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Journal of Virology, May 2000, p. 4898-4901, Vol. 74, No. 10
Departments of
Microbiology1 and
Neurosurgery,2 Kanazawa Medical
University, Uchinada, Ishikawa 920-0293, Japan
Received 28 July 1999/Accepted 14 February 2000
We sought to confirm the importance of L* protein for growth of
Theiler's murine encephalomyelitis virus (TMEV) in a
macrophage-like cell line, J774-1. The protein is out of frame with the
polyprotein and synthesized in DA but not GDVII subgroup strains of
TMEV. A recombinant virus, DANCL*/GD, which substitutes the DA 5'
noncoding and L* coding regions for the corresponding regions of GDVII
and synthesizes L* protein, grew with little restriction in J774-1 cells. In contrast, another recombinant virus, DANCL*-1/GD, which has
an ACG rather than an AUG as the starting codon of L* protein at
nucleotide 1079, resulting in no synthesis of L* protein, did not grow
well. No significant difference between the rates of adsorption to
J774-1 cells of these viruses was observed. RNase protection assay
demonstrated that DANCL*/GD viral RNA significantly increased, whereas
only a minimal increase was observed for DANCL*-1/GD. The present study
suggests that L* protein is required for virus growth in macrophages.
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
L* Protein of Theiler's Murine Encephalomyelitis
Virus Is Required for Virus Growth in a Murine Macrophage-Like
Cell Line
*
Corresponding author. Mailing address: Department of
Microbiology, Kanazawa Medical University, Uchinada, Ishikawa 920-0293, Japan. Phone: 81-76-286-2211, ext. 3011. Fax: 81-76-286-3961. E-mail:
ohara{at}kanazawa-med.ac.jp.
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