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Susceptibility of human T-lymphotropic virus type I infected cell line MT-2 to hepatitis C virus infection.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 1995 Jan 26; Vol. 206 (3), pp. 863-9. - Publication Year :
- 1995
-
Abstract
- To obtain a hepatitis C virus (HCV) proliferation system, we examined the susceptibility of various cultured cell lines to HCV infection. We found that a human T-lymphotropic virus type I infected cell line MT-2 was fairly sensitive to HCV infection. Using the polymerase chain reaction, intracellular positive-stranded HCV RNA was detected until at least 15 days postinoculation (p.i.). Intracellular negative-stranded HCV RNA was also detected at 10 days p.i., although not at 7 days p.i., suggesting that HCV is replicating in MT-2 cells 10 days p.i. Sequence analysis of hypervariable region 1 (HVR1) revealed that HVR1 sequences from cells 10 days p.i. had become homogeneous, although HVR1 sequences from the inoculum showed the typical quasi-species. We also found a lack of anti-HVR1 antibody against the HVR1 species which became homogeneous at 10 days p.i., although we easily detected antibody against the other HVR1 species obtained from the inoculum. These findings suggest that MT-2 cells are susceptible to HCV infection and are capable of supporting HCV replication.
- Subjects :
- Amino Acid Sequence
Animals
Base Sequence
Carcinoma, Hepatocellular
Cell Line
Hepacivirus genetics
Humans
Kidney
Leukemia
Liver Neoplasms
Molecular Sequence Data
Polymerase Chain Reaction
RNA, Viral analysis
Swine
Tumor Cells, Cultured
Viral Envelope Proteins analysis
Viral Envelope Proteins chemistry
Viral Envelope Proteins genetics
Virus Cultivation
Hepacivirus growth & development
Human T-lymphotropic virus 1 growth & development
Subjects
Details
- Language :
- English
- ISSN :
- 0006-291X
- Volume :
- 206
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 7832798
- Full Text :
- https://doi.org/10.1006/bbrc.1995.1123