Rapid cell division of Staphylococcus aureus during colonization of the human nose

Abstract Background Staphylococcus aureus is an important opportunistic pathogen and a commensal bacterium, thriving in the nasal cavities of 20% of the human population. Little is known about the dynamics of asymptomatic colonization and the occasional transition to infectious disease. Results In t...

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Main Authors: Anna K. Szafrańska, Vera Junker, Matthias Steglich, Ulrich Nübel
Format: Article
Language:English
Published: BMC 2019-03-01
Series:BMC Genomics
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12864-019-5604-6
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spelling doaj-66ffc1ada9854352bc4c4ca8b1a2d4b22020-11-25T02:01:17ZengBMCBMC Genomics1471-21642019-03-0120111310.1186/s12864-019-5604-6Rapid cell division of Staphylococcus aureus during colonization of the human noseAnna K. Szafrańska0Vera Junker1Matthias Steglich2Ulrich Nübel3Leibniz Institute DSMZ - German Collection of Microorganisms and Cell CulturesLeibniz Institute DSMZ - German Collection of Microorganisms and Cell CulturesLeibniz Institute DSMZ - German Collection of Microorganisms and Cell CulturesLeibniz Institute DSMZ - German Collection of Microorganisms and Cell CulturesAbstract Background Staphylococcus aureus is an important opportunistic pathogen and a commensal bacterium, thriving in the nasal cavities of 20% of the human population. Little is known about the dynamics of asymptomatic colonization and the occasional transition to infectious disease. Results In this study, we inferred that S. aureus cells replicate every one to three hours on average while colonizing the human nose, based on two independent lines of genomic evidence. First, we collected nasal swab samples from human subjects, extracted and sequenced metagenomic DNA, and analyzed the distribution of sequencing coverage along the staphylococcal chromosome. Calibration of this data by comparison to a laboratory culture enabled measuring S. aureus cell division rates in nasal samples. Second, we applied mutation accumulation experiments paired with genome sequencing to measure spontaneous mutation rates at a genome scale. Relating these mutation rates to annual evolutionary rates confirmed that nasal S. aureus continuously pass several thousand cell divisions per year when averaged over large, globally distributed populations and over many years, corresponding to generation times of less than two hours. Conclusions The cell division rates we determined were higher than the fastest documented rates during fulminant disease progression (in a mouse model of systemic infection) and much higher than those previously measured in expectorated sputum from cystic fibrosis patients. This paper supplies absolute in-vivo generation times for an important bacterial commensal, indicating that colonization of the human upper respiratory tract is characterized by a highly dynamic equilibrium between bacterial growth and removal.http://link.springer.com/article/10.1186/s12864-019-5604-6Commensal bacteriaNasal microbiomeReplication rateGeneration timeIn-vivo growth dynamicsMetagenome sequencing
collection DOAJ
language English
format Article
sources DOAJ
author Anna K. Szafrańska
Vera Junker
Matthias Steglich
Ulrich Nübel
spellingShingle Anna K. Szafrańska
Vera Junker
Matthias Steglich
Ulrich Nübel
Rapid cell division of Staphylococcus aureus during colonization of the human nose
BMC Genomics
Commensal bacteria
Nasal microbiome
Replication rate
Generation time
In-vivo growth dynamics
Metagenome sequencing
author_facet Anna K. Szafrańska
Vera Junker
Matthias Steglich
Ulrich Nübel
author_sort Anna K. Szafrańska
title Rapid cell division of Staphylococcus aureus during colonization of the human nose
title_short Rapid cell division of Staphylococcus aureus during colonization of the human nose
title_full Rapid cell division of Staphylococcus aureus during colonization of the human nose
title_fullStr Rapid cell division of Staphylococcus aureus during colonization of the human nose
title_full_unstemmed Rapid cell division of Staphylococcus aureus during colonization of the human nose
title_sort rapid cell division of staphylococcus aureus during colonization of the human nose
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2019-03-01
description Abstract Background Staphylococcus aureus is an important opportunistic pathogen and a commensal bacterium, thriving in the nasal cavities of 20% of the human population. Little is known about the dynamics of asymptomatic colonization and the occasional transition to infectious disease. Results In this study, we inferred that S. aureus cells replicate every one to three hours on average while colonizing the human nose, based on two independent lines of genomic evidence. First, we collected nasal swab samples from human subjects, extracted and sequenced metagenomic DNA, and analyzed the distribution of sequencing coverage along the staphylococcal chromosome. Calibration of this data by comparison to a laboratory culture enabled measuring S. aureus cell division rates in nasal samples. Second, we applied mutation accumulation experiments paired with genome sequencing to measure spontaneous mutation rates at a genome scale. Relating these mutation rates to annual evolutionary rates confirmed that nasal S. aureus continuously pass several thousand cell divisions per year when averaged over large, globally distributed populations and over many years, corresponding to generation times of less than two hours. Conclusions The cell division rates we determined were higher than the fastest documented rates during fulminant disease progression (in a mouse model of systemic infection) and much higher than those previously measured in expectorated sputum from cystic fibrosis patients. This paper supplies absolute in-vivo generation times for an important bacterial commensal, indicating that colonization of the human upper respiratory tract is characterized by a highly dynamic equilibrium between bacterial growth and removal.
topic Commensal bacteria
Nasal microbiome
Replication rate
Generation time
In-vivo growth dynamics
Metagenome sequencing
url http://link.springer.com/article/10.1186/s12864-019-5604-6
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