Bacterial Genomics and Evolution Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, India.
Department of Medical Microbiology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Genomics. 2020 Nov;112(6):4171-4178. doi: 10.1016/j.ygeno.2020.06.049. Epub 2020 Jul 10.
We report first complete genomic investigation of extensive drug resistance (XDR) in a nosocomial Stenotrophomonas maltophilia complex strain that is resistant to mainstream drugs (trimethoprim/sulfamethoxazole and levofloxacin). Comprehensive genomic investigation revealed its exclusive fourteen dynamic regions and highly enriched resistome comprising of two sulfonamide resistance genes on two diverse super-integrons of chromosomal origin. In addition, both these integrons harbour array of antibiotic resistance and commonly used disinfectant's resistance genes linked to ISCR elements. Isolation of a novel XDR strain from Indian tertiary care unit belonging to novel ST with diverse array of resistance genes on ISCR linked super-integrons indicates extent and nature of selection pressure in hospitals. Since, repetitive elements have major role in their spread and due to limitations of draft genomes, there is an urgent need to employ complete genome-based investigation for tracking the emergence of XDR at global level and designing strategies of antimicrobial stewardship and disinfection. IMPORTANCE: Hospital settings in India have one of the highest usages of antimicrobials and a heavy patient load. We hereby report a novel clinical isolate of S. maltophilia complex with two super-integrons that harbour array of antimicrobial resistance genes along with biocide and heavy metal resistance genes. Further, the presence of ISCR type of transposable elements on both the integrons indicates their propensity to transfer resistome while their chromosomal origin suggests possibilities for further genomic/phenotypic complexities according to selection pressure. Such complex mobile cassettes in a novel strain is a potential threat to global health care. Hence, to understand the evolution of opportunistic nosocomial pathogen, there is an urgent need to employ cost-effective long read technologies to keep vigilance on novel and XDR pathogens in populous countries. There is also need for surveillance of the usage of disinfectants and other antimicrobials for environmental hygiene and linked/rapid co-evolution of XDR in nosocomial pathogens. Repositories: Complete genome sequence of Stenotrophomonas maltophilia SM866: CP031058.
我们首次报道了一株医院获得性嗜麦芽窄食单胞菌复合菌株的广泛耐药性(XDR)的完整基因组调查结果,该菌株对主流药物(甲氧苄啶/磺胺甲恶唑和左氧氟沙星)具有耐药性。全面的基因组调查揭示了其独特的 14 个动态区域和高度丰富的耐药组,其中包括两个磺胺类耐药基因,位于两个不同的染色体起源的超级整合子上。此外,这两个整合子都含有抗生素耐药性和常用消毒剂耐药性基因的阵列,这些基因与 ISCR 元件相关。从印度三级护理病房分离出一株新型 XDR 菌株,该菌株属于新型 ST,具有不同的 ISCR 相关超级整合子上的耐药基因阵列,表明医院中存在的选择压力的程度和性质。由于重复元件在其传播中起着重要作用,并且由于草图基因组的限制,因此迫切需要采用基于全基因组的调查来跟踪全球范围内 XDR 的出现,并制定抗菌药物管理和消毒策略。
印度的医院环境是抗生素使用量最高和患者负担最重的环境之一。我们在此报告了一株新型嗜麦芽窄食单胞菌复合菌株的临床分离株,该菌株具有两个超级整合子,其中包含一系列抗生素耐药基因以及杀生物剂和重金属耐药基因。此外,两个整合子上都存在 ISCR 型转座元件,表明它们有转移耐药组的倾向,而它们的染色体起源表明根据选择压力可能会进一步产生基因组/表型复杂性。新型菌株中如此复杂的可移动盒是对全球卫生保健的潜在威胁。因此,为了了解机会性病原体的进化,迫切需要采用具有成本效益的长读技术来密切关注人口众多国家的新型和 XDR 病原体。还需要对消毒剂和其他抗菌药物的使用进行监测,以进行环境卫生,并对医院病原体的 XDR 进行快速共同进化。
嗜麦芽窄食单胞菌 SM866 的完整基因组序列:CP031058。