Evidence map›Paper›PMID 32320455›Full record

ArticlePloS one2020

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

Rendani I Manenzhe, Felix S Dube, Meredith Wright, Katie Lennard, Heather J Zar, Stephanie Mounaud, William C Nierman, Mark P Nicol, Clinton Moodley

Abstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Rendani I ManenzheDivision of Medical Microbiology, Faculty of Health Science, University of Cape Town, Cape Town, South Africa.ORCID 0000-0003-1384-4336
Felix S DubeDivision of Medical Microbiology, Faculty of Health Science, University of Cape Town, Cape Town, South Africa.
Meredith WrightJ. Craig Venter Institute, Rockville, MD, United States of America.
Katie LennardDivision of Computational Biology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Heather J ZarDepartment of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital and MRC unit on Child & Adolescent Health, University of Cape Town, Cape Town, South Africa.
Stephanie MounaudJ. Craig Venter Institute, Rockville, MD, United States of America.
William C NiermanJ. Craig Venter Institute, Rockville, MD, United States of America.
Mark P NicolDivision of Medical Microbiology, Faculty of Health Science, University of Cape Town, Cape Town, South Africa.
Clinton MoodleyDivision of Medical Microbiology, Faculty of Health Science, University of Cape Town, Cape Town, South Africa.ORCID 0000-0001-7547-9026

Funding

The nasopharyngeal microbiota of African children and lower respiratory tract infectionU54HG009824 · NHGRI · UNIVERSITY OF CAPE TOWN · PI NICOL, MARK PATRICK, ZAR, HEATHER JOY · 2017 to 2021
$2.9M
The nasopharyngeal microbiome and respiratory disease in African childrenU01AI110466 · NIAID · UNIVERSITY OF CAPE TOWN · PI NICOL, MARK PATRICK, ZAR, HEATHER JOY · 2013 to 2016
$1.4M
NHGRI NIH HHS U54 HG009824NIAID NIH HHS U01 AI110466
6 · The paper itself

Abstract

introductionNasopharyngeal (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.

methodsAs 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.

resultsAMR 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 blaOXA-60, blaOXA-22, and blaBRO-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.

conclusionThis 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.

Indexed as

MetagenomicsSequence Analysis, DNAAnti-Bacterial AgentsCohort StudiesFemaleHumansInfantLongitudinal StudiesMaleNasopharynxSouth AfricaStreptococcusAnti-Bacterial Agents

Identifiers

PMID32320455
PMCPMC7176138

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.