In recent years, nosocomial infections due to multidrug resistant strains have been increasing, associated with growing trend of resistance to beta-lactams and fluoroquinolones (FQs) worldwide. In this study, prevalence of beta-lactamase genes and resistance mechanisms to FQ were analyzed in 191 clinical isolates derived from respiratory tract infections in a teaching hospital in Yangon, Myanmar. The major extended-spectrum beta-lactamase gene was , which was detected in 33% of isolates, with CTX-M-15 being dominant. Fourteen isolates (7.3%) harbored carbapenemase genes that were genotyped as , , or . The most common plasmid-mediated quinolone resistance (PMQR) gene was (51.8%), followed by (41.9%), (23%), and (15.2%). In quinolone-resistance determining region of GyrA, eight different types of mutation were identified for FQ-resistant isolates, with double mutations at two positions (S83F, D87A) being most common (54.6%). Isolates with double mutations (three patterns) showed higher minimal inhibitory concentration to levofloxacin (LVX) (≥64 μg/mL) than those with a single mutation. PMQR gene profiles, including and any other gene(s), were generally related to higher resistance level to LVX. isolates with different profiles of beta-lactamase genes and FQ-resistance determinants were mostly classified into ST15 or its single-locus variant (SLV). The most common NDM gene, , was detected in ST975 (ST15-SLV) isolates and an ST4000 isolate. The present study revealed the wide spread of FQ-resistant clinical isolates acquiring various FQ-resistance determinants and beta-lactamases that were presumably derived from a single clonal lineage in a hospital in Myanmar.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1089/mdr.2019.0490 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!