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Increased bacterial taxonomic and functional diversity is associated with impaired rotavirus vaccine immunogenicity in infants from India and Malawi

The immunogenicity and effectiveness of oral rotavirus vaccines (ORVs) against severe rotavirus-associated gastroenteritis are impaired in low- and middle-income countries (LMICs) where the burden of disease is highest. Determining risk factors for impaired ORV response may help identify strategies...

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Autores principales: Cunningham-Oakes, Edward, Bronowski, Christina, Chinyama, End, Jere, Khuzwayo C., Sindhu, Kulandaipalayam Natarajan C., Kang, Gagandeep, Iturriza-Gómara, Miren, Darby, Alistair C., Parker, Edward P. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656894/
https://www.ncbi.nlm.nih.gov/pubmed/37980461
http://dx.doi.org/10.1186/s12866-023-03098-z
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author Cunningham-Oakes, Edward
Bronowski, Christina
Chinyama, End
Jere, Khuzwayo C.
Sindhu, Kulandaipalayam Natarajan C.
Kang, Gagandeep
Iturriza-Gómara, Miren
Darby, Alistair C.
Parker, Edward P. K.
author_facet Cunningham-Oakes, Edward
Bronowski, Christina
Chinyama, End
Jere, Khuzwayo C.
Sindhu, Kulandaipalayam Natarajan C.
Kang, Gagandeep
Iturriza-Gómara, Miren
Darby, Alistair C.
Parker, Edward P. K.
author_sort Cunningham-Oakes, Edward
collection PubMed
description The immunogenicity and effectiveness of oral rotavirus vaccines (ORVs) against severe rotavirus-associated gastroenteritis are impaired in low- and middle-income countries (LMICs) where the burden of disease is highest. Determining risk factors for impaired ORV response may help identify strategies to enhance vaccine effectiveness. In this study, we use metagenomic sequencing to provide a high-resolution taxonomic analysis of stool samples collected at 6 weeks of age (coinciding with the first ORV dose) during a prospective study of ORV immunogenicity in India and Malawi. We then analyse the functional capacity of the developing microbiome in these cohorts. Microbiome composition differed significantly between countries, although functional capacity was more similar than taxonomic composition. Our results confirm previously reported findings that the developing microbiome is more diverse in taxonomic composition in ORV non-seroconverters compared with seroconverters, and we additionally demonstrate a similar pattern in functional capacity. Although taxonomic or functional feature abundances are poor predictors of ORV response, we show that skews in the direction of associations within these microbiome data can be used to identify consistent markers of ORV response across LMIC infant cohorts. We also highlight the systemic under-representation of reference genes from LMICs that limit functional annotation in our study (7% and 13% annotation at pathway and enzyme commission level, respectively). Overall, higher microbiome diversity in early life may act as marker for impaired ORV response in India and Malawi, whilst a holistic perspective of functional capacity may be hidden in the “dark matter” of the microbiome. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-023-03098-z.
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spelling pubmed-106568942023-11-18 Increased bacterial taxonomic and functional diversity is associated with impaired rotavirus vaccine immunogenicity in infants from India and Malawi Cunningham-Oakes, Edward Bronowski, Christina Chinyama, End Jere, Khuzwayo C. Sindhu, Kulandaipalayam Natarajan C. Kang, Gagandeep Iturriza-Gómara, Miren Darby, Alistair C. Parker, Edward P. K. BMC Microbiol Research The immunogenicity and effectiveness of oral rotavirus vaccines (ORVs) against severe rotavirus-associated gastroenteritis are impaired in low- and middle-income countries (LMICs) where the burden of disease is highest. Determining risk factors for impaired ORV response may help identify strategies to enhance vaccine effectiveness. In this study, we use metagenomic sequencing to provide a high-resolution taxonomic analysis of stool samples collected at 6 weeks of age (coinciding with the first ORV dose) during a prospective study of ORV immunogenicity in India and Malawi. We then analyse the functional capacity of the developing microbiome in these cohorts. Microbiome composition differed significantly between countries, although functional capacity was more similar than taxonomic composition. Our results confirm previously reported findings that the developing microbiome is more diverse in taxonomic composition in ORV non-seroconverters compared with seroconverters, and we additionally demonstrate a similar pattern in functional capacity. Although taxonomic or functional feature abundances are poor predictors of ORV response, we show that skews in the direction of associations within these microbiome data can be used to identify consistent markers of ORV response across LMIC infant cohorts. We also highlight the systemic under-representation of reference genes from LMICs that limit functional annotation in our study (7% and 13% annotation at pathway and enzyme commission level, respectively). Overall, higher microbiome diversity in early life may act as marker for impaired ORV response in India and Malawi, whilst a holistic perspective of functional capacity may be hidden in the “dark matter” of the microbiome. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-023-03098-z. BioMed Central 2023-11-18 /pmc/articles/PMC10656894/ /pubmed/37980461 http://dx.doi.org/10.1186/s12866-023-03098-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 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
Cunningham-Oakes, Edward
Bronowski, Christina
Chinyama, End
Jere, Khuzwayo C.
Sindhu, Kulandaipalayam Natarajan C.
Kang, Gagandeep
Iturriza-Gómara, Miren
Darby, Alistair C.
Parker, Edward P. K.
Increased bacterial taxonomic and functional diversity is associated with impaired rotavirus vaccine immunogenicity in infants from India and Malawi
title Increased bacterial taxonomic and functional diversity is associated with impaired rotavirus vaccine immunogenicity in infants from India and Malawi
title_full Increased bacterial taxonomic and functional diversity is associated with impaired rotavirus vaccine immunogenicity in infants from India and Malawi
title_fullStr Increased bacterial taxonomic and functional diversity is associated with impaired rotavirus vaccine immunogenicity in infants from India and Malawi
title_full_unstemmed Increased bacterial taxonomic and functional diversity is associated with impaired rotavirus vaccine immunogenicity in infants from India and Malawi
title_short Increased bacterial taxonomic and functional diversity is associated with impaired rotavirus vaccine immunogenicity in infants from India and Malawi
title_sort increased bacterial taxonomic and functional diversity is associated with impaired rotavirus vaccine immunogenicity in infants from india and malawi
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656894/
https://www.ncbi.nlm.nih.gov/pubmed/37980461
http://dx.doi.org/10.1186/s12866-023-03098-z
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