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Genomic Evolution of Staphylococcus aureus During Artificial and Natural Colonization of the Human Nose

Staphylococcus aureus can colonize the human vestibulum nasi for many years. It is unknown whether and, how S. aureus adapts to this ecological niche during colonization. We determined the short (1 and 3 months) and mid-term (36 months) genomic evolution of S. aureus in natural carriers and artifici...

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Autores principales: Goyal, Manisha, Javerliat, Fabien, Palmieri, Mattia, Mirande, Caroline, van Wamel, Willem, Tavakol, Mehri, Verkaik, Nelianne J., van Belkum, Alex
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624446/
https://www.ncbi.nlm.nih.gov/pubmed/31333626
http://dx.doi.org/10.3389/fmicb.2019.01525
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author Goyal, Manisha
Javerliat, Fabien
Palmieri, Mattia
Mirande, Caroline
van Wamel, Willem
Tavakol, Mehri
Verkaik, Nelianne J.
van Belkum, Alex
author_facet Goyal, Manisha
Javerliat, Fabien
Palmieri, Mattia
Mirande, Caroline
van Wamel, Willem
Tavakol, Mehri
Verkaik, Nelianne J.
van Belkum, Alex
author_sort Goyal, Manisha
collection PubMed
description Staphylococcus aureus can colonize the human vestibulum nasi for many years. It is unknown whether and, how S. aureus adapts to this ecological niche during colonization. We determined the short (1 and 3 months) and mid-term (36 months) genomic evolution of S. aureus in natural carriers and artificially colonized volunteers. Eighty-five S. aureus strains were collected from 6 natural carriers during 3 years and 6 artificially colonized volunteers during 1 month. Multi-locus sequence typing (MLST) and single nucleotide polymorphism (SNP) analysis based on whole-genome sequencing (WGS) were carried out. Mutation frequencies within resident bacterial populations over time were quantified using core genome SNP counts (comparing groups of genomes) and pairwise SNP divergence assessment (comparing two genomes from strains originating from one host and sharing identical MLST). SNP counts (within 1–3 months) in all naturally colonizing strains varied from 0 to 757 (median 4). These strains showed random and independent patterns of pairwise SNP divergence (0 to 44 SNPs, median 7). When the different core genome SNP counts over a period of 3 years were considered, the median SNP count was 4 (range 0–26). Host-specific pairwise SNP divergence for the same period ranged from 9 to 57 SNPs (median 20). During short term artificial colonization the mutation frequency was even lower (0–7 SNPs, median 2) and the pairwise SNP distances were 0 to 5 SNPs (median 2). Quantifying mutation frequencies is important for the longitudinal follow-up of epidemics of infections and outbreak management. Random pattern of pairwise SNP divergence between the strains isolated from single carriers suggested that the WGS of multiple colonies is necessary in this context. Over periods up to 3 years, maximum median core genome SNP counts and SNP divergence for the strains studied were 4 and 20 SNPs or lower. During artificial colonization, where median core genome SNP and pairwise SNP distance scores were 2, there is no early stage selection of different genotypes. Therefore, we suggest an epidemiological cut off value of 20 SNPs as a marker of S. aureus strain identity during studies on nasal colonization and also outbreaks of infection.
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spelling pubmed-66244462019-07-22 Genomic Evolution of Staphylococcus aureus During Artificial and Natural Colonization of the Human Nose Goyal, Manisha Javerliat, Fabien Palmieri, Mattia Mirande, Caroline van Wamel, Willem Tavakol, Mehri Verkaik, Nelianne J. van Belkum, Alex Front Microbiol Microbiology Staphylococcus aureus can colonize the human vestibulum nasi for many years. It is unknown whether and, how S. aureus adapts to this ecological niche during colonization. We determined the short (1 and 3 months) and mid-term (36 months) genomic evolution of S. aureus in natural carriers and artificially colonized volunteers. Eighty-five S. aureus strains were collected from 6 natural carriers during 3 years and 6 artificially colonized volunteers during 1 month. Multi-locus sequence typing (MLST) and single nucleotide polymorphism (SNP) analysis based on whole-genome sequencing (WGS) were carried out. Mutation frequencies within resident bacterial populations over time were quantified using core genome SNP counts (comparing groups of genomes) and pairwise SNP divergence assessment (comparing two genomes from strains originating from one host and sharing identical MLST). SNP counts (within 1–3 months) in all naturally colonizing strains varied from 0 to 757 (median 4). These strains showed random and independent patterns of pairwise SNP divergence (0 to 44 SNPs, median 7). When the different core genome SNP counts over a period of 3 years were considered, the median SNP count was 4 (range 0–26). Host-specific pairwise SNP divergence for the same period ranged from 9 to 57 SNPs (median 20). During short term artificial colonization the mutation frequency was even lower (0–7 SNPs, median 2) and the pairwise SNP distances were 0 to 5 SNPs (median 2). Quantifying mutation frequencies is important for the longitudinal follow-up of epidemics of infections and outbreak management. Random pattern of pairwise SNP divergence between the strains isolated from single carriers suggested that the WGS of multiple colonies is necessary in this context. Over periods up to 3 years, maximum median core genome SNP counts and SNP divergence for the strains studied were 4 and 20 SNPs or lower. During artificial colonization, where median core genome SNP and pairwise SNP distance scores were 2, there is no early stage selection of different genotypes. Therefore, we suggest an epidemiological cut off value of 20 SNPs as a marker of S. aureus strain identity during studies on nasal colonization and also outbreaks of infection. Frontiers Media S.A. 2019-07-05 /pmc/articles/PMC6624446/ /pubmed/31333626 http://dx.doi.org/10.3389/fmicb.2019.01525 Text en Copyright © 2019 Goyal, Javerliat, Palmieri, Mirande, van Wamel, Tavakol, Verkaik and van Belkum. http://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 Microbiology
Goyal, Manisha
Javerliat, Fabien
Palmieri, Mattia
Mirande, Caroline
van Wamel, Willem
Tavakol, Mehri
Verkaik, Nelianne J.
van Belkum, Alex
Genomic Evolution of Staphylococcus aureus During Artificial and Natural Colonization of the Human Nose
title Genomic Evolution of Staphylococcus aureus During Artificial and Natural Colonization of the Human Nose
title_full Genomic Evolution of Staphylococcus aureus During Artificial and Natural Colonization of the Human Nose
title_fullStr Genomic Evolution of Staphylococcus aureus During Artificial and Natural Colonization of the Human Nose
title_full_unstemmed Genomic Evolution of Staphylococcus aureus During Artificial and Natural Colonization of the Human Nose
title_short Genomic Evolution of Staphylococcus aureus During Artificial and Natural Colonization of the Human Nose
title_sort genomic evolution of staphylococcus aureus during artificial and natural colonization of the human nose
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624446/
https://www.ncbi.nlm.nih.gov/pubmed/31333626
http://dx.doi.org/10.3389/fmicb.2019.01525
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