Efficacy of baloxavir marboxil against bovine H5N1 virus in mice

Since the first detection of highly pathogenic avian influenza (HPAI) H5N1 (clade 2.3.4.4b) in U.S. dairy cattle in early 2024, the virus has spread rapidly, posing a major public health concern as the number of human cases continues to rise. Although human-to-human transmission has not been confirmed, experimental data suggest that the bovine H5N1 virus can transmit via respiratory droplets in ferrets, highlighting its pandemic potential. With no vaccines currently available, antiviral drugs remain the only treatment option. Here, we investigate the efficacy of the polymerase inhibitor baloxavir marboxil (BXM) against this virus in mice. We find that early treatment post-infection is effective, but delayed treatment significantly reduces BXM efficacy and increases the risk of BXM resistance, underscoring the importance of timely BXM administration for effective treatment.

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Publication Details

Journal
Nature Communications
Published
2025-06-20
DOI
https://doi.org/10.1038/s41467-025-60791-5
Citations
10
Primary Topic
Influenza Virus Research Studies
Type
article
Field-Weighted Citation Impact
13.54

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article

Efficacy of baloxavir marboxil against bovine H5N1 virus in mice

Ryuta Uraki, Seiya Yamayoshi, Maki Kiso, Yoshihiro Kawaoka
10 citations
Nature Communications
Influenza Virus Research Studies
13.54
article

Efficacy of baloxavir marboxil against bovine H5N1 virus in mice

Ryuta Uraki, Seiya Yamayoshi, Maki Kiso, Yoshihiro Kawaoka
article en
10 citations

Abstract

Since the first detection of highly pathogenic avian influenza (HPAI) H5N1 (clade 2.3.4.4b) in U.S. dairy cattle in early 2024, the virus has spread rapidly, posing a major public health concern as the number of human cases continues to rise. Although human-to-human transmission has not been confirmed, experimental data suggest that the bovine H5N1 virus can transmit via respiratory droplets in ferrets, highlighting its pandemic potential. With no vaccines currently available, antiviral drugs remain the only treatment option. Here, we investigate the efficacy of the polymerase inhibitor baloxavir marboxil (BXM) against this virus in mice. We find that early treatment post-infection is effective, but delayed treatment significantly reduces BXM efficacy and increases the risk of BXM resistance, underscoring the importance of timely BXM administration for effective treatment.

Nature CommunicationsVol. 16(1)
University of Wisconsin–Madison (US), National Institute of Infectious Diseases (JP), National Center for Global Health and Medicine (JP), ClassNK (JP), The University of Tokyo (JP)
Japan Agency for Medical Research and Development, Shionogi, National Institute of Allergy and Infectious Diseases
Zero hunger
Openalex Percentile: Top 1%
Influenza Virus Research Studies
13.54
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