Quasispecies of Hepatitis C Virus Participate in Cell-Specific Infectivity

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作者
Takasuke Fukuhara
Satomi Yamamoto
Chikako Ono
Shota Nakamura
Daisuke Motooka
Hiroyuki Mori
Takeshi Kurihara
Asuka Sato
Tomokazu Tamura
Takashi Motomura
Toru Okamoto
Michio Imamura
Toru Ikegami
Tomoharu Yoshizumi
Yuji Soejima
Yoshihiko Maehara
Kazuaki Chayama
Yoshiharu Matsuura
机构
[1] Research Institute for Microbial Diseases,Department of Molecular Virology
[2] Osaka University,Department of Infection Metagenomics
[3] Laboratory of Veterinary Microbiology,Department of Surgery and Science
[4] School of Veterinary Medicine,Department of Gastroenterology and Metabolism
[5] Kitasato University,undefined
[6] Research Institute for Microbial Diseases,undefined
[7] Osaka University,undefined
[8] Graduate School of Medical Sciences,undefined
[9] Kyushu University,undefined
[10] Applied Life Sciences,undefined
[11] Institute of Biomedical & Health Sciences,undefined
[12] Hiroshima University,undefined
来源
Scientific Reports | / 7卷
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摘要
It is well documented that a variety of viral quasispecies are found in the patients with chronic infection of hepatitis C virus (HCV). However, the significance of quasispecies in the specific infectivity to individual cell types remains unknown. In the present study, we analyzed the role of quasispecies of the genotype 2a clone, JFH1 (HCVcc), in specific infectivity to the hepatic cell lines, Huh7.5.1 and Hep3B. HCV RNA was electroporated into Huh7.5.1 cells and Hep3B/miR-122 cells expressing miR-122 at a high level. Then, we adapted the viruses to Huh7 and Hep3B/miR-122 cells by serial passages and termed the resulting viruses HCVcc/Huh7 and HCVcc/Hep3B, respectively. Interestingly, a higher viral load was obtained in the homologous combination of HCVcc/Huh7 in Huh7.5.1 cells or HCVcc/Hep3B in Hep3B/miR-122 cells compared with the heterologous combination. By using a reverse genetics system and deep sequence analysis, we identified several adaptive mutations involved in the high affinity for each cell line, suggesting that quasispecies of HCV participate in cell-specific infectivity.
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