Functionally Overlapping Variants Control Tuberculosis Susceptibility in Collaborative Cross Mice
Clare M. Smith, Megan K. Proulx, Rocky Lai, Michael C Kiritsy, Timothy A. Bell, Pablo Hock, Fernando Pardo‐Manuel de Villena, Martin T. Ferris, et al. (11 authors)
mBio · 2019-11
Abstract
The variable outcome of Mycobacterium tuberculosis infection observed in natural populations is difficult to model in genetically homogeneous small-animal models. The newly developed Collaborative Cross (CC) represents a reproducible panel of genetically diverse mice that display a broad range of phenotypic responses to infection. We explored the genetic basis of this variation, focusing on a CC line that is highly susceptible to M. tuberculosis infection. This study identified multiple quantitative trait loci associated with bacterial control and cytokine production, including one that is caused by a novel loss-of-function mutation in the Itgal gene, which is necessary for T cell recruitment to the infected lung. These studies verify the multigenic control of mycobacterial disease in the CC panel, identify genetic loci controlling diverse aspects of pathogenesis, and highlight the utility of the CC resource.
MeSH terms
- Biology
- Tuberculosis
- Mycobacterium tuberculosis
- Phenotype
- Genetics
- Disease
- Gene
- Immunology
- Computational biology