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Enrichment of gut-derived Fusobacterium is associated with suboptimal immune recovery in HIV-infected individuals

We explored the gut microbiota profile among HIV-infected individuals with diverse immune recovery profiles following long-term suppressive ART and investigated the relationship between the altered bacteria with markers of immune dysfunction. The microbiota profile of rectal swabs from 26 HIV-infect...

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Autores principales: Lee, Soo Ching, Chua, Ling Ling, Yap, Siew Hwei, Khang, Tsung Fei, Leng, Chan Yoon, Raja Azwa, Raja Iskandar, Lewin, Sharon R., Kamarulzaman, Adeeba, Woo, Yin Ling, Lim, Yvonne Ai Lian, Loke, P’ng, Rajasuriar, Reena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155144/
https://www.ncbi.nlm.nih.gov/pubmed/30250162
http://dx.doi.org/10.1038/s41598-018-32585-x
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author Lee, Soo Ching
Chua, Ling Ling
Yap, Siew Hwei
Khang, Tsung Fei
Leng, Chan Yoon
Raja Azwa, Raja Iskandar
Lewin, Sharon R.
Kamarulzaman, Adeeba
Woo, Yin Ling
Lim, Yvonne Ai Lian
Loke, P’ng
Rajasuriar, Reena
author_facet Lee, Soo Ching
Chua, Ling Ling
Yap, Siew Hwei
Khang, Tsung Fei
Leng, Chan Yoon
Raja Azwa, Raja Iskandar
Lewin, Sharon R.
Kamarulzaman, Adeeba
Woo, Yin Ling
Lim, Yvonne Ai Lian
Loke, P’ng
Rajasuriar, Reena
author_sort Lee, Soo Ching
collection PubMed
description We explored the gut microbiota profile among HIV-infected individuals with diverse immune recovery profiles following long-term suppressive ART and investigated the relationship between the altered bacteria with markers of immune dysfunction. The microbiota profile of rectal swabs from 26 HIV-infected individuals and 20 HIV-uninfected controls were examined. Patients were classified as suboptimal responders, sIR (n = 10, CD4 T-cell <350 cells/ul) and optimal responders, oIR (n = 16, CD4 T-cell >500 cells/ul) after a minimum of 2 years on suppressive ART. Canonical correlation analysis(CCA) and multiple regression modelling were used to explore the association between fecal bacterial taxa abundance and immunological profiles in optimal and suboptimal responders. We found Fusobacterium was significantly enriched among the HIV-infected and the sIR group. CCA results showed that Fusobacterium abundance was negatively correlated with CD4 T-cell counts, but positively correlated with CD4 T-cell activation and CD4 Tregs. Multiple linear regression analysis adjusted for age, baseline CD4 T-cell count, antibiotic exposure and MSM status indicated that higher Fusobacterium relative abundance was independently associated with poorer CD4 T-cell recovery following ART. Enrichment of Fusobacterium was associated with reduced immune recovery and persistent immune dysfunction following ART. Modulating the abundance of this bacterial taxa in the gut may be a viable intervention to improve immune reconstitution in our setting.
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spelling pubmed-61551442018-09-28 Enrichment of gut-derived Fusobacterium is associated with suboptimal immune recovery in HIV-infected individuals Lee, Soo Ching Chua, Ling Ling Yap, Siew Hwei Khang, Tsung Fei Leng, Chan Yoon Raja Azwa, Raja Iskandar Lewin, Sharon R. Kamarulzaman, Adeeba Woo, Yin Ling Lim, Yvonne Ai Lian Loke, P’ng Rajasuriar, Reena Sci Rep Article We explored the gut microbiota profile among HIV-infected individuals with diverse immune recovery profiles following long-term suppressive ART and investigated the relationship between the altered bacteria with markers of immune dysfunction. The microbiota profile of rectal swabs from 26 HIV-infected individuals and 20 HIV-uninfected controls were examined. Patients were classified as suboptimal responders, sIR (n = 10, CD4 T-cell <350 cells/ul) and optimal responders, oIR (n = 16, CD4 T-cell >500 cells/ul) after a minimum of 2 years on suppressive ART. Canonical correlation analysis(CCA) and multiple regression modelling were used to explore the association between fecal bacterial taxa abundance and immunological profiles in optimal and suboptimal responders. We found Fusobacterium was significantly enriched among the HIV-infected and the sIR group. CCA results showed that Fusobacterium abundance was negatively correlated with CD4 T-cell counts, but positively correlated with CD4 T-cell activation and CD4 Tregs. Multiple linear regression analysis adjusted for age, baseline CD4 T-cell count, antibiotic exposure and MSM status indicated that higher Fusobacterium relative abundance was independently associated with poorer CD4 T-cell recovery following ART. Enrichment of Fusobacterium was associated with reduced immune recovery and persistent immune dysfunction following ART. Modulating the abundance of this bacterial taxa in the gut may be a viable intervention to improve immune reconstitution in our setting. Nature Publishing Group UK 2018-09-24 /pmc/articles/PMC6155144/ /pubmed/30250162 http://dx.doi.org/10.1038/s41598-018-32585-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lee, Soo Ching
Chua, Ling Ling
Yap, Siew Hwei
Khang, Tsung Fei
Leng, Chan Yoon
Raja Azwa, Raja Iskandar
Lewin, Sharon R.
Kamarulzaman, Adeeba
Woo, Yin Ling
Lim, Yvonne Ai Lian
Loke, P’ng
Rajasuriar, Reena
Enrichment of gut-derived Fusobacterium is associated with suboptimal immune recovery in HIV-infected individuals
title Enrichment of gut-derived Fusobacterium is associated with suboptimal immune recovery in HIV-infected individuals
title_full Enrichment of gut-derived Fusobacterium is associated with suboptimal immune recovery in HIV-infected individuals
title_fullStr Enrichment of gut-derived Fusobacterium is associated with suboptimal immune recovery in HIV-infected individuals
title_full_unstemmed Enrichment of gut-derived Fusobacterium is associated with suboptimal immune recovery in HIV-infected individuals
title_short Enrichment of gut-derived Fusobacterium is associated with suboptimal immune recovery in HIV-infected individuals
title_sort enrichment of gut-derived fusobacterium is associated with suboptimal immune recovery in hiv-infected individuals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155144/
https://www.ncbi.nlm.nih.gov/pubmed/30250162
http://dx.doi.org/10.1038/s41598-018-32585-x
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