SecDF as Part of the Sec-Translocase Facilitates Efficient Secretion of Bacillus cereus Toxins and Cell Wall-Associated Proteins
Identifieur interne : 001C82 ( Ncbi/Merge ); précédent : 001C81; suivant : 001C83SecDF as Part of the Sec-Translocase Facilitates Efficient Secretion of Bacillus cereus Toxins and Cell Wall-Associated Proteins
Auteurs : Aniko Vörös [Norvège] ; Roger Simm [Norvège] ; Leyla Slamti [France] ; Matthew J. Mckay [Australie] ; Ida K. Hegna [Norvège] ; Christina Nielsen-Leroux [France] ; Karl A. Hassan [Australie] ; Ian T. Paulsen [Australie] ; Didier Lereclus [France] ; Ole Andreas Kstad [Norvège] ; Mark P. Molloy [Australie] ; Anne-Brit Kolst [Norvège]Source :
- PLoS ONE [ 1932-6203 ] ; 2014.
Descripteurs français
- KwdFr :
- Analyse de profil d'expression de gènes, Animaux, Bacillus cereus (), Bacillus cereus (physiologie), Bacillus cereus (ultrastructure), Mutation, Papillons de nuit (microbiologie), Paroi cellulaire (métabolisme), Protéines bactériennes (génétique), Protéines bactériennes (métabolisme), Régulation de l'expression des gènes bactériens, Résistance bactérienne aux médicaments (génétique), Stress physiologique, Techniques de knock-out de gènes, Toxines bactériennes (biosynthèse), Transport biologique, Virulence (génétique), Xénobiotique (pharmacologie).
- MESH :
- biosynthèse : Toxines bactériennes.
- génétique : Protéines bactériennes, Résistance bactérienne aux médicaments, Virulence.
- microbiologie : Papillons de nuit.
- métabolisme : Paroi cellulaire, Protéines bactériennes.
- pharmacologie : Xénobiotique.
- physiologie : Bacillus cereus.
- Analyse de profil d'expression de gènes, Animaux, Bacillus cereus, Mutation, Régulation de l'expression des gènes bactériens, Stress physiologique, Techniques de knock-out de gènes, Transport biologique.
English descriptors
- KwdEn :
- Animals, Bacillus cereus (drug effects), Bacillus cereus (physiology), Bacillus cereus (ultrastructure), Bacterial Proteins (genetics), Bacterial Proteins (metabolism), Bacterial Toxins (biosynthesis), Biological Transport, Cell Wall (metabolism), Drug Resistance, Bacterial (genetics), Gene Expression Profiling, Gene Expression Regulation, Bacterial, Gene Knockout Techniques, Moths (microbiology), Mutation, Stress, Physiological, Virulence (genetics), Xenobiotics (pharmacology).
- MESH :
- chemical , biosynthesis : Bacterial Toxins.
- chemical , genetics : Bacterial Proteins.
- drug effects : Bacillus cereus.
- genetics : Drug Resistance, Bacterial, Virulence.
- chemical , metabolism : Bacterial Proteins, Cell Wall.
- microbiology : Moths.
- chemical , pharmacology : Xenobiotics.
- physiology : Bacillus cereus.
- ultrastructure : Bacillus cereus.
- Animals, Biological Transport, Gene Expression Profiling, Gene Expression Regulation, Bacterial, Gene Knockout Techniques, Mutation, Stress, Physiological.
Abstract
The aim of this study was to explore the role of SecDF in protein secretion in
Url:
DOI: 10.1371/journal.pone.0103326
PubMed: 25083861
PubMed Central: 4118872
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Links to Exploration step
PMC:4118872Le document en format XML
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term>
<term>Bacillus cereus (drug effects)</term>
<term>Bacillus cereus (physiology)</term>
<term>Bacillus cereus (ultrastructure)</term>
<term>Bacterial Proteins (genetics)</term>
<term>Bacterial Proteins (metabolism)</term>
<term>Bacterial Toxins (biosynthesis)</term>
<term>Biological Transport</term>
<term>Cell Wall (metabolism)</term>
<term>Drug Resistance, Bacterial (genetics)</term>
<term>Gene Expression Profiling</term>
<term>Gene Expression Regulation, Bacterial</term>
<term>Gene Knockout Techniques</term>
<term>Moths (microbiology)</term>
<term>Mutation</term>
<term>Stress, Physiological</term>
<term>Virulence (genetics)</term>
<term>Xenobiotics (pharmacology)</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Analyse de profil d'expression de gènes</term>
<term>Animaux</term>
<term>Bacillus cereus ()</term>
<term>Bacillus cereus (physiologie)</term>
<term>Bacillus cereus (ultrastructure)</term>
<term>Mutation</term>
<term>Papillons de nuit (microbiologie)</term>
<term>Paroi cellulaire (métabolisme)</term>
<term>Protéines bactériennes (génétique)</term>
<term>Protéines bactériennes (métabolisme)</term>
<term>Régulation de l'expression des gènes bactériens</term>
<term>Résistance bactérienne aux médicaments (génétique)</term>
<term>Stress physiologique</term>
<term>Techniques de knock-out de gènes</term>
<term>Toxines bactériennes (biosynthèse)</term>
<term>Transport biologique</term>
<term>Virulence (génétique)</term>
<term>Xénobiotique (pharmacologie)</term>
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<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Bacterial Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr"><term>Toxines bactériennes</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Bacillus cereus</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Drug Resistance, Bacterial</term>
<term>Virulence</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Protéines bactériennes</term>
<term>Résistance bactérienne aux médicaments</term>
<term>Virulence</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Bacterial Proteins</term>
<term>Cell Wall</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr"><term>Papillons de nuit</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Moths</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Paroi cellulaire</term>
<term>Protéines bactériennes</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Xénobiotique</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Xenobiotics</term>
</keywords>
<keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Bacillus cereus</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Bacillus cereus</term>
</keywords>
<keywords scheme="MESH" qualifier="ultrastructure" xml:lang="en"><term>Bacillus cereus</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Biological Transport</term>
<term>Gene Expression Profiling</term>
<term>Gene Expression Regulation, Bacterial</term>
<term>Gene Knockout Techniques</term>
<term>Mutation</term>
<term>Stress, Physiological</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Analyse de profil d'expression de gènes</term>
<term>Animaux</term>
<term>Bacillus cereus</term>
<term>Mutation</term>
<term>Régulation de l'expression des gènes bactériens</term>
<term>Stress physiologique</term>
<term>Techniques de knock-out de gènes</term>
<term>Transport biologique</term>
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<front><div type="abstract" xml:lang="en"><p>The aim of this study was to explore the role of SecDF in protein secretion in <italic>Bacillus cereus</italic>
ATCC 14579 by in-depth characterization of a markerless <italic>secDF</italic>
knock out mutant. Deletion of <italic>secDF</italic>
resulted in pleiotropic effects characterized by a moderately slower growth rate, aberrant cell morphology, enhanced susceptibility to xenobiotics, reduced virulence and motility. Most toxins, including food poisoning-associated enterotoxins Nhe, Hbl, and cytotoxin K, as well as phospholipase C were less abundant in the secretome of the Δ<italic>secDF</italic>
mutant as determined by label-free mass spectrometry. Global transcriptome studies revealed profound transcriptional changes upon deletion of <italic>secDF</italic>
indicating cell envelope stress. Interestingly, the addition of glucose enhanced the described phenotypes. This study shows that SecDF is an important part of the Sec-translocase mediating efficient secretion of virulence factors in the Gram-positive opportunistic pathogen <italic>B. cereus</italic>
, and further supports the notion that <italic>B. cereus</italic>
enterotoxins are secreted by the Sec-system.</p>
</div>
</front>
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Toxins and Cell Wall-Associated Proteins</title>
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</nlm:aff>
<country xml:lang="fr">Australie</country>
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<placeName><settlement type="city">Sydney</settlement>
<region type="état">Nouvelle-Galles du Sud</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Hegna, Ida K" sort="Hegna, Ida K" uniqKey="Hegna I" first="Ida K." last="Hegna">Ida K. Hegna</name>
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</nlm:aff>
<country xml:lang="fr">Norvège</country>
<wicri:regionArea>Laboratory for Microbial Dynamics (LaMDa), Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo</wicri:regionArea>
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<region nuts="2">Østlandet</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Nielsen Leroux, Christina" sort="Nielsen Leroux, Christina" uniqKey="Nielsen Leroux C" first="Christina" last="Nielsen-Leroux">Christina Nielsen-Leroux</name>
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</nlm:aff>
<country xml:lang="fr">France</country>
<wicri:regionArea>INRA, UMR1319 Micalis, Domaine de La Minière, Guyancourt</wicri:regionArea>
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</affiliation>
</author>
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</nlm:aff>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Department of Chemistry and Biomolecular Sciences, Macquarie University, Sydney</wicri:regionArea>
<placeName><settlement type="city">Sydney</settlement>
<region type="état">Nouvelle-Galles du Sud</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Paulsen, Ian T" sort="Paulsen, Ian T" uniqKey="Paulsen I" first="Ian T." last="Paulsen">Ian T. Paulsen</name>
<affiliation wicri:level="3"><nlm:aff id="aff5"><addr-line>Department of Chemistry and Biomolecular Sciences, Macquarie University, Sydney, Australia</addr-line>
</nlm:aff>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Department of Chemistry and Biomolecular Sciences, Macquarie University, Sydney</wicri:regionArea>
<placeName><settlement type="city">Sydney</settlement>
<region type="état">Nouvelle-Galles du Sud</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Lereclus, Didier" sort="Lereclus, Didier" uniqKey="Lereclus D" first="Didier" last="Lereclus">Didier Lereclus</name>
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</nlm:aff>
<country xml:lang="fr">France</country>
<wicri:regionArea>INRA, UMR1319 Micalis, Domaine de La Minière, Guyancourt</wicri:regionArea>
<wicri:noRegion>Guyancourt</wicri:noRegion>
<wicri:noRegion>Guyancourt</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1"><nlm:aff id="aff4"><addr-line>AgroParistech, UMR Micalis, Jouy-en-Josas, France</addr-line>
</nlm:aff>
<country xml:lang="fr">France</country>
<wicri:regionArea>AgroParistech, UMR Micalis, Jouy-en-Josas</wicri:regionArea>
<wicri:noRegion>Jouy-en-Josas</wicri:noRegion>
<wicri:noRegion>Jouy-en-Josas</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey=" Kstad, Ole Andreas" sort=" Kstad, Ole Andreas" uniqKey=" Kstad O" first="Ole Andreas" last=" Kstad">Ole Andreas Kstad</name>
<affiliation wicri:level="3"><nlm:aff id="aff1"><addr-line>Laboratory for Microbial Dynamics (LaMDa), Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo, Norway</addr-line>
</nlm:aff>
<country xml:lang="fr">Norvège</country>
<wicri:regionArea>Laboratory for Microbial Dynamics (LaMDa), Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo</wicri:regionArea>
<placeName><settlement type="city">Oslo</settlement>
<region nuts="2">Østlandet</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Molloy, Mark P" sort="Molloy, Mark P" uniqKey="Molloy M" first="Mark P." last="Molloy">Mark P. Molloy</name>
<affiliation wicri:level="3"><nlm:aff id="aff2"><addr-line>Australian Proteome Analysis Facility (APAF), Macquarie University, Sydney, Australia</addr-line>
</nlm:aff>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Australian Proteome Analysis Facility (APAF), Macquarie University, Sydney</wicri:regionArea>
<placeName><settlement type="city">Sydney</settlement>
<region type="état">Nouvelle-Galles du Sud</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Kolst, Anne Brit" sort="Kolst, Anne Brit" uniqKey="Kolst A" first="Anne-Brit" last="Kolst">Anne-Brit Kolst</name>
<affiliation wicri:level="3"><nlm:aff id="aff1"><addr-line>Laboratory for Microbial Dynamics (LaMDa), Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo, Norway</addr-line>
</nlm:aff>
<country xml:lang="fr">Norvège</country>
<wicri:regionArea>Laboratory for Microbial Dynamics (LaMDa), Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo</wicri:regionArea>
<placeName><settlement type="city">Oslo</settlement>
<region nuts="2">Østlandet</region>
</placeName>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PMC</idno>
<idno type="pmid">25083861</idno>
<idno type="pmc">4118872</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4118872</idno>
<idno type="RBID">PMC:4118872</idno>
<idno type="doi">10.1371/journal.pone.0103326</idno>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">SecDF as Part of the Sec-Translocase Facilitates Efficient Secretion of <italic>Bacillus cereus</italic>
Toxins and Cell Wall-Associated Proteins</title>
<author><name sortKey="Voros, Aniko" sort="Voros, Aniko" uniqKey="Voros A" first="Aniko" last="Vörös">Aniko Vörös</name>
<affiliation wicri:level="3"><nlm:aff id="aff1"><addr-line>Laboratory for Microbial Dynamics (LaMDa), Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo, Norway</addr-line>
</nlm:aff>
<country xml:lang="fr">Norvège</country>
<wicri:regionArea>Laboratory for Microbial Dynamics (LaMDa), Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo</wicri:regionArea>
<placeName><settlement type="city">Oslo</settlement>
<region nuts="2">Østlandet</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Simm, Roger" sort="Simm, Roger" uniqKey="Simm R" first="Roger" last="Simm">Roger Simm</name>
<affiliation wicri:level="3"><nlm:aff id="aff1"><addr-line>Laboratory for Microbial Dynamics (LaMDa), Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo, Norway</addr-line>
</nlm:aff>
<country xml:lang="fr">Norvège</country>
<wicri:regionArea>Laboratory for Microbial Dynamics (LaMDa), Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo</wicri:regionArea>
<placeName><settlement type="city">Oslo</settlement>
<region nuts="2">Østlandet</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Slamti, Leyla" sort="Slamti, Leyla" uniqKey="Slamti L" first="Leyla" last="Slamti">Leyla Slamti</name>
<affiliation wicri:level="1"><nlm:aff id="aff3"><addr-line>INRA, UMR1319 Micalis, Domaine de La Minière, Guyancourt, France</addr-line>
</nlm:aff>
<country xml:lang="fr">France</country>
<wicri:regionArea>INRA, UMR1319 Micalis, Domaine de La Minière, Guyancourt</wicri:regionArea>
<wicri:noRegion>Guyancourt</wicri:noRegion>
<wicri:noRegion>Guyancourt</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Mckay, Matthew J" sort="Mckay, Matthew J" uniqKey="Mckay M" first="Matthew J." last="Mckay">Matthew J. Mckay</name>
<affiliation wicri:level="3"><nlm:aff id="aff2"><addr-line>Australian Proteome Analysis Facility (APAF), Macquarie University, Sydney, Australia</addr-line>
</nlm:aff>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Australian Proteome Analysis Facility (APAF), Macquarie University, Sydney</wicri:regionArea>
<placeName><settlement type="city">Sydney</settlement>
<region type="état">Nouvelle-Galles du Sud</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Hegna, Ida K" sort="Hegna, Ida K" uniqKey="Hegna I" first="Ida K." last="Hegna">Ida K. Hegna</name>
<affiliation wicri:level="3"><nlm:aff id="aff1"><addr-line>Laboratory for Microbial Dynamics (LaMDa), Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo, Norway</addr-line>
</nlm:aff>
<country xml:lang="fr">Norvège</country>
<wicri:regionArea>Laboratory for Microbial Dynamics (LaMDa), Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo</wicri:regionArea>
<placeName><settlement type="city">Oslo</settlement>
<region nuts="2">Østlandet</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Nielsen Leroux, Christina" sort="Nielsen Leroux, Christina" uniqKey="Nielsen Leroux C" first="Christina" last="Nielsen-Leroux">Christina Nielsen-Leroux</name>
<affiliation wicri:level="1"><nlm:aff id="aff3"><addr-line>INRA, UMR1319 Micalis, Domaine de La Minière, Guyancourt, France</addr-line>
</nlm:aff>
<country xml:lang="fr">France</country>
<wicri:regionArea>INRA, UMR1319 Micalis, Domaine de La Minière, Guyancourt</wicri:regionArea>
<wicri:noRegion>Guyancourt</wicri:noRegion>
<wicri:noRegion>Guyancourt</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Hassan, Karl A" sort="Hassan, Karl A" uniqKey="Hassan K" first="Karl A." last="Hassan">Karl A. Hassan</name>
<affiliation wicri:level="3"><nlm:aff id="aff5"><addr-line>Department of Chemistry and Biomolecular Sciences, Macquarie University, Sydney, Australia</addr-line>
</nlm:aff>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Department of Chemistry and Biomolecular Sciences, Macquarie University, Sydney</wicri:regionArea>
<placeName><settlement type="city">Sydney</settlement>
<region type="état">Nouvelle-Galles du Sud</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Paulsen, Ian T" sort="Paulsen, Ian T" uniqKey="Paulsen I" first="Ian T." last="Paulsen">Ian T. Paulsen</name>
<affiliation wicri:level="3"><nlm:aff id="aff5"><addr-line>Department of Chemistry and Biomolecular Sciences, Macquarie University, Sydney, Australia</addr-line>
</nlm:aff>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Department of Chemistry and Biomolecular Sciences, Macquarie University, Sydney</wicri:regionArea>
<placeName><settlement type="city">Sydney</settlement>
<region type="état">Nouvelle-Galles du Sud</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Lereclus, Didier" sort="Lereclus, Didier" uniqKey="Lereclus D" first="Didier" last="Lereclus">Didier Lereclus</name>
<affiliation wicri:level="1"><nlm:aff id="aff3"><addr-line>INRA, UMR1319 Micalis, Domaine de La Minière, Guyancourt, France</addr-line>
</nlm:aff>
<country xml:lang="fr">France</country>
<wicri:regionArea>INRA, UMR1319 Micalis, Domaine de La Minière, Guyancourt</wicri:regionArea>
<wicri:noRegion>Guyancourt</wicri:noRegion>
<wicri:noRegion>Guyancourt</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1"><nlm:aff id="aff4"><addr-line>AgroParistech, UMR Micalis, Jouy-en-Josas, France</addr-line>
</nlm:aff>
<country xml:lang="fr">France</country>
<wicri:regionArea>AgroParistech, UMR Micalis, Jouy-en-Josas</wicri:regionArea>
<wicri:noRegion>Jouy-en-Josas</wicri:noRegion>
<wicri:noRegion>Jouy-en-Josas</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey=" Kstad, Ole Andreas" sort=" Kstad, Ole Andreas" uniqKey=" Kstad O" first="Ole Andreas" last=" Kstad">Ole Andreas Kstad</name>
<affiliation wicri:level="3"><nlm:aff id="aff1"><addr-line>Laboratory for Microbial Dynamics (LaMDa), Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo, Norway</addr-line>
</nlm:aff>
<country xml:lang="fr">Norvège</country>
<wicri:regionArea>Laboratory for Microbial Dynamics (LaMDa), Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo</wicri:regionArea>
<placeName><settlement type="city">Oslo</settlement>
<region nuts="2">Østlandet</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Molloy, Mark P" sort="Molloy, Mark P" uniqKey="Molloy M" first="Mark P." last="Molloy">Mark P. Molloy</name>
<affiliation wicri:level="3"><nlm:aff id="aff2"><addr-line>Australian Proteome Analysis Facility (APAF), Macquarie University, Sydney, Australia</addr-line>
</nlm:aff>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Australian Proteome Analysis Facility (APAF), Macquarie University, Sydney</wicri:regionArea>
<placeName><settlement type="city">Sydney</settlement>
<region type="état">Nouvelle-Galles du Sud</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Kolst, Anne Brit" sort="Kolst, Anne Brit" uniqKey="Kolst A" first="Anne-Brit" last="Kolst">Anne-Brit Kolst</name>
<affiliation wicri:level="3"><nlm:aff id="aff1"><addr-line>Laboratory for Microbial Dynamics (LaMDa), Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo, Norway</addr-line>
</nlm:aff>
<country xml:lang="fr">Norvège</country>
<wicri:regionArea>Laboratory for Microbial Dynamics (LaMDa), Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo</wicri:regionArea>
<placeName><settlement type="city">Oslo</settlement>
<region nuts="2">Østlandet</region>
</placeName>
</affiliation>
</author>
</analytic>
<series><title level="j">PLoS ONE</title>
<idno type="eISSN">1932-6203</idno>
<imprint><date when="2014">2014</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass></textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en"><p>The aim of this study was to explore the role of SecDF in protein secretion in <italic>Bacillus cereus</italic>
ATCC 14579 by in-depth characterization of a markerless <italic>secDF</italic>
knock out mutant. Deletion of <italic>secDF</italic>
resulted in pleiotropic effects characterized by a moderately slower growth rate, aberrant cell morphology, enhanced susceptibility to xenobiotics, reduced virulence and motility. Most toxins, including food poisoning-associated enterotoxins Nhe, Hbl, and cytotoxin K, as well as phospholipase C were less abundant in the secretome of the Δ<italic>secDF</italic>
mutant as determined by label-free mass spectrometry. Global transcriptome studies revealed profound transcriptional changes upon deletion of <italic>secDF</italic>
indicating cell envelope stress. Interestingly, the addition of glucose enhanced the described phenotypes. This study shows that SecDF is an important part of the Sec-translocase mediating efficient secretion of virulence factors in the Gram-positive opportunistic pathogen <italic>B. cereus</italic>
, and further supports the notion that <italic>B. cereus</italic>
enterotoxins are secreted by the Sec-system.</p>
</div>
</front>
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<wicri:regionArea>Department of Chemistry and Biomolecular Sciences, Macquarie University, Sydney</wicri:regionArea>
<placeName><settlement type="city">Sydney</settlement>
<region type="état">Nouvelle-Galles du Sud</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Paulsen, Ian T" sort="Paulsen, Ian T" uniqKey="Paulsen I" first="Ian T" last="Paulsen">Ian T. Paulsen</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Chemistry and Biomolecular Sciences, Macquarie University, Sydney, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Department of Chemistry and Biomolecular Sciences, Macquarie University, Sydney</wicri:regionArea>
<placeName><settlement type="city">Sydney</settlement>
<region type="état">Nouvelle-Galles du Sud</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Lereclus, Didier" sort="Lereclus, Didier" uniqKey="Lereclus D" first="Didier" last="Lereclus">Didier Lereclus</name>
<affiliation wicri:level="1"><nlm:affiliation>INRA, UMR1319 Micalis, Domaine de La Minière, Guyancourt, France; AgroParistech, UMR Micalis, Jouy-en-Josas, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>INRA, UMR1319 Micalis, Domaine de La Minière, Guyancourt, France; AgroParistech, UMR Micalis, Jouy-en-Josas</wicri:regionArea>
<wicri:noRegion>Jouy-en-Josas</wicri:noRegion>
<wicri:noRegion>Jouy-en-Josas</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey=" Kstad, Ole Andreas" sort=" Kstad, Ole Andreas" uniqKey=" Kstad O" first="Ole Andreas" last=" Kstad">Ole Andreas Kstad</name>
<affiliation wicri:level="3"><nlm:affiliation>Laboratory for Microbial Dynamics (LaMDa), Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo, Norway.</nlm:affiliation>
<country xml:lang="fr">Norvège</country>
<wicri:regionArea>Laboratory for Microbial Dynamics (LaMDa), Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo</wicri:regionArea>
<placeName><settlement type="city">Oslo</settlement>
<region nuts="2">Østlandet</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Molloy, Mark P" sort="Molloy, Mark P" uniqKey="Molloy M" first="Mark P" last="Molloy">Mark P. Molloy</name>
<affiliation wicri:level="3"><nlm:affiliation>Australian Proteome Analysis Facility (APAF), Macquarie University, Sydney, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Australian Proteome Analysis Facility (APAF), Macquarie University, Sydney</wicri:regionArea>
<placeName><settlement type="city">Sydney</settlement>
<region type="état">Nouvelle-Galles du Sud</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Kolst, Anne Brit" sort="Kolst, Anne Brit" uniqKey="Kolst A" first="Anne-Brit" last="Kolst">Anne-Brit Kolst</name>
<affiliation wicri:level="3"><nlm:affiliation>Laboratory for Microbial Dynamics (LaMDa), Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo, Norway.</nlm:affiliation>
<country xml:lang="fr">Norvège</country>
<wicri:regionArea>Laboratory for Microbial Dynamics (LaMDa), Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo</wicri:regionArea>
<placeName><settlement type="city">Oslo</settlement>
<region nuts="2">Østlandet</region>
</placeName>
</affiliation>
</author>
</analytic>
<series><title level="j">PloS one</title>
<idno type="eISSN">1932-6203</idno>
<imprint><date when="2014" type="published">2014</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term>
<term>Bacillus cereus (drug effects)</term>
<term>Bacillus cereus (physiology)</term>
<term>Bacillus cereus (ultrastructure)</term>
<term>Bacterial Proteins (genetics)</term>
<term>Bacterial Proteins (metabolism)</term>
<term>Bacterial Toxins (biosynthesis)</term>
<term>Biological Transport</term>
<term>Cell Wall (metabolism)</term>
<term>Drug Resistance, Bacterial (genetics)</term>
<term>Gene Expression Profiling</term>
<term>Gene Expression Regulation, Bacterial</term>
<term>Gene Knockout Techniques</term>
<term>Moths (microbiology)</term>
<term>Mutation</term>
<term>Stress, Physiological</term>
<term>Virulence (genetics)</term>
<term>Xenobiotics (pharmacology)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Analyse de profil d'expression de gènes</term>
<term>Animaux</term>
<term>Bacillus cereus ()</term>
<term>Bacillus cereus (physiologie)</term>
<term>Bacillus cereus (ultrastructure)</term>
<term>Mutation</term>
<term>Papillons de nuit (microbiologie)</term>
<term>Paroi cellulaire (métabolisme)</term>
<term>Protéines bactériennes (génétique)</term>
<term>Protéines bactériennes (métabolisme)</term>
<term>Régulation de l'expression des gènes bactériens</term>
<term>Résistance bactérienne aux médicaments (génétique)</term>
<term>Stress physiologique</term>
<term>Techniques de knock-out de gènes</term>
<term>Toxines bactériennes (biosynthèse)</term>
<term>Transport biologique</term>
<term>Virulence (génétique)</term>
<term>Xénobiotique (pharmacologie)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en"><term>Bacterial Toxins</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Bacterial Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr"><term>Toxines bactériennes</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Bacillus cereus</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Drug Resistance, Bacterial</term>
<term>Virulence</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Protéines bactériennes</term>
<term>Résistance bactérienne aux médicaments</term>
<term>Virulence</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Bacterial Proteins</term>
<term>Cell Wall</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr"><term>Papillons de nuit</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Moths</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Paroi cellulaire</term>
<term>Protéines bactériennes</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Xénobiotique</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Xenobiotics</term>
</keywords>
<keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Bacillus cereus</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Bacillus cereus</term>
</keywords>
<keywords scheme="MESH" qualifier="ultrastructure" xml:lang="en"><term>Bacillus cereus</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Biological Transport</term>
<term>Gene Expression Profiling</term>
<term>Gene Expression Regulation, Bacterial</term>
<term>Gene Knockout Techniques</term>
<term>Mutation</term>
<term>Stress, Physiological</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Analyse de profil d'expression de gènes</term>
<term>Animaux</term>
<term>Bacillus cereus</term>
<term>Mutation</term>
<term>Régulation de l'expression des gènes bactériens</term>
<term>Stress physiologique</term>
<term>Techniques de knock-out de gènes</term>
<term>Transport biologique</term>
</keywords>
</textClass>
</profileDesc>
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<front><div type="abstract" xml:lang="en">The aim of this study was to explore the role of SecDF in protein secretion in Bacillus cereus ATCC 14579 by in-depth characterization of a markerless secDF knock out mutant. Deletion of secDF resulted in pleiotropic effects characterized by a moderately slower growth rate, aberrant cell morphology, enhanced susceptibility to xenobiotics, reduced virulence and motility. Most toxins, including food poisoning-associated enterotoxins Nhe, Hbl, and cytotoxin K, as well as phospholipase C were less abundant in the secretome of the ΔsecDF mutant as determined by label-free mass spectrometry. Global transcriptome studies revealed profound transcriptional changes upon deletion of secDF indicating cell envelope stress. Interestingly, the addition of glucose enhanced the described phenotypes. This study shows that SecDF is an important part of the Sec-translocase mediating efficient secretion of virulence factors in the Gram-positive opportunistic pathogen B. cereus, and further supports the notion that B. cereus enterotoxins are secreted by the Sec-system.</div>
</front>
</TEI>
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