A novel locus on mouse chromosome 7 that influences survival after infection with tick-borne encephalitis virus
Abstract Background Tick-borne encephalitis (TBE) is the main tick-borne viral infection in Eurasia. Its manifestations range from inapparent infections and fevers with complete recovery to debilitating or fatal encephalitis. The basis of this heterogeneity is largely unknown, but part of this varia...
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2018-07-01
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Online Access: | http://link.springer.com/article/10.1186/s12868-018-0438-8 |
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language |
English |
format |
Article |
sources |
DOAJ |
author |
Martin Palus Yahya Sohrabi Karl W. Broman Hynek Strnad Matyáš Šíma Daniel Růžek Valeriya Volkova Martina Slapničková Jarmila Vojtíšková Lucie Mrázková Jiří Salát Marie Lipoldová |
spellingShingle |
Martin Palus Yahya Sohrabi Karl W. Broman Hynek Strnad Matyáš Šíma Daniel Růžek Valeriya Volkova Martina Slapničková Jarmila Vojtíšková Lucie Mrázková Jiří Salát Marie Lipoldová A novel locus on mouse chromosome 7 that influences survival after infection with tick-borne encephalitis virus BMC Neuroscience Tick-borne encephalitis virus (TBEV) Mouse model Survival Susceptibility locus Chromosome 7 Candidate gene |
author_facet |
Martin Palus Yahya Sohrabi Karl W. Broman Hynek Strnad Matyáš Šíma Daniel Růžek Valeriya Volkova Martina Slapničková Jarmila Vojtíšková Lucie Mrázková Jiří Salát Marie Lipoldová |
author_sort |
Martin Palus |
title |
A novel locus on mouse chromosome 7 that influences survival after infection with tick-borne encephalitis virus |
title_short |
A novel locus on mouse chromosome 7 that influences survival after infection with tick-borne encephalitis virus |
title_full |
A novel locus on mouse chromosome 7 that influences survival after infection with tick-borne encephalitis virus |
title_fullStr |
A novel locus on mouse chromosome 7 that influences survival after infection with tick-borne encephalitis virus |
title_full_unstemmed |
A novel locus on mouse chromosome 7 that influences survival after infection with tick-borne encephalitis virus |
title_sort |
novel locus on mouse chromosome 7 that influences survival after infection with tick-borne encephalitis virus |
publisher |
BMC |
series |
BMC Neuroscience |
issn |
1471-2202 |
publishDate |
2018-07-01 |
description |
Abstract Background Tick-borne encephalitis (TBE) is the main tick-borne viral infection in Eurasia. Its manifestations range from inapparent infections and fevers with complete recovery to debilitating or fatal encephalitis. The basis of this heterogeneity is largely unknown, but part of this variation is likely due to host genetic. We have previously found that BALB/c mice exhibit intermediate susceptibility to the infection of TBE virus (TBEV), STS mice are highly resistant, whereas the recombinant congenic strain CcS-11, carrying 12.5% of the STS genome on the background of the BALB/c genome is even more susceptible than BALB/c. Importantly, mouse orthologs of human TBE controlling genes Oas1b, Cd209, Tlr3, Ccr5, Ifnl3 and Il10, are in CcS-11 localized on segments derived from the strain BALB/c, so they are identical in BALB/c and CcS-11. As they cannot be responsible for the phenotypic difference of the two strains, we searched for the responsible STS-derived gene-locus. Of course the STS-derived genes in CcS-11 may operate through regulating or epigenetically modifying these non-polymorphic genes of BALB/c origin. Methods To determine the location of the STS genes responsible for susceptibility of CcS-11, we analyzed survival of TBEV-infected F2 hybrids between BALB/c and CcS-11. CcS-11 carries STS-derived segments on eight chromosomes. These were genotyped in the F2 hybrid mice and their linkage with survival was tested by binary trait interval mapping. We have sequenced genomes of BALB/c and STS using next generation sequencing and performed bioinformatics analysis of the chromosomal segment exhibiting linkage with TBEV survival. Results Linkage analysis revealed a novel suggestive survival-controlling locus on chromosome 7 linked to marker D7Nds5 (44.2 Mb). Analysis of this locus for polymorphisms between BALB/c and STS that change RNA stability and genes’ functions led to detection of 9 potential candidate genes: Cd33, Klk1b22, Siglece, Klk1b16, Fut2, Grwd1, Abcc6, Otog, and Mkrn3. One of them, Cd33, carried a nonsense mutation in the STS strain. Conclusions The robust genetic system of recombinant congenic strains of mice enabled detection of a novel suggestive locus on chromosome 7. This locus contains 9 candidate genes, which will be focus of future studies not only in mice but also in humans. |
topic |
Tick-borne encephalitis virus (TBEV) Mouse model Survival Susceptibility locus Chromosome 7 Candidate gene |
url |
http://link.springer.com/article/10.1186/s12868-018-0438-8 |
work_keys_str_mv |
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doaj-633680645c54450f98e56610ebc84b4e2020-11-25T00:59:17ZengBMCBMC Neuroscience1471-22022018-07-0119111110.1186/s12868-018-0438-8A novel locus on mouse chromosome 7 that influences survival after infection with tick-borne encephalitis virusMartin Palus0Yahya Sohrabi1Karl W. Broman2Hynek Strnad3Matyáš Šíma4Daniel Růžek5Valeriya Volkova6Martina Slapničková7Jarmila Vojtíšková8Lucie Mrázková9Jiří Salát10Marie Lipoldová11Institute of Parasitology, Biology Centre of the Czech Academy of SciencesDepartment of Molecular and Cellular Immunology, Institute of Molecular Genetics, Academy of Sciences of the Czech RepublicDepartment of Biostatistics and Medical InformaticsDepartment of Genomics and Bioinformatics, Institute of Molecular Genetics, Academy of Sciences of the Czech RepublicDepartment of Molecular and Cellular Immunology, Institute of Molecular Genetics, Academy of Sciences of the Czech RepublicInstitute of Parasitology, Biology Centre of the Czech Academy of SciencesDepartment of Molecular and Cellular Immunology, Institute of Molecular Genetics, Academy of Sciences of the Czech RepublicDepartment of Molecular and Cellular Immunology, Institute of Molecular Genetics, Academy of Sciences of the Czech RepublicDepartment of Molecular and Cellular Immunology, Institute of Molecular Genetics, Academy of Sciences of the Czech RepublicDepartment of Molecular and Cellular Immunology, Institute of Molecular Genetics, Academy of Sciences of the Czech RepublicDepartment of Virology, Veterinary Research InstituteDepartment of Molecular and Cellular Immunology, Institute of Molecular Genetics, Academy of Sciences of the Czech RepublicAbstract Background Tick-borne encephalitis (TBE) is the main tick-borne viral infection in Eurasia. Its manifestations range from inapparent infections and fevers with complete recovery to debilitating or fatal encephalitis. The basis of this heterogeneity is largely unknown, but part of this variation is likely due to host genetic. We have previously found that BALB/c mice exhibit intermediate susceptibility to the infection of TBE virus (TBEV), STS mice are highly resistant, whereas the recombinant congenic strain CcS-11, carrying 12.5% of the STS genome on the background of the BALB/c genome is even more susceptible than BALB/c. Importantly, mouse orthologs of human TBE controlling genes Oas1b, Cd209, Tlr3, Ccr5, Ifnl3 and Il10, are in CcS-11 localized on segments derived from the strain BALB/c, so they are identical in BALB/c and CcS-11. As they cannot be responsible for the phenotypic difference of the two strains, we searched for the responsible STS-derived gene-locus. Of course the STS-derived genes in CcS-11 may operate through regulating or epigenetically modifying these non-polymorphic genes of BALB/c origin. Methods To determine the location of the STS genes responsible for susceptibility of CcS-11, we analyzed survival of TBEV-infected F2 hybrids between BALB/c and CcS-11. CcS-11 carries STS-derived segments on eight chromosomes. These were genotyped in the F2 hybrid mice and their linkage with survival was tested by binary trait interval mapping. We have sequenced genomes of BALB/c and STS using next generation sequencing and performed bioinformatics analysis of the chromosomal segment exhibiting linkage with TBEV survival. Results Linkage analysis revealed a novel suggestive survival-controlling locus on chromosome 7 linked to marker D7Nds5 (44.2 Mb). Analysis of this locus for polymorphisms between BALB/c and STS that change RNA stability and genes’ functions led to detection of 9 potential candidate genes: Cd33, Klk1b22, Siglece, Klk1b16, Fut2, Grwd1, Abcc6, Otog, and Mkrn3. One of them, Cd33, carried a nonsense mutation in the STS strain. Conclusions The robust genetic system of recombinant congenic strains of mice enabled detection of a novel suggestive locus on chromosome 7. This locus contains 9 candidate genes, which will be focus of future studies not only in mice but also in humans.http://link.springer.com/article/10.1186/s12868-018-0438-8Tick-borne encephalitis virus (TBEV)Mouse modelSurvivalSusceptibility locusChromosome 7Candidate gene |