Tabriz Research Center of Infectious and Tropical Diseases, Tabriz University of Medical Sciences, Tabriz 5163639888, Iran.
Diagn Microbiol Infect Dis. 2013 Jul;76(3):330-4. doi: 10.1016/j.diagmicrobio.2013.04.003. Epub 2013 May 28.
We examined the prevalence of various cephalosporins' resistance mechanisms in Acinetobacter baumannii clinical isolates. Phenotypic and molecular detection of Ambler classes A, B and D β-lactamases was performed on 75 isolates. Clonal relatedness was defined using Repetitive Extragenic Palindromic PCR. PCR mapping was used to examine the linkage of insertion sequences and the ampC gene, and ampC expression was analyzed by TaqMan reverse transcriptase-PCR. Twenty-six (37%) isolates carried at least one of the blaPER-1 or blaTEM-1. Sixty-nine (98.5%) out of 70 cephalosporin-resistant isolates had insertions upstream of the ampC gene, of which 48 (69%) and 6 (8%) were identified as ISAba1and ISAba125, respectively. Higher level of expression was obtained in resistant isolates lacking ISAba1/ampC combination in comparison with that in positive ones. The ability to up-regulate the expression of ampC gene in association with different insertion elements has become an important factor in A. baumannii resistance to cephalosporins.
我们研究了鲍曼不动杆菌临床分离株中各种头孢菌素耐药机制的流行情况。对 75 株分离株进行了 Ambler 类 A、B 和 D β-内酰胺酶的表型和分子检测。采用重复外回文 PCR 定义克隆相关性。PCR 图谱用于检测插入序列和 ampC 基因的连锁关系,TaqMan 逆转录 PCR 用于分析 ampC 表达。26 株(37%)分离株携带至少一种 blaPER-1 或 blaTEM-1。70 株头孢菌素耐药株中有 69%(69%)和 8%(8%)分别为 ISAba1 和 ISAba125。与阳性者相比,缺乏 ISAba1/ampC 组合的耐药株表达水平更高。与不同插入元件相关的 ampC 基因表达上调能力已成为鲍曼不动杆菌对头孢菌素耐药的重要因素。