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Differential Signature of the Microbiome and Neutrophils in the Oral Cavity of HIV-Infected Individuals

HIV infection is associated with a wide range of changes in microbial communities and immune cell components of the oral cavity. The purpose of this study was to evaluate the oral microbiome in relationship to oral neutrophils in HIV-infected compared to healthy individuals. We evaluated oral washes...

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Autores principales: Perez Rosero, Eliana, Heron, Samantha, Jovel, Juan, O’Neil, Conar R., Turvey, Shannon Lee, Parashar, Pallavi, Elahi, Shokrollah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8630784/
https://www.ncbi.nlm.nih.gov/pubmed/34858437
http://dx.doi.org/10.3389/fimmu.2021.780910
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author Perez Rosero, Eliana
Heron, Samantha
Jovel, Juan
O’Neil, Conar R.
Turvey, Shannon Lee
Parashar, Pallavi
Elahi, Shokrollah
author_facet Perez Rosero, Eliana
Heron, Samantha
Jovel, Juan
O’Neil, Conar R.
Turvey, Shannon Lee
Parashar, Pallavi
Elahi, Shokrollah
author_sort Perez Rosero, Eliana
collection PubMed
description HIV infection is associated with a wide range of changes in microbial communities and immune cell components of the oral cavity. The purpose of this study was to evaluate the oral microbiome in relationship to oral neutrophils in HIV-infected compared to healthy individuals. We evaluated oral washes and saliva samples from HIV-infected individuals (n=52) and healthy controls (n=43). Using 16S-rRNA gene sequencing, we found differential β-diversity using Principal Coordinate Analysis (PCoA) with Bray-Curtis distances. The α-diversity analysis by Faith’s, Shannon, and observed OTUs indexes indicated that the saliva samples from HIV-infected individuals harbored significantly richer bacterial communities compared to the saliva samples from healthy individuals. Notably, we observed that five species of Spirochaeta including Spirochaetaceae, Spirochaeta, Treponema, Treponema amylovorum, and Treponema azotonutricum were significantly abundant. In contrast, Helicobacter species were significantly reduced in the saliva of HIV-infected individuals. Moreover, we found a significant reduction in the frequency of oral neutrophils in the oral cavity of HIV-infected individuals, which was positively related to their CD4(+) T cell count. In particular, we noted a significant decline in CD44 expressing neutrophils and the intensity of CD44 expression on oral neutrophils of HIV-infected individuals. This observation was supported by the elevation of soluble CD44 in the saliva of HIV-infected individuals. Overall, the core oral microbiome was distinguishable between HIV-infected individuals on antiretroviral therapy compared to the HIV-negative group. The observed reduction in oral neutrophils might likely be related to the low surface expression of CD44, resulting in a higher bacterial diversity and richness in HIV-infected individuals.
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spelling pubmed-86307842021-12-01 Differential Signature of the Microbiome and Neutrophils in the Oral Cavity of HIV-Infected Individuals Perez Rosero, Eliana Heron, Samantha Jovel, Juan O’Neil, Conar R. Turvey, Shannon Lee Parashar, Pallavi Elahi, Shokrollah Front Immunol Immunology HIV infection is associated with a wide range of changes in microbial communities and immune cell components of the oral cavity. The purpose of this study was to evaluate the oral microbiome in relationship to oral neutrophils in HIV-infected compared to healthy individuals. We evaluated oral washes and saliva samples from HIV-infected individuals (n=52) and healthy controls (n=43). Using 16S-rRNA gene sequencing, we found differential β-diversity using Principal Coordinate Analysis (PCoA) with Bray-Curtis distances. The α-diversity analysis by Faith’s, Shannon, and observed OTUs indexes indicated that the saliva samples from HIV-infected individuals harbored significantly richer bacterial communities compared to the saliva samples from healthy individuals. Notably, we observed that five species of Spirochaeta including Spirochaetaceae, Spirochaeta, Treponema, Treponema amylovorum, and Treponema azotonutricum were significantly abundant. In contrast, Helicobacter species were significantly reduced in the saliva of HIV-infected individuals. Moreover, we found a significant reduction in the frequency of oral neutrophils in the oral cavity of HIV-infected individuals, which was positively related to their CD4(+) T cell count. In particular, we noted a significant decline in CD44 expressing neutrophils and the intensity of CD44 expression on oral neutrophils of HIV-infected individuals. This observation was supported by the elevation of soluble CD44 in the saliva of HIV-infected individuals. Overall, the core oral microbiome was distinguishable between HIV-infected individuals on antiretroviral therapy compared to the HIV-negative group. The observed reduction in oral neutrophils might likely be related to the low surface expression of CD44, resulting in a higher bacterial diversity and richness in HIV-infected individuals. Frontiers Media S.A. 2021-11-09 /pmc/articles/PMC8630784/ /pubmed/34858437 http://dx.doi.org/10.3389/fimmu.2021.780910 Text en Copyright © 2021 Perez Rosero, Heron, Jovel, O’Neil, Turvey, Parashar and Elahi https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Perez Rosero, Eliana
Heron, Samantha
Jovel, Juan
O’Neil, Conar R.
Turvey, Shannon Lee
Parashar, Pallavi
Elahi, Shokrollah
Differential Signature of the Microbiome and Neutrophils in the Oral Cavity of HIV-Infected Individuals
title Differential Signature of the Microbiome and Neutrophils in the Oral Cavity of HIV-Infected Individuals
title_full Differential Signature of the Microbiome and Neutrophils in the Oral Cavity of HIV-Infected Individuals
title_fullStr Differential Signature of the Microbiome and Neutrophils in the Oral Cavity of HIV-Infected Individuals
title_full_unstemmed Differential Signature of the Microbiome and Neutrophils in the Oral Cavity of HIV-Infected Individuals
title_short Differential Signature of the Microbiome and Neutrophils in the Oral Cavity of HIV-Infected Individuals
title_sort differential signature of the microbiome and neutrophils in the oral cavity of hiv-infected individuals
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8630784/
https://www.ncbi.nlm.nih.gov/pubmed/34858437
http://dx.doi.org/10.3389/fimmu.2021.780910
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