Cargando…

Comparative genome analysis reveals niche-specific genome expansion in Acinetobacter baumannii strains

The nosocomial pathogen Acinetobacter baumannii acquired clinical significance due to the rapid development of its multi-drug resistant (MDR) phenotype. A. baumannii strains have the ability to colonize several ecological niches including soil, water, and animals, including humans. They also survive...

Descripción completa

Detalles Bibliográficos
Autores principales: Yakkala, Harshita, Samantarrai, Devyani, Gribskov, Michael, Siddavattam, Dayananda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6563999/
https://www.ncbi.nlm.nih.gov/pubmed/31194814
http://dx.doi.org/10.1371/journal.pone.0218204
_version_ 1783426635294310400
author Yakkala, Harshita
Samantarrai, Devyani
Gribskov, Michael
Siddavattam, Dayananda
author_facet Yakkala, Harshita
Samantarrai, Devyani
Gribskov, Michael
Siddavattam, Dayananda
author_sort Yakkala, Harshita
collection PubMed
description The nosocomial pathogen Acinetobacter baumannii acquired clinical significance due to the rapid development of its multi-drug resistant (MDR) phenotype. A. baumannii strains have the ability to colonize several ecological niches including soil, water, and animals, including humans. They also survive under extremely harsh environmental conditions thriving on rare and recalcitrant carbon compounds. However, the molecular basis behind such extreme adaptability of A. baumannii is unknown. We have therefore determined the complete genome sequence of A. baumannii DS002, which was isolated from agricultural soils, and compared it with 78 complete genome sequences of A. baumannii strains having complete information on the source of their isolation. Interestingly, the genome of A. baumannii DS002 showed high similarity to the genome of A. baumannii SDF isolated from the body louse. The environmental and clinical strains, which do not share a monophyletic origin, showed the existence of a strain-specific unique gene pool that supports niche-specific survival. The strains isolated from infected samples contained a genetic repertoire with a unique gene pool coding for iron acquisition machinery, particularly those required for the biosynthesis of acinetobactin. Interestingly, these strains also contained genes required for biofilm formation. However, such gene sets were either partially or completely missing in the environmental isolates, which instead harbored genes required for alternate carbon catabolism and a TonB-dependent transport system involved in the acquisition of iron via siderophores or xenosiderophores.
format Online
Article
Text
id pubmed-6563999
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-65639992019-06-20 Comparative genome analysis reveals niche-specific genome expansion in Acinetobacter baumannii strains Yakkala, Harshita Samantarrai, Devyani Gribskov, Michael Siddavattam, Dayananda PLoS One Research Article The nosocomial pathogen Acinetobacter baumannii acquired clinical significance due to the rapid development of its multi-drug resistant (MDR) phenotype. A. baumannii strains have the ability to colonize several ecological niches including soil, water, and animals, including humans. They also survive under extremely harsh environmental conditions thriving on rare and recalcitrant carbon compounds. However, the molecular basis behind such extreme adaptability of A. baumannii is unknown. We have therefore determined the complete genome sequence of A. baumannii DS002, which was isolated from agricultural soils, and compared it with 78 complete genome sequences of A. baumannii strains having complete information on the source of their isolation. Interestingly, the genome of A. baumannii DS002 showed high similarity to the genome of A. baumannii SDF isolated from the body louse. The environmental and clinical strains, which do not share a monophyletic origin, showed the existence of a strain-specific unique gene pool that supports niche-specific survival. The strains isolated from infected samples contained a genetic repertoire with a unique gene pool coding for iron acquisition machinery, particularly those required for the biosynthesis of acinetobactin. Interestingly, these strains also contained genes required for biofilm formation. However, such gene sets were either partially or completely missing in the environmental isolates, which instead harbored genes required for alternate carbon catabolism and a TonB-dependent transport system involved in the acquisition of iron via siderophores or xenosiderophores. Public Library of Science 2019-06-13 /pmc/articles/PMC6563999/ /pubmed/31194814 http://dx.doi.org/10.1371/journal.pone.0218204 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Yakkala, Harshita
Samantarrai, Devyani
Gribskov, Michael
Siddavattam, Dayananda
Comparative genome analysis reveals niche-specific genome expansion in Acinetobacter baumannii strains
title Comparative genome analysis reveals niche-specific genome expansion in Acinetobacter baumannii strains
title_full Comparative genome analysis reveals niche-specific genome expansion in Acinetobacter baumannii strains
title_fullStr Comparative genome analysis reveals niche-specific genome expansion in Acinetobacter baumannii strains
title_full_unstemmed Comparative genome analysis reveals niche-specific genome expansion in Acinetobacter baumannii strains
title_short Comparative genome analysis reveals niche-specific genome expansion in Acinetobacter baumannii strains
title_sort comparative genome analysis reveals niche-specific genome expansion in acinetobacter baumannii strains
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6563999/
https://www.ncbi.nlm.nih.gov/pubmed/31194814
http://dx.doi.org/10.1371/journal.pone.0218204
work_keys_str_mv AT yakkalaharshita comparativegenomeanalysisrevealsnichespecificgenomeexpansioninacinetobacterbaumanniistrains
AT samantarraidevyani comparativegenomeanalysisrevealsnichespecificgenomeexpansioninacinetobacterbaumanniistrains
AT gribskovmichael comparativegenomeanalysisrevealsnichespecificgenomeexpansioninacinetobacterbaumanniistrains
AT siddavattamdayananda comparativegenomeanalysisrevealsnichespecificgenomeexpansioninacinetobacterbaumanniistrains