Àá½Ã¸¸ ±â´Ù·Á ÁÖ¼¼¿ä. ·ÎµùÁßÀÔ´Ï´Ù.
KMID : 0880220100480040419
Journal of Microbiology
2010 Volume.48 No. 4 p.419 ~ p.425
Development of a Latex Agglutination Test for Norovirus Detection
Lee Hee-tae

Cheon Doo-Sung
Jee Young-Mee
Kim Mi-Soon
Ko Gwang-Pyo
Park Young-Bin
Jeong Hae-Sook
Abstract
Norovirus (NoV) is the leading cause of acute gastroenteritis worldwide. Currently, reverse transcription polymerase chain reaction (RT-PCR) is used commonly to detect NoVs in both clinical and environmental samples. However, RT-PCR requires expensive equipment and cannot be performed on site. In this study, a latex agglutination test (LAT) using antibody-labeled latex beads for detecting NoVs was developed. Two kinds of polyclonal antibodies, one generated from synthetic peptides and the other from E. coli-expressed NoV capsid proteins, were used to develop the LAT. Each of these polyclonal antibodies was immobilized on the surface of latex beads and tested for the ability to detect NoVs. Under optimized conditions, our LAT detected GII.4 NoV at concentrations as low as 3.3¡¿105 RT-PCR units/ml in stool samples. The detection limit for the LAT was approximately 1.7¡¿103 RT-PCR units. Forty-eight stool samples were tested for NoVs using this LAT. In comparison with an RT-PCR assay, the sensitivity and specificity of the LAT were 35% and 100%, respectively. With further optimization, this LAT used with appropriate antibodies could be applied for convenient detection of NoVs in clinical diagnosis and food monitoring.
KEYWORD
polyclonal antibody, latex agglutination test (LAT), norovirus, rapid detection, sensitivity, specificity
FullTexts / Linksout information
Listed journal information
MEDLINE ÇмúÁøÈïÀç´Ü(KCI) ´ëÇÑÀÇÇÐȸ ȸ¿ø