Department of Microbiology, School of Biological Sciences, Faculty of Natural and Agricultural Sciences, North-West University, Private Bag X2046, Mmabatho, 2735, South Africa.
Food Security and Safety Niche Area, Faculty of Natural and Agricultural Sciences, North-West University, Private Bag X2046, Mmabatho, 2735, South Africa.
Environ Sci Pollut Res Int. 2018 Nov;25(32):32694-32708. doi: 10.1007/s11356-018-3231-4. Epub 2018 Sep 22.
In this study, three hundred presumptive Salmonella strains isolated from cattle faeces and raw beef samples were subjected to both preliminary and confirmatory tests specific for Salmonella. PCR assays revealed that 100%, 20% and 26.7% of the isolates were positive for 16S rRNA, fliC and fljB gene fragments, respectively. Large proportions (62.4 to 94.3%) of these isolates were multiple antibiotic resistant (MAR) strains that were resistant to three or more antibiotics belonging to different classes. MAR phenotypes Ab1, Ab2, Ab3, Ab7, Ab8, Ab9, Ab26 and Ab27 were dominant among the isolates. Cluster analysis of antibiotic inhibition zone diameter data revealed two major clusters (clusters 1 and 2), and each cluster contained two sub-clusters (1A, 1B, 2A and 2B). PCR data revealed that 27.1% and 30.7% of the isolates possessed the spvC and invA virulent genes, respectively. There was a significant correlation between the possession of MAR phenotypes and virulent gene determinants. Analysis of restriction fragment length polymorphism (RFLP) of 16S rRNA gene fragments using EcoRI and HaeIII showed that large proportions of isolates from beef and cattle faeces produced similar genetic fingerprints. From these results, it is suggested that Salmonella species in cattle are transmitted to beef and, therefore, the consumption of undercooked beef could pose severe health complications on consumers. These findings provide baseline data that could be of great epidemiological importance and, thus, the need to utilise more sensitive typing tools in determining the genetic relatedness of isolates from different sources.
在这项研究中,从牛粪便和生牛肉样本中分离出的 300 株疑似沙门氏菌菌株分别进行了针对沙门氏菌的初步和确认试验。PCR 检测结果显示,16S rRNA、fliC 和 fljB 基因片段的阳性率分别为 100%、20%和 26.7%。这些分离株中很大一部分(62.4%至 94.3%)是对属于不同类别的三种或三种以上抗生素具有耐药性的多重抗生素耐药(MAR)菌株。MAR 表型 Ab1、Ab2、Ab3、Ab7、Ab8、Ab9、Ab26 和 Ab27 在分离株中占主导地位。抗生素抑菌圈直径数据的聚类分析显示出两个主要聚类(聚类 1 和 2),每个聚类包含两个亚聚类(1A、1B、2A 和 2B)。PCR 数据显示,27.1%和 30.7%的分离株分别携带 spvC 和 invA 毒力基因。MAR 表型和毒力基因决定簇之间存在显著相关性。对 16S rRNA 基因片段的 EcoRI 和 HaeIII 限制酶切片段长度多态性(RFLP)分析表明,来自牛肉和牛粪便的大量分离株产生了相似的遗传指纹。根据这些结果,表明牛中的沙门氏菌物种传播到牛肉中,因此,食用未煮熟的牛肉可能会对消费者造成严重的健康并发症。这些发现提供了基础数据,这些数据可能具有重要的流行病学意义,因此需要在确定来自不同来源的分离株的遗传相关性时使用更敏感的分型工具。