Aung Meiji Soe, Win Nyein Chan, San Nilar, Hlaing Myat Su, Myint Yi Yi, Thu Pyae Phyo, Aung Myint Thazin, Yaa Kyaw Thu, Maw Win Win, Urushibara Noriko, Kobayashi Nobumichi
Department of Hygiene, Sapporo Medical University School of Medicine, Sapporo, Japan.
Department of Medicine, University of Medicine 2, Yangon, Myanmar.
Microb Drug Resist. 2021 Jan;27(1):36-43. doi: 10.1089/mdr.2019.0490. Epub 2020 Jun 9.
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.
近年来,耐多药菌株引起的医院感染不断增加,这与全球范围内对β-内酰胺类和氟喹诺酮类(FQs)耐药性的增长趋势相关。在本研究中,对来自缅甸仰光一家教学医院呼吸道感染的191株临床分离株进行了β-内酰胺酶基因流行情况及对FQ耐药机制的分析。主要的超广谱β-内酰胺酶基因是 ,在33%的分离株中检测到,其中CTX-M-15占主导。14株分离株(7.3%)携带碳青霉烯酶基因,基因分型为 、 或 。最常见的质粒介导喹诺酮耐药(PMQR)基因是 (51.8%),其次是 (41.9%)、 (23%)和 (15.2%)。在GyrA的喹诺酮耐药决定区,对FQ耐药分离株鉴定出8种不同类型的突变,两个位置的双突变(S83F,D87A)最为常见(54.6%)。具有双突变(三种模式)的分离株对左氧氟沙星(LVX)的最低抑菌浓度(≥64μg/mL)高于单突变分离株。包括 和任何其他基因的PMQR基因谱通常与对LVX的更高耐药水平相关。具有不同β-内酰胺酶基因和FQ耐药决定因素谱的分离株大多归类为ST15或其单基因座变体(SLV)。最常见的NDM基因 ,在ST975(ST15-SLV)分离株和一株ST4000分离株中检测到。本研究揭示了在缅甸一家医院中,获得各种FQ耐药决定因素和β-内酰胺酶的FQ耐药临床分离株广泛传播,这些分离株可能源自单一克隆谱系。