The First Report of Phenotypic and Molecular Characterization of Extended-Spectrum Beta-Lactamase-Producing Uropathogens in Sikkim and Darjeeling Hills of India

Extended-spectrum β-lactamase (ESBL)-producing bacteria are a global health threat both in hospital and in community settings. The emergence of these organisms poses major difficulty in treating infections. This study was carried out to assess major ESBL-producing uropathogens in female patients of...

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Veröffentlicht in:Microbial drug resistance (Larchmont, N.Y.) N.Y.), 2018-11, Vol.24 (9), p.1284-1288
Hauptverfasser: Gajamer, Varsha Rani, Bhattacharjee, Amitabha, Paul, Deepjyoti, Kapil, Jyotsna, Sarkar, Arunabha, Singh, Ashish Kr, Pradhan, Nilu, Tiwari, Hare Krishna
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Sprache:eng
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Zusammenfassung:Extended-spectrum β-lactamase (ESBL)-producing bacteria are a global health threat both in hospital and in community settings. The emergence of these organisms poses major difficulty in treating infections. This study was carried out to assess major ESBL-producing uropathogens in female patients of Sikkim and Darjeeling by phenotypic and genotypic methods. Out of 1,516 urine samples, 454 uropathogens were isolated with a prevalence rate of 29.94%. Among them, Escherichia coli (74.3%) was the predominant type followed by Klebsiella pneumoniae (20.1%), Pseudomonas aeruginosa (2.4%), and Proteus mirabilis (1.98%). Four different ESBL genes were detected in 63 isolates, which included CTX-M ( n  = 32), CTX-M+OXA-2 ( n  = 15), CTX-M-15+OXA-2+TEM ( n  = 6), OXA-2 ( n  = 5), TEM+CTX-M-15 ( n  = 2), TEM+OXA-2+SHV-76 ( n  = 2), and TEM ( n  = 1). All ESBL genes ( bla genes) were found on a plasmid, which was mostly of HI1, I1, FIA+FIB, FIA, and Y types and was horizontally transferable. Among all ESBL genes, bla CTX-M-I5 group was the most prevalent. The study of urinary tract infection (UTI) caused by ESBL-producing bacteria needs to be studied in other high-altitude parts of India to understand the actual burden of UTI in the female.
ISSN:1076-6294
1931-8448
DOI:10.1089/mdr.2017.0159