Targeted Next Generation Sequencing Assay for Direct Detection and Serotyping of Salmonella from Enrichment

沙门氏菌 血清型 生物 DNA测序 计算生物学 微生物学 细菌 遗传学 基因
作者
Andrew Lin,Atul K. Singh,Adam Allred,Marc W. Allard,Doug Waltman,Behzad Imanian,Justin H. J. Ng,Yadollah Sanahmadi,Ramin Khaksar
出处
期刊:Journal of Food Protection [International Association for Food Protection]
卷期号:: 100256-100256
标识
DOI:10.1016/j.jfp.2024.100256
摘要

In this study, an automated, targeted next generation sequencing (tNGS) assay to detect and serotype Salmonella from sample enrichments was evaluated. The assay generates millions of reads to detect multiple Salmonella-specific genes and serotype-specific alleles, detecting all Salmonella spp. tested to date, and serotyping 62 common Salmonella serotypes. Accuracy was tested on 291 pure reference cultures (251 Salmonella, 40 non-Salmonella), 21 artificially contaminated poultry carcass rinse samples, and 363 naturally contaminated poultry environmental samples. Among the 291 pure reference cultures, the automated tNGS assay resulted in 100% detection accuracy, 100% serotyping accuracy for the claimed serotypes, and 0% false positives. The limit of detection was estimated at 5 x 104 CFU/mL by testing enumerated cultures of strains representative of six serotypes. In co-contamination studies with mixtures of two serotypes (Enteritidis, Typhimurium, Kentucky, Infantis, and Newport) at a 1:1 ratio, tNGS detected both serotypes with 100% accuracy. The assay demonstrated 100% accuracy in artificially contaminated poultry carcass rinse sample enrichments. Targeted NGS was highly effective in detecting Salmonella in samples collected from poultry production facilities. Results demonstrated that tNGS could detect Salmonella and provide accurate serotyping information consistent with conventional serology. These findings highlight reliable and efficient performance of a fully automated tNGS Salmonella assay in detecting and identifying Salmonella strains in complex matrices, reducing the time to results from 4-5 days required by the traditional isolation and serotyping to 10-12 hours for tNGS after primary enrichment.
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