4.7 Article

Antiviral Effect of Human Saliva Against Hantavirus

Journal

JOURNAL OF MEDICAL VIROLOGY
Volume 80, Issue 12, Pages 2122-2126

Publisher

WILEY-LISS
DOI: 10.1002/jmv.21332

Keywords

hantavirus; HFRS; HPS; saliva; antiviral effect; innate immunity; mucin

Categories

Funding

  1. Swedish Society of Medicine
  2. Svenska Sallskapet for Medicinsk Forskning
  3. Stiftelsen Goljes Minne, Magn
  4. Bergvalls Stiftelse
  5. Lars Hiertas Stiftelse
  6. Jeanssons Stiftelse
  7. Swedish Medical Research Council [12177, 12642]
  8. County Council of Vasterbotten
  9. Medical Faculty of Umea University
  10. EU 6th Framework Program [GOCE-CT-2003-010284 EDEN]
  11. EDEN Steering Committee [EDEN0082]

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Hemorrhagic fever with renal syndrome (HFRS) and Hantavirus pulmonary syndrome are zoonotic diseases caused by rodent borne hantaviruses. Transmission to humans occurs usually by inhalation of aerozolized virus-contaminated rodent excreta. Although human-to-human transmission of Andes hantavirus has been observed, the mode of transmission is currently not known. Saliva from Puumala hantavirus (PUUV)-infected patients was shown recently to contain viral RNA. To test if human saliva interferes with hantavirus replication, the effect of saliva and salivary proteins on hantavirus replication was studied. It was observed that saliva from healthy individuals reduced Hantaan hantavirus (HTNV) infectivity, although not completely. Furthermore, HTNV was resistant against the antiviral capacity of histatin 5, lysozyme, lactoferrin, and SLPI, but was inhibited by mucin. Inoculation of bank voles (Myodes glareolus) with HFRS-patient saliva, positive for PUUV-RNA, did not induce sero-conversion. In conclusion, no evidence of infectious virus in patient saliva was found. However, the in vitro experiments showed that HTNV, the prototype hantavirus, is insensitive to several antiviral salivary proteins, and is partly resistant to the antiviral effect of saliva. It therefore remains to be shown if human saliva might contain infectious virions early during infection, that is, before seroconversion. J. Med. Virol. 80:2122-2126, 2008. (C) 2008 Wiley-Liss, Inc.

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