Demonstration of spread by Mycobacterium tuberculosis bacilli in A549 epithelial cell monolayers
Abstract We developed an in vitro tissue-culture model to analyze the process involved in mycobacterial spread through lung epithelial cell monolayers. A549 cells were infected with low numbers of viable Mycobacterium tuberculosis bacilli expressing the gfp gene. Subsequent addition of a soft agaros...
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Veröffentlicht in: | FEMS microbiology letters 2002-07, Vol.212 (2), p.145-149 |
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description | Abstract
We developed an in vitro tissue-culture model to analyze the process involved in mycobacterial spread through lung epithelial cell monolayers. A549 cells were infected with low numbers of viable Mycobacterium tuberculosis bacilli expressing the gfp gene. Subsequent addition of a soft agarose overlay prevented the dispersal of the bacilli from the initial points of attachment. By fluorescence microscopy the bacteria were observed to infect and grow within the primary target cells; this was followed by lysis of the infected cells and subsequent infection of adjacent cells. This process repeated itself until an area of clearing (plaque formation) was observed. The addition of amikacin after initial infection did not prevent intracellular growth; however, subsequent plaque formation was not observed. Plaque formation was also observed after infection with Mycobacterium bovis BCG bacilli, but the plaques were smaller than those formed after infection with M. tuberculosis. These observations reinforce the possibility that cell-to-cell spreading of M. tuberculosis bacilli, particularly early in the course of infection within lung macrophages, pneumocytes, and other cells, may be an important component in the infectious process. |
doi_str_mv | 10.1111/j.1574-6968.2002.tb11258.x |
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We developed an in vitro tissue-culture model to analyze the process involved in mycobacterial spread through lung epithelial cell monolayers. A549 cells were infected with low numbers of viable Mycobacterium tuberculosis bacilli expressing the gfp gene. Subsequent addition of a soft agarose overlay prevented the dispersal of the bacilli from the initial points of attachment. By fluorescence microscopy the bacteria were observed to infect and grow within the primary target cells; this was followed by lysis of the infected cells and subsequent infection of adjacent cells. This process repeated itself until an area of clearing (plaque formation) was observed. The addition of amikacin after initial infection did not prevent intracellular growth; however, subsequent plaque formation was not observed. Plaque formation was also observed after infection with Mycobacterium bovis BCG bacilli, but the plaques were smaller than those formed after infection with M. tuberculosis. These observations reinforce the possibility that cell-to-cell spreading of M. tuberculosis bacilli, particularly early in the course of infection within lung macrophages, pneumocytes, and other cells, may be an important component in the infectious process.</description><identifier>ISSN: 0378-1097</identifier><identifier>EISSN: 1574-6968</identifier><identifier>DOI: 10.1111/j.1574-6968.2002.tb11258.x</identifier><identifier>PMID: 12113926</identifier><identifier>CODEN: FMLED7</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Amikacin ; Bacilli ; Bacillus Calmette-Guerin vaccine ; Bacteriology ; BCG ; Biological and medical sciences ; Cell culture ; Cell spreading ; Cells, Cultured ; Dispersal ; Epithelial cells ; Epithelial Cells - cytology ; Epithelial Cells - microbiology ; Fluorescence ; Fluorescence microscopy ; Fundamental and applied biological sciences. Psychology ; Genetics ; Green fluorescent protein ; Green Fluorescent Proteins ; Human lung epithelial cell ; Humans ; Indicators and Reagents - metabolism ; Infections ; Luminescent Proteins - genetics ; Lungs ; Lysis ; Macrophages ; Microbiology ; Monolayers ; Mycobacterium tuberculosis ; Mycobacterium tuberculosis - genetics ; Mycobacterium tuberculosis - growth & development ; Mycobacterium tuberculosis - pathogenicity ; Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains ; Plaque ; Plaques ; Pneumocytes ; Respiratory Mucosa - cytology ; Tissue culture ; Tuberculosis ; Tuberculosis, Pulmonary - microbiology ; Virulence</subject><ispartof>FEMS microbiology letters, 2002-07, Vol.212 (2), p.145-149</ispartof><rights>2002 Federation of European Microbiological Societies 2002</rights><rights>2002 Federation of European Microbiological Societies</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3525-57f7bed7d2d9936e685d34f5976c54e57eaaf1ed89dbae115262418093759cd03</citedby><cites>FETCH-LOGICAL-c3525-57f7bed7d2d9936e685d34f5976c54e57eaaf1ed89dbae115262418093759cd03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1574-6968.2002.tb11258.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1574-6968.2002.tb11258.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27922,27923,45572,45573</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14477017$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12113926$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Castro-Garza, Jorge</creatorcontrib><creatorcontrib>King, C.Harold</creatorcontrib><creatorcontrib>Swords, W.Edward</creatorcontrib><creatorcontrib>Quinn, Frederick D</creatorcontrib><title>Demonstration of spread by Mycobacterium tuberculosis bacilli in A549 epithelial cell monolayers</title><title>FEMS microbiology letters</title><addtitle>FEMS Microbiol Lett</addtitle><description>Abstract
We developed an in vitro tissue-culture model to analyze the process involved in mycobacterial spread through lung epithelial cell monolayers. A549 cells were infected with low numbers of viable Mycobacterium tuberculosis bacilli expressing the gfp gene. Subsequent addition of a soft agarose overlay prevented the dispersal of the bacilli from the initial points of attachment. By fluorescence microscopy the bacteria were observed to infect and grow within the primary target cells; this was followed by lysis of the infected cells and subsequent infection of adjacent cells. This process repeated itself until an area of clearing (plaque formation) was observed. The addition of amikacin after initial infection did not prevent intracellular growth; however, subsequent plaque formation was not observed. Plaque formation was also observed after infection with Mycobacterium bovis BCG bacilli, but the plaques were smaller than those formed after infection with M. tuberculosis. These observations reinforce the possibility that cell-to-cell spreading of M. tuberculosis bacilli, particularly early in the course of infection within lung macrophages, pneumocytes, and other cells, may be an important component in the infectious process.</description><subject>Amikacin</subject><subject>Bacilli</subject><subject>Bacillus Calmette-Guerin vaccine</subject><subject>Bacteriology</subject><subject>BCG</subject><subject>Biological and medical sciences</subject><subject>Cell culture</subject><subject>Cell spreading</subject><subject>Cells, Cultured</subject><subject>Dispersal</subject><subject>Epithelial cells</subject><subject>Epithelial Cells - cytology</subject><subject>Epithelial Cells - microbiology</subject><subject>Fluorescence</subject><subject>Fluorescence microscopy</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetics</subject><subject>Green fluorescent protein</subject><subject>Green Fluorescent Proteins</subject><subject>Human lung epithelial cell</subject><subject>Humans</subject><subject>Indicators and Reagents - metabolism</subject><subject>Infections</subject><subject>Luminescent Proteins - genetics</subject><subject>Lungs</subject><subject>Lysis</subject><subject>Macrophages</subject><subject>Microbiology</subject><subject>Monolayers</subject><subject>Mycobacterium tuberculosis</subject><subject>Mycobacterium tuberculosis - genetics</subject><subject>Mycobacterium tuberculosis - growth & development</subject><subject>Mycobacterium tuberculosis - pathogenicity</subject><subject>Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains</subject><subject>Plaque</subject><subject>Plaques</subject><subject>Pneumocytes</subject><subject>Respiratory Mucosa - cytology</subject><subject>Tissue culture</subject><subject>Tuberculosis</subject><subject>Tuberculosis, Pulmonary - microbiology</subject><subject>Virulence</subject><issn>0378-1097</issn><issn>1574-6968</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</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>eNqVkU-L1TAUxYMoznP0K0hQdNdnkuZP40IYxhkV3uBG1zFNbzGPtKlJi9Nvb8srMyCKmE0g-Z17z-Eg9IKSPV3Om-OeCsULqWW1Z4Sw_VhTykS1v32AdndfD9GOlKoqKNHqDD3J-UgI4YzIx-iMMkpLzeQOfXsPXezzmOzoY49ji_OQwDa4nvHN7GJt3QjJTx0epxqSm0LMPuPl2Yfgse_xheAaw-DH7xC8DdhBCHiZGYOdIeWn6FFrQ4Zn232Ovl5ffbn8WBw-f_h0eXEoXCmYKIRqVQ2NalijdSlBVqIpeSu0kk5wEAqsbSk0lW5qC5QKJhmnFdGlEto1pDxHr09zhxR_TJBH0_m8erE9xCkbRSsthdL_BGnFOVNMLeDL38BjnFK_hDCspERKsRhfqLcnyqWYc4LWDMl3Ns2GErPWZY5m7cSsnZi1LrPVZW4X8fNtxVR30NxLt34W4NUG2OxsaJPtnc_3HOdKEbp6fXfifvoA839YMNc3B8rXGOI0IE7DX-TFnxL8Ags6wUc</recordid><startdate>200207</startdate><enddate>200207</enddate><creator>Castro-Garza, Jorge</creator><creator>King, C.Harold</creator><creator>Swords, W.Edward</creator><creator>Quinn, Frederick D</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><general>Oxford University Press</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>7QL</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200207</creationdate><title>Demonstration of spread by Mycobacterium tuberculosis bacilli in A549 epithelial cell monolayers</title><author>Castro-Garza, Jorge ; King, C.Harold ; Swords, W.Edward ; Quinn, Frederick D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3525-57f7bed7d2d9936e685d34f5976c54e57eaaf1ed89dbae115262418093759cd03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Amikacin</topic><topic>Bacilli</topic><topic>Bacillus Calmette-Guerin vaccine</topic><topic>Bacteriology</topic><topic>BCG</topic><topic>Biological and medical sciences</topic><topic>Cell culture</topic><topic>Cell spreading</topic><topic>Cells, Cultured</topic><topic>Dispersal</topic><topic>Epithelial cells</topic><topic>Epithelial Cells - cytology</topic><topic>Epithelial Cells - microbiology</topic><topic>Fluorescence</topic><topic>Fluorescence microscopy</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetics</topic><topic>Green fluorescent protein</topic><topic>Green Fluorescent Proteins</topic><topic>Human lung epithelial cell</topic><topic>Humans</topic><topic>Indicators and Reagents - metabolism</topic><topic>Infections</topic><topic>Luminescent Proteins - genetics</topic><topic>Lungs</topic><topic>Lysis</topic><topic>Macrophages</topic><topic>Microbiology</topic><topic>Monolayers</topic><topic>Mycobacterium tuberculosis</topic><topic>Mycobacterium tuberculosis - genetics</topic><topic>Mycobacterium tuberculosis - growth & development</topic><topic>Mycobacterium tuberculosis - pathogenicity</topic><topic>Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains</topic><topic>Plaque</topic><topic>Plaques</topic><topic>Pneumocytes</topic><topic>Respiratory Mucosa - cytology</topic><topic>Tissue culture</topic><topic>Tuberculosis</topic><topic>Tuberculosis, Pulmonary - microbiology</topic><topic>Virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Castro-Garza, Jorge</creatorcontrib><creatorcontrib>King, C.Harold</creatorcontrib><creatorcontrib>Swords, W.Edward</creatorcontrib><creatorcontrib>Quinn, Frederick D</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</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>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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 One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>FEMS microbiology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Castro-Garza, Jorge</au><au>King, C.Harold</au><au>Swords, W.Edward</au><au>Quinn, Frederick D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Demonstration of spread by Mycobacterium tuberculosis bacilli in A549 epithelial cell monolayers</atitle><jtitle>FEMS microbiology letters</jtitle><addtitle>FEMS Microbiol Lett</addtitle><date>2002-07</date><risdate>2002</risdate><volume>212</volume><issue>2</issue><spage>145</spage><epage>149</epage><pages>145-149</pages><issn>0378-1097</issn><eissn>1574-6968</eissn><coden>FMLED7</coden><abstract>Abstract
We developed an in vitro tissue-culture model to analyze the process involved in mycobacterial spread through lung epithelial cell monolayers. A549 cells were infected with low numbers of viable Mycobacterium tuberculosis bacilli expressing the gfp gene. Subsequent addition of a soft agarose overlay prevented the dispersal of the bacilli from the initial points of attachment. By fluorescence microscopy the bacteria were observed to infect and grow within the primary target cells; this was followed by lysis of the infected cells and subsequent infection of adjacent cells. This process repeated itself until an area of clearing (plaque formation) was observed. The addition of amikacin after initial infection did not prevent intracellular growth; however, subsequent plaque formation was not observed. Plaque formation was also observed after infection with Mycobacterium bovis BCG bacilli, but the plaques were smaller than those formed after infection with M. tuberculosis. These observations reinforce the possibility that cell-to-cell spreading of M. tuberculosis bacilli, particularly early in the course of infection within lung macrophages, pneumocytes, and other cells, may be an important component in the infectious process.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>12113926</pmid><doi>10.1111/j.1574-6968.2002.tb11258.x</doi><tpages>5</tpages></addata></record> |
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source | MEDLINE; Oxford University Press Journals All Titles (1996-Current); Wiley Online Library All Journals; Alma/SFX Local Collection |
subjects | Amikacin Bacilli Bacillus Calmette-Guerin vaccine Bacteriology BCG Biological and medical sciences Cell culture Cell spreading Cells, Cultured Dispersal Epithelial cells Epithelial Cells - cytology Epithelial Cells - microbiology Fluorescence Fluorescence microscopy Fundamental and applied biological sciences. Psychology Genetics Green fluorescent protein Green Fluorescent Proteins Human lung epithelial cell Humans Indicators and Reagents - metabolism Infections Luminescent Proteins - genetics Lungs Lysis Macrophages Microbiology Monolayers Mycobacterium tuberculosis Mycobacterium tuberculosis - genetics Mycobacterium tuberculosis - growth & development Mycobacterium tuberculosis - pathogenicity Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains Plaque Plaques Pneumocytes Respiratory Mucosa - cytology Tissue culture Tuberculosis Tuberculosis, Pulmonary - microbiology Virulence |
title | Demonstration of spread by Mycobacterium tuberculosis bacilli in A549 epithelial cell monolayers |
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