Contribution of Veillonella parvula to Pseudomonas aeruginosa-mediated pathogenicity in a murine tumor model system
The recent finding that high numbers of strict anaerobes are present in the respiratory tract of cystic fibrosis (CF) patients has drawn attention to the pathogenic contribution of the CF microbiome to airway disease. In this study, we investigated the specific interactions of the most dominant bact...
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Veröffentlicht in: | Infection and immunity 2015-01, Vol.83 (1), p.417-429 |
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creator | Pustelny, Christian Komor, Uliana Pawar, Vinay Lorenz, Anne Bielecka, Agata Moter, Annette Gocht, Benjamin Eckweiler, Denitsa Müsken, Mathias Grothe, Claudia Lünsdorf, Heinrich Weiss, Siegfried Häussler, Susanne |
description | The recent finding that high numbers of strict anaerobes are present in the respiratory tract of cystic fibrosis (CF) patients has drawn attention to the pathogenic contribution of the CF microbiome to airway disease. In this study, we investigated the specific interactions of the most dominant bacterial CF pathogen, Pseudomonas aeruginosa, with the anaerobic bacterium Veillonella parvula, which has been recovered at comparable cell numbers from the respiratory tract of CF patients. In addition to growth competition experiments, transcriptional profiling, and analyses of biofilm formation by in vitro studies, we used our recently established in vivo murine tumor model to investigate mutual influences of the two pathogens during a biofilm-associated infection process. We found that P. aeruginosa and V. parvula colonized distinct niches within the tumor. Interestingly, significantly higher cell numbers of P. aeruginosa could be recovered from the tumor tissue when mice were coinfected with both bacterial species than when mice were monoinfected with P. aeruginosa. Concordantly, the results of in vivo transcriptional profiling implied that the presence of V. parvula supports P. aeruginosa growth at the site of infection in the host, and the higher P. aeruginosa load correlated with clinical deterioration of the host. Although many challenges must be overcome to dissect the specific interactions of coinfecting bacteria during an infection process, our findings exemplarily demonstrate that the complex interrelations between coinfecting microorganisms and the immune responses determine clinical outcome to a much greater extent than previously anticipated. |
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A.</contributor><creatorcontrib>Pustelny, Christian ; Komor, Uliana ; Pawar, Vinay ; Lorenz, Anne ; Bielecka, Agata ; Moter, Annette ; Gocht, Benjamin ; Eckweiler, Denitsa ; Müsken, Mathias ; Grothe, Claudia ; Lünsdorf, Heinrich ; Weiss, Siegfried ; Häussler, Susanne ; McCormick, B. A.</creatorcontrib><description>The recent finding that high numbers of strict anaerobes are present in the respiratory tract of cystic fibrosis (CF) patients has drawn attention to the pathogenic contribution of the CF microbiome to airway disease. In this study, we investigated the specific interactions of the most dominant bacterial CF pathogen, Pseudomonas aeruginosa, with the anaerobic bacterium Veillonella parvula, which has been recovered at comparable cell numbers from the respiratory tract of CF patients. In addition to growth competition experiments, transcriptional profiling, and analyses of biofilm formation by in vitro studies, we used our recently established in vivo murine tumor model to investigate mutual influences of the two pathogens during a biofilm-associated infection process. We found that P. aeruginosa and V. parvula colonized distinct niches within the tumor. Interestingly, significantly higher cell numbers of P. aeruginosa could be recovered from the tumor tissue when mice were coinfected with both bacterial species than when mice were monoinfected with P. aeruginosa. Concordantly, the results of in vivo transcriptional profiling implied that the presence of V. parvula supports P. aeruginosa growth at the site of infection in the host, and the higher P. aeruginosa load correlated with clinical deterioration of the host. Although many challenges must be overcome to dissect the specific interactions of coinfecting bacteria during an infection process, our findings exemplarily demonstrate that the complex interrelations between coinfecting microorganisms and the immune responses determine clinical outcome to a much greater extent than previously anticipated.</description><identifier>ISSN: 0019-9567</identifier><identifier>EISSN: 1098-5522</identifier><identifier>DOI: 10.1128/IAI.02234-14</identifier><identifier>PMID: 25385800</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Animals ; Bacterial Infections ; Bacterial Load ; Disease Models, Animal ; Female ; Gene Expression Profiling ; Mice, Inbred BALB C ; Microbial Interactions ; Neoplasms - complications ; Neoplasms - microbiology ; Pseudomonas aeruginosa ; Pseudomonas aeruginosa - pathogenicity ; Pseudomonas Infections - microbiology ; Veillonella - pathogenicity ; Veillonella parvula</subject><ispartof>Infection and immunity, 2015-01, Vol.83 (1), p.417-429</ispartof><rights>Copyright © 2015, American Society for Microbiology. All Rights Reserved.</rights><rights>Copyright © 2015, American Society for Microbiology. All Rights Reserved. 2015 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c460t-4e6c4f8afe7f234f30423f49c2484041c3d814ee4a8045566535c65c0fa21bf3</citedby><cites>FETCH-LOGICAL-c460t-4e6c4f8afe7f234f30423f49c2484041c3d814ee4a8045566535c65c0fa21bf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4288896/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4288896/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3188,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25385800$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>McCormick, B. A.</contributor><creatorcontrib>Pustelny, Christian</creatorcontrib><creatorcontrib>Komor, Uliana</creatorcontrib><creatorcontrib>Pawar, Vinay</creatorcontrib><creatorcontrib>Lorenz, Anne</creatorcontrib><creatorcontrib>Bielecka, Agata</creatorcontrib><creatorcontrib>Moter, Annette</creatorcontrib><creatorcontrib>Gocht, Benjamin</creatorcontrib><creatorcontrib>Eckweiler, Denitsa</creatorcontrib><creatorcontrib>Müsken, Mathias</creatorcontrib><creatorcontrib>Grothe, Claudia</creatorcontrib><creatorcontrib>Lünsdorf, Heinrich</creatorcontrib><creatorcontrib>Weiss, Siegfried</creatorcontrib><creatorcontrib>Häussler, Susanne</creatorcontrib><title>Contribution of Veillonella parvula to Pseudomonas aeruginosa-mediated pathogenicity in a murine tumor model system</title><title>Infection and immunity</title><addtitle>Infect Immun</addtitle><description>The recent finding that high numbers of strict anaerobes are present in the respiratory tract of cystic fibrosis (CF) patients has drawn attention to the pathogenic contribution of the CF microbiome to airway disease. In this study, we investigated the specific interactions of the most dominant bacterial CF pathogen, Pseudomonas aeruginosa, with the anaerobic bacterium Veillonella parvula, which has been recovered at comparable cell numbers from the respiratory tract of CF patients. In addition to growth competition experiments, transcriptional profiling, and analyses of biofilm formation by in vitro studies, we used our recently established in vivo murine tumor model to investigate mutual influences of the two pathogens during a biofilm-associated infection process. We found that P. aeruginosa and V. parvula colonized distinct niches within the tumor. Interestingly, significantly higher cell numbers of P. aeruginosa could be recovered from the tumor tissue when mice were coinfected with both bacterial species than when mice were monoinfected with P. aeruginosa. Concordantly, the results of in vivo transcriptional profiling implied that the presence of V. parvula supports P. aeruginosa growth at the site of infection in the host, and the higher P. aeruginosa load correlated with clinical deterioration of the host. Although many challenges must be overcome to dissect the specific interactions of coinfecting bacteria during an infection process, our findings exemplarily demonstrate that the complex interrelations between coinfecting microorganisms and the immune responses determine clinical outcome to a much greater extent than previously anticipated.</description><subject>Animals</subject><subject>Bacterial Infections</subject><subject>Bacterial Load</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>Gene Expression Profiling</subject><subject>Mice, Inbred BALB C</subject><subject>Microbial Interactions</subject><subject>Neoplasms - complications</subject><subject>Neoplasms - microbiology</subject><subject>Pseudomonas aeruginosa</subject><subject>Pseudomonas aeruginosa - pathogenicity</subject><subject>Pseudomonas Infections - microbiology</subject><subject>Veillonella - pathogenicity</subject><subject>Veillonella parvula</subject><issn>0019-9567</issn><issn>1098-5522</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkb1rHDEQxUWIic-XdKmDyhRZW9KOdrVNwBxJfGBwCpNW6LSjs8KudJG0hvvvI3_EJF2qYZgfj_fmEfKes3POhbrYXm7PmRAtNBxekRVng2qkFOI1WTHGh2aQXX9KznL-WVcAUG_IqZCtkoqxFcmbGEryu6X4GGh09Af6aYoBp8nQg0n3S50l0u8ZlzHOMZhMDaZl70PMpplx9KbgWNFyF_cYvPXlSH2ghs5L8gFpWeaY6BxHnGg-5oLzW3LizJTx3fNck9uvX243V831zbft5vK6sdCx0gB2FpwyDntX47mWgWgdDFaAAgbctqPigAhGMZCy62QrbSctc0bwnWvX5POT7GHZVZ8Wa1Az6UPys0lHHY3X_16Cv9P7eK9BKKWGrgp8fBZI8deCuejZZ_vwmYBxyZp3ErpByr7_D7Tth0HJmmBNPj2hNsWcE7oXR5zph0Z1bVQ_Nqo5VPzD3yle4D8Vtr8B5laenQ</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Pustelny, Christian</creator><creator>Komor, Uliana</creator><creator>Pawar, Vinay</creator><creator>Lorenz, Anne</creator><creator>Bielecka, Agata</creator><creator>Moter, Annette</creator><creator>Gocht, Benjamin</creator><creator>Eckweiler, Denitsa</creator><creator>Müsken, Mathias</creator><creator>Grothe, Claudia</creator><creator>Lünsdorf, Heinrich</creator><creator>Weiss, Siegfried</creator><creator>Häussler, Susanne</creator><general>American Society for Microbiology</general><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>7X8</scope><scope>7QL</scope><scope>7T5</scope><scope>C1K</scope><scope>H94</scope><scope>5PM</scope></search><sort><creationdate>20150101</creationdate><title>Contribution of Veillonella parvula to Pseudomonas aeruginosa-mediated pathogenicity in a murine tumor model system</title><author>Pustelny, Christian ; Komor, Uliana ; Pawar, Vinay ; Lorenz, Anne ; Bielecka, Agata ; Moter, Annette ; Gocht, Benjamin ; Eckweiler, Denitsa ; Müsken, Mathias ; Grothe, Claudia ; Lünsdorf, Heinrich ; Weiss, Siegfried ; Häussler, Susanne</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c460t-4e6c4f8afe7f234f30423f49c2484041c3d814ee4a8045566535c65c0fa21bf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Bacterial Infections</topic><topic>Bacterial Load</topic><topic>Disease Models, Animal</topic><topic>Female</topic><topic>Gene Expression Profiling</topic><topic>Mice, Inbred BALB C</topic><topic>Microbial Interactions</topic><topic>Neoplasms - complications</topic><topic>Neoplasms - microbiology</topic><topic>Pseudomonas aeruginosa</topic><topic>Pseudomonas aeruginosa - pathogenicity</topic><topic>Pseudomonas Infections - microbiology</topic><topic>Veillonella - pathogenicity</topic><topic>Veillonella parvula</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pustelny, Christian</creatorcontrib><creatorcontrib>Komor, Uliana</creatorcontrib><creatorcontrib>Pawar, Vinay</creatorcontrib><creatorcontrib>Lorenz, Anne</creatorcontrib><creatorcontrib>Bielecka, Agata</creatorcontrib><creatorcontrib>Moter, Annette</creatorcontrib><creatorcontrib>Gocht, Benjamin</creatorcontrib><creatorcontrib>Eckweiler, Denitsa</creatorcontrib><creatorcontrib>Müsken, Mathias</creatorcontrib><creatorcontrib>Grothe, Claudia</creatorcontrib><creatorcontrib>Lünsdorf, Heinrich</creatorcontrib><creatorcontrib>Weiss, Siegfried</creatorcontrib><creatorcontrib>Häussler, Susanne</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Infection and immunity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pustelny, Christian</au><au>Komor, Uliana</au><au>Pawar, Vinay</au><au>Lorenz, Anne</au><au>Bielecka, Agata</au><au>Moter, Annette</au><au>Gocht, Benjamin</au><au>Eckweiler, Denitsa</au><au>Müsken, Mathias</au><au>Grothe, Claudia</au><au>Lünsdorf, Heinrich</au><au>Weiss, Siegfried</au><au>Häussler, Susanne</au><au>McCormick, B. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Contribution of Veillonella parvula to Pseudomonas aeruginosa-mediated pathogenicity in a murine tumor model system</atitle><jtitle>Infection and immunity</jtitle><addtitle>Infect Immun</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>83</volume><issue>1</issue><spage>417</spage><epage>429</epage><pages>417-429</pages><issn>0019-9567</issn><eissn>1098-5522</eissn><abstract>The recent finding that high numbers of strict anaerobes are present in the respiratory tract of cystic fibrosis (CF) patients has drawn attention to the pathogenic contribution of the CF microbiome to airway disease. In this study, we investigated the specific interactions of the most dominant bacterial CF pathogen, Pseudomonas aeruginosa, with the anaerobic bacterium Veillonella parvula, which has been recovered at comparable cell numbers from the respiratory tract of CF patients. In addition to growth competition experiments, transcriptional profiling, and analyses of biofilm formation by in vitro studies, we used our recently established in vivo murine tumor model to investigate mutual influences of the two pathogens during a biofilm-associated infection process. We found that P. aeruginosa and V. parvula colonized distinct niches within the tumor. Interestingly, significantly higher cell numbers of P. aeruginosa could be recovered from the tumor tissue when mice were coinfected with both bacterial species than when mice were monoinfected with P. aeruginosa. Concordantly, the results of in vivo transcriptional profiling implied that the presence of V. parvula supports P. aeruginosa growth at the site of infection in the host, and the higher P. aeruginosa load correlated with clinical deterioration of the host. 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subjects | Animals Bacterial Infections Bacterial Load Disease Models, Animal Female Gene Expression Profiling Mice, Inbred BALB C Microbial Interactions Neoplasms - complications Neoplasms - microbiology Pseudomonas aeruginosa Pseudomonas aeruginosa - pathogenicity Pseudomonas Infections - microbiology Veillonella - pathogenicity Veillonella parvula |
title | Contribution of Veillonella parvula to Pseudomonas aeruginosa-mediated pathogenicity in a murine tumor model system |
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