波兰东北部比亚韦斯托克大学临床医院出现1类整合子携带blaVIM-2和blaVIM-4的铜绿假单胞菌。

Anna Michalska-Falkowska, Paweł Tomasz Sacha, Henryk Grześ, Tomasz Hauschild, Piotr Wieczorek, Dominika Ojdana, Elżbieta Anna Tryniszewska
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引用次数: 4

摘要

碳青霉烯类药物被认为是严重感染的最后抗菌剂,其有效性因细菌耐药性而受到损害。金属β-内酰胺酶(MBLs)的产生是铜绿假单胞菌中碳青霉烯类活性的最大威胁。本研究的目的是利用脉冲场凝胶电泳(PFGE)和多位点序列分型(MLST)技术,评估耐碳青霉烯类P. aeruginosa临床菌株中MBLs基因的存在和类型,确定MBLs基因的位置,并确定MBLs生产者之间的遗传相关性。首次鉴定的mbl阳性(blaVIM基因)铜绿假单胞菌菌株来自于2012年9月至2013年12月在比亚韦斯托克大学临床医院住院的患者。MBLs基因的变异和可变整合子区域通过PCR和测序进行了表征。用XbaI酶消化细菌基因组后进行PFGE。利用MLST分析了7个内务管理基因的序列类型。3株携带blaVIM-2基因,1株携带blaVIM-4基因。blaVIM基因位于1类整合子内。整合子的PCR图谱显示存在四种不同的盒式阵列。PFGE遗传相关性分析将vim阳性菌株分为4个不相关的脉冲型(A-D)。MLST显示存在四种不同的序列类型(ST 111、ST27和ST17),包括一种先前描述的新类型ST 2342。药敏试验结果显示,vim阳性菌株对碳青霉烯类、头孢菌素类、氨基糖苷类、喹诺酮类、氨曲南类中间药物耐药,仅对粘菌素敏感。整合子定位、PFGE和MLST结果可能指出这些菌株的不同来源和独立引入住院患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Emergence of Pseudomonas aeruginosa with class 1 integron carrying blaVIM-2 and blaVIM-4 in the University Clinical Hospital of Bialystok (northeastern Poland).

The effectiveness of carbapenems, considered as last-resort antimicrobials in severe infections, becomes compromised by bacterial resistance. The production of metallo-β-lactamases (MBLs) is the most significant threat to carbapenems activity among Pseudomonas aeruginosa. The aim of this study was to assess the presence and type of MBLs genes in carbapenem-resistant P. aeruginosa clinical strains, to identify the location of MBLs genes and to determine genetic relatedness between MBL-producers using pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST). The first identified MBL-positive (with blaVIM genes) P. aeruginosa strains were isolated from patients hospitalized in the University Clinical Hospital of Bialystok in the period from September 2012 to December 2013. Variants of MBLs genes and variable integron regions were characterized by PCR and sequencing. PFGE was performed after digesting of bacterial genomes by XbaI enzyme. By MLST seven housekeeping genes were analyzed for the determination of sequence type (ST). Three strains carried the blaVIM-2 gene and one harbored the blaVIM-4 gene. The blaVIM genes resided within class 1 integrons. PCR mapping of integrons revealed the presence of four different cassette arrays. Genetic relatedness analysis by PFGE classified VIM-positive strains into four unrelated pulsotypes (A-D). MLST demonstrated the presence of four (ST 111, ST27, and ST17) different sequence type including one previously undescribed new type of ST 2342. Antimicrobial susceptibility testing showed that VIM-positive strains were resistant to carbapenems, cephalosporins, aminoglycosides, and quinolones, intermediate to aztreonam, and susceptible only to colistin. Integrons mapping, PFGE, and MLST results may point to different origin of these strains and independent introduction into hospitalized patients.

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