Use of a TT virus ORF1 recombinant protein to detect anti-TT virus antibodies in human sera

被引:44
作者
Ott, C
Duret, L
Chemin, I
Trépo, C
Mandrand, B
Komurian-Pradel, F
机构
[1] Ecole Normale Super Lyon, CNRS BioMerieux, Unite Mixte Rech 2142, F-69364 Lyon 07, France
[2] Univ Lyon 1, Lab Biometrie Genet & Biol Populat, CNRS, UMR 5558, F-69622 Villeurbanne, France
[3] INSERM, U271, F-69424 Lyon 03, France
关键词
D O I
10.1099/0022-1317-81-12-2949
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
TT virus (TTV), isolated initially from a Japanese patient with hepatitis of unknown aetiology, has since been found to infect both healthy and diseased individuals and numerous prevalence studies have raised questions about its role in unexplained hepatitis. In order to determine the prevalence of ongoing TTV infection as well as resolved infection, a serological study was performed with a recombinant protein generated from the open reading frame 1 (ORF1) sequence isolated from a French patient infected by TTV. The C-terminal end of the ORF1 protein, containing a particularly hydrophilic region, was retained to be used as antigen to detect the presence of anti-TTV antibodies in serum samples by a Western blot analysis. For this purpose, the C-terminal ORF1 region was expressed in fusion with a hexahistidine tail in E. coli and purified by metal-chelate affinity chromatography. The serological screening of 70 human sera, including 30 patients with hepatitis of unknown aetiology, 30 blood donors and 10 healthy children, allowed the immune response of infected hosts to be identified by the detection of TTV-specific antibodies, with a very high prevalence of 98.6% in the human sera tested. In contrast, TTV DNA was detected by PCR in only 76.1% of the tested sera. The use of the ORF1 C-terminal recombinant protein thereby provided a diagnostic tool to follow the immune response of the host against TTV.
引用
收藏
页码:2949 / 2958
页数:10
相关论文
共 49 条
[1]   TT virus infection is widespread in the general populations from different geographic regions [J].
Abe, K ;
Inami, T ;
Asano, K ;
Miyoshi, C ;
Masaki, N ;
Hayashi, S ;
Ishikawa, KI ;
Takebe, Y ;
Win, KM ;
El-Zayadi, AR ;
Han, KH ;
Zhang, DY .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (08) :2703-2705
[2]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[3]   Determination and phylogenetic analysis of partial sequences from TT virus isolates [J].
Biagini, P ;
Gallian, P ;
Attoui, H ;
Cantaloube, JF ;
de Micco, P ;
de Lamballerie, X .
JOURNAL OF GENERAL VIROLOGY, 1999, 80 :419-424
[4]   TT-virus infection in North American blood donors, patients with fulminant hepatic failure, and cryptogenic cirrhosis [J].
Charlton, M ;
Adjei, P ;
Poterucha, J ;
Zein, N ;
Moore, B ;
Therneau, T ;
Krom, R ;
Wiesner, R .
HEPATOLOGY, 1998, 28 (03) :839-842
[5]   Prevalence of TT virus infection in US blood donors and populations at risk for acquiring parenterally transmitted viruses [J].
Desai, SM ;
Muerhoff, AS ;
Leary, TP ;
Erker, JC ;
Simons, JN ;
Chalmers, ML ;
Birkenmeyer, LG ;
Pilot-Matias, TJ ;
Mushahwar, IK .
JOURNAL OF INFECTIOUS DISEASES, 1999, 179 (05) :1242-1244
[6]   Analyses of TT virus full-length genomic sequences [J].
Erker, JC ;
Leary, TP ;
Desai, SM ;
Chalmers, ML ;
Mushahwar, IK .
JOURNAL OF GENERAL VIROLOGY, 1999, 80 :1743-1750
[7]   TT virus (TTV) is not associated with acute sporadic hepatitis [J].
Fukuda, Y ;
Nakano, I ;
Katano, Y ;
Kumada, T ;
Hayashi, K ;
Nakano, S ;
Hayakawa, T .
INFECTION, 1999, 27 (02) :125-127
[8]   Complete circular DNA genome of a TT virus variant (isolate name SANBAN) and 44 partial ORF2 sequences implicating a great degree of diversity beyond genotypes [J].
Hijikata, M ;
Takahashi, K ;
Mishiro, S .
VIROLOGY, 1999, 260 (01) :17-22
[9]  
Höhne M, 1998, J GEN VIROL, V79, P2761
[10]   PREDICTION OF PROTEIN ANTIGENIC DETERMINANTS FROM AMINO-ACID-SEQUENCES [J].
HOPP, TP ;
WOODS, KR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (06) :3824-3828