Literature DB >> 33713209

Cross-Resistance and the Mechanisms of Cephalosporin-Resistant Bacteria in Urinary Tract Infections Isolated in Indonesia.

Aya Ishii1, Katsumi Shigemura2,3,4, Koichi Kitagawa1,5, Mizuki Harada6, Yuki Kan7, Fuka Hayashi7, Kayo Osawa8, K Kuntaman9, Toshiro Shirakawa1,5, Masato Fujisawa10.   

Abstract

Urinary tract infection (UTI) by antibiotic-resistant strains has become increasingly problematic, with trends that differ from country to country. This study examined cross-resistance and the mechanisms of cephalosporin resistance in UTI-causative bacteria isolated in Indonesia. Antibiotic susceptibility tests based on Clinical Laboratory Standards Institute (CLSI) standards were done for UTI-causative strains (n = 50) isolated from patients in Indonesia in 2015-2016 and showed resistance against the third-generation cephalosporin. Mechanistic studies were carried out to confirm the presence of extended-spectrum β-lactamase (ESBL) genes, carbapenemase-related genes, the fosA3 gene related to fosfomycin resistance, and mutations of quinolone-resistance-related genes. Isolated UTI-causative bacteria included Escherichia coli (64.0%), Pseudomonas aeruginosa (16.0%), Klebsiella pneumoniae (10.0%), and others (10.0%). These strains showed 96.0% susceptibility to amikacin, 76.0% to fosfomycin, 90.0% to imipenem, 28.0% to levofloxacin, 92.0% to meropenem, and 74.0% to tazobactam/piperacillin. ESBL was produced by 68.0% of these strains. Mechanistic studies found no strains with carbapenemase genes but 6.0% of strains had the fosA3 gene. Seventy-two % of the strains had mutations in the gyrA gene and 74.0% in the parC gene. Most E. coli strains (87.5%) had Ser-83 → Leu and Asp-87 → Asn in gyrA and 93.8% of E. coli had Ser-80 → Ile in parC. There were significant correlations among mutations in gyrA and parC, and fosA3 gene detection (P < 0.05), respectively. To our knowledge, this is the first mechanistic study of antibiotic-cross-resistant UTI-causative bacteria in Indonesia. Further studies with a longer period of observation are necessary, especially for changes in carbapenem resistance without carbapenemase-related genes.

Entities:  

Year:  2021        PMID: 33713209     DOI: 10.1007/s00284-021-02415-x

Source DB:  PubMed          Journal:  Curr Microbiol        ISSN: 0343-8651            Impact factor:   2.188


  2 in total

1.  Mechanism for carbapenem resistance of clinical Enterobacteriaceae isolates.

Authors:  Yafei Ye; Lijuan Xu; Yanping Han; Zhe Chen; Cailin Liu; Liang Ming
Journal:  Exp Ther Med       Date:  2017-11-10       Impact factor: 2.447

2.  Association between mutations in gyrA and parC genes of Acinetobacter baumannii clinical isolates and ciprofloxacin resistance.

Authors:  Abdollah Ardebili; Abdolaziz Rastegar Lari; Maryam Beheshti; Elnaz Rastegar Lari
Journal:  Iran J Basic Med Sci       Date:  2015-06       Impact factor: 2.699

  2 in total

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