Cargando…
In vivo competition and horizontal gene transfer among distinct Staphylococcus aureus lineages as major drivers for adaptational changes during long-term persistence in humans
BACKGROUND: The airways of the majority of adolescent cystic fibrosis (CF) patients are persistently colonized or infected by Staphylococcus aureus. Using whole genome sequencing, we studied the evolutionary traits within a S. aureus population in the airways of a CF patient hypothesizing that horiz...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198438/ https://www.ncbi.nlm.nih.gov/pubmed/30348081 http://dx.doi.org/10.1186/s12866-018-1308-3 |
_version_ | 1783364966729908224 |
---|---|
author | Langhanki, Lars Berger, Petya Treffon, Janina Catania, Francesco Kahl, Barbara C. Mellmann, Alexander |
author_facet | Langhanki, Lars Berger, Petya Treffon, Janina Catania, Francesco Kahl, Barbara C. Mellmann, Alexander |
author_sort | Langhanki, Lars |
collection | PubMed |
description | BACKGROUND: The airways of the majority of adolescent cystic fibrosis (CF) patients are persistently colonized or infected by Staphylococcus aureus. Using whole genome sequencing, we studied the evolutionary traits within a S. aureus population in the airways of a CF patient hypothesizing that horizontal gene transfer (HGT) and inter-bacterial interaction play a major role in adaptation during long-term persistence. RESULTS: Whole genome sequencing of 21 S. aureus isolates spanning 13 years resulted in seven lineages defined by the spa types t012, t021, t331, t338, t364, t056, and t2351. Of these, the successfully persisting lineages t012 and t021 were closely related suggesting the evolution of t021 from t012, which was further corroborated by a nearly identical, syntenic set of mobile genetic elements. During transformation from t012 to t021, an increase of genomic changes including HGT from other S. aureus lineages was detected. CONCLUSIONS: In summary, our in vivo data enabled us to conceptualize an evolutionary model showing the impact of HGT and inter-bacterial interaction on bacterial long-term adaptation to the human host during CF. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-018-1308-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6198438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61984382018-10-31 In vivo competition and horizontal gene transfer among distinct Staphylococcus aureus lineages as major drivers for adaptational changes during long-term persistence in humans Langhanki, Lars Berger, Petya Treffon, Janina Catania, Francesco Kahl, Barbara C. Mellmann, Alexander BMC Microbiol Research Article BACKGROUND: The airways of the majority of adolescent cystic fibrosis (CF) patients are persistently colonized or infected by Staphylococcus aureus. Using whole genome sequencing, we studied the evolutionary traits within a S. aureus population in the airways of a CF patient hypothesizing that horizontal gene transfer (HGT) and inter-bacterial interaction play a major role in adaptation during long-term persistence. RESULTS: Whole genome sequencing of 21 S. aureus isolates spanning 13 years resulted in seven lineages defined by the spa types t012, t021, t331, t338, t364, t056, and t2351. Of these, the successfully persisting lineages t012 and t021 were closely related suggesting the evolution of t021 from t012, which was further corroborated by a nearly identical, syntenic set of mobile genetic elements. During transformation from t012 to t021, an increase of genomic changes including HGT from other S. aureus lineages was detected. CONCLUSIONS: In summary, our in vivo data enabled us to conceptualize an evolutionary model showing the impact of HGT and inter-bacterial interaction on bacterial long-term adaptation to the human host during CF. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-018-1308-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-10-22 /pmc/articles/PMC6198438/ /pubmed/30348081 http://dx.doi.org/10.1186/s12866-018-1308-3 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Langhanki, Lars Berger, Petya Treffon, Janina Catania, Francesco Kahl, Barbara C. Mellmann, Alexander In vivo competition and horizontal gene transfer among distinct Staphylococcus aureus lineages as major drivers for adaptational changes during long-term persistence in humans |
title | In vivo competition and horizontal gene transfer among distinct Staphylococcus aureus lineages as major drivers for adaptational changes during long-term persistence in humans |
title_full | In vivo competition and horizontal gene transfer among distinct Staphylococcus aureus lineages as major drivers for adaptational changes during long-term persistence in humans |
title_fullStr | In vivo competition and horizontal gene transfer among distinct Staphylococcus aureus lineages as major drivers for adaptational changes during long-term persistence in humans |
title_full_unstemmed | In vivo competition and horizontal gene transfer among distinct Staphylococcus aureus lineages as major drivers for adaptational changes during long-term persistence in humans |
title_short | In vivo competition and horizontal gene transfer among distinct Staphylococcus aureus lineages as major drivers for adaptational changes during long-term persistence in humans |
title_sort | in vivo competition and horizontal gene transfer among distinct staphylococcus aureus lineages as major drivers for adaptational changes during long-term persistence in humans |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198438/ https://www.ncbi.nlm.nih.gov/pubmed/30348081 http://dx.doi.org/10.1186/s12866-018-1308-3 |
work_keys_str_mv | AT langhankilars invivocompetitionandhorizontalgenetransferamongdistinctstaphylococcusaureuslineagesasmajordriversforadaptationalchangesduringlongtermpersistenceinhumans AT bergerpetya invivocompetitionandhorizontalgenetransferamongdistinctstaphylococcusaureuslineagesasmajordriversforadaptationalchangesduringlongtermpersistenceinhumans AT treffonjanina invivocompetitionandhorizontalgenetransferamongdistinctstaphylococcusaureuslineagesasmajordriversforadaptationalchangesduringlongtermpersistenceinhumans AT cataniafrancesco invivocompetitionandhorizontalgenetransferamongdistinctstaphylococcusaureuslineagesasmajordriversforadaptationalchangesduringlongtermpersistenceinhumans AT kahlbarbarac invivocompetitionandhorizontalgenetransferamongdistinctstaphylococcusaureuslineagesasmajordriversforadaptationalchangesduringlongtermpersistenceinhumans AT mellmannalexander invivocompetitionandhorizontalgenetransferamongdistinctstaphylococcusaureuslineagesasmajordriversforadaptationalchangesduringlongtermpersistenceinhumans |