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首页> 外文期刊>Advances in Microbiology >N-Acylhomoserine Lactones (AHLs), QseB/C Gene Detection, Virulence Factors and Antibiotics Resistance of &i&Aeromonas hydrophila&/i&
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N-Acylhomoserine Lactones (AHLs), QseB/C Gene Detection, Virulence Factors and Antibiotics Resistance of &i&Aeromonas hydrophila&/i&

机译:N-酰基高丝氨酸内酯(AHL),QseB / C基因检测,嗜水气单胞菌的致病因子和抗生素抗性。

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The aim of this research was to detect the N-acyl homoserine lactones (AHLs) production and QseB/C gene of Aeromonas hydrophila . We analyzed the potentials of these isolates of Aeromonas hydrophila in causing biofilm formation, hemolysis, protease, and lipase. The antibiotic susceptibility of the 15 Aeromonas hydrophila isolates was also investigated. The detection of AHLs was carried out using the Chromobacterium violaceum strain CV026 as biosensors. The isolated strains were tested for the reaction of C. violaceum CV026 by cross-streaking on an agar plate. Production of AHLs was determined by the diffusing via the agar plates and the tinge of the biosensor strains. All isolated strains produced AHLs. A polymerase chain reaction (PCR) showed the isolated strains had qseB and qseC genes. Susceptibility tests of A. hydrophila isolates were administered against 25 different antibiotic disks representing 12 classes of antibiotics. The strains were highly resistant to β -Lactam with 96.7% showing resistibility, whereas 97.7% susceptibility was found towards Aminoglycoside class of the antibiotic used. 60% showed intermediate resistant to Polypeptide. 100% of the strains showed no resistant to Aminoglycoside, Polypeptide, Monobactam, and Carbapenems class of antibiotics. Each of the isolates was found to be associated with at least one virulent factor. Our results clearly demonstrated that there is a presence of QseB/C genes in A. hydrophila and also produces AHLs molecule and virulence factors. The investigated isolates showed the pathogenic potential of Aeromonas hydrophila which makes it a serious threat to public health.
机译:这项研究的目的是检测嗜水气单胞菌的N-酰基高丝氨酸内酯(AHLs)产生和QseB / C基因。我们分析了这些嗜水气单胞菌分离物在引起生物膜形成,溶血,蛋白酶和脂肪酶方面的潜力。还研究了15种嗜水气单胞菌分离物的抗生素敏感性。 AOLs的检测是使用紫薇杆菌CV026菌株作为生物传感器进行的。测试分离的菌株的℃反应。通过在琼脂平板上交叉划线获得紫堇CV026。通过经由琼脂平板的扩散和生物传感器菌株的色调确定AHL的产生。所有分离的菌株均产生AHL。聚合酶链反应(PCR)显示分离的菌株具有qseB和qseC基因。 A的敏感性测试。针对代表12类抗生素的25种不同的抗生素圆盘施用亲水分离株。该菌株对β-内酰胺具有高度抗性,显示出96.7%的抗药性,而对所用抗生素的氨基糖苷类的药敏度为97.7%。 60%的人对多肽表现出中等抵抗力。 100%的菌株对氨糖苷,多肽,莫诺巴坦和碳青霉烯类抗生素无抗药性。发现每个分离物与至少一种毒性因子相关。我们的结果清楚地表明在 A中存在QseB / C基因。亲水,并产生AHL分子和毒力因子。被调查的菌株显示出嗜水气单胞菌的致病潜力,这使其对公共健康构成严重威胁。

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