婴儿奶粉蜡样芽孢杆菌中金属β-内酰胺酶基因blaIMP、blaVim、blaSPM-1的分子检测

C. Ghazaei
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引用次数: 0

摘要

背景:婴幼儿奶粉是蜡样芽孢杆菌等微生物生长的理想培养基。蜡样芽孢杆菌是一种孢子制造者,在巴氏灭菌过程中很容易存活,从而引起一些健康问题。目的:研究IMP样品中产生金属β-内酰胺酶(MBL)的蜡样芽孢杆菌的耐药模式。方法:制备50份IMP样品,培养检测蜡样芽孢杆菌的存在。采用Kirby-Bauer法测定抗生素敏感性,DDST法测定MBL酶表型。采用PCR方法对MBL基因blaVIM、blaSMP-1和blaIMP进行基因型检测。结果:与国家标准和国际标准相比,大多数IMP样品的蜡样芽孢杆菌污染水平较高。耐药比例最高的是头孢他啶和奥西林(100%),最低的是四环素(21.4%)和环丙沙星(26.3%)。在DDST试验中,所有蜡样芽孢杆菌分离株均产生MBL。所有分离株均未检测到blaSPM基因阳性。在其他MBL基因中,blaVIM基因存在于所有分离株中(100%),blaIMP基因存在于16株分离株中(84.21%)。结论:由于MBL酶的产生,研究区域的抗生素耐药性呈上升趋势。在产生mbl的分离株中,blaVIM基因的出现频率高于blaIMP和blaSPM-1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular Detection of Metallo-β-lactamase Genes blaIMP, blaVim,‎ ‎and blaSPM-1‎ in Bacillus cereus Strains Isolated from Infant Milk Powder Samples
Background: Infant milk powder (IMP) is a very suitable medium for the growth of ‎micro-organisms such as Bacillus cereus. B. cereus is a spore-producer that can ‎survive easily during the pasteurization process to cause some health problems. Objectives: This study was carried out to determine the antibiotic resistance pattern of B. ‎cereus isolates producing metallo-β-lactamase (MBL) enzymes in IMP samples‏.‏ Methods: After preparing 50 samples of IMP, they were cultured to detect the presence of B. cereus. The Kirby-Bauer method was used to determine antibiotic susceptibility and the DDST method to phenotypically detect MBL enzymes. MBL genes blaVIM, blaSMP-1, and blaIMP were genotypically examined in the isolates by the PCR method. Results: Most samples of IMP had a high level of contamination with B. cereus when compared to national and international standards. The highest percentage of resistance was related to ceftazidime and oxacillin (100%) and the lowest resistance to tetracycline (21.4%) and ciprofloxacin (26.3%). All B. cereus isolates were the producers of MBL in the DDST test. None of the isolates was positive for the blaSPM gene. Of the other MBL genes, the blaVIM gene was seen in all isolates (100%) and the blaIMP gene in 16 isolates (84.21%). Conclusions: Antibiotic resistance is on the rise in the study region due to the production of MBL enzymes. Among MBL-producing isolates, the frequency of the blaVIM gene was more than that of blaIMP and blaSPM-1.
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