Development and characterization of a pseudovirus system for human Aichi virus: in vitro and in vivo analysis

Abstract Human Aichi virus (AiV) (genus Kobuvirus, family Picornaviridae) has been described as a causative agent of human gastroenteritis since 1989. However, research on AiV at cellular and animal levels is limited. Utilizing a double reporter gene system, we constructed an AiV capsid protein plas...

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Main Authors: Ruojun Wu, Jingli Tian, Shunchang Fan, Minyi Liang, Yucheng Li, Ying Deng, Binbin Tang, Minyi Zhang, Qing Chen
Format: Article
Language:English
Published: BMC 2025-07-01
Series:Virology Journal
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Online Access:https://doi.org/10.1186/s12985-025-02839-y
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author Ruojun Wu
Jingli Tian
Shunchang Fan
Minyi Liang
Yucheng Li
Ying Deng
Binbin Tang
Minyi Zhang
Qing Chen
author_facet Ruojun Wu
Jingli Tian
Shunchang Fan
Minyi Liang
Yucheng Li
Ying Deng
Binbin Tang
Minyi Zhang
Qing Chen
author_sort Ruojun Wu
collection DOAJ
description Abstract Human Aichi virus (AiV) (genus Kobuvirus, family Picornaviridae) has been described as a causative agent of human gastroenteritis since 1989. However, research on AiV at cellular and animal levels is limited. Utilizing a double reporter gene system, we constructed an AiV capsid protein plasmid and genomic backbone Replicon. Subsequently, AiV pseudovirus (AiV PsV) particles were packaged using a three-plasmid co-transfection system. Eleven cell types were screened to identify those susceptible to AiV PsV. Mouse models were established with AiV PsV to determine the optimal mouse species, mode of infection, and detection time, and investigate distribution characteristics of AiVs in vivo. HeLa cells exhibited the highest sensitivity to AiV PsV. A BALB/c mouse model established with bioluminescence imaging performed 24 h after infection via intraperitoneal injection demonstrated that the bioluminescent signal was concentrated in the murine abdominal cavity. The AiV PsV system should advance understanding of the infectious features of AiVs.
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institution Kabale University
issn 1743-422X
language English
publishDate 2025-07-01
publisher BMC
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series Virology Journal
spelling doaj-art-7181caf05d6440f79e9cd16ed146c6e82025-08-20T03:42:19ZengBMCVirology Journal1743-422X2025-07-0122111010.1186/s12985-025-02839-yDevelopment and characterization of a pseudovirus system for human Aichi virus: in vitro and in vivo analysisRuojun Wu0Jingli Tian1Shunchang Fan2Minyi Liang3Yucheng Li4Ying Deng5Binbin Tang6Minyi Zhang7Qing Chen8Department of Epidemiology, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical UniversityDepartment of Epidemiology, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical UniversityDepartment of Epidemiology, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical UniversityDepartment of Epidemiology, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical UniversityDepartment of Epidemiology, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical UniversityDepartment of Epidemiology, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical UniversityDepartment of Epidemiology, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical UniversityDepartment of Epidemiology, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical UniversityDepartment of Epidemiology, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical UniversityAbstract Human Aichi virus (AiV) (genus Kobuvirus, family Picornaviridae) has been described as a causative agent of human gastroenteritis since 1989. However, research on AiV at cellular and animal levels is limited. Utilizing a double reporter gene system, we constructed an AiV capsid protein plasmid and genomic backbone Replicon. Subsequently, AiV pseudovirus (AiV PsV) particles were packaged using a three-plasmid co-transfection system. Eleven cell types were screened to identify those susceptible to AiV PsV. Mouse models were established with AiV PsV to determine the optimal mouse species, mode of infection, and detection time, and investigate distribution characteristics of AiVs in vivo. HeLa cells exhibited the highest sensitivity to AiV PsV. A BALB/c mouse model established with bioluminescence imaging performed 24 h after infection via intraperitoneal injection demonstrated that the bioluminescent signal was concentrated in the murine abdominal cavity. The AiV PsV system should advance understanding of the infectious features of AiVs.https://doi.org/10.1186/s12985-025-02839-yHuman Aichi virusPseudovirusesCellsMouse modelBioluminescent imaging
spellingShingle Ruojun Wu
Jingli Tian
Shunchang Fan
Minyi Liang
Yucheng Li
Ying Deng
Binbin Tang
Minyi Zhang
Qing Chen
Development and characterization of a pseudovirus system for human Aichi virus: in vitro and in vivo analysis
Virology Journal
Human Aichi virus
Pseudoviruses
Cells
Mouse model
Bioluminescent imaging
title Development and characterization of a pseudovirus system for human Aichi virus: in vitro and in vivo analysis
title_full Development and characterization of a pseudovirus system for human Aichi virus: in vitro and in vivo analysis
title_fullStr Development and characterization of a pseudovirus system for human Aichi virus: in vitro and in vivo analysis
title_full_unstemmed Development and characterization of a pseudovirus system for human Aichi virus: in vitro and in vivo analysis
title_short Development and characterization of a pseudovirus system for human Aichi virus: in vitro and in vivo analysis
title_sort development and characterization of a pseudovirus system for human aichi virus in vitro and in vivo analysis
topic Human Aichi virus
Pseudoviruses
Cells
Mouse model
Bioluminescent imaging
url https://doi.org/10.1186/s12985-025-02839-y
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