Menon Nitasha D, Somanath Priyanka, Jossart Jennifer, Vijayakumar Gayathri, Shetty Kavya, Baswe Manasi, Chatterjee Meghna, Hari Malavika B, Nair Samitha, Kumar V Anil, Nair Bipin G, Nizet Victor, Perry J Jefferson P, Kumar Geetha B
School of Biotechnology, Amrita Vishwa Vidyapeetham, Amritapuri, Kerala, India.
Antimicrobial Resistance, Tata Institute for Genetics and Society (TIGS), Bangalore, India.
JAC Antimicrob Resist. 2024 Jan 16;6(1):dlae001. doi: 10.1093/jacamr/dlae001. eCollection 2024 Feb.
We sought to analyse the antibiotic susceptibility profiles and molecular epidemiology of MDR clinical isolates from South India using non-MDR isolates as a reference.
We established a comprehensive clinical strain library consisting of 58 isolates collected from patients across the South Indian state of Kerala from March 2017 to July 2019. The strains were subject to antibiotic susceptibility testing, modified carbapenem inactivation method assay for carbapenemase production, PCR sequencing, comparative sequence analysis and quantitative PCR of MDR determinants associated with antibiotic efflux pump systems, fluoroquinolone resistance and carbapenem resistance. We performed modelling of MDR-specific SNPs.
Of our collection of South Indian clinical isolates, 74.1% were MDR and 55.8% were resistant to the entire panel of antibiotics tested. All MDR isolates were resistant to levofloxacin and 93% were resistant to meropenem. We identified seven distinct, MDR-specific mutations in , three of which are novel. was significantly overexpressed in strains that were resistant to the entire test antibiotic panel while and were overexpressed in MDR isolates. Mutations in fluoroquinolone determinants were significantly associated with MDR phenotype and a novel GyrA Y100C substitution was observed. Carbapenem resistance in MDR isolates was associated with loss-of-function mutations in and high prevalence of NDM () within our sample.
This study provides insight into MDR mechanisms adopted by clinical isolates, which may guide the potential development of therapeutic regimens to improve clinical outcomes.
我们试图以非多重耐药(MDR)菌株为参照,分析来自印度南部的MDR临床分离株的抗生素敏感性谱和分子流行病学特征。
我们建立了一个综合临床菌株库,其中包含2017年3月至2019年7月从印度南部喀拉拉邦各地患者身上收集的58株分离株。对这些菌株进行抗生素敏感性测试、改良碳青霉烯灭活方法检测碳青霉烯酶产生情况、PCR测序、比较序列分析以及与抗生素外排泵系统、氟喹诺酮耐药性和碳青霉烯耐药性相关的MDR决定因素的定量PCR。我们对MDR特异性单核苷酸多态性进行了建模。
在我们收集的印度南部临床分离株中,74.1%为MDR,55.8%对所测试的全部抗生素耐药。所有MDR分离株均对左氧氟沙星耐药,93%对美罗培南耐药。我们在[相关基因]中鉴定出7个不同的MDR特异性突变,其中3个是新发现的。[相关基因]在对全部测试抗生素耐药的菌株中显著过表达,而[另外两个相关基因]在MDR分离株中过表达。氟喹诺酮决定因素的突变与MDR表型显著相关,并且观察到一种新的GyrA Y100C替代。MDR分离株中的碳青霉烯耐药性与[相关基因]的功能丧失突变以及我们样本中较高的NDM([具体类型])流行率相关。
本研究深入了解了[相关细菌]临床分离株所采用的MDR机制,这可能为改善临床结果的治疗方案的潜在开发提供指导。