Replication competition between lactate dehydrogenase-elevating virus quasispecies in mice. Implications for quasispecies selection and evolution

• Published in: Archives of virology 2001-07, Vol.146 (7), p.1283-1296
• Main Authors: PLAGEMANN, P. G. W, CHEN, Z, LI, K
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Animal viral diseases; Animals; Arterivirus Infections - blood; Arterivirus Infections - immunology; Arterivirus Infections - virology; Biological and medical sciences; Cyclophosphamide - administration & dosage; Epidemiology; Fundamental and applied biological sciences. Psychology; Immunosuppressive Agents - administration & dosage; Infectious diseases; lactate dehydrogenase; Lactate dehydrogenase-elevating virus; Lactate dehydrogenase-elevating virus - genetics; Lactate dehydrogenase-elevating virus - pathogenicity; Lactate dehydrogenase-elevating virus - physiology; Medical sciences; Membrane Glycoproteins - genetics; Mice; Mice, Inbred BALB C; Mice, Nude; Mice, SCID; Microbiology; Molecular Sequence Data; Mutation; Reverse Transcriptase Polymerase Chain Reaction; Species Specificity; Time Factors; Viral diseases; Viral Envelope Proteins - genetics; Virology; Virus Replication; VP-3P protein; VP3P protein
• ISSN: 0304-8608; 1432-8798
• DOI: 10.1007/s007050170091

The common quasispecies of lactate dehydrogenase-elevating virus (LDV), LDV-P and LDV-vx, are highly resistant to the humoral host immune response because the single neutralization epitope on the ectodomain of the primary envelope glycoprotein, VP-3P, carries three large N-glycans. Two laboratory mutants, LDV-C and LDV-v, have lost two of the N-glycans on the VP-3P ectodomain, thereby gaining neuropathogenicity for AKR/C58 mice but at the same time, becoming susceptible to the humoral immune response of the host. In attempts to further assess the origins and evolution of these LDVs we have determined their competitiveness by monitoring their fate in mixed infections of wild type, SCID, nude, and cyclophosphamide-treated mice by reverse transcription/polymerase chain reaction assays that distinguish between them. In mixed infections with LDV-P and LDV-vx, LDV-C and LDV-v became rapidly lost even when present initially in large excess over the former. In mixed infections of mice unable to generate neutralizing antibodies, LDV-C and LDV-v also became replaced by LDV-P and LDV-vx as predominant quasispecies but more slowly than in immunocompetent mice. The results indicate that the humoral immune response plays an important role in the displacement of LDV-C and LDV-v by LDV-P and LDV-vx but that in addition, LDV-C and LDV-v possess an impaired ability to compete with LDV-P and LDV-vx in the productive infection of the subpopulation of macrophages that represents the host for all these LDVs. In addition, LDV-v outcompeted LDV-C in mixed infections and the same was the case for neutralization escape mutants of LDV-v and LDV-C which had regained all three N-glycosylation sites on the VP-3P ectodomain. Thus a hierarchy exists in replication fitness: LDV-P/LDV-vx>LDV-v>LDV-C, which is unrelated to the number of N-glycans on the VP-3P ectodomain. The implications of the results in relation to the evolution and selection of the LDV-quasispecies is discussed. LDV-P and LDV-vx are genetically highly stable and thus seem to have achieved evolutionary stasis with optimum ability to establish viremic persistent infections of mice that are unimpeded by the host immune responses.