Rapid Oligonucleotide Suspension Array-Based Multiplex Detection of Bacterial Pathogens

被引:4
|
作者
Zhao, Jinyin [1 ,2 ]
Kang, Lin [1 ]
Hu, Rui [3 ]
Gao, Shan [1 ]
Xin, Wenwen [1 ]
Chen, Weijun [1 ,2 ]
Wang, Jinglin [1 ]
机构
[1] Acad Mil Med Sci, Inst Microbiol & Epidemiol, State Key Lab Pathogen & Biosecur, Beijing 100071, Peoples R China
[2] Chinese Acad Sci, Beijing Inst Genom, Key Lab Genome Sci & Informat, Beijing 100029, Peoples R China
[3] Chinese Acad Sci, Inst Biophys, Key Lab Infect & Immunol, Beijing 100029, Peoples R China
关键词
POLYMERASE-CHAIN-REACTION; BEAD-BASED METHOD; VIBRIO-CHOLERAE; SHIGELLA-FLEXNERI; HIGH-THROUGHPUT; LEGIONELLA-PNEUMOPHILA; STAPHYLOCOCCUS-AUREUS; RESPIRATORY VIRUSES; ESCHERICHIA-COLI; FLOW-CYTOMETRY;
D O I
10.1089/fpd.2012.1476
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
A gene-specific microsphere suspension array coupled with 15-plex polymerase chain reaction (PCR) was developed to screen bacterial samples rapidly for 10 strains of bacteria: Shigella spp. (S. flexneri, S. dysenteriae, and S. sonnei), Staphylococcus aureus, Vibrio cholerae (serology O1 and O139), Legionella pneumophila, and Clostridium botulinum (types A, B, and E). Fifteen sets of highly validated primers were chosen to amplify target genes simultaneously. Corresponding oligonucleotide probes directly conjugated with microsphere sets were used to specifically identify PCR amplicons. Sensitivity tests revealed that the array coupled with single PCR was able to detect purified genomic DNA at concentrations as low as 10 copies/L, while the multiplex detection limit was 10-10(4) copies/L. The assay was validated using water samples artificially spiked with S. aureus and S. dysenteriae, as well as water specimens from swimming pools previously identified to contain S. aureus.
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页码:896 / 903
页数:8
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