Vancomycin-Resistant Enterococcus spp. Isolated From Mastitic cow’s milk

Marwa Abdali, A. Abdulrazzaq, R. Hamouda
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Abstract

This study assessed the recrudescence of Enterococci in mastitis cow's milk and investigated their resistance to vancomycin. 300 samples were compiled from separate places and fields in Kirkuk, Iraq during the period from February to May, 2022. The samples were ioculated on the surface of bile esculin agar plates with sodium azide and then incubated at 37°C for 24–48 h. The characteristic pin-point colonies with a zone of black precipitate and morphologically resembling Enterococci spp. were further subjected to presumptive identification by Gram’ staining, catalase, and oxidase tests. All isolates were kept in BHIB with 30% glycerol at −70°C for further molecular detection. Enterococci isolates were tested for their susceptibility to different antibiotics by a disc diffusion technique. Based on the results of the sensitivity test, the ten isolates with the highest level of multiple resistances were selected from each of E. faecalis and E. faecium to examine the van A, van B genes by cPCR. The results of the bacteriological examination revealed that, 61 isolates (20.3%) of Enterococci According to phenotypic criteria; 42 isolates were E. faecalis and 19 were E. faecium . Add this to the confirmatory tests that revealed 25 isolates (8.3%) were E. faecalis and 10 isolates (3.3%) were E. faecium detected by PCR. Antimicrobial susceptibility tests indicated high levels of multi-resistant E. faecalis and E. faecium strains. Vancomycin-resistant strains were 40% and 30% for E. faecalis and E. faecium, respectively. The genetic sequences of E. faecalis and E. faecium isolates and phylogenetic trees were established and registered in GenBank-NCBI. They obtained accession numbers (OP566382) for E. faecium and (OP566380) for E. faecalis, which became references in Iraq and around the world.
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从乳腺炎牛奶中分离的耐万古霉素肠球菌
本研究评估了乳腺炎牛奶中肠球菌的复发情况,并调查了它们对万古霉素的耐药性。2022年2月至5月期间,从伊拉克基尔库克的不同地点和田地采集了300份样本。将样品与叠氮化钠一起沉淀在胆汁esculin琼脂平板表面,然后在37°C下孵育24-48小时。通过革兰氏染色、过氧化氢酶和氧化酶测试,进一步对具有黑色沉淀区和形态类似肠球菌的特征性定点菌落进行推定鉴定。所有分离株都保存在含有30%甘油的BHIB中,温度为−70°C,用于进一步的分子检测。用纸片扩散法检测分离的肠球菌对不同抗生素的敏感性。根据敏感性试验结果,从粪大肠杆菌和粪大肠杆菌中分别筛选出10株多重耐药水平最高的菌株,用cPCR方法检测van A、van B基因。细菌检查结果显示,符合表型标准的肠球菌61株(20.3%);42个分离株为粪肠球菌,19个为粪肠球菌。将此添加到验证性测试中,通过PCR检测到25个分离株(8.3%)为粪便大肠杆菌,10个分离物(3.3%)为粪便芽孢杆菌。抗微生物药敏试验表明,耐多药粪大肠杆菌和粪大肠杆菌菌株水平较高。万古霉素抗性菌株对粪大肠杆菌和粪大肠杆菌的抗性分别为40%和30%。建立了粪大肠杆菌和粪大肠杆菌分离株的遗传序列和系统发育树,并在GenBank NCBI中进行了登记。他们获得了粪大肠杆菌的登录号(OP566382)和粪大肠杆菌(OP566380),这些编号在伊拉克和世界各地成为参考。
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来源期刊
CiteScore
1.10
自引率
0.00%
发文量
44
审稿时长
5 weeks
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