Bacterial fitness in chronic wounds appears to be mediated by the capacity for high-density growth, not virulence or biofilm functions
While much is known about acute infection pathogenesis, the understanding of chronic infections has lagged. Here we sought to identify the genes and functions that mediate fitness of the pathogen Pseudomonas aeruginosa in chronic wound infections, and to better understand the selective environment i...
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creator | Morgan, Sarah J Lippman, Soyeon I Bautista, Gilbert E Harrison, Joe J Harding, Christopher L Gallagher, Larry A Cheng, Ann-Chee Siehnel, Richard Ravishankar, Sumedha Usui, Marcia L Olerud, John E Fleckman, Philip Wolcott, Randall D Manoil, Colin Singh, Pradeep K |
description | While much is known about acute infection pathogenesis, the understanding of chronic infections has lagged. Here we sought to identify the genes and functions that mediate fitness of the pathogen Pseudomonas aeruginosa in chronic wound infections, and to better understand the selective environment in wounds. We found that clinical isolates from chronic human wounds were frequently defective in virulence functions and biofilm formation, and that many virulence and biofilm formation genes were not required for bacterial fitness in experimental mouse wounds. In contrast, genes involved in anaerobic growth, some metabolic and energy pathways, and membrane integrity were critical. Consistent with these findings, the fitness characteristics of some wound impaired-mutants could be represented by anaerobic, oxidative, and membrane-stress conditions ex vivo, and more comprehensively by high-density bacterial growth conditions, in the absence of a host. These data shed light on the bacterial functions needed in chronic wound infections, the nature of stresses applied to bacteria at chronic infection sites, and suggest therapeutic targets that might compromise wound infection pathogenesis. |
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Here we sought to identify the genes and functions that mediate fitness of the pathogen Pseudomonas aeruginosa in chronic wound infections, and to better understand the selective environment in wounds. We found that clinical isolates from chronic human wounds were frequently defective in virulence functions and biofilm formation, and that many virulence and biofilm formation genes were not required for bacterial fitness in experimental mouse wounds. In contrast, genes involved in anaerobic growth, some metabolic and energy pathways, and membrane integrity were critical. Consistent with these findings, the fitness characteristics of some wound impaired-mutants could be represented by anaerobic, oxidative, and membrane-stress conditions ex vivo, and more comprehensively by high-density bacterial growth conditions, in the absence of a host. These data shed light on the bacterial functions needed in chronic wound infections, the nature of stresses applied to bacteria at chronic infection sites, and suggest therapeutic targets that might compromise wound infection pathogenesis.</description><identifier>ISSN: 1553-7374</identifier><identifier>ISSN: 1553-7366</identifier><identifier>EISSN: 1553-7374</identifier><identifier>DOI: 10.1371/journal.ppat.1007511</identifier><identifier>PMID: 30893371</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adult ; Anaerobic conditions ; Animals ; Bacteria ; Bacteria - growth & development ; Bacterial Infections - metabolism ; Biofilms ; Biofilms - growth & development ; Biology and Life Sciences ; Cell Proliferation - physiology ; Chronic infection ; Clinical isolates ; Complications and side effects ; Cystic fibrosis ; Density ; Development and progression ; Disease Models, Animal ; Female ; Fitness ; Genes ; Genetic Fitness ; Genomes ; Genomics ; Growth conditions ; Health aspects ; Host Microbial Interactions - physiology ; House mouse ; Humans ; Infection ; Infections ; Male ; Medicine and Health Sciences ; Mice ; Microbial mats ; Microbiological research ; Mutants ; Pathogenesis ; Pathogens ; Pneumonia ; Pseudomonas aeruginosa ; Pseudomonas aeruginosa - growth & development ; Pseudomonas aeruginosa - metabolism ; Pseudomonas aeruginosa - pathogenicity ; Pseudomonas aeruginosa infections ; Pseudomonas Infections ; Supervision ; Therapeutic applications ; Virulence ; Virulence (Microbiology) ; Virulence - physiology ; Wound Healing - physiology ; Wound infection ; Wound Infection - metabolism ; Wound Infection - microbiology ; Wounds</subject><ispartof>PLoS pathogens, 2019-03, Vol.15 (3), p.e1007511-e1007511</ispartof><rights>COPYRIGHT 2019 Public Library of Science</rights><rights>2019 Morgan et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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Here we sought to identify the genes and functions that mediate fitness of the pathogen Pseudomonas aeruginosa in chronic wound infections, and to better understand the selective environment in wounds. We found that clinical isolates from chronic human wounds were frequently defective in virulence functions and biofilm formation, and that many virulence and biofilm formation genes were not required for bacterial fitness in experimental mouse wounds. In contrast, genes involved in anaerobic growth, some metabolic and energy pathways, and membrane integrity were critical. Consistent with these findings, the fitness characteristics of some wound impaired-mutants could be represented by anaerobic, oxidative, and membrane-stress conditions ex vivo, and more comprehensively by high-density bacterial growth conditions, in the absence of a host. These data shed light on the bacterial functions needed in chronic wound infections, the nature of stresses applied to bacteria at chronic infection sites, and suggest therapeutic targets that might compromise wound infection pathogenesis.</description><subject>Adult</subject><subject>Anaerobic conditions</subject><subject>Animals</subject><subject>Bacteria</subject><subject>Bacteria - growth & development</subject><subject>Bacterial Infections - metabolism</subject><subject>Biofilms</subject><subject>Biofilms - growth & development</subject><subject>Biology and Life Sciences</subject><subject>Cell Proliferation - physiology</subject><subject>Chronic infection</subject><subject>Clinical isolates</subject><subject>Complications and side effects</subject><subject>Cystic fibrosis</subject><subject>Density</subject><subject>Development and progression</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>Fitness</subject><subject>Genes</subject><subject>Genetic Fitness</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Growth conditions</subject><subject>Health aspects</subject><subject>Host Microbial Interactions - 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Here we sought to identify the genes and functions that mediate fitness of the pathogen Pseudomonas aeruginosa in chronic wound infections, and to better understand the selective environment in wounds. We found that clinical isolates from chronic human wounds were frequently defective in virulence functions and biofilm formation, and that many virulence and biofilm formation genes were not required for bacterial fitness in experimental mouse wounds. In contrast, genes involved in anaerobic growth, some metabolic and energy pathways, and membrane integrity were critical. Consistent with these findings, the fitness characteristics of some wound impaired-mutants could be represented by anaerobic, oxidative, and membrane-stress conditions ex vivo, and more comprehensively by high-density bacterial growth conditions, in the absence of a host. 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subjects | Adult Anaerobic conditions Animals Bacteria Bacteria - growth & development Bacterial Infections - metabolism Biofilms Biofilms - growth & development Biology and Life Sciences Cell Proliferation - physiology Chronic infection Clinical isolates Complications and side effects Cystic fibrosis Density Development and progression Disease Models, Animal Female Fitness Genes Genetic Fitness Genomes Genomics Growth conditions Health aspects Host Microbial Interactions - physiology House mouse Humans Infection Infections Male Medicine and Health Sciences Mice Microbial mats Microbiological research Mutants Pathogenesis Pathogens Pneumonia Pseudomonas aeruginosa Pseudomonas aeruginosa - growth & development Pseudomonas aeruginosa - metabolism Pseudomonas aeruginosa - pathogenicity Pseudomonas aeruginosa infections Pseudomonas Infections Supervision Therapeutic applications Virulence Virulence (Microbiology) Virulence - physiology Wound Healing - physiology Wound infection Wound Infection - metabolism Wound Infection - microbiology Wounds |
title | Bacterial fitness in chronic wounds appears to be mediated by the capacity for high-density growth, not virulence or biofilm functions |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T20%3A24%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Bacterial%20fitness%20in%20chronic%20wounds%20appears%20to%20be%20mediated%20by%20the%20capacity%20for%20high-density%20growth,%20not%20virulence%20or%20biofilm%20functions&rft.jtitle=PLoS%20pathogens&rft.au=Morgan,%20Sarah%20J&rft.date=2019-03-01&rft.volume=15&rft.issue=3&rft.spage=e1007511&rft.epage=e1007511&rft.pages=e1007511-e1007511&rft.issn=1553-7374&rft.eissn=1553-7374&rft_id=info:doi/10.1371/journal.ppat.1007511&rft_dat=%3Cgale_plos_%3EA580820335%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2251133255&rft_id=info:pmid/30893371&rft_galeid=A580820335&rft_doaj_id=oai_doaj_org_article_04a0e9429ad1465aa981669a15696103&rfr_iscdi=true |