Establishment and characterization of a cell line derived from eptesicus nilssonii

Journal of Veterinary Medical Science

Volumn 78, Issue 11, 2016, Pages 1727-1729

  Horie, Masayuki ^a,b   Akasaka, Takumi ^c   Matsuda, Sachiko ^c   Ogawa, Haruko ^c   Imai, Kunitoshi ^c  

^a KAGOSHIMA UNIVERSITY   (Japan)

^b YAMAGUCHI UNIVERSITY   (Japan)

^c OBIHIRO UNIVERSITY OF AGRICULTURE AND VETERINARY MEDICINE   (Japan)

Author keywords

Cell line; EEBLL 1; Endogenous bornavirus like element; Eptesicus nilssonii; RNA dependent RNA polymerase

Indexed keywords

ANIMAL; BAT; BORNAVIRIDAE; CELL LINE; CYTOLOGY; GENETICS; KIDNEY; METABOLISM; OPEN READING FRAME; VIRUS GENE; VIRUS GENOME;

ANIMALS; BORNAVIRIDAE; CELL LINE; CHIROPTERA; GENES, VIRAL; GENOME, VIRAL; KIDNEY; OPEN READING FRAMES;

EID: 85000977869     PISSN: 09167250     EISSN: 13477439     Source Type: Journal    
DOI: 10.1292/jvms.16-0274     Document Type: Note

References (13)

1. Belyi, V. A., Levine, A. J. and Skalka, A. M. 2010. Unexpected inheritance: multiple integrations of ancient bornavirus and ebolavirus/marburgvirus sequences in vertebrate genomes. PLoS Pathog. 6: e1001030.
2. Fort, P., Albertini, A., Van-Hua, A., Berthomieu, A., Roche, S., Delsuc, F., Pasteur, N., Capy, P., Gaudin, Y. and Weill, M. 2012. Fossil rhabdoviral sequences integrated into arthropod genomes: ontogeny, evolution, and potential functionality. Mol. Biol. Evol. 29: 381-390.
3. Fujino, K., Horie, M., Honda, T., Merriman, D. K. and Tomonaga, K. 2014. Inhibition of Borna disease virus replication by an endogenous bornavirus-like element in the ground squirrel genome. Proc. Natl. Acad. Sci. U.S.A. 111: 13175-13180.
4. He, X., Korytař, T., Schatz, J., Freuling, C. M., Müller, T. and Köllner, B. 2014. Anti-lyssaviral activity of interferons κ and ω from the serotine bat, Eptesicus serotinus. J. Virol. 88: 5444-5454.
5. Horie, M., Honda, T., Suzuki, Y., Kobayashi, Y., Daito, T., Oshida, T., Ikuta, K., Jern, P., Gojobori, T., Coffin, J. M. and Tomonaga, K. 2010. Endogenous non-retroviral RNA virus elements in mammalian genomes. Nature 463: 84-87.
6. Horie, M., Kobayashi, Y., Honda, T., Fujino, K., Akasaka, T., Kohl, C., Wibbelt, G., Mühldorfer, K., Kurth, A., Müller, M. A., Corman, V. M., Gillich, N., Suzuki, Y., Schwemmle, M. and Tomonaga, K. 2016. An RNA-dependent RNA polymerase gene in bat genomes derived from an ancient negative-strand RNA virus. Sci. Rep. 6: 25873.
7. Horie, M., Kobayashi, Y., Suzuki, Y. and Tomonaga, K. 2013. Comprehensive analysis of endogenous bornavirus-like elements in eukaryote genomes. Philos. Trans. R. Soc. Lond. B Biol. Sci. 368: 20120499.
8. Horie, M. and Tomonaga, K. 2011. Non-retroviral fossils in vertebrate genomes. Viruses 3: 1836-1848.
9. Imakawa, K., Nakagawa, S. and Miyazawa, T. 2015. Baton pass hypothesis: successive incorporation of unconserved endogenous retroviral genes for placentation during mammalian evolution. Genes Cells 20: 771-788.
10. Jern, P. and Coffin, J. M. 2008. Effects of retroviruses on host genome function. Annu. Rev. Genet. 42: 709-732.
11. Katzourakis, A. and Gifford, R. J. 2010. Endogenous viral elements in animal genomes. PLoS Genet. 6: e1001191.
12. Taylor, D. J., Dittmar, K., Ballinger, M. J. and Bruenn, J. A. 2011. Evolutionary maintenance of filovirus-like genes in bat genomes. BMC Evol. Biol. 11: 336.
13. Taylor, D. J., Leach, R. W. and Bruenn, J. 2010. Filoviruses are ancient and integrated into mammalian genomes. BMC Evol. Biol. 10: 193.