bioRxivMicrobiologyPreprint
Increased contact transmission of contemporary Human H5N1 compared to Bovine and Mountain Lion H5N1 in a hamster model
Reshma Koolaparambil MukeshiD, Franziska Karola KaiseriD, Jonathan E. SchulziD, Shane GalloglyiD, Jessica Prado-SmithiD, Arthur WickenhageniD, Kathleen Cordova, Brian J. SmithiD, Chad S. ClancyiD, Carl ShaiaiD, Greg A. SaturdayiD, Emmie de WitiD, Neeltje van DoremaleniD, Claude Kwe YindaiD, Vincent Jacobus MunsteriD
Abstract
The ongoing outbreak of highly pathogenic avian influenza virus (HPAIV) subtype H5N1 in the U.S. poses a significant public health threat. To date, 70 human cases have been confirmed in the United States, including two severe cases and one fatality. While suitable animal models are crucial for predicting the potential pandemic risk of newly emerging pathogens in humans, studies investigating contemporary HPAIV H5N1 transmission dynamics remain limited. Here, we investigated the pathogenicity and transmission efficiency of three recent clade 2.3.4.4b H5N1 viruses isolated from a bovine, mountain lion, and a human case using Syrian hamsters. Intranasal inoculation with 104 TCID50 resulted in productive virus replication in the respiratory tract and shedding for all three isolates. Transmission studies showed limited efficiency via direct contact and airborne routes for all three isolates. Although overall transmission was inefficient, the human H5N1 isolate demonstrated relatively greater contact transmissibility than the bovine and mountain lion isolates. Taken together, our data demonstrate that the Syrian hamster model complements existing animal models for influenza A virus research and expands the resources available for investigating the pathogenicity, transmissibility, and efficacy of countermeasures against HPAIV H5N1. One sentence summaryHuman HPAIV H5N1 exhibits comparatively higher contact transmissibility than bovine and mountain lion isolates, despite limited overall transmission.
- organism: mouse
- research focus: host-pathogen & immune response
- research focus: transcription & RNA processing
- research focus: cell type annotation
- research focus: differential expression
- approach: experimental assay
- Citations
- 0
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