Dynamics of Intrapulmonary Bacterial Growth in a Murine Model of Repeated Microaspiration
To study the change in intrapulmonary bacterial growth rate over time during Gram-negative pneumonia, a two-hit model of recurrent bacterial aspiration was developed in mice. A mutant of Klebsiella pneumoniae was isolated that could be distinguished from the wild type when cultured on appropriate me...
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Veröffentlicht in: | American journal of respiratory cell and molecular biology 2005-11, Vol.33 (5), p.476-482 |
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creator | Ben-David, Itzhak Price, Sarah E Bortz, David M Greineder, Colin F Cohen, Samuel E Bauer, Amy L Jackson, Trachette L Younger, John G |
description | To study the change in intrapulmonary bacterial growth rate over time during Gram-negative pneumonia, a two-hit model of recurrent bacterial aspiration was developed in mice. A mutant of Klebsiella pneumoniae was isolated that could be distinguished from the wild type when cultured on appropriate media. These strains were intranasally administered, 4 h apart, to mice whose lungs were quantitatively cultured 24 h later. The relative burden of each aspirated inoculum was determined, and, using the administered dose and the number of bacteria from each inoculum present at the end of the experiment, first-order growth constants for each inoculum were calculated. Results indicate that after an initial aspiration of this organism, subsequently aspirated bacteria proliferate more slowly. When two aspirations occurred 4 h apart, the bacteria aspirated first represented 96% of total lung burden at 24 h. The growth constant of the second inoculum was related to the magnitude of the first inoculum in an inverse, nonlinear fashion. When parallel experiments were performed in complement C3-deficient mice, no suppression of the second inoculum was noted, suggesting that early upregulation of antibacterial activity in the lung is a C3-mediated event. |
doi_str_mv | 10.1165/rcmb.2005-0053OC |
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A mutant of Klebsiella pneumoniae was isolated that could be distinguished from the wild type when cultured on appropriate media. These strains were intranasally administered, 4 h apart, to mice whose lungs were quantitatively cultured 24 h later. The relative burden of each aspirated inoculum was determined, and, using the administered dose and the number of bacteria from each inoculum present at the end of the experiment, first-order growth constants for each inoculum were calculated. Results indicate that after an initial aspiration of this organism, subsequently aspirated bacteria proliferate more slowly. When two aspirations occurred 4 h apart, the bacteria aspirated first represented 96% of total lung burden at 24 h. The growth constant of the second inoculum was related to the magnitude of the first inoculum in an inverse, nonlinear fashion. When parallel experiments were performed in complement C3-deficient mice, no suppression of the second inoculum was noted, suggesting that early upregulation of antibacterial activity in the lung is a C3-mediated event.</description><identifier>ISSN: 1044-1549</identifier><identifier>EISSN: 1535-4989</identifier><identifier>DOI: 10.1165/rcmb.2005-0053OC</identifier><identifier>PMID: 16014897</identifier><identifier>CODEN: AJRBEL</identifier><language>eng</language><publisher>United States: Am Thoracic Soc</publisher><subject>Animals ; Complement C3 - genetics ; Disease Models, Animal ; Galactose - genetics ; Klebsiella Infections - microbiology ; Klebsiella pneumoniae - genetics ; Klebsiella pneumoniae - growth & development ; Lung - microbiology ; Mice ; Mice, Mutant Strains ; Mutation ; Pneumonia, Bacterial - microbiology ; Serratia Infections - microbiology ; Serratia marcescens - growth & development</subject><ispartof>American journal of respiratory cell and molecular biology, 2005-11, Vol.33 (5), p.476-482</ispartof><rights>Copyright American Thoracic Society Nov 2005</rights><rights>Copyright © 2005, American Thoracic Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c454t-1edd87efd16be82a8111fcbfc6eaac17f910a7c2eb6d2f654feab4940c5df5bb3</citedby><cites>FETCH-LOGICAL-c454t-1edd87efd16be82a8111fcbfc6eaac17f910a7c2eb6d2f654feab4940c5df5bb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16014897$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ben-David, Itzhak</creatorcontrib><creatorcontrib>Price, Sarah E</creatorcontrib><creatorcontrib>Bortz, David M</creatorcontrib><creatorcontrib>Greineder, Colin F</creatorcontrib><creatorcontrib>Cohen, Samuel E</creatorcontrib><creatorcontrib>Bauer, Amy L</creatorcontrib><creatorcontrib>Jackson, Trachette L</creatorcontrib><creatorcontrib>Younger, John G</creatorcontrib><title>Dynamics of Intrapulmonary Bacterial Growth in a Murine Model of Repeated Microaspiration</title><title>American journal of respiratory cell and molecular biology</title><addtitle>Am J Respir Cell Mol Biol</addtitle><description>To study the change in intrapulmonary bacterial growth rate over time during Gram-negative pneumonia, a two-hit model of recurrent bacterial aspiration was developed in mice. A mutant of Klebsiella pneumoniae was isolated that could be distinguished from the wild type when cultured on appropriate media. These strains were intranasally administered, 4 h apart, to mice whose lungs were quantitatively cultured 24 h later. The relative burden of each aspirated inoculum was determined, and, using the administered dose and the number of bacteria from each inoculum present at the end of the experiment, first-order growth constants for each inoculum were calculated. Results indicate that after an initial aspiration of this organism, subsequently aspirated bacteria proliferate more slowly. When two aspirations occurred 4 h apart, the bacteria aspirated first represented 96% of total lung burden at 24 h. The growth constant of the second inoculum was related to the magnitude of the first inoculum in an inverse, nonlinear fashion. When parallel experiments were performed in complement C3-deficient mice, no suppression of the second inoculum was noted, suggesting that early upregulation of antibacterial activity in the lung is a C3-mediated event.</description><subject>Animals</subject><subject>Complement C3 - genetics</subject><subject>Disease Models, Animal</subject><subject>Galactose - genetics</subject><subject>Klebsiella Infections - microbiology</subject><subject>Klebsiella pneumoniae - genetics</subject><subject>Klebsiella pneumoniae - growth & development</subject><subject>Lung - microbiology</subject><subject>Mice</subject><subject>Mice, Mutant Strains</subject><subject>Mutation</subject><subject>Pneumonia, Bacterial - microbiology</subject><subject>Serratia Infections - microbiology</subject><subject>Serratia marcescens - growth & development</subject><issn>1044-1549</issn><issn>1535-4989</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpdkc2L1TAUxYsozofuXUlxIbPpmKRJ2m4Efeo4MI8B0YWrcJvezMsjTWrSOsx_b8p7-LUICeR3DvfcUxQvKLmkVIo3UY_9JSNEVPnUt5tHxSkVtah413aP85twXlHBu5PiLKU9IZS1lD4tTqgklLddc1p8__DgYbQ6lcGU136OMC1uDB7iQ_ke9IzRgiuvYrifd6X1JZTbJVqP5TYM6FbRF5wQZhzKrdUxQJpshNkG_6x4YsAlfH68z4tvnz5-3Xyubm6vrjfvbirNBZ8risPQNmgGKntsGeQBqdG90RIBNG1MRwk0mmEvB2ak4Aah5x0nWgxG9H19Xrw9-E5LP-KgcQ3h1BTtmEOoAFb9--PtTt2Fn4o1665ENnh9NIjhx4JpVqNNGp0Dj2FJSrYNqVktM_jqP3AfluhzOMVIIwVrJcsQOUB5GSlFNL8noUStpam1NLWWpg6lZcnLvxP8ERxbysDFAdjZu929jajSCM5lnCrYr351rYTijax_AevSpJQ</recordid><startdate>20051101</startdate><enddate>20051101</enddate><creator>Ben-David, Itzhak</creator><creator>Price, Sarah E</creator><creator>Bortz, David M</creator><creator>Greineder, Colin F</creator><creator>Cohen, Samuel E</creator><creator>Bauer, Amy L</creator><creator>Jackson, Trachette L</creator><creator>Younger, John G</creator><general>Am Thoracic Soc</general><general>American Thoracic Society</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20051101</creationdate><title>Dynamics of Intrapulmonary Bacterial Growth in a Murine Model of Repeated Microaspiration</title><author>Ben-David, Itzhak ; 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A mutant of Klebsiella pneumoniae was isolated that could be distinguished from the wild type when cultured on appropriate media. These strains were intranasally administered, 4 h apart, to mice whose lungs were quantitatively cultured 24 h later. The relative burden of each aspirated inoculum was determined, and, using the administered dose and the number of bacteria from each inoculum present at the end of the experiment, first-order growth constants for each inoculum were calculated. Results indicate that after an initial aspiration of this organism, subsequently aspirated bacteria proliferate more slowly. When two aspirations occurred 4 h apart, the bacteria aspirated first represented 96% of total lung burden at 24 h. The growth constant of the second inoculum was related to the magnitude of the first inoculum in an inverse, nonlinear fashion. When parallel experiments were performed in complement C3-deficient mice, no suppression of the second inoculum was noted, suggesting that early upregulation of antibacterial activity in the lung is a C3-mediated event.</abstract><cop>United States</cop><pub>Am Thoracic Soc</pub><pmid>16014897</pmid><doi>10.1165/rcmb.2005-0053OC</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Complement C3 - genetics Disease Models, Animal Galactose - genetics Klebsiella Infections - microbiology Klebsiella pneumoniae - genetics Klebsiella pneumoniae - growth & development Lung - microbiology Mice Mice, Mutant Strains Mutation Pneumonia, Bacterial - microbiology Serratia Infections - microbiology Serratia marcescens - growth & development |
title | Dynamics of Intrapulmonary Bacterial Growth in a Murine Model of Repeated Microaspiration |
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