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Avian Adenoviruses



          Juan Carlos Corredor and Eva Nagy*                                                          10




          Department of Pathobiology, Ontario Veterinary College, University of Guelph, Guelph, ON, Canada.

          *Correspondence: enagy@ovc.uoguelph.ca
          https://doi.org/10.21775/9781912530106.10






          Abstract                                              worldwide. Inclusion body hepatitis (IBH) is caused by fowl ade-
          Avian adenoviruses are ubiquitous worldwide in avian species.   noviruses (FAdVs), although they can be isolated from healthy
          Although many of these viruses are isolated from healthy birds,   chickens as well, and FAdVs are considered ubiquitous on poultry
          some cause diseases associated with significant economic losses   farms (Hess, 2013). Hydropericardium syndrome (HPS) is the
          in the poultry industry, including egg-drop syndrome (EDS),   result of infection with pathogenic serotype 4 FAdVs. Gizzard
          inclusion body hepatitis (IBH), inclusion body hepatitis/hydrop-  erosion, mainly attributed to FAdV-1, is more frequently seen in
          ericardium syndrome (IBH/HPS) in chickens and haemorrhagic   recent years (Gjevre et al., 2013; Ono et al., 2003). Quail bronchi-
          enteritis (HE) of turkeys. Avian adenoviruses are classified into   tis is an important disease of bobwhite quail. Egg drop syndrome
          three genera based on genome organization, phylogenetic rela-  (EDS) is caused by an atadenovirus, egg drop syndrome virus
          tionships and host: Aviadenovirus, Atadenovirus and Siadenovirus.   (EDSV). Haemorrhagic enteritis (HE) of turkeys is associ-
          The viral genome consists of genus-common and genus-specific   ated with turkey adenovirus 3 (TAdV-3) and together with the
          genes. Genus-common genes, such as those involved in DNA   causative agent of marble spleen disease of pheasants and avian
          replication and encoding structural proteins, are conserved and   adenovirus splenomegaly virus they belong to the siadenoviruses.
          present in all adenoviruses. Genus-specific genes, on the other   In addition, adenovirus infections have been described in turkeys,
          hand, are unique for each genus. The functions of most early viral   geese, ducks, pigeons, guinea fowls and wild birds. The descrip-
          genes of avian adenoviruses remain unknown. Some of these   tions of the diseases can be found in the appropriate chapters of
          genes, such as Gam-1 and ORF22, have functions similar to those   Diseases of Poultry (Swayne et al., 2013).
          described for human adenoviruses – stimulation of cell cycle   The first unintentional isolation of an avian adenovirus was
          progression, modulation of apoptosis and counteraction of the   in 1949, when material from a bovine case suspected for lumpy
          host’s innate immunity. Studies on virus–host interactions at the   skin disease was inoculated into embryonated chicken eggs
          molecular level are limited to a few viruses [e.g. fowl adenovirus   (Van Den Ende et al., 1949). The chicken embryo lethal orphan
          (FAdV)-1, FAdV-4 and FAdV-9]. The virulence determinants for   (CELO) virus, now designated FAdV-1, was first observed in
          these viruses are unknown. However, some candidate viral genes   1957 (Yates and Fry, 1957). Isolation of the first avian adeno-
          associated with virulence have been described in some aviad-  virus from a diseased bird, a bobwhite quail occurred in 1950
          enoviruses (e.g. FAdV-4 and FAdV-8) and a siadenovirus (duck   (Olson, 1951). IBH was first described in the USA in 1963
          adenovirus  1).  Non-pathogenic  aviadenoviruses,  such  as  fowl   by Helmboldt and Frazier (Helmboldt and Frazier, 1963).
          adenoviruses 1, 4, 8, 9 and 10, have been described as virus vec-  Isolation of aviadenovirus from broilers with hydropericardium
          tors for potential use as recombinant poultry vaccines and gene   syndrome was reported from Pakistan in 1988 (Cheema et al.,
          delivery.                                             1989) and very recently numerous outbreaks are identified in
                                                                China (Zhao et al., 2015; Niu et al., 2016). Egg drop syndrome
                                                                (EDS) was described in 1976 in the Netherlands (van Eck et al.,
          Introduction and history                              1976), and the viral aetiology was shown a year later (McFerran
          Adenoviruses can infect and be isolated from humans and a wide   et al., 1977). HE was first mentioned in 1937 (Pomeroy and
          range of mammals, birds and other vertebrate species, although   Fenstermacher, 1937), and its viral aetiology was considered
          they appear to be host specific and co-evolved with their hosts.   by Domermuth and Gross in 1971 (Domermuth and Gross,
          Adenoviruses were first mentioned in connection with human   1971), and since then the disease was reported in many coun-
          adenoid tissues by Rowe and colleagues in 1953 (Rowe et al.,   tries including North America (Carlson et al., 1974; Itakura et
          1953), hence the origin of the name of this group of viruses, sub-  al., 1974).
          sequently the virus was isolated in 1954 (Huebner et al., 1954).  The focus of this chapter is mainly on aviadenoviruses;
            The avian adenoviruses are associated with important clini-  however, other avian adenoviruses will be discussed where appro-
          cal diseases, causing substantial losses to the poultry industry   priate.
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