-
Je něco špatně v tomto záznamu ?
Infection caused by Klebsiella pneumoniae ST11 in a patient after craniectomy
D. Ojdana, J. Kochanowicz, P. Sacha, A. Sieńko, P. Wieczorek, P. Majewski, T. Hauschild, Z. Mariak, E. Tryniszewska,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu kazuistiky, časopisecké články
Grantová podpora
N/ST/ZB/15/006/2222
Uniwersytet Medyczny w Bialymstoku
- MeSH
- antibakteriální látky farmakologie terapeutické užití MeSH
- beta-laktamasy genetika MeSH
- fatální výsledek MeSH
- infekce bakteriemi rodu Klebsiella diagnostické zobrazování farmakoterapie mikrobiologie MeSH
- Klebsiella pneumoniae klasifikace účinky léků enzymologie MeSH
- kraniotomie škodlivé účinky MeSH
- lidé MeSH
- mikrobiální testy citlivosti MeSH
- mladý dospělý MeSH
- mnohočetná bakteriální léková rezistence * MeSH
- multilokusová sekvenční typizace MeSH
- počítačová rentgenová tomografie MeSH
- pulzní gelová elektroforéza MeSH
- techniky typizace bakterií MeSH
- Check Tag
- lidé MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
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 (blaTEM, blaSHV, blaCTX-M, blaVIM, blaIMP, blaNDM, blaKPC, blaOXA-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 blaSHV-11, blaTEM-1, and blaCTX-M-15 genes. Additionally, the strain from urine was blaKPC-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.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc20024238
- 003
- CZ-PrNML
- 005
- 20201208102220.0
- 007
- ta
- 008
- 201208s2020 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s12223-019-00718-y $2 doi
- 035 __
- $a (PubMed)31119589
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Ojdana, Dominika $u Department of Microbiological Diagnostics and Infectious Immunology, Medical University of Bialystok, 15a Waszyngtona Street, 15-269, Bialystok, Poland. dominika.ojdana@umb.edu.pl.
- 245 10
- $a Infection caused by Klebsiella pneumoniae ST11 in a patient after craniectomy / $c D. Ojdana, J. Kochanowicz, P. Sacha, A. Sieńko, P. Wieczorek, P. Majewski, T. Hauschild, Z. Mariak, E. Tryniszewska,
- 520 9_
- $a 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 (blaTEM, blaSHV, blaCTX-M, blaVIM, blaIMP, blaNDM, blaKPC, blaOXA-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 blaSHV-11, blaTEM-1, and blaCTX-M-15 genes. Additionally, the strain from urine was blaKPC-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.
- 650 _2
- $a antibakteriální látky $x farmakologie $x terapeutické užití $7 D000900
- 650 _2
- $a techniky typizace bakterií $7 D015373
- 650 _2
- $a kraniotomie $x škodlivé účinky $7 D003399
- 650 12
- $a mnohočetná bakteriální léková rezistence $7 D024901
- 650 _2
- $a pulzní gelová elektroforéza $7 D016521
- 650 _2
- $a fatální výsledek $7 D017809
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a infekce bakteriemi rodu Klebsiella $x diagnostické zobrazování $x farmakoterapie $x mikrobiologie $7 D007710
- 650 _2
- $a Klebsiella pneumoniae $x klasifikace $x účinky léků $x enzymologie $7 D007711
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a mikrobiální testy citlivosti $7 D008826
- 650 _2
- $a multilokusová sekvenční typizace $7 D058885
- 650 _2
- $a počítačová rentgenová tomografie $7 D014057
- 650 _2
- $a mladý dospělý $7 D055815
- 650 _2
- $a beta-laktamasy $x genetika $7 D001618
- 655 _2
- $a kazuistiky $7 D002363
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Kochanowicz, Jan $u Department of Neurosurgery, University Hospital of Bialystok, 24a M. Sklodowskiej-Cure Street, 15-276, Bialystok, Poland.
- 700 1_
- $a Sacha, Paweł $u Department of Microbiological Diagnostics and Infectious Immunology, Medical University of Bialystok, 15a Waszyngtona Street, 15-269, Bialystok, Poland.
- 700 1_
- $a Sieńko, Anna $u Department of Microbiological Diagnostics and Infectious Immunology, Medical University of Bialystok, 15a Waszyngtona Street, 15-269, Bialystok, Poland.
- 700 1_
- $a Wieczorek, Piotr $u Department of Microbiological Diagnostics and Infectious Immunology, Medical University of Bialystok, 15a Waszyngtona Street, 15-269, Bialystok, Poland.
- 700 1_
- $a Majewski, Piotr $u Department of Microbiological Diagnostics and Infectious Immunology, Medical University of Bialystok, 15a Waszyngtona Street, 15-269, Bialystok, Poland.
- 700 1_
- $a Hauschild, Tomasz $u Department of Microbiology, Institute of Biology, University of Bialystok, 1J Ciolkowskiego Street, 15-245, Bialystok, Poland.
- 700 1_
- $a Mariak, Zenon $u Department of Neurosurgery, University Hospital of Bialystok, 24a M. Sklodowskiej-Cure Street, 15-276, Bialystok, Poland.
- 700 1_
- $a Tryniszewska, Elżbieta $u Department of Microbiological Diagnostics and Infectious Immunology, Medical University of Bialystok, 15a Waszyngtona Street, 15-269, Bialystok, Poland.
- 773 0_
- $w MED00011005 $t Folia microbiologica $x 1874-9356 $g Roč. 65, č. 1 (2020), s. 205-209
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31119589 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20201208 $b ABA008
- 991 __
- $a 20201208102216 $b ABA008
- 999 __
- $a ok $b bmc $g 1593193 $s 1114919
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2020 $b 65 $c 1 $d 205-209 $e 20190522 $i 1874-9356 $m Folia microbiologica $n Folia microbiol. (Prague) $x MED00011005
- GRA __
- $a N/ST/ZB/15/006/2222 $p Uniwersytet Medyczny w Bialymstoku
- LZP __
- $a Pubmed-20201208