Mining of novel target genes through Pan-genome analysis for Conventional PCR and Real-Time PCR detection of Staphylococcus argenteus in food

被引:2
作者
Huang, Jiahui [1 ,2 ]
Dai, Jingsha [1 ,3 ]
Liu, Ming [1 ]
Huang, Shixuan [1 ]
Wu, Yuwei [1 ]
Rong, Dongli [1 ]
Li, Yuanyu [1 ]
Zhao, Miao [1 ]
Li, Ying [1 ]
Zhang, Jumei [1 ]
Wu, Shi [1 ,4 ]
Wu, Qingping [1 ,4 ]
机构
[1] Guangdong Acad Sci, State Key Lab Appl Microbiol Southern China, Guangdong Prov Key Lab Microbial Safety & Hlth, Inst Microbiol,Natl Hlth Commiss Sci & Technol Inn, Guangzhou 510070, Guangdong, Peoples R China
[2] Shaanxi Univ Sci & Technol, Sch Food Sci & Engn, Sch Biomed & Pharmaceut Sci, Xian 710000, Peoples R China
[3] South China Agr Univ, Coll Food Sci, Guangzhou 510642, Peoples R China
[4] Guangdong Inst Microbiol, 100 Cent Xianlie Rd, Guangzhou 510070, Peoples R China
关键词
Staphylococcus argenteus; Pan-genome analysis; Novel target gene; Multiply PCR; Real-time PCR; CLONAL COMPLEX 75; MASS-SPECTROMETRY; AUREUS; IDENTIFICATION; INFECTIONS; TREE;
D O I
10.1016/j.foodcont.2024.110550
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Staphylococcus argenteus is a novel species of coagulase-positive staphylococci which was separated from Staphylococcus aureus in 2015. It can threaten human health like S. aureus but cannot identify with conventional biochemical or other convenient methods. In order to develop a more convenient, specific and sensitive detection method for S. argenteus , this study screen several candidate target genes for detecting S. argenteus specifically and conveniently using Pan-genome analysis. As a result, 20 specific target sequences of S. argenteus were found and five novel target genes of S. argenteus ( S. arg_16901 , S. arg_21105 , S. arg_22757 , S. arg_22771 and S. arg_24206 ) were performed well after validated assays. Based on the novel target S. arg_16901 , conventional PCR and realtime fluorescence quantitative PCR methods were established to detect and identify S. argenteus strains. The specificity of these methods was robustly verified by S. argenteus and non - S. argenteus species. With extracting DNA of the dilution, the sensitivity of the PCR method was 9.8 x 10 6 CFU/mL, and it could differentiate and detect S. argenteus , in the 9.8 x 10 3 CFU/mL in the 10 -dilution liquid sample without extracting DNA. After that, a novel multiplex PCR based on novel target genes S. arg_16901 and S. aureus -specific gene ( nuc ) was designed. This method could simultaneously differentiate S. argenteus and S. aureus strains. The results of sensitivity and specificity assays indicate that the specific target fragment S. arg_16901 not only exhibits excellent performance in detecting and differentiating S. argenteus from S. aureus in food samples but also demonstrates higher accuracy than MALDI-TOF MS. Moreover, this is the first report on the detection of S. argenteus using a species -specific gene without relying on other phenotype -based methods. Our research demonstrated that these specific target genes can be mined efficiently through a pan-genome analysis tool, and the novel PCR assays developed in this study offer a promising technique for rapid and accurate detection of S. argenteus from S. aureus and other Staphylococcus .
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页数:13
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