铜绿假单胞菌临床分离株整合子基因的特征,这些基因可使这些菌株产生抗生素耐药性并形成生物膜

Q4 Biochemistry, Genetics and Molecular Biology
A.F. Alfarras, W.A. Al-Daraghi
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引用次数: 0

摘要

铜绿假单胞菌是一种具有重要临床和流行病学意义的细菌。它是免疫系统受损者机会性感染的主要病原体。众所周知,整合子对革兰氏阴性菌有显著的影响,尤其是对铜绿单胞菌,因为铜绿单胞菌具有对抗菌药物产生抗药性的能力。目的在分离的铜绿假单胞菌中系统鉴定和检测具有抗生素耐药性和生物膜形成能力的整合子基因(intI、intII、intIII)。研究方法从伊拉克巴格达市的阿尔亚穆克教学医院(Al Yarmouk Teaching Hospital)共采集 209 份样本,分离铜绿假单胞菌。通过表型和生化测试对细菌进行鉴定。使用 Vitek2 系统测量抗生素敏感性。生物膜定量采用微滴定法。采用 PCR 方法评估 1、2 和 3 类整合子的存在。结果通过结合形态学和生化检查,在 83 个分离物中鉴定出铜绿假单胞菌,所有分离物均能在西曲肽琼脂的铜绿假单胞菌选择性培养基上生长。结果还显示,一些样本和分离出的铜绿假单胞菌的百分比存在明显差异(p < 0.05)。烧伤和伤口感染铜绿假单胞菌阳性率最高(分别为 25% 和 19%),而烧伤和耳部感染铜绿假单胞菌阳性率最高(分别为 58% 和 50%)。此外,这些分离物还具有形成生物膜的能力,对多种抗生素产生耐药性的比例高达 68.7%。对多种药物耐药和敏感的铜绿微囊藻分离株的耐药率较高(分别为 49.4% 和 34.9%),而可能泛耐药和广泛耐药的分离株的耐药率较低(分别为 2.4% 和 13.3%)。聚合酶链式反应结果显示,整合素 I 的得分率最高(100%),而整合素 2 只在 3 个分离株(10%)中发现,没有在任何铜绿假单胞菌分离株中检测到 intI3 基因。结论总体而言,本次调查的结果表明,整合子和生物膜的发展被认为是导致铜绿假单胞菌产生抗生素耐药性的重要因素。在所有细菌分离物中,1 类整合子的发生率都很高,完全发生率为 100%。1 类整合子的高发生率与对关键抗生素(包括 β-内酰胺类、氨基糖苷类和头孢菌素类)产生耐药性有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Характеристика генів інтегронів клінічних ізолятів Pseudomonas aeruginosa, які реалізують резистентність до антибіотиків та біоплівкоутворення цими штамами
Pseudomonas aeruginosa is a bacterium that holds significant clinical and epidemiological significance. It serves as the principal etiological cause of opportunistic infections in individuals with impaired immune systems. Integrons are known to have a notable impact on Gram-negative bacteria, particularly in the context of P. aeruginosa, a bacterium recognized for its ability to develop resistance to antimicrobial drugs. Aim. To systematically characterize and detect integron genes (intI, intII, intIII) with antibiotic-resistant and biofilm-forming capabilities in isolated P. aeruginosa. Methods. A total of 209 samples were collected from Al Yarmouk Teaching Hospital in Baghdad City, Iraq to isolate P. aeruginosa. The process of bacterial identification was carried out phenotypically and by biochemical tests. Antibiotic susceptibility was measured using the Vitek2 system. Biofilm quantification was done by the microtiter method. The PCR approach was employed to assess the presence of class 1, 2, and 3 integrons. Results. P. aeruginosa was identified in 83 isolates by using a combination of morphological and biochemical examinations where all isolates showed the ability to grow a selective medium on cetrimide agar for P. aeruginosa. The results also showed significant variances (p < 0.05) among the percentage of a number of samples and isolated P. aeruginosa. The burn and wound infection scored the highest percentages (25% and 19%) based on the positivity of P. aeruginosa, whereas burn and ear sites scored the highest percentage (58% and 50%). Also, the isolates show the ability to form biofilm at a percentage of 68.7% with resistance to a high number of antibiotics. The multidrug-resistant and sensitive P. aeruginosa isolates scored high percentages (49.4% and 34.9%) whereas potentially pan drug-resistant and extensively drug-resistant isolates scored low percentages (2.4% and 13.3%). PCR results showed that integron I scored the highest percentage (100%) compared to integron 2 found in 3 (10%) isolates, and no intI3 gene was detected in any of the P. aeruginosa isolates. Conclusions. Overall, the findings of the present investigation indicate that integrons and biofilm development are recognized as significant factors contributing to antibiotic resistance in P. aeruginosa. The prevalence of class 1 integrons is shown to be significantly high in all bacterial isolates, with a complete occurrence rate of 100%. This high incidence of class 1 integrons is associated with the development of resistance to crucial antibiotics, including β-lactams, aminoglycosides, and cephalosporins.
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Mikrobiolohichnyi zhurnal
Mikrobiolohichnyi zhurnal Medicine-Microbiology (medical)
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