A novel Bacteroides metallo-beta-lactamase (MBL) and its gene (crxA) in Bacteroides xylanisolvens revealed by genomic sequencing and functional analysis

Objectives We sought to characterize the carbapenem resistance mechanism of Bacteroides xylanisolvens 14880, an imipenem-resistant strain from Germany, and assess its prevalence. Methods Antimicrobial susceptibilities were determined using agar dilution or Etest methodology and specific imipenemase...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Sóki József
Lang Uwe
Schumacher Ulrike
Nagy István
Berényi Ágnes
Fehér Tamás
Burián Katalin
Nagy Erzsébet
Dokumentumtípus: Cikk
Megjelent: 2022
Sorozat:JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY 77 No. 6
Tárgyszavak:
doi:10.1093/jac/dkac088

mtmt:32763246
Online Access:http://publicatio.bibl.u-szeged.hu/23961
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100 1 |a Sóki József 
245 1 2 |a A novel Bacteroides metallo-beta-lactamase (MBL) and its gene (crxA) in Bacteroides xylanisolvens revealed by genomic sequencing and functional analysis  |h [elektronikus dokumentum] /  |c  Sóki József 
260 |c 2022 
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490 0 |a JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY  |v 77 No. 6 
520 3 |a Objectives We sought to characterize the carbapenem resistance mechanism of Bacteroides xylanisolvens 14880, an imipenem-resistant strain from Germany, and assess its prevalence. Methods Antimicrobial susceptibilities were determined using agar dilution or Etest methodology and specific imipenemase activity was detected. The genomic sequence of B. xylanisolvens 14880 was determined and analysed for antibiotic resistance genes and genomic islands. We also used gene transfer to a carbapenem susceptible host, along with 5 '-RACE, conventional PCR with capillary sequencing and RT-PCR-based screening. Results B. xylanisolvens 14880 displayed resistance to carbapenems and produced high specific imipenemase activity. Its genomic sequence was 6.1 Mbp and a class B1 beta-lactamase gene (termed crxA) was detected in it. crxA was carried on a putative genomic island with insertion sequence (IS) elements and a putative GNAT (Gcn5-like acetyltransferase) toxin gene. Promoter localization by 5 '-RACE and gene targeting to an imipenem-susceptible Bacteroides host indicated that it is activated by an IS1380-like IS element and it can confer carbapenem resistance. The PCR screening of Bacteroides strains showed that crxA was specific to B. xylanisolvens with a carriage rate of 16.7%. Conclusions B. xylanisolvens strains can harbour a carbapenem resistance gene, which has many similarities to the 'cfiA system': metallo-beta-lactamase (MBL), IS element activation, carriage of a GNAT toxin gene, specific for a unique Bacteroides species with a significant prevalence. 
650 4 |a Biológiai tudományok 
650 4 |a Általános orvostudomány 
700 0 1 |a Lang Uwe  |e aut 
700 0 1 |a Schumacher Ulrike  |e aut 
700 0 1 |a Nagy István  |e aut 
700 0 1 |a Berényi Ágnes  |e aut 
700 0 1 |a Fehér Tamás  |e aut 
700 0 1 |a Burián Katalin  |e aut 
700 0 1 |a Nagy Erzsébet  |e aut 
856 4 0 |u http://publicatio.bibl.u-szeged.hu/23961/3/32763246.pdf  |z Dokumentum-elérés  
856 4 0 |u http://publicatio.bibl.u-szeged.hu/23961/1/dkac088.pdf  |z Dokumentum-elérés