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Genomic islands and molecular mechanisms relating to drug-resistance in Clostridioides (Clostridium) difficile PCR ribotype 176
M. Krutova, V. Kovarovic, M. Brajerova, F. Demay, J. Zikova, S. Prasad, A. Soltesova, E. Novakova, H. Pituch, E. Kuijper, WK. Smits, GB. Novotna
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 2012
Free Medical Journals
od 2012
PubMed Central
od 2012
Europe PubMed Central
od 2012
ProQuest Central
od 2022-01-01
Open Access Digital Library
od 2012-01-01
Open Access Digital Library
od 2012-01-01
Taylor & Francis Open Access
od 2014-01-01
Health & Medicine (ProQuest)
od 2022-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2012
- MeSH
- antibakteriální látky * farmakologie MeSH
- bakteriální léková rezistence * MeSH
- bakteriální proteiny genetika MeSH
- Clostridioides difficile * genetika účinky léků izolace a purifikace klasifikace MeSH
- genomové ostrovy * MeSH
- klostridiové infekce * mikrobiologie epidemiologie MeSH
- lidé MeSH
- methyltransferasy genetika MeSH
- mikrobiální testy citlivosti MeSH
- mnohočetná bakteriální léková rezistence * genetika MeSH
- multilokusová sekvenční typizace MeSH
- ribotypizace MeSH
- sekvenování celého genomu MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Geografické názvy
- Česká republika MeSH
- Polsko MeSH
OBJECTIVES: To analyse characteristics of Clostridioides difficile PCR ribotype 176 clinical isolates from Poland, the Czech Republic and Slovakia with regard to the differences in its epidemiology. METHODS: Antimicrobial susceptibility testing and whole genome sequencing were performed on a selected group of 22 clonally related isolates as determined by multilocus variable-number tandem repeat analysis (n = 509). Heterologous expression and functional analysis of the newly identified methyltransferase were performed. RESULTS: Core genome multilocus sequence typing found 10-37 allele differences. All isolates were resistant to fluoroquinolones (gyrA_p. T82I), aminoglycosides with aac(6')-Ie-aph(2'')-Ia in six isolates. Erythromycin resistance was detected in 21/22 isolates and 15 were also resistant to clindamycin with ermB gene. Fourteen isolates were resistant to rifampicin with rpoB_p. R505K or p. R505K/H502N, and five to imipenem with pbp1_p. P491L and pbp3_p. N537K. PnimBG together with nimB_p. L155I were detected in all isolates but only five were resistant to metronidazole on chocolate agar. The cfrE, vanZ1 and cat-like genes were not associated with linezolid, teicoplanin and chloramphenicol resistance, respectively. The genome comparison identified six transposons carrying antimicrobial resistance genes. The ermB gene was carried by new Tn7808, Tn6189 and Tn6218-like. The aac(6')-Ie-aph(2'')-Ia were carried by Tn6218-like and new Tn7806 together with cfrE gene. New Tn7807 carried a cat-like gene. Tn6110 and new Tn7806 contained an RlmN-type 23S rRNA methyltransferase, designated MrmA, associated with high-level macrolide resistance in isolates without ermB gene. CONCLUSIONS: Multidrug-resistant C. difficile PCR ribotype 176 isolates carry already described and unique transposons. A novel mechanism for erythromycin resistance in C. difficile was identified.
Department of Clinical Microbiology Unilabs Slovakia Inc Roznava Slovakia
Department of Medical Microbiology Medical University of Warsaw Warsaw Poland
European Society of Clinical Microbiology and Infectious Diseases Basel Switzerland
Institute of Microbiology The Czech Academy of Sciences BIOCEV Vestec Czech Republic
Citace poskytuje Crossref.org
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