食品科学 ›› 2022, Vol. 43 ›› Issue (6): 347-352.doi: 10.7506/spkx1002-6630-20210115-165

• 安全检测 • 上一篇    

高通量测序检测米线中的食源性致病菌

吴怡,刘露露,吴永民,代诗琼,商颖,曹建新,韩鹏   

  1. (昆明理工大学食品科学与工程学院,云南昆明 650500)
  • 出版日期:2022-03-25 发布日期:2022-03-28
  • 基金资助:
    云南食源性致病菌溯源技术及其风险评价的研究课题(2018BC006)

Analysis of Foodborne Pathogenic Bacteria in Rice Noodles by High-throughput 16S rDNA Sequencing

WU Yi, LIU Lulu, WU Yongmin, DAI Shiqiong, SHANG Ying, CAO Jianxin, HAN Peng   

  1. (Faculty of Food Science and Engineering, Kunming University of Science and Technology, Kunming 650500, China)
  • Online:2022-03-25 Published:2022-03-28

摘要: 为了解米线中食源性致病菌的污染情况,分析其细菌多样性随时间变化趋势,研究从原料到餐桌中各个环节米线样品中食源性致病菌的变化。采用高通量测序对10?个米线样本中细菌16S rDNA区域进行测序分析,测序结果一共注释到5?个门、11?个纲、19?个目、24?个科和29?个属的微生物信息。分析表明,在所有样品中,变形菌门均占据50%以上相对丰度,其次为厚壁菌门,沙门菌属和芽孢杆菌属在各样品中均有发现。同时在原料样品和米线样品中还检出了葡萄球菌属、埃希氏杆菌属和李斯特菌属。利用传统培养法对10 个样品进行检测,发现蜡样芽孢杆菌、沙门菌在各样品中均有检出,在原料和产品样品中也确实存在金黄色葡萄球菌、大肠杆菌O157:H7和单核细胞性李斯特菌,证明米线确实存在一定的食用风险。研究分析了不同阶段的米线样品中菌群的动态变化,为控制米线微生物污染,消除潜在的食用风险提供理论依据。

关键词: 米线;高通量测序;16S rDNA;传统培养;食源性致病菌;安全风险

Abstract: In order to understand foodborne pathogen contamination in rice noodles, the temporal trend in the bacterial flora structure in rice noodles from raw material to table was investigated. High-throughput 16S rDNA sequencing was used to analyze the bacterial community in ten rice noodle samples. The results showed that the sequencing data were annotated into 5 phyla, 11 classes, 19 orders, 24 families and 29 genera. Also, it was found that the relative abundance of Proteobacteria was more than 50% in all samples, followed by Firmicutes. Salmonella and Bacillus were found in all samples. Staphylococcus, Escherichia and Listeria were found in the raw materials and final products. Bacillus cereus and Salmonella were detected in each sample. Staphylococcus aureus, Escherichia coli O157:H7 and Listeria monocytogenes were also detected in the raw materials and products, suggesting that there is a safety risk on the consumption of rice noodles.

Key words: rice noodles; high-throughput sequencing; 16S rDNA; conventional bacterial culture; foodborne pathogenic bacteria; safety risk

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