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首页> 外文期刊>Indian Journal of Medical Microbiology >Investigation of Ureaplasma urealyticum biovars and their relationship with antimicrobial resistance
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Investigation of Ureaplasma urealyticum biovars and their relationship with antimicrobial resistance

机译:解脲脲原体生物变种及其与耐药性关系的研究

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Purpose: To develop Taqman fluorescence quantitative polymerase chain reaction (PCR) method for investigating the characteristics of the distributions of Ureaplasma urealyticum (UU) biovars and to explore the relationship between UU biovars and antimicrobial resistance. Materials and Methods: By the method of culture, Ureaplasma species were detected. Taqman fluorescence quantitative PCR for detecting UU biovars were developed and UU clinical isolates were detected to distinguish biovars. The broth micro-dilution susceptibility testing methods were used to determine UU susceptibility. Results: By Taqman PCR method, UU biovars was successfully detected. Of 126 samples, biovar 1 was found in 73 (57.94%). There was a statistical difference between genital-urinary tract infection group and asymptomatic group (P0.05). In the region, UU biovar 1 to 9 kinds of agents kept higher susceptibility rates, but biovar 2 maintained higher susceptibility rates only to tetracyclines. Compared with biovar 1, UU biovar 2 resistance rates to 7 kinds of agents were higher (P0.05). Conclusions: (1) Our new established Taqman PCR method is a useful tool for screening UU biovars. (2) UU biovar 1 predominated in asymptomatic population; whereas in genital-urinary tract infection population UU biovar 2 had a higher proportion. (3) The characteristics of drug resistance were different between UU biovars. Overall, both two biovars remained higher susceptibility rates to tetracyclines. A majority of biovor 1 strains were sensitive to macrolides and quinolones; while only a small number of biovar 2 strains kept sensitive to roxithromycin and quinolones, a large proportion of biovar 2 strains were found in intermediate ranges.
机译:目的:建立Taqman荧光定量聚合酶链反应(PCR)方法,研究解脲脲原体(UU)生物变种的分布特征,探讨UU生物变种与抗菌素耐药性的关系。材料与方法:采用培养的方法,检测出脲原体。开发了用于检测UU生物变种的Taqman荧光定量PCR,并检测了UU临床分离株以区分生物变种。肉汤微稀释敏感性测试方法用于确定UU敏感性。结果:通过Taqman PCR方法,成功检测到UU生物变种。在126个样本中,有73个(57.94%)被发现有biovar 1。生殖泌尿道感染组与无症状组比较差异有统计学意义(P <0.05)。在该地区,UU biovar 1至9种药剂保持较高的药敏率,而biovar 2仅对四环素保持较高的药敏率。与biovar 1相比,UU biovar 2对7种药物的耐药率更高(P <0.05)。结论:(1)我们新建立的Taqman PCR方法是筛选UU生物变种的有用工具。 (2)在无症状人群中,UU biovar 1占主导地位;而在生殖泌尿道感染人群中,UU biovar 2的比例更高。 (3)UU生物变种的耐药特性不同。总体而言,两个生物变种对四环素的敏感性仍然较高。大多数biovor 1菌株对大环内酯类和喹诺酮类药物敏感。虽然只有少数biovar 2菌株对罗红霉素和喹诺酮类药物保持敏感,但在中等范围内发现了大部分biovar 2菌株。

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