Evidence of interspecies transmission and reassortment among avian group A rotaviruses

Virology

Volumn 386, Issue 2, 2009, Pages 334-343

  Schumann, Thomas ^a   Hotzel, Helmut ^b   Otto, Peter ^b   Johne, Reimar ^a  

^a FEDERAL INSTITUTE FOR RISK ASSESSMENT   (Germany)

^b FEDERAL RESEARCH INSTITUTE FOR ANIMAL HEALTH   (Germany)

Author keywords

Avian virus; Epidemiology; Genome analysis; Interspecies transmission; Reassortment; Rotavirus

Indexed keywords

AMINO ACID;

AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; CONTROLLED STUDY; FOWL; GENE CLUSTER; GENE SEQUENCE; GENE STRUCTURE; GENETIC CODE; GENETIC REASSORTMENT; GENOTYPE; NONHUMAN; PHYLOGENY; PRIORITY JOURNAL; PROMOTER REGION; ROTAVIRUS; VIRUS GENE; VIRUS ISOLATION; VIRUS TRANSMISSION;

AMINO ACID SEQUENCE; ANIMALS; CAPSID PROTEINS; CHICKENS; EVOLUTION, MOLECULAR; GENOME, VIRAL; GENOTYPE; MOLECULAR SEQUENCE DATA; PHYLOGENY; RNA, VIRAL; ROTAVIRUS; ROTAVIRUS INFECTIONS; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS, RNA; TURKEYS;

AVES; GALLUS GALLUS; MAMMALIA; ROTAVIRUS; ROTAVIRUS A;

EID: 62749113376     PISSN: 00426822     EISSN: 10960341     Source Type: Journal    
DOI: 10.1016/j.virol.2009.01.040     Document Type: Article

References (61)

1. Aich P., Wilson H.L., Kaushik R.S., Potter A.A., Babiuk L.A., and Griebel P. Comparative analysis of innate immune responses following infection of newborn calves with bovine rotavirus and bovine coronavirus. J. Gen. Virol. 88 (2007) 2749-2761
2. Brüssow H., Nakagomi O., Gerna G., and Eichhorn W. Isolation of an avianlike group A rotavirus from a calf with diarrhea. J. Clin. Microbiol. 30 (1992) 67-73
3. Charpilienne A., Lepault J., Rey F., and Cohen J. Identification of rotavirus VP6 residues located at the interface with VP2 that are essential for capsid assembly and transcriptase activity. J. Virol. 76 (2002) 7822-7831
4. Choi A.H., Basu M., McNeal M.M., Flint J., VanCott J.L., Clements J.D., and Ward R.L. Functional mapping of protective domains and epitopes in the rotavirus VP6 protein. J. Virol. 74 (2000) 11574-11580
5. Cook N., Bridger J., Kendall K., Gomara M.I., El-Attar L., and Gray J. The zoonotic potential of rotavirus. J. Infect. 48 (2004) 289-302
6. Crawford S.E., Murkherjee S.K., Estes M.K., Lawton J.A., Shaw A.L., Ramig R.F., and Prasad B.V. Trypsin cleavage stabilizes the rotavirus VP4 spike. J. Virol. 75 (2001) 6052-6061
7. DeGrazia S., Martella V., Giammanco G.M., Iturriza-Gómara M., Ramirez S., Cascio A., Colomba C., and Arista S. Canine-origin G3P[3] rotavirus in child with acute gastroenteritis. Emerg. Infect. Dis. 13 (2007) 1091-1093
8. Day J.M., Spackman E., and Pantin-Jackwood M. A multiplex RT-PCR test for the differential identification of turkey astrovirus type 1, turkey astrovirus type 2, chicken astrovirus, avian nephritis virus, and avian rotavirus. Avian Dis. 51 (2007) 681-684
9. Dormitzer P.R., Sun Z.Y., Wagner G., and Harrison S.C. The rhesus rotavirus VP4 sialic acid binding domain has a galectin fold with a novel carbohydrate binding site. EMBO J. 21 (2002) 885-897
10. Eichwald C., Vascotto F., Faretti E., and Burrone O.R. Rotavirus NSP5: mapping phosphorylation sites and kinase activation and viroplasm localisation domains. J. Virol. 76 (2002) 3461-3470
11. Eichwald C., Jacob G., Muszynski B., Allende J.E., and Burrone O.R. Uncoupling substrate and activation functions of rotavirus NSP5: phosphorylation of Ser-67 by casein kinase 1 is essential for hyperphosphorylation. Proc. Natl. Acad. Sci. U. S. A. 101 (2004) 16304-16309
12. Elschner M., Hotzel H., Reetz J., Diller R., and Otto P. Isolation, identification and characterization of group A rotavirus from chicken: the inner capsid protein sequence shows only a distant phylogenetic relationship to most other avian group A rotaviruses. J. Vet. Med., Ser. B 52 (2005) 211-213
13. Erk I., Huet J.C., Duarte M., Duquerroy S., Rey F., Cohen J., and Lepault J. A zinc ion controls assembly and stability of the major capsid protein of rotavirus. J. Virol. 77 (2003) 3595-3601
14. Estes M.K., and Kapikian A.Z. Rotaviruses. In: Knipe D.M., Howley P.M., Griffin D.E., Lamb R.A., Martin M.A., Roizman B., and Straus S.E. (Eds). Fields Virology. fifth edition (2007), Lippincott, Williams and Wilkins, Philadelphia 1917-1974
15. Ghosh S., Varghese V., Samajdar S., Sinha M., Naik T.N., and Kobayashim N. Evidence for bovine origin of VP4 and VP7 genes of human group A rotavirus G6P[14] and G10P[14] strains. J. Clin. Microbiol. 45 (2007) 2751-2753
16. Gilbert J.M., and Greenberg H.B. Cleavage of rhesus rotavirus VP4 after arginine 247 is essential for rotavirus-like particle-induced fusion from without. J. Virol. 72 (1998) 5323-5327
17. Golantsova N.E., Gorbunova E.E., and Mackow E.R. Discrete domains within the rotavirus VP5* direct peripheral membrane association and membrane permeability. J. Virol. 78 (2004) 2037-2044
18. Gorziglia M., Nishikawa K., and Fukuhara N. Evidence of duplication and deletion in super short segment 11 of rabbit rotavirus Alabama strain. Virology 170 (1989) 587-590
19. Gorziglia M., Larralde G., Kapikian A.Z., and Chanock R.M. Antigenic relationships among human rotaviruses as determined by outer capsid protein VP4. Proc. Natl. Acad. Sci. U. S. A. 87 (1990) 7155-7159
20. Graham K.L., Halasz P., Tan Y., Hewish M.J., Takada Y., Mackow E.R., Robinson M.K., and Coulson B.S. Integrin-using rotaviruses bind alpha2beta1 integrin alpha 2 I domain via VP4 DGE sequence and recognize alphaXbeta2 and alphaVbeta3 by using VP7 during cell entry. J. Virol. 77 (2003) 9969-9978
21. Graham K.L., Takada Y., and Coulson B.S. Rotavirus spike protein VP5* binds alpha2beta1 integrin on the cell surface and competes with virus for cell binding and infectivity. J. Gen. Virol. 87 (2006) 1275-1283
22. Ito H., Sugiyama M., Masubuchi Y., Mori Y., and Minamoto N. Complete nucleotide sequence of a group A avian rotavirus genome and comparison with its counterparts of mammalian rotaviruses. Virus Res. 75 (2001) 123-138
23. Iturriza-Gómara M., Wong C., Blome S., Desselberger U., and Gray G. Molecular characterization of VP6 genes of human rotavirus isolates: correlation of genogroups with subgroups and evidence for independent segregation. J. Virol. 76 (2002) 6596-6601
24. Khamrin P., Maneekarn N., Peerakome S., Yagyu F., Okitsu S., and Ushijiama H. Molecular characterization of a rare G3P[3] human rotavirus reassortant strain reveals evidence for multiple human-animal interspecies transmissions. J. Med. Virol. 78 (2006) 986-994
25. Kojima K., Taniguchi K., Urasawa T., and Urasawa S. Sequence analysis of normal and rearranged NSP5 genes from human rotavirus strains isolated in nature: implications for the occurrence of the rearrangement at the step of plus strand synthesis. Virology 224 (1996) 446-452
26. Kool D.A., Matsui S.M., Greenberg H.B., and Holmes I.H. Isolation and characterization of a novel reassortant between avian Ty-1 and simian RRV rotaviruses. J. Virol. 66 (1992) 6836-6839
27. Mascarenhas J.D., Leite J.P., Lima J.C., Heinemann M.B., Oliveira D.S., Araujo I.T., Soares L.S., Gusmao R.H., Gabbay Y.B., and Linhares A.C. Detection of a neonatal human rotavirus strain with VP4 and NSP4 genes of porcine origin. J. Med. Microbiol. 56 (2007) 524-532
28. Mathieu M., Petittpas I., Navaza J., Lepault J., Kohli E., Pothier P., Prasad B.V., Cohen J., and Rey F.A. Atomic structure of the major capsid protein of rotavirus: implications for the architecture of the virion. EMBO J. 20 (2001) 1485-1497
29. Matthijnssens J., Rahman M., Martella V., Xuelei Y., De Vos S., De Leener K., Ciarlet M., Buonavoglia C., and Van Ranst M. Full genomic analysis of human rotavirus strain B4106 and lapine rotavirus strain 30/96 provides evidence for interspecies transmission. J. Virol. 80 (2006) 3801-3810
30. Matthijnssens J., Ciarlet M., Heiman E., Arijs I., Delbeke T., McDonald S.M., Palombo E.A., Iturriza-Gómara M., Maes P., Patton J.T., Rahman M., and Van Ranst M. Full genome-based classification of rotaviruses reveals common origin between human Wa-like and porcine rotavirus strains and human DS-1-like and bovine rotavirus strains. J. Virol. 82 (2008) 3204-3219
31. Matthijnssens J., Ciarlet M., Rahman M., Attoui H., Bányai K., Estes M.K., Gentsch J.R., Iturriza-Gómara M., Kirkwood C.D., Martella V., Mertens P.P., Nakagomi O., Patton J.T., Ruggeri F.M., Saif L.J., Santos N., Steyer A., Taniguchi K., Desselberger U., and Van Ranst M. Recommendations for the classification of group A rotaviruses using all 11 genomic RNA segments. Arch. Virol. 153 (2008) 1621-1629
32. Matthijnssens J., Rahman M., and Van Ranst M. Two out of 11 genes of an unusual human G6P[6] rotavirus isolate are of bovine origin. J. Gen. Virol. 89 (2008) 2630-2635
33. McNeal M.M., Basu M., Bean J.A., Clements J.D., Choi A.H., and Ward R.L. Identification of an immunodominant CD4+ T cell epitope in the VP6 protein of rotavirus following intranasal immunization of BALB/c mice. Virology 363 (2007) 410-418
34. McNulty M.S. Rotavirus infections. In: Saif Y.M. (Ed). Diseases of Poultry (2003), Iowa State University press, Ames, IA 308-320
35. McNulty M.S., Allan G.M., Todd D., and McFerran J.B. Isolation and cell culture propagation of rotaviruses from turkeys and chickens. Arch. Virol. 61 (1979) 13-21
36. McNulty M.S., Allan G.M., Todd D., McFerran J.B., McKillop E.R., Collins D.S., and McCracken R.M. Isolation of rotaviruses from turkeys and chickens: demonstration of distinct serotypes and RNA electropherotypes. Avian Pathol. 9 (1980) 363-375
37. Minamoto N., Sugimoto O., Yokota M., Tomita M., Goto H., Sugiyama M., and Kinjo T. Antigenic analysis of avian rotavirus VP6 using monoclonal antibodies. Arch. Virol. 131 (1993) 293-305
38. Mori Y., Sugiyama M., Takayama M., Atoji Y., Masegi T., and Minamoto N. Avian-to-mammal transmission of an avian rotavirus: analysis of its pathogenicity in a heterologous mouse model. Virology 288 (2001) 63-70
39. Mori Y., Borgan M.A., Takayama M., Ito N., Sugiyama M., and Minamoto N. Roles of outer capsid proteins as determinants of pathogenicity and host range of avian rotaviruses in a suckling mouse model. Virology 316 (2003) 126-134
40. Müller H., and Johne R. Rotaviruses: diversity and zoonotic potential - a brief review. Berl. Munch. Tierarztl. Wochenschr. 120 (2007) 108-112
41. Nishikawa K., Hoshino Y., and Gorziglia M. Sequence of the VP7 gene of chicken rotavirus Ch2 strain of serotype 7 rotavirus. Virology 185 (1991) 853-856
42. Nguyen T.A., Khamrin P., Trinh Q.D., Phan T.G., Pham l.e.D., Hoang l.e.P., Hoang K.T., Yagyu F., Okitsu S., and Ushijama U. Sequence analysis of Vietnamese P(6) rotavirus strains suggests evidence of interspecies transmission. J. Med. Virol. 79 (2007) 1959-1965
43. Otto P., Schulze P., and Herbst W. Demonstration of group C rotaviruses in fecal samples of diarrheic dogs in Germany. Arch. Virol. 144 (1999) 2467-2473
44. Otto P., Liebler-Tenorio E.M., Elschner M., Reetz J., Löhren U., and Diller R. Detection of rotaviruses and intestinal lesions in broiler chicks from flocks with runting and stunting syndrome (RSS). Avian Dis. 50 (2006) 411-418
45. Otto, P., Liebler-Tenorio, E.M., Löhren, U., Bachmeier, J., 2007. Occurrence of rotaviruses in broiler flocks from Northern and Southern Germany. Referatesammlung 72. Fachgespräch, Fachgruppe "Geflügelkrankheiten", Deutsche Veterinärmedizinische Gesellschaft e.V.
46. Palombo E.A. Genetic analysis of group A rotaviruses: evidence for interspecies transmission of rotavirus genes. Virus Genes 24 (2002) 11-20
47. Parashar U.D., Hummelman E.G., Bresee J.S., Miller M.A., and Glass R.I. Global illness and deaths caused by rotavirus disease in children. Emerg. Infect. Dis. 9 (2003) 565-572
48. Pantin-Jackwood M.J., Spackman E., Day J.M., and Rives D. Periodic monitoring of commercial turkeys for enteric viruses indicates continuous presence of astrovirus and rotavirus on the farms. Avian Dis. 51 (2007) 674-680
49. Rahman M., Matthijnssens J., Yang X., Delbeke T., Arijs I., Taniguchi K., Iturriza-Gómara M., Iftekharuddin N., Azim T., and Van Ranst M. Evolution history and global spread of the emerging G12 human rotaviruses. J. Virol. 81 (2007) 2382-2390
50. Rainsford E.W., and McCrae M.A. Characterization of the NSP6 protein product of rotavirus gene 11. Virus Res. 130 (2007) 193-201
51. Ramig R.F., Ciarlet M., Mertens P.P.C., and Dermody T.S. Genus Rotavirus. In: Fauquet C.M., Mayo M.A., Maniloff J., Desselberger U., and Ball L.A. (Eds). Virus Taxonomy. Eighth Report of the ICTV (2005), Elsevier Academic Press, Amsterdam etc. 484-496
52. Rohwedder A., Schütz K.I., Minamoto N., and Brüssow H. Sequence analysis of pigeon, turkey, and chicken rotavirus VP8* identifies rotavirus 993/83, isolated from calf feaces, as a pigeon rotavirus. Virology 210 (1995) 231-235
53. Ruiz-Palacios G.M., Perez-Schael I., Velazquez F.R., Abate H., Breuer T., Clemens S.C., Cheuvart B., Espinoza F., Gillard P., Innis B.L., Cervantes Y., Linhares A.C., Lopez P., Macias-Parra M., Ortega-Barria E., Richardson V., Rivera-Medina D.M., Rivera L., Salinas B., Pavia-Ruz N., Salmeron J., Rüttimann R., Tinoco J.C., Rubio P., Nunez E., Guerrero M.L., Yarzabal J.P., Damaso S., Tornieporth N., Saez-Llorens X., Vergara R.F., Vesikari T., Bouckenooghe A., Clemens R., De Vos B., O'Ryan M., and Human Rotavirus Vaccine Study Group. Safety and efficacy of an attenuated vaccine against severe rotavirus gastroenteritis. N. Engl. J. Med. 354 (2006) 11-22
54. Thompson J.D., Higgins D.G., and Gibson T.J. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucl. Acids Res. 22 (1994) 4673-4680
55. Torres-Vega M.A., Gonzalez R.A., Duarte M., Poncet D., Lopez S., and Arias C.F. The C-terminal domain of rotavirus NSP5 is essential for its multimerization, hyperphosphorylation and interaction with NSP6. J. Gen. Virol. 81 (2000) 821-830
56. Trojnar E., Otto P., and Johne R. The first complete genome sequence of a chicken group A rotavirus indicates independent evolution of mammalian and avian strains. Virology 386 (2009) 325-333
57. van der Heide R., Koopmans M.P.G., Shekary N., Houwers D.J., van Duynhofen Y.T.H.P., and van der Poel W.H.M. Molecular characterizations of human and animal group A rotaviruses in the Netherlands. J. Clin. Microbiol. 43 (2005) 669-675
58. Wani S.A., Bhat M.A., Ishag S.M., Ashrafi M.A., Buch A.S., and Haq M. Detection of a mammalian-like group A rotavirus in diarrhoeic chicken. Vet. Microbiol. 94 (2003) 13-18
59. Vesikari T., Matson D.O., Dennehy P., Van Damme P., Santosham M., Rodriguez Z., Dallas M.J., Heyse J.F., Goveia M.G., Black S.B., Shinefield H.R., Christie C.D., Ylitalo S., Itzler R.F., Coia M.L., Onorato M.T., Adeyi B.A., Marshall G.S., Gothefors L., Campens D., Karvonen A., Watt J.P., O'Brien K.L., DiNubile M.J., Clark H.F., Boslego J.W., Offit P.A., Heaton P.M., and Rotavirus Efficacy and Safety Trial (REST) Study Team. Safety and efficacy of a pentavalent human-bovine (WC3) reassortant rotavirus vaccine. N. Engl. J. Med. 354 (2006) 23-33
60. Vesikari T., Karvonen A., Prymula R., Schuster V., Tejedor J.C., Cohen R., Meurice F., Han H.H., Damaso S., and Bouckenooghe A. Efficacy of human rotavirus vaccine against rotavirus gastroenteritis during the first 2 years of life in European infants: randomised, double-blind controlled study. Lancet 370 (2007) 1757-1763
61. Zarate S., Romero P., Espinosa R., Arias C.F., and Lopez S. VP7 mediates the interaction of rotaviruses with integrin alphavbeta3 through a novel integrin-binding site. J. Virol. 78 (2004) 10839-10847