Disease threats to tigers and their prey

The contraction of the global tiger population over the last 100 years into small, often isolated subpopulations has made them increasingly vulnerable to the impact of disease. Despite this, the health of wild tigers continues to be insufficiently funded and explored. For example, canine distemper virus (CDV), has been associated with localized declines and increased risk of extinction, and yet has received little research attention in most tiger range countries. The emergence of new pathogenic threats has posed fresh challenges, including African swine fever virus (ASFV), which has the potential to devastate wild boar populations, and severe acute respiratory syndrome coronavirus (SARS-CoV2) with implications for tiger conservation that remain unknown. The objective of this review is to synthesize current research on the health of tigers and their prey that impacts the conservation of tigers in the wild. Published sources are interpreted based on three mechanisms through which disease can affect the viability of tiger populations: (1) by reducing the survival of adult tigers, (2) by reducing breeding productivity, and (3) by reducing the carrying capacity of tiger habitat through decreased prey abundance. Examples of CDV, SARS-CoV2, carnivore protoparvovirus 1 and ASFV are used to illustrate these processes and inform discussion of research and mitigation priorities. Copyright © 2023 Gilbert, Dvornicky-Raymond and Bodgener.

Rapid behavioral responses of endangered tigers to major roads during COVID-19 lockdown.

Roads pose a major, and growing, challenge for the conservation of endangered species. However, very little is known about how endangered species behaviorally respond to roads and what that means for road mitigation strategies. We used the nation-wide lockdown in Nepal during the COVID-19 pandemic as a natural experiment to investigate how dramatic reductions in traffic volume along the national highway affected movements of two GPS-collared tigers (Panthera tigris)-a globally endangered species. This work is the first systematic research on tigers in Nepal using radiotelemetry or GPS tracking data since the 1980s. We found that the highway more strongly constrained the space use and habitat selection of the male in Parsa National Park than the female in Bardia National Park. Over the entire study period, the female on average crossed 10 times more often per week than the male, and when he was near the highway, he was over 11 times more probable to not cross it than to cross during the day. However, we also found that the cessation of traffic during the pandemic lockdown relaxed tiger avoidance of roads and made the highway more permeable for both animals. They were 2-3 times more probable to cross the highway during the lockdown than before the lockdown. In the month following the lockdown, the space use area of the male tiger tripled in size (160-550 km2), whereas the female's shrunk to half its previous size (33-15 km2). These divergent patterns likely reflect differences between the two parks in their highway traffic volumes and regulations as well as ecological conditions. Our results provide clear evidence that vehicle traffic on major roads impede tiger movements, but also that tigers can respond quickly to reductions in human pressures. We conclude by identifying various actions to mitigate road impacts on tigers and other endangered species.

From People to Panthera: Natural SARS-CoV-2 Infection in Tigers and Lions at the Bronx Zoo.

Despite numerous barriers to transmission, zoonoses are the major cause of emerging infectious diseases in humans. Among these, severe acute respiratory syndrome (SARS), Middle East respiratory syndrome (MERS), and ebolaviruses have killed thousands; the human immunodeficiency virus (HIV) has killed millions. Zoonoses and human-to-animal cross-species transmission are driven by human actions and have important management, conservation, and public health implications. The current SARS-CoV-2 pandemic, which presumably originated from an animal reservoir, has killed more than half a million people around the world and cases continue to rise. In March 2020, New York City was a global epicenter for SARS-CoV-2 infections. During this time, four tigers and three lions at the Bronx Zoo, NY, developed mild, abnormal respiratory signs. We detected SARS-CoV-2 RNA in respiratory secretions and/or feces from all seven animals, live virus in three, and colocalized viral RNA with cellular damage in one. We produced nine whole SARS-CoV-2 genomes from the animals and keepers and identified different SARS-CoV-2 genotypes in the tigers and lions. Epidemiologic and genomic data indicated human-to-tiger transmission. These were the first confirmed cases of natural SARS-CoV-2 animal infections in the United States and the first in nondomestic species in the world. We highlight disease transmission at a nontraditional interface and provide information that contributes to understanding SARS-CoV-2 transmission across species.IMPORTANCE The human-animal-environment interface of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is an important aspect of the coronavirus disease 2019 (COVID-19) pandemic that requires robust One Health-based investigations. Despite this, few reports describe natural infections in animals or directly link them to human infections using genomic data. In the present study, we describe the first cases of natural SARS-CoV-2 infection in tigers and lions in the United States and provide epidemiological and genetic evidence for human-to-animal transmission of the virus. Our data show that tigers and lions were infected with different genotypes of SARS-CoV-2, indicating two independent transmission events to the animals. Importantly, infected animals shed infectious virus in respiratory secretions and feces. A better understanding of the susceptibility of animal species to SARS-CoV-2 may help to elucidate transmission mechanisms and identify potential reservoirs and sources of infection that are important in both animal and human health.