Rapid identification of Bacteroides dorei using novel specific target revealed by pan-genome analysis and its application in food

被引:0
|
作者
Xie, Zhiqing [1 ]
Huang, Aohuan [1 ,2 ]
Xie, Jihang [1 ,2 ]
Yu, Shubo [2 ]
Chen, Mengfei [1 ,2 ]
Cai, Jie [1 ,2 ]
Huang, Rong [1 ,2 ]
Zhu, Zhenjun [1 ]
Ding, Yu [1 ]
机构
[1] Jinan Univ, Inst Food Safety & Nutr, Coll Life Sci & Technol, Dept Food Sci & Engn, Guangzhou, Peoples R China
[2] Guangdong Acad Sci, Inst Microbiol, State Key Lab Appl Microbiol Southern China, Guangdong Prov Key Lab Microbial Safety & Hlth, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Bacteroides dorei; Novel molecular targets; Pan-genome analysis; Food detection; REAL-TIME PCR; ESCHERICHIA-COLI; FRAGILIS; PROTECTS;
D O I
10.1016/j.lwt.2024.116557
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Bacteroides dorei is a promising candidate for the next-generation probiotics (NGP), but its accurate identification remains challenging due to its close taxonomic relationship with other Bacteroides species. This study aimed to mine the novel specific molecular target for detecting Bacteroides dorei. Using pan-genome analysis and PCR validation, species-specific target genes with a size of 193 bp were identified, and the specificity of the designed primer pair (30 bp) for this molecular target was confirmed. The PCR assay demonstrated high applicability for detecting target and/or nontarget strains in three simulated food systems, yielding no false-positive or falsenegative results. Additionally, a qPCR method was developed for quantifying Bacteroides dorei, with a linear detection range from 1 x 108 to 1 x 101 CFU/mL and an R2 value greater than 0.98. This method exhibited accurate and sensitive detection capabilities suitable for both food and feces samples. Overall, our study established PCR and qPCR assays for the rapid identification of Bacteroides dorei, advancing the exploration of Bacteroides species and the application of detection for NGPs in functional foods across various product forms.
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页数:8
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