Asadollahi Khairollah, Taherikalani Morovat, Maleki Abbas, Alizadeh Eshrat, Valadbaigi Hasan, Soroush Setareh, Maleki Hossain, Asadollahi Parisa, Emaneini Mohammad
Department of Epidemiology, Ilam University of Medical Sciences, Ilam, Iran.
Acta Microbiol Immunol Hung. 2011 Dec;58(4):359-70. doi: 10.1556/AMicr.58.2011.4.11.
The aim of the present study was to investigate, for the first time, the diversity of the genes encoding aminoglycoside-modifying enzymes (AME) and their association with class 1 integrons in Iranian Acinetobacter baumannii strains. A total of 100 multidrug resistant A. baumannii, isolated from eight distinct hospitals in Tehran, were enrolled in this study. Susceptibility of these isolates to antimicrobial agents including gentamicin and amikacin was determined by E-test. Aminoglycoside resistant isolates were then tested by PCR for AME genes, including aphA6, aacC1, aacC2, aacA4, aadB, aadA1, classes 1 integron, 5'-CS-3' and typed by RAPD PCR. The rate of resistance to imipenem, meropenem, gentamicin and amikacin were 39%, 39%, 38% and 32%, respectively. Intermediate resistance phenotype to gentamicin and amikacin was observed in 2% and 5% of all the isolates, respectively. After aph6 with 90% (n = 36/40), aadA1, aacC1 and aadB with 82.5% (n = 33/40), 65% (n = 26/40) and 20% (n = 8/40) were the most prevalent AME genes among aminoglycosides resistant A. baumannii isolates. A combination of two to four different resistance genes was observed in 39 of 40 strains (97.5%), with a total of 7 different combinations. PCR of integrase genes revealed that AME gene was associated with 67% of class 1 integrons. RAPD analysis showed three predominant genotypes A (n = 20), B (n = 10) and 10 unrelated genotypes. The occurrence of identical resistance genes, gene combinations and class 1 integrons associated with these genes in clonally distinct strains indicates that horizontal gene transfer plays a major role in the dissemination of aminoglycoside resistance in A. baumannii.
本研究的目的是首次调查伊朗鲍曼不动杆菌菌株中编码氨基糖苷类修饰酶(AME)的基因多样性及其与1类整合子的关联。本研究纳入了从德黑兰八家不同医院分离出的100株多重耐药鲍曼不动杆菌。通过E-test测定这些分离株对包括庆大霉素和阿米卡星在内的抗菌药物的敏感性。然后,对氨基糖苷类耐药分离株进行PCR检测AME基因,包括aphA6、aacC1、aacC2、aacA4、aadB、aadA1、1类整合子、5'-CS-3',并通过RAPD PCR进行分型。对亚胺培南、美罗培南、庆大霉素和阿米卡星的耐药率分别为39%、39%、38%和32%。在所有分离株中,分别有2%和5%的菌株对庆大霉素和阿米卡星表现出中度耐药表型。在氨基糖苷类耐药鲍曼不动杆菌分离株中,aph6的检出率为90%(n = 36/40),aadA1、aacC1和aadB的检出率分别为82.5%(n = = 33/40)、65%(n = 26/40)和20%(n = 8/40),是最常见的AME基因。在40株菌株中的39株(97.5%)中观察到两种至四种不同耐药基因的组合,共有7种不同组合。整合酶基因的PCR结果显示,AME基因与67%的1类整合子相关。RAPD分析显示出三种主要基因型A(n = 20)、B(n = 10)和10种不相关的基因型。在克隆上不同的菌株中出现相同的耐药基因、基因组合以及与这些基因相关的1类整合子,表明水平基因转移在鲍曼不动杆菌氨基糖苷类耐药性传播中起主要作用。