Outer membrane protein A (OmpA): a new player in shigella flexneri protrusion formation and inter-cellular spreading
Outer membrane protein A (OmpA) is a multifaceted predominant outer membrane protein of Escherichia coli and other Enterobacteriaceae whose role in the pathogenesis of various bacterial infections has recently been recognized. Here, the role of OmpA on the virulence of Shigella flexneri has been inv...
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description | Outer membrane protein A (OmpA) is a multifaceted predominant outer membrane protein of Escherichia coli and other Enterobacteriaceae whose role in the pathogenesis of various bacterial infections has recently been recognized. Here, the role of OmpA on the virulence of Shigella flexneri has been investigated. An ompA mutant of wild-type S. flexneri 5a strain M90T was constructed (strain HND92) and it was shown to be severely impaired in cell-to-cell spreading since it failed to plaque on HeLa cell monolayers. The lack of OmpA significantly reduced the levels of IcsA while the levels of cell associated and released IcsP-cleaved 95 kDa amino-terminal portion of the mature protein were similar. Nevertheless, the ompA mutant displayed IcsA exposed across the entire bacterial surface. Surprisingly, the ompA mutant produced proper F-actin comet tails, indicating that the aberrant IcsA exposition at bacterial lateral surface did not affect proper activation of actin-nucleating proteins, suggesting that the absence of OmpA likely unmasks mature or cell associated IcsA at bacterial lateral surface. Moreover, the ompA mutant was able to invade and to multiply within HeLa cell monolayers, although internalized bacteria were found to be entrapped within the host cell cytoplasm. We found that the ompA mutant produced significantly less protrusions than the wild-type strain, indicating that this defect could be responsible of its inability to plaque. Although we could not definitely rule out that the ompA mutation might exert pleiotropic effects on other S. flexneri genes, complementation of the ompA mutation with a recombinant plasmid carrying the S. flexneri ompA gene clearly indicated that a functional OmpA protein is required and sufficient for proper IcsA exposition, plaque and protrusion formation. Moreover, an independent ompA mutant was generated. Since we found that both mutants displayed identical virulence profile, these results further supported the findings presented in this study. |
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Here, the role of OmpA on the virulence of Shigella flexneri has been investigated. An ompA mutant of wild-type S. flexneri 5a strain M90T was constructed (strain HND92) and it was shown to be severely impaired in cell-to-cell spreading since it failed to plaque on HeLa cell monolayers. The lack of OmpA significantly reduced the levels of IcsA while the levels of cell associated and released IcsP-cleaved 95 kDa amino-terminal portion of the mature protein were similar. Nevertheless, the ompA mutant displayed IcsA exposed across the entire bacterial surface. Surprisingly, the ompA mutant produced proper F-actin comet tails, indicating that the aberrant IcsA exposition at bacterial lateral surface did not affect proper activation of actin-nucleating proteins, suggesting that the absence of OmpA likely unmasks mature or cell associated IcsA at bacterial lateral surface. Moreover, the ompA mutant was able to invade and to multiply within HeLa cell monolayers, although internalized bacteria were found to be entrapped within the host cell cytoplasm. We found that the ompA mutant produced significantly less protrusions than the wild-type strain, indicating that this defect could be responsible of its inability to plaque. Although we could not definitely rule out that the ompA mutation might exert pleiotropic effects on other S. flexneri genes, complementation of the ompA mutation with a recombinant plasmid carrying the S. flexneri ompA gene clearly indicated that a functional OmpA protein is required and sufficient for proper IcsA exposition, plaque and protrusion formation. Moreover, an independent ompA mutant was generated. Since we found that both mutants displayed identical virulence profile, these results further supported the findings presented in this study.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0049625</identifier><identifier>PMID: 23166731</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Aberration ; Actin ; Actins - metabolism ; Antigens ; Bacteria ; Bacterial infections ; Bacterial Outer Membrane Proteins - genetics ; Bacterial Outer Membrane Proteins - metabolism ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Biology ; Cell Membrane Permeability - genetics ; Cell spreading ; Cell Surface Extensions - genetics ; Cell Surface Extensions - metabolism ; Comet tails ; Complementation ; Cytoplasm ; DNA-Binding Proteins - genetics ; DNA-Binding Proteins - metabolism ; E coli ; Enzyme Activation ; Escherichia coli ; Exposure ; Gene Expression Regulation, Bacterial ; Group IV Phospholipases A2 - metabolism ; Health aspects ; HeLa Cells ; Hostages ; Humans ; Infection ; Kinases ; Lipopolysaccharides - metabolism ; Membrane proteins ; Monolayers ; Monomolecular films ; Muscle proteins ; Mutants ; Mutation ; OmpA protein ; Pathogenesis ; Pathogens ; Phenotype ; Physics ; Plasmids ; Polymerization ; Protein A ; Proteins ; Shigella ; Shigella flexneri - genetics ; Shigella flexneri - metabolism ; Shigella flexneri - pathogenicity ; Spreading ; Transcription Factors - genetics ; Transcription Factors - metabolism ; Virulence ; Virulence (Microbiology) ; Virulence - genetics</subject><ispartof>PloS one, 2012-11, Vol.7 (11), p.e49625</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>2012. This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c593t-1adc5becf156417923b7970ff0e270375d5bf054247ce69679ad4978c6907633</citedby><cites>FETCH-LOGICAL-c593t-1adc5becf156417923b7970ff0e270375d5bf054247ce69679ad4978c6907633</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/PMC3498225/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3498225/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,862,883,2098,2917,23853,27911,27912,53778,53780,79355,79356</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23166731$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Chaves-Olarte, Esteban</contributor><creatorcontrib>Ambrosi, Cecilia</creatorcontrib><creatorcontrib>Pompili, Monica</creatorcontrib><creatorcontrib>Scribano, Daniela</creatorcontrib><creatorcontrib>Zagaglia, Carlo</creatorcontrib><creatorcontrib>Ripa, Sandro</creatorcontrib><creatorcontrib>Nicoletti, Mauro</creatorcontrib><title>Outer membrane protein A (OmpA): a new player in shigella flexneri protrusion formation and inter-cellular spreading</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Outer membrane protein A (OmpA) is a multifaceted predominant outer membrane protein of Escherichia coli and other Enterobacteriaceae whose role in the pathogenesis of various bacterial infections has recently been recognized. Here, the role of OmpA on the virulence of Shigella flexneri has been investigated. An ompA mutant of wild-type S. flexneri 5a strain M90T was constructed (strain HND92) and it was shown to be severely impaired in cell-to-cell spreading since it failed to plaque on HeLa cell monolayers. The lack of OmpA significantly reduced the levels of IcsA while the levels of cell associated and released IcsP-cleaved 95 kDa amino-terminal portion of the mature protein were similar. Nevertheless, the ompA mutant displayed IcsA exposed across the entire bacterial surface. Surprisingly, the ompA mutant produced proper F-actin comet tails, indicating that the aberrant IcsA exposition at bacterial lateral surface did not affect proper activation of actin-nucleating proteins, suggesting that the absence of OmpA likely unmasks mature or cell associated IcsA at bacterial lateral surface. Moreover, the ompA mutant was able to invade and to multiply within HeLa cell monolayers, although internalized bacteria were found to be entrapped within the host cell cytoplasm. We found that the ompA mutant produced significantly less protrusions than the wild-type strain, indicating that this defect could be responsible of its inability to plaque. Although we could not definitely rule out that the ompA mutation might exert pleiotropic effects on other S. flexneri genes, complementation of the ompA mutation with a recombinant plasmid carrying the S. flexneri ompA gene clearly indicated that a functional OmpA protein is required and sufficient for proper IcsA exposition, plaque and protrusion formation. Moreover, an independent ompA mutant was generated. Since we found that both mutants displayed identical virulence profile, these results further supported the findings presented in this study.</description><subject>Aberration</subject><subject>Actin</subject><subject>Actins - metabolism</subject><subject>Antigens</subject><subject>Bacteria</subject><subject>Bacterial infections</subject><subject>Bacterial Outer Membrane Proteins - genetics</subject><subject>Bacterial Outer Membrane Proteins - metabolism</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Biology</subject><subject>Cell Membrane Permeability - genetics</subject><subject>Cell spreading</subject><subject>Cell Surface Extensions - genetics</subject><subject>Cell Surface Extensions - metabolism</subject><subject>Comet tails</subject><subject>Complementation</subject><subject>Cytoplasm</subject><subject>DNA-Binding Proteins - genetics</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>E coli</subject><subject>Enzyme Activation</subject><subject>Escherichia coli</subject><subject>Exposure</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Group IV Phospholipases A2 - metabolism</subject><subject>Health aspects</subject><subject>HeLa Cells</subject><subject>Hostages</subject><subject>Humans</subject><subject>Infection</subject><subject>Kinases</subject><subject>Lipopolysaccharides - metabolism</subject><subject>Membrane proteins</subject><subject>Monolayers</subject><subject>Monomolecular films</subject><subject>Muscle proteins</subject><subject>Mutants</subject><subject>Mutation</subject><subject>OmpA protein</subject><subject>Pathogenesis</subject><subject>Pathogens</subject><subject>Phenotype</subject><subject>Physics</subject><subject>Plasmids</subject><subject>Polymerization</subject><subject>Protein A</subject><subject>Proteins</subject><subject>Shigella</subject><subject>Shigella flexneri - genetics</subject><subject>Shigella flexneri - metabolism</subject><subject>Shigella flexneri - pathogenicity</subject><subject>Spreading</subject><subject>Transcription Factors - genetics</subject><subject>Transcription Factors - metabolism</subject><subject>Virulence</subject><subject>Virulence (Microbiology)</subject><subject>Virulence - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ambrosi, Cecilia</au><au>Pompili, Monica</au><au>Scribano, Daniela</au><au>Zagaglia, Carlo</au><au>Ripa, Sandro</au><au>Nicoletti, Mauro</au><au>Chaves-Olarte, Esteban</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Outer membrane protein A (OmpA): a new player in shigella flexneri protrusion formation and inter-cellular spreading</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2012-11-14</date><risdate>2012</risdate><volume>7</volume><issue>11</issue><spage>e49625</spage><pages>e49625-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Outer membrane protein A (OmpA) is a multifaceted predominant outer membrane protein of Escherichia coli and other Enterobacteriaceae whose role in the pathogenesis of various bacterial infections has recently been recognized. Here, the role of OmpA on the virulence of Shigella flexneri has been investigated. An ompA mutant of wild-type S. flexneri 5a strain M90T was constructed (strain HND92) and it was shown to be severely impaired in cell-to-cell spreading since it failed to plaque on HeLa cell monolayers. The lack of OmpA significantly reduced the levels of IcsA while the levels of cell associated and released IcsP-cleaved 95 kDa amino-terminal portion of the mature protein were similar. Nevertheless, the ompA mutant displayed IcsA exposed across the entire bacterial surface. Surprisingly, the ompA mutant produced proper F-actin comet tails, indicating that the aberrant IcsA exposition at bacterial lateral surface did not affect proper activation of actin-nucleating proteins, suggesting that the absence of OmpA likely unmasks mature or cell associated IcsA at bacterial lateral surface. Moreover, the ompA mutant was able to invade and to multiply within HeLa cell monolayers, although internalized bacteria were found to be entrapped within the host cell cytoplasm. We found that the ompA mutant produced significantly less protrusions than the wild-type strain, indicating that this defect could be responsible of its inability to plaque. Although we could not definitely rule out that the ompA mutation might exert pleiotropic effects on other S. flexneri genes, complementation of the ompA mutation with a recombinant plasmid carrying the S. flexneri ompA gene clearly indicated that a functional OmpA protein is required and sufficient for proper IcsA exposition, plaque and protrusion formation. Moreover, an independent ompA mutant was generated. Since we found that both mutants displayed identical virulence profile, these results further supported the findings presented in this study.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23166731</pmid><doi>10.1371/journal.pone.0049625</doi><oa>free_for_read</oa></addata></record> |
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recordid | cdi_plos_journals_1339168672 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Public Library of Science (PLoS); PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Aberration Actin Actins - metabolism Antigens Bacteria Bacterial infections Bacterial Outer Membrane Proteins - genetics Bacterial Outer Membrane Proteins - metabolism Bacterial Proteins - genetics Bacterial Proteins - metabolism Biology Cell Membrane Permeability - genetics Cell spreading Cell Surface Extensions - genetics Cell Surface Extensions - metabolism Comet tails Complementation Cytoplasm DNA-Binding Proteins - genetics DNA-Binding Proteins - metabolism E coli Enzyme Activation Escherichia coli Exposure Gene Expression Regulation, Bacterial Group IV Phospholipases A2 - metabolism Health aspects HeLa Cells Hostages Humans Infection Kinases Lipopolysaccharides - metabolism Membrane proteins Monolayers Monomolecular films Muscle proteins Mutants Mutation OmpA protein Pathogenesis Pathogens Phenotype Physics Plasmids Polymerization Protein A Proteins Shigella Shigella flexneri - genetics Shigella flexneri - metabolism Shigella flexneri - pathogenicity Spreading Transcription Factors - genetics Transcription Factors - metabolism Virulence Virulence (Microbiology) Virulence - genetics |
title | Outer membrane protein A (OmpA): a new player in shigella flexneri protrusion formation and inter-cellular spreading |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T02%3A36%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Outer%20membrane%20protein%20A%20(OmpA):%20a%20new%20player%20in%20shigella%20flexneri%20protrusion%20formation%20and%20inter-cellular%20spreading&rft.jtitle=PloS%20one&rft.au=Ambrosi,%20Cecilia&rft.date=2012-11-14&rft.volume=7&rft.issue=11&rft.spage=e49625&rft.pages=e49625-&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0049625&rft_dat=%3Cgale_plos_%3EA477090661%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1339168672&rft_id=info:pmid/23166731&rft_galeid=A477090661&rft_doaj_id=oai_doaj_org_article_678aa14200f3432fa6730e4c5ed420b0&rfr_iscdi=true |