Evaluation of different phenotypic techniques in detection of metallo-betalactamases in pseudomonas aeruginosa

Aarushi Mangla, Hetal Vasani, M. Vegad
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Abstract

Metallo-beta-lactamase (MBL) producing Pseudomonas is a worrisome pathogen to hospital infection control due to production of resistance to multiple antibiotics. So, treatment options are narrowed down to only few antibiotics which will result in high morbidity and mortality. This study was conducted with the aim to detect prevalence of MBL producing Pseudomonas aeruginosa and to compare the different phenotypic methods for the detection of MBL production in Imipenem resistant clinical isolates of Pseudomonas aeruginosa. : In this prospective study total of 14,145 different clinical samples received from different wards. Out of which 804 Pseudomonas aeruginosa were isolated and antibiotic sensitivity testing was done by Kirby-Bauer disc diffusion method using CLSI guidelines. These were evaluated for Carbapenems resistance and MBL production. Imipenem resistant strains were subjected to screening tests like Double-disc synergy test, Combined disc diffusion test (CDT) and Modified-Hodge test. : In our study out of 804 isolates,153(19.02%) isolates are resistant to Imipenem. Out of 153 Imipenem resistant isolates, Combined disc diffusion test was positive in 100%, Double disc synergy test in 76.5% and Modified-hodge test in 84.15% isolates.: Combined disc diffusion test is very sensitive, cost effective and convenient screening test for detection of MBL producing Pseudomonas aeruginosa. So, all Imipenem resistant Pseudomonas isolates should be regularly screened for detection of MBL by Combined disc diffusion test (CDT) to prevent spread of resistance, longer hospital stay and treatment failure.
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铜绿假单胞菌金属- β -内酰胺酶不同表型检测技术的评价
产生金属内酰胺酶(MBL)的假单胞菌对多种抗生素产生耐药性,是医院感染控制的一个令人担忧的病原体。因此,治疗选择被缩小到只有几种抗生素,这将导致高发病率和死亡率。本研究旨在检测产生MBL的铜绿假单胞菌的患病率,并比较不同表型方法检测耐亚胺培南铜绿假单胞菌临床分离株MBL的产生。在这项前瞻性研究中,共收到来自不同病房的14145份不同的临床样本。其中铜绿假单胞菌804株,采用Kirby-Bauer圆盘扩散法,按照CLSI指南进行抗生素敏感性试验。对这些菌株的碳青霉烯类耐药性和MBL产量进行了评估。对耐亚胺培南菌株进行双盘协同试验、联合盘扩散试验(CDT)和改良霍奇试验等筛选。在我们的研究中,804株菌株中有153株(19.02%)对亚胺培南耐药。153株亚胺培南耐药菌株中,联合纸片扩散试验阳性率为100%,双纸片协同试验阳性率为76.5%,改良霍奇试验阳性率为84.15%。联合盘片扩散试验是一种灵敏、经济、方便的检测MBL产铜绿假单胞菌的筛选试验。因此,应定期对所有亚胺培南耐药假单胞菌分离株进行联合光盘扩散试验(CDT)筛查,以检测MBL,防止耐药性扩散、延长住院时间和治疗失败。
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