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Direct identification and molecular characterization of zoonotic hazards in raw milk by metagenomics using Brucella as a model pathogen

机译:使用布鲁氏菌作为模型病原体通过偏氧化物的直接鉴定和分子表征原料乳的含量危害

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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 Brucella 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 Brucella spp. in artificially and naturally contaminated raw milk from various ruminant species. With the depletion of eukaryotic cells prior to DNA extraction, Brucella was detectable at 10 bacterial cells ml?1, 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 Brucella 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.
机译:Metagenomics是一种有价值的诊断工具,用于增强微生物食品安全性,因为(i)它能够实现未明确的病原体检测,(ii)由于不需要微生物的原始分离,并且(iii)它具有高鉴别的动力用于病原体的详细分子表征。对于霰弹枪Metagenomics,从诸如食品的复杂样品中分离出总核酸(NAs)。随着微生物NAS,提取大量基质NAS,其在下一代测序期间可能在下一代测序期间递送微生物NAS,并且损害检测低丰度微生物的敏感性。敏感的实验方法对于检测Brucella SPP等高度致病性食源性细菌是必不可少的,因为由于污染的乳制品或肉类产品的消耗,低传染性剂量足以引起人类疾病。在我们的研究中,我们应用了Brucella SPP的鉴定和表征的霰弹枪Metagenomic测序。从各种反刍动物物种中人为而天然污染的原料乳。随着在DNA提取之前的真核细胞的耗尽,Brucella在10个细菌细胞ml-1中可检测,同时同时微生物培养和分离术语常见的细菌。此外,我们能够从偏见的数据集中检索Brucella分离物的基因型,表明使用SNP和核心基因组序列键入(CGMLST)的爆发调查的偏离调查的潜力。为了改善诊断应用,我们为基于SNP的应变预测开发了一种新的生物信息学方法,以识别正确的物种并限定一定的菌株,仅具有每种样本的特异性读数的少量留置。该管道原来是比Mash屏幕更敏感和特定的。在原料牛奶样品中,我们同时检测到许多其他动物区病原体,抗微生物抗性基因和毒力因子。我们的研究表明,Metagenomics是一种高度敏感的食品生物风险评估工具,特别是当病原体隔离是危险或挑战时。

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