Page 320 - Avian Virology: Current Research and Future Trends
P. 320

Avian Adenovirus |   311
            lesions in gizzards following experimental induction of gizzard erosion   100K-chaperone  protein  from  adenovirus  serotype  2  (Subgroup  C)
            in broilers. Vet. Res. 44, 38. https://doi.org/10.1186/1297-9716-44-38  assists in trimerization and nuclear localization of hexons from subgroups
          Grafl, B., Prokofieva, I., Wernsdorf, P., Steinborn, R., and Hess, M. (2014).   C and B adenoviruses. J. Mol. Biol. 352, 125–138.
            Infection  with  an  apathogenic fowl adenovirus serotype-1  strain   Howell, J., MacDonald, D.W., and Christian, R.G. (1970). Inclusion body
            (CELO) prevents adenoviral gizzard erosion in broilers. Vet. Microbiol.   hepatitis in chickens. Can. Vet. J. 11, 99–101.
            172, 177–185. https://doi.org/10.1016/j.vetmic.2014.05.020  Huang, W., Kiefer, J., Whalen, D., and Flint, S.J. (2003). DNA
          Grgić, H., Philippe, C., Ojkić, D., and Nagy, E. (2006). Study of vertical   synthesis-dependent relief of repression of transcription from the
            transmission of fowl adenoviruses. Can. J. Vet. Res. 70, 230–233.  adenovirus type 2 IVa2 promoter by a cellular protein. Virology 314,
          Grgić, H., Yang, D.H., and Nagy, E. (2011). Pathogenicity and complete   394–402.
            genome sequence of a fowl adenovirus serotype 8 isolate. Virus Res. 156,   Huebner, R.J., Rowe, W.P., Ward, T.G., Parrott, R.H., and Bell, J.A. (1954).
            91–97. https://doi.org/10.1016/j.virusres.2011.01.002  Adenoidal-pharyngeal-conjunctival agents: a newly recognized group
          Grgić, H., Poljak, Z., Sharif, S., and Nagy, É. (2013a). Pathogenicity and   of common viruses of the respiratory system. N. Engl. J. Med.  251,
            cytokine gene expression pattern of a serotype 4 fowl adenovirus isolate.   1077–1086. https://doi.org/10.1056/NEJM195412302512701
            PLOS ONE 8, e77601. https://doi.org/10.1371/journal.pone.0077601  Hussain, I., Choi, C.U., Rings, B.S., Shaw, D.P., and Nagaraja, K.V. (1993).
          Grgić, H., Sharif, S., Haghighi, H.R., and Nagy, É. (2013b). Cytokine patterns   Pathogenesis  of  hemorrhagic  enteritis  virus  infection in  turkeys.
            associated with a serotype 8 fowl adenovirus infection. Viral Immunol.   Zentralblatt Veterinarmedizin Reihe B 40, 715–726.
            26, 143–149. https://doi.org/10.1089/vim.2012.0078  Itakura, C., and Carlson, H.C. (1975). Electron microscopic findings of cells
          Grgić, H., Krell, P.J., and Nagy, E. (2014). Comparison of fiber gene   with inclusion bodies in experimental hemorrhagic enteritis of turkeys.
            sequences  of inclusion  body hepatitis  (IBH)  and non-IBH strains of   Can. J. Comp. Med. 39, 299–304.
            serotype 8 and 11 fowl adenoviruses. Virus Genes 48, 74–80. https://  Itakura, C., Carlson, H.C., and Lang, G.N. (1974). Experimental transmission
            doi.org/10.1007/s11262-013-0995-y                     of haemorrhagic enteritis of turkeys. Avian Pathol. 3, 279–292.
          Griffin, B.D., and Nagy, É. (2011). Coding potential and transcript analysis   Itakura, C., Matsushita, S., and Goto, M. (1977). Fine structure of inclusion
            of fowl adenovirus 4: insight into upstream ORFs as common sequence   bodies in hepatic cells of chickens naturally affected with inclusion body
            features in adenoviral transcripts. J. Gen. Virol. 92, 1260–1272.  hepatitis. Avian Pathol. 6, 19–32.
          Grimes, T.M., King, D.J., Kleven, S.H., and Fletcher, O.J. (1977). Involvement   Ivanics, E., Palya, V., Glavits, R., Dan, A., Palfi, V., Revesz, T., and Benko,
            of a type-8 avian adenovirus in the etiology of inclusion body hepatitis.   M. (2001). The role of egg drop syndrome virus in acute respiratory
            Avian Dis. 21, 26–38.                                 disease of goslings. Avian Pathol.  30, 201–208. https://doi.
          Gross, W.B. (1967). Lesions of hemorrhagic enteritis. Avian Dis.  11,   org/10.1080/03079450120054604
            684–693.                                            Ivanics, E., Palya, V., Markos, B., Dán, A., Ursu, K., Harrach, B., Kaján, G.,
          Gulka, C.M., Piela, T.H., Yates, V.J., and Bagshaw, C. (1984). Evidence of   and Glávits, R. (2010). Hepatitis and hydropericardium syndrome
            exposure of waterfowl and other aquatic birds to the hemagglutinating   associated with adenovirus infection in goslings. Acta Vet. Hung.  58,
            duck adenovirus identical to EDS-76 virus. J. Wildl. Dis. 20, 1–5.  47–58. https://doi.org/10.1556/AVet.58.2010.1.5
          Gutter, B., Fingerut, E., Gallili, G., Eliahu, D., Perelman, B., Finger, A., and   Jiang, P., Ojkic, D., Tuboly, T., Huber, P., and Nagy, E. (1999). Application
            Pitcovski, J. (2008). Recombinant egg drop syndrome subunit vaccine   of the polymerase chain reaction to detect fowl adenoviruses. Can. J. Vet.
            offers an alternative to virus propagation in duck eggs. Avian Pathol. 37,   Res. 63, 124–128.
            33–37. https://doi.org/10.1080/03079450701784867    Johnson, M.A., Pooley, C., and Lowenthal, J.W. (2000). Delivery of avian
          Guy, J.S. (1998). Virus infections of the gastrointestinal tract of poultry.   cytokines by adenovirus vectors. Dev. Comp. Immunol. 24, 343–354.
            Poult. Sci. 77, 1166–1175. https://doi.org/10.1093/ps/77.8.1166  Johnson, M.A., Pooley, C., Ignjatovic, J., and Tyack, S.G. (2003). A
          Hansen, T.H., and Bouvier, M. (2009). MHC class I antigen presentation:   recombinant  fowl  adenovirus  expressing  the  S1  gene  of  infectious
            learning from viral evasion strategies. Nat. Rev. Immunol. 9, 503–513.   bronchitis virus protects against challenge with infectious bronchitis
            https://doi.org/10.1038/nri2575                       virus. Vaccine 21, 2730–2736.
          Harakuni, T., Andoh, K., Sakamoto, R.I., Tamaki, Y., Miyata, T., Uefuji, H.,   Jones, R.C., and Georgiou, K. (1984). Experimental infection of chickens
            Yamazaki, K.I., and Arakawa, T. (2016). Fiber knob domain lacking the   with adenoviruses isolated from tenosynovitis. Avian Pathol. 13, 13–23.
            shaft sequence but fused to a coiled coil is a candidate subunit vaccine   Jordan, I., John, K., Höwing, K., Lohr, V., Penzes, Z., Gubucz-Sombor, E.,
            against egg-drop syndrome. Vaccine 34, 3184–3190.     Fu, Y., Gao, P., Harder, T., Zádori, Z., et al. (2016). Continuous cell lines
          Harrach, B., Benkö, M., Both, G., Brown, M., Davison, A., Echavarría, M.,   from the Muscovy duck as potential replacement for primary cells in the
            Hess, M., Jones, M.S., Kajon, A., Lehmkuhl, H., et al. (2011). Family   production of avian vaccines. Avian Pathol. 45, 137–155. https://doi.org
            Adenoviridae. In Virus Taxonomy: Ninth Report of the International   /10.1080/03079457.2016.1138280
            Committee on Taxonomy of Viruses, A. King, M. Adams, E. Carstens,   Jucker, M.T., McQuiston, J.R., van den Hurk, J.V., Boyle, S.M., and Pierson,
            and E. Lefkowitz, eds (Elsevier Academic Press, San Diego, CA), pp.   F.W. (1996). Characterization of the haemorrhagic enteritis virus genome
            125–141.                                              and the sequence of the putative penton base and core protein genes. J.
          Helmboldt, C.F., and Frazier, M.N. (1963). Avian hepatic inclusion bodies   Gen. Virol. 77, 469–479. https://doi.org/10.1099/0022-1317-77-3-469
            of unknown significance. Avian Dis. 7, 446–450.     Kaján, G.L., Davison, A.J., Palya, V., Harrach, B., and Benko, M. (2012).
          Hess,  M.  (2000).  Detection  and  differentiation  of  avian  Genome sequence of a waterfowl aviadenovirus, goose adenovirus 4. J.
            adenoviruses: a review. Avian Pathol.  29, 195–206. https://doi.  Gen. Virol. 93, 2457–2465.
            org/10.1080/03079450050045440                       Kaján, G.L., Kecskeméti, S., Harrach, B., and Benkő, M. (2013). Molecular
          Hess, M. (2013). Aviadenovirus infections. In Diseases of Poultry, V.   typing of fowl adenoviruses, isolated in Hungary recently, reveals high
            Swayne, D. E., McDougald, L. R., Nolan, L. K., Suarez, D. L., Nair, eds   diversity. Vet. Microbiol.  167, 357–363. https://doi.org/10.1016/j.
            (Wiley-Blackwell, Ames, IA), pp. 289–300.             vetmic.2013.09.025
          Hess, M., Cuzange, A., Ruigrok, R.W., Chroboczek, J., and Jacrot, B. (1995).   Kaleta, E.F., Khalaf, S.E., and Siegmann, O. (1980). Antibodies to egg-drop
            The avian adenovirus penton: two fibres and one base. J. Mol. Biol. 252,   syndrome 76 virus in wild birds in possible conjunction with egg-shell
            379–385.                                              problems. Avian Pathol. 9, 587–590.
          Hess, M., Blöcker, H., and Brandt, P. (1997). The complete nucleotide   Kälin, S., Amstutz, B., Gastaldelli, M., Wolfrum, N., Boucke, K., Havenga,
            sequence of the egg drop syndrome virus: an intermediate between   M., DiGennaro, F., Liska, N., Hemmi, S., and Greber, U.F. (2010).
            mastadenoviruses and aviadenoviruses. Virology 238, 145–156.  Macropinocytotic uptake and infection of human epithelial cells with
          Hess, M., Raue, R., and Prusas, C. (1999). Epidemiological studies on fowl   species B2 adenovirus type 35. J. Virol.  84, 5336–5350. https://doi.
            adenoviruses isolated from cases of infectious hydropericardium. Avian   org/10.1128/JVI.02494-09
            Pathol. 28, 433–439. https://doi.org/10.1080/03079459994443  Kang, M., Cha, S.Y., and Jang, H.K. (2017). Tropism and infectivity of
          Hong, S.S., Szolajska, E., Schoehn, G., Franqueville, L., Myhre, S., Lindholm,   duck-derived  egg  drop  syndrome virus  in chickens.  PLOS  ONE  12,
            L., Ruigrok, R.W., Boulanger, P., and Chroboczek, J. (2005). The   e0177236. https://doi.org/10.1371/journal.pone.0177236
   315   316   317   318   319   320   321   322   323   324   325