TY - JOUR
T1 - Replication of hepatitis C virus in ascitic mononuclear cells with development of distinct viral quasispecies
AU - Hsu, Chao Wei
AU - Yeh, Chau Ting
AU - Chen, Peggy Guey Chi
AU - Liaw, Yun Fan
PY - 1999
Y1 - 1999
N2 - To investigate whether distinct compositions of viral quasispecies developed in the ascitic fluid of patients with late-stage chronic hepatitis C virus (HCV) infection, samples of various origins, including ascitic fluid and ascitic mononuclear cells (AMCs), were analyzed by the method of single- strand conformation polymorphism (SSCP). Subsequently, the major species were isolated, sequenced, and subjected to phylogenetic analysis. Of 42 patients analyzed, HCV-RNA was detectable in the AMCs of 25 patients. SSCP analysis indicated that the compositions of viral quasispecies among samples of different origins were markedly different in this group of patients. Phylogenetic analysis revealed that the ascitic-fluid-derived clones were most closely related to the AMC-derived clones. Minus-strand HCV-RNA was detectable in 5 of them. Our data suggest that HCV can replicate in the AMCs of patients with late-stage chronic HCV, which results in the development of distinct viral quasispecies.
AB - To investigate whether distinct compositions of viral quasispecies developed in the ascitic fluid of patients with late-stage chronic hepatitis C virus (HCV) infection, samples of various origins, including ascitic fluid and ascitic mononuclear cells (AMCs), were analyzed by the method of single- strand conformation polymorphism (SSCP). Subsequently, the major species were isolated, sequenced, and subjected to phylogenetic analysis. Of 42 patients analyzed, HCV-RNA was detectable in the AMCs of 25 patients. SSCP analysis indicated that the compositions of viral quasispecies among samples of different origins were markedly different in this group of patients. Phylogenetic analysis revealed that the ascitic-fluid-derived clones were most closely related to the AMC-derived clones. Minus-strand HCV-RNA was detectable in 5 of them. Our data suggest that HCV can replicate in the AMCs of patients with late-stage chronic HCV, which results in the development of distinct viral quasispecies.
UR - http://www.scopus.com/inward/record.url?scp=0033383717&partnerID=8YFLogxK
U2 - 10.1086/315035
DO - 10.1086/315035
M3 - 文章
C2 - 10479123
AN - SCOPUS:0033383717
SN - 0022-1899
VL - 180
SP - 992
EP - 1000
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 4
ER -