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Breast Milk Virome and Bacterial Microbiome Resilience in Kenyan Women Living with HIV
Breast milk is nutritionally and immunologically beneficial in early life but is also a potential source of infection. Little is known about breast milk microbiota of women living with HIV (WLHIV), the impact of severe immunosuppression, and the contribution to mortality of HIV-exposed infants. Here...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8546991/ https://www.ncbi.nlm.nih.gov/pubmed/33727396 http://dx.doi.org/10.1128/mSystems.01079-20 |
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author | Maqsood, Rabia Reus, Joshua B. Wu, Lily I. Holland, LaRinda A. Nduati, Ruth Mbori-Ngacha, Dorothy Maleche-Obimbo, Elizabeth Begnel, Emily R. Gantt, Soren Ojee, Ednah Wamalwa, Dalton John-Stewart, Grace Slyker, Jennifer Lehman, Dara A. Lim, Efrem S. |
author_facet | Maqsood, Rabia Reus, Joshua B. Wu, Lily I. Holland, LaRinda A. Nduati, Ruth Mbori-Ngacha, Dorothy Maleche-Obimbo, Elizabeth Begnel, Emily R. Gantt, Soren Ojee, Ednah Wamalwa, Dalton John-Stewart, Grace Slyker, Jennifer Lehman, Dara A. Lim, Efrem S. |
author_sort | Maqsood, Rabia |
collection | PubMed |
description | Breast milk is nutritionally and immunologically beneficial in early life but is also a potential source of infection. Little is known about breast milk microbiota of women living with HIV (WLHIV), the impact of severe immunosuppression, and the contribution to mortality of HIV-exposed infants. Here, we performed metagenomic sequencing to characterize the bacterial microbiome and DNA virome of breast milk samples at 1 month postpartum from Kenyan WLHIV who were not receiving combination antiretroviral therapy (cART), 23 women with CD4 counts of <250 and 30 women with CD4 of >500; and additionally, 19 WLHIV with infants that lived and 26 WLHIV with infants that died during the first 2 years of life were included. We found that breast milk bacterial microbiomes in this study population were highly diverse but shared a core community composed of the Streptococcaceae, Staphylococcaceae, Moraxellaceae, and Eubacteriaceae families. The breast milk virome was dominated by human cytomegalovirus (CMV) and included the bacteriophage families Myoviridae, Siphoviridae, and Podoviridae. Bacterial microbiome and virome profiles and diversity were not significantly altered by HIV immunosuppression, as defined by a CD4 of <250. CMV viral load was not associated with maternal CD4 counts or infant mortality. In conclusion, we show that the core bacterial and viral communities are resilient in breast milk despite immunosuppression in WLHIV. IMPORTANCE Breastfeeding plays an important role in seeding the infant gut microbiome and mammary health. Although most studies focus on the diverse breast milk bacterial communities, little is known about the viral communities harbored in breast milk. We performed the first breast milk virome study of an HIV population. In this study cohort of Kenyan women living with HIV from the pre-antiretroviral therapy era, we found that breast milk harbors a core bacterial microbiome and a virome dominated by human cytomegalovirus. The virome and bacterial microbiome were not substantially altered by immunosuppression or associated with infant mortality. Together, these findings indicate resilience of the microbial community in breast milk compartmentalization. These findings advance out fundamental understanding of the breast milk core microbiome and virome interactions in the context of HIV disease. |
format | Online Article Text |
id | pubmed-8546991 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-85469912021-10-27 Breast Milk Virome and Bacterial Microbiome Resilience in Kenyan Women Living with HIV Maqsood, Rabia Reus, Joshua B. Wu, Lily I. Holland, LaRinda A. Nduati, Ruth Mbori-Ngacha, Dorothy Maleche-Obimbo, Elizabeth Begnel, Emily R. Gantt, Soren Ojee, Ednah Wamalwa, Dalton John-Stewart, Grace Slyker, Jennifer Lehman, Dara A. Lim, Efrem S. mSystems Research Article Breast milk is nutritionally and immunologically beneficial in early life but is also a potential source of infection. Little is known about breast milk microbiota of women living with HIV (WLHIV), the impact of severe immunosuppression, and the contribution to mortality of HIV-exposed infants. Here, we performed metagenomic sequencing to characterize the bacterial microbiome and DNA virome of breast milk samples at 1 month postpartum from Kenyan WLHIV who were not receiving combination antiretroviral therapy (cART), 23 women with CD4 counts of <250 and 30 women with CD4 of >500; and additionally, 19 WLHIV with infants that lived and 26 WLHIV with infants that died during the first 2 years of life were included. We found that breast milk bacterial microbiomes in this study population were highly diverse but shared a core community composed of the Streptococcaceae, Staphylococcaceae, Moraxellaceae, and Eubacteriaceae families. The breast milk virome was dominated by human cytomegalovirus (CMV) and included the bacteriophage families Myoviridae, Siphoviridae, and Podoviridae. Bacterial microbiome and virome profiles and diversity were not significantly altered by HIV immunosuppression, as defined by a CD4 of <250. CMV viral load was not associated with maternal CD4 counts or infant mortality. In conclusion, we show that the core bacterial and viral communities are resilient in breast milk despite immunosuppression in WLHIV. IMPORTANCE Breastfeeding plays an important role in seeding the infant gut microbiome and mammary health. Although most studies focus on the diverse breast milk bacterial communities, little is known about the viral communities harbored in breast milk. We performed the first breast milk virome study of an HIV population. In this study cohort of Kenyan women living with HIV from the pre-antiretroviral therapy era, we found that breast milk harbors a core bacterial microbiome and a virome dominated by human cytomegalovirus. The virome and bacterial microbiome were not substantially altered by immunosuppression or associated with infant mortality. Together, these findings indicate resilience of the microbial community in breast milk compartmentalization. These findings advance out fundamental understanding of the breast milk core microbiome and virome interactions in the context of HIV disease. American Society for Microbiology 2021-03-16 /pmc/articles/PMC8546991/ /pubmed/33727396 http://dx.doi.org/10.1128/mSystems.01079-20 Text en Copyright © 2021 Maqsood et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Maqsood, Rabia Reus, Joshua B. Wu, Lily I. Holland, LaRinda A. Nduati, Ruth Mbori-Ngacha, Dorothy Maleche-Obimbo, Elizabeth Begnel, Emily R. Gantt, Soren Ojee, Ednah Wamalwa, Dalton John-Stewart, Grace Slyker, Jennifer Lehman, Dara A. Lim, Efrem S. Breast Milk Virome and Bacterial Microbiome Resilience in Kenyan Women Living with HIV |
title | Breast Milk Virome and Bacterial Microbiome Resilience in Kenyan Women Living with HIV |
title_full | Breast Milk Virome and Bacterial Microbiome Resilience in Kenyan Women Living with HIV |
title_fullStr | Breast Milk Virome and Bacterial Microbiome Resilience in Kenyan Women Living with HIV |
title_full_unstemmed | Breast Milk Virome and Bacterial Microbiome Resilience in Kenyan Women Living with HIV |
title_short | Breast Milk Virome and Bacterial Microbiome Resilience in Kenyan Women Living with HIV |
title_sort | breast milk virome and bacterial microbiome resilience in kenyan women living with hiv |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8546991/ https://www.ncbi.nlm.nih.gov/pubmed/33727396 http://dx.doi.org/10.1128/mSystems.01079-20 |
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