Episodic evolution mediates interspecies transfer of a murine coronavirus

Journal of Virology

Volumn 71, Issue 3, 1997, Pages 1946-1955

  Baric, Ralph S ^a,b   Yount, Boyd ^a   Hensley, Lisa ^a   Peel, Sheila A ^a   Chen, Wan ^a  

^a IL   (United States)

^b UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

VIRUS PROTEIN; VIRUS RNA;

ANIMAL CELL; ARTICLE; CAT; CELL STRAIN BHK; CHO CELL; CONTROLLED STUDY; EVOLUTION; HUMAN; HUMAN CELL; MOUSE; MURINE HEPATITIS CORONAVIRUS; NATURAL SELECTION; NONHUMAN; PRIORITY JOURNAL; SPECIES; SWINE; VERO CELL; VIRUS CELL INTERACTION; VIRUS RECOMBINANT; VIRUS REPLICATION;

EID: 0031041457     PISSN: 0022538X     EISSN: None     Source Type: Journal    
DOI: 10.1128/jvi.71.3.1946-1955.1997     Document Type: Article

References (67)

1. Allan, J. S. 1992. Viral evolution and AIDS. J. NIH Res. 4:51-54.
2. Ampel, N. M. 1991. Plagues - what's past is present: thoughts on the origin and history of new infectious diseases. Rev. Infect. Dis. 13:658-665.
3. Armstrong, J., H. Niemann, S. Smeekens, P. Rottier, and G. Warren. 1984. Sequence and topology of a model intracellular membrane protein, E1 glycoprotein, from a coronavirus. Nature 308:751-752.
4. Baric, R. S., K. S. Fu, M. C. Schaad, and S. A. Stohlman. 1990. Establishing a genetic recombination map for MHV-A59 complementation groups. Virology 177:646-656.
5. Bridgen, A., M. Duarte, K. Tobber, H. Laude, and M. Ackermann. 1993. Sequence determination of the nucleocapsid gene of a porcine epidemic diarrhea virus confirms that it is closely related to human coronavirus 229E and TGEV. J. Gen. Virol. 74:1795-1804.
6. Brown, E. G. 1990. Increased virulence of a mouse-adapted variant of influenza A/FM/1/47 virus is controlled by mutations in genome segments 4, 5, 7, and 8. J. Virol. 64:4523-4533.
7. Burks, J. S., B. L. Pelletier, V. Calvez, and F. Colbere-Garapin. 1980. Two coronaviruses isolated from central nervous system tissue of two multiple sclerosis patients. Science 209:933-934.
8. Burns, D. P. W., and R. C. Desrosiers. 1991. Selection of genetic variants of simian immunodeficiency virus in persistently infected rhesus monkeys. J. Virol. 65:1843-1854.
9. Chen, W., and R. S. Baric. 1996. Molecular anatomy of MHV persistence: coevolution of increased host resistance and virus virulence. J. Virol. 70: 3947-3960.
10. Clarke, D. K., E. A. Duarte, A. Moya, S. F. Elena, E. Domingo, and J. Holland. 1993. Genetic bottlenecks and population passages cause profound fitness differences in RNA viruses. J. Virol. 67:222-228.
11. Diez, J., M. Davila, C. Escarmis, M. G. Mateu, J. Dominguez, J. J. Perez, E. Giralt, J. A. Melero, and E. Domingo. 1990. Unique amino acid substitutions in the capsid proteins of foot-and-mouth disease virus from a persistent infection in cell culture. J. Virol. 60:5519-5528.
12. Dveksler, G. S., C. W. Pensiero, C. B. Cardellichio, K. McCuaig, M. N. Pensiero, G.-S. Jiang, N. Beauchemin, and K. V. Holmes. 1993. Several members of the mouse carcinoembryonic antigen-related glycoprotein family are functional receptors for the coronavirus mouse hepatitis virus-A59. J. Virol. 67:1-8.
13. Dveksler, G. S., M. N. Pensiero, C. B. Cardellichio, R. K. Williams, G.-S. Jiang, K. V. Holmes, and C. W. Dieffenbach. 1991. Cloning of the mouse hepatitis virus (MHV) receptor: expression in human and hamster cell lines confers susceptibility to MHV. J. Virol. 65:6881-6891.
14. Eldredge, N., and S. J. Gould. 1977. Punctuated equilibria: an alternative phyletic gradualism, p. 82-115. In T. J. M. Schopf (ed.), Models in paleobiology. Freeman and Cooper, San Francisco, Calif.
15. Ewald, P. W. 1990. Transmission modes and the evolution of virulence. Hum. Nat. 2:1-30.
16. Fernandez-Cuartero, B., J. Burgyan, M. A. Aranda, K. Salanki, E. Moriones, and F. Garcia-Arenal. 1994. Increase in the relative fitness of a plant virus RNA associated with its recombinant nature. Virology 203:373-377.
17. Fitch, W. M., J. M. E. Leiter, X. Li, and P. Palese. 1991. Positive Darwinian evolution in human influenza A virus. Proc. Natl. Acad. Sci. USA 88:4270-4274.
18. Fu, K., and R. S. Baric. 1994. Map locations of mouse hepatitis virus temperature sensitive mutants: confirmation of variable rates of recombination. J. Virol. 68:7458-7466.
19. Gallagher, T. M., M. J. Buchmeier, and S. Perlman. 1992. Cell receptor independent infection by a neurotropic coronavirus. Virology 91:517-522.
20. Gillespie, J. H. 1995. On Ohta's hypothesis: most amino acid substitutions are deleterious. J. Mol. Evol. 40:64-69.
21. Gillespie, J. H. 1984. The molecular clock may be an episodic clock. Proc. Natl. Acad. Sci. USA 81:8009-8013.
22. th Century avian ancestor. Mol. Biol. Evol. 7:194-200.
23. Geraci, J. R., D. J. Aubin, and I. K. Baker. 1982. Mass mortality of harbor seals: pneumonia associated with influenza A virus. Science 215:1129-1131.
24. Gojobori, T., E. N. Moriyama, and M. Kimura. 1990. Molecular clock of viral evolution, and the neutral theory. Proc. Natl. Acad. Sci. USA 87:10015-10018.
25. Gombold, J. E., S. T. Thingley, and S. R. Weiss. 1993. Fusion defective mutants of mouse hepatitis virus A59 contain a mutation in the spike protein cleavage signal. J. Virol. 67:4504-4512.
26. Holland, J. J., J. C. De La Torre, and D. A. Steinhauer. 1992. RNA virus populations as quasispecies. Curr. Top. Microbiol. Immunol. 176:1-43.
27. Kimura, M. 1989. The neutral theory of molecular evolution and the world view of the neutralists. Genome 31:24-31.
28. Lai, M. M. C. 1990. Coronaviruses: organization, replication and expression of genome. Annu. Rev. Microbiol. 44:303-333.
29. Lai, M. M. C. 1992. Genetic recombination in RNA viruses. Curr. Top. Microbiol. Immunol. 176:21-32.
30. Lin, S.-H., and G. Guidotti. 1989. Cloning and expression of a cDNA coding for a rat liver plasma membrane ecto-ATPase. The primary structure of the ecto-ATPase is similar to that of the human biliary glycoprotein I. J. Biol. Chem. 264:14408-14414.
31. Luytjes, W., P. J. Bredenbeek, A. F. H. Noten, M. C. Horzinek, and W. J. M. Spaan. 1988. Sequence of mouse hepatitis virus A59 mRNA 2: indications for RNA recombination between coronavirus and influenza C virus. Virology 166:415-422.
32. Luytjes, W., P. J. Bredenbeek, J. Charite, B. A. van der Zeijst, M. C. Horzinek, and W. J. Spaan. 1987. Primary structure of the glycoprotein E2 of coronavirus MHV-A59 and identification of the trypsin cleavage site. Virology 161:479-487.
33. Makino, S., J. G. Keck, S. A. Stohlman, and M. M. C. Lai. 1986. High frequency RNA recombination of murine coronaviruses. J. Virol. 57:729-737.
34. Mayer, E. 1994. Driving forces in evolution. An analysis of natural selection, p. 29-48. In S. S. Morse (ed.), The evolutionary biology of viruses. Raven Press, New York, N.Y.
35. Michler, R. E. 1996. Xenotransplantation: risks, clinical potential and future prospects. Emerging Infect. Dis. 2:64-70.
36. Morse, S. S., and A. Schluederberg. 1990. Emerging viruses: the evolution of viruses and viral diseases. J. Infect. Dis. 162:1-15.
37. Mounir, S., and P. J. Talbot. 1992. Sequence analysis of the membrane protein gene of human coronavirus OC43 and evidence of O-glycosylation. J. Gen. Virol. 73:2731-2736.
38. Mounir, S., and P. J. Talbot. 1993. Molecular characterization of the S protein gene of human coronavirus. J. Gen. Virol. 74:1981-1989.
39. Murphy, F. A. 1994. New emerging and reemerging infectious diseases. Adv. Virus Res. 43:1-52.
40. Murray, K., P. Selleck, P. Hooper, A. Hyatt, A. Gould, L. Gleeson, H. Westbury, L. Hiley, L. Selvey, B. Rodwell, and P. Ketterer. 1995. A morbillivirus that caused fatal disease in horses and humans. Science 268:94-97.
41. Murray, M. G., J. Bradley, X.-F. Yang, E. Wimmer, E. G. Moss, and V. R. Racaniello. 1988. Poliovirus host range is determined by a short amino acid sequence in neutralization antigenic site I. Science 241:213-215.
42. Murray, R. S., B. Brown, D. Brian, and G. F. Gabirac. 1992. Detection of coronavirus-RNA and antigen in multiple sclerosis brain. Ann. Neurol. 31:525-533.
43. Murray, R. S., G.-Y. Cal, K. Hoel, J.-Y. Zhang, K. F. Soike, and G. F. Cabirac. 1992. Coronavirus infects and causes demyelination in the primate central nervous system. Virology 188:274-284.
44. Nichol, S. T., J. D. Rowe, and W. M. Fitch. 1993. Punctuated equilibrium and positive Darwinian evolution in vesicular stomatitis virus. Proc. Natl. Acad. Sci. USA 90:10424-10428.
45. Ohta, T. 1995. Synonymous and nonsynonymous substitutions in mammalian genes and the nearly neutral theory. J. Mol. Evol. 40:56-63.
46. Parish, C. R. 1994. The emergence and evolution of canine parvovirus - an example of recent host range mutation. Semin. Virology 5:121-132.
47. Parker, M. M., and P. S. Masters. 1990. Sequence comparison of the N genes of five strains of the coronavirus mouse hepatitis virus suggests a three domain structure for the nucteocapsid protein. Virology 179:463-468.
48. Parker, S. E., T. M. Gallagher, and M. J. Buchmeier. 1989. Sequence analysis reveals extensive polymorphism and evidence of deletions within the E2 glycoprotein gene of several strains of murine hepatitis virus. Virology 173: 664-673.
49. Rasschaert, D., M. Duarte, and H. Laude. 1990. Porcine respiratory coronavirus differs from transmissible gastroenteritis virus by a few genomic deletions. J. Gen. Virol. 71:2599-2607.
50. Schmidt, I., M. A. Skinner, and S. G. Siddell. 1987. Nucleotide sequence of the gene encoding the surface projection glycoprotein of coronavirus MHV-JHM. J. Gen. Virol. 68:47-56.
51. Scholtissek, C., I. Koennecke, and R. Rott. 1978. Host range recombinants of fowl plaque (influenza A) virus. Virology 91:79-85.
52. Shope, R. E. 1931. Swine influenza. III. Filtration experiments and etiology. J. Exp. Med. 54:373-380.
53. Shope, R. E. 1958. Swine influenza, p. 81-91. In H. W. Dunne (ed.), Diseases of swine, 1st ed. Iowa State University Press, Ames.
54. Skinner, M. A., D. Ebner, and S. G. Siddell. 1985. Coronavirus MHV-JHM mRNA 5 has a sequence arrangement which potentially allows translation of a second, downstream open reading frame. J. Gen. Virol. 66:581-592.
55. Stewart, J. N., S. Mounir, and P. J. Talbot. 1992. Human coronavirus gene expression in the brains of multiple sclerosis patients. Virology 191:502-505.
56. Subbarao, E. K., W. London, and B. R. Murphy. 1993. A single amino acid in the PB2 gene of influenza A virus is a determinant of host range. J. Virol. 67:1761-1764.
57. Suzuki, H., and F. Taguchi. 1996. Analysis of the receptor binding site of murine coronavirus spike glycoprotein. J. Virol. 70:2632-2636.
58. Tian, S.-F., A. J. Buckler-White, W. T. London, L. J. Reck, R. M. Chanock, and B. R. Murphy. 1985. Nucleoprotein and membrane protein genes are associated with restriction of replication of influenza A/Mallard?NY/78 virus and its reassortants in squirrel monkey respiratory tract. J. Virol. 53:771-775.
59. Truyen, U., J. F. Evermann, E. Vieler, and C. R. Parrish. 1996. Evolution of canine parvovirus involved loss and gain of feline host range. Virology 215:186-189.
60. Vlasak, R., W. Luytjes, W. J. M. Spaan, and P. Palese. 1988. Human and bovine coronaviruses recognize sialic acid containing receptors similar to those of influenza viruses. Proc. Natl. Acad. Sci. USA 85:4526-4529.
61. Weaver, S. C., T. W. Scott, and R. Rico-Hesse. 1991. Molecular evolution of eastern equine encephalomyelitis virus in North America. Virology 182:774-781.
62. Webster, R. G., J. R. Geraci, G. Petursson, and K. Skirnmission. 1981. Conjunctivitis in human beings caused by influenza A virus of seals. N. Engl. J. Med. 304:911-914.
63. Wimmer, E. 1994. Cellular receptors for viruses, p. 1-14. In E. Wimmer (ed.), Cellular receptors for viruses. Cold Spring Harbor Laboratory Press, Plainview, N.Y.
64. Yin, F. H., and N. B. Lomax. 1983. Host range mutants of human rhinoviruses in which nonstructural genes are altered. J. Virol. 48:410-418.
65. Yokomori, K., and M. M. C. Lai. 1991. Mouse hepatitis virus S RNA sequence reveals that nonstructural proteins ns4 and ns5a are not essential for murine coronavirus replication. J. Virol. 65:5605-5608.
66. Yokomori, K., L. R. Banner, and M. M. C. Lai. 1991. Heterogeneity of gene expression of the hemagglutinin-esterase (HE) protein of murine coronaviruses. Virology 183:647-657.
67. Zhang, X., K. G. Kousoulas, and J. Storz. 1992. The hemagglutinin gene of human coronavirus OC43: Phylogenetic relationships to bovine and murine coronaviruses and influenza C virus. Virology 180:221-228.