4.5 Article

Phenotypic and genotypic identification of carbapenem resistance in Bacteroides fragilis clinical strains

Journal

MEDICAL MICROBIOLOGY AND IMMUNOLOGY
Volume 212, Issue 3, Pages 231-240

Publisher

SPRINGER
DOI: 10.1007/s00430-023-00765-w

Keywords

Bacteroides fragilis; Carba NP; Carbapenemase; CfiA; Meropenem

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The aim of this study was to determine the prevalence of cfiA-positive isolates in B. fragilis infections and investigate the carbapenemase activity in B. fragilis strains through the Carba NP test. The study found that 5.2% of B. fragilis isolates were phenotypically resistant to meropenem and 6.1% of B. fragilis isolates carried the cfiA gene. The meropenem minimum inhibitory concentrations were significantly higher in cfiA-positive strains.
Bacteroides fragilis is an important etiological agent of serious infections in humans. Rapid methods, readily adaptable to use in medical laboratories, are needed to detect antibiotic resistance and decrease the likelihood of therapy failure. The aim of this study was to determine the prevalence of B. fragilis cfiA-positive isolates. The second purpose was to investigate the carbapenemase activity in B. fragilis strains by Carba NP test. In the study, 5.2% of B. fragilis isolates are phenotypically resistant to meropenem. The cfiA gene was identified in 6.1% of B. fragilis isolates. The MICs of meropenem were significantly higher in cfiA-positive strains. The presence of the cfiA gene along with the IS1186 was detected in one B. fragilis strain which was resistant to meropenem (MIC 1.5 mg/L). The Carba NP test results were positive for all the cfiA-positive strains, including those susceptible to carbapenems based on their MIC values. A review of the literature revealed that the rate of B. fragilis with the cfiA gene varies from 7.6 to 38.9% worldwide. Presented results are in line with the other European studies. Phenotypic testing with the Carba NP test, it seems to be a viable alternative for the cfiA gene detection in B. fragilis isolates. The positive result obtained is of greater clinical importance than the detection of the gene cfiA.

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