Page 321 - Avian Virology: Current Research and Future Trends

312 | Corredor and Nagy
Karen, K.A., and Hearing, P. (2011). Adenovirus core protein VII protects the Ma, H.C., and Hearing, P. (2011). Adenovirus structural protein IIIa is
viral genome from a DNA damage response at early times after infection. involved in the serotype specificity of viral DNA packaging. J. Virol. 85,
J. Virol. 85, 4135–4142. https://doi.org/10.1128/JVI.02540-10 7849–7855. https://doi.org/10.1128/JVI.00467-11
Keestra, A.M., de Zoete, M.R., Bouwman, L.I., and van Putten, J.P. Macpherson, I., McDougall, J.S., and Laursen-Jones, A.P. (1974). Inclusion
(2010). Chicken TLR21 is an innate CpG DNA receptor distinct from body hepatitis in a broiler integration. Vet. Rec. 95, 286–289.
mammalian TLR9. J. Immunol. 185, 460–467. https://doi.org/10.4049/ Mahsoub, H.M., Evans, N.P., Beach, N.M., Yuan, L., Zimmerman, K., and
jimmunol.0901921 Pierson, F.W. (2017). Real-time PCR-based infectivity assay for the
Khawaja, D.A., Ahmad, S., Rauf, M.A., Zulfiqar, M.Z., Mahmood, S.M., and titration of turkey hemorrhagic enteritis virus, an adenovirus, in live
Hassan, M. (1988). Isolation of an adenovirus from hydropericardium vaccines. J. Virol. Methods 239, 42–49.
syndrome in broiler chicks. Pak. J. Vet. Res. 1, 2–17. Mangel, W.F., and San Martín, C. (2014). Structure, function and
Kim, J.N., Byun, S.H., Kim, M.J., Kim, J.j., Sung, H.W., and Mo, I.P. dynamics in adenovirus maturation. Viruses 6, 4536–4570. https://doi.
(2008). Outbreaks of hydropericardium syndrome and molecular org/10.3390/v6114536
characterization of Korean fowl adenoviral isolates. Avian Dis. 52, Mansoor, M.K., Hussain, I., Arshad, M., and Muhammad, G. (2011).
526–530. https://doi.org/10.1637/8178-112207-Case Preparation and evaluation of chicken embryo-adapted fowl adenovirus
Kleine, A., Hafez, H.M., and Lüschow, D. (2017). Investigations on serotype 4 vaccine in broiler chickens. Trop. Anim. Health Prod. 43,
aviadenoviruses isolated from turkey flocks in Germany. Avian Pathol. 331–338. https://doi.org/10.1007/s11250-010-9694-z
46, 181–187. https://doi.org/10.1080/03079457.2016.1237013 Marek, A., Günes, A., Schulz, E., and Hess, M. (2010a). Classification of
Ko, J.H., Asano, A., Kon, Y., Watanabe, T., and Agui, T. (2004). fowl adenoviruses by use of phylogenetic analysis and high-resolution
Characterization of the chicken PKR: polymorphism of the gene and melting-curve analysis of the hexon L1 gene region. J. Virol. Methods
antiviral activity against vesicular stomatitis virus. Jpn. J. Vet. Res. 51, 170, 147–154. https://doi.org/10.1016/j.jviromet.2010.09.019
123–133. Marek, A., Schulz, E., Hess, C., and Hess, M. (2010b). Comparison of the
Kovács, E.R., and Benko, M. (2011). Complete sequence of raptor fibers of Fowl adenovirus A serotype 1 isolates from chickens with
adenovirus 1 confirms the characteristic genome organization of gizzard erosions in Europe and apathogenic reference strains. J. Vet.
siadenoviruses. Infect. Genet. Evol. 11, 1058–1065. https://doi. Diagn. Invest. 22, 937–941.
org/10.1016/j.meegid.2011.03.021 Marek, A., Nolte, V., Schachner, A., Berger, E., Schlötterer, C., and Hess,
Kumar, R., Mohanty, G.C., Verma, K.C., and Ram-Kumar (1992). M. (2012). Two fiber genes of nearly equal lengths are a common and
Epizootiological studies on egg drop syndrome in poultry. Indian J. distinctive feature of Fowl adenovirus C members. Vet. Microbiol. 156,
Anim. Sci. 62, 497–501. 411–417. https://doi.org/10.1016/j.vetmic.2011.11.003
Kümin, D., Hofmann, C., Uckert, W., Both, G.W., and Löser, P. (2004). Marek, A., Kosiol, C., Harrach, B., Kaján, G.L., Schlötterer, C., and Hess,
Identification of an ovine atadenovirus gene whose product activates the M. (2013). The first whole genome sequence of a fowl adenovirus B
viral E2 promoter: possible involvement of E2F-1. Virology 318, 79–89. strain enables interspecies comparisons within the genus aviadenovirus.
https://doi.org/10.1016/j.virol.2003.09.002 Vet. Microbiol. 166, 250–256. https://doi.org/10.1016/j.
Lal, B., Maiti, N.K., Oberoi, M.S., and Sharma, S.N. (1991). Cell mediated vetmic.2013.05.017
immune response of chicks following fowl adenovirus type-1 infection. Marek, A., Kaján, G.L., Kosiol, C., Harrach, B., Schlötterer, C., and Hess,
Comp. Immunol. Microbiol. Infect. Dis. 14, 55–58. M. (2014a). Complete genome sequences of pigeon adenovirus 1
Larsson, S., Bellett, A., and Akusjärvi, G. (1986). VA RNAs from avian and and duck adenovirus 2 extend the number of species within the genus
human adenoviruses: dramatic differences in length, sequence, and gene Aviadenovirus. Virology 462-463, 107–114. https://doi.org/10.1016/j.
location. J. Virol. 58, 600–609. virol.2014.04.033
Latimer, K.S., Niagro, F.D., Williams, O.C., Ramis, A., Goodwin, M.A., Marek, A., Ballmann, M.Z., Kosiol, C., Harrach, B., Schlotterer, C., and
Ritchie, B.W., and Campagnoli, R.P. (1997). Diagnosis of avian Hess, M. (2014b). Whole-genome sequences of two turkey adenovirus
adenovirus infections using DNA in situ hybridization. Avian Dis. 41, types reveal the existence of two unknown lineages that merit the
773–782. establishment of novel species within the genus Aviadenovirus. J Gen
Le Goff, F., Mederle-Mangeot, I., Jestin, A., and Langlois, P. (2005). Deletion Virol 95, 156–170.
of open reading frames 9, 10 and 11 from the avian adenovirus CELO Marek, A., Kaján, G.L., Kosiol, C., Benkő, M., Schachner, A., and Hess, M.
genome: effect on biodistribution and humoral responses. J. Gen. Virol. (2016). Genetic diversity of species fowl aviadenovirus D and Fowl
86, 2019–2027. aviadenovirus E. J. Gen. Virol. 97, 2323–2332. https://doi.org/10.1099/
Lehrmann, H., and Cotten, M. (1999). Characterization of CELO virus jgv.0.000519
proteins that modulate the pRb/E2F pathway. J. Virol. 73, 6517–6525. Mase, M., Nakamura, K., and Imada, T. (2010). Characterization of fowl
Leopold, P.L., Kreitzer, G., Miyazawa, N., Rempel, S., Pfister, K.K., adenovirus serotype 4 isolated from chickens with hydropericardium
Rodriguez-Boulan, E., and Crystal, R.G. (2000). Dynein- and syndrome based on analysis of the short fiber protein gene. J. Vet. Diagn.
microtubule-mediated translocation of adenovirus serotype 5 occurs Invest. 22, 218–223.
after endosomal lysis. Hum. Gene Ther. 11, 151–165. https://doi. Matczuk, A.K., Niczyporuk, J.S., Kuczkowski, M., Woźniakowski, G.,
org/10.1089/10430340050016238 Nowak, M., and Wieliczko, A. (2017). Whole genome sequencing of
Li, H., Wang, J., Qiu, L., Han, Z., and Liu, S. (2016). Fowl adenovirus species fowl aviadenovirus A - a causative agent of gizzard erosion and ulceration,
C serotype 4 is attributed to the emergence of hepatitis-hydropericardium in adult laying hens. Infect. Genet. Evol. 48, 47–53.
syndrome in chickens in China. Infect. Genet. Evol. 45, 230–241. Matos, M., Grafl, B., Liebhart, D., and Hess, M. (2016a). The outcome
Lim, T.H., Kim, B.Y., Kim, M.S., Jang, J.H., Lee, D.H., Kwon, Y.K., Lee, J.B., of experimentally induced inclusion body hepatitis (IBH) by fowl
Park, S.Y., Choi, I.S., and Song, C.S. (2012). Outbreak of gizzard erosion aviadenoviruses (FAdVs) is crucially influenced by the genetic
associated with fowl adenovirus infection in Korea. Poult. Sci. 91, background of the host. Vet. Res. 47, 69. https://doi.org/10.1186/
1113–1117. https://doi.org/10.3382/ps.2011-02050 s13567-016-0350-0
Liu, Y., Wan, W., Gao, D., Li, Y., Yang, X., Liu, H., Yao, H., Chen, L., Wang, C., Matos, M., Grafl, B., Liebhart, D., Schwendenwein, I., and Hess, M. (2016b).
and Zhao, J. (2016). Genetic characterization of novel fowl aviadenovirus Selected clinical chemistry analytes correlate with the pathogenesis of
4 isolates from outbreaks of hepatitis-hydropericardium syndrome in inclusion body hepatitis experimentally induced by fowl aviadenoviruses.
broiler chickens in China. Emerg. Microbes Infect. 5, e117. https://doi. Avian Pathol. 45, 520–529. https://doi.org/10.1080/03079457.2016.1
org/10.1038/emi.2016.115 168513
Lüschow, D., Prusas, C., Lierz, M., Gerlach, H., Soike, D., and Hafez, H.M. Mazaheri, A., Prusas, C., Voss, M., and Hess, M. (1998). Some strains
(2007). Adenovirus of psittacine birds: investigations on isolation of serotype 4 fowl adenoviruses cause inclusion body hepatitis and
and development of a real-time polymerase chain reaction for specific hydropericardium syndrome in chickens. Avian Pathol. 27, 269–276.
detection. Avian Pathol. 36, 487–494. https://doi.org/10.1080/03079459808419335