Ultrastructural Changes in Clinical and Microbiota Isolates of Klebsiella pneumoniae Carriers of Genes blaSHV, blaTEM, blaCTX-M, or blaKPC When Subject to β-Lactam Antibiotics

The aim of this study was to characterize the ultrastructural effects caused by β-lactam antibiotics in Klebsiella pneumoniae isolates. Three K. pneumoniae clinical isolates were selected for the study with resistance profiles for third-generation cephalosporins, aztreonam, and/or imipenem and with...

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Main Authors: Dyana Leal Veras, Ana Catarina de Souza Lopes, Grasielle Vaz da Silva, Gabriel Gazzoni Araújo Gonçalves, Catarina Fernandes de Freitas, Fernanda Cristina Gomes de Lima, Maria Amélia Vieira Maciel, Ana Paula Sampaio Feitosa, Luiz Carlos Alves, Fábio André Brayner
Format: Article
Language:English
Published: Hindawi Limited 2015-01-01
Series:The Scientific World Journal
Online Access:http://dx.doi.org/10.1155/2015/572128
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spelling doaj-d43e13aa077a4f11a55bdb54807599882020-11-24T21:37:52ZengHindawi LimitedThe Scientific World Journal2356-61401537-744X2015-01-01201510.1155/2015/572128572128Ultrastructural Changes in Clinical and Microbiota Isolates of Klebsiella pneumoniae Carriers of Genes blaSHV, blaTEM, blaCTX-M, or blaKPC When Subject to β-Lactam AntibioticsDyana Leal Veras0Ana Catarina de Souza Lopes1Grasielle Vaz da Silva2Gabriel Gazzoni Araújo Gonçalves3Catarina Fernandes de Freitas4Fernanda Cristina Gomes de Lima5Maria Amélia Vieira Maciel6Ana Paula Sampaio Feitosa7Luiz Carlos Alves8Fábio André Brayner9Setor de Microscopia Eletrônica, Laboratório de Imunopatologia Keizo Asami (LIKA), Universidade Federal de Pernambuco (UFPE), Avenida Professor Moraes Rego, s/n, Cidade Universitária, 50670-901 Recife, PE, BrazilDepartamento de Medicina Tropical, Universidade Federal de Pernambuco (UFPE), Avenida Professor Moraes Rego, s/n, Cidade Universitária, 50670-901 Recife, PE, BrazilSetor de Microscopia Eletrônica, Laboratório de Imunopatologia Keizo Asami (LIKA), Universidade Federal de Pernambuco (UFPE), Avenida Professor Moraes Rego, s/n, Cidade Universitária, 50670-901 Recife, PE, BrazilSetor de Microscopia Eletrônica, Laboratório de Imunopatologia Keizo Asami (LIKA), Universidade Federal de Pernambuco (UFPE), Avenida Professor Moraes Rego, s/n, Cidade Universitária, 50670-901 Recife, PE, BrazilDepartamento de Parasitologia, Centro de Pesquisas Aggeu Magalhães (CPqAM)-Fiocruz, Avenida Professor Moraes Rego, s/n, Caixa Postal 7472, Cidade Universitária, 50670-420 Recife, PE, BrazilDepartamento de Parasitologia, Centro de Pesquisas Aggeu Magalhães (CPqAM)-Fiocruz, Avenida Professor Moraes Rego, s/n, Caixa Postal 7472, Cidade Universitária, 50670-420 Recife, PE, BrazilDepartamento de Medicina Tropical, Universidade Federal de Pernambuco (UFPE), Avenida Professor Moraes Rego, s/n, Cidade Universitária, 50670-901 Recife, PE, BrazilSetor de Microscopia Eletrônica, Laboratório de Imunopatologia Keizo Asami (LIKA), Universidade Federal de Pernambuco (UFPE), Avenida Professor Moraes Rego, s/n, Cidade Universitária, 50670-901 Recife, PE, BrazilSetor de Microscopia Eletrônica, Laboratório de Imunopatologia Keizo Asami (LIKA), Universidade Federal de Pernambuco (UFPE), Avenida Professor Moraes Rego, s/n, Cidade Universitária, 50670-901 Recife, PE, BrazilSetor de Microscopia Eletrônica, Laboratório de Imunopatologia Keizo Asami (LIKA), Universidade Federal de Pernambuco (UFPE), Avenida Professor Moraes Rego, s/n, Cidade Universitária, 50670-901 Recife, PE, BrazilThe aim of this study was to characterize the ultrastructural effects caused by β-lactam antibiotics in Klebsiella pneumoniae isolates. Three K. pneumoniae clinical isolates were selected for the study with resistance profiles for third-generation cephalosporins, aztreonam, and/or imipenem and with different resistance genes for extended-spectrum β-lactamases (ESBL) or Klebsiella pneumoniae carbapenemase (KPC). Two K. pneumoniae isolates obtained from the microbiota, which were both resistant to amoxicillin and ampicillin, were also analyzed. In accordance with the susceptibility profile, the clinical isolates were subjected to subminimum inhibitory concentrations (sub-MICs) of cefotaxime, ceftazidime, aztreonam, and imipenem and the isolates from the microbiota to ampicillin and amoxicillin, for analysis by means of scanning and transmission electron microscopy. The K. pneumoniae isolates showed different morphological and ultrastructural changes after subjection to β-lactams tested at different concentrations, such as cell filamentation, loss of cytoplasmic material, and deformation of dividing septa. Our results demonstrate that K. pneumoniae isolates harboring different genes that encode for β-lactamases show cell alterations when subjected to different β-lactam antibiotics, thus suggesting that they possess residual activity in vitro, despite the phenotypic resistance presented in the isolates analyzed.http://dx.doi.org/10.1155/2015/572128
collection DOAJ
language English
format Article
sources DOAJ
author Dyana Leal Veras
Ana Catarina de Souza Lopes
Grasielle Vaz da Silva
Gabriel Gazzoni Araújo Gonçalves
Catarina Fernandes de Freitas
Fernanda Cristina Gomes de Lima
Maria Amélia Vieira Maciel
Ana Paula Sampaio Feitosa
Luiz Carlos Alves
Fábio André Brayner
spellingShingle Dyana Leal Veras
Ana Catarina de Souza Lopes
Grasielle Vaz da Silva
Gabriel Gazzoni Araújo Gonçalves
Catarina Fernandes de Freitas
Fernanda Cristina Gomes de Lima
Maria Amélia Vieira Maciel
Ana Paula Sampaio Feitosa
Luiz Carlos Alves
Fábio André Brayner
Ultrastructural Changes in Clinical and Microbiota Isolates of Klebsiella pneumoniae Carriers of Genes blaSHV, blaTEM, blaCTX-M, or blaKPC When Subject to β-Lactam Antibiotics
The Scientific World Journal
author_facet Dyana Leal Veras
Ana Catarina de Souza Lopes
Grasielle Vaz da Silva
Gabriel Gazzoni Araújo Gonçalves
Catarina Fernandes de Freitas
Fernanda Cristina Gomes de Lima
Maria Amélia Vieira Maciel
Ana Paula Sampaio Feitosa
Luiz Carlos Alves
Fábio André Brayner
author_sort Dyana Leal Veras
title Ultrastructural Changes in Clinical and Microbiota Isolates of Klebsiella pneumoniae Carriers of Genes blaSHV, blaTEM, blaCTX-M, or blaKPC When Subject to β-Lactam Antibiotics
title_short Ultrastructural Changes in Clinical and Microbiota Isolates of Klebsiella pneumoniae Carriers of Genes blaSHV, blaTEM, blaCTX-M, or blaKPC When Subject to β-Lactam Antibiotics
title_full Ultrastructural Changes in Clinical and Microbiota Isolates of Klebsiella pneumoniae Carriers of Genes blaSHV, blaTEM, blaCTX-M, or blaKPC When Subject to β-Lactam Antibiotics
title_fullStr Ultrastructural Changes in Clinical and Microbiota Isolates of Klebsiella pneumoniae Carriers of Genes blaSHV, blaTEM, blaCTX-M, or blaKPC When Subject to β-Lactam Antibiotics
title_full_unstemmed Ultrastructural Changes in Clinical and Microbiota Isolates of Klebsiella pneumoniae Carriers of Genes blaSHV, blaTEM, blaCTX-M, or blaKPC When Subject to β-Lactam Antibiotics
title_sort ultrastructural changes in clinical and microbiota isolates of klebsiella pneumoniae carriers of genes blashv, blatem, blactx-m, or blakpc when subject to β-lactam antibiotics
publisher Hindawi Limited
series The Scientific World Journal
issn 2356-6140
1537-744X
publishDate 2015-01-01
description The aim of this study was to characterize the ultrastructural effects caused by β-lactam antibiotics in Klebsiella pneumoniae isolates. Three K. pneumoniae clinical isolates were selected for the study with resistance profiles for third-generation cephalosporins, aztreonam, and/or imipenem and with different resistance genes for extended-spectrum β-lactamases (ESBL) or Klebsiella pneumoniae carbapenemase (KPC). Two K. pneumoniae isolates obtained from the microbiota, which were both resistant to amoxicillin and ampicillin, were also analyzed. In accordance with the susceptibility profile, the clinical isolates were subjected to subminimum inhibitory concentrations (sub-MICs) of cefotaxime, ceftazidime, aztreonam, and imipenem and the isolates from the microbiota to ampicillin and amoxicillin, for analysis by means of scanning and transmission electron microscopy. The K. pneumoniae isolates showed different morphological and ultrastructural changes after subjection to β-lactams tested at different concentrations, such as cell filamentation, loss of cytoplasmic material, and deformation of dividing septa. Our results demonstrate that K. pneumoniae isolates harboring different genes that encode for β-lactamases show cell alterations when subjected to different β-lactam antibiotics, thus suggesting that they possess residual activity in vitro, despite the phenotypic resistance presented in the isolates analyzed.
url http://dx.doi.org/10.1155/2015/572128
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