Prevalence of SXT/R391-like integrative and conjugative elements carrying blaC MY-2 in Proteus mirabilis

Objectives: To characterize the vectors involved in the dissemination of bla CMY-2 genes in clinical isolates of Proteus mirabilis collected between 1999 and 2007. Methods: Plasmid analysis of 19 P. mirabilis carrying ampC genes was performed by PCR-based replicon typing, S1-PFGE and Southern hybrid...

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Autores: Mata C., Navarro F., Miró E., Walsh T.R., Mirelis B., Toleman M.
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2011
País:España
Recursos:Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)
Repositorio:r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
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https://www.scopus.com/inward/record.uri?eid=2-s2.0-79960963278&doi=10.1093%2fjac%2fdkr286&partnerID=40&md5=62e3be4a3b566844c60e96ccab389d04
Access Level:acceso abierto
Palavra-chave:antitoxin
bacterial protein
beta lactamase AmpC
beta lactamase CMY 2
beta lactamase CTX M
carbapenemase
extended spectrum beta lactamase
integrase
R391 integrative conjugative elements
SXT integrative conjugative element
unclassified drug
article
bacterial gene
bacterium isolate
genetic organization
hybridization
nonhuman
plasmid
polymerase chain reaction
Proteus mirabilis
Southern blotting
Bacterial Proteins
beta-Lactamases
Conjugation, Genetic
DNA, Bacterial
Drug Resistance, Multiple, Bacterial
Humans
Integrases
Interspersed Repetitive Sequences
Microbial Sensitivity Tests
Plasmids
Proteus Infections
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repository_id_str
spelling Prevalence of SXT/R391-like integrative and conjugative elements carrying blaC MY-2 in Proteus mirabilisMata C.Navarro F.Miró E.Walsh T.R.Mirelis B.Toleman M.antitoxinbacterial proteinbeta lactamase AmpCbeta lactamase CMY 2beta lactamase CTX Mcarbapenemaseextended spectrum beta lactamaseintegraseR391 integrative conjugative elementsSXT integrative conjugative elementunclassified drugarticlebacterial genebacterium isolategenetic organizationhybridizationnonhumanplasmidpolymerase chain reactionProteus mirabilisSouthern blottingBacterial Proteinsbeta-LactamasesConjugation, GeneticDNA, BacterialDrug Resistance, Multiple, BacterialHumansIntegrasesInterspersed Repetitive SequencesMicrobial Sensitivity TestsPlasmidsProteus InfectionsProteus mirabilisObjectives: To characterize the vectors involved in the dissemination of bla CMY-2 genes in clinical isolates of Proteus mirabilis collected between 1999 and 2007. Methods: Plasmid analysis of 19 P. mirabilis carrying ampC genes was performed by PCR-based replicon typing, S1-PFGE and Southern hybridization with ampC and replicon probes. Isolates that could not be characterized were examined for the presence of SXT/R391-like elements. To demonstrate the involvement of these elements in the dissemination of bla CMY-2, we performed a PCR amplification of the integrase (int) and toxin/antitoxin (TA) genes from SXT/R391-like integrative conjugative elements (ICEs). Later on, I-Ceu-I PFGE gels and hybridization with bla CMY-2, int and prfC probes were performed. The genetic organization of bla CMY-2 was also studied. Results: ampC genes were located on large conjugative plasmids in 11 of the 19 (58%) P. mirabilis studied. However, in eight of these isolates a plasmid was not involved in the mobilization of ampC genes. I-Ceu-I PFGE and hybridization analyses revealed thatbla CMY-2 were chromosomally located in these eight P. mirabilis isolates. The genetic organization of bla CMY-2 and hybridization analyses revealed that bla CMY-2 was carried by an ICE almost identical to ICEPmiJpan1 in seven out of these eight isolates. Conclusions: The prevalence of ICEs carrying bla CMY-2 was surprisingly high [37% (7 out of 19)]. This is the first study giving prevalence data on ICEs carrying bla CMY-2 genes. These results suggest the need to study these mobile genetic elements in the context of dissemination of acquired AmpC ß-lactamases and also of other ß-lactamases, such as extended-spectrum ß-lactamases and carbapenemases. © The Author 2011. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved.OXFORD UNIV PRESS2011info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttps://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=10501https://www.scopus.com/inward/record.uri?eid=2-s2.0-79960963278&doi=10.1093%2fjac%2fdkr286&partnerID=40&md5=62e3be4a3b566844c60e96ccab389d04JOURNAL OF ANTIMICROBIAL CHEMOTHERAPYISSN: 03057453ISSNe: 14602091reponame:r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pauinstname:Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)Inglésinfo:eu-repo/semantics/openAccessoai:iibsantpau.fundanetsuite.com:p105012026-06-14T12:41:47Z
dc.title.none.fl_str_mv Prevalence of SXT/R391-like integrative and conjugative elements carrying blaC MY-2 in Proteus mirabilis
title Prevalence of SXT/R391-like integrative and conjugative elements carrying blaC MY-2 in Proteus mirabilis
spellingShingle Prevalence of SXT/R391-like integrative and conjugative elements carrying blaC MY-2 in Proteus mirabilis
Mata C.
antitoxin
bacterial protein
beta lactamase AmpC
beta lactamase CMY 2
beta lactamase CTX M
carbapenemase
extended spectrum beta lactamase
integrase
R391 integrative conjugative elements
SXT integrative conjugative element
unclassified drug
article
bacterial gene
bacterium isolate
genetic organization
hybridization
nonhuman
plasmid
polymerase chain reaction
Proteus mirabilis
Southern blotting
Bacterial Proteins
beta-Lactamases
Conjugation, Genetic
DNA, Bacterial
Drug Resistance, Multiple, Bacterial
Humans
Integrases
Interspersed Repetitive Sequences
Microbial Sensitivity Tests
Plasmids
Proteus Infections
Proteus mirabilis
title_short Prevalence of SXT/R391-like integrative and conjugative elements carrying blaC MY-2 in Proteus mirabilis
title_full Prevalence of SXT/R391-like integrative and conjugative elements carrying blaC MY-2 in Proteus mirabilis
title_fullStr Prevalence of SXT/R391-like integrative and conjugative elements carrying blaC MY-2 in Proteus mirabilis
title_full_unstemmed Prevalence of SXT/R391-like integrative and conjugative elements carrying blaC MY-2 in Proteus mirabilis
title_sort Prevalence of SXT/R391-like integrative and conjugative elements carrying blaC MY-2 in Proteus mirabilis
dc.creator.none.fl_str_mv Mata C.
Navarro F.
Miró E.
Walsh T.R.
Mirelis B.
Toleman M.
author Mata C.
author_facet Mata C.
Navarro F.
Miró E.
Walsh T.R.
Mirelis B.
Toleman M.
author_role author
author2 Navarro F.
Miró E.
Walsh T.R.
Mirelis B.
Toleman M.
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv antitoxin
bacterial protein
beta lactamase AmpC
beta lactamase CMY 2
beta lactamase CTX M
carbapenemase
extended spectrum beta lactamase
integrase
R391 integrative conjugative elements
SXT integrative conjugative element
unclassified drug
article
bacterial gene
bacterium isolate
genetic organization
hybridization
nonhuman
plasmid
polymerase chain reaction
Proteus mirabilis
Southern blotting
Bacterial Proteins
beta-Lactamases
Conjugation, Genetic
DNA, Bacterial
Drug Resistance, Multiple, Bacterial
Humans
Integrases
Interspersed Repetitive Sequences
Microbial Sensitivity Tests
Plasmids
Proteus Infections
Proteus mirabilis
topic antitoxin
bacterial protein
beta lactamase AmpC
beta lactamase CMY 2
beta lactamase CTX M
carbapenemase
extended spectrum beta lactamase
integrase
R391 integrative conjugative elements
SXT integrative conjugative element
unclassified drug
article
bacterial gene
bacterium isolate
genetic organization
hybridization
nonhuman
plasmid
polymerase chain reaction
Proteus mirabilis
Southern blotting
Bacterial Proteins
beta-Lactamases
Conjugation, Genetic
DNA, Bacterial
Drug Resistance, Multiple, Bacterial
Humans
Integrases
Interspersed Repetitive Sequences
Microbial Sensitivity Tests
Plasmids
Proteus Infections
Proteus mirabilis
description Objectives: To characterize the vectors involved in the dissemination of bla CMY-2 genes in clinical isolates of Proteus mirabilis collected between 1999 and 2007. Methods: Plasmid analysis of 19 P. mirabilis carrying ampC genes was performed by PCR-based replicon typing, S1-PFGE and Southern hybridization with ampC and replicon probes. Isolates that could not be characterized were examined for the presence of SXT/R391-like elements. To demonstrate the involvement of these elements in the dissemination of bla CMY-2, we performed a PCR amplification of the integrase (int) and toxin/antitoxin (TA) genes from SXT/R391-like integrative conjugative elements (ICEs). Later on, I-Ceu-I PFGE gels and hybridization with bla CMY-2, int and prfC probes were performed. The genetic organization of bla CMY-2 was also studied. Results: ampC genes were located on large conjugative plasmids in 11 of the 19 (58%) P. mirabilis studied. However, in eight of these isolates a plasmid was not involved in the mobilization of ampC genes. I-Ceu-I PFGE and hybridization analyses revealed thatbla CMY-2 were chromosomally located in these eight P. mirabilis isolates. The genetic organization of bla CMY-2 and hybridization analyses revealed that bla CMY-2 was carried by an ICE almost identical to ICEPmiJpan1 in seven out of these eight isolates. Conclusions: The prevalence of ICEs carrying bla CMY-2 was surprisingly high [37% (7 out of 19)]. This is the first study giving prevalence data on ICEs carrying bla CMY-2 genes. These results suggest the need to study these mobile genetic elements in the context of dissemination of acquired AmpC ß-lactamases and also of other ß-lactamases, such as extended-spectrum ß-lactamases and carbapenemases. © The Author 2011. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved.
publishDate 2011
dc.date.none.fl_str_mv 2011
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=10501
https://www.scopus.com/inward/record.uri?eid=2-s2.0-79960963278&doi=10.1093%2fjac%2fdkr286&partnerID=40&md5=62e3be4a3b566844c60e96ccab389d04
url https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=10501
https://www.scopus.com/inward/record.uri?eid=2-s2.0-79960963278&doi=10.1093%2fjac%2fdkr286&partnerID=40&md5=62e3be4a3b566844c60e96ccab389d04
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv OXFORD UNIV PRESS
publisher.none.fl_str_mv OXFORD UNIV PRESS
dc.source.none.fl_str_mv JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
ISSN: 03057453
ISSNe: 14602091
reponame:r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname:Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)
instname_str Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)
reponame_str r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
collection r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
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repository.mail.fl_str_mv
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