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Assessment of 16srRNA Methylase Genes Among Non-ESBL and ESBL-Producing Klebsiella pneumoniae Isolates

机译:评估非ESBL和ESBL和ESBL的Klebsiella肺炎分离物中的16SRRNA甲基酶基因

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The aim of our study was to investigate mechanisms of aminoglycoside resistance in extended-spectrum beta-lactamases (ESBL)-producing Klebsiella pneumoniae (K. pneumoniae) isolates from Iran. To this end, 154 clinical isolates of K. pneumoniae were collectedfrom two hospitals in Ilam city, Iran. The Kirby-Bauer (agar diffusion) antibiotic testing method was used to determine the susceptibilitypattern of the isolates against kanamycin, gentamicin, tobramycin, netilmicin and amikacin. Aminoglycoside acetyltransferases(aac(3)-IIa, aac(6’)-Ib, and aac(3)-Ia), 16SrRNA methylase genes (armA and rmtB) and ESBL genes (blaTEM, blaSHV , and blaCTX-M)were detected by PCR amplification. 59.1% (n = 91) of K. pneumoniae isolates were detected ESBL producers with the phenotypic test.Moreover, blaTEM, blaSHV and blaCTX-M were detected in 83.5% (n=76), 52.7% (n=48) and 26.4% (n=24) of the ESBL-producing isolates,respectively. Among 52 resistant or intermediate isolates against aminoglycosides, the aac(3)-IIa, aac(6’)-Ib and rmtB genes were detectedin 55.8% (n = 29), 80.8% (n = 42) and 1.9% (n = 1) of the isolates, respectively; none of the isolates, however, had the aac(3)-Iaand armA genes. Therefore, the results showed the high prevalence of aminoglycosides resistance in the K. pneumoniae isolates. Asobserved, the acetyltransferase modifying enzymes (aac genes) played major roles in determining this resistance. However, the rateof 16srRNA methylase genes was extremely low in K. pneumoniae.
机译:我们的研究目的是研究延长光谱β-内酰胺酶(ESBL)的氨基糖苷类抗性的机制 - 从伊朗分离出来的Klebsiella肺炎(K.Pneumoniae)分离物。为此,从伊朗伊兰市的两家医院收集了154名K.Pneumoniae的临床分离株。 Kirby-Bauer(琼脂扩散)抗生素检测方法用于确定对卡那霉素,庆大霉素,染发蛋白,Netilmicin和Amikacin的分离物的易感性。氨基甘氨酸乙酰转移酶(AAC(3)-IIa,AAC(6') - IB和AAC(3)-IA),16SRRNA甲基酶基因(ARMA和RMTB)和ESBL基因(BLATEM,BLAPHV和BLACTX-M)通过PCR扩增。将59.1%(n = 91)的K.肺炎群分离物检测ESBL生产者,以表型试验检测。在83.5%(n = 76)中,检测到,现实,BlAPHV和Blactx-m,52.7%(n = 48)和26.4分别产生ESBL的分离株%(n = 24)。在针对氨基糖苷的52个抗性或中间分离物中,检测AAC(3)-IIa,AAC(6') - IB和RMTB基因55.8%(n = 29),80.8%(n = 42)和1.9%(n = 1)分离物质;然而,没有一个分离物具有AAC(3) - AIRAMA ARAMA基因。因此,结果表明,K.肺炎群分离物中的氨基糖苷抗性的高普遍性。 Asobserved,乙酰转移酶改性酶(AAC基因)在确定这种阻力时发挥了重要作用。然而,16SRRNA甲基酶基因的速率极低,K.肺炎。

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