J Virol. 1993 April; 67(4): 2055-2063
Cells and viruses with mutations affecting viral entry are selected during persistent infections of L cells with mammalian reoviruses.
T S Dermody,
M L Nibert,
J D Wetzel,
X Tong and
B N Fields
Department of Pediatrics, Vanderbilt Medical School, Nashville, Tennessee 37232.
ABSTRACT
Previous studies demonstrated that both cellular and viral mutants are selected during maintenance of persistent infections established in murine L cells with high-passage stocks of mammalian reoviruses. In particular, when one culture was cured of persistent infection, the resulting cells were found to support the growth of viruses isolated from persistently infected cultures (termed PI viruses here) better than that of wild-type (wt) viruses (R. Ahmed, W. M. Canning, R. S. Kauffman, A. H. Sharpe, J. V. Hallum, and B. N. Fields, Cell 25:325-332, 1981). To address the nature of cellular and viral mutations selected during maintenance of persistent reovirus infections, we established independent, persistently infected cultures with L cells and high-passage stocks of wt reovirus. These cultures served as sources of new PI viruses and cured cells for study. We found that although wt viruses grew poorly in cured cells when infection was initiated with intact virions, they grew well in cured cells when infection was initiated with infectious subvirion particles generated from virions by in vitro treatment with chymotrypsin. This finding indicates that the block to growth of wt viruses in cured cells involves an early step that is unique to infection by virions, such as proteolytic processing in an endocytic compartment. We also found that PI viruses grew better than wt viruses in L cells treated with ammonium chloride, a weak base that inhibits the pH decrease in endosomes and lysosomes. Because ammonium chloride blocks an early step in infection by intact virions, probably the proteolytic processing of viral outer capsid proteins by acid-dependent cellular proteases in late endosomes or lysosomes, this finding indicates that PI viruses differ from wt viruses with respect to viral entry into cells. Therefore, these results indicate that both cells and viruses evolve mutations that affect one or more early steps in the viral growth cycle during maintenance of L-cell cultures persistently infected with reoviruses.
J Virol. 1993 April; 67(4): 2055-2063
This article has been cited by other articles:
-
Herrera, M., Grande-Perez, A., Perales, C., Domingo, E.
(2008). Persistence of foot-and-mouth disease virus in cell culture revisited: implications for contingency in evolution. J. Gen. Virol.
89: 232-244
[Abstract]
[Full Text]
-
Zhong, J., Gastaminza, P., Chung, J., Stamataki, Z., Isogawa, M., Cheng, G., McKeating, J. A., Chisari, F. V.
(2006). Persistent Hepatitis C Virus Infection In Vitro: Coevolution of Virus and Host. J. Virol.
80: 11082-11093
[Abstract]
[Full Text]
-
Wetzel, J. D., Barton, E. S., Chappell, J. D., Baer, G. S., Mochow-Grundy, M., Rodgers, S. E., Shyr, Y., Powers, A. C., Thomas, J. W., Dermody, T. S.
(2006). Reovirus Delays Diabetes Onset but Does Not Prevent Insulitis in Nonobese Diabetic Mice. J. Virol.
80: 3078-3082
[Abstract]
[Full Text]
-
Clark, K. M., Wetzel, J. D., Gu, Y., Ebert, D. H., McAbee, S. A., Stoneman, E. K., Baer, G. S., Zhu, Y., Wilson, G. J., Prasad, B. V. V., Dermody, T. S.
(2006). Reovirus Variants Selected for Resistance to Ammonium Chloride Have Mutations in Viral Outer-Capsid Protein {sigma}3. J. Virol.
80: 671-681
[Abstract]
[Full Text]
-
Ebert, D. H., Kopecky-Bromberg, S. A., Dermody, T. S.
(2004). Cathepsin B Is Inhibited in Mutant Cells Selected during Persistent Reovirus Infection. J. Biol. Chem.
279: 3837-3851
[Abstract]
[Full Text]
-
Becker, M. M., Peters, T. R., Dermody, T. S.
(2003). Reovirus {sigma}NS and {micro}NS Proteins Form Cytoplasmic Inclusion Structures in the Absence of Viral Infection. J. Virol.
77: 5948-5963
[Abstract]
[Full Text]
-
Wilson, G. J., Nason, E. L., Hardy, C. S., Ebert, D. H., Wetzel, J. D., Venkataram Prasad, B. V., Dermody, T. S.
(2002). A Single Mutation in the Carboxy Terminus of Reovirus Outer-Capsid Protein {sigma}3 Confers Enhanced Kinetics of {sigma}3 Proteolysis, Resistance to Inhibitors of Viral Disassembly, and Alterations in {sigma}3 Structure. J. Virol.
76: 9832-9843
[Abstract]
[Full Text]
-
Ebert, D. H., Deussing, J., Peters, C., Dermody, T. S.
(2002). Cathepsin L and Cathepsin B Mediate Reovirus Disassembly in Murine Fibroblast Cells. J. Biol. Chem.
277: 24609-24617
[Abstract]
[Full Text]
-
Golden, J. W., Linke, J., Schmechel, S., Thoemke, K., Schiff, L. A.
(2002). Addition of Exogenous Protease Facilitates Reovirus Infection in Many Restrictive Cells. J. Virol.
76: 7430-7443
[Abstract]
[Full Text]
-
Jane-Valbuena, J., Breun, L. A., Schiff, L. A., Nibert, M. L.
(2002). Sites and Determinants of Early Cleavages in the Proteolytic Processing Pathway of Reovirus Surface Protein {sigma}3. J. Virol.
76: 5184-5197
[Abstract]
[Full Text]
-
Ebert, D. H., Wetzel, J. D., Brumbaugh, D. E., Chance, S. R., Stobie, L. E., Baer, G. S., Dermody, T. S.
(2001). Adaptation of Reovirus to Growth in the Presence of Protease Inhibitor E64 Segregates with a Mutation in the Carboxy Terminus of Viral Outer-Capsid Protein {sigma}3. J. Virol.
75: 3197-3206
[Abstract]
[Full Text]
-
Baer, G. S., Ebert, D. H., Chung, C. J., Erickson, A. H., Dermody, T. S.
(1999). Mutant Cells Selected during Persistent Reovirus Infection Do Not Express Mature Cathepsin L and Do Not Support Reovirus Disassembly. J. Virol.
73: 9532-9543
[Abstract]
[Full Text]
-
Baric, R. S., Sullivan, E., Hensley, L., Yount, B., Chen, W.
(1999). Persistent Infection Promotes Cross-Species Transmissibility of Mouse Hepatitis Virus. J. Virol.
73: 638-649
[Abstract]
[Full Text]
-
Chappell, J. D., Barton, E. S., Smith, T. H., Baer, G. S., Duong, D. T., Nibert, M. L., Dermody, T. S.
(1998). Cleavage Susceptibility of Reovirus Attachment Protein sigma 1 during Proteolytic Disassembly of Virions Is Determined by a Sequence Polymorphism in the sigma 1 Neck. J. Virol.
72: 8205-8213
[Abstract]
[Full Text]
-
Mrukowicz, J. Z., Wetzel, J. D., Goral, M. I., Fogo, A. B., Wright, P. F., Dermody, T. S.
(1998). Viruses and Cells with Mutations Affecting Viral Entry Are Selected during Persistent Rotavirus Infections of MA104 Cells. J. Virol.
72: 3088-3097
[Abstract]
[Full Text]
-
Rao, P. V., Gallagher, T. M.
(1998). Intracellular Complexes of Viral Spike and Cellular Receptor Accumulate during Cytopathic Murine Coronavirus Infections. J. Virol.
72: 3278-3288
[Abstract]
[Full Text]
Copyright © 1993 by the American Society for Microbiology. All rights reserved.