UreC and ZapA virulence genes amplification in clinical specimen of Proteus mirabilis in Bayelsa state, Nigeria

Itodo Sunday Ewaoche, A. Tolulope, Arikekpar Ibemologi, Ekanem Edmund
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引用次数: 3

Abstract

Background and objective: Proteus mirabilis is part of the Enterobacteriaceae family, Gram negative bacterium which typically lives in the human gut, which means when it causes illness it can be a serious bloodstream infection, urinary tract infection or disseminated infection. UreC and ZapA virulent genes constitute the major pathogenicity of this organism as well as its resistance to antibiotics. This study was carried out to detect the presence of UreC and ZapA genes in Proteus mirabilis isolates sourced from Federal Medical Centre and Niger Delta University teaching hospital in Bayelsa State. Materials and methods: A total of one hundred and forty (140) clinical samples were collected from Federal Medical Centre (FMC) Yenagoa and Niger Delta University Teaching Hospital (NDUTH) Okolobiri, Bayelsa State. Of the 140 samples collected, 64(45.7%) were from males while 76(54.3%) were from females. The samples were Urine, Sputum, High vaginal swab, Urethral swab, Ear swab and Wound swab. The samples were inoculated in different laboratory media and incubated at 37°C for 48 hours. Morphological, cultural, biochemical characteristics and Polymerase Chain Reaction (PCR) technique were noted appropriately. Means and corresponding standard deviations were calculated for continuous data while proportions, along with the 95% confidence intervals, were calculated for categorical data. Results: A total of 81 bacterial isolates were obtained from these samples, of which 17(20.9%), 22(27.2%), 8(10.0%), 10(12.3%) and 24(29.6%) were Proteus mirabilis , Escherichia coli , Pseudomonas aeruginosa , Klebsiella pneumoniae and Staphylococcus aureus respectively. Fifteen (15) out of the 17(20.9%) P. mirabilis isolates were subjected to single-plex PCR amplification using specific primers after extraction of bacterial DNA from the samples. Out of the 15 samples, 14(93.3%) were positive for UreC gene while 15(100%) were positive to ZapA gene. Conclusion : The present study revealed that virulent genes-UreC and ZapA are highly present in P. mirabilis isolates obtained from clinical specimens from FMC and NDUTH in Bayelsa state, thus making them more pathogenic and resistant to antibiotics curing effect.
尼日利亚巴耶尔萨州奇异变形杆菌临床标本UreC和ZapA毒力基因扩增
背景和目的:奇异变形杆菌属于肠杆菌科,革兰氏阴性菌,通常生活在人体肠道中,这意味着当它致病时,可能是严重的血液感染、尿路感染或播散性感染。UreC和ZapA毒力基因构成了该生物的主要致病性及其对抗生素的耐药性。本研究旨在检测来自联邦医疗中心和尼日尔三角洲大学巴耶尔萨州教学医院的奇异变形杆菌分离株中UreC和ZapA基因的存在。材料和方法:共从联邦医疗中心(FMC)叶纳戈阿和尼日尔三角洲大学教学医院(NDUTH)巴耶尔萨州奥科洛比里收集了一百四十(140)份临床样本。在收集的140份样本中,64份(45.7%)来自男性,76份(54.3%)来自女性。样本为尿液、痰液、高位阴道拭子、尿道拭子、耳拭子和伤口拭子。将样品接种在不同的实验室培养基中,并在37°C下孵育48小时。对其形态、培养、生化特性和聚合酶链式反应(PCR)技术进行了适当的观察。计算连续数据的平均值和相应的标准差,同时计算分类数据的比例和95%置信区间。结果:共分离到81株细菌,其中奇异变形杆菌17株(20.9%),肺炎克雷伯菌22株(27.2%),金黄色葡萄球菌8株(10.0%),大肠杆菌10株(12.3%),绿脓杆菌24株(29.6%)。从样品中提取细菌DNA后,使用特异性引物对17个(20.9%)奇异紫外假单胞菌分离株中的15个进行了单重PCR扩增。在15个样本中,14个(93.3%)对UreC基因呈阳性,15个(100%)对ZapA基因呈阳性。结论:本研究表明,从巴耶尔萨州FMC和NDUTH的临床标本中获得的奇异紫外假单胞菌分离株中,毒力基因UreC和ZapA高度存在,从而使其更具致病性和抗抗生素治疗效果。
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