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PLOS Neglected Tropical Diseases logoLink to PLOS Neglected Tropical Diseases
. 2021 Nov 2;15(11):e0009909. doi: 10.1371/journal.pntd.0009909

The burden of zoonoses in Paraguay: A systematic review

Liz Paola Noguera Zayas 1,2,*, Simon Rüegg 1, Paul Torgerson 1
Editor: Christine A Petersen3
PMCID: PMC8589157  PMID: 34727113

Abstract

Introduction

Underestimation of zoonoses is exacerbated in low and middle-income countries due mainly to inequalities with serious consequences in healthcare. This is difficult to gauge and reduce the impact of those diseases. Our study focuses on Paraguay, where the livestock industry is one of the major components of the country’s economy. Therefore, the rationale of this study was to develop a case study in Paraguay to estimate the dual impact of zoonotic diseases on both the human health and animal health sector and thus determine the societal burden of such diseases.

Methodology/Principal findings

We conducted a systemic review (including a meta-analysis) to assess the burden of zoonoses in Paraguay, including official reports and grey literature of disease incidence and prevalence. We estimated the Disability Adjusted Life Years (DALYs) and Zoonosis Disability Adjusted Life Years (zDALYs) to measure the difference between the current health status and the desired health situation of animals and the Paraguayan population based on 50 zoonotic diseases suggested by the WHO (World Health Organization), OIE (World Organization for Animal Health) and the National Health in Paraguay. The total DALYs represent 19,384 (95% CI: from 15,805 to 29,733), and zDALYs, 62,178 (95% CI: from 48,696 to 77,188). According to the results, the priority pathogens for DALYs are E. coli, Trypanosoma cruzi, Leishmania spp, and Toxoplasma gondii. When we include the additional animal health burden, the most important pathogens are Brucella spp, E. coli, Trypanosoma cruzi, and Fasciola hepatica for zDALYs.

Conclusion/Significance

This is the first study to integrate DALYs and zDALYs with important clues related to the health status of Paraguay. Through DALYs and zDALYs, our perspective becomes more complete because we consider not only human health but also animal health. This is important for setting priorities in disease control, especially in a society where livestock contribute significantly to the economy and to human well-being.

Author summary

Zoonotic diseases in man are more likely to occur where there is a close association between man and animals. The control of zoonotic diseases requires a “One Health” approach to reduce the risk of such transmission. This represents a challenge in low and middle-income countries, due to inequalities and limited resources, especially in healthcare. For that reason, we need to quantify the impact of zoonoses in those countries such as Paraguay, a major exporter of beef and agricultural products, so that disease control priorities can be set. Through a systematic review, we estimate the Disability Adjusted Life Years (DALYs) and the Zoonosis Disability Adjusted Life Years (zDALYs) based on incidence and prevalence of zoonoses to find gaps between the real and the desired health status of both animals and humans in Paraguay. The zDALY ensures the total societal burden of disease, rather than just the direct human disease burden. We have through zDALYs a more equitable method for disease burden analysis that has a dual impact on human and animal health. Accordingly, we have found that those diseases with the highest zDALY are brucellosis, colibacillosis and Chagas disease.

Introduction

It has been suggested that 61% of human infectious diseases are zoonoses [1]. Transmission pathways could be by direct or indirect contact, including air, food, and vectors. Presently, disease transmission is exacerbated by anthropogenic activities and global changes (climate change, globalization), causing a high socioeconomic impact [2]. Moreover, low and middle-income countries suffer from major inequalities, especially in healthcare, making people in poverty more vulnerable to easily preventable diseases with hygiene and good food quality.

The Republic of Paraguay is a landlocked, subtropical, and developing country in South America, where the main economic activities are agriculture and livestock production. The country is divided into the Occidental (Western) or Chaco region (with three departments) and the Oriental (Eastern) region (with 14 departments). Paraguay’s population is estimated at 7 million (in 406,752 km2) with 112,000 births in 2018. In the same period, the Ministry of Public Health and Social Welfare registered 31,000 deaths, but the General Directorate of Statistics, Surveys and Censuses estimated 40,000 deaths per year [3]. According to the World Bank, Paraguay has increased its population life expectancy from 2000 (being 70,5 years) to 2018 (74 years old for both sexes).

In 2017, livestock production represented 12.1% of the GDP, and consequently, animal diseases, including zoonoses, represent substantial potential losses to the country’s economy [4]. The main animal production corresponded to poultry (24 million from January to April), cattle (13.5 million registered), pigs (0.4 million), sheep (0.3 million), horses (0.2 million) and goats (0.1 million) in 2018 [5]. In 2017, Paraguay exported to more than 140 countries. With such a large livestock sector, the contact between humans and animals results in a higher risk of the transmission of zoonoses. In Paraguay, further (wild) animal-human contact occurs due to deforestation, unplanned urbanization, population growth, invasion of wild habitats, bushmeat, hunting, loss of biodiversity, introduction of exotic (alien) species, certain natural phenomena such as flooding, unequal resource distribution, lack of adequate basic hygiene measures, lack of infrastructure and planning. All these factors provide additional risks for the transmission of zoonotic diseases. Because of this high risk for diseases at the human-animal interface, we hypothesize that zoonoses cause a substantial proportion of the burden of infectious diseases, this being 149,196 DALYs in 2019 [6]. Our study aims to estimate the burden of zoonoses using disability-adjusted life years (DALYs), as well as an adjusted indicator, zoonotic DALY (zDALY), to include animal loss equivalents in the estimate [7].

These indicators can help prioritize health interventions from a more holistic perspective. They may reveal some opportunities to improve health in Paraguay by harnessing synergies between human and animal health based on a “well-being economy.”

Methods

We identified 50 zoonotic diseases in Paraguay based on the lists of the World Health Organization (WHO), the World Organization for Animal Health (OIE). We also included a list of notifiable zoonoses issued by the government of Paraguay, and other diseases with zoonotic potential that exist in Paraguay and/or South America but which are not considered a priority by the Paraguayan government (S1 Table). As Paraguay is a highly productive country, the priorities related to animal health are mainly of economic interest.

We have considered the lists of all these organizations because they are slightly different, since their objectives vary in relation to their priorities and their concepts (e.g., vectors, reservoirs, target, etc.). By combining these lists, we searched for a more comprehensive view on the influence of zoonoses on several areas, such as human and animal health, socio-economic impact, national and international importance.

Systematic review

We followed the guidelines for “Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA)” (S1 Prisma checklist) to conduct the systematic review, as depicted in Fig 1 [8,9]. We collected data on incidences and prevalences in Paraguay between January 2000 and December 2019. The information was gathered through five global databases (Web of Science, Scopus, Ebscohost, Pubmed, and Google Scholar) and two Paraguayan databases (Scielo Paraguay, and theses shared by the library of Veterinary Sciences and the Central Library of the National University of Asunción) accessible via websites (details in the S2 Table).

Fig 1. Flow diagram of the results of the systematic review for the burden of zoonoses in Paraguay, adapted from PRISMA guidelines.

Fig 1

We used Boolean search syntax (OR, AND) to join the scientific nomenclature and popular name(s) of each zoonosis in English and Spanish on the five global databases. For example, Paraguay AND (“scientific name of the causative agent” OR “common disease name in Spanish” OR “common disease name in English” OR “an alternative name if needed”). In the local databases, we only used the scientific name of the zoonotic agent with the disease name in Spanish. We specified the terms and the syntax construction for each search engine in the S1 Text. We complemented the resulting information on these databases to reports published on the websites of the WHO, PAHO, WAHIS, FAOSTAT, CDC, Global Health Data Exchange, the Health Sciences Research Institute in Paraguay, the Ministry of Public Health and Social Welfare and the National Service of Quality and Animal Health (SENACSA). The corresponding links are listed in S2 Table.

We included articles considering the title and the abstracts with the following criteria: reports from Paraguay, any Paraguayan department, city, area, or hospital. We also selected articles of zoonosis with the following terms: “triple border”, “South America”, “Latin America”, “southern cone”, “tropical country” (although Paraguay is a subtropical country, it is often confused with a tropical country), “subtropical region”, “Neotropical”, “the Americas”, the “New World”, “worldwide”, “western hemisphere”, diseases in developing countries and diseases in low-and middle-income countries. We also considered reviews and overviews of zoonoses and the presentation of symptoms of undetermined diseases (e.g., pneumonia, kidney injury or parasitic infections).

We excluded articles meeting the following criteria: case studies of frequent diseases when we had enough data, zoonoses occurring outside of Paraguay, Paraguayan emigrants who presented zoonosis cases abroad, laboratory studies without incidence and prevalence, mathematical modelling, questionnaires related to the level of knowledge about certain diseases and information out of the specified period. After article screening, first by title and then by abstracts, we read the eligible papers’ full text. Finally, we included the studies in this systematic review with a critical appraisal to estimate DALYs and zDALYs [8,10].

DALY and zDALY calculation

To assess the burden of zoonoses in Paraguay, we used the DALY incidence-based approach.

DALY=YLL+YLD

The DALY’s burden consists of the sum of Years of Life Lost (YLL) due to early death in the population and Years Lost due to Disability (YLD) for those who are sick or have sequelae of a certain disease. We estimated the YLL based on the product of the number of deaths (N) multiplied and residual of the life expectancy (L) of the population in Paraguay.

YLL=NxL

To obtain the YLD, we multiplied the number of cases (I), the duration of the disease with sequelae zoonosis (L), and the disability weight (DW) representing the disease severity from 0 to 1 (where zero = perfect health, and one = death) [11].

YLD=IxLxDW.

We obtained the residual life expectancy information from the WHO Standard Life Table for Years of Life Lost 2000–2016 (WHO 2018) [12]. When we had no data to estimate DALY, we filled these gaps with global information found on literature and official websites (WHO, CDC, OIE, FAO), such as fatality rate, sequelae, and the disease duration—the URLs are specified in the S2 Table. To calculate the duration of each zoonosis, we considered the total average of the incubation period, the treatment, time to recover, and the sequela (if needed). Regarding tuberculosis, since the reports in human cases did not determine if they were due to Mycrobacterium tuberculosis or Mycobacterium bovis, we used the estimates for the proportion of human tuberculosis due to M. bovis infections in humans as a median of 0.3% (range 0%– 33.9%) in the Americas [13]. With respect to zoonotic diarrheal diseases, we applied the methodology of the Foodborne Disease Burden Epidemiology Reference Group (FERG), consisting of a proportion of diarrhea cases due to various etiologies (colibacillosis, salmonellosis, campylobacteriosis), combining with diarrhea data from the Global Burden of Disease (GBD) estimations [1418]. For cysticercosis, the FERG methodology assumes that 29% of epilepsy cases in at-risk populations will be caused by cysticercosis and the population at higher risk has no access to improved sanitation in countries where pigs are reared. According to the latest data for Paraguay, 11% of the population do not have access to improved sanitation [14,19]. To calculate the cysticercosis burden, we used the DALYs reported for epilepsy for Paraguay on the Institute for Health Metrics and Evaluation (IHME) website [16]. According to its estimates, the epilepsy burden for Paraguay is 12,163 (CI 5,917–21,760).

The zDALY consists of the sum of the DALYs and the animal loss equivalents (ALEs) and represents the burden of disease in society due to zoonoses. This is calculated as [7]:

zDALY=YLL+YLD+ALE

ALEs are the equivalent impact as the DALY on animal owners. This is estimated through time trade-offs (i.e., the time taken to earn money to replace the animal loss and hence converted to a DALY equivalent). Thus, DALYs and ALEs are integrated. To estimate the ALEs, we considered the annual monetary impact of the animal loss in Paraguay divided by its gross national per capita income (GNI) in US$ [20]. We estimated the average animal loss value per category in Paraguay based on information provided by the website of the SENACSA [21]. Regarding the economic value of cattle, we obtained the prices in US$ from the Rural Association of Paraguay website [22]. For pets (dogs and cats), we estimate the average of the purebred pets’ prices, from zero to the mean value based on expert advice who manage market prices in Paraguay and Paraguayan pet selling websites on the internet and social media (further details in the S1 and S2 Tables, and S1 Text). Then, we converted Paraguayan Guarani to US$ at the most recent value at the time of the study [23].

We estimated the 95% probability to account for uncertainty using Monte Carlo analysis. We applied Beta, Gamma, Dirichlet, and Binomial distributions according to the data available. For example, we used beta distributions for the proportions such as incidence and prevalence of diseases; gamma distributions for right-skewed data with a small sample. We used Dirichlet distribution for multinomial or categorical observations, such as leishmaniasis being its main forms: visceral, cutaneous, and mucocutaneous. We performed binomial distributions when the number of observations was fixed, e.g., when researchers selected a determined number of patients to test for a disease. The distributions and employed data parameters are reported in S3 and S4 Tables.

For each zoonotic disease, we sampled 10,000 iterations from the probability distribution of the parameters, and these samples were summed to give us values to estimate the DALY and zDALY for each zoonotic disease. The median and 95% confidence intervals of DALY and zDALY are reported as the 50, 2.5 and 97.5 percentiles of the 10,000 estimates of the DALY and zDALY. We performed the calculations in R version 3.6.0 using the packages MCMCpack, Prevalence, epiR and rjags.

For the burden of disease estimates, initially, most sensitivity analyses were undertaken for age-weighting and discount rate values, but it is not relevant since these are no longer used. Mathers et al. undertook a sensitivity analysis which essentially ranked the risk factors according to the % of the burden to see how much the total burden will be affected by the uncertainty in estimating any one risk factor [24]. We examined the relative contribution to the total burden by each disease and the relative contributions of the human health effects and the animal health equivalents using the method of Mathers et al. 2006 [24]. Thus, can be seen which diseases and sectors (human or animal health) have the greatest influence on the total burden and hence which would be affected by uncertainty in the data.

Meta-analysis

According to suitable data previously described, we performed a meta-analysis to get an overall effect size based on the prevalence of the following animal diseases: leishmaniasis, rabies, leptospirosis, ehrlichiosis, scabies, and babesiosis. For human diseases, we performed the meta-analysis of leishmaniasis, leptospirosis, and toxoplasmosis. We applied a random-effect model approach to pool the effect sizes in our meta-analysis (24). In this approach, the model parameters are random variables. We used the funnel plot and Duval & Tweedie’s trim-and-fill procedure to gauge publication bias (25). We used R packages: "meta", "metafor" and “forestplot" (18, 19).

Results

Systematic review

We identified 43,193 citations between 2000 and 2019 and excluded 43,018 by title and abstract screening, according to the exclusion criteria. We fully assessed 175 articles, resulting in 55 eligible manuscripts that were included in the qualitative synthesis (Fig 1). We performed the meta-analysis of disease prevalence based on 30 articles (those with more than two publications). The results are summarised in the S1 File. We also noticed a substantial increase in scientific publications and reports after 2010, illustrated in Fig 2.

Fig 2. Diseases publications per year (2000–2019).

Fig 2

Burden assessment

We estimated the DALYs of 20 zoonotic diseases and the zDALYs of 25 diseases in Paraguay reported in Table 1. Although the PAHO has recognized Paraguay as free from urban Chagas in 2018, we included it in this work since we found several cases reported in recent years, especially on chronic Chagas [25].

Table 1. Estimated DALYs, YLD and YLL, ALEs and zDALYs of burden of zoonoses in Paraguay with corresponding 95% uncertainty intervals.

Disease DALYs (95% CI) YLDs (95% CI) YLLs (95% CI) Species ALE (95% CI) zDALYs (95% CI)
Babesiosis Cattle 331 (213–450) 735 (491–991)
Horse 300 (191–410)
Dogs 104 (21–207)
Brucellosis 245 (49–505) 48 (6–60) 198 (0–463) 7,291 (6,930–7,678)
Cattle 6,978 (6,684–7,275)
Dogs 69 (14–124)
Campylobacteriosis 678 (144–2150) 64 (13–216) 614 (131–1,935) 678 (144–2,150)
Chagas 5,386 (5,281–5,587) 5,339 (5,254–5,428) 39 (1.1–231) 5,386 (5,281–5,587)
Colibacillosis 5,412 (1,991–15,531) 42 (13–92) 5,349 (1,977–15,465) Cattle (meat) 947 (0–2,209) 6,343 (2,826–16,651)
Cryptosporidiosis 688 (369–1259) 7 (4–13) 681 (365–1,248) Sheep 175 (120–230) 865 (543–1,443)
Cystic echinococcosis 375 (249–541) 181 (120–259) 194 (128–281) 375 (249–541)
Cysticercosis 388 (188–694) 388 (188–694)
Dermatophytosis (M. canis) 3 (2–3.4) 3 (2–3.4) 0 Cats 22 (18–27) 25 (21–30)
Dioctophymosis Dogs 95 (69–128) 95 (69–128)
Ehrlichiosis 132 (0.2–331) 0.3 (0.1–0.6) 132 (0–330) Dogs 437 (417–458) 565 (427–775)
Fascioliasis 0 0 0 Cattle 2970 (1,909–4,030) 3576 (2,512–4,639)
Sheep 606 (600–612)
Giardiasis 35 (34–36) 35 (34–36) 0 35 (34–36)
Hantavirus pulmonary syndrome 597 (278–933) 70 (54–88) 529 (198–859) 597 (278–933)
Leishmaniasis 2,129 (1,992–2,386) 2,014 (1,929–2,101) 110 (16–364) Dogs 445 (438–452) 2,576 (2,438–2,831)
Leptospirosis 671 (338–1,068) 10 (7–13) 661 (330–1057) 2,702 (2,293–3,150)
Cattle 1,743 (1,567–1,914)
Horse 292 (215–370)
Myiasis 9 (8.7–62) 9 (8.7–9.33) 6.4e-03 (6.3e-19–54) 9 (8.7–62)
Rabies 148 (114–189) 9 (8–10) 139 (105–180) 159 (125–199)
Cattle 10 (8–13)
Dogs 0.8 (0.7–0.9)
Salmonellosis (non–typhoidal) 949 (550–1475) 21 (18–26) 925 (529–1454) 949 (550–1475)
Scabies 228 (226–230) 228 (226–230) 0 Dogs 6 (2–10) 234 (230–239)
Staphylococcosis Cattle 6 (5–8) 6 (5–8)
Streptococcosis Cattle 3 (2–6) 3 (2–6)
Toxocariasis 15 (13–17) 15 (13–16) 0
80 (76–85)
Dogs 39 (37–41)
Cats 26 (25–28)
Toxoplasmosis 1,139 (1,003–1,342) 1,098 (979–1,232) 28 (0.34–200) 1,139 (100–342)
Bovine Tuberculosis 764 (707–823) 16 (15.9–17) 793 (397–1,256) Cattle 761 (687–842) 1,561 (1,162–2,027)
Total 18,424 (14,859–28,750) 408 (334–500) 10,034 (6,500–20,349) 43,123 (31,501–54,558) 62,178 (48,696–77,188)

The total DALYs represents 18,424 (14,859–28,750) and zDALYs 62,178 (48,696–77,188) (Table 1). The five pathogens causing the highest burden of disease in decreasing order of DALYs constitute E. coli, Trypanosoma cruzi, Leishmania spp, Toxoplasma gondii and Salmonella spp (Fig 3). They are responsible for 75% of the disease burden. Considering the ALEs, we obtained the following priority (in decreasing order) of pathogens: Brucella spp, Fasciola hepatica, Leishmania spp, Ehrlichia spp, and Leptospira spp (Table 1).

Fig 3. Relative burden of diseases in Paraguay: DALYs.

Fig 3

Regarding zDALYs, it suggests the following priority for zoonoses in Paraguay: Brucella spp, Escherichia coli, Trypanosoma cruzi, Fasciola hepatica, and Leptospira spp (Fig 4). These high priority diseases would have the greatest influence on the total burden. The burden of disease is also sensitive to the inclusion of ALEs into the total burden estimates (Fig 5).

Fig 4. Relative burden of diseases in Paraguay: zDALYs.

Fig 4

Fig 5. Relative burden of diseases in Paraguay: ALEs.

Fig 5

The number in the right upper corner of each rectangle represents the percentage of the corresponding disease in the total burden of diseases in Paraguay.

Meta-analysis

Table 2 shows the overall effect of each disease in the meta-analysis with its respective heterogeneity. Among all diseases in the meta-analysis, leishmaniasis in dogs has larger studies, so smaller standard errors.

Table 2. Summary of the meta-analysis.

Disease Overall effect (95% range) Tau2 I2 Q P–value
Leishmaniasis (animal) 0.33 (0.18–0.44) 0.041 (SE = 0.024) 99.85% 1788 < .0001
Leishmaniasis (human) 0.60 (0.29–0.91) 0.0740 (SE = 0.0758) 98.26% 58 < .0001
Brucellosis (animal) 0.03 (0.01–0.05) 0.0002 (SE = 0.0003) 99.80% 502 < .0001
Rabies (animal) 0.62 (0.20–1.03) 0.089 (SE = 0.13) 98.05% 51 < .0001
Leptospirosis (animal) 0.29 (0.12–0.46) 0.022 (SE = 0.023) 98.00% 80 < .0001
Leptospirosis (human) 0.06 (0.02–0.11) 0.0008 (SE = 0.0016) 70.46% 3.9 0.066
Ehrlichiosis (animal) 0.33 (0.09–0.57) 0.059 (SE = 0.0496) 99.71% 1875 < .0001
Scabies (animal) 0.11 (0.08–0.14) 0 (SE = 0.0020) 0.18% 1.9 0.3943
Babesiosis (animal) 0.21 (0.05–0.38) 0.025 (SE = 0.0230) 91.14% 21.11 < .0001
Toxoplasmosis 0.4 (0.09–0.71) 0.12 (SE = 0.088) 99.54% 1005 < .0001

Cochran’s Q test would be underpowered in cases of only two studies, such as rabies. We complement this extent with P-value to determine statistical heterogeneity.

We found a high heterogeneity (I2) across diseases, except scabies (but it is not significant).

We have no evidence of publication bias according to trim-and-fill procedures. See figures in S1 File.

Discussion

This work represents the first study to integrate the burden of zoonoses to society through DALYs and zDALYs (DALYs + ALEs), using real data from a country and complemented with conservative assumptions and stochastic modelling. According to the data available and our conservative estimations, zoonoses causing the major burden attributed directly to human diseases in Paraguay were colibacillosis, chagas, leishmaniasis, toxoplasmosis and salmonellosis, whereas the burden attributed to animal health losses (ALE) were brucellosis, fasciolosis, leishmaniasis, ehrlichiosis, and leptospirosis. The total disease burden, combining the burden attributed to human and animal burden of zoonotic diseases (zDALYs), has resulted in a change of priorities to brucellosis, colibacillosis, Chagas, fasciolosis and leptospirosis. We observed slightly different results according to the approach, being not opposed but complementary. A high burden of zoonotic diseases in animals means a higher risk of spreading disease to humans if preventive measures are not taken. Our dataset may suffer bias, namely the lack of available data from several geographical areas, diseases, vulnerable human populations, and neglected animal populations. We chose Monte Carlo method for stochastic modelling since it has been widely used to model the probability distribution of diseases due to its simplicity and flexibility. All the outputs consist of estimations based on data that we found through the systematic review.

We assume an underestimation of the total burden of zoonoses in Paraguay due to underreporting, under-ascertainment, underdiagnoses, and misdiagnoses. According to the Ministry of Public Health and Social Welfare, 8,971 of 31,258 deaths (28.7%) occurred without medical assistance in 2018, and similar cases happen every year. It is estimated that approximately 8,598 deaths per year are not registered in this country [3]. The cause of several of those deaths would have a high probability of under-reporting and under-ascertainment. Currently in Paraguay, zoonotic diseases with surveillance program lead by the Ministry of Health are bovine tuberculosis (National Program for Tuberculosis Control–PNCT), rabies (National Program of Zoonotic Diseases and National Rabies Center–CAN), Chagas, and leishmaniasis [26]. Our observation suggests underreporting from rural areas and inland Paraguay since most scientific articles correspond to the capital, Asunción (or metropolitan area), and the Central Department due to infrastructures and resources are mainly in this area. This illustrates the challenge of Paraguay, being a “centralized” country where most services (especially health, sciences, infrastructure, and resources) are in “Gran Asunción” and the Central department, leaving other departments and most rural areas neglected. Among studies outside Central Department, they are primarily contained in theses that are not easily accessible.

Another factor that would increase zoonosis under-ascertainment is illiteracy, in addition to contributing to the spread of zoonoses. Until 2018, 6% of the Paraguayan population remained illiterate [27]. The challenge to prevent zoonoses (especially foodborne diseases) is even more critical with an illiterate population. For instance in 2017, in Caaguazú (the main dairy producer and supplier of the country), 720 workers in 360 dairy herds were interviewed, 11.7% of them were illiterate, 64% stated that they did not know what brucellosis is, and 73.3% had no knowledge of how to prevent brucellosis. All of them also used to consume unpasteurized dairy by-products, mainly Paraguayan cheese [28]. Dairy farm owners, the Ministry of Health and the National Service of Quality and Animal Health (SENACSA) are primarily responsible for educating and sensitizing dairy workers to follow preventive practices. A law (Nr. 5804) established in 2017, imposes a national system to prevent labor risks in public and private entities [29]. Another issue is that workers from informal sectors are difficult to protect, so they are more vulnerable to injustices and diseases. In 2014, Paraguay registered 78% of informality rate being 88.6% in rural areas [30]. Informal sectors and poverty are frequently associated; approximately 5.9% of the Paraguayan population lived in poverty with an income below US$ 3.20 per day in 2018. This sector is the most vulnerable to hunger and diseases in the country [31].

Paraguay is a major food exporter, but malnutrition and hunger are still a concern. The Nutritional Food Surveillance System (SISVAN) in Paraguay reported that 11.4% of children under five years old suffer from chronic malnutrition. According to the FAO, undernourishment has increased over the last three years in this country as well as obesity. Based on the reported data, Paraguay has reduced poverty in the last years, increased food production, but undernourishment has also increased, proving that inequalities are part of this process. Currently, Paraguay is the third country in South America with the most inequalities after Brazil and Colombia [32].

Part of the zoonoses under-ascertainment would be related to demographic characteristics of the current Paraguayan population, which are only based on estimates since the national census carried out in 2012 was not completed as established. According to the international standards, a census should cover at least 90–95% of the population to be valid, but in Paraguay, it was only covered 74.4% of the population [33]. In addition, UNICEF estimated in 2013 that one in four children was not registered in Paraguay [34]. This condition increases our uncertainty of gauging the true impact of zoonoses in Paraguay. In our search, we observed that certain diagnoses are symptomatic (e.g., diarrhea, fever) rather than etiologic resulting in underdiagnosis of zoonoses. For instance, some reports on heart disease do not explain the etiologic cause, such as cases of “dilated cardiomyopathy” can be related to toxoplasmosis, Chagas, histoplasmosis, Lyme disease, rickettsial diseases, nutritional causes, among others [3537].

Misdiagnoses contribute to the underestimation due to several causes, such as cross-reactivity in diagnostic tests, e.g., serological leishmaniasis test [38,39]. Furthermore, not all people can afford a gold standard test, pay for a test repetition, or spend money on a second medical opinion. In case of leishmaniasis, positive pets are euthanized as a disposition of Ministry of Health in Paraguay. This represents an inconvenience when the definitive diagnosis is not confirmed by a gold standard test. As a result, the risk of facing other pathologies that we ignore is higher, and owners would lose needlessly lives of sick pets caused by other diseases, even non-zoonotic ones. The National Program of Zoonoses Control in Paraguay manages the diagnosis of leishmaniosis without a gold standard test. In 2016, as a routine exam of leishmaniosis in 6,672 dogs, using rK39 test, 1,586 resulted positive of which 1,038 positive dogs were culled without a gold standard test (as data reported in the 6th World Congress on Leishmaniasis). Taking into account that an rK39 test has a specificity of approximately 82% [40]; applying to the previous case, 851 dogs would have been culled unnecessarily by misdiagnosis.

In 2018, the Pan American Health Organization certified Paraguay as a “country free of domiciliary vector transmission of Chagas disease caused by Trypanosoma cruzi”. Despite this certification, Chagas represents one of the highest DALYs among zoonoses, especially those due to chronic Chagas. Moreover, we also found acute cases of Chagas, but the reports did not specify the transmission form (whether they were urban or sylvatic). Although Paraguay is a “country free of domiciliary vector transmission of Chagas”, the work related to this disease has not finished yet, and it must not be neglected. The WHO has estimated that approximately 6 to 7 million people are infected by T. cruzi worldwide, being the most affected Latin America. The triatomine bug is the vector that transmitted this disease. Chagas is not only considered a vector-borne disease but also a foodborne, bloodborne and congenital disease. Over centuries, the vector of Chagas or American trypanosomiasis has had an “evolution” or adaption, affecting at the beginning only wild mammals until also spreading to domestic mammals. In the past, Chagas was usual in rural areas but the urban cases have been increasing lately due mainly to the migration of infected people and anthropogenic activities that cause changes in the environment, increasing the risk of contact with the vector. Chagas or American trypanosomiasis is endemic in Latin America, and since 1990, the WHO has reported a reduction of transmissions. The most affected countries in South America are Brazil (174,194.22 DALYs), followed by Venezuela (27,037.40 DALYs), and Argentina (23,552.58 DALYs); Uruguay being the least affected (350.72 DALYs) based on the estimations of the Global Burden of Diseases [41]. Concerning Chagas in pets, there were a few studies of seroprevalence of Chagas in dogs in Latin America such as Argentina, Brazil, Chile, Colombia, Ecuador, Mexico, Venezuela but none in Paraguay [4248]. Several other mammals are a potential reservoir of Chagas. This is one of the reasons that eradication of this disease is not feasible, but its impact can be reduced not only by taking care of the animal and human health but also of the environment.

Foodborne zoonoses are the most frequently underreported since they principally cause diarrhea, and the treatments are mainly symptomatic. Paraguay registered 92,466 cases of diarrhea, being 83,140 classified as parasitic origin, 216 as food poisoning, and the remaining 9,110 were unspecified, according to Paraguay statistical yearbook 2017. Since diarrhea cases are frequently underreported, we used the estimates of diarrhea for Paraguay of 10.3 million (9.5 million—11 million) [49]. The most common bacterial zoonotic diseases were colibacillosis, non-typhoidal salmonellosis, and campylobacteriosis [50]. In Paraguay, colibacillosis cases were mainly reported in children and condemned beef in abattoirs through certain theses. Worldwide, Shiga toxin-producing E. coli (STEC) causes outbreaks mainly associated with undercooked or raw beef and its products; also, fecal contamination of vegetables and water. The reservoirs of E. coli are mainly cattle, goats, sheep, and deer. Other animals can be infected by this pathogen, such as dogs, cats, chicken, horses, pigs, rabbits, and turkeys. Besides being E. coli, a foodborne and waterborne disease, it can also be transmitted from person to person (through unwashed hands). The O157:H7 serotype is the main related to STEC and can cause hemolytic uremic syndrome (HUS). Lately, it seems a lack of updated outbreaks of E. coli in Latin America, whereas for the USA, the E. coli infections and outbreaks are constantly updated by the CDC. Therefore, we easily found more cases in the latter country.

In Paraguay, we only found cases of campylobacteriosis and salmonellosis in children. The WHO affirms that worldwide, campylobacteriosis and salmonellosis are one of the main causes of diarrhea of approximately 1 in 10 people yearly. Both foodborne and waterborne diseases usually cause mild symptoms, but they can generate some complications. In the case of campylobacteriosis, among its complications are bacteraemia, hepatitis, pancreatitis, and abortion. Rare cases manifest post-infection complications, including reactive arthritis for several months, Guillain-Barré syndrome, a polio-like form of paralysis. Campylobacter spp can be found in chicken, cattle, pigs, sheep, shellfish, ostriches, cats, and dogs. In the case of salmonellosis, the transmission can also be from person-to-person (fecal-oral route)–besides contaminated food. Salmonella spp is in chicken, cattle, pigs, dogs, cats, and wild animals such as birds and reptiles. Most of the cases of salmonellosis are considered sporadic, according to the WHO. E. coli, Campylobacter spp, and Salmonella spp have increased antimicrobial resistance as well as awareness about this issue. WHO and FAO formed an alliance to prevent foodborne diseases creating the International Network of Food Safety Authorities (INFOSAN) and to contribute to early detection and response they created an Advisory Group on Integrated Surveillance of Antimicrobial Resistance (AGISAR). Only at the end of 2018 was banned the sale of antibiotics without a prescription in Paraguay.

Within the parasitic causes of diarrhea, we identified giardiasis primarily in children [51]. Giardia intestinalis, lamblia or duodenalis is distributed worldwide, but with a low report because most infections are asymptomatic. Other parasitic zoonoses found in Paraguay with different symptoms were cystic echinococcosis (Echinococcus granulosus)–identified as surgically treated cases—and toxocariasis (Toxocara canis) in children. There are low reports of these diseases in Paraguay, only in five countries of South America (Argentina, Chile, Peru, Uruguay, and Brazil) cystic echinococcosis is considered endemic as stated by PAHO from 2009 to 2014. Paraguay is likely to have more echinococcosis cases than those found, but we have almost no data due to missing official reports or surveillance of this disease. Cases of giardiasis, echinococcosis, and toxocariasis can be prevented with good hygiene practices that are difficult to apply in deprived places without safe drinking water or lack of access to improved sanitation. The presence of stray dogs aggravates the risk in urban settings, and the same problem occurs in rural areas where certain farm animals are free to roam.

We did not find any report of cysticercosis in Paraguay. Although the Institute for Health Metrics and Evaluation (IHME) data estimated for cysticercosis a DALY of 2,531 (1,395–4,002), we consider this figure represents an overestimation. In 2018, only 359,604 pigs were registered in Paraguay, most of them corresponded to intensive farms with a low transmission risk. Based on the Foodborne Disease Burden Epidemiology Reference Group (FERG) methodology [52], we estimated 388 (188–694) DALYs instead, and recommend studies on neurocysticercosis, especially in areas that lack basic sanitation with free-range pigs. The PAHO estimates 14.9 million people with neurocysticercosis and 1.35 million with epilepsy due to this disease in Latin American and the Caribbean.

Another important parasitic foodborne disease among the priorities is fascioliasis or liver fluke (Fasciola hepatica) that was only reported in cattle and sheep in Paraguay, and it is the sole foodborne trematode infection registered in this country. We have not found human cases, but the risk is higher since the burden in animals is also high. The WHO affirms that about 2.4 million people are infected worldwide. The PAHO has declared that the most affected places by this disease in South America are the Andean highlands, mainly indigenous communities. Paraguay declared in its census that the estimated indigenous population was 112,848 people in 2012. However, there are no studies or surveillance in these communities about this disease.

With respect to leishmaniasis, it was difficult to identify if the reported cases were part of a coinfection or a primary infection. This information would help assess the extent of the specific disease burden, and how much is attributable to coinfection in patients with HIV or other immunosuppressive diseases [53]. Comorbidities of zoonoses were not common to find, but zoonotic infections such as toxoplasmosis and cryptosporidiosis with HIV co-infections were more frequent. According to the Global Health Data Exchange, the HIV burden of Paraguay was 69,576 (45,151–96,058) in 2017 [41], which is still higher than the estimated total burden of zoonoses in people and animals (zDALYs)—62,178 (48,696–77,188).

Toxoplasmosis in humans represents one of Paraguay’s most studied infectious diseases, especially in pregnant women and children (congenital toxoplasmosis, being the most common transmission form). Ocular toxoplasmosis is usually reported and, to a lesser extent, cerebral toxoplasmosis as co-infections mainly with HIV [54,55]. Cats are the primary host of Toxoplasma gondii, but it can infect a wide range of wild and domestic animals, including dogs. Toxoplasmosis is one of the diseases that can be mainly prevented with good hygienic practices, especially related to food.

We identified a high human tuberculosis incidence of 36.7 per 100,000 inhabitants in Paraguay [56]. Since zoonotic tuberculosis is mainly due to Mycobacterium bovis, we were interested in finding the infections caused by this pathogen. However, reports on human tuberculosis in Paraguay did not specify if they were caused by M. tuberculosis or M. bovis. For that reason, we used the estimates for the proportion of human tuberculosis due to M. bovis as a median of 0.3% (range 0%– 33.9%) in the Americas [13]–since Paraguay does not count for this proportion. Our estimates for bovine tuberculosis in human cases are 764 (707–823) DALYs and when we include all the cases of human tuberculosis the DALYs sum 25,460 (23,590–27,383) in Paraguay. We only considered the results of bovine tuberculosis because our focus was on zoonotic tuberculosis. In the future, it will be useful a study about tuberculosis as an anthropozoonosis to understand better the dynamic of this disease since there are almost no data globally about it, and this is an important approach in prevention.

Leptospirosis has a high prevalence, predominantly in the most disadvantaged areas and sectors of the country. In Paraguay, its incidence is related to flooding and living conditions of people in poverty (aggravated by the lack of infrastructure). Poverty is also associated with other zoonoses such as scabies, larva migrans, fungal skin diseases, vector-borne diseases (dengue and other arboviruses), and animal-related problems; namely animal bites and contact with poisonous animals [5759]. All these diseases mentioned above are underreported in Paraguay and low- and middle-income countries, underestimating their actual impact.

Hantaviruses (spreading mainly by rodents) present two main forms: hemorrhagic fever with renal syndrome (HFRS)—reported in Asia and Europe—and hantavirus pulmonary syndrome (HPS) in the Americas. The first registered outbreak of hantaviruses in Paraguay was in 1995 in the Chaco region [60,61]. As a result, most studies of HPS have been conducted in this region. Currently, hantavirus is considered endemic of Paraguay’s main ecological regions: the Chaco and the Atlantic Forest [62]. We notice certain fluctuations in hantaviruses case records, such as in 2011, 74 HPS cases, and none in 2012. In 2017, the Paraguayan statistical yearbook reported 10 HPS cases, whereas the WAHIS (World Animal Health Information System-OIE) did not specify the number of cases. We consider that the reporting systems need to be improved. Countries in Latin America such as Argentina, Chile, and Panama have registered increased cases of hantavirus infection in the last years.

With respect to animal diseases, Paraguay has larger amount of data about productive and reproductive animal diseases due to the traceability system of its livestock, playing a fundamental key in the economy of this country. We found more data on tuberculosis in cattle, leptospirosis in livestock, brucellosis in cattle, E. coli in beef products, rabies in various species and leishmaniosis in dogs. The animal health service in Paraguay (SENACSA) has registries at national level of rabies, tuberculosis, and brucellosis in cattle. We observed that cattle tested for tuberculosis (< 30,000 per year on average) are less than those tested for brucellosis (100,000 per year), being also another possible source of bias since some diseases are under surveillance more than others. As beef is the main exported meat, this country spends most of its resources for surveillance of cattle diseases and inevitably neglects other important species. In Paraguay, the least studied farm animals but with a considerable number per inhabitants are chicken (the most produced in the country) and pigs (the third largest local production, after cattle)—see Fig 6. In this aspect, it is crucial to adjust lenses and refocus the priorities to control diseases. Although livestock production is indeed a priority because it contributes to the country’s economic growth, it can also contribute to poverty if diseases of surrounding species are not controlled and prevented (this factor may also affect the economy directly and indirectly). Another risk consists of bushmeat consumed by a small proportion of the Paraguayan population. Some farmers breed wild animals for consumption without any veterinary control or regulations in the country. Also, activities related to hunting have a higher risk of zoonotic infections due to wild animals are not under food quality control. Therefore, more education and control are needed in this regard.

Fig 6. Diagram of the human and livestock population related to their proportion of publications and studies in Paraguay.

Fig 6

The zDALYs metric is intended to estimate the burden of zoonoses combining the burden of disease due to human and animal morbidity and mortality. For zDALYs, we consider the time lost in years of life that zoonotic diseases cause through human morbidity and mortality and the time trade-off to “recover” the animal loss due to those diseases. This makes estimates of the animal loss equivalents (ALE) on pets and wildlife challenging, because market values do not reflect the complex relationship between people and pets or wildlife, and their value in the ecosystem. For a robust estimation of the time trade-off, the moral and emotional factors require further research. This indicates that we may have underestimated the ALEs of zoonoses in pets; and for the moment, we cannot estimate ALEs for wild animals [6367]. For DALYs, the emotional value is not directly estimated but this is intrinsically included in the disability weight estimations.

We estimated for the first time the DALYs on ehrlichiosis, scabies, and dermatophytosis (Microsporum canis). These diseases affect animal and human life quality, and zoonoses such as ehrlichiosis can even be a fatal tick-borne disease if it is not treated. According to our estimations, ehrlichiosis causes the second highest burden in animals (mainly in dogs) but it is not even included among the disease priorities of Paraguay. In this country, the first ehrlichiosis cases reported in scientific studies were from 2013–2014 in dogs, and in the last years some cases in humans. This disease has been reported in most countries of South America.

Certain fungal diseases are considered sapronoses but to some extent its origin is related to animals, such as their feces. Fungal diseases are mainly manifested as coinfections in patients with immunosuppression. We found cases of Histoplasma capsulatum (endemic in Paraguay), Sporothrix schenckii complex (report of a family case transmitted by a cat), and Crytococcus neoformans with insufficient data to estimate DALYs [53,55,68,69]. Although histoplasmosis is considered endemic in South America, only in Brazil, Argentina, and Colombia have published studies about this disease transmitted mainly through bat and bird droppings and associated with HIV- positive patients [70].

Animal bites are not zoonoses but contribute to the burden of diseases through injuries causing zoonotic infections and deaths in cases not treated in time. In 2013, 5799 patients were treated for animal bites (dogs, cats, monkeys, bats and rodents) and in 2015, Paraguay registered 169 cases of snakebites (Bothrops, Crotalus, and other unidentified species) [7173]. In addition, snakebites cause significant losses to livestock in some countries. However, there is no evidence of how much livestock farmers lose due to snakebites in Paraguay [74], and how much these agricultural activities damage the environment. To study the impact of animal bites, surveillance is needed, especially for snakebites (venomous animal contact). Although the last case of human rabies was in 2004 and the last rabies cases in dogs were in 2015, Paraguay should be vigilant due to cases of rabies have recently been reported in Argentina. The PAHO reported in 2017 that canine rabies was still endemic in Bolivia (another country bordering Paraguay), Guatemala, Haiti and the Dominican Republic [75]. A study in 2011 in Paraguay, after two confirmed cases of rabies in dogs, demonstrated that 78% of pets have not been vaccinated (49/63) in Loma Plata, Chaco [76]. Unfortunately, unvaccinated animals are common in various parts of the country, especially in peripherical and rural areas, representing a higher risk for rabies outbreaks [77]. Despite no cases in humans, it remains a burden of rabies due to the use of post-exposure prophylaxis (PEP) following animal bites. Although the costs related to rabies are higher and more than the PEP, when we also consider the pre-exposure prophylaxis (PreEP) which varies according to the country. For Paraguay, we did not find official figures that represent that cost. We assume that if we include more costs for rabies prevention, the burden will increase as well as all the zoonotic diseases under surveillance in the country. However, we cannot add any extra amount that is not official since, in low and middle-income countries such as Paraguay, owners are in charge of the rabies vaccination and sterilization of their pets in most cases. Another source of rabies in livestock is wildlife, in particular bats and foxes [78]. Consequently, rabies incidence has increased in cattle [79]. In 2002, a case of human rabies transmitted by a bat was reported in Paraguay [80]. In the process of recent anthropogenic activities, wildlife has fewer natural habitats and Paraguay has lost biodiversity resulting in an increased risk of zoonoses [8183]. Paraguay has lost a vast area of its humid primary forest, being decreased by 31% from 2002 to 2020.

We only found a single outbreak of yellow fever in 2008 (after 40 years without reported cases of this disease) in the department of San Pedro, Caaguazú, and Central (San Lorenzo) [84,85]. The same year in San Pedro and Central Departments, researchers tested some primates for yellow fever (Cebus sp: 31) and (Alouatta caraya: 13), with negative results [86]. In South America, yellow fever is mainly sylvatic with non-human primates being the principal reservoir. This is in contrast to Africa where it is primarily human-to-human transmission, via vectors [87]. According to the latest report of the PAHO, only Bolivia, Peru, and Brazil registered cases of yellow fever, being the latter country with the highest seasonal cases in 2019 in South America [88].

Another disease present in Paraguay and poorly studied is tungiasis (Tunga penetrans and Tunga trimamillata). There is evidence that this disease has been present since pre-hispanic America [89]. However, it is ironically one of the least studied disease in this continent. The most affected population is in extreme poverty and lacks medical assistance [90]. Certain affected people remove Tunga penetrans themselves, leading to an underestimation of the incidence. Furthermore, tungiasis does not represent a disease of major concern, but it could lead to more severe infections such as tetanus. In Paraguay, myiasis is a frequent parasitic infestation in animals, especially in warm seasons (the predominant climate in this subtropical country). However, veterinarians usually do not report it. Regarding human cases of myiasis, we found some records, but they did not specify what part of the body was affected, making it difficult to properly estimate the disability weight. As a result, for the DALYs of myiasis estimations, we do not consider any sequelae since it varies considerably according to where the infestation is located. In South America besides Paraguay, a few cases of myiasis were reported in Argentina, Brazil, Equator, Peru, Uruguay, and Venezuela; some of the registered cases were about travellers returning from one of the mentioned countries [9194]. Other zoonoses that are rarely reported hence of low risk include sparganosis, and dirofilariosis [95,96]. Diphyllobothrioisis has not been reported in Paraguay, but it is present in neighbouring countries [97].

Among zoonotic influenza, Paraguay was also part of the swine influenza (H1N1) pandemic in 2009. Between 2009 and 2010, Paraguay reported 1025 cases and 47 deaths according to the PAHO. The vaccination helped to control this disease as well as a national response plan to an eventual influenza pandemic created in 2003. After 2010, it has not been published reports of outbreaks. Concerning avian influenza (H5N1), Paraguay has no reports as well as any country in South America.

Until now, the notifiable diseases that seem still absent in Paraguay or at least without reports are: Q fever, tularaemia, venezuelan equine encephalitis virus, rift valley fever—all of them are vectorial—and, nipah virus encephalomyelitis (non-vectorial). Concerning the epidemiological information of Q fever (Coxiella burnetii), it has been considered that its distribution is worldwide. However, Q fever is not commonly reported in neighboring countries of Paraguay either, there were only some cases reported in Brazil, and evidence of circulation in Argentina [98101]. Brazil identified more cases of Q fever when they started including this disease as part of the differential diagnoses list for flu-like diseases such as dengue [102]. Tularaemia has not been reported in South America thus far. Venezuelan equine encephalitis has been more diagnosed in the past in South America. One of the speculations is that it is misdiagnosed as dengue among other flu-like disease. The rift valley fever is more frequent in sub-Saharan Africa, and this disease has not been reported in the Americas up to the present. Whereas Nipah virus encephalomyelitis has been only reported in Asian countries and Ghana so far.

We observed that the most reported zoonoses are parasitic diseases. This might be because parasitic diseases are cheaper to diagnose compared to other diseases such as bacterial, viral, or fungal. Nevertheless, they consist of one of the more under-ascertained infections since parasites do not always cause symptoms (or alarming symptoms). We observed an increment of scientific publications from 2010, which is possibly due to the historical economic growth that Paraguay experimented the same year. This economic improvement was helped by higher exportation of agricultural products (mainly soy and beef), and likely influenced by the new presidential administration that started in 2008. After 2010, the GDP was slowly growing with some relapses in 2012, 2016 and 2019. Paraguay has had since 2014 a National Development Plan 2030 to align and achieve objectives of the “Sustainable development goals” promoted by the United Nations. Paraguay is working on three main axes supported by public politics to become a competitive and efficient country: 1) poverty reduction and social development, 2) inclusive economic growth, and 3) insertion of Paraguay in the world [103]. This plan gives Paraguayans some hope, despite the situation.

Conclusion

In terms of DALYs, we have shown that zoonoses represent a substantial proportion of the burden of infectious diseases in Paraguay. This is further illustrated when the direct effects on animal health are also included as zDALYs. The utility of the zDALY is further supported by comparing the prioritization of diseases in terms of DALYs and zDALYs. Thus, disease prioritization varies if we consider only the human burden of diseases (DALYs) compared to the additional burden when the effects of animal diseases are also included (zDALYs). This is a clear example that we need to focus on both human and animal diseases since the zDALY provides more holistic information for disease prioritization and prevention and confirms an initial step of the “One-Health” approach to disease control. Improving data quality remains a challenge in Paraguay and crucial to approach the Paraguayan Development Plan 2030. Our results show that interdepartmental and inter-institutional communication in this country, mainly between veterinary and medical sectors, then with other related institutions such as the environment should be improved. The registration systems of diseases at national and international levels must also be improved to avoid disparities and underreporting. This country should invest in a common database for zoonoses to ease the “decision-making” and policies based on evidence in health area, including more digitalization of resources (e.g., theses) to document what is already available.

We consider that the local list of "emerging diseases" and zoonoses priorities should be updated, adding diseases such as ehrlichiosis, among other vectorial diseases.

Although DALYs and zDALYs contribute to a more holistic approach to the health losses in a population, these health metrics continue to be a challenge in terms of social and environmental impacts to make them part of an actual One Health metric.

Supporting information

S1 Prisma checklist

(DOCX)

S1 Alternative Language Abstract

(DOCX)

S1 Table. List of selected zoonoses for the systematic review.

(XLSX)

S2 Table. Databases and other sources searched.

(XLSX)

S3 Table. Monte Carlo Analysis applied to modelling of zoonotic diseases.

(XLSX)

S4 Table. Auxiliary information of zoonoses used to estimate the YLL, YLD and DALYs.

(DOCX)

S1 Text. Complete search term used according to each database.

(DOCX)

S1 File

Fig A: Meta-analysis plots of zoonoses in Paraguay: forest plot and funnel plot of babesiosis in animals. Fig B: Meta-analysis plots of zoonoses in Paraguay: forest plot and funnel plot of ehrlichiosis in animals (dogs). Fig C: Meta-analysis plots of zoonoses in Paraguay: forest plot and funnel plot of leishmaniasis in animals (dogs). Fig D: Meta-analysis plots of zoonoses in Paraguay: forest plot and funnel plot of leishmaniasis in humans. Fig E: Meta-analysis plots of zoonoses in Paraguay: forest plot and funnel plot of leptospirosis in animals. Fig F: Meta-analysis plots of zoonoses in Paraguay: forest plot and funnel plot of leptospirosis in humans. Fig G: Meta-analysis plots of zoonoses in Paraguay: forest plot and funnel plot of rabies in animals. Fig H: Meta-analysis plots of zoonoses in Paraguay: forest plot and funnel plot of scabies in animals. Fig I: Meta-analysis plots of zoonoses in Paraguay: forest plot and funnel plot of toxoplasmosis in humans

(ZIP)

Acknowledgments

Liz thanks Romina Marini, Sergio Escobar, Arami Santacruz, and Florian Graf for answering her messages and send her their work. Paraguay needs more people like you, altruistic and concerned for a better situation. Aguyje!

Data Availability

All relevant data are within the manuscript and its Supporting Information files.

Funding Statement

LPNZ received research funding from BECAL (“Becas Don Carlos Antonio López”). BECAL (https://www.becal.gov.py/) funded this study partially as a part of the Paraguayan National Development Plan 2030. The funders had no role in study design, data collection, analysis, decision to publish, or manuscript preparation.

References

PLoS Negl Trop Dis. doi: 10.1371/journal.pntd.0009909.r001

Decision Letter 0

Christine A Petersen, Peter Horby

2 Apr 2021

Dear Mrs Noguera Zayas,

Thank you very much for submitting your manuscript "The Burden of Zoonoses in Paraguay: A Systematic Review" for consideration at PLOS Neglected Tropical Diseases. As with all papers reviewed by the journal, your manuscript was reviewed by members of the editorial board and by several independent reviewers. In light of the reviews (below this email), we would like to invite the resubmission of a significantly-revised version that takes into account the reviewers' comments.

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Reviewer's Responses to Questions

Key Review Criteria Required for Acceptance?

As you describe the new analyses required for acceptance, please consider the following:

Methods

-Are the objectives of the study clearly articulated with a clear testable hypothesis stated?

-Is the study design appropriate to address the stated objectives?

-Is the population clearly described and appropriate for the hypothesis being tested?

-Is the sample size sufficient to ensure adequate power to address the hypothesis being tested?

-Were correct statistical analysis used to support conclusions?

-Are there concerns about ethical or regulatory requirements being met?

Reviewer #1: The objectives are stated in L76-82.

The hypothesis is weakly stated as "zoonoses represent a substantial health burden in Paraguay" but to my liking this is not testable. Reference to GDP or other cost impact would have relevance for the costs of zoonoses.

The PRISM approach describes the population of literature surveyed, and demographics for Paraguay are described. The sample size is adequate; statistical testing was not applied nor appropriate.

No ethical or regulatory concerns.

Reviewer #2: objectives are clear and the study design is in agreement with the stated objectives

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Results

-Does the analysis presented match the analysis plan?

-Are the results clearly and completely presented?

-Are the figures (Tables, Images) of sufficient quality for clarity?

Reviewer #1: The analysis approaches the intended objective of the article (valuation of zoonoses) but there could be more made of the results.

For example, I don’t see how the results from calculating DALYs and ALEs are integrated or at least assessed in unison. In other words, how did these results from ALEs inform our knowledge of DALYs? Surely there is more of a story to tell other than adding to the total financial impact. If the authors feel this was addressed in the article, it needs to be summarized and highlighted in the Discussion towards the end or in the Conclusions.

For the most part the results are clear and the tables and images of sufficient quality for clarity.

However, I find that the discussion on the impact on livelihoods is thin other than to summarize that the diseases are present, recorded, and the authors can confirm that their findings reflect what is in the literature they cite (or in medical records from Paraguay). There is no wider discussion on the social burden of animal diseases in terms of direct or indirect influence on daily decision making that impacts livelihoods for example (e.g., avoidance of some species due disease risk could have economic impact on family income), or impact on family nutrition. Those are just two ideas, but those wider implications of the GBADs seem to be missing in the discussion.

I also wonder why the distributions presented in the results were not discussed in more detail. Are the authors satisfied with those distributions, do they match other findings, is there more particular work to do with regards to simulating distributions, what are the shortcomings of applying those distributions to policy work, etc. There was also no apparent effort to apply sensitivity analysis - a critical feature of robust simulation studies that is missing as far as I can tell.

Reviewer #2: results are clearley presented.

Fig 1 map is wrong and not very useful, other countries in the region are missing, labeling is hard to read. A more informative map should be not only more complete, but should incorporate geographical data correlating to the data discussed in the text. Paraguayan regions are mentioned throughout the manuscript and it would be helpful for the reader to easily locate them on this map.

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Conclusions

-Are the conclusions supported by the data presented?

-Are the limitations of analysis clearly described?

-Do the authors discuss how these data can be helpful to advance our understanding of the topic under study?

-Is public health relevance addressed?

Reviewer #1: See some of my previous comments.

Conclusions are very general and supported by the data but seem cursory relative to what else might be addressed.

Use of these data to advance our understanding falls short of what is promised in L79-82 although this is woven into the discussion of misdiagnosis, under estimation, under ascertainment and (this was not clearly noted but was suggested) access to health care for marginalized and remote communities. Those are all good points that need to be brought to conclusion - can these results influence policy in some way to correct those problems?

Public health relevance is addressed throughout the paper.

Reviewer #2: (No Response)

--------------------

Editorial and Data Presentation Modifications?

Use this section for editorial suggestions as well as relatively minor modifications of existing data that would enhance clarity. If the only modifications needed are minor and/or editorial, you may wish to recommend “Minor Revision” or “Accept”.

Reviewer #1: Grammar and punctuation:

There are many small punctuation and occasional grammatical errors that should be addressed by a fluent speaker/writer of English. For example, line 11 is not a proper sentence, “One Health” is not hyphenated and should be capitalized, numbers greater than 100 should use commas, “31 thousand” etc. should be written as 31,000 (million is acceptable as a word), “/year” in the text should be spelled out as “per year”, disease names are not capitalized unless proper nouns are used, “decision making” is not hyphenated, “12 %” should have no space as in “12%”, “potential loses” should read “potential losses”, “and in less quantity sheep” is awkward and simply not stated, line 68 probably refers to livestock product exports but needs to state so, conjunctions and prepositions are missing or incorrect throughout the document, etc. There are far too many edits to list them all – please have someone review and correct these errors.

Reviewer #2: (No Response)

--------------------

Summary and General Comments

Use this section to provide overall comments, discuss strengths/weaknesses of the study, novelty, significance, general execution and scholarship. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. If requesting major revision, please articulate the new experiments that are needed.

Reviewer #1: This research has promise to present more robust and extended findings if my comments are taken into consideration. As it stands is presents more as a catalogue of estimations with reflection on which diseases are already noted as zoonotic and a burden in Paraguay. That seems to be the overall weakness of the paper.

The strength is the wide search for data in the literature and an effort to model disease distributions and impact using simulation.

L57: I don’t think Fig 1 is particularly helpful considering how much page space this colour illustration occupies. Readers will either know where Paraguay is located, or can find this quickly on the internet. There is nothing to indicate livestock density on this map or relative economic value compared to neighbours, which might have made it more interesting.

L85: A few of the zoonoses chosen could be more narrowly defined (E. coli, tuberculosis, and avian influenza for example). You do note that for some diseases this is not available but surely you there is some reference to these distinctions in the literature. For a paper that addresses zoonoses, this seems a critical point of interest. Tuberculosis from M. bovis vs. M. tuberculosis, or HPAI vs. non-pathogenic AI will change weighting factors and output measurements. This should be addressed in general somewhere in your article (cf. my comment L148).

L98: Your PRISMA approach is a well accepted approach and you have conducted what appears to be an extensive search. However, with so many diseases listed compared to the number of articles, I wonder if you might consider a figure that shows clusters of disease over time (e.g., bacterial, viral, common, rare, self-limiting, fatal without intervention, etc.)

L133, L146: Equations would help here. These are not complicated concepts but the explanations are hard to follow for someone not familiar with the equations.

L148: Further to my comment L85, do you not have this distinction for Paraguay? It would be good to know if that is the case. Using all of the Americas as a reference is a pretty wide reference base.

L170: I am not sure from reference where your pet values came from – no mention pet market sources or of social media that I can see in your S2 info. (The livestock sources seem reliable and reasonable.)

L172: With respect to simulation, your terminology gets a bit sloppy. Technically, uncertainty cannot be estimated because you do not know either probability or outcome, but you could estimate risk (the product of probability and outcome). What are you estimating? Risk of …? This needs to be stated clearly in the first sentence of the paragraph starting at L172.

L172: Why did you decide on beta, gamma, etc. distributions? Expert opinion, best fit (and then how and of what other distributions), past experience? Why were some diseases modeled under two or more distributions and others only one? A lot of assumptions seem to be missing here. Seed, underlying estimator (MLE, etc.), etc.

L174: I believe what you state as “draws” should be iterations.

L182: Is this in reference to data you refer to previously or is this a new reference? Please clarify and if new, information regarding those sources is needed.

L184: Why were these particular diseases selected?

L185: Is the “random effect model” approach something all readers should know? Some clarity is needed here.

L195: Unless you tested for significance, replace that word with “substantial”. Is there a reason to account for this substantial increase?

L234: … as well as differentiation between bacterial species and their relative impact on human vs. animal populations. It seems to me this is the Achilles heel of the research – interesting from a global conclusion but weak specificity of local conclusions (to use the modeling reference to global vs. local optima points).

L241: Can this not be incorporated into your estimation of the impact of “tuberculosis” somehow, or perhaps model both TB and bTB? I see you have approached that notion in L337-338.

L249-252: I don’t see the point of this paragraph if these individuals emigrated (out of Paraguay). Please add clarification of relevance.

L373: Agreed, but neither is the emotional value of human life incorporated into DALYs. As for wild animals, you could have estimated marketable valuation or value based on economic substitution.

L392-400: A substantial burden from rabies is the cost to the public sector or PEP treatment as well as dog capture, neuter, vaccinate, and release programs. Lots of articles in the rabies literature to draw on from S. America that you could use just to note that is a cost not incorporated in your study. You might start with: de Carval et al. (2018) Rabies in the Americas: 1998-2014. PNTD. https://doi.org/10.1371/journal.pntd.0006271. Chile is now considered free of dog rabies, but it took a strong and costly campaign to get there – should be data on that too.

Reviewer #2: In this paper, the authors assess the burden of zoonoses in Paraguay. They address the influence of zoonoses on both human and animal health and its socioeconomic impact, also they discuss its national/international importance in terms of economic interest and healthcare priorities.

A systematic review is performed based on the previously reported systematic review and meta analyses: PRISMA. Obtained data was used to estimate DALY and zDALY, useful parameters to assess the burden of zoonoses in Paraguay.

I would like to discuss some points that were not clear for me: In cases of comorbidity due to more than one infection, how was the employed criteria?

I agree that “The five most important pathogens of DALYs in decreasing order constitutes E. coli, Trypanosoma cruzi, Leishmania spp, Toxoplasma gondii and Campylobacter spp.. They are responsible for 75% of the disease burden.” However, E. coli and T. cruzi are by far, the most important pathogens, they should be discussed separately since these two pathogens represent a half of the total disease burden.

Should be considered T. cruzi to discuss zDALY? As far as I know, Chagas disease doesn’t affect cattle, poultry, pigs, sheep, horses, goats or any other economically important animal.

More detail is necessary to establish Paraguay as a unique case for this study. When appropriate, available information from other countries should be included for comparison. If it is the purpose of the authors, as stated, to uncover clues in order to set disease control priorities, cross-country comparisons become even more essential. What is the burden of the analyzed zoonoses in neighboring countries? What is the disease burden in non-neighboring countries which share the same type of economy heavily skewed towards agricultural production?

Minor comments:

Large sections (particularly in the introduction) should be revised for grammar and syntax. Oxford commas are inconsistently used throughout.

Line 11: Change “this difficult to gauge”… by “it is difficult to gauge…”

Line 65: losses

Line 166: Was the economic value of cattle estimated in export prices or prices for the local market, or a combination of both?

Line 167: “In respect of pets” change by “with respect to pets”

257. Replace “have been interviewed” with “were interviewed”

262. It would be useful to mention the legal status of disclosure of risks to workers in the country in this context.

Line 285: lose

Line 383: Discussion of animal bites seems out of place outside of the context of rabies.

--------------------

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Reviewer #1: No

Reviewer #2: Yes: Leticia Perez-Diaz

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PLoS Negl Trop Dis. doi: 10.1371/journal.pntd.0009909.r003

Decision Letter 1

Christine A Petersen, Peter Horby

3 Sep 2021

Dear Mrs Noguera Zayas,

Thank you very much for submitting your manuscript "The Burden of Zoonoses in Paraguay: A Systematic Review" for consideration at PLOS Neglected Tropical Diseases. As with all papers reviewed by the journal, your manuscript was reviewed by members of the editorial board and by several independent reviewers. The reviewers appreciated the attention to an important topic. Based on the reviews, we are likely to accept this manuscript for publication, providing that you modify the manuscript according to the review recommendations.

Please prepare and submit your revised manuscript within 30 days. If you anticipate any delay, please let us know the expected resubmission date by replying to this email.

When you are ready to resubmit, please upload the following:

[1] A letter containing a detailed list of your responses to all review comments, and a description of the changes you have made in the manuscript.

Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out

[2] Two versions of the revised manuscript: one with either highlights or tracked changes denoting where the text has been changed; the other a clean version (uploaded as the manuscript file).

Important additional instructions are given below your reviewer comments.

Thank you again for your submission to our journal. We hope that our editorial process has been constructive so far, and we welcome your feedback at any time. Please don't hesitate to contact us if you have any questions or comments.

Sincerely,

Peter Horby

Associate Editor

PLOS Neglected Tropical Diseases

Christine Petersen

Deputy Editor

PLOS Neglected Tropical Diseases

***********************

Reviewer's Responses to Questions

Key Review Criteria Required for Acceptance?

As you describe the new analyses required for acceptance, please consider the following:

Methods

-Are the objectives of the study clearly articulated with a clear testable hypothesis stated?

-Is the study design appropriate to address the stated objectives?

-Is the population clearly described and appropriate for the hypothesis being tested?

-Is the sample size sufficient to ensure adequate power to address the hypothesis being tested?

-Were correct statistical analysis used to support conclusions?

-Are there concerns about ethical or regulatory requirements being met?

Reviewer #1: I am finding it difficult to locate the changes, but I think I succeeded. The version I was sent has no changes indicated in any way. Nor do the authors indicate on what line(s) changes were incorporated in the new manuscript. This would have been helpful.

I will refer to my previous comments and author replies.

The authors' response focusing on GDP misses my earlier point - I did not suggest you measure GDP (which, by the way, is an economic metric, not monetary metric). I suggest you need to incorporate some sort of standardized cost measure which would be consistent with your frequent reference to the economic value and market valuation of animals and their use. This to me is one of the weaknesses in general of adopting DALYs or modified DALYs - animals are property with market value but people are not.

This boils down to a philosophical and intellectual debate regarding how to measure and incorporate market valuation. DALYs and your zDALY certainly help, but the wider social impact of the market losses is not captured (e.g., food security and all the other SDGs). I suggest you simply add a line that notes that somewhere in your paper (end of Discussion or Conclusions perhaps). No one has achieved that in a single index and that is your challenge.

Reviewer #2: objectives are clear and the study design is in agreement with the stated objectives. The population is adequate to test the hypothesis.

In the new version submitted, the methodology employed is better explained which makes it clearer.

--------------------

Results

-Does the analysis presented match the analysis plan?

-Are the results clearly and completely presented?

-Are the figures (Tables, Images) of sufficient quality for clarity?

Reviewer #1: Again, it's quite difficult to find the specific changes without either TrackChanges or author reference to the line(s) where changes were made. In future, I suggest the lead author indicate to reviewers what lines in the new manuscript incorporate changes.

I cannot see where you discuss the social burden of disease in your discussion or conclusion. It may well be beyond the scope of your study, but I do think it bears mentioning as a weakness of current methods of estimation of GBADs. If not already incorporated, please add to the Discussion in a clearly stated sentence. There are many such methods used in development/ growth/ welfare economics, but just mentioning that weakness (absence) I think is important.

Reviewer #2: to clarify, new graph and figure were added to show clusters of disease (publications) from 2000 to 2020 and the relative impact of diseases in the country (DALY, ALE and zDALY)

--------------------

Conclusions

-Are the conclusions supported by the data presented?

-Are the limitations of analysis clearly described?

-Do the authors discuss how these data can be helpful to advance our understanding of the topic under study?

-Is public health relevance addressed?

Reviewer #1: I think your Conclusions is better stated in your revised manuscript.

Reviewer #2: Conclusions were rewritten and looks more clear. They are supported by presented data

--------------------

Editorial and Data Presentation Modifications?

Use this section for editorial suggestions as well as relatively minor modifications of existing data that would enhance clarity. If the only modifications needed are minor and/or editorial, you may wish to recommend “Minor Revision” or “Accept”.

Reviewer #1: (No Response)

Reviewer #2: (No Response)

--------------------

Summary and General Comments

Use this section to provide overall comments, discuss strengths/weaknesses of the study, novelty, significance, general execution and scholarship. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. If requesting major revision, please articulate the new experiments that are needed.

Reviewer #1: Other changes to the manuscript (e.g., added graph, equations, etc.) have improved the manuscript.

Reviewer #2: In this paper, the authors quantify the impact of different pathogens in human and animal disease burden in Paraguay, through the estimation of DALY and DALYz parameters respectively.

The methodology is now better explained and clearer in this new version of the manuscript.

The Discussion Section has been also improved. The authors well discuss the limitations of the methods and the different possible causes of underestimation or overestimation of the presented data. Moreover, each one of the pathogens causing the studied zoonoses are now described in the discussion. In this context, I think that the discussion is now quite long (too much). The authors should focus on the description of the most relevant zoonoses (the high priority) in the study, those with higher DALY and DALYz values.

The study of the burden of zoonosis diseases and the interconnection between people and animals will help to develop optimal health outcomes, prioritizing those illness with higher impact in human and animal health minimizing economic losses. For that reason I think that this work is very interesting to be published but I strongly suggest shortening the section Discussion to accept the manuscript.

minor comments:

E coli must be defined by Escherichia coli by the first time

Lane 234. From results in Table 1, one the most relevant pathogens, considering the zDALY calculation was T. cruzi, however, there is no ALE data in the table (from dogs) so in this case, zDALY is the same as DALY. Is zDALY discussion relevant in this case?

In figure 3a, 3b and 3c, What is the meaning of the numbers in the right upper corner? are they percentages of the estimated total DALY, Ale and zDALY respectively? Please, explain

--------------------

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Reviewer #1: Yes: David C. Hall

Reviewer #2: Yes: Leticia Pérez-Díaz

Figure Files:

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email us at figures@plos.org.

Data Requirements:

Please note that, as a condition of publication, PLOS' data policy requires that you make available all data used to draw the conclusions outlined in your manuscript. Data must be deposited in an appropriate repository, included within the body of the manuscript, or uploaded as supporting information. This includes all numerical values that were used to generate graphs, histograms etc.. For an example see here: http://www.plosbiology.org/article/info%3Adoi%2F10.1371%2Fjournal.pbio.1001908#s5.

Reproducibility:

To enhance the reproducibility of your results, we recommend that you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. Additionally, PLOS ONE offers an option to publish peer-reviewed clinical study protocols. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols

References

Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article's retracted status in the References list and also include a citation and full reference for the retraction notice.

PLoS Negl Trop Dis. doi: 10.1371/journal.pntd.0009909.r005

Decision Letter 2

Christine A Petersen

15 Oct 2021

Dear Mrs Noguera Zayas,

We are pleased to inform you that your manuscript 'The Burden of Zoonoses in Paraguay: A Systematic Review' has been provisionally accepted for publication in PLOS Neglected Tropical Diseases.

Before your manuscript can be formally accepted you will need to complete some formatting changes, which you will receive in a follow up email. A member of our team will be in touch with a set of requests.

Please note that your manuscript will not be scheduled for publication until you have made the required changes, so a swift response is appreciated.

IMPORTANT: The editorial review process is now complete. PLOS will only permit corrections to spelling, formatting or significant scientific errors from this point onwards. Requests for major changes, or any which affect the scientific understanding of your work, will cause delays to the publication date of your manuscript.

Should you, your institution's press office or the journal office choose to press release your paper, you will automatically be opted out of early publication. We ask that you notify us now if you or your institution is planning to press release the article. All press must be co-ordinated with PLOS.

Thank you again for supporting Open Access publishing; we are looking forward to publishing your work in PLOS Neglected Tropical Diseases.

Best regards,

Christine A Petersen

Deputy Editor

PLOS Neglected Tropical Diseases

Christine Petersen

Deputy Editor

PLOS Neglected Tropical Diseases

***********************************************************

Reviewer's Responses to Questions

Key Review Criteria Required for Acceptance?

As you describe the new analyses required for acceptance, please consider the following:

Methods

-Are the objectives of the study clearly articulated with a clear testable hypothesis stated?

-Is the study design appropriate to address the stated objectives?

-Is the population clearly described and appropriate for the hypothesis being tested?

-Is the sample size sufficient to ensure adequate power to address the hypothesis being tested?

-Were correct statistical analysis used to support conclusions?

-Are there concerns about ethical or regulatory requirements being met?

Reviewer #1: (No Response)

**********

Results

-Does the analysis presented match the analysis plan?

-Are the results clearly and completely presented?

-Are the figures (Tables, Images) of sufficient quality for clarity?

Reviewer #1: (No Response)

**********

Conclusions

-Are the conclusions supported by the data presented?

-Are the limitations of analysis clearly described?

-Do the authors discuss how these data can be helpful to advance our understanding of the topic under study?

-Is public health relevance addressed?

Reviewer #1: (No Response)

**********

Editorial and Data Presentation Modifications?

Use this section for editorial suggestions as well as relatively minor modifications of existing data that would enhance clarity. If the only modifications needed are minor and/or editorial, you may wish to recommend “Minor Revision” or “Accept”.

Reviewer #1: (No Response)

**********

Summary and General Comments

Use this section to provide overall comments, discuss strengths/weaknesses of the study, novelty, significance, general execution and scholarship. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. If requesting major revision, please articulate the new experiments that are needed.

Reviewer #1: (No Response)

**********

PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

PLoS Negl Trop Dis. doi: 10.1371/journal.pntd.0009909.r006

Acceptance letter

Christine A Petersen

28 Oct 2021

Dear Mrs Noguera Zayas,

We are delighted to inform you that your manuscript, "The Burden of Zoonoses in Paraguay: A Systematic Review," has been formally accepted for publication in PLOS Neglected Tropical Diseases.

We have now passed your article onto the PLOS Production Department who will complete the rest of the publication process. All authors will receive a confirmation email upon publication.

The corresponding author will soon be receiving a typeset proof for review, to ensure errors have not been introduced during production. Please review the PDF proof of your manuscript carefully, as this is the last chance to correct any scientific or type-setting errors. Please note that major changes, or those which affect the scientific understanding of the work, will likely cause delays to the publication date of your manuscript. Note: Proofs for Front Matter articles (Editorial, Viewpoint, Symposium, Review, etc...) are generated on a different schedule and may not be made available as quickly.

Soon after your final files are uploaded, the early version of your manuscript will be published online unless you opted out of this process. The date of the early version will be your article's publication date. The final article will be published to the same URL, and all versions of the paper will be accessible to readers.

Thank you again for supporting open-access publishing; we are looking forward to publishing your work in PLOS Neglected Tropical Diseases.

Best regards,

Shaden Kamhawi

co-Editor-in-Chief

PLOS Neglected Tropical Diseases

Paul Brindley

co-Editor-in-Chief

PLOS Neglected Tropical Diseases

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 Prisma checklist

    (DOCX)

    S1 Alternative Language Abstract

    (DOCX)

    S1 Table. List of selected zoonoses for the systematic review.

    (XLSX)

    S2 Table. Databases and other sources searched.

    (XLSX)

    S3 Table. Monte Carlo Analysis applied to modelling of zoonotic diseases.

    (XLSX)

    S4 Table. Auxiliary information of zoonoses used to estimate the YLL, YLD and DALYs.

    (DOCX)

    S1 Text. Complete search term used according to each database.

    (DOCX)

    S1 File

    Fig A: Meta-analysis plots of zoonoses in Paraguay: forest plot and funnel plot of babesiosis in animals. Fig B: Meta-analysis plots of zoonoses in Paraguay: forest plot and funnel plot of ehrlichiosis in animals (dogs). Fig C: Meta-analysis plots of zoonoses in Paraguay: forest plot and funnel plot of leishmaniasis in animals (dogs). Fig D: Meta-analysis plots of zoonoses in Paraguay: forest plot and funnel plot of leishmaniasis in humans. Fig E: Meta-analysis plots of zoonoses in Paraguay: forest plot and funnel plot of leptospirosis in animals. Fig F: Meta-analysis plots of zoonoses in Paraguay: forest plot and funnel plot of leptospirosis in humans. Fig G: Meta-analysis plots of zoonoses in Paraguay: forest plot and funnel plot of rabies in animals. Fig H: Meta-analysis plots of zoonoses in Paraguay: forest plot and funnel plot of scabies in animals. Fig I: Meta-analysis plots of zoonoses in Paraguay: forest plot and funnel plot of toxoplasmosis in humans

    (ZIP)

    Attachment

    Submitted filename: Response to reviewers BZD Paraguay.docx

    Attachment

    Submitted filename: Response to reviewers BDZ in Paraguay.docx

    Data Availability Statement

    All relevant data are within the manuscript and its Supporting Information files.


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