Abstract
Background
The COVID-19 pandemic has induced unprecedented reductions in human mobility and social contacts throughout the world. Because dengue virus (DENV) transmission is strongly driven by human mobility, behavioral changes associated with the pandemic have been hypothesized to impact dengue incidence. By discouraging human contact, COVID-19 control measures have also disrupted dengue vector control interventions, the most effective of which require entry into homes. We sought to investigate how and why dengue incidence could differ under a lockdown scenario with a proportion of the population sheltered at home.
Methodology & principal findings
We used an agent-based model with a realistic treatment of human mobility and vector control. We found that a lockdown in which 70% of the population sheltered at home and which occurred in a season when a new serotype invaded could lead to a small average increase in cumulative DENV infections of up to 10%, depending on the time of year lockdown occurred. Lockdown had a more pronounced effect on the spatial distribution of DENV infections, with higher incidence under lockdown in regions with higher mosquito abundance. Transmission was also more focused in homes following lockdown. The proportion of people infected in their own home rose from 54% under normal conditions to 66% under lockdown, and the household secondary attack rate rose from 0.109 to 0.128, a 17% increase. When we considered that lockdown measures could disrupt regular, city-wide vector control campaigns, the increase in incidence was more pronounced than with lockdown alone, especially if lockdown occurred at the optimal time for vector control.
Conclusions & significance
Our results indicate that an unintended outcome of lockdown measures may be to adversely alter the epidemiology of dengue. This observation has important implications for an improved understanding of dengue epidemiology and effective application of dengue vector control. When coordinating public health responses during a syndemic, it is important to monitor multiple infections and understand that an intervention against one disease may exacerbate another.
Author summary
Dengue virus causes substantial suffering in the tropical and subtropical regions of the world, with roughly 400 million infections and 40,000 deaths each year. In 2020, we witnessed unprecedented changes in human movement as the world tried to combat the COVID-19 pandemic, including in countries that regularly experience dengue epidemics, such as Thailand and Peru. These changes could affect transmission of dengue virus, though it is unclear whether transmission will decrease, as people reduce their movements between houses, or increase, as people spend more time at home and campaigns to control the mosquito vector of dengue virus are interrupted. We used a simulation model to estimate the impact of these changes on dengue virus transmission. Our model describes the locations of buildings and the movement of people between them, allowing us to directly estimate what happens when human movement patterns change. We found that as people spend more time at home, transmission is likely to increase moderately. If these changes also lead to disruption to vector control, the magnitude of the increase is greater. Our results reinforce concerns about the complexity of public health responses to multiple overlapping epidemics and support the need for policy makers and health authorities to think holistically in their intervention planning.
Introduction
Interventions to combat the COVID-19 pandemic have had unprecedented effects on the lives of people around the world. While measures like social distancing and stay-at-home orders have been successful in reducing transmission, morbidity, and mortality associated with SARS-CoV-2 [1], they are likely to have also had an effect on the incidence of other diseases. For example, lockdown measures are predicted to increase the burden of tuberculosis, HIV, and malaria by reducing access to essential services [2,3].
Dengue is a mosquito-borne viral disease endemic across much of the tropics, with an estimated 400 million infections and 40,000 deaths each year [4,5]. A number of countries with particularly severe COVID-19 epidemics regularly experience dengue epidemics (e.g., Peru, Brazil, and Indonesia), and there have been reports of 2020 being an above-average year for dengue in South America [6]. A number of warnings have been raised regarding the potential dangers of overlapping dengue and COVID-19 epidemics; e.g., both diseases can result in similar symptoms and there have been reports of serological cross-reaction, which increases the chance of misdiagnosis [7–13]. At least five cases of dengue-COVID-19 co-infection have been reported, one of which resulted in death by stroke [8,13–17]. Some researchers have raised concerns about the possible impact of interrupted vector control campaigns and called for efforts to overcome this adverse impact [18,19].
Dengue virus (DENV) transmission is influenced by multiple overlapping drivers, including human and mosquito movement; climate and environmental factors that affect mosquito abundance, contact with human hosts, and vector-virus interactions; human host immunity; and virus genotype [20–25]. Hence, predicting the epidemiological impact of drastic changes in human mobility on DENV transmission is difficult because of the large number of other potentially influential variables that interact in complex ways. It is understood that daily routine movement between houses is a key driver of DENV transmission, and it is this type of movement that has been most affected by COVID-19 lockdown measures [23]. While on the one hand reductions in house-to-house movements could be expected to reduce DENV transmission, on the other hand increased opportunities for intra-household transmission coupled with local mosquito movement and imperfect compliance with lockdown could heighten transmission. Hence, it is unclear in which direction transmission will change in response to lockdown.
We used an established, agent-based model of DENV transmission [26] to explore the impact of lockdown on dengue incidence. Our model incorporates a detailed, realistic, and spatially explicit representation of human mobility and spatiotemporal patterns of mosquito abundance. It is calibrated to dengue incidence in the city of Iquitos, Peru, and has been previously used to answer a number of questions of public health significance beyond that specific setting [27,28]. In this study, we compared the effects of initiating lockdown in different DENV transmission seasons and at different times within a transmission season. Rather than seeking to model the actual patterns of dengue in Iquitos in 2020, our study uses reconstructions of past dengue seasons, and asks the hypothetical question of what these seasons would have looked like with changes in mobility similar to those we might expect under lockdown, or with disrupted vector control campaigns. This enables us to isolate the effect of those modifications and to present general principles from our assessments. We focused on lockdown effects on (1) the incidence and spatial distribution of DENV infections, (2) local transmission by calculating household secondary attack rates, and (3) disrupted vector control campaigns. Our approach yields predictions for how lockdown could affect dengue and the mechanisms by which it could do so.
Methods
Model overview
A detailed explanation of all features of the model is given in the S1 Text and previous publications [26–29]. In brief, we used an established agent-based model of DENV transmission [26], with a detailed and realistic model of human movement [30], to explore how preventive measures taken against COVID-19 could affect DENV transmission. Our model is based on the city of Iquitos, in the Peruvian Amazon. Human agents in the model move around the city according to individualized movement trajectories, calibrated to data on movement patterns in Iquitos from semi-structured resident interviews [30]. The average distribution of mosquito agents in the model follows spatio-temporal estimates of abundance based on household entomological surveys [31]. The distribution of household sizes matches the demography observed in population surveys [30]. Mosquito agents also move, but much less than human agents. Each mosquito determines when to bite based on a temperature dependent gonotrophic rate parameter, and who to bite based on the body sizes of humans present at that time (see S1 Text for more details). Transmission occurs between mosquito and human agents when one agent (either mosquito or human) is susceptible and the other infectious, a blood-meal is taken by the mosquito, and the infection establishes in the susceptible agent, which occurs with a fixed probability. Transmission in the model is partially driven by time series of imported infections, which were calibrated to estimates of the time-varying, serotype-specific force of infection over an 11-year time period (S1 Fig). See Fig in Perkins et al. and S1 Fig in Cavany et al. for a visual representation of the calibration [26,27]. We do not alter these importation patterns between simulations. In reality, importation patterns almost certainly decreased during lockdown. However, we used baseline importation patterns because epidemic timing in our model is driven by the importation time series. Moreover, our aim was to isolate the effects of mobility changes and disruptions in vector control, and for these aims the baseline importation patterns served as a valid baseline. Other differences between what actually happened in Iquitos and our simulated scenarios likely include the length and level of compliance with lockdown–these differences are discussed in more detail in the Discussion.
Simulations
To understand the impact that lockdown could have on dengue, we simulated historical transmission under typical movement patterns and those that might be expected under lockdown. We defined lockdown as 70% of the population staying at home instead of undertaking their typical movement trajectory for that day. That is, 30% of individuals do not comply with lockdown, either because they choose not to or because they have an essential job. We explored different values of compliance in a sensitivity analysis. We chose three representative seasons from empirical data for the period 2000–2010 that span a range of seasonal dynamics, including a season with low incidence (2004–2005, “low” hereafter), a season with high incidence but no new serotype invasion (2000–2001, “high” hereafter), and a season with high incidence due to a new serotype invasion (2001–2002, invasion of DENV-3, “serotype invasion” hereafter) (Fig 1). Seasons were defined to begin on July 1 and end on June 30 [32]. In each of these scenarios, we initiated lockdown on the first of each month to explore the effect of initiating lockdown at different times of year. (Fig 1). For our baseline setting, we simulated lockdowns lasting for three months, though we also explored different values of this timespan in a second sensitivity analysis. We explored starting lockdown in different months to understand how lockdown interplays with the seasonality of dengue. Except where stated otherwise, we started lockdown on March 17, which was the date lockdown began during 2020 in Peru. This showed a moderate effect in the serotype invasion season. We simulated vector control as a city-wide campaign in which all houses that complied (70%) were sprayed three times in a three-week period; approximately 11,000 houses per day. In baseline simulations and for the calibration, vector control did not take place. The ultra-low volume insecticide treatment had no residuality and increased the mortality rate of mosquitoes in the household by 1.5 day-1 on the day when spraying occurred [27,33]. We ran each simulation 400 times, because increasing the number of simulations past that point did not reduce the coefficient of variation in the number of DENV infections by more than 0.1% [34].
Analysis
For each scenario, we analyzed the distribution across simulations of the number of human DENV infections in the transmission seasons including and immediately following the initiation of lockdown, and compared this to the same period in simulations without lockdown. We calculated the following outcomes:
The total number of infections through space and time. Where cumulative incidence is reported in the results, it is over two seasons: the season of the lockdown and the following season. When location is shown, we assign infections to the home of the infected individual.
The number of unique individuals each mosquito bites during its lifetime.
The average secondary attack rate by location, defined as the average proportion of household contacts infected in a season, excluding the first infection in the household.
In all figures except Fig 1, we show the incidence of local infections (those infected in Iquitos), because imported infections (those infected outside Iquitos) do not differ (on average) between simulations and excluding them makes differences more visible.
The movement trajectories are calculated prior to simulating the agent-based models, and are then used as inputs to the model. By comparing the movement trajectories directly, i.e. without simulating the model, we analyzed the effect of changing these trajectories so that people spend all of their time at home. We quantified this impact by calculating the number of locations where the average number of people present was greater under lockdown These outcomes are based purely on the modified activity spaces of individuals in the model, without directly simulating movement or transmission, and are presented in the “Changing distributions of people and blood-meals section.”
We undertook three sensitivity analyses: varying lockdown compliance, lockdown length, and mosquito movement probability. In all three cases, we swept across 2,000 parameter values, calculated the cumulative number of infections across two seasons, and fitted a generalized additive model (GAM) to the output using the mgcv package in R [35,36].
Results
Effect of lockdown timing on dengue incidence
The effect of the month in which lockdown was initiated varied across scenarios (Figs 2 and S2–S4). In the low and high scenarios, lockdown had little effect on the incidence of DENV infection; i.e. the timing of lockdown was not important (Fig 2). In the serotype invasion scenario, the timing of lockdown was much more important. Initiating lockdown early in the season (July–October) led to similar local two-year cumulative incidence of infections as the no-lockdown scenario; e.g., initiating in July led to 130,434 infections (95% uncertainty interval (UI): 122,674–150,995), a 0.2% decrease (Figs 2 and S5). Conversely, initiating lockdown just after the seasonal peak in infections (June) led to many more infections; e.g., 144,668 infections (95% UI: 136,812–162,403) over two years, an 11% increase. This part of the season follows the period of highest incidence, when prevalence and force of infection are at their highest.
Spatial and locational effects of lockdown
When we initiated a three-month lockdown in mid-March in the serotype invasion scenario, lockdown changed the spatial distribution of infections; i.e. the home of the person infected (Fig 3). Mid-March was chosen because that is when COVID-19 mobility restrictions were put in place in 2020 and because we observed a moderate effect of lockdown initiated in March in the serotype invasion scenario (Fig 2). In 20 of 35 Ministry of Health zones, infections rose, with the greatest increases in the northeast and southwest of the city. Notably, the zones with the greatest increases were those zones with the highest average Ae. aegypti abundance. Those with a decrease had the lowest average Ae. aegypti abundance (Pearson’s correlation, r = 0.946 (95% UI: 0.923, 0.955)). The correlation between cumulative incidence and average mosquito abundance was r = 0.925 (95% UI: 0.893, 0.938) when no lockdown occurred, compared to r = 0.946 with lockdown. This indicates that spatial abundance of mosquitoes may have a slightly stronger effect on dengue incidence when human mobility is reduced. Neither human population density (r = - 0.344) nor changes in the total number of person-days spent in each zone (r = 0.056) were strongly correlated with changes in incidence.
While some zones where people spend more time under lockdown were those where there was also greater mosquito abundance (e.g., in the northeast), other zones with high mosquito abundance saw reductions in the amount of time spent there (e.g., in the southwest) (Fig 3B and 3D). Notably, these southwest zones saw increases in incidence despite, in most cases, fewer person-days being spent there (Fig 3A and 3D). This is due to the fact that while fewer people were visiting this region, resulting in an overall decrease in person-hours, the people who live in this region were spending more time in homes with relatively high mosquito abundance.
The type of location where infections took place noticeably changed under lockdown. In the baseline scenario, 54.5% (95% UI: 54.3%– 55.0%) of infections occurred in the home of the infected individual. In contrast, when a lockdown occurred in mid-March in the serotype invasion season, 66.3% (95% UI: 58.9%– 70.2%) of infections occurred in the infected person’s home. This had an effect on the household secondary attack rate, which increased from a mean of 0.109 (95% UI: 0.0999, 0.126) in the baseline scenario to 0.128 (95% UI: 0.119, 0.146) in the lockdown scenario, a 17% increase. In our model, lockdown had a negligible impact on the total number of mosquito bites on humans because the time when mosquitoes take blood-meals is determined by the temperature-driven gonotrophic cycle period, not the number of humans present.
Changing distributions of people and blood-meals
According to the most recent available information from reports of past city-wide spraying campaigns (which are not publicly available), there are 92,896 buildings in Iquitos [27] (Amy Morrison & Helvio Astete, personal communication). Comparing typical patterns of human mobility in Iquitos with those under lockdown (assuming each person spends more time at home), we would expect 78,562 (85%) buildings to have more people inside them during lockdown. Every location that was expected to have more people under lockdown was a residential location, while all non-residential locations had fewer people, on average, under lockdown. There were 9,761 residential locations (11% of all 88,323 residential locations) that had a lower average number of people under lockdown.
Model simulations in the absence of vector control showed that the number of unique individuals bitten by a single mosquito increased under lockdown. In the serotype invasion scenario with a three-month lockdown beginning in mid-March, the number of unique individuals each mosquito bit in its lifetime rose from 2.54 to 2.64 (3.9%). In all three scenarios, the number of unique bites rose by 0.09–0.10 bites. This increase in the number of unique bites was due to heterogeneity in the number of people per location. In the baseline scenario, the Gini coefficient of the number of people in each house was 0.635, whereas under lockdown it was 0.402. As a smaller Gini coefficient implies greater homogeneity, this suggests that the number of people per house was more homogeneous under lockdown. In turn, this implies that in the baseline scenario there was more heterogeneity in the number of unique individuals available for each mosquito to bite, resulting in fewer bites on unique individuals on average.
Importance of vector control
In addition to the effects of lockdown on incidence caused by changes in mosquito-human encounters, lockdown can affect incidence by disrupting vector control. If an early-season vector-control campaign (July or August) was interrupted by public health measures against COVID-19, the impact of lockdown and the interrupted campaign was small, but still more than double the incidence of infection immediately following lockdown (Figs 4 and S5, Jul and Aug panels). If the lockdown instead took place just prior to the seasonal peak (e.g., March), this led to a large increase in the size of the epidemic by a factor of greater than 10 at the peak of the season (Figs 4 and S5, Mar panels). In the alternative scenario in which vector control proceeded as planned during lockdown, there was a large rebound in infections the following season, due to low population immunity. That rebound could be mitigated partially by a delayed campaign following lockdown, or a city-wide campaign in the subsequent year (S6–S8 Figs).
Sensitivity analysis
In all baseline analyses, we used values of 70% compliance with lockdown orders and a lockdown length of three months. We explored changing these values in a one-at-a-time sensitivity analysis in the serotype invasion season beginning lockdown in mid-March (S9–10 Figs). Compliance had a non-linear, non-monotonic relationship with the cumulative number of infections (S9 Fig). The cumulative number of infections peaked at slightly below 90% compliance. This indicates that while lockdown tends to increase DENV incidence, the optimal conditions for transmission require some amount of human mobility. Even if compliance were 100%, however, our results indicate that incidence would still rise compared to typical movement patterns. Longer lockdowns appeared to increase cumulative DENV incidence, though this effect saturated at around 150 days (S10 Fig).
Because human mobility was severely curtailed during lockdown and mosquito distribution patterns were correlated with changes in DENV incidence, the role of mosquito movement in transmission may have been heightened in our model. We explored this by varying the daily probability of mosquito movement in simulations with and without lockdown (Fig 5). Irrespective of whether lockdown occurred, incidence peaked when the daily probability of mosquitoes moving from a house was around 0.2; i.e. each day, each mosquito moves to a new house with probability 0.2. Regardless of lockdown, there was no transmission when mosquitoes did not move between houses, because house-level mosquito extinctions could not be replenished. As mosquito movement increased, so did the proportional change in the number of infections in lockdown compared to no lockdown (Fig 5B). This indicates that the role of mosquito movement is heightened under lockdown. If its role were the same in both situations, we would expect this ratio to remain at 1 across the range of mosquito movement probabilities.
Discussion
We found that lockdown movement restrictions led to an increase in DENV transmission in our model output, if these restrictions occurred during a season in which incidence was high due to a new serotype invasion. Though the increase was relatively modest, the effect was most pronounced when lockdown occurred during periods of time when the prevalence of infection, and hence the force of infection, was highest. In this study, that scenario occurred at the end of a novel serotype invasion season, following several months of heightened transmission. Lockdown had a more pronounced effect in changing the locations where transmission occurred and the spatial distribution of infections. Specifically, more infections occurred in people’s homes than at other types of locations, which increased the household secondary attack rate by 17%. This meant that more infections occurred where mosquito abundance was highest, amplifying hyperlocal transmission due to incomplete compliance with lockdown and mosquito movement among nearby houses. Mosquito movement between houses seems particularly important to enable some inter-household transmission in the context of reduced human mobility. If mosquitoes moved less, the effect of lockdown would in fact be to reduce transmission overall. When we considered the effect of potential interruptions to vector control, lockdown led to much greater increases in DENV transmission.
Our results identified three factors contributing to the direct effect of lockdown on DENV transmission apart from interruption of vector control. First, lockdown causes infections to become more concentrated in locations where mosquito abundance is highest, facilitating more transmission than might occur otherwise. Second, people spending more time at home causes an increase in the household secondary attack rate. Under non-lockdown circumstances, uninfected household members spend more time outside the home and thereby reduce their exposure. Third, lockdown results in a more homogeneous distribution of person-hours across locations, which leads to an increase in the number of unique individuals that each mosquito bites because there are fewer mosquitoes with no-one to bite and many mosquitoes have more options of who to bite. This increases the chance that a mosquito becomes infected within its lifetime, as well as the chance that a mosquito gets infected by one person and later bites and infects a different person.
These direct effects of lockdown are likely to be greatest in settings where transmission predominantly occurs in homes and where household-level mosquito abundance is typically high. In Iquitos, this assumption is supported both by pupal surveys of Aedes aegypti mosquitoes in non-residential locations [37] and epidemiological investigations of contact-site clusters [23,38]. Rather than to model the interaction between COVID-19 and dengue as it unfolded in Iquitos, however, our goal was to use a model previously developed for Iquitos to address a general question about the effect of lockdown on dengue. We used hypothetical scenarios with altered mobility patterns and vector control campaigns, which were not intended to directly represent the reality of what happened in Iquitos or any other city in 2020, but to gain mechanistic understanding of the effect of these type of mobility changes. Even so, it is worth noting that Iquitos did experience a large COVID-19 epidemic beginning in March 2020, which severely strained health services there [39]. Just before then, the city experienced a relatively large dengue epidemic in December 2019 through March 2020 [40]. Extensive disruption of health services thereafter for illnesses other than COVID-19 makes it difficult to know what the course of that dengue epidemic was once COVID-19 arrived [39]. Given how large the COVID-19 epidemic in Iquitos appears to have been [41], compliance with lockdown there may have been low. On the other hand, Google mobility data from Maynas province shows a 30% increase from baseline in household mobility and a 60% decrease from baseline in workplace mobility during April and May, suggesting substantial changes in mobility patterns [42]. Although low compliance with lockdown would reduce the direct effects of lockdown on dengue that we demonstrated with our model, reductions to vector control services may have had effects on dengue incidence that went unnoticed by surveillance and that could have implications for the next dengue transmission season. If we were to use our model to attempt to reconstruct what actually happened in Iquitos, we need data from serological surveys and mosquito household surveys from 2010 up to 2021, alongside detailed mobility data for the city. Once these former data become available, such a study could prove a valuable contribution.
Globally, there have been reports of both rising [7,43,44] and falling [45,46] dengue incidence since the COVID-19 pandemic began [47]. A study from Thailand was able to associate increases in dengue incidence with interventions against COVID-19 [48], consistent with our findings. The observational nature of that study did not allow for the mechanisms behind that association to be understood, but the authors hypothesized that it may have been due to heightened exposure to vectors while people spent more time in their homes [48]. Our analysis adds value by testing that hypothesis through simulation experiments and elucidating how the strength of those effects is modulated by other factors, such as spatial heterogeneity in mosquito abundance, the spatial scale of mosquito movement, compliance with lockdown, and the seasonal timing of lockdown. Our study is also inline with a statistical analysis from Brazil finding a positive association of mobility restrictions with dengue cases 20 days later [49], and is similar to the finding that reductions in mobility due to the effects of fever can increase transmission [50]. Conversely, a study from Sri Lanka found a decreased risk of dengue during lockdown [51].
A factor that could be important in modulating effects of lockdown on dengue is the extent to which DENV transmission occurs at other types of locations, such as schools [52,53]. In settings where schools or other non-residential locations are important for DENV transmission, lockdown measures could have a qualitatively different effect by reducing the number of people in those high-risk locations. Nonetheless, homes and their vicinity remain a key site of transmission in many settings, and we expect that our finding that lockdown further increases transmission in such locations will be robust [54–59]. Spatio-temporal heterogeneity in compliance with lockdown may also impact dengue transmission. While we modeled some heterogeneity by randomly choosing who will comply with lockdown, there is no spatial or temporal structure to this aspect of our approach. If certain districts within a city have lower compliance with lockdown, there may be a reduced effect of lockdown in those districts.
The scale of the non-pharmaceutical interventions undertaken to combat the COVID-19 epidemic have likely impacted a number of other diseases, either directly or indirectly. Some of these effects may be positive. For instance, due to the shared route of transmission, interventions against COVID-19 impact influenza in a similar way, and likely contributed to very low flu seasons during the Southern Hemisphere winter and in Hong Kong [60,61]. On the other hand, disruption of key services and reductions in care-seeking behavior are projected to have negative effects on the burden of TB, malaria, HIV/AIDS, and a range of vaccine-preventable diseases [2,3,62–65]. Our results align more closely with the latter pattern, showing a potentially large negative effect if dengue vector control campaigns are interrupted. To mitigate this, public health authorities could encourage or assist people to spray their own homes, by providing them with self-use insecticide treatments [66]. This would mitigate the impact of reduced vector control activities and reduce the impact of changes in mobility on dengue transmission.
A significant strength of our study is our spatially explicit treatment of human mobility, which allowed us to isolate the effect of lockdown in ways that a simpler model could not. Moreover, our model’s direct inclusion of mosquito movement and individual biting behavior allowed us to understand the changing role of these factors in DENV transmission when movement restrictions were imposed. Our study also has at least five limitations. First, it is difficult to know the exact response people made to lockdown measures, such as the level of compliance and how the nature of their movements changed. Our sensitivity analysis of lockdown compliance and duration found that reduced compliance linearly decreased the change in incidence due to lockdown. Second, we assumed that mosquito behavior was unaffected by changes in human mobility. Lockdown has been associated with increased vector indices in India [67]. Third, we did not assess the impact of changing DENV importation patterns into Iquitos. Because our model predicts the biggest impact of lockdown is late in the season, a time when the epidemic is predominantly driven by local transmission, we would not expect changes in imported infections to qualitatively affect this result. Changing importations may, however, have a significant impact if they prevent an imported infection from seeding a new outbreak, particularly if the introduced virus was a new serotype. Fourth, we did not assess impact in terms of severe disease; e.g., dengue hemorrhagic fever (DHF). We made this decision because of severe dengue’s dependence on the local immunity profile and circulating serotype, which would mean DHF results would be difficult to generalize. Our model was also calibrated to a statistical reconstruction of incidence of infection [25] rather than disease. Nonetheless, increased incidence of DENV infection would, all else being equal, be expected to translate to higher rates of severe disease; a very concerning situation in the context of already strained health systems due to COVID-19. Fifth, in order to simplify the analysis we did not incorporate structured spatial heterogeneity in compliance. While we do model heterogeneity in compliance between individuals, structured differences between regions may lead to effects not captured in our analysis.
Our findings illustrate why, during a syndemic, public health officials must consider the implications of an action to prevent one disease on other concurrent diseases [68]. Thus, a holistic approach to infectious disease mitigation is needed. Research and policy efforts should focus on ways to retain the positive effects of lockdown on diseases like COVID-19, influenza, and pneumonia while mitigating the negative effects on dengue, malaria, and TB. Vector control activities which people can do themselves in their own homes, such handheld over-the-counter insecticide treatments, should be encouraged and supported during lockdown. Whenever there is risk of DENV transmission, efforts must be made to avoid disrupting effective control practises and provide carefully planned alternative means of making interventions possible. More communication, creativity, and inter-sectorial collaboration will be needed to ensure the continuation of meaningful interventions than to rely solely on providing vector control staff with personal protective equipment to carry out existing forms of control [18].
Supporting information
Acknowledgments
We thank Amy Morrison (University of California, Davis) for helpful discussion and commentary on the manuscript. We also thank the Proyecto Dengue team in Iquitos for performing research over many years that informed the development of our model. This research made extensive use of computing resources provided by the Center for Research Computing at the University of Notre Dame.
Data Availability
All model code and synthetic data are available at github.com/scavany/dengue_shelter_in_place.
Funding Statement
All authors were supported by grant P01AI098670 (TWS, PI) from the National Institutes of Health, National Institute for Allergy and Infectious Disease (https://www.niaid.nih.gov). GE and TAP were also supported by a RAPID grant from the National Science Foundation (DEB 2027718). The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.
References
- 1.Flaxman S, Mishra S, Gandy A, Unwin HJT, Mellan TA, Coupland H, et al. Estimating the effects of non-pharmaceutical interventions on COVID-19 in Europe. Nature. 2020. doi: 10.1038/s41586-020-2405-7 [DOI] [PubMed] [Google Scholar]
- 2.Hogan AB, Jewell BL, Sherrard-Smith E, Vesga JF, Watson OJ, Whittaker C, et al. Potential impact of the COVID-19 pandemic on HIV, tuberculosis, and malaria in low-income and middle-income countries: a modelling study. The Lancet Global Health. 2020;0. doi: 10.1016/S2214-109X(20)30288-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.McQuaid CF, McCreesh N, Read JM, Sumner T, Houben RMGJ, White RG, et al. The potential impact of COVID-19-related disruption on tuberculosis burden. European Respiratory Journal. 2020. [cited 7 Jul 2020]. doi: 10.1183/13993003.01718-2020 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Stanaway JD, Shepard DS, Undurraga EA, Halasa YA, Coffeng LE, Brady OJ, et al. The global burden of dengue: an analysis from the Global Burden of Disease Study 2013. The Lancet Infectious Diseases. 2016;16: 712–723. doi: 10.1016/S1473-3099(16)00026-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Bhatt S, Gething PW, Brady OJ, Messina JP, Farlow AW, Moyes CL, et al. The global distribution and burden of dengue. Nature. 2013;496: 504–507. doi: 10.1038/nature12060 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Dengue in the Americas: 20 countries reporting higher-than-usual numbers prompting CDC travel notice. In: Outbreak News Today [Internet]. 4 Oct 2020 [cited 5 Oct 2020]. Available: http://outbreaknewstoday.com/dengue-in-the-americas-20-countries-reporting-higher-than-usual-numbers-prompting-cdc-travel-notice-76746/
- 7.Cardona-Ospina JA, Arteaga-Livias K, Villamil-Gómez WE, Pérez-Díaz CE, Katterine Bonilla-Aldana D, Mondragon-Cardona Á, et al. Dengue and COVID-19, overlapping epidemics? An Analysis from Colombia. J Med Virol. 2020. doi: 10.1002/jmv.26194 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Epelboin L, Blondé R, Nacher M, Combe P, Collet L. COVID-19 and dengue co-infection in a returning traveller. J Travel Med. 2020. doi: 10.1093/jtm/taaa114 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Haqqi A, Awan UA, Ali M, Saqib MAN, Ahmed H, Afzal MS. COVID-19 and dengue virus co-epidemics in Pakistan: A dangerous combination for overburdened healthcare system. J Med Virol. 2020. doi: 10.1002/jmv.26144 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Miah MA, Husna A. Co-infection, co-epidemics of Covid-19 and Dengue in dengue endemic countries: a serious health concern. J Med Virol. 2020. doi: 10.1002/jmv.26269 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Ridwan R. COVID-19 and dengue: a deadly duo. Trop Doct. 2020; 49475520936874. doi: 10.1177/0049475520936874 [DOI] [PubMed] [Google Scholar]
- 12.Wee LE, Cherng BPZ, Conceicao EP, Goh KC-M, Wan WY, Ko KKK, et al. Experience of a Tertiary Hospital in Singapore with Management of a Dual Outbreak of COVID-19 and Dengue. Am J Trop Med Hyg. 2020. doi: 10.4269/ajtmh.20-0703 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Masyeni S, Santoso MS, Widyaningsih PD, Wedha Asmara DG, Nainu F, Harapan H, et al. Serological cross-reaction and co-infection of dengue and COVID-19 in Asia: Experience from Indonesia. Int J Infect Dis. 2020. doi: 10.1016/j.ijid.2020.10.043 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Verduyn M, Allou N, Gazaille V, Andre M, Desroche T, Jaffar M-C, et al. Co-infection of dengue and COVID-19: A case report. PLoS Negl Trop Dis. 2020;14: e0008476. doi: 10.1371/journal.pntd.0008476 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Estofolete CF, Machado LF, Zini N, Luckemeyer GD, Moraes MM, Dos Santos TNIL, et al. Fatal stroke as presentation of SARS-CoV-2 and dengue virus coinfection. J Med Virol. 2020. doi: 10.1002/jmv.26476 [DOI] [PubMed] [Google Scholar]
- 16.Bicudo N, Bicudo E, Costa JD, Castro JALP, Barra GB. Co-infection of SARS-CoV-2 and dengue virus: a clinical challenge. Braz J Infect Dis. 2020. doi: 10.1016/j.bjid.2020.07.008 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Pontes RL, de Brito BB, da Silva FAF, Correia TML, Teixeira AF, Oliveira MV, et al. Coinfection by SARS-CoV-2 and dengue virus in a dual viral circulation setting. Travel Med Infect Dis. 2020; 101862. doi: 10.1016/j.tmaid.2020.101862 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Seelig F, Bezerra H, Cameron M, Hii J, Hiscox A, Irish S, et al. The COVID-19 pandemic should not derail global vector control efforts. PLOS Neglected Tropical Diseases. 2020;14: e0008606. doi: 10.1371/journal.pntd.0008606 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Olive M-M, Baldet T, Devillers J, Fite J, Paty M-C, Paupy C, et al. The COVID-19 pandemic should not jeopardize dengue control. PLoS Negl Trop Dis. 2020;14: e0008716. doi: 10.1371/journal.pntd.0008716 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Oidtman RJ, Lai S, Huang Z, Yang J, Siraj AS, Reiner RC, et al. Inter-annual variation in seasonal dengue epidemics driven by multiple interacting factors in Guangzhou, China. Nat Commun. 2019;10: 1148. doi: 10.1038/s41467-019-09035-x [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Brito AF, Machado LC, Siconelli MJL, Oidtman RJ, Fauver JR, Carvalho RD de O, et al. Lying in wait: the resurgence of dengue virus after the Zika epidemic in Brazil. medRxiv. 2020;2020.08.10.20172247. doi: 10.1101/2020.08.10.20172247 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Wearing HJ, Rohani P. Ecological and immunological determinants of dengue epidemics. PNAS. 2006;103: 11802–11807. doi: 10.1073/pnas.0602960103 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Stoddard ST, Forshey BM, Morrison AC, Paz-Soldan VA, Vazquez-Prokopec GM, Astete H, et al. House-to-house human movement drives dengue virus transmission. Proceedings of the National Academy of Sciences. 2013;110: 994–999. doi: 10.1073/pnas.1213349110 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Bosch QA ten Singh BK, Hassan MRA Chadee DD, Michael E. The Role of Serotype Interactions and Seasonality in Dengue Model Selection and Control: Insights from a Pattern Matching Approach. PLOS Neglected Tropical Diseases. 2016;10: e0004680. doi: 10.1371/journal.pntd.0004680 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Reiner RC, Stoddard ST, Forshey BM, King AA, Ellis AM, Lloyd AL, et al. Time-varying, serotype-specific force of infection of dengue virus. Proc Natl Acad Sci USA. 2014;111: E2694–2702. doi: 10.1073/pnas.1314933111 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Perkins TA, Reiner RC, España G, Ten Bosch QA, Verma A, Liebman KA, et al. An agent-based model of dengue virus transmission shows how uncertainty about breakthrough infections influences vaccination impact projections. PLoS Comput Biol. 2019;15: e1006710. doi: 10.1371/journal.pcbi.1006710 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Cavany SM, España G, Lloyd AL, Waller LA, Kitron U, Astete H, et al. Optimizing the deployment of ultra-low volume and targeted indoor residual spraying for dengue outbreak response. PLOS Computational Biology. 2020;16: e1007743. doi: 10.1371/journal.pcbi.1007743 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.España G, Yao Y, Anderson KB, Fitzpatrick MC, Smith DL, Morrison AC, et al. Model-based assessment of public health impact and cost-effectiveness of dengue vaccination following screening for prior exposure. PLoS Negl Trop Dis. 2019;13: e0007482. doi: 10.1371/journal.pntd.0007482 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Flasche S, Jit M, Rodríguez-Barraquer I, Coudeville L, Recker M, Koelle K, et al. The Long-Term Safety, Public Health Impact, and Cost-Effectiveness of Routine Vaccination with a Recombinant, Live-Attenuated Dengue Vaccine (Dengvaxia): A Model Comparison Study. PLOS Medicine. 2016;13: e1002181. doi: 10.1371/journal.pmed.1002181 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Perkins TA, Garcia AJ, Paz-Soldán VA, Stoddard ST, Reiner RC, Vazquez-Prokopec G, et al. Theory and data for simulating fine-scale human movement in an urban environment. J R Soc Interface. 2014;11. doi: 10.1098/rsif.2014.0642 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Reiner RC, Stoddard ST, Vazquez-Prokopec GM, Astete H, Perkins TA, Sihuincha M, et al. Estimating the impact of city-wide Aedes aegypti population control: An observational study in Iquitos, Peru. PLoS Negl Trop Dis. 2019;13: e0007255. doi: 10.1371/journal.pntd.0007255 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Stoddard ST, Wearing HJ, Reiner RC, Morrison AC, Astete H, Vilcarromero S, et al. Long-Term and Seasonal Dynamics of Dengue in Iquitos, Peru. Barrera R, editor. PLoS Neglected Tropical Diseases. 2014;8: e3003. doi: 10.1371/journal.pntd.0003003 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Gunning CE, Okamoto KW, Astete H, Vasquez GM, Erhardt E, Del Aguila C, et al. Efficacy of Aedes aegypti control by indoor Ultra Low Volume (ULV) insecticide spraying in Iquitos, Peru. Barrera R, editor. PLOS Neglected Tropical Diseases. 2018;12: e0006378. doi: 10.1371/journal.pntd.0006378 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Lee J-S, Filatova T, Ligmann-Zielinska A, Hassani-Mahmooei B, Stonedahl F, Lorscheid I, et al. The Complexities of Agent-Based Modeling Output Analysis. JASSS. 2015;18: 4. doi: 10.18564/jasss.2760 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.R Core Team. R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing; 2018. [Google Scholar]
- 36.Wood S. mgcv: Mixed GAM Computation Vehicle with Automatic Smoothness Estimation. 2020. Available: https://CRAN.R-project.org/package=mgcv [Google Scholar]
- 37.Morrison AC, Gray K, Getis A, Astete H, Sihuincha M, Focks D, et al. Temporal and Geographic Patterns of Aedes aegypti (Diptera: Culicidae) Production in Iquitos, Peru. J Med Entomol. 2004;41: 1123–1142. doi: 10.1603/0022-2585-41.6.1123 [DOI] [PubMed] [Google Scholar]
- 38.Reiner RC, Stoddard ST, Scott TW. Socially structured human movement shapes dengue transmission despite the diffusive effect of mosquito dispersal. Epidemics. 2014;6: 30–36. doi: 10.1016/j.epidem.2013.12.003 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Fraser B. COVID-19 strains remote regions of Peru. The Lancet. 2020;395: 1684. doi: 10.1016/S0140-6736(20)31236-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Torres K, Alava F, Soto-Calle V, Llanos-Cuentas A, Rodriguez H, Llacsahuanga L, et al. Malaria Situation in the Peruvian Amazon during the COVID-19 Pandemic. The American Journal of Tropical Medicine and Hygiene. 2020;103: 1773–1776. doi: 10.4269/ajtmh.20-0889 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Chafloque-Vásquez RA, Pampa-Espinoza L, Celis Salinas JC. Seroprevalencia de COVID-19 en trabajadores de un hospital de la Amazonía peruana. Acta Med Peru. 2020;37. doi: 10.35663/amp.2020.373.1050 [DOI] [Google Scholar]
- 42.COVID-19 Community Mobility Report. In: COVID-19 Community Mobility Report [Internet]. 26 Mar 2021 [cited 26 Mar 2021]. Available: https://www.google.com/covid19/mobility?hl=en
- 43.Nacher M, Douine M, Gaillet M, Flamand C, Rousset D, Rousseau C, et al. Simultaneous dengue and COVID-19 epidemics: Difficult days ahead? PLOS Neglected Tropical Diseases. 2020;14: e0008426. doi: 10.1371/journal.pntd.0008426 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Huang E. Outbreak of dengue fever in Southeast Asia is “exploding” amid the coronavirus fight. In: CNBC [Internet]. 10 Jul 2020 [cited 16 Jul 2020]. Available: https://www.cnbc.com/2020/07/10/outbreak-of-dengue-fever-in-southeast-asia-is-exploding-amid-the-coronavirus-fight.html
- 45.Mascarenhas MDM, Batista FM de A, Rodrigues MTP, Barbosa O de AA, Barros VC, Mascarenhas MDM, et al. Ocorrência simultânea de COVID-19 e dengue: o que os dados revelam? Cadernos de Saúde Pública. 2020;36. doi: 10.1590/0102-311x00126520 [DOI] [PubMed] [Google Scholar]
- 46.Dantés HG, Manrique-Saide P, Vazquez-Prokopec G, Morales FC, Siqueira Junior JB, Pimenta F, et al. Prevention and control of Aedes transmitted infections in the post-pandemic scenario of COVID-19: challenges and opportunities for the region of the Americas. Memórias do Instituto Oswaldo Cruz. 2020;115. doi: 10.1590/0074-02760200284 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Brady O, Wilder-Smith A. What Is the Impact of Lockdowns on Dengue? Curr Infect Dis Rep. 2021;23: 2. doi: 10.1007/s11908-020-00744-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Lim JT, Dickens BSL, Chew LZX, Choo ELW, Koo JR, Aik J, et al. Impact of sars-cov-2 interventions on dengue transmission. PLOS Neglected Tropical Diseases. 2020;14: e0008719. doi: 10.1371/journal.pntd.0008719 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Conceição GM de S, Barbosa GL, Lorenz C, Bocewicz ACD, Santana LMR, Marques CC de A, et al. Effect of social isolation in dengue cases in the state of Sao Paulo, Brazil: an analysis during the COVID-19 pandemic. arXiv:210308669 [stat]. 2021 [cited 22 Mar 2021]. Available: http://arxiv.org/abs/2103.08669 [DOI] [PMC free article] [PubMed]
- 50.Schaber KL, Perkins TA, Lloyd AL, Waller LA, Kitron U, Paz-Soldan VA, et al. Disease-driven reduction in human mobility influences human-mosquito contacts and dengue transmission dynamics. PLoS Comput Biol. 2021;17: e1008627. doi: 10.1371/journal.pcbi.1008627 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Liyanage P, Rocklöv J, Tissera HA. The impact of COVID–19 lockdown on dengue transmission in Sri Lanka; A natural experiment for understanding the influence of human mobility. PLOS Neglected Tropical Diseases. 2021;15: e0009420. doi: 10.1371/journal.pntd.0009420 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Parra B, Rengifo G, Méndez F, Burbano ME, Arias JF, Muñoz J, et al. HUMAN AND MOSQUITO INFECTIONS BY DENGUE VIRUSES DURING AND AFTER EPIDEMICS IN A DENGUE–ENDEMIC REGION OF COLOMBIA. The American Journal of Tropical Medicine and Hygiene. 2006;74: 678–683. doi: 10.4269/ajtmh.2006.74.678 [DOI] [PubMed] [Google Scholar]
- 53.Ratanawong P, Kittayapong P, Olanratmanee P, Wilder-Smith A, Byass P, Tozan Y, et al. Spatial Variations in Dengue Transmission in Schools in Thailand. PLOS ONE. 2016;11: e0161895. doi: 10.1371/journal.pone.0161895 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54.Sujariyakul A, Prateepko S, Chongsuvivatwong V, Thammapalo S. Transmission of Dengue Haemorrhagic Fever: At Home or School? 2005;29: 9. [Google Scholar]
- 55.Waterman SH, Novak RJ, Sather GE, Bailey RE, Rios I, Gubler DJ. Dengue Transmission in Two Puerto Rican Communities in 1982. The American Journal of Tropical Medicine and Hygiene. 1985;34: 625–632. doi: 10.4269/ajtmh.1985.34.625 [DOI] [PubMed] [Google Scholar]
- 56.Koopman JS, Prevots DR, Mann MAV, Dantes HG, Aquino MLZ, Longini IM, et al. Determinants and Predictors of Dengue Infection in Mexico. Am J Epidemiol. 1991;133: 1168–1178. doi: 10.1093/oxfordjournals.aje.a115829 [DOI] [PubMed] [Google Scholar]
- 57.Ko Y-C, Chen M-J, Yeh S-M. The Predisposing and Protective Factors against Dengue Virus Transmission by Mosquito Vector. American Journal of Epidemiology. 1992;136: 214–220. doi: 10.1093/oxfordjournals.aje.a116487 [DOI] [PubMed] [Google Scholar]
- 58.Anders KL, Nga LH, Thuy NTV, Ngoc TV, Tam CT, Tai LTH, et al. Households as Foci for Dengue Transmission in Highly Urban Vietnam. PLOS Neglected Tropical Diseases. 2015;9: e0003528. doi: 10.1371/journal.pntd.0003528 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 59.McBride WJH, Mullner H, Muller R, Labrooy J, Wronski I. Determinants of Dengue 2 Infection among Residents of Charters Towers, Queensland, Australia. American Journal of Epidemiology. 1998;148: 1111–1116. doi: 10.1093/oxfordjournals.aje.a009589 [DOI] [PubMed] [Google Scholar]
- 60.Cowling BJ, Ali ST, Ng TWY, Tsang TK, Li JCM, Fong MW, et al. Impact assessment of non-pharmaceutical interventions against coronavirus disease 2019 and influenza in Hong Kong: an observational study. The Lancet Public Health. 2020;5: e279–e288. doi: 10.1016/S2468-2667(20)30090-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 61.Olsen SJ. Decreased Influenza Activity During the COVID-19 Pandemic—United States, Australia, Chile, and South Africa, 2020. MMWR Morb Mortal Wkly Rep. 2020;69. doi: 10.15585/mmwr.mm6937a6 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 62.Sherrard-Smith E, Hogan AB, Hamlet A, Watson OJ, Whittaker C, Winskill P, et al. The potential public health consequences of COVID-19 on malaria in Africa. Nature Medicine. 2020; 1–6. doi: 10.1038/s41591-019-0740-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 63.Weiss DJ, Bertozzi-Villa A, Rumisha SF, Amratia P, Arambepola R, Battle KE, et al. Indirect effects of the COVID-19 pandemic on malaria intervention coverage, morbidity, and mortality in Africa: a geospatial modelling analysis. The Lancet Infectious Diseases. 2020;0. doi: 10.1016/S1473-3099(20)30700-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 64.Abbas K, Procter SR, van Zandvoort K, Clark A, Funk S, Mengistu T, et al. Routine childhood immunisation during the COVID-19 pandemic in Africa: a benefit-risk analysis of health benefits versus excess risk of SARS-CoV-2 infection. The Lancet Global Health. 2020;8: e1264–e1272. doi: 10.1016/S2214-109X(20)30308-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 65.Jenness SM, Guillou AL, Chandra C, Mann LM, Sanchez T, Westreich D, et al. Projected HIV and Bacterial STI Incidence Following COVID-Related Sexual Distancing and Clinical Service Interruption. medRxiv. 2020; 2020.09.30.20204529. doi: 10.1101/2020.09.30.20204529 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 66.Dzib-Florez S, Ponce-García G, Medina-Barreiro A, González-Olvera G, Contreras-Perera Y, Castillo-Centeno FD, et al. Evaluating Over-the-Counter Household Insecticide Aerosols for Rapid Vector Control of Pyrethroid-Resistant Aedes aegypti. 2020; tpmd200515. doi: 10.4269/ajtmh.20-0515 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 67.Daniel Reegan A, Rajiv Gandhi M, Cruz Asharaja A, Devi C, Shanthakumar SP. COVID-19 lockdown: impact assessment on Aedes larval indices, breeding habitats, effects on vector control programme and prevention of dengue outbreaks. Heliyon. 2020;6: e05181. doi: 10.1016/j.heliyon.2020.e05181 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 68.Horton R. Offline: COVID-19 is not a pandemic. The Lancet. 2020;396: 874. doi: 10.1016/S0140-6736(20)32000-6 [DOI] [PMC free article] [PubMed] [Google Scholar]