Literature DB >> 2536983

Glycoprotein evolution of vesicular stomatitis virus New Jersey.

S T Nichol1, J E Rowe, W M Fitch.   

Abstract

A T1 ribonuclease fingerprinting study of a large number of virus isolates had previously demonstrated that considerable genetic variability existed among natural isolates of the vesicular stomatitis virus (VSV) New Jersey (NJ) serotype [S.T. Nichol (1988) J. Virol. 62, 572-579]. Based on these results, 34 virus isolates were chosen as representing the extent of genetic diversity within the VSV NJ serotype. We report the entire glycoprotein (G) gene nucleotide sequence and the deduced amino acid sequence for each of these viruses. Up to 19.8% G gene sequence differences could be seen among NJ serotype isolates. Analysis of the distribution of nucleotide substitutions relative to nucleotide codon position revealed that third position changes were distributed randomly throughout the gene. Third base changes constituted 84% of the observed nucleotide substitutions and affected 89% of the third base positions located in the G gene. Only three short oligonucleotide stretches of complete sequence conservation were observed. The remaining nucleotide changes located in the first and second positions were not distributed randomly, indicating that most of the amino acids coded by the G gene cannot be altered without reducing the fitness of the VSV NJ serotype viruses. Despite these constraints, up to 8.5% amino acid differences were observed between virus isolates. These differences were located throughout the G protein including regions adjacent to defined major antibody neutralization epitopes. Apparent clusters of amino acid substitutions were present in the hydrophobic signal sequence, transmembrane domain, and within the cytoplasmic domain of the G protein. A maximum parsimony analysis of the G gene nucleotide sequences allowed construction of a phylogram indicating the evolutionary relationship of these viruses. The VSV NJ serotype appears to contain at least three distinct lineages or subtypes. All recent virus isolates from the United States and Mexico are within subtype I and appear to have evolved from an ancestor more closely related to the Hazelhurst historic strain than other older strains. The implications of these findings for the evolution, epizootiology, and classification of these viruses are discussed.

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Year:  1989        PMID: 2536983     DOI: 10.1016/0042-6822(89)90268-7

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  19 in total

1.  Quantitation of relative fitness and great adaptability of clonal populations of RNA viruses.

Authors:  J J Holland; J C de la Torre; D K Clarke; E Duarte
Journal:  J Virol       Date:  1991-06       Impact factor: 5.103

2.  Efficient export of the vesicular stomatitis virus G protein from the endoplasmic reticulum requires a signal in the cytoplasmic tail that includes both tyrosine-based and di-acidic motifs.

Authors:  C S Sevier; O A Weisz; M Davis; C E Machamer
Journal:  Mol Biol Cell       Date:  2000-01       Impact factor: 4.138

3.  RNA virus quasispecies populations can suppress vastly superior mutant progeny.

Authors:  J C de la Torre; J J Holland
Journal:  J Virol       Date:  1990-12       Impact factor: 5.103

4.  Polymerase errors accumulating during natural evolution of the glycoprotein gene of vesicular stomatitis virus Indiana serotype isolates.

Authors:  P A Bilsel; S T Nichol
Journal:  J Virol       Date:  1990-10       Impact factor: 5.103

5.  Very high frequency of reversion to guanidine resistance in clonal pools of guanidine-dependent type 1 poliovirus.

Authors:  J C de la Torre; E Wimmer; J J Holland
Journal:  J Virol       Date:  1990-02       Impact factor: 5.103

6.  Phosphoprotein and nucleocapsid protein evolution of vesicular stomatitis virus New Jersey.

Authors:  P A Bilsel; J E Rowe; W M Fitch; S T Nichol
Journal:  J Virol       Date:  1990-06       Impact factor: 5.103

7.  Virus mutation frequencies can be greatly underestimated by monoclonal antibody neutralization of virions.

Authors:  J J Holland; J C de la Torre; D A Steinhauer; D Clarke; E Duarte; E Domingo
Journal:  J Virol       Date:  1989-12       Impact factor: 5.103

Review 8.  The glycoprotein G of rhabdoviruses.

Authors:  J M Coll
Journal:  Arch Virol       Date:  1995       Impact factor: 2.574

9.  Evolutionary analysis of the picornavirus family.

Authors:  M J Rodrigo; J Dopazo
Journal:  J Mol Evol       Date:  1995-04       Impact factor: 2.395

10.  Punctuated equilibrium and positive Darwinian evolution in vesicular stomatitis virus.

Authors:  S T Nichol; J E Rowe; W M Fitch
Journal:  Proc Natl Acad Sci U S A       Date:  1993-11-15       Impact factor: 11.205

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