TY - JOUR
T1 - ELISA for IgG-class antibody to hepatitis E virus based on a highly conserved, conformational epitope expressed in Eschericia coli
AU - Anderson, David A.
AU - Li, Fan
AU - Riddell, Michaela
AU - Howard, Teresa
AU - Seow, Heng Fong
AU - Torresi, Joseph
AU - Perry, Gillian
AU - Sumarsidi, Didi
AU - Shrestha, Santosh Man
AU - Shrestha, Iswar Lal
PY - 1999/8/1
Y1 - 1999/8/1
N2 - In assays based on most recombinant hepatitis E virus (HEV) antigens, the IgG antibody responses to HEV are observed commonly to wane or disappear after the acute phase of infection. Such IgG assays have therefore been used for the diagnosis of acute HEV infection, but they have limited usefulness in seroepidemiological studies. Using western immunoblotting, it was shown previously that the open reading frame (ORF) 2.1 antigen, representing the carboxy-terminal 267 amino acids (aa) of the capsid protein, exposes a conformational epitope which allows optimal detection of convalescent antibody compared to other proteins expressed in Eschericia coli. This conformational epitope is shown to be highly conserved between divergent human HEV isolates, and the development of a sensitive and highly specific enzyme immunoassay (ELISA) based on this recombinant antigen is described. The ORF2.1 ELISA allows the detection and quantitation of both acute- and convalescent phase HEV-specific IgG, and will help to define better the antibody responses to the virus and the prevalence of HEV infection worldwide. Copyright (C) 1999 Elsevier Science B.V.
AB - In assays based on most recombinant hepatitis E virus (HEV) antigens, the IgG antibody responses to HEV are observed commonly to wane or disappear after the acute phase of infection. Such IgG assays have therefore been used for the diagnosis of acute HEV infection, but they have limited usefulness in seroepidemiological studies. Using western immunoblotting, it was shown previously that the open reading frame (ORF) 2.1 antigen, representing the carboxy-terminal 267 amino acids (aa) of the capsid protein, exposes a conformational epitope which allows optimal detection of convalescent antibody compared to other proteins expressed in Eschericia coli. This conformational epitope is shown to be highly conserved between divergent human HEV isolates, and the development of a sensitive and highly specific enzyme immunoassay (ELISA) based on this recombinant antigen is described. The ORF2.1 ELISA allows the detection and quantitation of both acute- and convalescent phase HEV-specific IgG, and will help to define better the antibody responses to the virus and the prevalence of HEV infection worldwide. Copyright (C) 1999 Elsevier Science B.V.
KW - Conformational epitopes
KW - Convalescent reactivity
KW - Enzyme immunoassay
KW - HEV
KW - Seroprevalence
UR - http://www.scopus.com/inward/record.url?scp=0032779258&partnerID=8YFLogxK
U2 - 10.1016/S0166-0934(99)00069-5
DO - 10.1016/S0166-0934(99)00069-5
M3 - Article
C2 - 10488771
AN - SCOPUS:0032779258
SN - 0166-0934
VL - 81
SP - 131
EP - 142
JO - Journal of Virological Methods
JF - Journal of Virological Methods
IS - 1-2
ER -