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Antibiotic-induced gut bacteria depletion has no effect on HBV replication in HBV immune tolerance mouse model

Commensal microbiota is closely related to Hepatitis B virus (HBV) infection. Gut bacteria maturation accelerates HBV immune clearance in hydrodynamic injection (HDI) HBV mouse model. However, the effect of gut bacteria on HBV replication in recombinant adeno-associated virus (AAV)-HBV mouse model w...

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Autores principales: Bu, Yanan, Zhao, Kaitao, Xu, Zaichao, Zheng, Yingcheng, Hua, Rong, Wu, Chuanjian, Zhu, Chengliang, Xia, Yuchen, Cheng, Xiaoming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wuhan Institute of Virology, Chinese Academy of Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311260/
https://www.ncbi.nlm.nih.gov/pubmed/37141990
http://dx.doi.org/10.1016/j.virs.2023.04.010
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author Bu, Yanan
Zhao, Kaitao
Xu, Zaichao
Zheng, Yingcheng
Hua, Rong
Wu, Chuanjian
Zhu, Chengliang
Xia, Yuchen
Cheng, Xiaoming
author_facet Bu, Yanan
Zhao, Kaitao
Xu, Zaichao
Zheng, Yingcheng
Hua, Rong
Wu, Chuanjian
Zhu, Chengliang
Xia, Yuchen
Cheng, Xiaoming
author_sort Bu, Yanan
collection PubMed
description Commensal microbiota is closely related to Hepatitis B virus (HBV) infection. Gut bacteria maturation accelerates HBV immune clearance in hydrodynamic injection (HDI) HBV mouse model. However, the effect of gut bacteria on HBV replication in recombinant adeno-associated virus (AAV)-HBV mouse model with immune tolerance remains obscure. We aim to investigate its role on HBV replication in AAV-HBV mouse model. C57BL/6 mice were administrated with broad-spectrum antibiotic mixtures (ABX) to deplete gut bacteria and intravenously injected with AAV-HBV to establish persistent HBV replication. Gut microbiota community was analyzed by fecal qPCR assay and 16S ribosomal RNA (rRNA) gene sequencing. HBV replication markers in blood and liver were determined by ELISA, qPCR assay and Western blot at indicated time points. Immune response in AAV-HBV mouse model was activated through HDI of HBV plasmid or poly(I:C) and then detected by quantifying the percentage of IFN-γ(+)/CD8(+) T cells in the spleen via flow cytometry as well as the splenic IFN-γ mRNA level via qPCR assay. We found that antibiotic exposure remarkably decreased gut bacteria abundance and diversity. Antibiotic treatment failed to alter the levels of serological HBV antigens, intrahepatic HBV RNA transcripts and HBc protein in AAV-HBV mouse model, but contributed to HBsAg increase after breaking of immune tolerance. Overall, our data uncovered that antibiotic-induced gut bacteria depletion has no effect on HBV replication in immune tolerant AAV-HBV mouse model, providing new thoughts for elucidating the correlation between gut bacteria dysbiosis by antibiotic abuse and clinical chronic HBV infection.
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spelling pubmed-103112602023-07-01 Antibiotic-induced gut bacteria depletion has no effect on HBV replication in HBV immune tolerance mouse model Bu, Yanan Zhao, Kaitao Xu, Zaichao Zheng, Yingcheng Hua, Rong Wu, Chuanjian Zhu, Chengliang Xia, Yuchen Cheng, Xiaoming Virol Sin Research Article Commensal microbiota is closely related to Hepatitis B virus (HBV) infection. Gut bacteria maturation accelerates HBV immune clearance in hydrodynamic injection (HDI) HBV mouse model. However, the effect of gut bacteria on HBV replication in recombinant adeno-associated virus (AAV)-HBV mouse model with immune tolerance remains obscure. We aim to investigate its role on HBV replication in AAV-HBV mouse model. C57BL/6 mice were administrated with broad-spectrum antibiotic mixtures (ABX) to deplete gut bacteria and intravenously injected with AAV-HBV to establish persistent HBV replication. Gut microbiota community was analyzed by fecal qPCR assay and 16S ribosomal RNA (rRNA) gene sequencing. HBV replication markers in blood and liver were determined by ELISA, qPCR assay and Western blot at indicated time points. Immune response in AAV-HBV mouse model was activated through HDI of HBV plasmid or poly(I:C) and then detected by quantifying the percentage of IFN-γ(+)/CD8(+) T cells in the spleen via flow cytometry as well as the splenic IFN-γ mRNA level via qPCR assay. We found that antibiotic exposure remarkably decreased gut bacteria abundance and diversity. Antibiotic treatment failed to alter the levels of serological HBV antigens, intrahepatic HBV RNA transcripts and HBc protein in AAV-HBV mouse model, but contributed to HBsAg increase after breaking of immune tolerance. Overall, our data uncovered that antibiotic-induced gut bacteria depletion has no effect on HBV replication in immune tolerant AAV-HBV mouse model, providing new thoughts for elucidating the correlation between gut bacteria dysbiosis by antibiotic abuse and clinical chronic HBV infection. Wuhan Institute of Virology, Chinese Academy of Sciences 2023-05-02 /pmc/articles/PMC10311260/ /pubmed/37141990 http://dx.doi.org/10.1016/j.virs.2023.04.010 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Bu, Yanan
Zhao, Kaitao
Xu, Zaichao
Zheng, Yingcheng
Hua, Rong
Wu, Chuanjian
Zhu, Chengliang
Xia, Yuchen
Cheng, Xiaoming
Antibiotic-induced gut bacteria depletion has no effect on HBV replication in HBV immune tolerance mouse model
title Antibiotic-induced gut bacteria depletion has no effect on HBV replication in HBV immune tolerance mouse model
title_full Antibiotic-induced gut bacteria depletion has no effect on HBV replication in HBV immune tolerance mouse model
title_fullStr Antibiotic-induced gut bacteria depletion has no effect on HBV replication in HBV immune tolerance mouse model
title_full_unstemmed Antibiotic-induced gut bacteria depletion has no effect on HBV replication in HBV immune tolerance mouse model
title_short Antibiotic-induced gut bacteria depletion has no effect on HBV replication in HBV immune tolerance mouse model
title_sort antibiotic-induced gut bacteria depletion has no effect on hbv replication in hbv immune tolerance mouse model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311260/
https://www.ncbi.nlm.nih.gov/pubmed/37141990
http://dx.doi.org/10.1016/j.virs.2023.04.010
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