Page 282 - Avian Virology: Current Research and Future Trends
P. 282
Chicken Infectious Anaemia Virus | 275
International Committee on Taxonomy of Viruses (2016). Arch. Virol. Chandratilleke, D., O’Connell, P., and Schat, K.A. (1991). Characterization
161, 2921–2949. https://doi.org/10.1007/s00705-016-2977-6 of proteins of chicken infectious anemia virus with monoclonal
Allan, G.M., Phenix, K.V., Todd, D., and McNulty, M.S. (1994). Some antibodies. Avian Dis. 35, 854–862.
biological and physico-chemical properties of porcine circovirus. Chansiripornchai, N. (2016). Field study of seroconversion of three
Zentralblatt Veterinarmedizin Reihe B 41, 17–26. commercial vaccines of chicken infectious anemia virus in Thailand. Thai
Backendorf, C., and Noteborn, M.H. (2014). Apoptin towards safe and J. Vet. Med. 46, 699–704.
efficient anticancer therapies. Adv. Exp. Med. Biol. 818, 39–59. https:// Cheng, J.H., Sheu, S.C., Lien, Y.Y., Lee, M.S., Chen, H.J., Su, W.H.,
doi.org/10.1007/978-1-4471-6458-6_3 and Lee, M.S. (2012). Identification of the NLS and NES motifs
Backendorf, C., Visser, A.E., de Boer, A.G., Zimmerman, R., Visser, of VP2 from chicken anemia virus and the interaction of VP2 with
M., Voskamp, P., Zhang, Y.H., and Noteborn, M. (2008). Apoptin: mini-chromosome maintenance protein 3. BMC Vet. Res. 8, 15. https://
therapeutic potential of an early sensor of carcinogenic transformation. doi.org/10.1186/1746-6148-8-15
Annu. Rev. Pharmacol. Toxicol. 48, 143–169. https://doi.org/10.1146/ Chettle, N.J., Eddy, R.K., Wyeth, P.J., and Lister, S.A. (1989). An outbreak of
annurev.pharmtox.48.121806.154910 disease due to chicken anaemia agent in broiler chickens in England. Vet.
Biagini, P. (2009). Classification of TTV and related viruses (anelloviruses). Rec. 124, 211–215.
Curr. Top. Microbiol. Immunol. 331, 21–33. Chu, D.K., Poon, L.L., Chiu, S.S., Chan, K.H., Ng, E.M., Bauer, I., Cheung,
Biagini, P. (2015). Taxonomic proposal to the ICTV Executive Committee: T.K., Ng, I.H., Guan, Y., Wang, D., et al. (2012). Characterization of a
Create the family Anelloviridae containing 9 new genera and 47 species. novel gyrovirus in human stool and chicken meat. J. Clin. Virol. 55,
Code 2007.075a-xxV (Marseille, France), pp. 1–34. 209–213. https://doi.org/10.1016/j.jcv.2012.07.001
Biagini, P., Bédarida, S., Touinssi, M., Galicher, V., and de Micco, P. (2013). Claessens, J.A., Schrier, C.C., Mockett, A.P., Jagt, E.H., and Sondermeijer,
Human gyrovirus in healthy blood donors, France. Emerging Infect. Dis. P.J. (1991). Molecular cloning and sequence analysis of the genome
19, 1014–1015. https://doi.org/10.3201/eid1906.130228 of chicken anaemia agent. J. Gen. Virol. 72, 2003–2006. https://doi.
Bounous, D.I., Goodwin, M.A., Brooks, R.L., Lamichhane, C.M., Campagnoli, org/10.1099/0022-1317-72-8-2003
R.P., Brown, J., and Snyder, D.B. (1995). Immunosuppression and Connor, T.J., McNeilly, F., Firth, G.A., and McNulty, M.S. (1991). Biological
intracellular calcium signaling in splenocytes from chicks infected with characterisation of Australian isolates of chicken anaemia agent. Aust.
chicken anemia virus, CL-1 isolate. Avian Dis. 39, 135–140. Vet. J. 68, 199–201.
Bouzari, M., and Salmanizadeh, S.h. (2015). Detection of Torque teno midi Crowther, R.A., Berriman, J.A., Curran, W.L., Allan, G.M., and Todd, D.
virus/Small anellovirus (TTMDV/SAV) in the sera of domestic village (2003). Comparison of the structures of three circoviruses: chicken
chickens and its vertical transmission from hen to eggs. Iran. J. Vet. Res. anemia virus, porcine circovirus type 2, and beak and feather disease
16, 110–113. virus. J. Virol. 77, 13036–13041.
Bouzari, M., and Shaykh Baygloo, N. (2013). Detection of torque teno virus Danen-Van Oorschot, A.A., Fischer, D.F., Grimbergen, J.M., Klein, B.,
(TTV) in domestic village chickens in Iran. Vet. Res. Forum 4, 55–58. Zhuang, S., Falkenburg, J.H., Backendorf, C., Quax, P.H., Van der Eb,
Brentano, L., Lazzarin, S., Bassi, S.S., Klein, T.A., and Schat, K.A. (2005). A.J., and Noteborn, M.H. (1997). Apoptin induces apoptosis in human
Detection of chicken anemia virus in the gonads and in the progeny transformed and malignant cells but not in normal cells. PNAS 94,
of broiler breeder hens with high neutralizing antibody titers. Vet. 5843–5847.
Microbiol. 105, 65–72. Danen-Van Oorschot, A.A., Zhang, Y.H., Leliveld, S.R., Rohn, J.L., Seelen,
Bullenkamp, J., and Tavassoli, M. (2014). Signalling of Apoptin. Adv. Exp. M.C., Bolk, M.W., Van Zon, A., Erkeland, S.J., Abrahams, J.P., Mumberg,
Med. Biol. 818, 11–37. https://doi.org/10.1007/978-1-4471-6458-6_2 D., et al. (2003). Importance of nuclear localization of apoptin for
Bullenkamp, J., Cole, D., Malik, F., Alkhatabi, H., Kulasekararaj, A., tumor-specific induction of apoptosis. J. Biol. Chem. 278, 27729–27736.
Odell, E.W., Farzaneh, F., Gäken, J., and Tavassoli, M. (2012). Human https://doi.org/10.1074/jbc.M303114200
Gyrovirus Apoptin shows a similar subcellular distribution pattern and Davidson, I., and Shulman, L.M. (2008). Unraveling the puzzle of human
apoptosis induction as the chicken anaemia virus derived VP3/Apoptin. anellovirus infections by comparison with avian infections with the
Cell Death Dis. 3, e296. https://doi.org/10.1038/cddis.2012.34 chicken anemia virus. Virus Res. 137, 1–15. https://doi.org/10.1016/j.
Bullenkamp, J., Gäken, J., Festy, F., Chong, E.Z., Ng, T., and Tavassoli, M. virusres.2008.06.014
(2015). Apoptin interacts with and regulates the activity of protein Davidson, I., Kedem, M., Borochovitz, H., Kass, N., Ayali, G., Hamzani,
kinase C beta in cancer cells. Apoptosis 20, 831–842. https://doi. E., Perelman, B., Smith, B., and Perk, S. (2004). Chicken infectious
org/10.1007/s10495-015-1120-6 anemia virus infection in Israeli commercial flocks: virus amplification,
Calnek, B.W., Harris, R.W., Buscaglia, C., Schat, K.A., and Lucio, B. (1998). clinical signs, performance, and antibody status. Avian Dis. 48, 108–118.
Relationship between the immunosuppressive potential and the https://doi.org/10.1637/7072
pathotype of Marek’s disease virus isolates. Avian Dis. 42, 124–132. Davidson, I., Loeb, E., Lublin, A., Shkoda, I., and Schat, K.A. (2007).
Calnek, B.W., Lucio-Martinez, B., Cardona, C., Harris, R.W., Schat, K.A., Assessment of various criteria to determine the chicken anemia virus
and Buscaglia, C. (2000). Comparative susceptibility of Marek’s disease pathogenicity in embryonated eggs and in day-old chicks. Curr. Top.
cell lines to chicken infectious anemia virus. Avian Dis. 44, 114–124. Virol. 6, 95–111.
Campbell, G. (2001). Investigation into evidence of exposure to infectious Davidson, I., Artzi, N., Shkoda, I., Lublin, A., Loeb, E., and Schat, K.A. (2008).
bursal disease virus (IBDV) and chick infectious anaemia virus (CIAV) The contribution of feathers in the spread of chicken anemia virus. Virus
in wild birds in Ireland. In Proceedings of 2nd International Symposium Res. 132, 152–159. https://doi.org/10.1016/j.virusres.2007.11.012
on Infectious Bursal Disease and Chicken Infectious Anaemia De Boer, G.F., Van Roozelaar, D.J., Moormann, R.J., Jeurissen, S.H.,
(Rauischholzhausen, Germany), pp. 230–233. Wijngaard, J.C., Hilbink, F., and Koch, G. (1994). Interaction between
Cardona, C., Lucio, B., O’Connell, P., Jagne, J., and Schat, K.A. (2000a). chicken anaemia virus and live Newcastle disease vaccine. Avian Pathol.
Humoral immune responses to chicken infectious anemia virus in three 23, 263–275.
strains of chickens in a closed flock. Avian Dis. 44, 661–667. De Herdt, P., Van den Bosch, G., Ducatelle, R., Uyttebroek, E., and Schrier,
Cardona, C.J., Oswald, W.B., and Schat, K.A. (2000b). Distribution of chicken C. (2001). Epidemiology and significance of chicken infectious anemia
anaemia virus in the reproductive tissues of specific-pathogen-free virus infections in broilers and broiler parents under nonvaccinated
chickens. J. Gen. Virol. 81 2067–2075. European circumstances. Avian Dis. 45, 706–708.
Carlson, H.C., Sweeny, P.R., and Tokaryk, J.M. (1968). Demonstration de Smit, M.H., and Noteborn, M.H. (2009). Apoptosis-inducing proteins
of phagocytic and trephocytic activities of chicken thrombocytes by in chicken anemia virus and TT virus. Curr. Top. Microbiol. Immunol.
microscopy and vital staining techniques. Avian Dis. 12, 700–715. 331, 131–149.
Catroxo, M.H.B., Nishiya, A., Sabino, E., Teixeira, P.S., Petrella, S., Milanelo, de Villiers, E.M., Borkosky, S.S., Kimmel, R., Gunst, K., and Fei, J.W. (2011).
L., Vieira, J.C.F., and ZDiaz, R.S. (2008). Research of torque teno virus The diversity of torque teno viruses: in vitro replication leads to the
(TTV) in serum and total blood of Brazilian non-hyman primates and in formation of additional replication-competent subviral molecules. J.
chicken plasma (Gallus gallus domesticus) by the PCR N22 region. Int. Virol. 85, 7284–7295. https://doi.org/10.1128/JVI.02472-10
J. Morphol. 26, 377–384.