Difference of Intrahost Dynamics of the Second Human Pegivirus and Hepatitis C Virus in HPgV-2/HCV-Coinfected Patients
BackgroundThe second human pegivirus (HPgV-2) and hepatitis C virus (HCV) belong to the Flaviviridae family and share some common genome features. However, the two viruses exhibit significantly different genetic diversity. The comparison of intrahost dynamics of HPgV-2 and HCV that mainly reflect vi...
| 出版年: | Frontiers in Cellular and Infection Microbiology |
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| 主要な著者: | , , , , , , , , , , |
| フォーマット: | 論文 |
| 言語: | 英語 |
| 出版事項: |
Frontiers Media S.A.
2021-08-01
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| 主題: | |
| オンライン・アクセス: | https://www.frontiersin.org/articles/10.3389/fcimb.2021.728415/full |
| _version_ | 1852784646884950016 |
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| author | Yuanhao Liang Fengyu Hu Hang Fan Linghua Li Zhengwei Wan Haiying Wang Jingwei Shui Yuanping Zhou Yigang Tong Weiping Cai Shixing Tang Shixing Tang |
| author_facet | Yuanhao Liang Fengyu Hu Hang Fan Linghua Li Zhengwei Wan Haiying Wang Jingwei Shui Yuanping Zhou Yigang Tong Weiping Cai Shixing Tang Shixing Tang |
| author_sort | Yuanhao Liang |
| collection | DOAJ |
| container_title | Frontiers in Cellular and Infection Microbiology |
| description | BackgroundThe second human pegivirus (HPgV-2) and hepatitis C virus (HCV) belong to the Flaviviridae family and share some common genome features. However, the two viruses exhibit significantly different genetic diversity. The comparison of intrahost dynamics of HPgV-2 and HCV that mainly reflect virus-host interactions is needed to elucidate their intrahost difference of genetic diversity and the possible mechanisms.MethodsIntrahost single nucleotide variations (iSNVs) were identified by means of next-generation sequencing from both cross-sectional and longitudinal samples from HPgV-2- and HCV-coinfected patients. The levels of human cytokines were quantified in the patient before and after HCV elimination by the treatment of direct-acting antivirals (DAA).ResultsUnlike HCV, the viral sequences of HPgV-2 are highly conserved among HPgV-2-infected patients. However, iSNV analysis confirmed the intrahost variation or quasispecies of HPgV-2. Almost all iSNVs of HPgV-2 did not accumulate or transmit within host over time, which may explain the highly conserved HPgV-2 consensus sequence. Intrahost variation of HPgV-2 mainly causes nucleotide transition in particular at the 3rd codon position and synonymous substitutions, indicating purifying or negative selection posed by host immune system. Cytokine data further indicate that HPgV-2 infection alone may not efficiently stimulate innate immune responses since proinflammatory cytokine expression dramatically decreased with elimination of HCV.ConclusionThis study provided new insights into the intrahost genomic variations and evolutionary dynamics of HPgV-2 as well as the impact of host immune selection and virus polymerase on virus evolution. The different genetic diversity of HPgV-2 and HCV makes HPgV-2 a potential new model to investigate RNA virus diversity and the mechanism of viral polymerase in modulating virus replication. |
| format | Article |
| id | doaj-art-149e13b793364e8f8aa3d1efbe94fa2c |
| institution | Directory of Open Access Journals |
| issn | 2235-2988 |
| language | English |
| publishDate | 2021-08-01 |
| publisher | Frontiers Media S.A. |
| record_format | Article |
| spelling | doaj-art-149e13b793364e8f8aa3d1efbe94fa2c2025-08-19T20:46:30ZengFrontiers Media S.A.Frontiers in Cellular and Infection Microbiology2235-29882021-08-011110.3389/fcimb.2021.728415728415Difference of Intrahost Dynamics of the Second Human Pegivirus and Hepatitis C Virus in HPgV-2/HCV-Coinfected PatientsYuanhao Liang0Fengyu Hu1Hang Fan2Linghua Li3Zhengwei Wan4Haiying Wang5Jingwei Shui6Yuanping Zhou7Yigang Tong8Weiping Cai9Shixing Tang10Shixing Tang11Department of Epidemiology, School of Public Health, Southern Medical University, Guangzhou, ChinaGuangzhou Eighth People’s Hospital, Guangzhou Medical University, Guangzhou, ChinaState Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, ChinaGuangzhou Eighth People’s Hospital, Guangzhou Medical University, Guangzhou, ChinaDepartment of Epidemiology, School of Public Health, Southern Medical University, Guangzhou, ChinaDepartment of Epidemiology, School of Public Health, Southern Medical University, Guangzhou, ChinaDepartment of Epidemiology, School of Public Health, Southern Medical University, Guangzhou, ChinaDepartment of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, ChinaSchool of Life Science and Technology, Beijing University of Chemical Technology, Beijing, ChinaGuangzhou Eighth People’s Hospital, Guangzhou Medical University, Guangzhou, ChinaDepartment of Epidemiology, School of Public Health, Southern Medical University, Guangzhou, ChinaWenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, ChinaBackgroundThe second human pegivirus (HPgV-2) and hepatitis C virus (HCV) belong to the Flaviviridae family and share some common genome features. However, the two viruses exhibit significantly different genetic diversity. The comparison of intrahost dynamics of HPgV-2 and HCV that mainly reflect virus-host interactions is needed to elucidate their intrahost difference of genetic diversity and the possible mechanisms.MethodsIntrahost single nucleotide variations (iSNVs) were identified by means of next-generation sequencing from both cross-sectional and longitudinal samples from HPgV-2- and HCV-coinfected patients. The levels of human cytokines were quantified in the patient before and after HCV elimination by the treatment of direct-acting antivirals (DAA).ResultsUnlike HCV, the viral sequences of HPgV-2 are highly conserved among HPgV-2-infected patients. However, iSNV analysis confirmed the intrahost variation or quasispecies of HPgV-2. Almost all iSNVs of HPgV-2 did not accumulate or transmit within host over time, which may explain the highly conserved HPgV-2 consensus sequence. Intrahost variation of HPgV-2 mainly causes nucleotide transition in particular at the 3rd codon position and synonymous substitutions, indicating purifying or negative selection posed by host immune system. Cytokine data further indicate that HPgV-2 infection alone may not efficiently stimulate innate immune responses since proinflammatory cytokine expression dramatically decreased with elimination of HCV.ConclusionThis study provided new insights into the intrahost genomic variations and evolutionary dynamics of HPgV-2 as well as the impact of host immune selection and virus polymerase on virus evolution. The different genetic diversity of HPgV-2 and HCV makes HPgV-2 a potential new model to investigate RNA virus diversity and the mechanism of viral polymerase in modulating virus replication.https://www.frontiersin.org/articles/10.3389/fcimb.2021.728415/fullHPgV-2HCVHCV/HPgV-2 coinfectionintrahost variantscytokine |
| spellingShingle | Yuanhao Liang Fengyu Hu Hang Fan Linghua Li Zhengwei Wan Haiying Wang Jingwei Shui Yuanping Zhou Yigang Tong Weiping Cai Shixing Tang Shixing Tang Difference of Intrahost Dynamics of the Second Human Pegivirus and Hepatitis C Virus in HPgV-2/HCV-Coinfected Patients HPgV-2 HCV HCV/HPgV-2 coinfection intrahost variants cytokine |
| title | Difference of Intrahost Dynamics of the Second Human Pegivirus and Hepatitis C Virus in HPgV-2/HCV-Coinfected Patients |
| title_full | Difference of Intrahost Dynamics of the Second Human Pegivirus and Hepatitis C Virus in HPgV-2/HCV-Coinfected Patients |
| title_fullStr | Difference of Intrahost Dynamics of the Second Human Pegivirus and Hepatitis C Virus in HPgV-2/HCV-Coinfected Patients |
| title_full_unstemmed | Difference of Intrahost Dynamics of the Second Human Pegivirus and Hepatitis C Virus in HPgV-2/HCV-Coinfected Patients |
| title_short | Difference of Intrahost Dynamics of the Second Human Pegivirus and Hepatitis C Virus in HPgV-2/HCV-Coinfected Patients |
| title_sort | difference of intrahost dynamics of the second human pegivirus and hepatitis c virus in hpgv 2 hcv coinfected patients |
| topic | HPgV-2 HCV HCV/HPgV-2 coinfection intrahost variants cytokine |
| url | https://www.frontiersin.org/articles/10.3389/fcimb.2021.728415/full |
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