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Burkholderia cepacia Complex Regulation of Virulence Gene Expression: A Review

Burkholderia cepacia complex (Bcc) bacteria emerged as opportunistic pathogens in cystic fibrosis and immunocompromised patients. Their eradication is very difficult due to the high level of intrinsic resistance to clinically relevant antibiotics. Bcc bacteria have large and complex genomes, compose...

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Detalles Bibliográficos
Autores principales: Sousa, Sílvia A., Feliciano, Joana R., Pita, Tiago, Guerreiro, Soraia I., Leitão, Jorge H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295037/
https://www.ncbi.nlm.nih.gov/pubmed/28106859
http://dx.doi.org/10.3390/genes8010043
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author Sousa, Sílvia A.
Feliciano, Joana R.
Pita, Tiago
Guerreiro, Soraia I.
Leitão, Jorge H.
author_facet Sousa, Sílvia A.
Feliciano, Joana R.
Pita, Tiago
Guerreiro, Soraia I.
Leitão, Jorge H.
author_sort Sousa, Sílvia A.
collection PubMed
description Burkholderia cepacia complex (Bcc) bacteria emerged as opportunistic pathogens in cystic fibrosis and immunocompromised patients. Their eradication is very difficult due to the high level of intrinsic resistance to clinically relevant antibiotics. Bcc bacteria have large and complex genomes, composed of two to four replicons, with variable numbers of insertion sequences. The complexity of Bcc genomes confers a high genomic plasticity to these bacteria, allowing their adaptation and survival to diverse habitats, including the human host. In this work, we review results from recent studies using omics approaches to elucidate in vivo adaptive strategies and virulence gene regulation expression of Bcc bacteria when infecting the human host or subject to conditions mimicking the stressful environment of the cystic fibrosis lung.
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spelling pubmed-52950372017-02-10 Burkholderia cepacia Complex Regulation of Virulence Gene Expression: A Review Sousa, Sílvia A. Feliciano, Joana R. Pita, Tiago Guerreiro, Soraia I. Leitão, Jorge H. Genes (Basel) Review Burkholderia cepacia complex (Bcc) bacteria emerged as opportunistic pathogens in cystic fibrosis and immunocompromised patients. Their eradication is very difficult due to the high level of intrinsic resistance to clinically relevant antibiotics. Bcc bacteria have large and complex genomes, composed of two to four replicons, with variable numbers of insertion sequences. The complexity of Bcc genomes confers a high genomic plasticity to these bacteria, allowing their adaptation and survival to diverse habitats, including the human host. In this work, we review results from recent studies using omics approaches to elucidate in vivo adaptive strategies and virulence gene regulation expression of Bcc bacteria when infecting the human host or subject to conditions mimicking the stressful environment of the cystic fibrosis lung. MDPI 2017-01-19 /pmc/articles/PMC5295037/ /pubmed/28106859 http://dx.doi.org/10.3390/genes8010043 Text en © 2017 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Sousa, Sílvia A.
Feliciano, Joana R.
Pita, Tiago
Guerreiro, Soraia I.
Leitão, Jorge H.
Burkholderia cepacia Complex Regulation of Virulence Gene Expression: A Review
title Burkholderia cepacia Complex Regulation of Virulence Gene Expression: A Review
title_full Burkholderia cepacia Complex Regulation of Virulence Gene Expression: A Review
title_fullStr Burkholderia cepacia Complex Regulation of Virulence Gene Expression: A Review
title_full_unstemmed Burkholderia cepacia Complex Regulation of Virulence Gene Expression: A Review
title_short Burkholderia cepacia Complex Regulation of Virulence Gene Expression: A Review
title_sort burkholderia cepacia complex regulation of virulence gene expression: a review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295037/
https://www.ncbi.nlm.nih.gov/pubmed/28106859
http://dx.doi.org/10.3390/genes8010043
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