Literature DB >> 6296277

Murine coronaviruses: isolation and characterization of two plaque morphology variants of the JHM neurotropic strain.

S A Stohlman, P R Brayton, J O Fleming, L P Weiner, M M Lai.   

Abstract

Two plaque-size variants of the neurotropic JHM strain of mouse hepatitis virus have been isolated from the virus stock after eight serial passages in suckling mouse brain. One variant, JHM-DL, produces large plaques, while the other, JHM-DS, produces small plaques in tissue culture. DS replicates more slowly, has a lower virus yield in vitro, and is less virulent for mice than DL. They also differ in their pathogenicity for mice: JHM-DL infection results in acute encephalomyelitis while JHM-DS infection results in demyelination. Oligonucleotide fingerprint analysis of the RNA genomes of these two variants revealed that they had almost identical genetic sequences. Each variant, however, had a unique oligonucleotide spot not found in the other. The unique spot of the large plaque variant, JHM-DL, was localized at approximately 3 to 5 kb from the 3' end, while the JHM-DS unique spot was mapped at 14 to 15 kb from the 3' end of the genome. We have further shown that these oligonucleotide changes are not correlated with the plaque morphology. These two viruses may be useful for studying the molecular basis of virus-induced demyelination.

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Year:  1982        PMID: 6296277     DOI: 10.1099/0022-1317-63-2-265

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  53 in total

1.  Role of viral persistence in retaining CD8(+) T cells within the central nervous system.

Authors:  N W Marten; S A Stohlman; C C Bergmann
Journal:  J Virol       Date:  2000-09       Impact factor: 5.103

2.  Matrix metalloproteinase expression correlates with virulence following neurotropic mouse hepatitis virus infection.

Authors:  Jiehao Zhou; Stephen A Stohlman; Roscoe Atkinson; David R Hinton; Norman W Marten
Journal:  J Virol       Date:  2002-08       Impact factor: 5.103

3.  Neutralization-resistant variants of a neurotropic coronavirus are generated by deletions within the amino-terminal half of the spike glycoprotein.

Authors:  T M Gallagher; S E Parker; M J Buchmeier
Journal:  J Virol       Date:  1990-02       Impact factor: 5.103

4.  Alteration of the pH dependence of coronavirus-induced cell fusion: effect of mutations in the spike glycoprotein.

Authors:  T M Gallagher; C Escarmis; M J Buchmeier
Journal:  J Virol       Date:  1991-04       Impact factor: 5.103

5.  Effective clearance of mouse hepatitis virus from the central nervous system requires both CD4+ and CD8+ T cells.

Authors:  J S Williamson; S A Stohlman
Journal:  J Virol       Date:  1990-09       Impact factor: 5.103

6.  Mouse hepatitis virus is cleared from the central nervous systems of mice lacking perforin-mediated cytolysis.

Authors:  M T Lin; S A Stohlman; D R Hinton
Journal:  J Virol       Date:  1997-01       Impact factor: 5.103

7.  Structure of the intracellular defective viral RNAs of defective interfering particles of mouse hepatitis virus.

Authors:  S Makino; N Fujioka; K Fujiwara
Journal:  J Virol       Date:  1985-05       Impact factor: 5.103

8.  Sequence analysis reveals extensive polymorphism and evidence of deletions within the E2 glycoprotein gene of several strains of murine hepatitis virus.

Authors:  S E Parker; T M Gallagher; M J Buchmeier
Journal:  Virology       Date:  1989-12       Impact factor: 3.616

9.  Defective interfering particles of mouse hepatitis virus.

Authors:  S Makino; F Taguchi; K Fujiwara
Journal:  Virology       Date:  1984-02       Impact factor: 3.616

10.  Heterogeneity of the polyribocytidylic acid tract in aphthovirus: biochemical and biological studies of viruses carrying polyribocytidylic acid tracts of different lengths.

Authors:  M P Costa Giomi; I E Bergmann; E A Scodeller; P Augé de Mello; I Gomez; J L La Torre
Journal:  J Virol       Date:  1984-09       Impact factor: 5.103

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