Pakbin Babak, Amani Zahra, Allahyari Samaneh, Mousavi Shaghayegh, Mahmoudi Razzagh, Brück Wolfram Manuel, Peymani Amir
Medical Microbiology Research Center Qazvin University of Medical Sciences Qazvin Iran.
Institute for Life Technologies University of Applied Sciences Western Switzerland Valais-Wallis Switzerland.
Food Sci Nutr. 2021 Sep 23;9(11):6362-6371. doi: 10.1002/fsn3.2603. eCollection 2021 Nov.
The emergence of multidrug-resistant is a significant threat to global public health. Limited studies have investigated the incidence, antimicrobial susceptibility, and genetic diversity of isolated from food products. Conventional culture-based, serologic, molecular, disk diffusion, PCR, and RAPD-PCR methods were used to determine the prevalence rate, phenotypic and genotypic antibiotic resistance profile, and genetic diversity of the isolates from food samples including vegetable salad, ground meat, and raw cow's milk (405 samples). The prevalence rate of in food samples was 4.44%. The incidence of (3.7%) was higher than that of (0.74%). and were not detected in food samples examined. Also, no were recovered from raw cow's milk. This study showed that the isolates were resistant to sulfamethoxazole/trimethoprim (83.3%), amoxicillin (66.6%), streptomycin (66.6%), tetracycline (61.1%), ampicillin (50%), amoxicillin-clavulanic acid (50%), azithromycin (50%), and chloramphenicol (50%) and completely sensitive to cefoxitin, cefepime, amikacin, and gentamicin. All isolates were multidrug-resistant. We detected resistance gene in all isolates; however, no isolate harbored gene. RAPD-PCR categorized the isolates into five main clusters. The highest antibiotic resistance was observed in the isolates of cluster R4. The finding of this study also indicated an association between antimicrobial resistance profiles and genotyping properties of the isolates. Novel food monitoring systems, including surveillance of multidrug-resistant foodborne pathogens, especially in developing countries, are required to control the foodborne diseases.
多重耐药菌的出现对全球公共卫生构成重大威胁。针对从食品中分离出的此类细菌的发病率、抗菌药敏性和遗传多样性的研究有限。采用传统的基于培养的方法、血清学方法、分子方法、纸片扩散法、聚合酶链反应(PCR)和随机扩增多态性DNA-PCR(RAPD-PCR)方法,以确定从蔬菜沙拉、碎肉和生牛奶(共405份样品)等食品样品中分离出的此类细菌的流行率、表型和基因型抗生素耐药谱以及遗传多样性。食品样品中此类细菌的流行率为4.44%。该类细菌(3.7%)的发病率高于另一类细菌(0.74%)。在所检测的食品样品中未检测到其他两类细菌。此外,未从生牛奶中分离出该类细菌。本研究表明,此类细菌分离株对磺胺甲恶唑/甲氧苄啶(83.3%)、阿莫西林(66.6%)、链霉素(66.6%)、四环素(61.1%)、氨苄西林(50%)、阿莫西林-克拉维酸(50%)、阿奇霉素(50%)和氯霉素(50%)耐药,而对头孢西丁、头孢吡肟、阿米卡星和庆大霉素完全敏感。所有此类细菌分离株均为多重耐药。我们在所有分离株中均检测到某耐药基因;然而,没有分离株携带另一基因。RAPD-PCR将此类细菌分离株分为五个主要簇。在簇R4的分离株中观察到最高的抗生素耐药性。本研究结果还表明,分离株的抗菌耐药谱与基因分型特性之间存在关联。需要新型食品监测系统,包括对多重耐药食源性病原体的监测,尤其是在发展中国家,以控制食源性疾病。