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Gut microbiota and their putative metabolic functions in fragmented Bengal tiger population of Nepal.
Karmacharya, Dibesh; Manandhar, Prajwol; Manandhar, Sulochana; Sherchan, Adarsh M; Sharma, Ajay N; Joshi, Jyoti; Bista, Manisha; Bajracharya, Shailendra; Awasthi, Nagendra P; Sharma, Netra; Llewellyn, Bronwyn; Waits, Lisette P; Thapa, Kanchan; Kelly, Marcella J; Vuyisich, Momchilo; Starkenburg, Shawn R; Hero, Jean-Marc; Hughes, Jane; Wultsch, Claudia; Bertola, Laura; Fountain-Jones, Nicholas M; Sinha, Amit K.
Afiliação
  • Karmacharya D; Center for Molecular Dynamics Nepal, Kathmandu, Nepal.
  • Manandhar P; School of Environment, Griffith University, Brisbane, Queensland, Australia.
  • Manandhar S; Center for Molecular Dynamics Nepal, Kathmandu, Nepal.
  • Sherchan AM; Center for Molecular Dynamics Nepal, Kathmandu, Nepal.
  • Sharma AN; Center for Molecular Dynamics Nepal, Kathmandu, Nepal.
  • Joshi J; Center for Molecular Dynamics Nepal, Kathmandu, Nepal.
  • Bista M; Center for Molecular Dynamics Nepal, Kathmandu, Nepal.
  • Bajracharya S; Center for Molecular Dynamics Nepal, Kathmandu, Nepal.
  • Awasthi NP; Center for Molecular Dynamics Nepal, Kathmandu, Nepal.
  • Sharma N; Center for Molecular Dynamics Nepal, Kathmandu, Nepal.
  • Llewellyn B; Environment Team, U.S. Agency for International Development, Kathmandu, Nepal.
  • Waits LP; Environment Team, U.S. Agency for International Development, Kathmandu, Nepal.
  • Thapa K; Department of Fish and Wildlife Sciences, University of Idaho, Moscow, Idaho, United States of America.
  • Kelly MJ; Department of Fish and Wildlife Conservation, Virginia Tech, Blacksburg, Virginia, United States of America.
  • Vuyisich M; Department of Fish and Wildlife Conservation, Virginia Tech, Blacksburg, Virginia, United States of America.
  • Starkenburg SR; Applied Genomics, Los Alamos National Lab, Los Alamos, New Mexico, United States of America.
  • Hero JM; Applied Genomics, Los Alamos National Lab, Los Alamos, New Mexico, United States of America.
  • Hughes J; School of Science & Education, University of the Sunshine Coast, Sunshine Coast, Queensland, Australia.
  • Wultsch C; School of Environment, Griffith University, Brisbane, Queensland, Australia.
  • Bertola L; Sackler Institute for Comparative Genomics, American Museum of Natural History, New York, United States of America.
  • Fountain-Jones NM; Bioinformatics and Computational Genomics Laboratory, Hunter College, City University of New York, New York, United States of America.
  • Sinha AK; Department of Biology, City College of New York, New York, United States of America.
PLoS One ; 14(8): e0221868, 2019.
Article em En | MEDLINE | ID: mdl-31465520
ABSTRACT
Bengal tigers (Panthera tigris tigris) serve a pivotal role as an apex predator in forest ecosystems. To increase our knowledge on factors impacting the viability and health of this endangered species, we studied the gut microbiota in 32 individual Bengal tigers from three geographically separated areas (Chitwan National Park (CNP), Bardia National Park (BNP) and Suklaphanta Wildlife Reserve (SWR)) in Nepal, using noninvasive genetic sampling methods. Gut microbiota influence the immune system, impact various physiological functions, and modulates metabolic reactions, that ultimately impact the host health, behavior and development. Across the tiger populations in Nepal, we found significant differences in the composition of microbial communities based on their geographic locations. Specifically, we detected significant differences between CNP and the other two protected areas (CNP vs BNP pseudo t = 1.944, P = 0.006; CNP vs SWR pseudo t = 1.9942, P = 0.0071), but no differences between BNP and SWR. This mirrors what has been found for tiger gene flow in the same populations, suggesting gut microbiota composition and host gene flow may be linked. Furthermore, predictive metagenome functional content analysis (PICRUSt) revealed a higher functional enrichment and diversity for significant gut microbiota in the Chitwan tiger population and the lowest enrichment and diversity in Suklaphanta. The CNP tiger population contained higher proportions of microbiota that are associated with predicted functions relevant for metabolism of amino acid, lipid, xenobiotics biodegradation, terpenoides and polyketides than the SWR population. We conclude the tiger population structure, gut microbiota profile and associated functional metabolic categories are correlated, with geographically most separated CNP and SWR tiger population having the most distinct and different host genotype and microbiota profiles. Our work dramatically expands the understanding of tiger microbiota in wild populations and provides a valuable case study on how to investigate genetic diversity at different hierarchical levels, including hosts as well as their microbial communities.
Assuntos

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Tigres / Metabolômica / Microbioma Gastrointestinal Tipo de estudo: Prognostic_studies Limite: Animals País/Região como assunto: Asia Idioma: En Revista: PLoS One Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Tigres / Metabolômica / Microbioma Gastrointestinal Tipo de estudo: Prognostic_studies Limite: Animals País/Região como assunto: Asia Idioma: En Revista: PLoS One Ano de publicação: 2019 Tipo de documento: Article