Caracterização fenotípica e molecular dos mecanismos de resistência aos beta-lactâmicos em linhagens clínicas de Klebsiella pneumoniae isoladas do Amazonas

Detalhes bibliográficos
Autor(a) principal: Souza, Rosineide Cardoso de
Data de Publicação: 2018
Tipo de documento: Tese
Idioma: por
Título da fonte: Repositório Institucional da UFSCAR
Texto Completo: https://repositorio.ufscar.br/handle/ufscar/11839
Resumo: Klebsiella pneumoniae resistant to beta-lactams are present in hospitals worldwide and reduce treatment alternatives. In this study, 40 K. pneumoniae isolates were characterized. All of them were resistant to beta-lactam antibiotics and classified as multidrug resistant. Among these, eight isolates were resistant to carbapenems and six of which had the gene blaKPC-2, encoding the enzyme Klebsiella pneumoniae carbapenemase (KPC). The blaTEM and blaCTX-M genes were found in 80% of the samples. The 40 isolates were grouped into 12 pulses (A to L) according to the genetic similarity determined by the DNA macro-restriction followed by pulsed-field gel electrophoresis. A total of 20 isolates were classified as pulsotype A, which was subdivided into 13 subtypes (A1 to A13), with subtype A1 being the most prevalent. Representatives of pulsotype A belong to the ST11, clonal complex CC258. In this study, we identified four new STs: ST2540, ST2308, ST2258, and ST2307. AMKP5 and AMKP2, belonging to subtypes A7 and A8, respectively, are resistant to carbapenems but did not present the blaKPC gene. Sequencing of the AMKP5 genome indicated mutations in the C-terminal region of the OmpK36 porin which may alter the entry of carbapenems into the cell. Genome sequencing of the AMKP10 isolate identified the plasmid pAMKP10, with 48.454 bp belonging to the IncX5 incompatibility group. In this plasmid, the blaKPC-2 gene was found in a non-Tn4401 genetic element (NTEKPC) containing tnpA-ISEc63-like / tnpR-Tn3 / tnpA-ISKpn27 / blaKPC-2 / ΔISKpn6, based on Tn1722. All isolates with the blaKPC-2 gene had the same plasmid. Conjugation of this plasmid to Escherichia coli J53 occurred from ST11 isolates with low conjugation frequencies (8.23 x 10-12 to 1.31 x 10-7) resulting in resistance to carbapenems. Finally, the outbreak of carbapenem-resistant K. pneumoniae resistant of this Amazonian hospital involved the transfer of the NTEKPC-containing pAMKP10 between two lineages (ST11 and ST2302) but was largely due to the clonal dissemination of the ST11 endemic lineage.
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spelling Souza, Rosineide Cardoso deCamargo, Ilana Lopes Baratella da Cunhahttp://lattes.cnpq.br/4104096171600845http://lattes.cnpq.br/5739753892325187ff125bc7-7846-4cdf-8c1b-c73b9a8413e92019-09-13T19:50:32Z2019-09-13T19:50:32Z2018-10-25SOUZA, Rosineide Cardoso de. Caracterização fenotípica e molecular dos mecanismos de resistência aos beta-lactâmicos em linhagens clínicas de Klebsiella pneumoniae isoladas do Amazonas. 2018. Tese (Doutorado em Genética Evolutiva e Biologia Molecular) – Universidade Federal de São Carlos, São Carlos, 2018. Disponível em: https://repositorio.ufscar.br/handle/ufscar/11839.https://repositorio.ufscar.br/handle/ufscar/11839Klebsiella pneumoniae resistant to beta-lactams are present in hospitals worldwide and reduce treatment alternatives. In this study, 40 K. pneumoniae isolates were characterized. All of them were resistant to beta-lactam antibiotics and classified as multidrug resistant. Among these, eight isolates were resistant to carbapenems and six of which had the gene blaKPC-2, encoding the enzyme Klebsiella pneumoniae carbapenemase (KPC). The blaTEM and blaCTX-M genes were found in 80% of the samples. The 40 isolates were grouped into 12 pulses (A to L) according to the genetic similarity determined by the DNA macro-restriction followed by pulsed-field gel electrophoresis. A total of 20 isolates were classified as pulsotype A, which was subdivided into 13 subtypes (A1 to A13), with subtype A1 being the most prevalent. Representatives of pulsotype A belong to the ST11, clonal complex CC258. In this study, we identified four new STs: ST2540, ST2308, ST2258, and ST2307. AMKP5 and AMKP2, belonging to subtypes A7 and A8, respectively, are resistant to carbapenems but did not present the blaKPC gene. Sequencing of the AMKP5 genome indicated mutations in the C-terminal region of the OmpK36 porin which may alter the entry of carbapenems into the cell. Genome sequencing of the AMKP10 isolate identified the plasmid pAMKP10, with 48.454 bp belonging to the IncX5 incompatibility group. In this plasmid, the blaKPC-2 gene was found in a non-Tn4401 genetic element (NTEKPC) containing tnpA-ISEc63-like / tnpR-Tn3 / tnpA-ISKpn27 / blaKPC-2 / ΔISKpn6, based on Tn1722. All isolates with the blaKPC-2 gene had the same plasmid. Conjugation of this plasmid to Escherichia coli J53 occurred from ST11 isolates with low conjugation frequencies (8.23 x 10-12 to 1.31 x 10-7) resulting in resistance to carbapenems. Finally, the outbreak of carbapenem-resistant K. pneumoniae resistant of this Amazonian hospital involved the transfer of the NTEKPC-containing pAMKP10 between two lineages (ST11 and ST2302) but was largely due to the clonal dissemination of the ST11 endemic lineage.Klebsiella pneumoniae resistentes aos beta-lactâmicos estão presentes em hospitais do mundo todo e reduzem as alternativas de tratamento. Nesse estudo, 40 isolados de K. pneumoniae foram caracterizados. Todos foram classificados como multirresistentes e com resistência aos antibióticos beta-lactâmicos. Dentre estes, oito amostras são resistentes aos carbapenêmicos e seis delas têm o gene blaKPC-2, que codifica a enzima Klebsiella pneumoniae carbapenemase (KPC). Os genes blaTEM e blaCTX-M foram encontrados em 80% das amostras. Os 40 isolados foram agrupados em 12 pulsotipos (A a L) de acordo com a similaridade genética determinada pela macrorrestrição do DNA seguida de eletroforese em gel de campos pulsados. Um total de 20 isolados foram classificados como pulsotipo A, o qual foi subdividido em 13 subtipos (A1 a A13), sendo o subtipo A1 o prevalente. Representantes do pulsotipo A pertencem ao ST11, complexo clonal CC258. Neste estudo, quatro novos STs foram identificados: ST2540, ST2308, ST2258 e ST2307. AMKP5 e AMKP2, dos subtipos A7 e A8, respectivamente, são resistentes aos carbapenêmicos, mas não apresentaram o gene blaKPC. O sequenciamento do genoma da AMKP5 indicou mutações na região C-terminal da porina OmpK36 que pode alterar a entrada dos carbapenêmicos na célula. O sequenciamento do genoma da amostra AMKP10 identificou o plasmídeo pAMKP10, com 48,454 pb pertencente ao grupo de incompatibilidade IncX5. Neste plasmídeo, o gene blaKPC foi encontrado em um ambiente genético diferente do Tn4401 (NTEKPC do inglês, non-Tn4401 genetic element) contendo tnpA-ISEc63-like/tnpR-Tn3/tnpA-ISKpn27/blaKPC-2/ΔISKpn6, baseado no Tn1722. Todos os isolados com o gene blaKPC-2 apresentaram o mesmo plasmídeo. A conjugação deste plasmídeo para Escherichia coli J53 ocorreu a partir dos isolados ST11 com baixas frequências de conjugação (de 8,23 x 10-12 a 1,31 x 10-7) resultando em resistência aos carbapenêmicos. Por fim, observou-se que o surto de K. pneumoniae resistentes aos carbapenêmicos deste hospital Amazonense envolveu a transferência do pAMKP10 contendo NTEKPC entre duas linhagens (ST11 e ST2302), mas ocorreu em grande parte devido à disseminação clonal da linhagem endêmica ST11.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Fundação de Amparo à Pesquisa do Estado do Amazonas (FAPEAM)FAPEAM: 24868.484.14650.07112014-35526FAPESP: 13/07600-l3CNPq: 131314/2018-1porUniversidade Federal de São CarlosCâmpus São CarlosPrograma de Pós-Graduação em Genética Evolutiva e Biologia Molecular - PPGGEvUFSCarKlebsiella pneumoniaeblaKPC-2NTEKPCIncX5CarbapenemCIENCIAS BIOLOGICAS::BIOQUIMICACIENCIAS BIOLOGICAS::GENETICACIENCIAS BIOLOGICAS::MICROBIOLOGIACaracterização fenotípica e molecular dos mecanismos de resistência aos beta-lactâmicos em linhagens clínicas de Klebsiella pneumoniae isoladas do AmazonasPhenotypic and molecular characterization of beta-lactam resistance mechanisms in clinical strains of Klebsiella pneumoniae isolated from Amazonasinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesis6 meses após a data da defesa22028037-951f-464b-bc2d-bce3c9e94ea4info:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFSCARinstname:Universidade Federal de São Carlos (UFSCAR)instacron:UFSCARORIGINALRosineide Cardoso de Souza.pdfRosineide Cardoso de Souza.pdfapplication/pdf1974442https://repositorio.ufscar.br/bitstream/ufscar/11839/1/Rosineide%20Cardoso%20de%20Souza.pdfa0c9abc2cb3da25daf526e606d7495d8MD51carta-comprovante 2.pdfcarta-comprovante 2.pdfCarta comprovante de deposito da versão final da teseapplication/pdf89372https://repositorio.ufscar.br/bitstream/ufscar/11839/3/carta-comprovante%202.pdf33c79ecc26d904fcfd130c4bbba8733cMD53LICENSElicense.txtlicense.txttext/plain; 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dc.title.por.fl_str_mv Caracterização fenotípica e molecular dos mecanismos de resistência aos beta-lactâmicos em linhagens clínicas de Klebsiella pneumoniae isoladas do Amazonas
dc.title.alternative.eng.fl_str_mv Phenotypic and molecular characterization of beta-lactam resistance mechanisms in clinical strains of Klebsiella pneumoniae isolated from Amazonas
title Caracterização fenotípica e molecular dos mecanismos de resistência aos beta-lactâmicos em linhagens clínicas de Klebsiella pneumoniae isoladas do Amazonas
spellingShingle Caracterização fenotípica e molecular dos mecanismos de resistência aos beta-lactâmicos em linhagens clínicas de Klebsiella pneumoniae isoladas do Amazonas
Souza, Rosineide Cardoso de
Klebsiella pneumoniae
blaKPC-2
NTEKPC
IncX5
Carbapenem
CIENCIAS BIOLOGICAS::BIOQUIMICA
CIENCIAS BIOLOGICAS::GENETICA
CIENCIAS BIOLOGICAS::MICROBIOLOGIA
title_short Caracterização fenotípica e molecular dos mecanismos de resistência aos beta-lactâmicos em linhagens clínicas de Klebsiella pneumoniae isoladas do Amazonas
title_full Caracterização fenotípica e molecular dos mecanismos de resistência aos beta-lactâmicos em linhagens clínicas de Klebsiella pneumoniae isoladas do Amazonas
title_fullStr Caracterização fenotípica e molecular dos mecanismos de resistência aos beta-lactâmicos em linhagens clínicas de Klebsiella pneumoniae isoladas do Amazonas
title_full_unstemmed Caracterização fenotípica e molecular dos mecanismos de resistência aos beta-lactâmicos em linhagens clínicas de Klebsiella pneumoniae isoladas do Amazonas
title_sort Caracterização fenotípica e molecular dos mecanismos de resistência aos beta-lactâmicos em linhagens clínicas de Klebsiella pneumoniae isoladas do Amazonas
author Souza, Rosineide Cardoso de
author_facet Souza, Rosineide Cardoso de
author_role author
dc.contributor.authorlattes.por.fl_str_mv http://lattes.cnpq.br/5739753892325187
dc.contributor.author.fl_str_mv Souza, Rosineide Cardoso de
dc.contributor.advisor1.fl_str_mv Camargo, Ilana Lopes Baratella da Cunha
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/4104096171600845
dc.contributor.authorID.fl_str_mv ff125bc7-7846-4cdf-8c1b-c73b9a8413e9
contributor_str_mv Camargo, Ilana Lopes Baratella da Cunha
dc.subject.eng.fl_str_mv Klebsiella pneumoniae
blaKPC-2
NTEKPC
IncX5
Carbapenem
topic Klebsiella pneumoniae
blaKPC-2
NTEKPC
IncX5
Carbapenem
CIENCIAS BIOLOGICAS::BIOQUIMICA
CIENCIAS BIOLOGICAS::GENETICA
CIENCIAS BIOLOGICAS::MICROBIOLOGIA
dc.subject.cnpq.fl_str_mv CIENCIAS BIOLOGICAS::BIOQUIMICA
CIENCIAS BIOLOGICAS::GENETICA
CIENCIAS BIOLOGICAS::MICROBIOLOGIA
description Klebsiella pneumoniae resistant to beta-lactams are present in hospitals worldwide and reduce treatment alternatives. In this study, 40 K. pneumoniae isolates were characterized. All of them were resistant to beta-lactam antibiotics and classified as multidrug resistant. Among these, eight isolates were resistant to carbapenems and six of which had the gene blaKPC-2, encoding the enzyme Klebsiella pneumoniae carbapenemase (KPC). The blaTEM and blaCTX-M genes were found in 80% of the samples. The 40 isolates were grouped into 12 pulses (A to L) according to the genetic similarity determined by the DNA macro-restriction followed by pulsed-field gel electrophoresis. A total of 20 isolates were classified as pulsotype A, which was subdivided into 13 subtypes (A1 to A13), with subtype A1 being the most prevalent. Representatives of pulsotype A belong to the ST11, clonal complex CC258. In this study, we identified four new STs: ST2540, ST2308, ST2258, and ST2307. AMKP5 and AMKP2, belonging to subtypes A7 and A8, respectively, are resistant to carbapenems but did not present the blaKPC gene. Sequencing of the AMKP5 genome indicated mutations in the C-terminal region of the OmpK36 porin which may alter the entry of carbapenems into the cell. Genome sequencing of the AMKP10 isolate identified the plasmid pAMKP10, with 48.454 bp belonging to the IncX5 incompatibility group. In this plasmid, the blaKPC-2 gene was found in a non-Tn4401 genetic element (NTEKPC) containing tnpA-ISEc63-like / tnpR-Tn3 / tnpA-ISKpn27 / blaKPC-2 / ΔISKpn6, based on Tn1722. All isolates with the blaKPC-2 gene had the same plasmid. Conjugation of this plasmid to Escherichia coli J53 occurred from ST11 isolates with low conjugation frequencies (8.23 x 10-12 to 1.31 x 10-7) resulting in resistance to carbapenems. Finally, the outbreak of carbapenem-resistant K. pneumoniae resistant of this Amazonian hospital involved the transfer of the NTEKPC-containing pAMKP10 between two lineages (ST11 and ST2302) but was largely due to the clonal dissemination of the ST11 endemic lineage.
publishDate 2018
dc.date.issued.fl_str_mv 2018-10-25
dc.date.accessioned.fl_str_mv 2019-09-13T19:50:32Z
dc.date.available.fl_str_mv 2019-09-13T19:50:32Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.citation.fl_str_mv SOUZA, Rosineide Cardoso de. Caracterização fenotípica e molecular dos mecanismos de resistência aos beta-lactâmicos em linhagens clínicas de Klebsiella pneumoniae isoladas do Amazonas. 2018. Tese (Doutorado em Genética Evolutiva e Biologia Molecular) – Universidade Federal de São Carlos, São Carlos, 2018. Disponível em: https://repositorio.ufscar.br/handle/ufscar/11839.
dc.identifier.uri.fl_str_mv https://repositorio.ufscar.br/handle/ufscar/11839
identifier_str_mv SOUZA, Rosineide Cardoso de. Caracterização fenotípica e molecular dos mecanismos de resistência aos beta-lactâmicos em linhagens clínicas de Klebsiella pneumoniae isoladas do Amazonas. 2018. Tese (Doutorado em Genética Evolutiva e Biologia Molecular) – Universidade Federal de São Carlos, São Carlos, 2018. Disponível em: https://repositorio.ufscar.br/handle/ufscar/11839.
url https://repositorio.ufscar.br/handle/ufscar/11839
dc.language.iso.fl_str_mv por
language por
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dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Universidade Federal de São Carlos
Câmpus São Carlos
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Genética Evolutiva e Biologia Molecular - PPGGEv
dc.publisher.initials.fl_str_mv UFSCar
publisher.none.fl_str_mv Universidade Federal de São Carlos
Câmpus São Carlos
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFSCAR
instname:Universidade Federal de São Carlos (UFSCAR)
instacron:UFSCAR
instname_str Universidade Federal de São Carlos (UFSCAR)
instacron_str UFSCAR
institution UFSCAR
reponame_str Repositório Institucional da UFSCAR
collection Repositório Institucional da UFSCAR
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