A Rapid Method to Screen for Multi Drug Resistance (MDR) Trait in Clinical Isolates of Acinetobacter baumannii-Acyl Homoserine Lactone (AHL) Screening in CRAB and CSAB Isolates

Saipriya Kamaraju, V. Sritharan
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Abstract

Aims: Our proposal aimed to evaluate Acyl Homoserine Lactones (AHL) as a functional marker for Multi drug resistant (MDR) potential in clinical isolates of Acinetobacter baumannii. We investigated the AHL production potential of clinical isolates using a biosensor assay directly on a commonly used agar media. Place and Duration of Study: Department of Molecular Diagnostics and Biomarkers, Gleneagles Global Hospitals, Lakdikapul, Hyderabad-500004. Methodology: Antimicrobial drug sensitivity testing (AST) was performed on 72 clinical isolates of A. baumannii against two front-line antibiotics, Imipenem (10µg) and Meropenem (10µg), by Kirby-Bauer disk diffusion method. Production of long chain Acyl Homoserine lactone (AHLs) in the clinical isolates of A. baumannii was tested by cross streaking with the biosensor Chromobacterium violaceum mutant strain CV026 and Agrobacterium tumefaciens (NTL4pZLR4) by agar plate diffusion assay. Screening and identification of the quorum sensing mediator gene abaI was done by PCR to confirm its presence in all the 72 clinical isolates. Results: Out of the 72 clinical isolates, 58 were Carbapenem resistant Acinetobacter baumannii (CRAB) and 14 were Carbapenem sensitive Acinetobacter baumannii (CSAB) for AST by agar disc diffusion method. None of our isolates produced short chain AHLs whereas all the isolates could produce varying amounts of long chain AHLs. Genotypic confirmation of AHL gene was obtained by abaI gene PCR. Conclusion: Carbapenems are the front-line antibiotics used to treat gram negative bacterial infections in emergencies and in the critical care units of hospitals. Clinical isolates A. baumannii has innate resistance to several antibiotics due to various mechanisms, biofilms forming the first line of defense against antibiotics for the bacterium. Our study used AST to carbapenem as the leading marker for MDR, assuming the innate resistance of A. baumannii to other beta lactam antibiotics. Our study brought out certain important observations namely: a) All clinical isolates of A. baumannii produced Quorum Sensing signal molecules, the AHLs b) the clinical isolates of A. baumannii did not produce any short chain AHLs b) All the clinical isolates of A. baumannii produced long chain AHLs c) AHL production is not specific to carbapenem drug resistance because even CSAB isolates produced AHL d) AHL production is inherent to all clinical isolates of A. baumannii and it apparently indicates an underlying biofilm potential and MDR trait in these A. baumannii isolates. e) AHLs could be a universal marker for revealing MDR trait and biofilm potential in clinical microbiology AST profiling protocols. 
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鲍曼不动杆菌临床分离株多重耐药特性的快速筛选方法——acyl同型丝氨酸内酯(AHL)在CRAB和CSAB分离株中的筛选
目的:我们的建议旨在评估酰基同丝氨酸内酯(AHL)作为鲍曼不动杆菌临床分离株多重耐药(MDR)潜力的功能标记物。我们使用生物传感器直接在常用的琼脂培养基上检测临床分离株的AHL生产潜力。研究地点和时间:格伦伊格尔斯全球医院分子诊断和生物标志物部,拉迪卡普尔,海得拉巴-500004。方法:采用Kirby-Bauer纸片扩散法对临床分离的72株鲍曼不动杆菌对亚胺培南(10µg)和美罗培南(10µg)两种一线抗菌药物进行药物敏感性试验。采用琼脂平板扩散法,用生物传感器紫色色杆菌(Chromobacterium violaceum)突变株CV026和农杆菌(Agrobacterium tummefaciens)突变株NTL4pZLR4进行交叉实验,检测鲍曼不动杆菌临床分离株长链酰基高丝氨酸内酯(AHLs)的产生。采用PCR方法对群体感应中介基因abaI进行筛选和鉴定,证实其存在于全部72株临床分离株中。结果:72株临床分离菌株中,琼脂盘扩散法检测AST为耐碳青霉烯鲍曼不动杆菌(CRAB) 58株,CSAB 14株。我们的分离株均未产生短链ahl,而所有分离株均可产生不同数量的长链ahl。用abaI基因PCR法确定AHL基因的基因型。结论:碳青霉烯类抗生素是急诊和医院重症监护病房治疗革兰氏阴性菌感染的一线抗生素。临床分离的鲍曼不动杆菌由于各种机制对几种抗生素具有先天耐药性,生物膜形成了细菌抵抗抗生素的第一道防线。我们的研究使用AST对碳青霉烯作为MDR的主要标记物,假设鲍曼不动杆菌对其他β -内酰胺类抗生素具有先天耐药。我们的研究得出了一些重要的观察结果,即:a)鲍曼不动杆菌临床分离株均产生群体感应信号分子;b)鲍曼不动杆菌临床分离株不产生任何短链AHL b)鲍曼不动杆菌临床分离株都产生长链AHL c) AHL的产生并非碳青霉烯类耐药性所特有,因为即使是CSAB分离株也会产生AHL d) AHL的产生是鲍曼不动杆菌临床分离株所固有的,这显然表明这些鲍曼不动杆菌分离株具有潜在的生物膜潜力和耐多药性状。e) ahl可作为临床微生物AST谱分析方案中揭示MDR特征和生物膜潜力的通用标记物。
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