A surrogate BSL2-compliant infection model recapitulating key aspects of human Marburg virus disease

Marburg virus disease (MVD) is a severe infectious disease caused by the Marburg virus (MARV), posing a significant threat to humans. MARV needs to be operated under strict biosafety Level 4 (BSL-4) laboratory conditions. Therefore, accessible and practical animal models are urgently needed to advan...

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Main Authors: Wanying Yang, Wujie Zhou, Bo Liang, Xiaojun Hu, Shen Wang, Zhenshan Wang, Tiecheng Wang, Xianzhu Xia, Na Feng, Yongkun Zhao, Feihu Yan
Format: Article
Language:English
Published: Taylor & Francis Group 2025-12-01
Series:Emerging Microbes and Infections
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Online Access:https://www.tandfonline.com/doi/10.1080/22221751.2024.2449083
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author Wanying Yang
Wujie Zhou
Bo Liang
Xiaojun Hu
Shen Wang
Zhenshan Wang
Tiecheng Wang
Xianzhu Xia
Na Feng
Yongkun Zhao
Feihu Yan
author_facet Wanying Yang
Wujie Zhou
Bo Liang
Xiaojun Hu
Shen Wang
Zhenshan Wang
Tiecheng Wang
Xianzhu Xia
Na Feng
Yongkun Zhao
Feihu Yan
author_sort Wanying Yang
collection DOAJ
description Marburg virus disease (MVD) is a severe infectious disease caused by the Marburg virus (MARV), posing a significant threat to humans. MARV needs to be operated under strict biosafety Level 4 (BSL-4) laboratory conditions. Therefore, accessible and practical animal models are urgently needed to advance prophylactic and therapeutic strategies for MARV. In this study, we constructed a recombinant vesicular stomatitis virus (VSV) expressing the Marburg virus glycoprotein (VSV-MARV/GP). Syrian hamsters infected with VSV-MARV/GP presented symptoms such as thrombocytopenia, lymphopenia, haemophilia, and multiorgan failure, developing a severe systemic disease akin to that observed in human MARV patients. Notably, the pathogenicity was found to be species-specific, age-related, sex-associated, and challenge route-dependent. Subsequently, the therapeutic efficacy of the MR191 monoclonal antibody was validated in this model. In summary, this alternative model is an effective tool for rapidly screening medical countermeasures against MARV GP in vivo under BSL-2 conditions.
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institution Kabale University
issn 2222-1751
language English
publishDate 2025-12-01
publisher Taylor & Francis Group
record_format Article
series Emerging Microbes and Infections
spelling doaj-art-3b7a70580abc4f38b90b742d42a9fbcd2025-01-12T19:46:58ZengTaylor & Francis GroupEmerging Microbes and Infections2222-17512025-12-0114110.1080/22221751.2024.2449083A surrogate BSL2-compliant infection model recapitulating key aspects of human Marburg virus diseaseWanying Yang0Wujie Zhou1Bo Liang2Xiaojun Hu3Shen Wang4Zhenshan Wang5Tiecheng Wang6Xianzhu Xia7Na Feng8Yongkun Zhao9Feihu Yan10State Key Laboratory of Pathogenic Microorganisms, Key Laboratory of Jilin Province for Zoonosis Prevention and Control, Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, People’s Republic of ChinaState Key Laboratory of Pathogenic Microorganisms, Key Laboratory of Jilin Province for Zoonosis Prevention and Control, Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, People’s Republic of ChinaState Key Laboratory of Pathogenic Microorganisms, Key Laboratory of Jilin Province for Zoonosis Prevention and Control, Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, People’s Republic of ChinaState Key Laboratory of Pathogenic Microorganisms, Key Laboratory of Jilin Province for Zoonosis Prevention and Control, Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, People’s Republic of ChinaState Key Laboratory of Pathogenic Microorganisms, Key Laboratory of Jilin Province for Zoonosis Prevention and Control, Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, People’s Republic of ChinaState Key Laboratory of Pathogenic Microorganisms, Key Laboratory of Jilin Province for Zoonosis Prevention and Control, Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, People’s Republic of ChinaState Key Laboratory of Pathogenic Microorganisms, Key Laboratory of Jilin Province for Zoonosis Prevention and Control, Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, People’s Republic of ChinaState Key Laboratory of Pathogenic Microorganisms, Key Laboratory of Jilin Province for Zoonosis Prevention and Control, Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, People’s Republic of ChinaState Key Laboratory of Pathogenic Microorganisms, Key Laboratory of Jilin Province for Zoonosis Prevention and Control, Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, People’s Republic of ChinaState Key Laboratory of Pathogenic Microorganisms, Key Laboratory of Jilin Province for Zoonosis Prevention and Control, Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, People’s Republic of ChinaState Key Laboratory of Pathogenic Microorganisms, Key Laboratory of Jilin Province for Zoonosis Prevention and Control, Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, People’s Republic of ChinaMarburg virus disease (MVD) is a severe infectious disease caused by the Marburg virus (MARV), posing a significant threat to humans. MARV needs to be operated under strict biosafety Level 4 (BSL-4) laboratory conditions. Therefore, accessible and practical animal models are urgently needed to advance prophylactic and therapeutic strategies for MARV. In this study, we constructed a recombinant vesicular stomatitis virus (VSV) expressing the Marburg virus glycoprotein (VSV-MARV/GP). Syrian hamsters infected with VSV-MARV/GP presented symptoms such as thrombocytopenia, lymphopenia, haemophilia, and multiorgan failure, developing a severe systemic disease akin to that observed in human MARV patients. Notably, the pathogenicity was found to be species-specific, age-related, sex-associated, and challenge route-dependent. Subsequently, the therapeutic efficacy of the MR191 monoclonal antibody was validated in this model. In summary, this alternative model is an effective tool for rapidly screening medical countermeasures against MARV GP in vivo under BSL-2 conditions.https://www.tandfonline.com/doi/10.1080/22221751.2024.2449083Marburg virusrecombinant vesicular stomatitis virusSyrian hamstersurrogate modelrecurrence of classic symptomsvaccine evaluation and drug screening
spellingShingle Wanying Yang
Wujie Zhou
Bo Liang
Xiaojun Hu
Shen Wang
Zhenshan Wang
Tiecheng Wang
Xianzhu Xia
Na Feng
Yongkun Zhao
Feihu Yan
A surrogate BSL2-compliant infection model recapitulating key aspects of human Marburg virus disease
Emerging Microbes and Infections
Marburg virus
recombinant vesicular stomatitis virus
Syrian hamster
surrogate model
recurrence of classic symptoms
vaccine evaluation and drug screening
title A surrogate BSL2-compliant infection model recapitulating key aspects of human Marburg virus disease
title_full A surrogate BSL2-compliant infection model recapitulating key aspects of human Marburg virus disease
title_fullStr A surrogate BSL2-compliant infection model recapitulating key aspects of human Marburg virus disease
title_full_unstemmed A surrogate BSL2-compliant infection model recapitulating key aspects of human Marburg virus disease
title_short A surrogate BSL2-compliant infection model recapitulating key aspects of human Marburg virus disease
title_sort surrogate bsl2 compliant infection model recapitulating key aspects of human marburg virus disease
topic Marburg virus
recombinant vesicular stomatitis virus
Syrian hamster
surrogate model
recurrence of classic symptoms
vaccine evaluation and drug screening
url https://www.tandfonline.com/doi/10.1080/22221751.2024.2449083
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