Seroepidemiology of Reovirus in Healthy Dogs in Six Prefectures in Japan

Reovirus infection is common in mammals. However, seroepidemiological data of reovirus neutralizing antibodies are limited in dogs. In this study, sera of 65 healthy dogs from six prefectures across Japan were tested for neutralizing antibodies against reovirus serotype 1 strain Lang (T1L), serotype...

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Published inJournal of Veterinary Medical Science Vol. 76; no. 3; pp. 471 - 475
Main Authors HWANG, Chung Chew, MOCHIZUKI, Masami, MAEDA, Ken, OKUDA, Masaru, MIZUNO, Takuya
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Published Japan JAPANESE SOCIETY OF VETERINARY SCIENCE 2014
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Abstract Reovirus infection is common in mammals. However, seroepidemiological data of reovirus neutralizing antibodies are limited in dogs. In this study, sera of 65 healthy dogs from six prefectures across Japan were tested for neutralizing antibodies against reovirus serotype 1 strain Lang (T1L), serotype 2 strain Amy (T2A) and serotype 3 strain Dearing (T3D) using plaque reduction neutralization test (PRNT). Seropositivity against reovirus T1L, T2A and T3D was 53.85%, 33.85% and 46.15%, respectively. Distribution of reovirus seropositive samples displayed no distinguishable geographical pattern. However, reovirus seropositivity increased with age and in dogs housed outdoor. Co-infection of multiple reovirus serotypes in dogs was also detected. These data will provide valuable insights towards the usage of reovirus in oncolytic virotherapy in canine cancers.
AbstractList Reovirus infection is common in mammals. However, seroepidemiological data of reovirus neutralizing antibodies are limited in dogs. In this study, sera of 65 healthy dogs from six prefectures across Japan were tested for neutralizing antibodies against reovirus serotype 1 strain Lang (T1L), serotype 2 strain Amy (T2A) and serotype 3 strain Dearing (T3D) using plaque reduction neutralization test (PRNT). Seropositivity against reovirus T1L, T2A and T3D was 53.85%, 33.85% and 46.15%, respectively. Distribution of reovirus seropositive samples displayed no distinguishable geographical pattern. However, reovirus seropositivity increased with age and in dogs housed outdoor. Co-infection of multiple reovirus serotypes in dogs was also detected. These data will provide valuable insights towards the usage of reovirus in oncolytic virotherapy in canine cancers.Reovirus infection is common in mammals. However, seroepidemiological data of reovirus neutralizing antibodies are limited in dogs. In this study, sera of 65 healthy dogs from six prefectures across Japan were tested for neutralizing antibodies against reovirus serotype 1 strain Lang (T1L), serotype 2 strain Amy (T2A) and serotype 3 strain Dearing (T3D) using plaque reduction neutralization test (PRNT). Seropositivity against reovirus T1L, T2A and T3D was 53.85%, 33.85% and 46.15%, respectively. Distribution of reovirus seropositive samples displayed no distinguishable geographical pattern. However, reovirus seropositivity increased with age and in dogs housed outdoor. Co-infection of multiple reovirus serotypes in dogs was also detected. These data will provide valuable insights towards the usage of reovirus in oncolytic virotherapy in canine cancers.
Reovirus infection is common in mammals. However, seroepidemiological data of reovirus neutralizing antibodies are limited in dogs. In this study, sera of 65 healthy dogs from six prefectures across Japan were tested for neutralizing antibodies against reovirus serotype 1 strain Lang (T1L), serotype 2 strain Amy (T2A) and serotype 3 strain Dearing (T3D) using plaque reduction neutralization test (PRNT). Seropositivity against reovirus T1L, T2A and T3D was 53.85%, 33.85% and 46.15%, respectively. Distribution of reovirus seropositive samples displayed no distinguishable geographical pattern. However, reovirus seropositivity increased with age and in dogs housed outdoor. Co-infection of multiple reovirus serotypes in dogs was also detected. These data will provide valuable insights towards the usage of reovirus in oncolytic virotherapy in canine cancers.
Reovirus infection is common in mammals. However, seroepidemiological data of reovirus neutralizing antibodies are limited in dogs. In this study, sera of 65 healthy dogs from six prefectures across Japan were tested for neutralizing antibodies against reovirus serotype 1 strain Lang (T1L), serotype 2 strain Amy (T2A) and serotype 3 strain Dearing (T3D) using plaque reduction neutralization test (PRNT). Seropositivity against reovirus T1L, T2A and T3D was 53.85%, 33.85% and 46.15%, respectively. Distribution of reovirus seropositive samples displayed no distinguishable geographical pattern. However, reovirus seropositivity increased with age and in dogs housed outdoor. Co-infection of multiple reovirus serotypes in dogs was also detected. These data will provide valuable insights towards the usage of reovirus in oncolytic virotherapy in canine cancers.
Author MOCHIZUKI, Masami
MIZUNO, Takuya
MAEDA, Ken
HWANG, Chung Chew
OKUDA, Masaru
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  organization: Laboratory of Veterinary Internal Medicine, The United Graduate School of Veterinary Science, Yamaguchi University, 1677–1 Yoshida, Yamaguchi 753–8515, Japan
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  organization: Laboratory of Veterinary Microbiology, Joint Faculty of Veterinary Medicine, Yamaguchi University, 1677–1 Yoshida, Yamaguchi 753–8515, Japan
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  organization: Laboratory of Veterinary Internal Medicine, The United Graduate School of Veterinary Science, Yamaguchi University, 1677–1 Yoshida, Yamaguchi 753–8515, Japan
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References_xml – reference: 24. Rosen, L., Abinanti, F. R. and Hovis, J. F. 1963. Further observations on the natural infection of cattle with reoviruses. Am. J. Hyg. 77: 38–48.
– reference: 31. Taylor-Robinson, D. 1965. Respiratory virus antibodies in human sera from different regions of the world. Bull. World Health Org. 32: 833–847.
– reference: 11. Lou, T. Y. and Wenner, H. A. 1963. Natural and experimental infection of dogs with reovirus type 1: pathogenecity of the strain for other animals. Am. J. Hyg. 77: 293–304.
– reference: 25. Sabin, A. B. 1959. Reoviruses. Science 130: 1387–1389.
– reference: 7. Hirahara, T., Yasuhara, H., Matsui, O., Kodama, K., Nakai, M. and Sasaki, N. 1988. Characteristics of reovirus type 1 from the respiratory tract of pigs in Japan. Jpn. J. Vet. Sci. 50: 353–361.
– reference: 32. Weiner, H. L. and Fields, B. N. 1977. Neutralization of reovirus: the gene responsible for the neutralization antigen. J. Exp. Med. 146: 1305–1310.
– reference: 29. Tai, J. H., Williams, J. V., Edwards, K. M., Wright, P. F., Crowe, J. E. J. and Dermody, T. S. 2005. Prevalence of reovirus-specific antibodies in young children in Nashville, Tennessee. J. Infect. Dis. 191: 1221–1224.
– reference: 4. Csiza, C. K. 1974. Characterization and serotyping of three feline reovirus isolates. Infect. Immun. 9: 159–166.
– reference: 21. Pal, S. R. and Agarwal, S. C. 1968. Sero-epidemiological study of reovirus infection amongst the normal population of the Chandigarh area- northern India. J. Hyg. (Lond.) 66: 519–529.
– reference: 20. Ouattara, L. A., Barin, F., Barthez, M. A., Bonnaud, B., Roingeard, P., Goudeau, A., Castelnau, P., Vernet, G., Paranhos-Baccalà, G. and Komurian-Pradel, F. 2011. Novel human reovirus isolated from children with acute necrotizing encephalopathy. Emerg. Infect. Dis. 17: 1436–1444.
– reference: 17. Murakami, T. and Kato, H. 1975. Reovirus antibody patterns in dogs: a trial for the application of principal component analysis to seroepidemiology. Natl. Inst. Anim. Health Q (Tokyo) 15: 8–14.
– reference: 26. Schiff, L. A., Nibert, M. L. and Tyler, K. L. 2007. Orthoreoviruses and their replication. pp. 1853–1915. In: Fields Virology, 5th ed. (Knipe, D. M. and Howley, P. M. eds), Lippincott Williams & Wilkins, Philadelphia.
– reference: 18. Muscillo, M., La Rosa, G., Marianelli, C., Zaniratti, S., Capobianchi, M. R., Cantiani, L. and Carducci, A. 2001. A new RT-PCR method for the identification of reoviruses in seawater samples. Water Res. 35: 548–556.
– reference: 22. Rosen, L. 1960. Serologic grouping of reoviruses by hemagglutination-inhibition. Am. J. Hyg. 71: 242–249.
– reference: 5. Decaro, N., Campolo, M., Desario, C., Ricci, D., Camero, M., Lorusso, E., Elia, G., Lavazza, A., Martella, V. and Buonavoglia, C. 2005. Virological and molecular characterization of a mammalian orthoreovirus type 3 strain isolated from a dog in Italy. Vet. Microbiol. 109: 19–27.
– reference: 2. Binn, L. N., Marchwicki, R. H., Keenan, K. P., Strano, A. J. and Engler, W. F. 1977. Recovery of reovirus type 2 from an immature dog with respiratory tract disease. Am. J. Vet. Res. 38: 927–929.
– reference: 33. White, C. L., Twigger, K. R., Vidal, L., De Bono, J. S., Coffey, M., Heinemann, L., Morgan, R., Merrick, A., Errington, F., Vile, R. G., Melcher, A. A., Pandha, H. S. and Harrington, K. J. 2008. Characterization of the adaptive and innate immune response to intravenous oncolytic reovirus (Dearing type 3) during a phase I clinical trial. Gene Ther. 15: 911–920.
– reference: 9. Kokubu, T., Takahashi, T., Takamura, K., Yasuda, H., Hiramatsu, K. and Nakai, M. 1993. Isolation of reovirus type 3 from dogs with diarrhea. J. Vet. Med. Sci. 55: 453–454.
– reference: 27. Scott, F. W., Kahn, D. E. and Gillespie, J. H. 1970. Feline viruses: isolation, characterization, and pathogenicity of a feline reovirus. Am. J. Vet. Res. 31: 11–20.
– reference: 28. Selb, B. and Weber, B. 1994. A study of human reovirus IgG and IgA antibodies by ELISA and western blot. J. Virol. Methods 47: 15–25.
– reference: 15. Matsuura, K., Hasegawa, S., Nakayama, T., Morita, O. and Uetake, H. 1984. Viral pollution of the rivers in Toyama City. Microbiol. Immunol. 28: 575–588.
– reference: 16. Mochizuki, M. and Uchizono, S. 1993. Experimental infections of feline reovirus serotype 2 isolates. J. Vet. Med. Sci. 55: 469–470.
– reference: 23. Rosen, L. 1962. Reoviruses in animals other than man. Ann. N. Y. Acad. Sci. 101: 461–465.
– reference: 8. Hwang, C. C., Umeki, S., Kubo, M., Hayashi, T., Shimoda, H., Mochizuki, M., Maeda, K., Baba, K., Hiraoka, H., Coffey, M., Okuda, M. and Mizuno, T. 2013. Oncolytic reovirus in canine mast cell tumor. PLoS ONE 8: e73555.
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Snippet Reovirus infection is common in mammals. However, seroepidemiological data of reovirus neutralizing antibodies are limited in dogs. In this study, sera of 65...
Reovirus infection is common in mammals. However, seroepidemiological data of reovirus neutralizing antibodies are limited in dogs. In this study, sera of 65...
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SubjectTerms Age Factors
Animals
Antibodies, Neutralizing - blood
canine
Clinical Patholog
Dog Diseases - epidemiology
Dog Diseases - virology
Dogs
Japan - epidemiology
Neutralization Tests - veterinary
neutralizing antibody
plaque reduction neutralization test
Reoviridae Infections - epidemiology
Reoviridae Infections - veterinary
reovirus
Seroepidemiologic Studies
seroepidemiology
Title Seroepidemiology of Reovirus in Healthy Dogs in Six Prefectures in Japan
URI https://www.jstage.jst.go.jp/article/jvms/76/3/76_13-0472/_article/-char/en
https://www.ncbi.nlm.nih.gov/pubmed/24284973
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https://www.proquest.com/docview/1513048389
https://pubmed.ncbi.nlm.nih.gov/PMC4013379
Volume 76
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