Pseudomonas aeruginosa Microevolution during Cystic Fibrosis Lung Infection Establishes Clones with Adapted Virulence
During long-term lung infection in patients with cystic fibrosis (CF), Pseudomonas aeruginosa strains develop mutations leading to clonal expansion. This microevolution is believed to be correlated with a reduced virulence. We tested this hypothesis in models of lung infection, using mice with diffe...
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Veröffentlicht in: | American journal of respiratory and critical care medicine 2009-07, Vol.180 (2), p.138-145 |
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creator | Bragonzi, Alessandra Paroni, Moira Nonis, Alessandro Cramer, Nina Montanari, Sara Rejman, Joanna Di Serio, Clelia Doring, Gerd Tummler, Burkhard |
description | During long-term lung infection in patients with cystic fibrosis (CF), Pseudomonas aeruginosa strains develop mutations leading to clonal expansion. This microevolution is believed to be correlated with a reduced virulence.
We tested this hypothesis in models of lung infection, using mice with different genetic backgrounds.
From infected airways of six patients with CF, 25 P. aeruginosa clones were isolated during a period of up to 16.3 years and genotypically and phenotypically characterized. Virulence of the 8 early, 6 intermediate, and 11 late CF isolates and 5 environmental strains was assessed by monitoring acute mortality versus survival and P. aeruginosa chronic persistence versus lung clearance in mice of different genetic backgrounds, including CF mice.
Different patients harbored clonally unrelated strains, but early, intermediate, and late P. aeruginosa isolates from single patients were clonally related, allowing comparative in vivo analysis. Although late isolates were attenuated in causing acute mortality in the mouse models, compared with early and intermediate clonal isolates and environmental strains, they did not differ from early and intermediate clonal isolates in their capacity to establish chronic infection and cause extensive inflammation in the murine respiratory tract.
Our findings indicate that clonal expansion of P. aeruginosa strains during microevolution within CF lungs leads to populations with altered but not reduced virulence. These P. aeruginosa clones with adapted virulence play a critical role in the pathogenesis of chronic infections and may serve to define virulence determinants as targets for novel therapies. |
doi_str_mv | 10.1164/rccm.200812-1943OC |
format | Article |
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We tested this hypothesis in models of lung infection, using mice with different genetic backgrounds.
From infected airways of six patients with CF, 25 P. aeruginosa clones were isolated during a period of up to 16.3 years and genotypically and phenotypically characterized. Virulence of the 8 early, 6 intermediate, and 11 late CF isolates and 5 environmental strains was assessed by monitoring acute mortality versus survival and P. aeruginosa chronic persistence versus lung clearance in mice of different genetic backgrounds, including CF mice.
Different patients harbored clonally unrelated strains, but early, intermediate, and late P. aeruginosa isolates from single patients were clonally related, allowing comparative in vivo analysis. Although late isolates were attenuated in causing acute mortality in the mouse models, compared with early and intermediate clonal isolates and environmental strains, they did not differ from early and intermediate clonal isolates in their capacity to establish chronic infection and cause extensive inflammation in the murine respiratory tract.
Our findings indicate that clonal expansion of P. aeruginosa strains during microevolution within CF lungs leads to populations with altered but not reduced virulence. These P. aeruginosa clones with adapted virulence play a critical role in the pathogenesis of chronic infections and may serve to define virulence determinants as targets for novel therapies.</description><identifier>ISSN: 1073-449X</identifier><identifier>EISSN: 1535-4970</identifier><identifier>DOI: 10.1164/rccm.200812-1943OC</identifier><identifier>PMID: 19423715</identifier><language>eng</language><publisher>New York, NY: Am Thoracic Soc</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Animals ; Biological and medical sciences ; Chronic Disease ; Chronic illnesses ; Clone Cells - physiology ; Cloning ; Cystic fibrosis ; Cystic Fibrosis - microbiology ; Cystic Fibrosis - pathology ; Disease Models, Animal ; Emergency and intensive respiratory care ; Genes ; Humans ; Hypotheses ; Infections ; Intensive care medicine ; Laboratories ; Lungs ; Male ; Medical sciences ; Mice ; Mice, Inbred C57BL ; Mice, Inbred CFTR ; Mortality ; Mutation ; Pseudomonas aeruginosa - isolation & purification ; Pseudomonas aeruginosa - pathogenicity ; Pseudomonas Infections - microbiology ; Pseudomonas Infections - pathology ; Respiratory Tract Infections - microbiology ; Respiratory Tract Infections - pathology ; Virulence</subject><ispartof>American journal of respiratory and critical care medicine, 2009-07, Vol.180 (2), p.138-145</ispartof><rights>2009 INIST-CNRS</rights><rights>Copyright American Thoracic Society Jul 15, 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-d57931779c0cd03fbeabf81cc9babffa0c6ae75f13608d84dc6efc1b066183f53</citedby><cites>FETCH-LOGICAL-c417t-d57931779c0cd03fbeabf81cc9babffa0c6ae75f13608d84dc6efc1b066183f53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,4026,4027,27928,27929</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21708553$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19423715$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bragonzi, Alessandra</creatorcontrib><creatorcontrib>Paroni, Moira</creatorcontrib><creatorcontrib>Nonis, Alessandro</creatorcontrib><creatorcontrib>Cramer, Nina</creatorcontrib><creatorcontrib>Montanari, Sara</creatorcontrib><creatorcontrib>Rejman, Joanna</creatorcontrib><creatorcontrib>Di Serio, Clelia</creatorcontrib><creatorcontrib>Doring, Gerd</creatorcontrib><creatorcontrib>Tummler, Burkhard</creatorcontrib><title>Pseudomonas aeruginosa Microevolution during Cystic Fibrosis Lung Infection Establishes Clones with Adapted Virulence</title><title>American journal of respiratory and critical care medicine</title><addtitle>Am J Respir Crit Care Med</addtitle><description>During long-term lung infection in patients with cystic fibrosis (CF), Pseudomonas aeruginosa strains develop mutations leading to clonal expansion. This microevolution is believed to be correlated with a reduced virulence.
We tested this hypothesis in models of lung infection, using mice with different genetic backgrounds.
From infected airways of six patients with CF, 25 P. aeruginosa clones were isolated during a period of up to 16.3 years and genotypically and phenotypically characterized. Virulence of the 8 early, 6 intermediate, and 11 late CF isolates and 5 environmental strains was assessed by monitoring acute mortality versus survival and P. aeruginosa chronic persistence versus lung clearance in mice of different genetic backgrounds, including CF mice.
Different patients harbored clonally unrelated strains, but early, intermediate, and late P. aeruginosa isolates from single patients were clonally related, allowing comparative in vivo analysis. Although late isolates were attenuated in causing acute mortality in the mouse models, compared with early and intermediate clonal isolates and environmental strains, they did not differ from early and intermediate clonal isolates in their capacity to establish chronic infection and cause extensive inflammation in the murine respiratory tract.
Our findings indicate that clonal expansion of P. aeruginosa strains during microevolution within CF lungs leads to populations with altered but not reduced virulence. These P. aeruginosa clones with adapted virulence play a critical role in the pathogenesis of chronic infections and may serve to define virulence determinants as targets for novel therapies.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Chronic Disease</subject><subject>Chronic illnesses</subject><subject>Clone Cells - physiology</subject><subject>Cloning</subject><subject>Cystic fibrosis</subject><subject>Cystic Fibrosis - microbiology</subject><subject>Cystic Fibrosis - pathology</subject><subject>Disease Models, Animal</subject><subject>Emergency and intensive respiratory care</subject><subject>Genes</subject><subject>Humans</subject><subject>Hypotheses</subject><subject>Infections</subject><subject>Intensive care medicine</subject><subject>Laboratories</subject><subject>Lungs</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Inbred CFTR</subject><subject>Mortality</subject><subject>Mutation</subject><subject>Pseudomonas aeruginosa - isolation & purification</subject><subject>Pseudomonas aeruginosa - pathogenicity</subject><subject>Pseudomonas Infections - microbiology</subject><subject>Pseudomonas Infections - pathology</subject><subject>Respiratory Tract Infections - microbiology</subject><subject>Respiratory Tract Infections - pathology</subject><subject>Virulence</subject><issn>1073-449X</issn><issn>1535-4970</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpdkUFv1DAQhSMEoqXwBzigCKlIHFI8cRwnxypqodKicgDEzXIce9crx148MVX_PV6yAonTjEbfvDeaVxSvgVwBtM2HqNR8VRPSQV1B39D74UlxDoyyquk5eZp7wmnVNP2Ps-IF4p4QqDsgz4uzTNeUAzsv0hfUaQpz8BJLqWPaWh9Qlp-tikH_Ci4tNvhyStH6bTk84mJVeWvHGNBiuUl5eOeNVn-oG1zk6CzuNJaDCz6XB7vsyutJHhY9ld9tTE57pV8Wz4x0qF-d6kXx7fbm6_Cp2tx_vBuuN5VqgC_VxHhPgfNeETURakYtR9OBUv2YGyOJaqXmzABtSTd1zaRabRSMpG2ho4bRi-LdqnuI4WfSuIjZotLOSa9DQtHypmn7us7g2__AfUjR59sE9H1LWP5khuoVyq9BjNqIQ7SzjI8CiDgmIo6JiDURsSaSl96clNM46-nfyimCDFyeAIlKOhOlVxb_cjVw0jF2dH-_cju73T3YqAXO0rksC0Luj87QEZF9aUd_A9Wxpew</recordid><startdate>20090715</startdate><enddate>20090715</enddate><creator>Bragonzi, Alessandra</creator><creator>Paroni, Moira</creator><creator>Nonis, Alessandro</creator><creator>Cramer, Nina</creator><creator>Montanari, Sara</creator><creator>Rejman, Joanna</creator><creator>Di Serio, Clelia</creator><creator>Doring, Gerd</creator><creator>Tummler, Burkhard</creator><general>Am Thoracic Soc</general><general>American Thoracic Society</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20090715</creationdate><title>Pseudomonas aeruginosa Microevolution during Cystic Fibrosis Lung Infection Establishes Clones with Adapted Virulence</title><author>Bragonzi, Alessandra ; Paroni, Moira ; Nonis, Alessandro ; Cramer, Nina ; Montanari, Sara ; Rejman, Joanna ; Di Serio, Clelia ; Doring, Gerd ; Tummler, Burkhard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-d57931779c0cd03fbeabf81cc9babffa0c6ae75f13608d84dc6efc1b066183f53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Chronic Disease</topic><topic>Chronic illnesses</topic><topic>Clone Cells - physiology</topic><topic>Cloning</topic><topic>Cystic fibrosis</topic><topic>Cystic Fibrosis - microbiology</topic><topic>Cystic Fibrosis - pathology</topic><topic>Disease Models, Animal</topic><topic>Emergency and intensive respiratory care</topic><topic>Genes</topic><topic>Humans</topic><topic>Hypotheses</topic><topic>Infections</topic><topic>Intensive care medicine</topic><topic>Laboratories</topic><topic>Lungs</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Inbred CFTR</topic><topic>Mortality</topic><topic>Mutation</topic><topic>Pseudomonas aeruginosa - isolation & purification</topic><topic>Pseudomonas aeruginosa - pathogenicity</topic><topic>Pseudomonas Infections - microbiology</topic><topic>Pseudomonas Infections - pathology</topic><topic>Respiratory Tract Infections - microbiology</topic><topic>Respiratory Tract Infections - pathology</topic><topic>Virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bragonzi, Alessandra</creatorcontrib><creatorcontrib>Paroni, Moira</creatorcontrib><creatorcontrib>Nonis, Alessandro</creatorcontrib><creatorcontrib>Cramer, Nina</creatorcontrib><creatorcontrib>Montanari, Sara</creatorcontrib><creatorcontrib>Rejman, Joanna</creatorcontrib><creatorcontrib>Di Serio, Clelia</creatorcontrib><creatorcontrib>Doring, Gerd</creatorcontrib><creatorcontrib>Tummler, Burkhard</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of respiratory and critical care medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bragonzi, Alessandra</au><au>Paroni, Moira</au><au>Nonis, Alessandro</au><au>Cramer, Nina</au><au>Montanari, Sara</au><au>Rejman, Joanna</au><au>Di Serio, Clelia</au><au>Doring, Gerd</au><au>Tummler, Burkhard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pseudomonas aeruginosa Microevolution during Cystic Fibrosis Lung Infection Establishes Clones with Adapted Virulence</atitle><jtitle>American journal of respiratory and critical care medicine</jtitle><addtitle>Am J Respir Crit Care Med</addtitle><date>2009-07-15</date><risdate>2009</risdate><volume>180</volume><issue>2</issue><spage>138</spage><epage>145</epage><pages>138-145</pages><issn>1073-449X</issn><eissn>1535-4970</eissn><abstract>During long-term lung infection in patients with cystic fibrosis (CF), Pseudomonas aeruginosa strains develop mutations leading to clonal expansion. This microevolution is believed to be correlated with a reduced virulence.
We tested this hypothesis in models of lung infection, using mice with different genetic backgrounds.
From infected airways of six patients with CF, 25 P. aeruginosa clones were isolated during a period of up to 16.3 years and genotypically and phenotypically characterized. Virulence of the 8 early, 6 intermediate, and 11 late CF isolates and 5 environmental strains was assessed by monitoring acute mortality versus survival and P. aeruginosa chronic persistence versus lung clearance in mice of different genetic backgrounds, including CF mice.
Different patients harbored clonally unrelated strains, but early, intermediate, and late P. aeruginosa isolates from single patients were clonally related, allowing comparative in vivo analysis. Although late isolates were attenuated in causing acute mortality in the mouse models, compared with early and intermediate clonal isolates and environmental strains, they did not differ from early and intermediate clonal isolates in their capacity to establish chronic infection and cause extensive inflammation in the murine respiratory tract.
Our findings indicate that clonal expansion of P. aeruginosa strains during microevolution within CF lungs leads to populations with altered but not reduced virulence. These P. aeruginosa clones with adapted virulence play a critical role in the pathogenesis of chronic infections and may serve to define virulence determinants as targets for novel therapies.</abstract><cop>New York, NY</cop><pub>Am Thoracic Soc</pub><pmid>19423715</pmid><doi>10.1164/rccm.200812-1943OC</doi><tpages>8</tpages></addata></record> |
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subjects | Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Animals Biological and medical sciences Chronic Disease Chronic illnesses Clone Cells - physiology Cloning Cystic fibrosis Cystic Fibrosis - microbiology Cystic Fibrosis - pathology Disease Models, Animal Emergency and intensive respiratory care Genes Humans Hypotheses Infections Intensive care medicine Laboratories Lungs Male Medical sciences Mice Mice, Inbred C57BL Mice, Inbred CFTR Mortality Mutation Pseudomonas aeruginosa - isolation & purification Pseudomonas aeruginosa - pathogenicity Pseudomonas Infections - microbiology Pseudomonas Infections - pathology Respiratory Tract Infections - microbiology Respiratory Tract Infections - pathology Virulence |
title | Pseudomonas aeruginosa Microevolution during Cystic Fibrosis Lung Infection Establishes Clones with Adapted Virulence |
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