion and redistribution of Aedes-borne virus transmission risk with climate change. PLoS Negl. Trop. Dis 13, e0007213 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]

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