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Antimicrobial Susceptibility of Western Hemisphere Isolates of Burkholderia pseudomallei: Phenotypic and Genomic Analyses.
- Source :
-
Microbial Drug Resistance: Mechanism, Epidemiology, & Disease . Sep2021, Vol. 27 Issue 9, p1176-1185. 10p. - Publication Year :
- 2021
-
Abstract
- Current antimicrobial treatment recommendations for melioidosis, the disease caused by Burkholderia pseudomallei, are largely based on studies of strains isolated from the Eastern Hemisphere (EH), where most human cases are identified and reported. In this study, we evaluated the antimicrobial susceptibility of 26 strains in the CDC (Centers for Diseases Control and Prevention) collection from the Western Hemisphere (WH) isolated from 1960 to 2015. Minimal inhibitory concentration (MIC) values were measured by standard broth microdilution for 16 antimicrobials following Clinical and Laboratory Standards Institute (CLSI) guidelines. Twenty-four of the 26 WH strains were susceptible to the six antimicrobials with CLSI-defined MIC susceptibility interpretive criteria for B. pseudomallei: amoxicillin/clavulanate, ceftazidime, imipenem, doxycycline, tetracycline, and trimethoprim/sulfamethoxazole. One WH strain demonstrated intermediate amoxicillin/clavulanate resistance and another strain had intermediate resistance to tetracycline. For all antimicrobials tested, the susceptibility profiles of WH isolates were comparable with previously reported MIC results of EH strains. The overall similarities suggest that the same antimicrobials are useful for melioidosis treatment in both the WH and EH. Using in silico analyses of WH genomes, we identified a novel amino acid substitution P258S in the beta-lactamase PenA, which may contribute to decreased susceptibility to amoxicillin/clavulanate in B. pseudomallei. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 10766294
- Volume :
- 27
- Issue :
- 9
- Database :
- Academic Search Index
- Journal :
- Microbial Drug Resistance: Mechanism, Epidemiology, & Disease
- Publication Type :
- Academic Journal
- Accession number :
- 152444606
- Full Text :
- https://doi.org/10.1089/mdr.2020.0362