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Comparative Genomics and Transcriptomics of Propionibacterium acnes

The anaerobic Gram-positive bacterium Propionibacterium acnes is a human skin commensal that is occasionally associated with inflammatory diseases. Recent work has indicated that evolutionary distinct lineages of P. acnes play etiologic roles in disease while others are associated with maintenance o...

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Autores principales: Brzuszkiewicz, Elzbieta, Weiner, January, Wollherr, Antje, Thürmer, Andrea, Hüpeden, Jennifer, Lomholt, Hans B., Kilian, Mogens, Gottschalk, Gerhard, Daniel, Rolf, Mollenkopf, Hans-Joachim, Meyer, Thomas F., Brüggemann, Holger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3124536/
https://www.ncbi.nlm.nih.gov/pubmed/21738717
http://dx.doi.org/10.1371/journal.pone.0021581
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author Brzuszkiewicz, Elzbieta
Weiner, January
Wollherr, Antje
Thürmer, Andrea
Hüpeden, Jennifer
Lomholt, Hans B.
Kilian, Mogens
Gottschalk, Gerhard
Daniel, Rolf
Mollenkopf, Hans-Joachim
Meyer, Thomas F.
Brüggemann, Holger
author_facet Brzuszkiewicz, Elzbieta
Weiner, January
Wollherr, Antje
Thürmer, Andrea
Hüpeden, Jennifer
Lomholt, Hans B.
Kilian, Mogens
Gottschalk, Gerhard
Daniel, Rolf
Mollenkopf, Hans-Joachim
Meyer, Thomas F.
Brüggemann, Holger
author_sort Brzuszkiewicz, Elzbieta
collection PubMed
description The anaerobic Gram-positive bacterium Propionibacterium acnes is a human skin commensal that is occasionally associated with inflammatory diseases. Recent work has indicated that evolutionary distinct lineages of P. acnes play etiologic roles in disease while others are associated with maintenance of skin homeostasis. To shed light on the molecular basis for differential strain properties, we carried out genomic and transcriptomic analysis of distinct P. acnes strains. We sequenced the genome of the P. acnes strain 266, a type I-1a strain. Comparative genome analysis of strain 266 and four other P. acnes strains revealed that overall genome plasticity is relatively low; however, a number of island-like genomic regions, encoding a variety of putative virulence-associated and fitness traits differ between phylotypes, as judged from PCR analysis of a collection of P. acnes strains. Comparative transcriptome analysis of strains KPA171202 (type I-2) and 266 during exponential growth revealed inter-strain differences in gene expression of transport systems and metabolic pathways. In addition, transcript levels of genes encoding possible virulence factors such as dermatan-sulphate adhesin, polyunsaturated fatty acid isomerase, iron acquisition protein HtaA and lipase GehA were upregulated in strain 266. We investigated differential gene expression during exponential and stationary growth phases. Genes encoding components of the energy-conserving respiratory chain as well as secreted and virulence-associated factors were transcribed during the exponential phase, while the stationary growth phase was characterized by upregulation of genes involved in stress responses and amino acid metabolism. Our data highlight the genomic basis for strain diversity and identify, for the first time, the actively transcribed part of the genome, underlining the important role growth status plays in the inflammation-inducing activity of P. acnes. We argue that the disease-causing potential of different P. acnes strains is not only determined by the phylotype-specific genome content but also by variable gene expression.
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spelling pubmed-31245362011-07-07 Comparative Genomics and Transcriptomics of Propionibacterium acnes Brzuszkiewicz, Elzbieta Weiner, January Wollherr, Antje Thürmer, Andrea Hüpeden, Jennifer Lomholt, Hans B. Kilian, Mogens Gottschalk, Gerhard Daniel, Rolf Mollenkopf, Hans-Joachim Meyer, Thomas F. Brüggemann, Holger PLoS One Research Article The anaerobic Gram-positive bacterium Propionibacterium acnes is a human skin commensal that is occasionally associated with inflammatory diseases. Recent work has indicated that evolutionary distinct lineages of P. acnes play etiologic roles in disease while others are associated with maintenance of skin homeostasis. To shed light on the molecular basis for differential strain properties, we carried out genomic and transcriptomic analysis of distinct P. acnes strains. We sequenced the genome of the P. acnes strain 266, a type I-1a strain. Comparative genome analysis of strain 266 and four other P. acnes strains revealed that overall genome plasticity is relatively low; however, a number of island-like genomic regions, encoding a variety of putative virulence-associated and fitness traits differ between phylotypes, as judged from PCR analysis of a collection of P. acnes strains. Comparative transcriptome analysis of strains KPA171202 (type I-2) and 266 during exponential growth revealed inter-strain differences in gene expression of transport systems and metabolic pathways. In addition, transcript levels of genes encoding possible virulence factors such as dermatan-sulphate adhesin, polyunsaturated fatty acid isomerase, iron acquisition protein HtaA and lipase GehA were upregulated in strain 266. We investigated differential gene expression during exponential and stationary growth phases. Genes encoding components of the energy-conserving respiratory chain as well as secreted and virulence-associated factors were transcribed during the exponential phase, while the stationary growth phase was characterized by upregulation of genes involved in stress responses and amino acid metabolism. Our data highlight the genomic basis for strain diversity and identify, for the first time, the actively transcribed part of the genome, underlining the important role growth status plays in the inflammation-inducing activity of P. acnes. We argue that the disease-causing potential of different P. acnes strains is not only determined by the phylotype-specific genome content but also by variable gene expression. Public Library of Science 2011-06-27 /pmc/articles/PMC3124536/ /pubmed/21738717 http://dx.doi.org/10.1371/journal.pone.0021581 Text en Brzuszkiewicz et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Brzuszkiewicz, Elzbieta
Weiner, January
Wollherr, Antje
Thürmer, Andrea
Hüpeden, Jennifer
Lomholt, Hans B.
Kilian, Mogens
Gottschalk, Gerhard
Daniel, Rolf
Mollenkopf, Hans-Joachim
Meyer, Thomas F.
Brüggemann, Holger
Comparative Genomics and Transcriptomics of Propionibacterium acnes
title Comparative Genomics and Transcriptomics of Propionibacterium acnes
title_full Comparative Genomics and Transcriptomics of Propionibacterium acnes
title_fullStr Comparative Genomics and Transcriptomics of Propionibacterium acnes
title_full_unstemmed Comparative Genomics and Transcriptomics of Propionibacterium acnes
title_short Comparative Genomics and Transcriptomics of Propionibacterium acnes
title_sort comparative genomics and transcriptomics of propionibacterium acnes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3124536/
https://www.ncbi.nlm.nih.gov/pubmed/21738717
http://dx.doi.org/10.1371/journal.pone.0021581
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