Affiliations 

  • 1 Department of Pathology, University of Texas Medical Branch, Galveston
  • 2 Department of Pathology and Immunology, Washington University School of Medicine, St Louis, Missouri
  • 3 Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston
  • 4 Institute for Human Infections and Immunity, University of Texas Medical Branch, Galveston
  • 5 Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, New York
J Infect Dis, 2018 10 05;218(10):1602-1610.
PMID: 29912426 DOI: 10.1093/infdis/jiy357

Abstract

Background: Nipah virus (NiV) is a paramyxovirus (genus Henipavirus) that can cause severe respiratory illness and encephalitis in humans. Transmission occurs through consumption of NiV-contaminated foods, and contact with NiV-infected animals or human body fluids. However, it is unclear whether aerosols derived from aforesaid sources or others also contribute to transmission, and current knowledge on NiV-induced pathogenicity after small-particle aerosol exposure is still limited.

Methods: Infectivity, pathogenicity, and real-time dissemination of aerosolized NiV in Syrian hamsters was evaluated using NiV-Malaysia (NiV-M) and/or its recombinant expressing firefly luciferase (rNiV-FlucNP).

Results: Both viruses had an equivalent pathogenicity in hamsters, which developed respiratory and neurological symptoms of disease, similar to using intranasal route, with no direct correlations to the dose. We showed that virus replication was predominantly initiated in the lower respiratory tract and, although delayed, also intensely in the oronasal cavity and possibly the brain, with gradual increase of signal in these regions until at least day 5-6 postinfection.

Conclusion: Hamsters infected with small-particle aerosolized NiV undergo similar clinical manifestations of the disease as previously described using liquid inoculum, and exhibit histopathological lesions consistent with NiV patient reports. NiV droplets could therefore play a role in transmission by close contact.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.