首页> 外文期刊>British Microbiology Research Journal >Concomitant Detection of Biofilm Formation andMBL Production in Meropenem Resistant Isolates ofPseudomonas aeruginosa
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Concomitant Detection of Biofilm Formation andMBL Production in Meropenem Resistant Isolates ofPseudomonas aeruginosa

机译:铜绿假单胞菌抗美罗培南分离株的生物膜形成和MBL产生的伴随检测。

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The purpose of this study was to detect biofilm formation and to examine the correlation between biofilm and Metallo-β-lactamases (MBL) production in Pseudomonas aeruginosa. A total of 64 P. aeruginosa isolates were identified using standard microbiological methods and antimicrobial susceptibility testing (AST) was performed on them according to Clinical and Laboratory Standards Institute (CLSI) guidelines. The isolates were screened for biofilm production using both qualitative and quantitative methods. The presence of MBL genes were checked by multiplex PCR assay. Out of all 30 meropenem resistant P. aeruginosa, 2 isolates were found producing all the three genes (i.e. blaIMP, blaVIM, blaSIM) for MBL production and they were found to produce biofilm. Resistant to four antibiotics such as aztreonam (85.7% vs 11.1%, P< 0.000), Cefepime (82.1% vs 2.8%, P<0.000) gentamycin (82.1% vs 27.8%, P< 0.000) and Pipercillin/Tazobactum was also high (28.6% vs 2.8% P< 0.003) was comparatively higher among biofilm producers than non biofilm producers. In biofilm production, both qualitative method and quantitative plate method showed 16 isolates (53.3%) as biofilm producers for MBL genes. Out of these 16, only 9 isolates showed MBL production along with biofilm production having significant association (P<0.004).The prevalence of MBLs has been increasing worldwide, particularly among P. aeruginosa, leading to severe limitations in the therapeutic options for the management. Presence of MBL genes has a role in inducing biofilm production and significant association in P. aeruginosa isolates. Overall, drug resistance was found to be more in biofilm producing isolates than non biofilm isolates.
机译:这项研究的目的是检测铜绿假单胞菌中生物膜的形成并检查生物膜与金属β-内酰胺酶(MBL)产生之间的相关性。使用标准微生物学方法鉴定出总共64种铜绿假单胞菌分离物,并根据临床和实验室标准协会(CLSI)指南对其进行了抗菌药敏试验(AST)。使用定性和定量方法筛选分离物的生物膜生产。通过多重PCR测定检查MBL基因的存在。在所有30个耐美罗培南的铜绿假单胞菌中,发现2个分离株产生了用于MBL产生的所有三个基因(即blaIMP,blaVIM,blaSIM),并且发现它们会产生生物膜。对氨曲南(85.7%/ 11.1%,P <0.000),头孢吡肟(82.1%/ 2.8%,P <0.000)庆大霉素(82.1%/ 27.8%,P <0.000)和四种抗生素具有抗性生物膜生产商中的哌尔西林/他唑巴坦也较高(28.6%/ 2.8%,P <0.003)相对高于非生物膜生产商。在生物膜生产中,定性方法和定量平板方法均显示有16个分离物(占53.3%)是MBL基因的生物膜生产者。在这16个菌株中,只有9个菌株显示MBL产生以及生物膜产生具有显着的关联性(P <0.004).MBL的流行在全世界范围内呈上升趋势,特别是在铜绿假单胞菌中,导致该治疗的治疗选择受到严重限制。 。 MBL基因的存在在铜绿假单胞菌分离物中诱导生物膜产生和显着关联中具有作用。总体而言,发现在产生生物膜的分离物中的耐药性要比非在生物膜中的分离株高。

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