The first whole genome sequence and pathogenicity characterization of a fowl adenovirus 4 isolated from ducks associated with inclusion body hepatitis and hydropericardium syndrome

References

• Asthana, M., Chandra, R. & Kumar, R. (2013). Hydropericardium syndrome: current state and future developments. Archives of Virology, 158, 921–931. doi: 10.1007/s00705-012-1570-x
   PubMed Web of Science ®Google Scholar
• Chen, H., Dou, Y., Zheng, X., Tang, Y., Zhang, M., Zhang, Y., Wang, Z. & Diao, Y. (2016). Hydropericardium hepatitis syndrome emerged in cherry valley ducks in China. Transboundary and Emerging Diseases. [Epub ahead of print]. doi:10.1111/tbed.12500.
   Web of Science ®Google Scholar
• Eregae, M.E., Dewey, C.E., McEwen, S.A., Ouckama, R., Ojkić, D. & Guerin, M.T. (2014). Flock prevalence of exposure to avian adeno-associated virus, chicken anemia virus, fowl adenovirus, and infectious bursal disease virus among Ontario broiler chicken flocks. Avian Diseases, 58, 71–77. doi: 10.1637/10612-071113-Reg.1
   PubMed Web of Science ®Google Scholar
• Francois, A., Chevalier, C., Delmas, B., Eterradossi, N., Toquin, D., Rivallan, G. & Langlois, P. (2004). Avian adenovirus CELO recombinants expressing VP2 of infectious bursal disease virus induce protection against bursal disease in chickens. Vaccine, 22, 2351–2360. doi: 10.1016/j.vaccine.2003.10.039
   PubMed Web of Science ®Google Scholar
• Ganesh, K., Suryanarayana, V., Raghavan, R. & Gowda, S. (2001). Nucleotide sequence of L1 and part of P1 of hexon gene of fowl adenovirus associated with hydropericardium hepatitis syndrome differs with the corresponding region of other fowl adenoviruses. Veterinary Microbiology, 78, 1–11. doi: 10.1016/S0378-1135(00)00288-1
   PubMed Web of Science ®Google Scholar
• Hess M. (2000). Detection and differentiation of avian adenoviruses: a review. Avian Pathology, 29, 195–206. doi: 10.1080/03079450050045440
   PubMed Web of Science ®Google Scholar
• Jiang, L., Qi, X., Gao, Y., Hua, Y., Li, K., Deng, X., Wang, Q., Zhang, L., Chai, H., Chen, Y., Yin, C., Gao, H., Qin, L., Wang, Y., Qu, Y., Chen, Q., Fan, Z. & Wang, X. (2013). Molecular characterization and phylogenetic analysis of the reticuloendotheliosis virus isolated from wild birds in northeast China. Veterinary Microbiology, 166, 68–75. doi: 10.1016/j.vetmic.2013.05.008
   PubMed Web of Science ®Google Scholar
• Johnson, M.A., Pooley, C., Ignjatovic, J. & Tyack, S.G. (2003). A recombinant fowl adenovirus expressing the S1 gene of infectious bronchitis virus protects against challenge with infectious bronchitis virus. Vaccine, 21, 2730–2736. doi: 10.1016/S0264-410X(03)00227-5
   PubMed Web of Science ®Google Scholar
• Kaján, G.L., Kecskeméti, S., Harrach, B. & Benkő, M. (2013). Molecular typing of fowl adenoviruses, isolated in Hungary recently, reveals high diversity. Veterinary Microbiology, 167, 357–363. doi: 10.1016/j.vetmic.2013.09.025
   PubMed Web of Science ®Google Scholar
• Li, L., Luo, L., Luo, Q., Zhang, T., Zhao, K., Wang, H., Zhang, R., Lu, Q., Pan, Z., Shao, H., Zhang, W. & Wen, G. (2016). Genome sequence of a fowl adenovirus serotype 4 strain lethal to chickens, isolated from China. Genome Announcements, 4, e00140–16.
   PubMedGoogle Scholar
• Li, Y., Li, C., Liu, L., Wang, H., Wang, C., Tian, G., Webster, R.G., Yu, K. & Chen, H. (2006). Characterization of an avian influenza virus of subtype H7N2 isolated from chickens in northern China. Virus Genes, 33, 117–122. doi: 10.1007/s11262-005-0042-8
   PubMed Web of Science ®Google Scholar
• Lu, Z., Zhang, L., Wang, N., Chen, Y., Gao, L., Wang, Y., Gao, H., Gao, Y., Li, K., Qi, X. & Wang, X. (2015). Naturally occurring reassortant infectious bursal disease virus in northern China. Virus Research, 203, 92–95. doi: 10.1016/j.virusres.2015.04.003
   PubMed Web of Science ®Google Scholar
• Lv, H., Zhang, Y., Sun, G., Bao, K., Gao, Y., Qi, X., Cui, H., Wang, Y., Li, K., Gao, L., Pan, Q., Wang, X. & Liu, C. (2016). Genetic evolution of Gallid herpesvirus 2 isolated in China. Infection, Genetic and Evolution, 51, 263–274. doi: 10.1016/j.meegid.2016.04.027
   PubMed Web of Science ®Google Scholar
• Marek, A., Kosiol, C., Harrach, B., Kaján, G.L., Schlötterer, C. & Hess, M. (2013). The first whole genome sequence of a Fowl adenovirus B strain enables interspecies comparisons within the genus Aviadenovirus. Veterinary Microbiology, 166(1–2), 250–256. doi: 10.1016/j.vetmic.2013.05.017
   PubMed Web of Science ®Google Scholar
• Mase, M., Nakamura, K. & Minami, F. (2012). Fowl adenoviruses isolated from chickens with inclusion body hepatitis in Japan, 2009–2010. Journal of Veterinary Medicine Science, 74, 1087–1089. doi: 10.1292/jvms.11-0443
   PubMed Web of Science ®Google Scholar
• Mazaheri, A., Prusas, C., Voss, M. & Hess, M. (1998). Some strains of serotype 4 fowl adenoviruses cause inclusion body hepatitis and hydropericardium syndrome in chickens. Avian Pathology, 27, 269–276. doi: 10.1080/03079459808419335
   PubMed Web of Science ®Google Scholar
• Mittal, D., Jindal, N., Tiwari, A.K. & Khokhar, R.S. (2014). Characterization of fowl adenoviruses associated with hydropericardium syndrome and inclusion body hepatitis in broiler chickens. VirusDisease, 25, 114–119. doi: 10.1007/s13337-013-0183-7
   PubMedGoogle Scholar
• Rahimi, M. & Minoosh, S.H.Z. (2015). Adenovirus-like inclusion body hepatitis in a flock of broiler chickens in Kermanshah province, Iran. Veterinary Research Forum, 6, 95–98.
   PubMed Web of Science ®Google Scholar
• Reed, L.J. & Muench, H. (1938). A simple method of estimation of 50% end points. American Journal of Hygiene, 27, 493–497.
   Google Scholar
• Sheppard, M., McCoy, R.J. & Werner, W. (1995). Genomic mapping and sequence analysis of the fowl adenovirus serotype 10 hexon gene. Journal of General Virology, 76, 2595–2600. doi: 10.1099/0022-1317-76-10-2595
   PubMed Web of Science ®Google Scholar
• Vera-Hernández, P.F., Morales-Garzón, A., Cortés-Espinosa, D.V., Galiote-Flores, A., García-Barrera, L.J., Rodríguez-Galindo, E.T., Toscano-Contreras, A., Lucio-Decanini, E. & Absalon, A.E. (2015). Clinicopathological characterization and genomic sequence differences observed in a highly virulent fowl aviadenovirus serotype 4. Avian Pathology, 27, 1–32.
   Google Scholar
• Wang, Q., Li, X., Ji, X., Wang, J., Shen, N., Gao, Y., Qi, X., Wang, Y., Gao, H., Zhang, S. & Wang, X. (2014). A recombinant avian leukosis virus subgroup J for directly monitoring viral infection and the selection of neutralizing antibodies. PLoS One, 9, e115422. doi: 10.1371/journal.pone.0115422
   PubMed Web of Science ®Google Scholar
• Ye, J., Liang, G., Zhang, J., Wang, W., Song, N., Wang, P., Zheng, W., Xie, Q., Shao, H., Wan, Z., Wang, C., Chen, H., Gao, W. & Qin, A. (2016). Outbreaks of serotype 4 fowl adenovirus with novel genotype, China. Emerging Microbes and Infections, 5, e50. doi: 10.1038/emi.2016.50
   PubMed Web of Science ®Google Scholar
• Zhao, J., Zhong, Q., Zhao, Y., Hu, Y.X. & Zhang, G.Z. (2015). Pathogenicity and complete genome characterization of fowl adenoviruses isolated from chickens associated with inclusion body hepatitis and hydropericardium syndrome in China. PLoS One, 10, e0133073. doi: 10.1371/journal.pone.0133073
   PubMed Web of Science ®Google Scholar
• Zhong, L., Gao, L., Liu, Y., Li, K., Wang, M., Qi, X., Gao, Y. & Wang, X. (2016). Genetic and pathogenic characterisation of 11 avian reovirus isolates from northern China suggests continued evolution of virulence. Scientific Reports, 6, 35271. doi: 10.1038/srep35271
   PubMed Web of Science ®Google Scholar
• Zhu, J., Hu, S., Xu, H., Liu, J., Zhao, Z., Wang, X. & Liu, X. (2016). Characterization of virulent Newcastle disease viruses from vaccinated chicken flocks in Eastern China. BMC Veterinary Research, 12, 113. doi: 10.1186/s12917-016-0732-6
   PubMed Web of Science ®Google Scholar