| Literature DB >> 31042467 |
Ichiro Misumi1, Kevin D Cook2, Joseph E Mitchell2, Makayla M Lund2, Sarah C Vick3, Robert H Lee4, Toru Uchimura5, Wolfgang Bergmeier4, Piotr Mieczkowski6, Fernando Pardo-Manuel de Villena6, Jenny P Y Ting7, Jason K Whitmire8.
Abstract
Arenaviruses can cause severe hemorrhagic disease in humans, which can progress to organ failure and death. The underlying mechanisms causing lethality and person-to-person variation in outcome remain incompletely explained. Herein, we characterize a mouse model that recapitulates many features of pathogenesis observed in humans with arenavirus-induced hemorrhagic disease, including thrombocytopenia, severe vascular leakage, lung edema, and lethality. The susceptibility of congenic B6.PL mice to lymphocytic choriomeningitis virus (LCMV) infection is associated with increased antiviral T cell responses in B6.PL mice compared with C57BL/6 mice and is T cell dependent. Pathogenesis imparted by the causative locus is inherited in a semi-dominant manner in F1 crosses. The locus includes PL-derived sequence variants in both poorly annotated genes and genes known to contribute to immune responses. This model can be used to further interrogate how limited genetic differences in the host can remarkably alter the disease course of viral infection.Entities:
Keywords: CD8(+) T cells; LCMV; arenavirus; forward genetic mapping; mouse genetics; thrombocytopenia; viral hemorrhagic disease; viral pathogenesis
Mesh:
Year: 2019 PMID: 31042467 PMCID: PMC6508094 DOI: 10.1016/j.celrep.2019.04.004
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423