Influence pH on virulence genes of Pseudomonas aeruginosa analyzed by RT-PCR method

Q4 Business, Management and Accounting
Ahmed Attalah Hassan Al-Fhdawi, A. M. Rabee
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引用次数: 0

Abstract

PurposeThe purpose of this study was to determine the influence of environmental pH on production of biofilms and virulence genes expression in Pseudomonas aeruginosa.Design/methodology/approachAmong 303 clinical and environmental samples 109 (61 + 48) isolates were identified as clinical and environmental P. aeruginosa isolates, respectively. Clinical samples were obtained from patients in the Al-Yarmouk hospital in Baghdad city, Iraq. Waste water from Al-Yarmouk hospital was used from site before treatment unit to collect environmental samples. The ability of producing biofilm at various pH levels was examined by microtiter plate and the prevalence of Alg D, Psl A and Pel A was determined by quantitative real time-polymerase chain reaction (qRT-PCR).FindingsThis study showed that the ability of clinical and environmental isolates to biofilm development was observed in 86.9% and 85.42% of clinical and environmental isolates, respectively. As well as, the environmental P. aeruginosa isolates showed the highest biofilm production at pH 7. Clinical isolates showed the highest genes expression of Alg D, Psl A and Pel A as compared to environmental isolates with pH change. In general, both clinical and environmental isolates formed biofilm and carried AlgD, PslA and PelA genes. Also, alkaline pH was favored for biofilm production.Originality/valueThere are very few studies done to find out the influence of environmental pH on production of biofilms and virulence genes expression in Pseudomonas aeruginosa. This study is unique as it has highlighted the influence of environmental pH on the ability of clinical and environmental isolates to biofilm development and genes expression.
采用RT-PCR方法分析pH值对铜绿假单胞菌毒力基因的影响
目的研究环境pH值对铜绿假单胞菌生物膜生成及毒力基因表达的影响。设计/方法/方法在303份临床和环境样本中,分别鉴定109(61 + 48)株为临床和环境铜绿假单胞菌。临床样本取自伊拉克巴格达市Al-Yarmouk医院的病人。Al-Yarmouk医院的废水在处理单位之前从现场使用,以收集环境样本。采用微滴板检测不同pH水平下产生生物膜的能力,采用定量实时聚合酶链反应(qRT-PCR)检测Alg D、Psl A和Pel A的流行率。结果临床分离株和环境分离株的生物膜发育能力分别为86.9%和85.42%。此外,环境铜绿假单胞菌分离株在pH为7时生物膜产量最高。临床分离株Alg D、Psl A和Pel A基因表达量高于pH变化的环境分离株。一般情况下,临床分离株和环境分离株均形成生物膜并携带AlgD、PslA和PelA基因。同时,碱性pH有利于生物膜的生成。原创性/价值环境pH值对铜绿假单胞菌生物膜生成及毒力基因表达的影响研究甚少。这项研究的独特之处在于它强调了环境pH对临床和环境分离株对生物膜发育和基因表达能力的影响。
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来源期刊
Arab Gulf Journal of Scientific Research
Arab Gulf Journal of Scientific Research 综合性期刊-综合性期刊
CiteScore
1.00
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Information not localized
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