Resumen
Dysbiosis and impaired gut barrier integrity contribute to chronic immune activation associated with both obesity and HIV infection. Given the increased incidence of obesity in people living with HIV, we explored the impact of obesity on the gut microbiome and microbial translocation (MT) biomarkers during HIV infection and antiretroviral therapy (ART). Lean and obese rhesus macaques were infected with simian immunodeficiency virus (SIV) and subsequently treated with ART. Obese animals exhibited higher initial MT and inflammation biomarkers that remained constant throughout the study, while lean animals exhibited significant increases in these biomarkers that approached levels observed in obese animals. Lean and obese animals exhibited similar observed amplicon sequence variants (ASVs) at baseline, with obese animals exhibiting reduced ASVs during acute SIV infection that rebounded after 39 weeks of ART treatment. Beta diversity differed between groups and was longitudinally altered in obese animals. Obese animals exhibited significant changes in differential abundance in four times as many bacterial genera compared to lean animals. Our finding that MT and inflammation biomarkers significantly changed in lean animals, while obese animals exhibited significant alterations in microbial diversity, suggests that microbiome changes and systemic inflammation may not directly correlate during SIV infection and ART.
| Idioma original | English |
|---|---|
| Páginas (desde-hasta) | 1-18 |
| Número de páginas | 18 |
| Publicación | Microbiology spectrum |
| Volumen | 13 |
| N.º | 10 |
| DOI | |
| Estado | Published - oct 7 2025 |
Nota bibliográfica
Publisher Copyright:© 2025 McGuire et al
Financiación
This work was supported by NIH grants DK123115 to P.K. and DK122843 to J.B.S., P.K., and C.T.R., as well as OD11092 for operation of the Oregon National Primate Research Center. The OncoGenomics Shared Resource Facility of the University of Kentucky Markey Cancer Center (P30CA177558) supported this research. The research reported in this publication used computational infrastructure supported by the Office of Research Infrastructure Programs, Office of the Director, of the National Institutes of Health under Award Number S10OD034224. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. This work was supported by NIH grants DK123115 to P.K. and DK122843 to J.B.S., P.K., and C.T.R., as well as OD11092 for operation of the Oregon National Primate Research Center. The OncoGenomics Shared Resource Facility of the University of Kentucky Markey Cancer Center (P30CA177558) supported this research. The research reported in this publication used computational infrastructure supported by the of Research Infrastructure Programs, of the Director, of the National Institutes of Health under Award Number S10OD034224. The content is solely the responsibility of the authors and does not necessarily represent the views of the National Institutes of Health.
| Financiadores | Número del financiador |
|---|---|
| Oregon National Primate Research Center | |
| NIH Office of Research Infrastructure Programs | |
| University of Kentucky Markey Comprehensive Cancer Center | P30CA177558 |
| National Institutes of Health (NIH) | DK123115, DK122843, S10OD034224, OD11092 |
ODS de las Naciones Unidas
Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible
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Good health and well being
ASJC Scopus subject areas
- Physiology
- Ecology
- Genetics
- General Immunology and Microbiology
- Cell Biology
- Microbiology (medical)
- Infectious Diseases
Huella
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