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Avian Adenovirus | 315
Schloer, G.M., Dardiri, A.H., Butterfield, W.K., Yates, V., and Breese, S.S. Steer, P.A., Kirkpatrick, N.C., O’Rourke, D., and Noormohammadi,
(1978). Isolation of a virus indistinguishable from adenovirus 127 from A.H. (2009). Classification of fowl adenovirus serotypes by use of
chickens in the United States. Proc. Annu. Meet. U. S. Anim. Health high-resolution melting-curve analysis of the hexon gene region. J. Clin.
Assoc. 82, 332–345. Microbiol. 47, 311–321. https://doi.org/10.1128/JCM.01567-08.
Schoenborn, J.R., and Wilson, C.B. (2007). Regulation of interferon-gamma Steer, P.A., O’Rourke, D., Ghorashi, S.A., and Noormohammadi, A.H.
during innate and adaptive immune responses. Adv. Immunol. 96, (2011). Application of high-resolution melting curve analysis for typing
41–101. of fowl adenoviruses in field cases of inclusion body hepatitis. Aust. Vet. J.
Schonewille, E., Singh, A., Göbel, T.W., Gerner, W., Saalmüller, A., and 89, 184–192. https://doi.org/10.1111/j.1751-0813.2011.00695.x.
Hess, M. (2008). Fowl adenovirus (FAdV) serotype 4 causes depletion Steer, P.A., Sandy, J.R., O’Rourke, D., Scott, P.C., Browning, G.F., and
of B and T-cells in lymphoid organs in specific pathogen-free chickens Noormohammadi, A.H. (2015). Chronological analysis of gross and
following experimental infection. Vet. Immunol. Immunopathol. 121, histological lesions induced by field strains of fowl adenovirus serotypes
130–139. 1, 8b and 11 in 1-day-old chickens. Avian Pathol. 44, 106–113. https://
Schonewille, E., Jaspers, R., Paul, G., and Hess, M. (2010). doi.org/10.1080/03079457.2015.1007919.
Specific-pathogen-free chickens vaccinated with a live FAdV-4 vaccine Suresh, M., and Sharma, J.M. (1995). Hemorrhagic enteritis virus induced
are fully protected against a severe challenge even in the absence changes in the lymphocyte subpopulations in turkeys and the effect of
of neutralizing antibodies. Avian Dis. 54, 905–910. https://doi. experimental immunodeficiency on viral pathogenesis. Vet. Immunol.
org/10.1637/8999-072309-Reg.1. Immunopathol. 45, 139–150.
Schybli, M., Sigrist, B., Hess, M., van Leerdam, B., Hoop, R.K., and Vögtlin, Suresh, M., and Sharma, J.M. (1996). Pathogenesis of type II avian
A. (2014). Development of a new real-time polymerase chain reaction adenovirus infection in turkeys: in vivo immune cell tropism and tissue
assay to detect Duck adenovirus A DNA and application to samples distribution of the virus. J. Virol. 70, 30–36.
from Swiss poultry flocks. J. Vet. Diagn. Invest. 26, 189–194. https://doi. Swaminathan, S., and Thimmapaya, B. (1996). Transactivation of
org/10.1177/1040638714523426. adenovirus E2-early promoter by E1A and E4 6/7 in the context of viral
Senne, D.A. (1998). Virus propagation in embryonating eggs. In A chromosome. J. Mol. Biol. 258, 736–746.
Laboratory Manual for the Isolation and Identification of Avian Swayne, D.E., Glisson, J.R., McDougald, L.R., Nolan, L., Suarez, D.L., and
Pathogens, Swayne, D., Glisson, J.R., Jackwood, M.W., Pearson, J.E., and Nair, V. (2013). Diseases of Poultry (Wiley-Blackwell, Ames, IA).
Reed, W.M., eds (American Association of Avian Pathologists, Kennett Taharaguchi, S., Kono, Y., Ohta, H., and Takase, K. (2007). Putative host
Square, PA), pp. 235–247. cell receptor for fowl adenovirus detected in gizzard. J. Vet. Med. Sci. 69,
Shah, M.S., Ashraf, A., Rahman, M., Khan, M.I., and Qureshi, J.A. 1203–1205.
(2012). A subunit vaccine against hydropericardium syndrome using Tan, P.K., Michou, A.I., Bergelson, J.M., and Cotten, M. (2001). Defining
adenovirus penton capsid protein. Vaccine 30, 7153–7156. https://doi. CAR as a cellular receptor for the avian adenovirus CELO using a genetic
org/10.1016/j.vaccine.2012.10.013. analysis of the two viral fibre proteins. J. Gen. Virol. 82, 1465–1472.
Shah, M.S., Ashraf, A., Khan, M.I., Rahman, M., Habib, M., Chughtai, M.I., Temperley, N.D., Berlin, S., Paton, I.R., Griffin, D.K., and Burt, D.W.
and Qureshi, J.A. (2017). Fowl adenovirus: history, emergence, biology (2008). Evolution of the chicken toll-like receptor gene family: A
and development of a vaccine against hydropericardium syndrome. Arch. story of gene gain and gene loss. BMC Genomics 9, 62. https://doi.
Virol. 162, 1833–1843. https://doi.org/10.1007/s00705-017-3313-5. org/10.1186/1471-2164-9-62.
Shashkova, E.V., Cherenova, L.V., Kazansky, D.B., and Doronin, K. (2005). Teske, L., Rubbenstroth, D., Meixner, M., Liere, K., Bartels, H., and
Avian adenovirus vector CELO-TK displays anticancer activity in human Rautenschlein, S. (2017). Identification of a novel aviadenovirus,
cancer cells and suppresses established murine melanoma tumors. designated pigeon adenovirus 2 in domestic pigeons (Columba livia).
Cancer Gene Ther. 12, 617–626. Virus Res. 227, 15–22.
Sheppard, M., Werner, W., McCoy, R.J., and Johnson, M.A. (1998a). The Thaci, B., Ulasov, I.V., Wainwright, D.A., and Lesniak, M.S. (2011). The
major late promoter and bipartite leader sequence of fowl adenovirus. challenge for gene therapy: innate immune response to adenoviruses.
Arch. Virol. 143, 537–548. Oncotarget 2, 113–121.
Sheppard, M., Werner, W., Tsatas, E., McCoy, R., Prowse, S., and Johnson, Todd, D., and McNulty, M.S. (1978). Biochemical studies on a virus
M. (1998b). Fowl adenovirus recombinant expressing VP2 of infectious associated with egg drop syndrome 1976. J. Gen. Virol. 40, 63–75.
bursal disease virus induces protective immunity against bursal disease. Toro, H., Prusas, C., Raue, R., Cerda, L., Geisse, C., González, C., and Hess,
Arch. Virol. 143, 915–930. M. (1999). Characterization of fowl adenoviruses from outbreaks of
Shivaprasad, H.L., Woolcock, P.R., and McFarland, M.D. (2001). Group inclusion body hepatitis/hydropericardium syndrome in Chile. Avian
I avian adenovirus and avian adeno-associated virus in turkey poults Dis. 43, 262–270.
with inclusion body hepatitis. Avian Pathol. 30, 661–666. https://doi. Toro, H., González, O., Escobar, C., Cerda, L., Morales, M.A., and
org/10.1080/03079450120092152. Gonzalez, C. (2001). Vertical induction of the inclusion body hepatitis/
Singh, A., Grewal, G.S., Maiti, N.K., and Oberoi, M.S. (2006). Effect of fowl hydropericardium syndrome with fowl adenovirus and chicken anemia
adenovirus-1 (IBH isolate) on humoral and cellular immune competency virus. Avian Dis. 45, 215–222.
of broiler chicks. Comp. Immunol. Microbiol. Infect. Dis. 29, 315–321. Toro, H., González, C., Cerda, L., Morales, M.A., Dooner, P., and Salamero,
Singh, A., Bekele, A.Z., Patnayak, D.P., Jindal, N., Porter, R.E., Mor, S.K., and M. (2002). Prevention of inclusion body hepatitis/hydropericardium
Goyal, S.M. (2016). Molecular characterization of quail bronchitis virus syndrome in progeny chickens by vaccination of breeders with fowl
isolated from bobwhite quail in Minnesota. Poult. Sci. 95, 2815–2818. adenovirus and chicken anemia virus. Avian Dis. 46, 547–554. https://
Slaine, P.D., Ackford, J.G., Kropinski, A.M., Kozak, R.A., Krell, P.J., and Nagy, doi.org/10.1637/0005-2086(2002)046[0547:POIBHH]2.0.CO;2.
É. (2016). Molecular characterization of pathogenic and nonpathogenic Totsuka, M., Goda, M., Isogai, K., Yamamoto, Y., Sukigara, S., and Suzuki,
fowl aviadenovirus serotype 11 isolates. Can. J. Microbiol. 62, 993–1002. T. (2015). Gizzard erosion of brown layer chicken with fowl adenovirus
https://doi.org/10.1139/cjm-2016-0297. infection. J. Japanese Soc. Poult. Dis. 51, 11–12.
Smyth, J.A.A. (2013). Atadenovirus (egg drop syndrome and related Trampel, D.W., Meteyer, C.U., and Bickford, A.A. (1992). Hemorrhagic
infections). In Diseases of Poultry, Swayne, D.E., Glisson, J.R., enteritis virus inclusions in turkey renal tubular epithelium. Avian Dis.
McDougald, L.R., L.. Nolan, Suarez, D.L., and Nair, V., eds 36, 1086–1091.
(Wiley-Blackwell, Ames, IA), pp. 289–332. Umesh, Kumar, K., Krishnaswamy, S., and Venkata Reddy, T. (1989).
Smyth, J.A., and Adair, B.M. (1988). Lateral transmission of egg drop Cell-mediated immune response to egg drop syndrome-76 (EDS-76)
syndrome-76 virus by the egg. Avian Pathol. 17, 193–200. virus infection in chickens. Curr. Sci. 58, 431–433.
Smyth, J.A., Platten, M.A., and McFerran, J.B. (1988). A study of the Van Den Ende, M., Don, P.A., and Kipps, A. (1949). The isolation in eggs of a
pathogenesis of egg drop syndrome in laying hens. Avian Pathol. 17, new filtrable agent which may be the cause of bovine lumpy skin disease.
653–666. J. Gen. Microbiol. 3, 174–183. https://doi.org/10.1099/00221287-3-2-
Solyom, F., Nemesi, M., Forgacs, A., Balla, E., and Perenyi, T. (1982). Studies 174.
on EDS vaccine. Dev. Biol. Stand. 51, 105–121.