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Gut microbiota and plasma metabolites associated with diabetes in women with, or at high risk for, HIV infection

BACKGROUND: Gut microbiota alteration has been implicated in HIV infection and metabolic disorders. The relationship between gut microbiota and diabetes has rarely been studied in HIV-infected individuals, who have excess risk of metabolic disorders. METHODS: Our study during 2015–2016 enrolled pred...

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Autores principales: Moon, Jee-Young, Zolnik, Christine P., Wang, Zheng, Qiu, Yunping, Usyk, Mykhaylo, Wang, Tao, Kizer, Jorge R., Landay, Alan L., Kurland, Irwin J., Anastos, Kathryn, Kaplan, Robert C., Burk, Robert D., Qi, Qibin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286648/
https://www.ncbi.nlm.nih.gov/pubmed/30366816
http://dx.doi.org/10.1016/j.ebiom.2018.10.037
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author Moon, Jee-Young
Zolnik, Christine P.
Wang, Zheng
Qiu, Yunping
Usyk, Mykhaylo
Wang, Tao
Kizer, Jorge R.
Landay, Alan L.
Kurland, Irwin J.
Anastos, Kathryn
Kaplan, Robert C.
Burk, Robert D.
Qi, Qibin
author_facet Moon, Jee-Young
Zolnik, Christine P.
Wang, Zheng
Qiu, Yunping
Usyk, Mykhaylo
Wang, Tao
Kizer, Jorge R.
Landay, Alan L.
Kurland, Irwin J.
Anastos, Kathryn
Kaplan, Robert C.
Burk, Robert D.
Qi, Qibin
author_sort Moon, Jee-Young
collection PubMed
description BACKGROUND: Gut microbiota alteration has been implicated in HIV infection and metabolic disorders. The relationship between gut microbiota and diabetes has rarely been studied in HIV-infected individuals, who have excess risk of metabolic disorders. METHODS: Our study during 2015–2016 enrolled predominantly African Americans and Hispanics in the Women's Interagency HIV Study. We studied 28 women with long-standing HIV infection under antiretroviral therapy and 20 HIV-uninfected, but at high risk of infection, women (16 HIV+ and 6 HIV- with diabetes). Fecal samples were analyzed by sequencing prokaryotic16S rRNA gene. Plasma metabolomics profiling was performed by liquid chromatography-tandem mass spectrometry. FINDINGS: No significant differences in bacterial α- or β-diversity were observed by diabetes or HIV serostatus (all P > .1). Relative abundances of four genera (Finegoldia, Anaerococcus, Sneathia, and Adlercreutzia) were lower in women with diabetes compared to those without diabetes (all P < .01). In women with diabetes, plasma levels of several metabolites in tryptophan catabolism (e,g., kynurenine/tryptophan ratio), branched-chain amino acid and proline metabolism pathways were higher, while glycerophospholipids were lower (all P < .05). Results were generally consistent between HIV-infected and HIV-uninfected women, and no significant modification effects by HIV serostatus were observed (all P(interaction) > 0.05). Anaerococcus, known to produce butyrate which is involved in anti-inflammation and glucose metabolism, showed an inverse correlation with kynurenine/tryptophan ratio (r = −0.38, P < .01). INTERPRETATION: Among women with or at high risk for HIV infection, diabetes is associated with gut microbiota and plasma metabolite alteration, including depletion of butyrate-producing bacterial population along with higher tryptophan catabolism. FUND: NHLBI (K01HL129892, R01HL140976) and FMF.
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spelling pubmed-62866482018-12-19 Gut microbiota and plasma metabolites associated with diabetes in women with, or at high risk for, HIV infection Moon, Jee-Young Zolnik, Christine P. Wang, Zheng Qiu, Yunping Usyk, Mykhaylo Wang, Tao Kizer, Jorge R. Landay, Alan L. Kurland, Irwin J. Anastos, Kathryn Kaplan, Robert C. Burk, Robert D. Qi, Qibin EBioMedicine Research paper BACKGROUND: Gut microbiota alteration has been implicated in HIV infection and metabolic disorders. The relationship between gut microbiota and diabetes has rarely been studied in HIV-infected individuals, who have excess risk of metabolic disorders. METHODS: Our study during 2015–2016 enrolled predominantly African Americans and Hispanics in the Women's Interagency HIV Study. We studied 28 women with long-standing HIV infection under antiretroviral therapy and 20 HIV-uninfected, but at high risk of infection, women (16 HIV+ and 6 HIV- with diabetes). Fecal samples were analyzed by sequencing prokaryotic16S rRNA gene. Plasma metabolomics profiling was performed by liquid chromatography-tandem mass spectrometry. FINDINGS: No significant differences in bacterial α- or β-diversity were observed by diabetes or HIV serostatus (all P > .1). Relative abundances of four genera (Finegoldia, Anaerococcus, Sneathia, and Adlercreutzia) were lower in women with diabetes compared to those without diabetes (all P < .01). In women with diabetes, plasma levels of several metabolites in tryptophan catabolism (e,g., kynurenine/tryptophan ratio), branched-chain amino acid and proline metabolism pathways were higher, while glycerophospholipids were lower (all P < .05). Results were generally consistent between HIV-infected and HIV-uninfected women, and no significant modification effects by HIV serostatus were observed (all P(interaction) > 0.05). Anaerococcus, known to produce butyrate which is involved in anti-inflammation and glucose metabolism, showed an inverse correlation with kynurenine/tryptophan ratio (r = −0.38, P < .01). INTERPRETATION: Among women with or at high risk for HIV infection, diabetes is associated with gut microbiota and plasma metabolite alteration, including depletion of butyrate-producing bacterial population along with higher tryptophan catabolism. FUND: NHLBI (K01HL129892, R01HL140976) and FMF. Elsevier 2018-10-23 /pmc/articles/PMC6286648/ /pubmed/30366816 http://dx.doi.org/10.1016/j.ebiom.2018.10.037 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research paper
Moon, Jee-Young
Zolnik, Christine P.
Wang, Zheng
Qiu, Yunping
Usyk, Mykhaylo
Wang, Tao
Kizer, Jorge R.
Landay, Alan L.
Kurland, Irwin J.
Anastos, Kathryn
Kaplan, Robert C.
Burk, Robert D.
Qi, Qibin
Gut microbiota and plasma metabolites associated with diabetes in women with, or at high risk for, HIV infection
title Gut microbiota and plasma metabolites associated with diabetes in women with, or at high risk for, HIV infection
title_full Gut microbiota and plasma metabolites associated with diabetes in women with, or at high risk for, HIV infection
title_fullStr Gut microbiota and plasma metabolites associated with diabetes in women with, or at high risk for, HIV infection
title_full_unstemmed Gut microbiota and plasma metabolites associated with diabetes in women with, or at high risk for, HIV infection
title_short Gut microbiota and plasma metabolites associated with diabetes in women with, or at high risk for, HIV infection
title_sort gut microbiota and plasma metabolites associated with diabetes in women with, or at high risk for, hiv infection
topic Research paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286648/
https://www.ncbi.nlm.nih.gov/pubmed/30366816
http://dx.doi.org/10.1016/j.ebiom.2018.10.037
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