Reintroduction of the PLB1 gene into Candida albicans restores virulence in vivo

Center for Medical Mycology, University Hospitals of Cleveland and Department of Dermatology, Case Western Reserve University, Cleveland, OH 44106-5028, USA 1 Department of Microbiology and Immunology, Medical College of Ohio, Toledo, OH 43614-5806, USA 2 Author for correspondence: Mahmoud A. Ghanno...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Microbiology (Society for General Microbiology) 2001-09, Vol.147 (9), p.2585-2597
Hauptverfasser: Mukherjee, Pranab K, Seshan, K. R, Leidich, S. D, Chandra, Jyotsna, Cole, Garry T, Ghannoum, Mahmoud A
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2597
container_issue 9
container_start_page 2585
container_title Microbiology (Society for General Microbiology)
container_volume 147
creator Mukherjee, Pranab K
Seshan, K. R
Leidich, S. D
Chandra, Jyotsna
Cole, Garry T
Ghannoum, Mahmoud A
description Center for Medical Mycology, University Hospitals of Cleveland and Department of Dermatology, Case Western Reserve University, Cleveland, OH 44106-5028, USA 1 Department of Microbiology and Immunology, Medical College of Ohio, Toledo, OH 43614-5806, USA 2 Author for correspondence: Mahmoud A. Ghannoum. Tel: +1 216 844 8580. Fax: +1 216 844 1076. e-mail: mag3{at}po.cwru.edu Phospholipases have been proposed to contribute to the virulence of Candida albicans . Recently, a candidal strain deleted for PLB1 , the gene encoding the predominant phospholipase B (Plb1) secreted by C. albicans , was constructed and its virulence in an intravenous murine model of disseminated candidiasis was evaluated. In the present study, the PLB1 gene was reintroduced back into the plb1 null mutant to generate the revertant strain, which showed similar growth and morphology to its isogenic parent strain. Virulence of the revertant strain was found to be comparable to that of the parent strain in an intravenous murine model of disseminated candidiasis. To compare the abilities of the plb1 null mutant, the revertant and the isogenic parent strains to cross the gastrointestinal (GI) tract and cause systemic infection, an oral–intragastric infant mouse model of candidiasis was used. Histological examinations and analysis of c.f.u. of the pathogen in liver homogenates revealed that the parental and revertant strains were able to invade and traverse the GI mucosa to a significantly greater extent than the plb1 null mutant. Immunofluorescence and immunoelectron microscopic studies of infected host tissue using anti-Plb1 antibody showed that Plb1 is secreted during invasion of the gastric mucosa by the parental and revertant strains. In contrast, little or no labelling was observed in the null mutant strain. The results indicate that the Plb1 secreted by C. albicans enhances the ability of this organism to cross the GI tract and disseminate haematogenously. These studies provide unequivocal evidence supporting a role for Plb1 during the course of infection by C. albicans . Keywords: phospholipase B, virulence factor, candidal transmigration, in vivo localization of Plb1 Abbreviations: GI, gastrointestinal; PAS, periodic acid–Schiff reagent a These authors contributed equally to this work.
doi_str_mv 10.1099/00221287-147-9-2585
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_71142141</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>18196635</sourcerecordid><originalsourceid>FETCH-LOGICAL-c441t-3e7d0fb8e2fb5415ee9a0fa60fe2a2d8a8f4d2736e47268a692d10a858a499ba3</originalsourceid><addsrcrecordid>eNqFkE2LFDEQhoMo7of-AkFyUdhDayqddCdHd_ALBlxEz6E6XdmJ9HTWpHvFf2-GGVlvXvJBPfVW8TD2AsQbENa-FUJKkKZvQPWNbaQ2-hE7B9XpRgojHtd3q0UjTC_P2EUpP4SoRQFP2RmAbnVv7Tm7-UpxXnIaV7_ENPMU-LIjfrO9Bn5LM_FaTXyD8xhH5DgN0eNceKaypHrw-5jXiWZ_AOvnPj1jTwJOhZ6f7kv2_cP7b5tPzfbLx8-bd9vGKwVL01I_ijAYkmHQCjSRRRGwE4EkytGgCWqUfduR6mVnsLNyBIFGG1TWDthestfH3Lucfq51HbePxdM04UxpLa4HUBIU_BcEA7brWl3B9gj6nErJFNxdjnvMvx0IdzDu_hp31biz7mC8dr08xa_DnsaHnpPiCrw6AVg8TiHj7GN54BTU6d0h6OrI7eLt7lfM5Kr_fazLDDHVnf0_Q_8AViiWYA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>18196635</pqid></control><display><type>article</type><title>Reintroduction of the PLB1 gene into Candida albicans restores virulence in vivo</title><source>MEDLINE</source><source>PubMed Central</source><creator>Mukherjee, Pranab K ; Seshan, K. R ; Leidich, S. D ; Chandra, Jyotsna ; Cole, Garry T ; Ghannoum, Mahmoud A</creator><creatorcontrib>Mukherjee, Pranab K ; Seshan, K. R ; Leidich, S. D ; Chandra, Jyotsna ; Cole, Garry T ; Ghannoum, Mahmoud A</creatorcontrib><description>Center for Medical Mycology, University Hospitals of Cleveland and Department of Dermatology, Case Western Reserve University, Cleveland, OH 44106-5028, USA 1 Department of Microbiology and Immunology, Medical College of Ohio, Toledo, OH 43614-5806, USA 2 Author for correspondence: Mahmoud A. Ghannoum. Tel: +1 216 844 8580. Fax: +1 216 844 1076. e-mail: mag3{at}po.cwru.edu Phospholipases have been proposed to contribute to the virulence of Candida albicans . Recently, a candidal strain deleted for PLB1 , the gene encoding the predominant phospholipase B (Plb1) secreted by C. albicans , was constructed and its virulence in an intravenous murine model of disseminated candidiasis was evaluated. In the present study, the PLB1 gene was reintroduced back into the plb1 null mutant to generate the revertant strain, which showed similar growth and morphology to its isogenic parent strain. Virulence of the revertant strain was found to be comparable to that of the parent strain in an intravenous murine model of disseminated candidiasis. To compare the abilities of the plb1 null mutant, the revertant and the isogenic parent strains to cross the gastrointestinal (GI) tract and cause systemic infection, an oral–intragastric infant mouse model of candidiasis was used. Histological examinations and analysis of c.f.u. of the pathogen in liver homogenates revealed that the parental and revertant strains were able to invade and traverse the GI mucosa to a significantly greater extent than the plb1 null mutant. Immunofluorescence and immunoelectron microscopic studies of infected host tissue using anti-Plb1 antibody showed that Plb1 is secreted during invasion of the gastric mucosa by the parental and revertant strains. In contrast, little or no labelling was observed in the null mutant strain. The results indicate that the Plb1 secreted by C. albicans enhances the ability of this organism to cross the GI tract and disseminate haematogenously. These studies provide unequivocal evidence supporting a role for Plb1 during the course of infection by C. albicans . Keywords: phospholipase B, virulence factor, candidal transmigration, in vivo localization of Plb1 Abbreviations: GI, gastrointestinal; PAS, periodic acid–Schiff reagent a These authors contributed equally to this work.</description><identifier>ISSN: 1350-0872</identifier><identifier>EISSN: 1465-2080</identifier><identifier>DOI: 10.1099/00221287-147-9-2585</identifier><identifier>PMID: 11535799</identifier><language>eng</language><publisher>Reading: Soc General Microbiol</publisher><subject>Animals ; Bacteriology ; Biological and medical sciences ; Candida albicans ; Candida albicans - enzymology ; Candida albicans - genetics ; Candida albicans - pathogenicity ; Candidiasis - etiology ; Candidiasis - pathology ; Disease Models, Animal ; Fundamental and applied biological sciences. Psychology ; Fungal Proteins - genetics ; Fungal Proteins - metabolism ; Gastric Mucosa - microbiology ; Gastric Mucosa - pathology ; Genes, Fungal ; Genetics ; Humans ; Liver - microbiology ; Liver - pathology ; Lysophospholipase - genetics ; Lysophospholipase - metabolism ; Mice ; Microbiology ; Microscopy, Electron ; Mutation ; Mycology ; Pathogenicity, host-agent relations, miscellaneous strains, epidemiology ; PLB1 gene ; Virulence - genetics</subject><ispartof>Microbiology (Society for General Microbiology), 2001-09, Vol.147 (9), p.2585-2597</ispartof><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-3e7d0fb8e2fb5415ee9a0fa60fe2a2d8a8f4d2736e47268a692d10a858a499ba3</citedby><cites>FETCH-LOGICAL-c441t-3e7d0fb8e2fb5415ee9a0fa60fe2a2d8a8f4d2736e47268a692d10a858a499ba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=14166365$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11535799$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mukherjee, Pranab K</creatorcontrib><creatorcontrib>Seshan, K. R</creatorcontrib><creatorcontrib>Leidich, S. D</creatorcontrib><creatorcontrib>Chandra, Jyotsna</creatorcontrib><creatorcontrib>Cole, Garry T</creatorcontrib><creatorcontrib>Ghannoum, Mahmoud A</creatorcontrib><title>Reintroduction of the PLB1 gene into Candida albicans restores virulence in vivo</title><title>Microbiology (Society for General Microbiology)</title><addtitle>Microbiology</addtitle><description>Center for Medical Mycology, University Hospitals of Cleveland and Department of Dermatology, Case Western Reserve University, Cleveland, OH 44106-5028, USA 1 Department of Microbiology and Immunology, Medical College of Ohio, Toledo, OH 43614-5806, USA 2 Author for correspondence: Mahmoud A. Ghannoum. Tel: +1 216 844 8580. Fax: +1 216 844 1076. e-mail: mag3{at}po.cwru.edu Phospholipases have been proposed to contribute to the virulence of Candida albicans . Recently, a candidal strain deleted for PLB1 , the gene encoding the predominant phospholipase B (Plb1) secreted by C. albicans , was constructed and its virulence in an intravenous murine model of disseminated candidiasis was evaluated. In the present study, the PLB1 gene was reintroduced back into the plb1 null mutant to generate the revertant strain, which showed similar growth and morphology to its isogenic parent strain. Virulence of the revertant strain was found to be comparable to that of the parent strain in an intravenous murine model of disseminated candidiasis. To compare the abilities of the plb1 null mutant, the revertant and the isogenic parent strains to cross the gastrointestinal (GI) tract and cause systemic infection, an oral–intragastric infant mouse model of candidiasis was used. Histological examinations and analysis of c.f.u. of the pathogen in liver homogenates revealed that the parental and revertant strains were able to invade and traverse the GI mucosa to a significantly greater extent than the plb1 null mutant. Immunofluorescence and immunoelectron microscopic studies of infected host tissue using anti-Plb1 antibody showed that Plb1 is secreted during invasion of the gastric mucosa by the parental and revertant strains. In contrast, little or no labelling was observed in the null mutant strain. The results indicate that the Plb1 secreted by C. albicans enhances the ability of this organism to cross the GI tract and disseminate haematogenously. These studies provide unequivocal evidence supporting a role for Plb1 during the course of infection by C. albicans . Keywords: phospholipase B, virulence factor, candidal transmigration, in vivo localization of Plb1 Abbreviations: GI, gastrointestinal; PAS, periodic acid–Schiff reagent a These authors contributed equally to this work.</description><subject>Animals</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Candida albicans</subject><subject>Candida albicans - enzymology</subject><subject>Candida albicans - genetics</subject><subject>Candida albicans - pathogenicity</subject><subject>Candidiasis - etiology</subject><subject>Candidiasis - pathology</subject><subject>Disease Models, Animal</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fungal Proteins - genetics</subject><subject>Fungal Proteins - metabolism</subject><subject>Gastric Mucosa - microbiology</subject><subject>Gastric Mucosa - pathology</subject><subject>Genes, Fungal</subject><subject>Genetics</subject><subject>Humans</subject><subject>Liver - microbiology</subject><subject>Liver - pathology</subject><subject>Lysophospholipase - genetics</subject><subject>Lysophospholipase - metabolism</subject><subject>Mice</subject><subject>Microbiology</subject><subject>Microscopy, Electron</subject><subject>Mutation</subject><subject>Mycology</subject><subject>Pathogenicity, host-agent relations, miscellaneous strains, epidemiology</subject><subject>PLB1 gene</subject><subject>Virulence - genetics</subject><issn>1350-0872</issn><issn>1465-2080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE2LFDEQhoMo7of-AkFyUdhDayqddCdHd_ALBlxEz6E6XdmJ9HTWpHvFf2-GGVlvXvJBPfVW8TD2AsQbENa-FUJKkKZvQPWNbaQ2-hE7B9XpRgojHtd3q0UjTC_P2EUpP4SoRQFP2RmAbnVv7Tm7-UpxXnIaV7_ENPMU-LIjfrO9Bn5LM_FaTXyD8xhH5DgN0eNceKaypHrw-5jXiWZ_AOvnPj1jTwJOhZ6f7kv2_cP7b5tPzfbLx8-bd9vGKwVL01I_ijAYkmHQCjSRRRGwE4EkytGgCWqUfduR6mVnsLNyBIFGG1TWDthestfH3Lucfq51HbePxdM04UxpLa4HUBIU_BcEA7brWl3B9gj6nErJFNxdjnvMvx0IdzDu_hp31biz7mC8dr08xa_DnsaHnpPiCrw6AVg8TiHj7GN54BTU6d0h6OrI7eLt7lfM5Kr_fazLDDHVnf0_Q_8AViiWYA</recordid><startdate>20010901</startdate><enddate>20010901</enddate><creator>Mukherjee, Pranab K</creator><creator>Seshan, K. R</creator><creator>Leidich, S. D</creator><creator>Chandra, Jyotsna</creator><creator>Cole, Garry T</creator><creator>Ghannoum, Mahmoud A</creator><general>Soc General Microbiol</general><general>Society for General Microbiology</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>M7N</scope><scope>7X8</scope></search><sort><creationdate>20010901</creationdate><title>Reintroduction of the PLB1 gene into Candida albicans restores virulence in vivo</title><author>Mukherjee, Pranab K ; Seshan, K. R ; Leidich, S. D ; Chandra, Jyotsna ; Cole, Garry T ; Ghannoum, Mahmoud A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-3e7d0fb8e2fb5415ee9a0fa60fe2a2d8a8f4d2736e47268a692d10a858a499ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Animals</topic><topic>Bacteriology</topic><topic>Biological and medical sciences</topic><topic>Candida albicans</topic><topic>Candida albicans - enzymology</topic><topic>Candida albicans - genetics</topic><topic>Candida albicans - pathogenicity</topic><topic>Candidiasis - etiology</topic><topic>Candidiasis - pathology</topic><topic>Disease Models, Animal</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fungal Proteins - genetics</topic><topic>Fungal Proteins - metabolism</topic><topic>Gastric Mucosa - microbiology</topic><topic>Gastric Mucosa - pathology</topic><topic>Genes, Fungal</topic><topic>Genetics</topic><topic>Humans</topic><topic>Liver - microbiology</topic><topic>Liver - pathology</topic><topic>Lysophospholipase - genetics</topic><topic>Lysophospholipase - metabolism</topic><topic>Mice</topic><topic>Microbiology</topic><topic>Microscopy, Electron</topic><topic>Mutation</topic><topic>Mycology</topic><topic>Pathogenicity, host-agent relations, miscellaneous strains, epidemiology</topic><topic>PLB1 gene</topic><topic>Virulence - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mukherjee, Pranab K</creatorcontrib><creatorcontrib>Seshan, K. R</creatorcontrib><creatorcontrib>Leidich, S. D</creatorcontrib><creatorcontrib>Chandra, Jyotsna</creatorcontrib><creatorcontrib>Cole, Garry T</creatorcontrib><creatorcontrib>Ghannoum, Mahmoud A</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>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>Microbiology (Society for General Microbiology)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mukherjee, Pranab K</au><au>Seshan, K. R</au><au>Leidich, S. D</au><au>Chandra, Jyotsna</au><au>Cole, Garry T</au><au>Ghannoum, Mahmoud A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reintroduction of the PLB1 gene into Candida albicans restores virulence in vivo</atitle><jtitle>Microbiology (Society for General Microbiology)</jtitle><addtitle>Microbiology</addtitle><date>2001-09-01</date><risdate>2001</risdate><volume>147</volume><issue>9</issue><spage>2585</spage><epage>2597</epage><pages>2585-2597</pages><issn>1350-0872</issn><eissn>1465-2080</eissn><abstract>Center for Medical Mycology, University Hospitals of Cleveland and Department of Dermatology, Case Western Reserve University, Cleveland, OH 44106-5028, USA 1 Department of Microbiology and Immunology, Medical College of Ohio, Toledo, OH 43614-5806, USA 2 Author for correspondence: Mahmoud A. Ghannoum. Tel: +1 216 844 8580. Fax: +1 216 844 1076. e-mail: mag3{at}po.cwru.edu Phospholipases have been proposed to contribute to the virulence of Candida albicans . Recently, a candidal strain deleted for PLB1 , the gene encoding the predominant phospholipase B (Plb1) secreted by C. albicans , was constructed and its virulence in an intravenous murine model of disseminated candidiasis was evaluated. In the present study, the PLB1 gene was reintroduced back into the plb1 null mutant to generate the revertant strain, which showed similar growth and morphology to its isogenic parent strain. Virulence of the revertant strain was found to be comparable to that of the parent strain in an intravenous murine model of disseminated candidiasis. To compare the abilities of the plb1 null mutant, the revertant and the isogenic parent strains to cross the gastrointestinal (GI) tract and cause systemic infection, an oral–intragastric infant mouse model of candidiasis was used. Histological examinations and analysis of c.f.u. of the pathogen in liver homogenates revealed that the parental and revertant strains were able to invade and traverse the GI mucosa to a significantly greater extent than the plb1 null mutant. Immunofluorescence and immunoelectron microscopic studies of infected host tissue using anti-Plb1 antibody showed that Plb1 is secreted during invasion of the gastric mucosa by the parental and revertant strains. In contrast, little or no labelling was observed in the null mutant strain. The results indicate that the Plb1 secreted by C. albicans enhances the ability of this organism to cross the GI tract and disseminate haematogenously. These studies provide unequivocal evidence supporting a role for Plb1 during the course of infection by C. albicans . Keywords: phospholipase B, virulence factor, candidal transmigration, in vivo localization of Plb1 Abbreviations: GI, gastrointestinal; PAS, periodic acid–Schiff reagent a These authors contributed equally to this work.</abstract><cop>Reading</cop><pub>Soc General Microbiol</pub><pmid>11535799</pmid><doi>10.1099/00221287-147-9-2585</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1350-0872
ispartof Microbiology (Society for General Microbiology), 2001-09, Vol.147 (9), p.2585-2597
issn 1350-0872
1465-2080
language eng
recordid cdi_proquest_miscellaneous_71142141
source MEDLINE; PubMed Central
subjects Animals
Bacteriology
Biological and medical sciences
Candida albicans
Candida albicans - enzymology
Candida albicans - genetics
Candida albicans - pathogenicity
Candidiasis - etiology
Candidiasis - pathology
Disease Models, Animal
Fundamental and applied biological sciences. Psychology
Fungal Proteins - genetics
Fungal Proteins - metabolism
Gastric Mucosa - microbiology
Gastric Mucosa - pathology
Genes, Fungal
Genetics
Humans
Liver - microbiology
Liver - pathology
Lysophospholipase - genetics
Lysophospholipase - metabolism
Mice
Microbiology
Microscopy, Electron
Mutation
Mycology
Pathogenicity, host-agent relations, miscellaneous strains, epidemiology
PLB1 gene
Virulence - genetics
title Reintroduction of the PLB1 gene into Candida albicans restores virulence in vivo
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T21%3A27%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Reintroduction%20of%20the%20PLB1%20gene%20into%20Candida%20albicans%20restores%20virulence%20in%20vivo&rft.jtitle=Microbiology%20(Society%20for%20General%20Microbiology)&rft.au=Mukherjee,%20Pranab%20K&rft.date=2001-09-01&rft.volume=147&rft.issue=9&rft.spage=2585&rft.epage=2597&rft.pages=2585-2597&rft.issn=1350-0872&rft.eissn=1465-2080&rft_id=info:doi/10.1099/00221287-147-9-2585&rft_dat=%3Cproquest_cross%3E18196635%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=18196635&rft_id=info:pmid/11535799&rfr_iscdi=true