Department of Biological Safety, German Federal Institute for Risk Assessment, Berlin, Germany.
Department of Hygiene and Zoonoses, Faculty of Veterinary Medicine, Mansoura University, Mansoura, Egypt.
Microb Genom. 2021 May;7(5). doi: 10.1099/mgen.0.000552.
Metagenomics is a valuable diagnostic tool for enhancing microbial food safety because (i) it enables the untargeted detection of pathogens, (ii) it is fast since primary isolation of micro-organisms is not required, and (iii) it has high discriminatory power allowing for a detailed molecular characterization of pathogens. For shotgun metagenomics, total nucleic acids (NAs) are isolated from complex samples such as foodstuff. Along with microbial NAs, high amounts of matrix NAs are extracted that might outcompete microbial NAs during next-generation sequencing and compromise sensitivity for the detection of low abundance micro-organisms. Sensitive laboratory methods are indispensable for detecting highly pathogenic foodborne bacteria like spp., because a low infectious dose is sufficient to cause human disease through the consumption of contaminated dairy or meat products. In our study, we applied shotgun metagenomic sequencing for the identification and characterization of spp. in artificially and naturally contaminated raw milk from various ruminant species. With the depletion of eukaryotic cells prior to DNA extraction, was detectable at 10 bacterial cells ml, while at the same time microbiological culture and isolation of the fastidious bacteria commonly failed. Moreover, we were able to retrieve the genotype of a isolate from a metagenomic dataset, indicating the potential of metagenomics for outbreak investigations using SNPs and core-genome multilocus sequence typing (cgMLST). To improve diagnostic applications, we developed a new bioinformatics approach for strain prediction based on SNPs to identify the correct species and define a certain strain with only low numbers of genus-specific reads per sample. This pipeline turned out to be more sensitive and specific than Mash Screen. In raw milk samples, we simultaneously detected numerous other zoonotic pathogens, antimicrobial resistance genes and virulence factors. Our study showed that metagenomics is a highly sensitive tool for biological risk assessment of foodstuffs, particularly when pathogen isolation is hazardous or challenging.
宏基因组学是一种增强微生物食品安全的有价值的诊断工具,因为 (i) 它能够非靶向检测病原体,(ii) 它速度快,因为不需要对微生物进行初步分离,以及 (iii) 它具有高鉴别力,能够对病原体进行详细的分子特征分析。对于鸟枪法宏基因组学,从食品等复杂样本中分离总核酸 (NAs)。与微生物 NAs 一起,提取出大量的基质 NAs,这些 NAs 可能会在下一代测序过程中与微生物 NAs 竞争,并降低对低丰度微生物检测的敏感性。为了检测像 这样的高致病性食源性病原体,敏感的实验室方法是必不可少的,因为通过食用受污染的乳制品或肉类产品,低感染剂量就足以导致人类疾病。在我们的研究中,我们应用鸟枪法宏基因组测序来鉴定和表征来自不同反刍动物物种的人工和自然污染的生奶中的 。通过在 DNA 提取前耗尽真核细胞,在 10 个细菌细胞 ml 时可检测到 ,而同时微生物培养和常见的苛养菌分离通常会失败。此外,我们能够从宏基因组数据集中检索到一个 分离株的基因型,表明宏基因组学在使用 SNP 和核心基因组多位点序列分型 (cgMLST) 进行暴发调查方面具有潜力。为了改进诊断应用,我们开发了一种基于 SNP 的新生物信息学方法用于菌株预测,以识别正确的物种并仅使用每个样本中少量属特异性读段来定义特定菌株。该方法比 Mash Screen 更敏感和特异。在生奶样本中,我们同时检测到许多其他的人畜共患病原体、抗微生物药物耐药基因和毒力因子。我们的研究表明,宏基因组学是一种高度敏感的食品生物风险评估工具,特别是在病原体分离具有危害性或挑战性时。