Pragasam A K, Vijayakumar S, Bakthavatchalam Y D, Kapil A, Das B K, Ray P, Gautam V, Sistla S, Parija S C, Walia K, Ohri V C, Anandan S, Veeraraghavan B
Department of Clinical Microbiology, Christian Medical College, Vellore, Tamil Nadu, India.
Department of Microbiology, All Institute of Medical Sciences, New Delhi, India.
Indian J Med Microbiol. 2016 Oct-Dec;34(4):433-441. doi: 10.4103/0255-0857.195376.
Surveillance of antimicrobial resistance (AMR) is of great importance. Pseudomonas aeruginosa and Acinetobacter baumannii are important pathogens and emergence of resistance in these have increased the morbidity and mortality rates. This surveillance study was initiated by the Government of India - Indian Council of Medical Research. The aim of this study is to determine the antimicrobial susceptibility profile and to characterise the enzyme mediated antimicrobial resistance such as extended spectrum beta-lactamases (ESBLs) and carbapenemases among multidrug-resistant (MDR) P. aeruginosa and A. baumannii.
A multi-centric study was conducted from January 2014 to December 2015 with a total number of 240 MDR P. aeruginosa and 312 MDR A. baumannii isolated from blood, cerebrospinal fluid, respiratory, pus, urine and intra-abdominal infections. Kirby-Bauer disc diffusion was done to determine the antimicrobial susceptibility profile. Further, MDR isolates were characterised by multiplex polymerase chain reaction to determine the resistance genes for ESBLs and carbapenemases.
Among the ESBLs, blaVEB (23%), blaTEM (5%) and blaSHV (0.4%) in P. aeruginosa and blaPER (54%), blaTEM (16%) and blaSHV (1%) in A. baumannii were the most prevalent. Likewise, blaVIM (37%), blaNDM (14%), blaGES (8%) and blaIMP (2%) in P. aeruginosa and blaOXA-23like (98%), blaOXA-58like (2%), blaNDM (22%) and blaVIM (3%) in A. baumannii were found to be the most prevalent carbapenemases. blaOXA-51like gene, intrinsic to A. baumannii was present in all the isolates tested.
The data shown highlight the wide difference in the molecular mechanisms of AMR profile between P. aeruginosa and A. baumannii. In P. aeruginosa, plasmid-mediated mechanisms are much lesser than the chromosomal mediated mechanisms. In A. baumannii, class D oxacillinases are more common than other mechanisms. Continuous surveillance to monitor the trends in AMR among MDR pathogens is important for implementation of infection control and to guide appropriate empirical antimicrobial therapy.
抗菌药物耐药性监测至关重要。铜绿假单胞菌和鲍曼不动杆菌是重要病原体,其耐药性的出现增加了发病率和死亡率。这项监测研究由印度政府 - 印度医学研究理事会发起。本研究的目的是确定多重耐药铜绿假单胞菌和鲍曼不动杆菌的抗菌药物敏感性概况,并对酶介导的抗菌药物耐药性进行特征分析,如超广谱β-内酰胺酶(ESBLs)和碳青霉烯酶。
2014年1月至2015年12月进行了一项多中心研究,共分离出240株多重耐药铜绿假单胞菌和312株多重耐药鲍曼不动杆菌,分别来自血液、脑脊液、呼吸道、脓液、尿液和腹腔感染。采用 Kirby-Bauer 纸片扩散法确定抗菌药物敏感性概况。此外,通过多重聚合酶链反应对多重耐药菌株进行特征分析,以确定ESBLs和碳青霉烯酶的耐药基因。
在ESBLs中,铜绿假单胞菌中的blaVEB(23%)、blaTEM(5%)和blaSHV(0.4%)以及鲍曼不动杆菌中的blaPER(54%)、blaTEM(16%)和blaSHV(1%)最为常见。同样,铜绿假单胞菌中的blaVIM(37%)、blaNDM(14%)、blaGES(8%)和blaIMP(2%)以及鲍曼不动杆菌中的blaOXA-23样(98%)、blaOXA-58样(2%)、blaNDM(22%)和blaVIM(3%)被发现是最常见的碳青霉烯酶。鲍曼不动杆菌固有的blaOXA-51样基因存在于所有测试菌株中。
所示数据突出了铜绿假单胞菌和鲍曼不动杆菌之间抗菌药物耐药性分子机制的巨大差异。在铜绿假单胞菌中,质粒介导的机制远少于染色体介导的机制。在鲍曼不动杆菌中,D类苯唑西林酶比其他机制更为常见。持续监测多重耐药病原体的抗菌药物耐药性趋势对于实施感染控制和指导适当的经验性抗菌治疗至关重要。