Integrating immunomagnetic bead enrichment with immunochromatography for the detection of in-fluenza A virus
10.3760/cma.j.issn.0254-5101.2016.04.015
- VernacularTitle:免疫磁珠富集与免疫层析一体化检测甲型流感病毒的研究
- Author:
Xuemin WU
;
Liping ZHANG
;
Xuezheng MA
;
Yong ZHAO
;
Jimin GAO
;
Kongxin HU
- Publication Type:Journal Article
- Keywords:
Influenza A virus;
Immunomagnetic beads;
Immunochromatography;
Rapid detection
- From:
Chinese Journal of Microbiology and Immunology
2016;36(4):310-315
- CountryChina
- Language:Chinese
-
Abstract:
Objective To establish a novel method by integrating immunomagnetic bead enrich-ment with immunochromatography for the detection of influenza A virus. Methods The immunomagnetic beads were prepared by using EDC/NHS method and then coupled with monoclonal antibodies against influ-enza A virus. A direct immunomagnetic beads-based immunochromatography for the detection of influenza A virus was developed by using double-antibody sandwich method and immunochromatography, which was fur-ther combined with immunomagnetic separation to establish the novel integrated method of immunomagnectic bead enrichment and immunochromatography. Clinical throat swab samples collected from patients with influ-enza A virus infection and healthy subjects were analyzed by the novel method and the results were compared with those by using the conventional colloidal gold immunochromatography to evaluate the specificity, sensi-tivity and positive coincidence rate of this established method. Results The direct immunomagnetic beads-based immunochromatography and the colloidal gold immunochromatography showed no significant differences in specificity and sensitivity and could be used to identify influenza A virus-positive samples with cycle threshold ( Ct) values less than or equal to 22 obtained by real-time PCR assay. The integrated method could identify positive samples with Ct values less than or equal to 28, indicating that the novel method was more sensitive. Conclusion The novel method by integrating immunomagnetic bead enrichment with immunochroma-tography was successfully established and suitable for the rapid and on-site detection of influenza A virus.
