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1.
Viruses ; 10(10)2018 09 23.
Article in English | MEDLINE | ID: mdl-30249047

ABSTRACT

Inflammatory bowel disease (IBD) and Clostridium difficile infection cause gastrointestinal (GI) distension and, in severe cases, toxic megacolon with risk of perforation and death. Herpesviruses have been linked to severe GI dilatation. MHV-68 is a model for human gamma herpesvirus infection inducing GI dilatation in interleukin-10 (IL-10)-deficient mice but is benign in wildtype mice. MHV-68 also causes lethal vasculitis and pulmonary hemorrhage in interferon gamma receptor-deficient (IFNγR-/-) mice, but GI dilatation has not been reported. In prior work the Myxomavirus-derived anti-inflammatory serpin, Serp-1, improved survival, reducing vasculitis and pulmonary hemorrhage in MHV-68-infected IFNγR-/- mice with significantly increased IL-10. IL-10 has been investigated as treatment for GI dilatation with variable efficacy. We report here that MHV-68 infection produces severe GI dilatation with inflammation and gut wall degradation in 28% of INFγR-/- mice. Macrophage invasion and smooth muscle degradation were accompanied by decreased concentrations of T helper (Th2), B, monocyte, and dendritic cells. Plasma and spleen IL-10 were significantly reduced in mice with GI dilatation, while interleukin-1 beta (IL-1ß), IL-6, tumor necrosis factor alpha (TNFα) and INFγ increased. Treatment of gamma herpesvirus-infected mice with exogenous IL-10 prevents severe GI inflammation and dilatation, suggesting benefit for herpesvirus-induced dilatation.


Subject(s)
Gastric Dilatation/therapy , Gastric Dilatation/virology , Herpesviridae Infections/complications , Interleukin-10/therapeutic use , Receptors, Interferon/genetics , Rhadinovirus , Animals , Cytokines/blood , Cytokines/immunology , Disease Models, Animal , Gastric Dilatation/genetics , Gastric Dilatation/pathology , Interleukin-10/genetics , Mice , Mice, Knockout , Receptors, Interferon/metabolism , Statistics, Nonparametric , Interferon gamma Receptor
2.
J Virol ; 86(12): 7023, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22628404

ABSTRACT

Avian bornaviruses (ABV) were first detected and described in 2008. They are the etiologic agents of proventricular dilatation disease (PDD), a frequently fatal neurologic disease of captive parrots. Seven ABV genogroups have been identified worldwide from a variety of sources, and that number may increase as surveillance for novel bornaviruses continues. Here, we report the first complete sequence of a genogroup 1 avian bornavirus (ABV1).


Subject(s)
Bird Diseases/virology , Bornaviridae/genetics , Gastric Dilatation/veterinary , Genome, Viral , Parrots , Proventriculus/virology , Animals , Base Sequence , Bornaviridae/classification , Bornaviridae/isolation & purification , Gastric Dilatation/virology , Genotype , Molecular Sequence Data , Parrots/virology
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