Host genetic background influences diverse neurological responses to viral infection in mice

被引:26
作者
Brinkmeyer-Langford, Candice L. [1 ]
Rech, Raquel [2 ]
Amstalden, Katia [2 ]
Kochan, Kelli J. [3 ]
Hillhouse, Andrew E. [3 ]
Young, Colin [1 ]
Welsh, C. Jane [1 ,2 ]
Threadgill, David W. [2 ,3 ,4 ]
机构
[1] Texas A&M Univ, Dept Vet Integrat Biosci, College Stn, TX 77843 USA
[2] Texas A&M Univ, Dept Vet Pathobiol, College Stn, TX 77843 USA
[3] Texas A&M Univ, Texas A&M Inst Genom Sci & Soc, College Stn, TX 77843 USA
[4] Texas A&M Univ, Dept Mol & Cellular Med, College Stn, TX 77843 USA
关键词
THEILERS-VIRUS-INFECTION; GUILLAIN-BARRE-SYNDROME; SUBSEQUENT DEMYELINATING DISEASE; AMYOTROPHIC-LATERAL-SCLEROSIS; CHRONIC RESTRAINT STRESS; MULTIPLE-SCLEROSIS; COLLABORATIVE CROSS; PARKINSONS-DISEASE; RISK-FACTORS; PERSISTENT INFECTION;
D O I
10.1038/s41598-017-12477-2
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Infection by Theiler's murine encephalomyelitis virus (TMEV) is a model for neurological outcomes caused by virus infection because it leads to diverse neurological conditions in mice, depending on the strain infected. To extend knowledge on the heterogeneous neurological outcomes caused by TMEV and identify new models of human neurological diseases associated with antecedent infections, we analyzed the phenotypic consequences of TMEV infection in the Collaborative Cross (CC) mouse population. We evaluated 5 different CC strains for outcomes of long-term infection (3 months) and acute vs. early chronic infection (7 vs. 28 days post-infection), using neurological and behavioral phenotyping tests and histology. We correlated phenotypic observations with haplotypes of genomic regions previously linked to TMEV susceptibility to test the hypothesis that genomic diversity within CC mice results in variable disease phenotypes in response to TMEV. None of the 5 strains analyzed had a response identical to that of any other CC strain or inbred strain for which prior data are available, indicating that strains of the CC can produce novel models of neurological disease. Thus, CC strains can be a powerful resource for studying how viral infection can cause different neurological outcomes depending on host genetic background.
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页数:17
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