A longitudinal study of a novel dot-enzyme-linked immunosorbent assay for detection of avian influenza virus

H Lu - Avian diseases, 2003 - meridian.allenpress.com
Avian diseases, 2003meridian.allenpress.com
A monoclonal antibody (MAb)-based dot-enzyme-linked immunosorbent assay (ELISA) has
been developed that detected the epitopes specifically associated with avian influenza virus
(AIV). The dot-ELISA detected the antigens of AIV directly from clinical and field specimens.
Data obtained from experimentally AIV-infected specific-pathogen-free chickens and also
the 2001/02 AIV outbreak of serotype H7N2 positive flocks in Pennsylvania indicated that
the mean sensitivity (Se) of the dot-ELISA ranged between 45% and 68% and the mean …
Abstract
A monoclonal antibody (MAb)-based dot-enzyme-linked immunosorbent assay (ELISA) has been developed that detected the epitopes specifically associated with avian influenza virus (AIV). The dot-ELISA detected the antigens of AIV directly from clinical and field specimens. Data obtained from experimentally AIV-infected specific-pathogen-free chickens and also the 2001/02 AIV outbreak of serotype H7N2 positive flocks in Pennsylvania indicated that the mean sensitivity (Se) of the dot-ELISA ranged between 45% and 68% and the mean specificity (Sp), between 85% and 90%. The values were derived from various clinical and field specimens when compared with virus isolation with embryonating chicken eggs. On routine AIV surveillance samples, the dot-ELISA achieved a 92%–100% Sp on the basis of testing over 1500 AIV surveillance samples that were confirmed negative by virus isolation. The dot-ELISA detected AIV antigens with a 5-µl allantoic fluid sample that contained a concentration of 0.4 hemagglutinating units. Furthermore, the dot-ELISA retained its specificity for AIV because no cross-reactions were obtained with various other avian viruses. The findings in this study indicated that the dot-ELISA was highly sensitive and specific and comparable with the commercial Directigen® test in the detection of AIV obtained from clinical and field specimens.
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