Detection of exopolysaccharides (algD, pelF, and pslD) genes in burn wound Pseudomonas aeruginosa isolates

Q4 Medicine
Z. Alwan, R. Lilo, Z. AL-Taee, Liqaa Mohsen, F. Al-Alaq
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引用次数: 0

Abstract

Background: Pseudomonas aeruginosa biofilm is an essential component of virulence that plays a significant role in antimicrobial resistance and chronic burn wound infections. Objective: This study aimed to investigate the biofilm formation capacity of P. aeruginosa isolated from chronic burn wound from January to May 2022 by biochemical and molecular techniques. Materials and Methods: Quantification of biofilm was performed based on tube method for local isolates of P. aeruginosa after growing on brain heart Broth. The genes encoding exopolysaccharides (algD, pelF, and pslD) were targeted by using conventional polymerase chain reaction (PCR). Results: The results showed that 92.6% of isolates were biofilm former, interestingly 68% of isolates were considered as strong former comparing with other biofilm categories. Gel electrophoresis result of PCR products presented clear bands for algD and psID genes with percentages (96%) and (3.7%) respectively. However, there was no PCR product for pelf gene among all isolates. Conclusion: The prevalence of algD, the large operon necessary for alginate production, was high among P. aeruginosa biofilm producer in this study and it can be an essential agent in the pathogenicity of P. aeruginosa burn wound infections comparing with other biofilm genes (pelF and pslD) of exopolysaccharide structure.
检测烧伤伤口铜绿假单胞菌分离物中的外多糖(algD、pelF 和 pslD)基因
背景:铜绿假单胞菌生物膜是铜绿假单胞菌毒力的重要组成部分,在抗菌药耐药性和慢性烧伤伤口感染中发挥着重要作用。研究目的本研究旨在通过生化和分子技术研究 2022 年 1 月至 5 月从慢性烧伤创面分离的铜绿假单胞菌的生物膜形成能力。材料与方法:采用试管法对当地分离的铜绿假单胞菌在脑心肉汤上培养后进行生物膜定量。使用传统聚合酶链反应(PCR)对编码外多糖的基因(algD、pelF 和 pslD)进行靶向分析。结果显示结果表明,92.6%的分离物是生物膜前体,有趣的是,与其他生物膜类别相比,68%的分离物被认为是强生物膜前体。PCR 产物的凝胶电泳结果显示,algD 和 psID 基因的条带清晰,分别占 96% 和 3.7%。然而,所有分离物中都没有 pelf 基因的 PCR 产物。结论与其他外多糖结构的生物膜基因(pelF 和 pslD)相比,该基因可能是铜绿假单胞菌烧伤创面感染致病的关键因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.90
自引率
0.00%
发文量
21
审稿时长
8 weeks
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