Lymphotropism and host responses during acute wild-type canine distemper virus infections in a highly susceptible natural host

The mechanisms behind the in vivo virulence of immunosuppressive wild-type morbillivirus infections are still not fully understood. To investigate lymphotropism and host responses, we have selected the natural host model of canine distemper virus (CDV) infection in mink. This model displays multisys...

Full description

Saved in:
Bibliographic Details
Published inJournal of general virology Vol. 90; no. 9; pp. 2157 - 2165
Main Authors Nielsen, Line, Søgaard, Mette, Jensen, Trine Hammer, Andersen, Mads Klindt, Aasted, Bent, Blixenkrone-Møller, Merete
Format Journal Article
LanguageEnglish
Published Reading Soc General Microbiol 01.09.2009
Society for General Microbiology
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The mechanisms behind the in vivo virulence of immunosuppressive wild-type morbillivirus infections are still not fully understood. To investigate lymphotropism and host responses, we have selected the natural host model of canine distemper virus (CDV) infection in mink. This model displays multisystemic infection, similar to measles virus and rinderpest virus infections in their susceptible natural hosts. The wild-type CDVs investigated provoked marked virulence differences, inducing mild versus marked to severe acute disease. The mildly virulent wild-type virus induced transient lymphopenia, despite the development of massive infection of peripheral blood mononuclear cells (PBMCs) exceeding that determined for the highly virulent wild-type virus, indicating an inverse relationship between acute virulence and the extent of viraemia in the investigated wild-type viruses. Single-cell cytokine production in PBMCs was investigated throughout the acute infections. We observed Th1- and Th2-type cytokine responses beginning in the prodromal phase, and late inflammatory responses were shared between the wild-type infections.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ObjectType-Article-1
ObjectType-Feature-2
ISSN:0022-1317
1465-2099
DOI:10.1099/vir.0.010744-0