Issue |
Vet. Res.
Volume 41, Number 5, September–October 2010
|
|
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Number of page(s) | 12 | |
DOI | https://doi.org/10.1051/vetres/2010038 | |
Published online | 15 June 2010 | |
How to cite this article | Vet. Res. (2010) 41:66 |
Original article
The mouse model is suitable for the study of viral factors governing transmission and pathogenesis of highly pathogenic avian influenza (HPAI) viruses in mammals
1
OIE/FAO and National Reference Laboratory for Avian Influenza and Newcastle disease, OIE Collaborating Centre for Diseases at the Animal-Human Interface, Research & Development Department, Istituto Zooprofilattico Sperimentale delle Venezie, Viale dell’Università 10, 35020
Legnaro, Padova, Italy
2
Public Health and Risk Analysis Department, Istituto Zooprofilattico Sperimentale delle Venezie,Viale dell’Università 10, 35020, Legnaro, Padova, Italy
* Corresponding author: mrigoni@izsvenezie.it
Received:
4
January
2010
Accepted:
11
June
2010
Highly pathogenic avian influenza (HPAI) viruses of the H5 and H7 subtype pose a major public health threat due to their capacity to cross the species barrier and infect mammals, for example dogs, cats and humans. In the present study we tested the capacity of selected H7 and H5 HPAI viruses to infect and to be transmitted from infected BALB/c mice to contact sentinels. Previous experiments have shown that viruses belonging to both H5 and H7 subtypes replicate in the respiratory tract and central nervous system of experimentally infected mice. In this study we show that selected H7N1 and H5N1 HPAI viruses can be transmitted from mouse-to-mouse by direct contact, and that in experimentally infected animals they exhibit a different pattern of replication and transmission. Our results can be considered as a starting point for transmission experiments involving other influenza A viruses with α 2-3 receptor affinity in order to better understand the viral factors influencing transmissibility of these viruses in selected mammalian species.
Key words: highly pathogenic avian influenza virus / mouse / transmission / H7 / H5
© INRA, EDP Sciences, 2010