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
Hauptverfasser: Castro-Garza, Jorge, King, C.Harold, Swords, W.Edward, Quinn, Frederick D
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creator Castro-Garza, Jorge
King, C.Harold
Swords, W.Edward
Quinn, Frederick D
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.
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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. 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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 &amp; 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&amp;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. 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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. 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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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