Molecular typing of fowl adenoviruses, isolated in Hungary recently, reveals high diversity

Veterinary Microbiology

Volumn 167, Issue 3-4, 2013, Pages 357-363

  Kaján, Gyozo L ^a   Kecskeméti, Sándor ^b   Harrach, Balázs ^a   Benko, Mária ^a  

^a INSTITUTE OF EXPERIMENTAL MEDICINE   (Hungary)

^b CENTRAL VETERINARY INSTITUTE   (Hungary)

Author keywords

Emerging pathogen; Fowl adenovirus; Genotyping; Gizzard erosion; Inclusion body hepatitis; Taxonomy

Indexed keywords

ADENOVIRUS; AMPLICON; ARTICLE; CHICKEN; EMBRYO; FOWL; FOWL ADENOVIRUS; GENE AMPLIFICATION; HUNGARY; MICROBIAL DIVERSITY; NONHUMAN; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS; VIRUS ISOLATION;

ADENOVIRIDAE; GALLUS GALLUS;

EMERGING PATHOGEN; FOWL ADENOVIRUS; GENOTYPING; GIZZARD EROSION; INCLUSION BODY HEPATITIS; TAXONOMY;

ADENOVIRIDAE INFECTIONS; ANIMALS; AVIADENOVIRUS; CELLS, CULTURED; CHICK EMBRYO; CHICKENS; GENETIC VARIATION; HUNGARY; MOLECULAR SEQUENCE DATA; MOLECULAR TYPING; PHYLOGENY; POULTRY DISEASES; SEQUENCE HOMOLOGY, NUCLEIC ACID;

EID: 84888052549     PISSN: 03781135     EISSN: 18732542     Source Type: Journal    
DOI: 10.1016/j.vetmic.2013.09.025     Document Type: Article

References (40)

1. Adair B.M., Fitzgerald S.D. Adenovirus infections. Group I adenovirus infections. Diseases of Poultry 2008, 252-266. Wiley-Blackwell. Y.M. Saif, A.M. Fadly, J.R. Glisson, L.R. McDougald, L.K. Nolan, D.E. Swayne (Eds.).
2. Both G.W. Atadenovirus. The Springer Index of Viruses 2012, 1-12. Springer-Verlag, New York. C.A. Tidona, G. Darai (Eds.).
3. Choi K.S., Kye S.J., Kim J.Y., Jeon W.J., Lee E.K., Park K.Y., Sung H.W. Epidemiological investigation of outbreaks of fowl adenovirus infection in commercial chickens in Korea. Poult. Sci. 2012, 91:2502-2506.
4. Davison A.J., Harrach B. Siadenovirus. The Springer Index of Viruses 2011, 49-56. Springer, New York. C.A. Tidona, G. Darai (Eds.).
5. Domanska-Blicharz K., Tomczyk G., Smietanka K., Kozaczynski W., Minta Z. Molecular characterization of fowl adenoviruses isolated from chickens with gizzard erosions. Poult. Sci. 2011, 90:983-989.
6. Günes A., Marek A., Grafl B., Berger E., Hess M. Real-time PCR assay for universal detection and quantitation of all five species of fowl adenoviruses (FAdV-A to FAdV-E). J. Virol. Methods 2012, 183:147-153.
7. Hanson L.A., Rudis M.R., Vasquez-Lee M., Montgomery R.D. A broadly applicable method to characterize large DNA viruses and adenoviruses based on the DNA polymerase gene. Virol. J. 2006, 3:28.
8. Harrach B., Benko M., Both G.W., Brown M., Davison A.J., Echavarría M., Hess M., Jones M.S., Kajon A., Lehmkuhl H.D., Mautner V., Mittal S., Wadell G. Family Adenoviridae. Virus Taxonomy: IXth Report of the International Committee on Taxonomy of Viruses 2011, 125-141. Elsevier, San Diego. A.M.Q. King, E. Lefkowitz, M.J. Adams, E.B. Carstens (Eds.).
9. Harrach B., Kaján G.L. Aviadenovirus. The Springer Index of Viruses 2011, 13-28. Springer, New York. C.A. Tidona, G. Darai (Eds.).
10. Harrach B., Meehan B., Benko M., Adair B., Todd D. Close phylogenetic relationship between egg drop syndrome virus, bovine adenovirus serotype 7, and ovine adenovirus strain 287. Virology 1997, 229:302-308.
11. Jones R.C. Avian reovirus infections. Rev. Sci. Tech. 2000, 19:614-625.
12. Kaján G.L., Kecskeméti S. First Hungarian isolation of an adenovirus type belonging to species Fowl adenovirus B. Magyar Állatorvosok Lapja 2011, 133:347-352.
13. Kaján G.L., Sameti S., Benko M. Partial sequence of the DNA-dependent DNA polymerase gene of fowl adenoviruses: a reference panel for a general diagnostic PCR in poultry. Acta Vet. Hung. 2011, 59:279-285.
14. Kawamura H., Shimizu F., Tsubahara H. Avian adenovirus: its properties and serological classification. Natl. Inst. Anim. Health Quart. 1964, 4:183-193.
15. Kecskeméti S., Bistyák A., Matiz K., Glávits R., Kaján G., Benko M. Observations on gizzard ulcers caused by adenovirus in chickens. Magyar Állatorvosok Lapja 2012, 134:145-149.
16. Lim T.H., Lee H.J., Lee D.H., Lee Y.N., Park J.K., Youn H.N., Kim M.S., Youn H.S., Lee J.B., Park S.Y., Choi I.S., Song C.S. Identification and virulence characterization of fowl adenoviruses in Korea. Avian Dis. 2011, 55:554-560.
17. Marek A., Günes A., Schulz E., Hess M. Classification of fowl adenoviruses by use of phylogenetic analysis and high-resolution melting-curve analysis of the hexon L1 gene region. J. Virol. Methods 2010, 170:147-154.
18. Marek A., Kosiol C., Harrach B., Kaján G.L., Schlötterer C., Hess M. The first whole genome sequence of a Fowl adenovirus B strain enables interspecies comparisons within the genus Aviadenovirus. Vet. Microbiol. 2013, 166:250-256.
19. Marek A., Schulz E., Hess C., Hess M. Comparison of the fibers of Fowl adenovirus A serotype 1 isolates from chickens with gizzard erosions in Europe and apathogenic reference strains. J. Vet. Diagn. Invest. 2010, 22:937-941.
20. Mase M., Mitake H., Inoue T., Imada T. Identification of group I-III avian adenovirus by PCR coupled with direct sequencing of the hexon gene. J. Vet. Med. Sci. 2009, 71:1239-1242.
21. Mase M., Nakamura K., Minami F. Fowl adenoviruses isolated from chickens with inclusion body hepatitis in Japan, 2009-2010. J. Vet. Med. Sci. 2012, 74:1087-1089.
22. McFerran J.B., Clarke J.K., Connor T.J. Serological classification of avian adenoviruses. Arch. Gesamte Virusforsch. 1972, 39:132-139.
23. McFerran J.B., Connor T.J. Further studies on the classification of fowl adenoviruses. Avian Dis. 1977, 21:585-595.
24. McFerran J.B., Connor T.J., McCracken R.M. Isolation of adenoviruses and reoviruses from avian species other than domestic fowl. Avian Dis. 1976, 20:519-524.
25. McFerran J.B., Smyth J.A. Avian adenoviruses. Rev. Sci. Tech. 2000, 19:589-601.
26. Meulemans G., Couvreur B., Decaesstecker M., Boschmans M., van den Berg T. Phylogenetic analysis of fowl adenoviruses. Avian Pathol. 2004, 33:164-170.
27. Nakamura K., Mase M., Yamamoto Y., Takizawa K., Kabeya M., Wakuda T., Matsuda M., Chikuba T., Ohyama T., Takahashi K., Sato N., Akiyama N., Honma H., Imai K. Inclusion body hepatitis caused by fowl adenovirus in broiler chickens in Japan, 2009-2010. Avian Dis. 2011, 55:719-723.
28. Ojkić D., Krell P., Tuboly T., Nagy E. Characterization of fowl adenoviruses isolated in Ontario and Quebec, Canada. Can. J. Vet. Res. 2008, 72:236-241.
29. Ojkić D., Martin E., Swinton J., Vaillancourt J., Boulianne M., Gomis S. Genotyping of Canadian isolates of fowl adenoviruses. Avian Pathol. 2008, 37:95-100.
30. Okuda Y., Ono M., Shibata I., Sato S., Akashi H. Comparison of the polymerase chain reaction-restriction fragment length polymorphism pattern of the fiber gene and pathogenicity of serotype-1 fowl adenovirus isolates from gizzard erosions and from feces of clinically healthy chickens in Japan. J. Vet. Diagn. Invest. 2006, 18:162-167.
31. Ono M., Okuda Y., Yazawa S., Shibata I., Tanimura N., Kimura K., Haritani M., Mase M., Sato S. Epizootic outbreaks of gizzard erosion associated with adenovirus infection in chickens. Avian Dis. 2001, 45:268-275.
32. Pizzuto M.S., De Battisti C., Marciano S., Capua I., Cattoli G. Pyrosequencing analysis for a rapid classification of fowl adenovirus species. Avian Pathol. 2010, 39:391-398.
33. Raue R., Gerlach H., Müller H. Phylogenetic analysis of the hexon loop 1 region of an adenovirus from psittacine birds supports the existence of a new psittacine adenovirus (PsAdV). Arch. Virol. 2005, 150:1933-1943.
34. Raue R., Hess M. Hexon based PCRs combined with restriction enzyme analysis for rapid detection and differentiation of fowl adenoviruses and egg drop syndrome virus. J. Virol. Methods 1998, 73:211-217.
35. Smyth J.A., McNulty M.S. Adenoviridae. Poultry Diseases 2007, 367-381. Elsevier, Edinburgh. M. Pattison, P.F. McMullin, J.M. Bradbury, D.J. Alexander (Eds.).
36. Steer P., Kirkpatrick N., O'Rourke D., Noormohammadi A. Classification of fowl adenovirus serotypes by use of high-resolution melting-curve analysis of the hexon gene region. J. Clin. Microbiol. 2009, 47:311-321.
37. Steer P.A., O'Rourke D., Ghorashi S.A., Noormohammadi A.H. Application of high-resolution melting curve analysis for typing of fowl adenoviruses in field cases of inclusion body hepatitis. Aust. Vet. J. 2011, 89:184-192.
38. Wellehan J., Johnson A., Harrach B., Benko M., Pessier A., Johnson C., Garner M., Childress A., Jacobson E. Detection and analysis of six lizard adenoviruses by consensus primer PCR provides further evidence of a reptilian origin for the atadenoviruses. J. Virol. 2004, 78:13366-13369.
39. Xie Z., Tang Y., Fan Q., Liu J., Pang Y., Deng X., Peng Y., Xie L., Khan M.I. Rapid detection of group I avian adenoviruses by a loop-mediated isothermal amplification. Avian Dis. 2011, 55:575-579.
40. Zsák L., Kisary J. Grouping of fowl adenoviruses based upon the restriction patterns of DNA generated by BamHI and HindIII. Intervirology 1984, 22:110-114.