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Requirements for Pseudomonas aeruginosa Acute Burn and Chronic Surgical Wound Infection

Opportunistic infections caused by Pseudomonas aeruginosa can be acute or chronic. While acute infections often spread rapidly and can cause tissue damage and sepsis with high mortality rates, chronic infections can persist for weeks, months, or years in the face of intensive clinical intervention....

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Autores principales: Turner, Keith H., Everett, Jake, Trivedi, Urvish, Rumbaugh, Kendra P., Whiteley, Marvin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4109851/
https://www.ncbi.nlm.nih.gov/pubmed/25057820
http://dx.doi.org/10.1371/journal.pgen.1004518
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author Turner, Keith H.
Everett, Jake
Trivedi, Urvish
Rumbaugh, Kendra P.
Whiteley, Marvin
author_facet Turner, Keith H.
Everett, Jake
Trivedi, Urvish
Rumbaugh, Kendra P.
Whiteley, Marvin
author_sort Turner, Keith H.
collection PubMed
description Opportunistic infections caused by Pseudomonas aeruginosa can be acute or chronic. While acute infections often spread rapidly and can cause tissue damage and sepsis with high mortality rates, chronic infections can persist for weeks, months, or years in the face of intensive clinical intervention. Remarkably, this diverse infectious capability is not accompanied by extensive variation in genomic content, suggesting that the genetic capacity to be an acute or a chronic pathogen is present in most P. aeruginosa strains. To investigate the genetic requirements for acute and chronic pathogenesis in P. aeruginosa infections, we combined high-throughput sequencing-mediated transcriptome profiling (RNA-seq) and genome-wide insertion mutant fitness profiling (Tn-seq) to characterize gene expression and fitness determinants in murine models of burn and non-diabetic chronic wound infection. Generally we discovered that expression of a gene in vivo is not correlated with its importance for fitness, with the exception of metabolic genes. By combining metabolic models generated from in vivo gene expression data with mutant fitness profiles, we determined the nutritional requirements for colonization and persistence in these infections. Specifically, we found that long-chain fatty acids represent a major carbon source in both chronic and acute wounds, and P. aeruginosa must biosynthesize purines, several amino acids, and most cofactors during infection. In addition, we determined that P. aeruginosa requires chemotactic flagellar motility for fitness and virulence in acute burn wound infections, but not in non-diabetic chronic wound infections. Our results provide novel insight into the genetic requirements for acute and chronic P. aeruginosa wound infections and demonstrate the power of using both gene expression and fitness profiling for probing bacterial virulence.
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spelling pubmed-41098512014-07-29 Requirements for Pseudomonas aeruginosa Acute Burn and Chronic Surgical Wound Infection Turner, Keith H. Everett, Jake Trivedi, Urvish Rumbaugh, Kendra P. Whiteley, Marvin PLoS Genet Research Article Opportunistic infections caused by Pseudomonas aeruginosa can be acute or chronic. While acute infections often spread rapidly and can cause tissue damage and sepsis with high mortality rates, chronic infections can persist for weeks, months, or years in the face of intensive clinical intervention. Remarkably, this diverse infectious capability is not accompanied by extensive variation in genomic content, suggesting that the genetic capacity to be an acute or a chronic pathogen is present in most P. aeruginosa strains. To investigate the genetic requirements for acute and chronic pathogenesis in P. aeruginosa infections, we combined high-throughput sequencing-mediated transcriptome profiling (RNA-seq) and genome-wide insertion mutant fitness profiling (Tn-seq) to characterize gene expression and fitness determinants in murine models of burn and non-diabetic chronic wound infection. Generally we discovered that expression of a gene in vivo is not correlated with its importance for fitness, with the exception of metabolic genes. By combining metabolic models generated from in vivo gene expression data with mutant fitness profiles, we determined the nutritional requirements for colonization and persistence in these infections. Specifically, we found that long-chain fatty acids represent a major carbon source in both chronic and acute wounds, and P. aeruginosa must biosynthesize purines, several amino acids, and most cofactors during infection. In addition, we determined that P. aeruginosa requires chemotactic flagellar motility for fitness and virulence in acute burn wound infections, but not in non-diabetic chronic wound infections. Our results provide novel insight into the genetic requirements for acute and chronic P. aeruginosa wound infections and demonstrate the power of using both gene expression and fitness profiling for probing bacterial virulence. Public Library of Science 2014-07-24 /pmc/articles/PMC4109851/ /pubmed/25057820 http://dx.doi.org/10.1371/journal.pgen.1004518 Text en © 2014 Turner 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
Turner, Keith H.
Everett, Jake
Trivedi, Urvish
Rumbaugh, Kendra P.
Whiteley, Marvin
Requirements for Pseudomonas aeruginosa Acute Burn and Chronic Surgical Wound Infection
title Requirements for Pseudomonas aeruginosa Acute Burn and Chronic Surgical Wound Infection
title_full Requirements for Pseudomonas aeruginosa Acute Burn and Chronic Surgical Wound Infection
title_fullStr Requirements for Pseudomonas aeruginosa Acute Burn and Chronic Surgical Wound Infection
title_full_unstemmed Requirements for Pseudomonas aeruginosa Acute Burn and Chronic Surgical Wound Infection
title_short Requirements for Pseudomonas aeruginosa Acute Burn and Chronic Surgical Wound Infection
title_sort requirements for pseudomonas aeruginosa acute burn and chronic surgical wound infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4109851/
https://www.ncbi.nlm.nih.gov/pubmed/25057820
http://dx.doi.org/10.1371/journal.pgen.1004518
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