Cargando…
Antenatal gut microbiome profiles and effect on pregnancy outcome in HIV infected and HIV uninfected women in a resource limited setting
BACKGROUND: Human immunodeficiency virus (HIV) severely damages the epithelial cells of the gut lining leading to an inflamed leaky gut, translocation of microbial products, and dysbiosis resulting in systemic immune activation. Also, microbiota composition and maternal gut function can be altered i...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9817306/ https://www.ncbi.nlm.nih.gov/pubmed/36604616 http://dx.doi.org/10.1186/s12866-022-02747-z |
_version_ | 1784864726276112384 |
---|---|
author | Chandiwana, Panashe Munjoma, Privilege Tendai Mazhandu, Arthur John Li, Jiaqi Baertschi, Isabel Wyss, Jacqueline Jordi, Sebastian Bruno Ulrich Mazengera, Lovemore Ronald Yilmaz, Bahtiyar Misselwitz, Benjamin Duri, Kerina |
author_facet | Chandiwana, Panashe Munjoma, Privilege Tendai Mazhandu, Arthur John Li, Jiaqi Baertschi, Isabel Wyss, Jacqueline Jordi, Sebastian Bruno Ulrich Mazengera, Lovemore Ronald Yilmaz, Bahtiyar Misselwitz, Benjamin Duri, Kerina |
author_sort | Chandiwana, Panashe |
collection | PubMed |
description | BACKGROUND: Human immunodeficiency virus (HIV) severely damages the epithelial cells of the gut lining leading to an inflamed leaky gut, translocation of microbial products, and dysbiosis resulting in systemic immune activation. Also, microbiota composition and maternal gut function can be altered in pregnancy through changes in the immune system and intestinal physiology. The aim of this study was to investigate the gut microbiota in HIV-infected and HIV-uninfected pregnant women and to compare and identify the association between gut microbial composition and adverse birth outcomes. RESULTS: A total of 94 pregnant women (35 HIV-infected and 59 HIV-uninfected controls) were recruited in Harare from 4 polyclinics serving populations with relatively poor socioeconomic status. Women were of a median age of 28 years (interquartile range, IQR: 22.3–32.0) and 55% of women were 35 weeks gestational age at enrolment (median 35.0 weeks, IQR: 32.5–37.2). Microbiota profiling in these participants showed that species richness was significantly lower in the HIV-infected pregnant women compared to their HIV-uninfected peers and significant differences in β-diversity using Bray–Curtis dissimilarity were observed. In contrast, there was no significant difference in α-diversity between immune-compromised (CD4(+) < 350 cells/µL) and immune-competent HIV-infected women (CD4(+) ≥ 350 cells/µL) even after stratification by viral load suppression. HIV infection was significantly associated with a reduced abundance of Clostridium, Turicibacter, Ruminococcus, Parabacteroides, Bacteroides, Bifidobacterium, Treponema, Oscillospira, and Faecalibacterium and a higher abundance of Actinomyces, and Succinivibrio. Low infant birth weight (< 2500 g) was significantly associated with high abundances of the phylum Spirochaetes, the families Spirochaeteceae, Veillonellaceae, and the genus Treponema. CONCLUSION: The results reported here show that the species richness and taxonomy composition of the gut microbiota is altered in HIV-infected pregnant women, possibly reflecting intestinal dysbiosis. Some of these taxa were also associated with low infant birth weight. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-022-02747-z. |
format | Online Article Text |
id | pubmed-9817306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-98173062023-01-07 Antenatal gut microbiome profiles and effect on pregnancy outcome in HIV infected and HIV uninfected women in a resource limited setting Chandiwana, Panashe Munjoma, Privilege Tendai Mazhandu, Arthur John Li, Jiaqi Baertschi, Isabel Wyss, Jacqueline Jordi, Sebastian Bruno Ulrich Mazengera, Lovemore Ronald Yilmaz, Bahtiyar Misselwitz, Benjamin Duri, Kerina BMC Microbiol Research BACKGROUND: Human immunodeficiency virus (HIV) severely damages the epithelial cells of the gut lining leading to an inflamed leaky gut, translocation of microbial products, and dysbiosis resulting in systemic immune activation. Also, microbiota composition and maternal gut function can be altered in pregnancy through changes in the immune system and intestinal physiology. The aim of this study was to investigate the gut microbiota in HIV-infected and HIV-uninfected pregnant women and to compare and identify the association between gut microbial composition and adverse birth outcomes. RESULTS: A total of 94 pregnant women (35 HIV-infected and 59 HIV-uninfected controls) were recruited in Harare from 4 polyclinics serving populations with relatively poor socioeconomic status. Women were of a median age of 28 years (interquartile range, IQR: 22.3–32.0) and 55% of women were 35 weeks gestational age at enrolment (median 35.0 weeks, IQR: 32.5–37.2). Microbiota profiling in these participants showed that species richness was significantly lower in the HIV-infected pregnant women compared to their HIV-uninfected peers and significant differences in β-diversity using Bray–Curtis dissimilarity were observed. In contrast, there was no significant difference in α-diversity between immune-compromised (CD4(+) < 350 cells/µL) and immune-competent HIV-infected women (CD4(+) ≥ 350 cells/µL) even after stratification by viral load suppression. HIV infection was significantly associated with a reduced abundance of Clostridium, Turicibacter, Ruminococcus, Parabacteroides, Bacteroides, Bifidobacterium, Treponema, Oscillospira, and Faecalibacterium and a higher abundance of Actinomyces, and Succinivibrio. Low infant birth weight (< 2500 g) was significantly associated with high abundances of the phylum Spirochaetes, the families Spirochaeteceae, Veillonellaceae, and the genus Treponema. CONCLUSION: The results reported here show that the species richness and taxonomy composition of the gut microbiota is altered in HIV-infected pregnant women, possibly reflecting intestinal dysbiosis. Some of these taxa were also associated with low infant birth weight. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-022-02747-z. BioMed Central 2023-01-06 /pmc/articles/PMC9817306/ /pubmed/36604616 http://dx.doi.org/10.1186/s12866-022-02747-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Chandiwana, Panashe Munjoma, Privilege Tendai Mazhandu, Arthur John Li, Jiaqi Baertschi, Isabel Wyss, Jacqueline Jordi, Sebastian Bruno Ulrich Mazengera, Lovemore Ronald Yilmaz, Bahtiyar Misselwitz, Benjamin Duri, Kerina Antenatal gut microbiome profiles and effect on pregnancy outcome in HIV infected and HIV uninfected women in a resource limited setting |
title | Antenatal gut microbiome profiles and effect on pregnancy outcome in HIV infected and HIV uninfected women in a resource limited setting |
title_full | Antenatal gut microbiome profiles and effect on pregnancy outcome in HIV infected and HIV uninfected women in a resource limited setting |
title_fullStr | Antenatal gut microbiome profiles and effect on pregnancy outcome in HIV infected and HIV uninfected women in a resource limited setting |
title_full_unstemmed | Antenatal gut microbiome profiles and effect on pregnancy outcome in HIV infected and HIV uninfected women in a resource limited setting |
title_short | Antenatal gut microbiome profiles and effect on pregnancy outcome in HIV infected and HIV uninfected women in a resource limited setting |
title_sort | antenatal gut microbiome profiles and effect on pregnancy outcome in hiv infected and hiv uninfected women in a resource limited setting |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9817306/ https://www.ncbi.nlm.nih.gov/pubmed/36604616 http://dx.doi.org/10.1186/s12866-022-02747-z |
work_keys_str_mv | AT chandiwanapanashe antenatalgutmicrobiomeprofilesandeffectonpregnancyoutcomeinhivinfectedandhivuninfectedwomeninaresourcelimitedsetting AT munjomaprivilegetendai antenatalgutmicrobiomeprofilesandeffectonpregnancyoutcomeinhivinfectedandhivuninfectedwomeninaresourcelimitedsetting AT mazhanduarthurjohn antenatalgutmicrobiomeprofilesandeffectonpregnancyoutcomeinhivinfectedandhivuninfectedwomeninaresourcelimitedsetting AT lijiaqi antenatalgutmicrobiomeprofilesandeffectonpregnancyoutcomeinhivinfectedandhivuninfectedwomeninaresourcelimitedsetting AT baertschiisabel antenatalgutmicrobiomeprofilesandeffectonpregnancyoutcomeinhivinfectedandhivuninfectedwomeninaresourcelimitedsetting AT wyssjacqueline antenatalgutmicrobiomeprofilesandeffectonpregnancyoutcomeinhivinfectedandhivuninfectedwomeninaresourcelimitedsetting AT jordisebastianbrunoulrich antenatalgutmicrobiomeprofilesandeffectonpregnancyoutcomeinhivinfectedandhivuninfectedwomeninaresourcelimitedsetting AT mazengeralovemoreronald antenatalgutmicrobiomeprofilesandeffectonpregnancyoutcomeinhivinfectedandhivuninfectedwomeninaresourcelimitedsetting AT yilmazbahtiyar antenatalgutmicrobiomeprofilesandeffectonpregnancyoutcomeinhivinfectedandhivuninfectedwomeninaresourcelimitedsetting AT misselwitzbenjamin antenatalgutmicrobiomeprofilesandeffectonpregnancyoutcomeinhivinfectedandhivuninfectedwomeninaresourcelimitedsetting AT durikerina antenatalgutmicrobiomeprofilesandeffectonpregnancyoutcomeinhivinfectedandhivuninfectedwomeninaresourcelimitedsetting |