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首页> 外文期刊>Journal of Nanjing Medical University >Class Ⅰ integron with a novel cassette array in an ESBL-producing multidrug-resistant Klebsiella pneumoniae isolate
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Class Ⅰ integron with a novel cassette array in an ESBL-producing multidrug-resistant Klebsiella pneumoniae isolate

机译:带有ESBL产生多药耐药性肺炎克雷伯菌的新型盒带阵列的Ⅰ类整合子

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Objective: To analyze the molecular mechanism of integron mediated multi-resistance in an ESBL-producing K. pneumoniae NJ 12 isolate. Methods: Susceptibility test was carried out by Kirby-Bauer method. Class Ⅰ , Ⅱ and Ⅲ integrons were detected by integrase gene PCR with primers that annealed to conserved regions of integron-encoded integrase genes intI1, intI2 and intI3. The variable region of integron was amplified by integron PCR with primers that targeted the conserved flanking regions, and the PCR product was sequenced. Six aminoglycoside modifying-enzyme genes, including ant(2″)-Ⅰ , ant(3″)-Ⅰ , aac(3)-Ⅰ , aac(3)-Ⅱ , aac (6′)-Ⅰ , and aac (6′)-Ⅱ , were detected. Results: K. pneumoniae NJ 12 was resistant to nine antibiotics, including piperacillin, ampicillin, cefuroxime, ceftazidime, cefotaxime, aztreonam, streptomycin, gentamicin and amikacin. This isolate was shown that there was positive with class I integron, ant(2″)-Ⅰ , ant(3″)-Ⅰ , aac(3)-Ⅱ andaac(6′)-Ⅰ modifying-enzyme genes. Neither class Ⅱ nor Ⅲ integron was detected; DNA sequencing of the fragment amplified by integron PCR revealed a novel cassette array aadB-cat-bla_(oxa-10/) aadAl. Conclusion: Class Ⅰ integron with a novel cassette array in an ESBL-producing multidrug-resistant K. pneumoniae NJ 12 isolate was reported from Nanjing area of China, with the GenBank accession number DQ141319.
机译:目的:分析整合素介导的多重耐药在产ESBL的肺炎克雷伯菌NJ 12分离株中的分子机制。方法:采用Kirby-Bauer方法进行药敏试验。通过整合酶基因PCR,通过与整合子编码的整合酶基因intI1,intI2和intI3的保守区域退火的引物,检测出Ⅰ,Ⅱ和Ⅲ类整合素。整合子的可变区通过整合子PCR用靶向保守的侧翼区的引物扩增,并测序PCR产物。六个氨基糖苷修饰酶基因,包括ant(2″)-Ⅰ,ant(3″)-Ⅰ,aac(3)-Ⅰ,aac(3)-Ⅱ,aac(6′)-Ⅰ和​​aac(6 ')-Ⅱ,被检测到。结果:肺炎克雷伯菌NJ 12对9种抗生素具有抗药性,包括哌拉西林,氨苄西林,头孢呋辛,头孢他啶,头孢噻肟,氨曲南,链霉素,庆大霉素和丁胺卡那霉素。该分离株显示出I类整合子,ant(2″)-Ⅰ,ant(3″)-Ⅰ,aac(3)-Ⅱ和aac(6′)-Ⅰ修饰酶基因阳性。均未检出Ⅱ类和Ⅲ类整合子。整合子PCR扩增的片段的DNA测序揭示了一种新颖的盒式阵列aadB-cat-bla_(oxa-10 /)aadA1。结论:从中国南京地区报道了在产ESBL的耐多药肺炎克雷伯菌NJ 12分离株中具有新型盒阵列的Ⅰ类整合子。GenBank登录号为DQ141319。

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