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Succession and determinants of the early life nasopharyngeal microbiota in a South African birth cohort
BACKGROUND: Bacteria colonizing the nasopharynx play a key role as gatekeepers of respiratory health. Yet, dynamics of early life nasopharyngeal (NP) bacterial profiles remain understudied in low- and middle-income countries (LMICs), where children have a high prevalence of risk factors for lower re...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240772/ https://www.ncbi.nlm.nih.gov/pubmed/37271810 http://dx.doi.org/10.1186/s40168-023-01563-5 |
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author | Claassen-Weitz, Shantelle Gardner-Lubbe, Sugnet Xia, Yao Mwaikono, Kilaza S. Mounaud, Stephanie Harris Nierman, William C. Workman, Lesley Zar, Heather J. Nicol, Mark P. |
author_facet | Claassen-Weitz, Shantelle Gardner-Lubbe, Sugnet Xia, Yao Mwaikono, Kilaza S. Mounaud, Stephanie Harris Nierman, William C. Workman, Lesley Zar, Heather J. Nicol, Mark P. |
author_sort | Claassen-Weitz, Shantelle |
collection | PubMed |
description | BACKGROUND: Bacteria colonizing the nasopharynx play a key role as gatekeepers of respiratory health. Yet, dynamics of early life nasopharyngeal (NP) bacterial profiles remain understudied in low- and middle-income countries (LMICs), where children have a high prevalence of risk factors for lower respiratory tract infection. We investigated longitudinal changes in NP bacterial profiles, and associated exposures, among healthy infants from low-income households in South Africa. METHODS: We used short fragment (V4 region) 16S rRNA gene amplicon sequencing to characterize NP bacterial profiles from 103 infants in a South African birth cohort, at monthly intervals from birth through the first 12 months of life and six monthly thereafter until 30 months. RESULTS: Corynebacterium and Staphylococcus were dominant colonizers at 1 month of life; however, these were rapidly replaced by Moraxella- or Haemophilus-dominated profiles by 4 months. This succession was almost universal and largely independent of a broad range of exposures. Warm weather (summer), lower gestational age, maternal smoking, no day-care attendance, antibiotic exposure, or low height-for-age z score at 12 months were associated with higher alpha and beta diversity. Summer was also associated with higher relative abundances of Staphylococcus, Streptococcus, Neisseria, or anaerobic gram-negative bacteria, whilst spring and winter were associated with higher relative abundances of Haemophilus or Corynebacterium, respectively. Maternal smoking was associated with higher relative abundances of Porphyromonas. Antibiotic therapy (or isoniazid prophylaxis for tuberculosis) was associated with higher relative abundance of anerobic taxa (Porphyromonas, Fusobacterium, and Prevotella) and with lower relative abundances of health associated-taxa Corynebacterium and Dolosigranulum. HIV-exposure was associated with higher relative abundances of Klebsiella or Veillonella and lower relative abundances of an unclassified genus within the family Lachnospiraceae. CONCLUSIONS: In this intensively sampled cohort, there was rapid and predictable replacement of early profiles dominated by health-associated Corynebacterium and Dolosigranulum with those dominated by Moraxella and Haemophilus, independent of exposures. Season and antibiotic exposure were key determinants of NP bacterial profiles. Understudied but highly prevalent exposures prevalent in LMICs, including maternal smoking and HIV-exposure, were associated with NP bacterial profiles. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01563-5. |
format | Online Article Text |
id | pubmed-10240772 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102407722023-06-06 Succession and determinants of the early life nasopharyngeal microbiota in a South African birth cohort Claassen-Weitz, Shantelle Gardner-Lubbe, Sugnet Xia, Yao Mwaikono, Kilaza S. Mounaud, Stephanie Harris Nierman, William C. Workman, Lesley Zar, Heather J. Nicol, Mark P. Microbiome Research BACKGROUND: Bacteria colonizing the nasopharynx play a key role as gatekeepers of respiratory health. Yet, dynamics of early life nasopharyngeal (NP) bacterial profiles remain understudied in low- and middle-income countries (LMICs), where children have a high prevalence of risk factors for lower respiratory tract infection. We investigated longitudinal changes in NP bacterial profiles, and associated exposures, among healthy infants from low-income households in South Africa. METHODS: We used short fragment (V4 region) 16S rRNA gene amplicon sequencing to characterize NP bacterial profiles from 103 infants in a South African birth cohort, at monthly intervals from birth through the first 12 months of life and six monthly thereafter until 30 months. RESULTS: Corynebacterium and Staphylococcus were dominant colonizers at 1 month of life; however, these were rapidly replaced by Moraxella- or Haemophilus-dominated profiles by 4 months. This succession was almost universal and largely independent of a broad range of exposures. Warm weather (summer), lower gestational age, maternal smoking, no day-care attendance, antibiotic exposure, or low height-for-age z score at 12 months were associated with higher alpha and beta diversity. Summer was also associated with higher relative abundances of Staphylococcus, Streptococcus, Neisseria, or anaerobic gram-negative bacteria, whilst spring and winter were associated with higher relative abundances of Haemophilus or Corynebacterium, respectively. Maternal smoking was associated with higher relative abundances of Porphyromonas. Antibiotic therapy (or isoniazid prophylaxis for tuberculosis) was associated with higher relative abundance of anerobic taxa (Porphyromonas, Fusobacterium, and Prevotella) and with lower relative abundances of health associated-taxa Corynebacterium and Dolosigranulum. HIV-exposure was associated with higher relative abundances of Klebsiella or Veillonella and lower relative abundances of an unclassified genus within the family Lachnospiraceae. CONCLUSIONS: In this intensively sampled cohort, there was rapid and predictable replacement of early profiles dominated by health-associated Corynebacterium and Dolosigranulum with those dominated by Moraxella and Haemophilus, independent of exposures. Season and antibiotic exposure were key determinants of NP bacterial profiles. Understudied but highly prevalent exposures prevalent in LMICs, including maternal smoking and HIV-exposure, were associated with NP bacterial profiles. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01563-5. BioMed Central 2023-06-05 /pmc/articles/PMC10240772/ /pubmed/37271810 http://dx.doi.org/10.1186/s40168-023-01563-5 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 Claassen-Weitz, Shantelle Gardner-Lubbe, Sugnet Xia, Yao Mwaikono, Kilaza S. Mounaud, Stephanie Harris Nierman, William C. Workman, Lesley Zar, Heather J. Nicol, Mark P. Succession and determinants of the early life nasopharyngeal microbiota in a South African birth cohort |
title | Succession and determinants of the early life nasopharyngeal microbiota in a South African birth cohort |
title_full | Succession and determinants of the early life nasopharyngeal microbiota in a South African birth cohort |
title_fullStr | Succession and determinants of the early life nasopharyngeal microbiota in a South African birth cohort |
title_full_unstemmed | Succession and determinants of the early life nasopharyngeal microbiota in a South African birth cohort |
title_short | Succession and determinants of the early life nasopharyngeal microbiota in a South African birth cohort |
title_sort | succession and determinants of the early life nasopharyngeal microbiota in a south african birth cohort |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240772/ https://www.ncbi.nlm.nih.gov/pubmed/37271810 http://dx.doi.org/10.1186/s40168-023-01563-5 |
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