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Infection caused by Klebsiella pneumoniae ST11 in a patient after craniectomy

Klebsiella pneumoniae infections have always been an important problem in public health, but today, the increasing resistance of these bacteria to antibiotics due to β-lactamases production has renewed interest in K. pneumoniae infections. The aim of the study was to present a case of a neurosurgica...

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Autores principales: Ojdana, Dominika, Kochanowicz, Jan, Sacha, Paweł, Sieńko, Anna, Wieczorek, Piotr, Majewski, Piotr, Hauschild, Tomasz, Mariak, Zenon, Tryniszewska, Elżbieta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971140/
https://www.ncbi.nlm.nih.gov/pubmed/31119589
http://dx.doi.org/10.1007/s12223-019-00718-y
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author Ojdana, Dominika
Kochanowicz, Jan
Sacha, Paweł
Sieńko, Anna
Wieczorek, Piotr
Majewski, Piotr
Hauschild, Tomasz
Mariak, Zenon
Tryniszewska, Elżbieta
author_facet Ojdana, Dominika
Kochanowicz, Jan
Sacha, Paweł
Sieńko, Anna
Wieczorek, Piotr
Majewski, Piotr
Hauschild, Tomasz
Mariak, Zenon
Tryniszewska, Elżbieta
author_sort Ojdana, Dominika
collection PubMed
description Klebsiella pneumoniae infections have always been an important problem in public health, but today, the increasing resistance of these bacteria to antibiotics due to β-lactamases production has renewed interest in K. pneumoniae infections. The aim of the study was to present a case of a neurosurgical patient with multidrug-resistant K. pneumoniae ST11 infection after craniectomy. Four K. pneumoniae isolates from various clinical materials of the patient undergone identification and susceptibility testing with the Vitek2 system. Tests for β-lactamases production were performed according to EUCAST guidelines. Strains were analyzed for bla genes responsible for β-lactamase production (bla(TEM), bla(SHV), bla(CTX-M), bla(VIM), bla(IMP), bla(NDM), bla(KPC), bla(OXA-48)) using PCR. Moreover, the genetic relatedness of these isolates was determined by pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST). All tested strain presented multidrug resistance. The highest susceptibility was observed for imipenem, meropenem, and ertapenem. The strain isolated from the nervous system was ESBL-positive with bla(SHV-11), bla(TEM-1), and bla(CTX-M-15) genes. Additionally, the strain from urine was bla(KPC-3)-positive. Molecular typing revealed that all strains belonged to the same clone and identified two PFGE profiles. The analysis of MLST allelic profile showed that tested K. pneumoniae strains belonged to ST11. Identification of ST11 K. pneumoniae as etiological factor of infection unfavorably impacts on prognosis among neurosurgical patient after craniectomy.
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spelling pubmed-69711402020-01-31 Infection caused by Klebsiella pneumoniae ST11 in a patient after craniectomy Ojdana, Dominika Kochanowicz, Jan Sacha, Paweł Sieńko, Anna Wieczorek, Piotr Majewski, Piotr Hauschild, Tomasz Mariak, Zenon Tryniszewska, Elżbieta Folia Microbiol (Praha) Short Communication Klebsiella pneumoniae infections have always been an important problem in public health, but today, the increasing resistance of these bacteria to antibiotics due to β-lactamases production has renewed interest in K. pneumoniae infections. The aim of the study was to present a case of a neurosurgical patient with multidrug-resistant K. pneumoniae ST11 infection after craniectomy. Four K. pneumoniae isolates from various clinical materials of the patient undergone identification and susceptibility testing with the Vitek2 system. Tests for β-lactamases production were performed according to EUCAST guidelines. Strains were analyzed for bla genes responsible for β-lactamase production (bla(TEM), bla(SHV), bla(CTX-M), bla(VIM), bla(IMP), bla(NDM), bla(KPC), bla(OXA-48)) using PCR. Moreover, the genetic relatedness of these isolates was determined by pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST). All tested strain presented multidrug resistance. The highest susceptibility was observed for imipenem, meropenem, and ertapenem. The strain isolated from the nervous system was ESBL-positive with bla(SHV-11), bla(TEM-1), and bla(CTX-M-15) genes. Additionally, the strain from urine was bla(KPC-3)-positive. Molecular typing revealed that all strains belonged to the same clone and identified two PFGE profiles. The analysis of MLST allelic profile showed that tested K. pneumoniae strains belonged to ST11. Identification of ST11 K. pneumoniae as etiological factor of infection unfavorably impacts on prognosis among neurosurgical patient after craniectomy. Springer Netherlands 2019-05-22 2020 /pmc/articles/PMC6971140/ /pubmed/31119589 http://dx.doi.org/10.1007/s12223-019-00718-y Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Short Communication
Ojdana, Dominika
Kochanowicz, Jan
Sacha, Paweł
Sieńko, Anna
Wieczorek, Piotr
Majewski, Piotr
Hauschild, Tomasz
Mariak, Zenon
Tryniszewska, Elżbieta
Infection caused by Klebsiella pneumoniae ST11 in a patient after craniectomy
title Infection caused by Klebsiella pneumoniae ST11 in a patient after craniectomy
title_full Infection caused by Klebsiella pneumoniae ST11 in a patient after craniectomy
title_fullStr Infection caused by Klebsiella pneumoniae ST11 in a patient after craniectomy
title_full_unstemmed Infection caused by Klebsiella pneumoniae ST11 in a patient after craniectomy
title_short Infection caused by Klebsiella pneumoniae ST11 in a patient after craniectomy
title_sort infection caused by klebsiella pneumoniae st11 in a patient after craniectomy
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971140/
https://www.ncbi.nlm.nih.gov/pubmed/31119589
http://dx.doi.org/10.1007/s12223-019-00718-y
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