Detection of PCR amplicons from bacterial pathogens using microsphere agglutination

被引:18
作者
Wu, SJ
Chan, A
Kado, CI
机构
[1] Natl Cent Univ, Dept Life Sci, Jhong Li City 320, Taoyuan, Taiwan
[2] Avenir Genet Technol Inc, Sacramento, CA 95818 USA
关键词
PCR amplicons; bacterial pathogens; microsphere agglutination; detection;
D O I
10.1016/j.mimet.2003.11.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
For rapid and inexpensive detection of polymerase chain reaction (PCR) amplicons, a novel microsphere agglutination assay has been developed. PCR is carried out using biotinylated forward and reverse primers, and the amplified DNA fragments are able to agglutinate streptavidin-coated microspheres (5.7 mum in diameter). Purification of PCR amplicons is unnecessary when initial primer concentrations are 250 nM. Agglutination can be identified visually within 2 min without any additional equipment or reagents. Using listeriolysin (lisA)-specific biotinylated primers, we have successfully detected and identified Listeria monocytogenes lisA(+) cells among Salmonella typhimurium, Staphylococcus aureus, Campylobacter jejuni and Escherichia coli O157:H7 cells. The simplicity of this protocol considerably reduces the time and cost of diagnostic PCR experiments. This procedure is potentially useful for various studies and field applications. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:395 / 400
页数:6
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