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DOI 10.1016/j.jviromet.2007.09.007

Медицинская библиотека · Journal of virological methods · 2007

Evaluation of immunochromatography and commercial enzyme-linked immunosorbent assay for rapid detection of norovirus antigen in stool samples.

Khamrin Pattara, Nguyen Tuan Anh, Phan Tung Gia, Satou Kenji, Masuoka Yuichi, Okitsu Shoko, Maneekarn Niwat, Nishio Osamu, Ushijima Hiroshi

Сравнительное исследованиеОценочное исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

The efficiency of immunochromatography and commercial enzyme-linked immunosorbent assay (ELISA) kit (Denka Seiken Co. Ltd., Tokyo, Japan) were evaluated for rapid detection of norovirus (NoV) from stool specimens. A total of 503 stool specimens collected from infants and young children who suffered from acute gastroenteritis were tested for NoV by the NoV-immunochromatography kit, Denka ELISA kit, and by a monoplex RT-PCR method. The NoV-immunochromatography revealed 78.9% sensitivity, 96.4% specificity, and 92.4% efficiency with the monoplex RT-PCR method. The Denka ELISA kit had a sensitivity of 90.4%, specificity of 96.4%, and an efficiency level of 95%. The findings indicate that the newly developed NoV-immunochromatography kit provides the specificity equal to that of the Denka ELISA kit, even through the sensitivity of detection was lower. However, the advantage of the NoV-immunochromatography kit is less time consuming and simpler. The data show that both the Denka ELISA and the NoV-immunochromatography kits may be used as an alternative method for screening of NoV in stool samples.

Для цитирования: Khamrin Pattara, Nguyen Tuan Anh, Phan Tung Gia, Satou Kenji, Masuoka Yuichi, Okitsu Shoko, Maneekarn Niwat, Nishio Osamu, Ushijima Hiroshi. Evaluation of immunochromatography and commercial enzyme-linked immunosorbent assay for rapid detection of norovirus antigen in stool samples.. Journal of virological methods. 2007. DOI: 10.1016/j.jviromet.2007.09.007.

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