Western Blot Detection of Human Anti-Chikungunya Virus Antibody with Recombinant Envelope 2 Protein
0
조회
0
다운로드
0
인용
0
참고문헌
키워드
초록
Chikungunya virus (CHIKV), a tropical pathogen, has re-emerged and has massive outbreaks abruptly all over the world. Containing many dominant epitopes, the envelope E2 protein of CHIKV has been explored for the vaccination or diagnosis. In the present study, the antigenicity of a recombinant expressed intrinsically disorder domain (IUD) of E2 was tested for the detection of the antibody against CHIKV through western blot method. The gene of the IUD of E2 was inserted into 2 different vectors and expressed as recombinant GST-E2 and recombinant MBP-E2 fusion protein, respectively. Two kinds of fusion proteins were tested with 30 CHIKV patient sera and 30 normal sera, respectively. Both proteins were detected by 25 patients sera (83.3%) and 1 normal serum (3.3%). This test showed a relatively high sensitivity and very high specificity of the recombinant E2 proteins to be used as diagnostic antigens against CHIKV infection.
Abstract
Chikungunya virus (CHIKV), a tropical pathogen, has re-emerged and has massive outbreaks abruptly all over the world. Containing many dominant epitopes, the envelope E2 protein of CHIKV has been explored for the vaccination or diagnosis. In the present study, the antigenicity of a recombinant expressed intrinsically disorder domain (IUD) of E2 was tested for the detection of the antibody against CHIKV through western blot method. The gene of the IUD of E2 was inserted into 2 different vectors and expressed as recombinant GST-E2 and recombinant MBP-E2 fusion protein, respectively. Two kinds of fusion proteins were tested with 30 CHIKV patient sera and 30 normal sera, respectively. Both proteins were detected by 25 patients sera (83.3%) and 1 normal serum (3.3%). This test showed a relatively high sensitivity and very high specificity of the recombinant E2 proteins to be used as diagnostic antigens against CHIKV infection.
참고문헌 (10)
- Burt FJ, "Mahalingam S, Heise MT. Chikungunya: a re-emerging virus", Lancet, 379, pp.662~671 (2012)
- Parida MM, "Rapid and real-time detection of Chikungunya virus by reverse transcription loop-mediated isothermal amplification assay", J Clin Microbiol, 45, pp.351~357 (2007)
- Kam YW, "Sero-prevalence and cross-reactivity of chikungunya virus specific anti-E2EP3 antibodies in arbovirus-infected patients", PLoS Negl Trop Dis, 9, pp.e3445~ (2015)
- Dudha N, "Host-pathogen interactome analysis of Chikungunya virus envelope proteins E1 and E2", Virus Genes, 50, pp.200~209 (2015)
- Goh LY, "A sensitive epitope-blocking ELISA for the detection of Chikungunya virus-specific antibodies in patients", J Virol Methods, 222, pp.55~61 (2015)
- Okabayashi T, "Detection of chikungunya virus antigen by a novel rapid immunochromatographic test", J Clin Microbiol, 53, pp.382~388 (2015)
- Tripathi NK, "Production of recombinant Chikungunya virus envelope 2 protein in Escherichia coli", Appl Microbiol Biotechnol, 98, pp.2461~2471 (2014)
- Kumar S, "Development of novel antibodies against non-structural proteins nsP1, nsP3 and nsP4 of chikungunya virus: potential use in basic research", Arch Virol (2015)
- Bhatnagar S, "Evaluation of multiple antigenic peptides based on the Chikungunya E2 protein for improved serological diagnosis of infection", Viral Immunol, 28, pp.107~112 (2015)
- 송경주, "A Rapid Diagnostic Test for Toxoplasmosis using Recombinant Antigenic N-terminal Half of SAG1 Linked with Intrinsically Unstructured Domain of GRA2 Protein", The Korean Journal of Parasitology, 51(5), pp.503~510 (2013), 대한기생충학ㆍ열대의학회
