Infection with mpox virus via the genital mucosae increases shedding and transmission in the multimammate rat (Mastomys natalensis)

Julia R. Port,Jade C. Riopelle, Samuel G. Smith, Lara Myers, Franziska K. Kaiser,Matthew C. Lewis, Shane Gallogly,Atsushi Okumura, Trent Bushmaker,Jonathan E. Schulz, Rebecca Rosenke, Jessica Prado-Smith,Aaron Carmody, Sidy Bane,Brian J. Smith, Greg Saturday,Heinz Feldmann, Kyle Rosenke,Vincent J. Munster

NATURE MICROBIOLOGY(2024)

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摘要
The 2022 mpox virus (MPXV) outbreak was sustained by human-to-human transmission; however, it is currently unclear which factors lead to sustained transmission of MPXV. Here we present Mastomys natalensis as a model for MPXV transmission after intraperitoneal, rectal, vaginal, aerosol and transdermal inoculation with an early 2022 human outbreak isolate (Clade IIb). Virus shedding and tissue replication were route dependent and occurred in the presence of self-resolving localized skin, lung, reproductive tract or rectal lesions. Mucosal inoculation via the rectal, vaginal and aerosol routes led to increased shedding, replication and a pro-inflammatory T cell profile compared with skin inoculation. Contact transmission was higher from rectally inoculated animals. This suggests that transmission might be sustained by increased susceptibility of the anal and genital mucosae for infection and subsequent virus release.
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