U. S. Food and Drug Administration, Center for Food Safety and Applied Nutrition, Office of Applied Research and Safety Assessment, Laurel, MD 20708 USA.
U. S. Food and Drug Administration, Center for Food Safety and Applied Nutrition, Office of Applied Research and Safety Assessment, Laurel, MD 20708 USA.
Int J Food Microbiol. 2018 Nov 2;284:31-39. doi: 10.1016/j.ijfoodmicro.2018.06.016. Epub 2018 Jun 27.
Bacillus cereus strains were isolated from dried foods, which included international brands of spices from South East Asia, Mexico and India purchased from several retail stores, samples of powdered infant formula (PIF), medicated fish feed and dietary supplements. The genetic diversity of 64 strains from spices and PIF was determined using a multiplex endpoint PCR assay designed to identify hemolysin BL, nonhemolytic enterotoxin, cytotoxin K, and enterotoxin FM toxin genes. Thirteen different B. cereus toxigenic gene patterns or profiles were identified among the strains. Randomly selected B. cereus strains were sequenced and compared with reference Genomic Groups from National Center Biotechnology Information using bioinformatics tools. A comprehensive multi-loci sequence analysis (MLSA) was designed using alleles from 25 known MLST genes specifically tailored for use with whole genome assemblies. A cohort of representative genomes of strains from a few FDA regulated commodities like dry foods and medicated fish feed was used to demonstrate the utility of the 25-MLSA approach for rapid clustering and identification of Genome Groups. The analysis clustered the strains from medicated fish feed, dry foods, and dietary supplements into phylogenetically-related groups. 25-MLSA also pointed to a greater diversity of B. cereus strains from foods and feed than previously recognized. Our integrated approach of toxin gene PCR, and to our knowledge, whole genome sequencing (WGS) based sequence analysis, may be the first of its kind that demonstrates enterotoxigenic potential and genomic diversity in parallel.
蜡样芽胞杆菌菌株从干燥食品中分离出来,这些食品包括从几家零售店购买的来自东南亚、墨西哥和印度的国际品牌香料、粉状婴儿配方奶粉(PIF)、药用鱼饲料和膳食补充剂。使用设计用于鉴定溶血素 BL、非溶血肠毒素、细胞毒素 K 和肠毒素 FM 毒素基因的多重终点 PCR 检测法,确定了来自香料和 PIF 的 64 株菌的遗传多样性。在这些菌株中,确定了 13 种不同的蜡样芽胞杆菌产毒基因模式或图谱。随机选择的蜡样芽胞杆菌菌株进行测序,并使用生物信息学工具与美国国立生物技术信息中心的参考基因组群进行比较。使用专门针对全基因组组装设计的来自 25 个已知 MLST 基因的等位基因,设计了全面的多位点序列分析(MLSA)。使用来自 FDA 监管的几种商品(如干燥食品和药用鱼饲料)的代表性菌株的队列来证明 25-MLSA 方法用于快速聚类和鉴定基因组群的实用性。该分析将来自药用鱼饲料、干燥食品和膳食补充剂的菌株聚类到系统发育相关的组中。25-MLSA 还指出,食品和饲料中的蜡样芽胞杆菌菌株比以前认为的具有更大的多样性。我们的毒素基因 PCR 综合方法,以及据我们所知,基于全基因组测序(WGS)的序列分析,可能是首例同时证明产肠毒素潜力和基因组多样性的方法。