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Longitudinal changes in the nasopharyngeal resistome of South African infants using shotgun metagenomic sequencing

INTRODUCTION: Nasopharyngeal (NP) colonization with antimicrobial-resistant bacteria is a global public health concern. Antimicrobial-resistance (AMR) genes carried by the resident NP microbiota may serve as a reservoir for transfer of resistance elements to opportunistic pathogens. Little is known...

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Autores principales: Manenzhe, Rendani I., Dube, Felix S., Wright, Meredith, Lennard, Katie, Zar, Heather J., Mounaud, Stephanie, Nierman, William C., Nicol, Mark P., Moodley, Clinton
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7176138/
https://www.ncbi.nlm.nih.gov/pubmed/32320455
http://dx.doi.org/10.1371/journal.pone.0231887
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author Manenzhe, Rendani I.
Dube, Felix S.
Wright, Meredith
Lennard, Katie
Zar, Heather J.
Mounaud, Stephanie
Nierman, William C.
Nicol, Mark P.
Moodley, Clinton
author_facet Manenzhe, Rendani I.
Dube, Felix S.
Wright, Meredith
Lennard, Katie
Zar, Heather J.
Mounaud, Stephanie
Nierman, William C.
Nicol, Mark P.
Moodley, Clinton
author_sort Manenzhe, Rendani I.
collection PubMed
description INTRODUCTION: Nasopharyngeal (NP) colonization with antimicrobial-resistant bacteria is a global public health concern. Antimicrobial-resistance (AMR) genes carried by the resident NP microbiota may serve as a reservoir for transfer of resistance elements to opportunistic pathogens. Little is known about the NP antibiotic resistome. This study longitudinally investigated the composition of the NP antibiotic resistome in Streptococcus-enriched samples in a South African birth cohort. METHODS: As a proof of concept study, 196 longitudinal NP samples were retrieved from a subset of 23 infants enrolled as part of broader birth cohort study. These were selected on the basis of changes in serotype and antibiogram over time. NP samples underwent short-term enrichment for streptococci prior to total nucleic acid extraction and whole metagenome shotgun sequencing (WMGS). Reads were assembled and aligned to pneumococcal reference genomes for the extraction of streptococcal and non-streptococcal bacterial reads. Contigs were aligned to the Antibiotic Resistance Gene-ANNOTation database of acquired AMR genes. RESULTS: AMR genes were detected in 64% (125/196) of the samples. A total of 329 AMR genes were detected, including 36 non-redundant genes, ranging from 1 to 14 genes per sample. The predominant AMR genes detected encoded resistance mechanisms to beta-lactam (52%, 172/329), macrolide-lincosamide-streptogramin (17%, 56/329), and tetracycline antibiotics (12%, 38/329). MsrD, ermB, and mefA genes were only detected from streptococcal reads. The predominant genes detected from non- streptococcal reads included bla(OXA-60), bla(OXA-22), and bla(BRO-1). Different patterns of carriage of AMR genes were observed, with only one infant having a stable carriage of mefA, msrD and tetM over a long period. CONCLUSION: This study demonstrates that WMGS can provide a broad snapshot of the NP resistome and has the potential to provide a comprehensive assessment of resistance elements present in this niche.
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spelling pubmed-71761382020-05-12 Longitudinal changes in the nasopharyngeal resistome of South African infants using shotgun metagenomic sequencing Manenzhe, Rendani I. Dube, Felix S. Wright, Meredith Lennard, Katie Zar, Heather J. Mounaud, Stephanie Nierman, William C. Nicol, Mark P. Moodley, Clinton PLoS One Research Article INTRODUCTION: Nasopharyngeal (NP) colonization with antimicrobial-resistant bacteria is a global public health concern. Antimicrobial-resistance (AMR) genes carried by the resident NP microbiota may serve as a reservoir for transfer of resistance elements to opportunistic pathogens. Little is known about the NP antibiotic resistome. This study longitudinally investigated the composition of the NP antibiotic resistome in Streptococcus-enriched samples in a South African birth cohort. METHODS: As a proof of concept study, 196 longitudinal NP samples were retrieved from a subset of 23 infants enrolled as part of broader birth cohort study. These were selected on the basis of changes in serotype and antibiogram over time. NP samples underwent short-term enrichment for streptococci prior to total nucleic acid extraction and whole metagenome shotgun sequencing (WMGS). Reads were assembled and aligned to pneumococcal reference genomes for the extraction of streptococcal and non-streptococcal bacterial reads. Contigs were aligned to the Antibiotic Resistance Gene-ANNOTation database of acquired AMR genes. RESULTS: AMR genes were detected in 64% (125/196) of the samples. A total of 329 AMR genes were detected, including 36 non-redundant genes, ranging from 1 to 14 genes per sample. The predominant AMR genes detected encoded resistance mechanisms to beta-lactam (52%, 172/329), macrolide-lincosamide-streptogramin (17%, 56/329), and tetracycline antibiotics (12%, 38/329). MsrD, ermB, and mefA genes were only detected from streptococcal reads. The predominant genes detected from non- streptococcal reads included bla(OXA-60), bla(OXA-22), and bla(BRO-1). Different patterns of carriage of AMR genes were observed, with only one infant having a stable carriage of mefA, msrD and tetM over a long period. CONCLUSION: This study demonstrates that WMGS can provide a broad snapshot of the NP resistome and has the potential to provide a comprehensive assessment of resistance elements present in this niche. Public Library of Science 2020-04-22 /pmc/articles/PMC7176138/ /pubmed/32320455 http://dx.doi.org/10.1371/journal.pone.0231887 Text en © 2020 Manenzhe et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Manenzhe, Rendani I.
Dube, Felix S.
Wright, Meredith
Lennard, Katie
Zar, Heather J.
Mounaud, Stephanie
Nierman, William C.
Nicol, Mark P.
Moodley, Clinton
Longitudinal changes in the nasopharyngeal resistome of South African infants using shotgun metagenomic sequencing
title Longitudinal changes in the nasopharyngeal resistome of South African infants using shotgun metagenomic sequencing
title_full Longitudinal changes in the nasopharyngeal resistome of South African infants using shotgun metagenomic sequencing
title_fullStr Longitudinal changes in the nasopharyngeal resistome of South African infants using shotgun metagenomic sequencing
title_full_unstemmed Longitudinal changes in the nasopharyngeal resistome of South African infants using shotgun metagenomic sequencing
title_short Longitudinal changes in the nasopharyngeal resistome of South African infants using shotgun metagenomic sequencing
title_sort longitudinal changes in the nasopharyngeal resistome of south african infants using shotgun metagenomic sequencing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7176138/
https://www.ncbi.nlm.nih.gov/pubmed/32320455
http://dx.doi.org/10.1371/journal.pone.0231887
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