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首页> 外文期刊>Applied Microbiology >Use of Metagenomic Shotgun Sequencing Technology To Detect Foodborne Pathogens within the Microbiome of the Beef Production Chain
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Use of Metagenomic Shotgun Sequencing Technology To Detect Foodborne Pathogens within the Microbiome of the Beef Production Chain

机译:使用超基因组Shot弹枪测序技术来检测牛肉生产链微生物组中的食源性病原体

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Foodborne illnesses associated with pathogenic bacteria are a global public health and economic challenge. The diversity of microorganisms (pathogenic and nonpathogenic) that exists within the food and meat industries complicates efforts to understand pathogen ecology. Further, little is known about the interaction of pathogens within the microbiome throughout the meat production chain. Here, a metagenomic approach and shotgun sequencing technology were used as tools to detect pathogenic bacteria in environmental samples collected from the same groups of cattle at different longitudinal processing steps of the beef production chain: cattle entry to feedlot, exit from feedlot, cattle transport trucks, abattoir holding pens, and the end of the fabrication system. The log read counts classified as pathogens per million reads for Salmonella enterica , Listeria monocytogenes , Escherichia coli , Staphylococcus aureus , Clostridium spp. ( C. botulinum and C. perfringens ), and Campylobacter spp. ( C. jejuni , C. coli , and C. fetus ) decreased over subsequential processing steps. Furthermore, the normalized read counts for S. enterica , E. coli , and C. botulinum were greater in the final product than at the feedlots, indicating that the proportion of these bacteria increased (the effect on absolute numbers was unknown) within the remaining microbiome. From an ecological perspective, data indicated that shotgun metagenomics can be used to evaluate not only the microbiome but also shifts in pathogen populations during beef production. Nonetheless, there were several challenges in this analysis approach, one of the main ones being the identification of the specific pathogen from which the sequence reads originated, which makes this approach impractical for use in pathogen identification for regulatory and confirmation purposes.
机译:与病原菌相关的食源性疾病是全球公共卫生和经济挑战。食品和肉类行业中存在的微生物(致病性和非致病性)多样性使了解病原体生态的努力变得复杂。此外,关于整个肉类生产链中微生物组内病原体之间相互作用的了解甚少。在这里,宏基因组学方法和shot弹枪测序技术被用作检测在牛肉生产链的不同纵向加工步骤从同一组牛中采集的环境样品中的病原细菌的工具:牛进入饲养场,从饲养场退出,运牛车,屠宰场候宰栏和制作系统的结尾。原木读数计数被分类为每百万读数中的病原体,包括小肠沙门氏菌,单核细胞增生性李斯特菌,大肠杆菌,金黄色葡萄球菌,梭状芽孢杆菌。 (肉毒梭菌和产气荚膜梭菌)和弯曲杆菌属。 (空肠弯曲杆菌,大肠杆菌和胎儿弯曲杆菌)在后续加工步骤中减少了。此外,最终产品中肠炎链球菌,大肠杆菌和肉毒梭菌的标准化读取计数比饲养场要大,这表明这些细菌的比例在剩余物中增加了(对绝对数的影响未知)微生物组。从生态学的角度来看,数据表明shot弹枪宏基因组学不仅可以用于评估微生物组,而且可以用于评估牛肉生产过程中病原体种群的变化。尽管如此,这种分析方法仍存在一些挑战,其中主要的挑战之一是鉴定从其读取序列的特定病原体,这使得该方法在用于监管和确认目的的病原体鉴定中不切实际。

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