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Abstract BackgroundTrypanosomaare protozoa parasites that infect animals and can cause economic losses in cattle production.Trypanosomalive in the blood and are transmitted by hematophagous insects, such as flies in the genusTabanus.Using ecological niche models, we explored the current geography of six commonTabanusspecies in Brazil, which are considered vectors ofTrypanosoma vivaxandTr. evansiin the Neotropics. MethodsWe used georeferenced data and biotic and abiotic variables integrated using a fundamental ecological niche modeling approach. Modeling results from sixTabanusspecies were used to identify risk areas ofTrypanosomatransmission in Latin America accounting for area predicted, landscape conditions, and density of livestock. We performed Jaccard, Schoener, and Hellinger metrics to indicate the ecological niche similarities of pairs ofTabanusspecies to identify known and likely vectors overlapping in distribution across geographies. ResultsOur results revealed significant ecological niche similarities for twoTabanusspecies (T. pungensandT. sorbillans), whereasT. triangulumandT. importunushave low ecological similarity. Ecological niche models predicted risk ofTrypanosomatransmission across Neotropical countries, with the highest risk in southern South America, Venezuela, and central Mexico. ConclusionsMore than 1.6 billion cattle and 38 million horses are under a threat category for infection risk. Furthermore, we identified specific areas and livestock populations at high risk of trypanosomiasis in Latin America. This study reveals the areas, landscapes, and populations at risk ofTrypanosomainfections in livestock in the Americas. Graphical Abstract 

Abstract Interactions among humans, livestock, and wildlife within disturbed ecosystems, such as those impacted by climate change, can facilitate pathogen spillover transmission and increase disease emergence risks. The study of future climate change impacts on the distribution of free-ranging bats is therefore relevant for forecasting potential disease burden. This study used current and future climate data and historic occurrence locations of the vampire bat speciesDesmodus rotundus, a reservoir of the rabies virus to assess the potential impacts of climate change on disease reservoir distribution. Analyses included a comprehensive comparison of different climate change periods, carbon emission scenarios, and global circulation models (GCMs) on final model outputs. Models revealed that, although climatic scenarios and GCMs used have a significant influence on model outputs, there was a consistent signal of range expansion across the future climates analyzed. Areas suitable forD. rotundusrange expansion include the southern United States and south-central portions of Argentina and Chile. Certain areas in the Amazon Rainforest, which currently rests at the geographic center ofD. rotundus’ range, may become climatically unsuitable for this species within the context of niche conservatism. While the impacts of rabies virus transmitted byD. rotunduson livestock are well known, an expansion ofD. rotundusinto novel areas may impact new mammalian species and livestock with unexpected consequences. Some areas in the Americas may benefit from an assessment of their preparedness to deal with an expectedD. rotundusrange expansion. 

ABSTRACT BackgroundIn Latin America, there is a high incidence of vampire bat‐transmitted rabies in cattle causing increased mortality of livestock, which heavily impacts the agricultural sector. Anticoagulants‐based control methods for the common vampire bat (Desmodus rotundus) have been employed continuously since the 1970s with various methods of application, presentations, doses and active ingredients. Studies from half a century ago still serve as a reference for the current use of anticoagulants for bat‐borne rabies control in Latin America. The objective of this study was to structurally and bibliometrically review literature on the use of anticoagulants for the control ofD. rotundusas a means of rabies control. Materials & MethodsScientific literature on the use of anticoagulant products forD. rotunduscontrol was obtained, reviewed and analysed. Articles were retrieved from Scopus and Web of Science databases. Research articles from 1971 to 2021 in Spanish, English and Portuguese were included in the review. Results were visualised using RStudio, Bibliometrix and VOSviewer. ResultsThe body of literature indicates effectiveness of up to 100% in the use of anticoagulants to induce bat mortality. The effectiveness of anticoagulants for rabies control, however, remains uncertain. No evidence was found to support or refute the use of anticoagulants for rabies control. DiscussionInstead, literature suggests that disturbing bat colonies increases rabies prevalence. This finding suggests that anticoagulants may have the opposite intended effect on rabies control and highlights the importance of further research on the practical methods for bat‐borne rabies prevention. ConclusionField experimental studies that include control groups over areas and periods that account forD. rotundusecology are needed to determine the effectiveness of anticoagulants for rabies control in livestock. In conclusion, the use of anticoagulants for rabies control is questionable. 

Abstract BackgroundCache Valley virus (CVV) is an understudiedOrthobunyaviruswith a high spillover transmission potential due to its wide geographical distribution and large number of associated hosts and vectors. Although CVV is known to be widely distributed throughout North America, no studies have explored its geography or employed computational methods to explore the mammal and mosquito species likely participating in the CVV sylvatic cycle. MethodsWe used a literature review and online databases to compile locality data for CVV and its potential vectors and hosts. We linked location data points with climatic data via ecological niche modeling to estimate the geographical range of CVV and hotspots of transmission risk. We used background similarity tests to identify likely CVV mosquito vectors and mammal hosts to detect ecological signals from CVV sylvatic transmission. ResultsCVV distribution maps revealed a widespread potential viral occurrence throughout North America. Ecological niche models identified areas with climate, vectors, and hosts suitable to maintain CVV transmission. Our background similarity tests identifiedAedes vexans,Culiseta inornata, andCulex tarsalisas the most likely vectors andOdocoileus virginianus(white-tailed deer) as the most likely host sustaining sylvatic transmission. ConclusionsCVV has a continental-level, widespread transmission potential. Large areas of North America have suitable climate, vectors, and hosts for CVV emergence, establishment, and spread. We identified geographical hotspots that have no confirmed CVV reports to date and, in view of CVV misdiagnosis or underreporting, can guide future surveillance to specific localities and species. Graphical Abstract 

Abstract In North America, the rodent‐borne hantavirus pulmonary syndrome is predominantly caused by the Sin Nombre virus, typically associated with the deer mousePeromyscus maniculatus. Utilizing data from the National Ecological Observatory Network (NEON) hantavirus program, we assessed factors that may influence the spatial and temporal distribution of hantavirus in rodent populations across the United States. Between 2014 and 2019, the NEON hantavirus program conducted 104,379 small mammal captures and collected 14,004 blood samples from 49 species at 45 field sites. Our study identified 296 seropositive samples across 15 rodent species, including 8Peromyscusspecies. We describe six new species with hantavirus seropositive samples not previously reported as hantavirus hosts. The highest number of seropositive samples was obtained fromPe. maniculatus(n = 116; 2.9% seroprevalence), followed byPeromyscus leucopus(n = 96; 2.8%) andMicrotus pennsylvanicus(n = 33; 4.2%). Hantavirus seroprevalence showed an uneven spatial distribution, with the highest seroprevalence found in Virginia (7.8%, 99 seropositive samples), Colorado (5.7%,n = 37), and Texas (4.8%,n = 19). Hantavirus seropositive samples were obtained from 32 sites, 10 of which presented seropositive samples in species other thanPe. maniculatusorPe. leucopus. Seroprevalence was inconsistent across years but showed intra‐annual bimodal trends, and inPe. maniculatusandPe. leucopus, the number of captures correlated with seroprevalence in the following months. Seroprevalence was higher in adult males, with only one seropositive sample obtained from a juvenilePeromyscus truei. Higher body mass, presence of scrotal testes, and nonpregnant status were associated with higher seropositivity. The NEON dataset, derived from a multiyear and structured surveillance system, revealed the extensive distribution of hantavirus across broad taxonomic and environmental ranges. Future research should consider winter season surveillance and continued analyses of stored samples for a comprehensive spatiotemporal study of hantavirus circulation in wildlife. Global changes are expected to affect the dynamics of rodent populations by affecting their availability of resources and demography and, consequently, may modify transmission rates of rodent‐borne zoonotic pathogens such as hantavirus. This study can be considered a baseline to assess hantavirus patterns across host taxa, geographies, and seasons in the United States. 

Abstract Pathogen spillover corresponds to the transmission of a pathogen or parasite from an original host species to a novel host species, preluding disease emergence. Understanding the interacting factors that lead to pathogen transmission in a zoonotic cycle could help identify novel hosts of pathogens and the patterns that lead to disease emergence. We hypothesize that ecological and biogeographic factors drive host encounters, infection susceptibility, and cross‐species spillover transmission. Using a rodent–ectoparasite system in the Neotropics, with shared ectoparasite associations as a proxy for ecological interaction between rodent species, we assessed relationships between rodents using geographic range, phylogenetic relatedness, and ectoparasite associations to determine the roles of generalist and specialist hosts in the transmission cycle of hantavirus. A total of 50 rodent species were ranked on their centrality in a network model based on ectoparasites sharing. Geographic proximity and phylogenetic relatedness were predictors for rodents to share ectoparasite species and were associated with shorter network path distance between rodents through shared ectoparasites. The rodent–ectoparasite network model successfully predicted independent data of seven known hantavirus hosts. The model predicted five novel rodent species as potential, unrecognized hantavirus hosts in South America. Findings suggest that ectoparasite data, geographic range, and phylogenetic relatedness of wildlife species could help predict novel hosts susceptible to infection and possible transmission of zoonotic pathogens. Hantavirus is a high‐consequence zoonotic pathogen with documented animal‐to‐animal, animal‐to‐human, and human‐to‐human transmission. Predictions of new rodent hosts can guide active epidemiological surveillance in specific areas and wildlife species to mitigate hantavirus spillover transmission risk from rodents to humans. This study supports the idea that ectoparasite relationships among rodents are a proxy of host species interactions and can inform transmission cycles of diverse pathogens circulating in wildlife disease systems, including wildlife viruses with epidemic potential, such as hantavirus. 

Rabies is a zoonotic infectious disease of global distribution that impacts human and animal health. In rural Latin America, rabies negatively impacts food security and the economy due to losses in livestock production. The common vampire bat,Desmodus rotundus, is the main reservoir and transmitter of rabies virus (RABV) to domestic animals in Latin America.Desmodus rotundusRABV is known to impact the cattle industry, from small farmers to large corporations. We assessed the main patterns of rabies in cattle attributed toD.rotundusRABV across Latin America. Epidemiological data on rabies from Latin America were collected from the Pan American Health Organization spanning the 1970–2023 period. Analyses revealed an average of 450 outbreaks annually for the countries whereD.rotundusis distributed, with at least 6 animals dying in each outbreak. Brazil, Colombia, Peru, and Mexico were the Latin American countries with the highest number of rabies outbreaks during the study period and are the most affected countries in recent years. Findings suggest a re-emergence of bat-borne rabies in the region with more outbreaks reported in recent years, especially during the 2003–2020 period. Rabies outbreaks in cattle in the 2000–2020 period were significantly more frequent than in previous decades, with an increase in cross-species transmission after 2002. The size of outbreaks, however, was smaller in recent years, involving lower cattle mortality. Peru, El Salvador, and Brazil showed a strong association (R = 0.73,p= 0.01) between rabies incidence inD.rotundus(rates per million humans: 1.61, 0.94, and 1.09, respectively) and rabies outbreaks in cattle (rates per million cattle: 465.85, 351.01, and 48.22, respectively). A sustained, standardized, and widespread monitoring ofD.rotundusdemography and health could serve to inform an early warning system for the early detection of RABV and other bat-borne pathogens in Latin America. Current data can be used to forecast when, where, and in which intensity RABV outbreaks are more likely to occur in subtropical and tropical Latin America. A decrease in the size of outbreaks could suggest that strategies for epidemic management (e.g., education, early diagnosis, vaccination) have been effective. The increase in the number of outbreaks could suggest that the factors facilitating cross-species transmission could be on the rise. 

Mpox is an emerging, infectious disease that has caused outbreaks in at least 91 countries from May to August 2022. We assessed the link between international air travel patterns and Mpox transmission risk, and the relationship between the translocation of Mpox and human mobility dynamics after travel restrictions due to the COVID-19 pandemic had been lifted. Our three novel observations were that: i) more people traveled internationally after the removal of travel restrictions in the summer of 2022 compared to pre-pandemic levels; ii) countries with a high concentration of global air travel have the most recorded Mpox cases; and iii) Mpox transmission includes a number of previously nonendemic regions. These results suggest that international airports should be a primary location for monitoring the risk of emerging communicable diseases. Findings highlight the need for global collaboration concerning proactive measures emphasizing realtime surveillance. 

Bat‐borne pathogens are a threat to global health and in recent history have had major impacts on human morbidity and mortality. Examples include diseases such as rabies, Nipah virus encephalitis, and severe acute respiratory syndrome (SARS). Climate change may exacerbate the emergence of bat‐borne pathogens by affecting the ecology of bats in tropical ecosystems. Here, we report the impacts of climate change on the distributional ecology of the common vampire batDesmodus rotundusacross the last century. Our retrospective analysis revealed a positive relationship between changes in climate and the northern expansion of the distribution ofD. rotundusin North America. Furthermore, we also found a reduction in the standard deviation of temperatures atD. rotunduscapture locations during the last century, expressed as more consistent, less‐seasonal climate in recent years. These results elucidate an association betweenD. rotundusrange expansion and a continental‐level rise in rabies virus spillover transmission fromD. rotundusto cattle in the last 50 years of the 120‐year study period. This correlative study, based on field observations, offers empirical evidence supporting previous statistical and mathematical simulation‐based studies reporting a likely increase of bat‐borne diseases in response to climate change. We conclude that theD. rotundusrabies system exemplifies the consequences of climate change augmentation at the wildlife–livestock–human interface, demonstrating how global change acts upon these complex and interconnected systems to drive increased disease emergence.