Gonzalez-Escalona Narjol, Kwon Hee Jin, Chen Yi
Genomics Development and Applications Branch, Division of Food Safety Genomics, Office of Applied Microbiology and Technology (OAMT), Office of Laboratory Operations and Applied Science (OLOAS), Human Foods Program, Food & Drug Administration, College Park, MD 20740, USA.
Microbial Methods Development Branch, Division of Food and Environmental Safety, Office of Applied Microbiology and Technology (OAMT), Office of Laboratory Operations and Applied Science (OLOAS), Human Foods Program, Food & Drug Administration, College Park, MD 20740, USA.
Microorganisms. 2024 Nov 22;12(12):2389. doi: 10.3390/microorganisms12122389.
Precision metagenomic approaches using Oxford Nanopore Technology (ONT) sequencing has been shown to allow recovery of complete genomes of foodborne bacteria from overnight enrichments of agricultural waters. This study tests the applicability of a similar approach for genome recovery from powdered infant formula (PIF) overnight enrichments, where typically dominates the overall microbiome (>90%). This study aimed to test whether using ONT sequencing of overnight PIF enrichments could recover a completely closed genome for further genomic characterization. Ten PIF samples, each inoculated with different strains, covering , , , , and , were processed according to the Bacteriological Analytical Manual (BAM) protocol. Real-time quantitative PCR (qPCR) was used for initial screening (detection and quantification) of the overnight enrichments and confirmed that the inoculated PIF samples after the overnight enrichment had high levels of (10 to 10 CFU/mL). DNA from overnight PIF enrichments was extracted from the enrichment broth and sequenced using ONT. Results showed that ONT sequencing could accurately identify, characterize, and close the genomes of strains from overnight PIF enrichments in 3 days, much faster than the nearly 2 weeks required by the current BAM method. Complete genome recovery and species differentiation were achieved. This suggests that combining qPCR with ONT sequencing provides a rapid, cost-effective alternative for detecting and characterizing in PIF, enabling timely corrective actions during outbreaks.
使用牛津纳米孔技术(ONT)测序的精准宏基因组学方法已被证明能够从农业用水的过夜富集培养物中获得食源细菌的完整基因组。本研究测试了一种类似方法从婴儿配方奶粉(PIF)过夜富集培养物中进行基因组恢复的适用性,其中 通常在总体微生物组中占主导地位(>90%)。本研究旨在测试对PIF过夜富集培养物进行ONT测序是否能够获得一个完全封闭的基因组用于进一步的基因组特征分析。按照《细菌学分析手册》(BAM)方案处理了10个PIF样本,每个样本接种不同的菌株,涵盖 、 、 、 以及 。实时定量PCR(qPCR)用于过夜富集培养物的初始筛选(检测和定量),并确认过夜富集后的接种PIF样本含有高水平的 (10至10 CFU/mL)。从过夜PIF富集培养物的富集肉汤中提取DNA,并使用ONT进行测序。结果表明,ONT测序能够在3天内准确识别、表征并封闭过夜PIF富集培养物中 菌株的基因组,比当前BAM方法所需的近2周时间快得多。实现了完整基因组的恢复和物种分化。这表明将qPCR与ONT测序相结合为检测和表征PIF中的 提供了一种快速、经济高效的替代方法,能够在疫情爆发期间及时采取纠正措施。