Altered gut microbiota is associated with different immunologic responses to antiretroviral therapy in HIV‐infected men who have sex with men

Author:

Zhao Heping1,Feng Anping1,Luo Dan1,Wu Hao2,Zhang Ge3,Zhang Lin456,Yuan Jinqiu789,Lin Yi‐Fan1,Li Linghua10,Zou Huachun111ORCID

Affiliation:

1. School of Public Health (Shenzhen) Sun Yat‐sen University Shenzhen China

2. Guangzhou Center for Disease Control and Prevention Guangzhou China

3. Department of Microbial and Biochemical Pharmacy, School of Pharmaceutical Sciences Sun Yat‐sen University Guangzhou China

4. Department of Anesthesia and Intensive Care The Chinese University of Hong Kong Hong Kong P. R. China

5. Department of Medicine and Therapeutics The Chinese University of Hong Kong Hong Kong P. R. China

6. CUHK Shenzhen Research Institute Shenzhen P. R. China

7. Big Data Center, The Seventh Affiliated Hospital Sun Yat‐sen University Shenzhen Guangdong China

8. Clinical Research Center, The Seventh Affiliated Hospital Sun Yat‐sen University Shenzhen Guangdong China

9. Guangdong Provincial Key Laboratory of Gastrointestinal Cancers, Center for Digestive Disease, The Seventh Affiliated Hospital Sun Yat‐sen University Shenzhen Guangdong China

10. Guangzhou Eighth People's Hospital Guangzhou Medical University Guangzhou China

11. Kirby Institute University of New South Wales Sydney Australia

Abstract

AbstractThe association between gut microbiota and immunologic nonresponse among people living with HIV (PLHIV) on antiretroviral therapy (ART) is not well documented. This study aimed to characterize gut microbiota among HIV‐infected men who have sex with men (MSM) with different immunologic responses. We recruited HIV‐infected MSM and HIV‐uninfected MSM (healthy controls, HC) in Guangzhou, June–October 2021. HIV‐infected MSM were grouped into good immunological responders (GIR) (CD4 + T cell count ≥ 350 cells/μL) and poor immunological responders (PIR) (<350 cells/μL). Blood and stool samples were collected. Microbial translocation in serum was performed using enzyme‐linked immunosorbent assay (ELISA). Bacterial 16S ribosomal DNA sequencing was performed on stool samples, and microbial metabolites were obtained through gas chromatography‐mass spectrometry. 56 GIR, 41 PIR, and 51 HC were included. Microbial translocation marker soluble cluster of differentiation 14 (sCD14) in both GIR and PIR groups was significantly higher than that in HC. Compared with PIR or HC groups, the genera of Coprococcus, Blautia, Clostridium, and SMB53 were decreased, whereas Megamonas and Megasphaera were more abundant in GIR group. Compared with GIR or PIR groups, Bifidobacterium, Collinsella, Faecalibacterium, Oscillospira, and Roseburia were more abundant, whereas Escherichia was decreased in HC group. The levels of benzenoids, imidazoles, phenylpropanoic acids, phenylpropanoids, and pyridines showed strongly significant correlations between differential genera. This study presented a comprehensive landscape of gut microbiota in PLHIV with different treatment outcomes. Megamonas, Coprococcus and Blautia were the major genera correlated with different immunologic responses in PLHIV.

Publisher

Wiley

Subject

Infectious Diseases,Virology

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