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...

Full description

Bibliographic Details
Main Authors: 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
Format: Article
Language:English
Published: BMC 2018-07-01
Series:BMC Neuroscience
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12868-018-0438-8
id doaj-633680645c54450f98e56610ebc84b4e
record_format Article
collection DOAJ
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 AT martinpalus anovellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT yahyasohrabi anovellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT karlwbroman anovellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT hynekstrnad anovellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT matyassima anovellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT danielruzek anovellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT valeriyavolkova anovellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT martinaslapnickova anovellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT jarmilavojtiskova anovellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT luciemrazkova anovellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT jirisalat anovellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT marielipoldova anovellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT martinpalus novellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT yahyasohrabi novellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT karlwbroman novellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT hynekstrnad novellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT matyassima novellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT danielruzek novellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT valeriyavolkova novellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT martinaslapnickova novellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT jarmilavojtiskova novellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT luciemrazkova novellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT jirisalat novellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
AT marielipoldova novellocusonmousechromosome7thatinfluencessurvivalafterinfectionwithtickborneencephalitisvirus
_version_ 1725218214161416192
spelling 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