Basu Shreya, Mukherjee Sandip Kumar, Hazra Avijit, Mukherjee Mandira
Junior Research Fellow, Department of Biochemistry and Medical Biotechnology, School of Tropical Medicine , Kolkata, West Bengal, India .
Associate Professor, Department of Pharmacology, IPGMER , Kolkata, West Bengal, India .
J Clin Diagn Res. 2013 Dec;7(12):2727-31. doi: 10.7860/JCDR/2013/6613.3744. Epub 2013 Dec 15.
A proficient pathogen should be virulent, resistant to antibiotics, and epidemic. However, the interplay between resistance and virulence is poorly understood. Perhaps, the most commonly accepted view is that resistance to quinolones is linked to a loss of virulence factors. However, the low virulent phylogenetic groups may be more prone to acquire resistance to quinolones. The aim of this study was to identify and characterise the Nalidixic Acid (NA) and ciprofloxacin (CIP) resistant uropathogenic Escherichia coli (UPEC) isolates with respect to virulence and phylogenetic background, from hospital settings in Kolkata, an eastern region in India. Research based on these bacterial populations will help in understanding the molecular mechanisms underlying the association between resistance and virulence, that in turn, may help in managing the future disseminations of UTIs in their entirety.
One hundred and ten E. coli isolates were screened against NA and CIP using Kirby-Bauer disk diffusion technique, following CLSI guidelines. Prevalence of virulent factor genes and distribution of phylogenetic groups amongst the isolates was determined by PCR, using gene specific primers against the different virulent factors and DNA markers (chuA, yjaA and DNA fragment, TSPE4.C2) respectively. Statistical analysis of the data was performed using SPSS software.
Resistance to both NA and CIP was reported in 75.5 % of the isolates which were analysed. The virulent determinants, papC, pap GII, papEF, afa, cnf1, hlyA and iroN were significantly predominant in the drug susceptible than the resistant isolates. A significant reduction of phylogroup B2 in NA (85.7% versus 64.6%, χ(2)P<0.001) and CIP (85.2 % versus 61.4%, χ(2)P<0.001) resistant UPEC isolates, followed by increase in predominance of non-B2 phylotypes (group D and group B1), were observed.
This is the first report from India that has indicated possible evidence on horizontal gene transfer from pathogenic to commensal strains and selection of the latter, on extensive usage of this group of antimicrobials in hospital settings, where these drugs were routinely prescribed for treating urinary tract infection. Therefore, this information necessitates surveillance programs and administration of effective strategies, to put an end to random prescription policies involving this group of antimicrobials.
一种成功的病原体应具备致病性、抗生素耐药性且具有流行性。然而,耐药性与致病性之间的相互作用却鲜为人知。或许,最普遍接受的观点是喹诺酮类耐药性与毒力因子的丧失有关。然而,低毒力的系统发育群体可能更容易获得对喹诺酮类的耐药性。本研究的目的是从印度东部加尔各答的医院环境中,鉴定和表征耐萘啶酸(NA)和环丙沙星(CIP)的尿路致病性大肠杆菌(UPEC)分离株的毒力和系统发育背景。基于这些细菌群体的研究将有助于理解耐药性与致病性之间关联的分子机制,进而有助于全面管理未来尿路感染的传播。
按照CLSI指南,采用 Kirby-Bauer 纸片扩散法对110株大肠杆菌分离株进行 NA 和 CIP 耐药性筛选。分别使用针对不同毒力因子的基因特异性引物和 DNA 标记(chuA、yjaA 和 DNA 片段 TSPE4.C2),通过 PCR 确定分离株中毒力因子基因的流行情况和系统发育群体的分布。使用 SPSS 软件对数据进行统计分析。
在分析的分离株中,75.5%的菌株对 NA 和 CIP 均耐药。与耐药分离株相比,毒力决定因素 papC、pap GII、papEF、afa、cnf1、hlyA 和 iroN 在药敏分离株中显著占优势。耐 NA(85.7%对64.6%,χ(2)P<0.001)和耐 CIP(85.2%对61.4%,χ(2)P<¬0.001)的 UPEC 分离株中 B2 系统发育群显著减少,随后非 B2 系统发育型(D 群和 B1 群)的优势增加。
这是来自印度的首份报告,表明在医院环境中广泛使用这类抗菌药物治疗尿路感染时,可能存在从致病菌株向共生菌株水平基因转移以及后者被选择的证据。因此,这些信息需要监测计划并实施有效策略,以终止涉及这类抗菌药物的随意处方政策。