Expression and purification of recombinant H5HA1 protein of H5N1 avian influenza virus in E. coli and its application in indirect ELISA

Y. T. Redda, G. Venkatesh, S. Kalaiyarasu, S. Bhatia, D. S. Kumar, S. Nagarajan, A. Pillai, S. Tripathi, D. D. Kulkarni, S. C. Dubey
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Abstract

ABSTRACT The PCR amplified HA1 fragment of H5N1 (H5HA1) avian influenza virus (AIV) hemagglutinin gene was cloned into pET28a (+) expression vector and expressed in Rosetta Blue (DE3) pLysS cells. The recombinant H5HA1 (rH5HA1) protein purified by passive gel elution after SDS-PAGE of the inclusion bodies reacted specifically with H5N1 serum in Western blot analysis. A subtype specific indirect enzyme linked immunosorbent assay (iELISA) using the rH5HA1 protein as the coating antigen was developed for detecting antibodies to H5 subtype of AIV. The assay had 89.04% sensitivity and 95.95% specificity when compared with haemagglutination inhibition test. The Kappa value of 0.842 indicated a perfect agreement between the tests. The iELISA developed can be used for serosurveillance of avian influenza in chickens.
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H5N1禽流感病毒重组H5HA1蛋白在大肠杆菌中的表达纯化及其间接ELISA应用
将PCR扩增的H5N1 (H5HA1)禽流感病毒(AIV)血凝素基因HA1片段克隆到pET28a(+)表达载体中,在Rosetta Blue (DE3) pLysS细胞中表达。包涵体SDS-PAGE与H5N1血清特异性反应后,采用被动凝胶洗脱纯化重组H5HA1 (rH5HA1)蛋白。建立了以rH5HA1蛋白为包被抗原的AIV H5亚型特异性间接酶联免疫吸附试验(iELISA)。与血凝抑制试验相比,灵敏度为89.04%,特异性为95.95%。Kappa值为0.842,表明试验结果完全一致。开发的iELISA可用于鸡的禽流感血清监测。
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