HN GLYCOPROTEIN ROLE IN MUMPS VIRUS NEUROVIRULENCE
HN GLYCOPROTEIN ROLE IN MUMPS VIRUS NEUROVIRULENCE
批准号:
3407139
负责人:
M. NEAL WAXHAM
金额:
$12.26万
依托单位国家:
美国
项目类别:
财政年份:
1986
资助国家:
美国
项目状态:
已结题
起止时间:
1986-04-01 至 1989-03-31
关键词:
affinity chromatography antiantibody electrophoresis enzyme linked immunosorbent assay genetic library genetic strain monoclonal antibody mumps mumps virus neurotropic virus newborn animals radiotracer synthetic peptide tissue /cell culture viral meningitis virulence virus classification virus cytopathogenic effect
中文摘要
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英文摘要
Mumps virus is a common human pathogen that frequently invades the central
nervous system (CNS). Strains of mumps virus differ in their
cytopathogenicity (the degree of cytopathology that they cause in vitro)
and their neurovirulence (the ability to invade the CNS and infect neurons)
and there appears to be a correlation between the in vitro and in vivo
biological effects. The molecular basis for these strain-dependent
differences is not known and is the focus of the proposed experiments.
Preliminary evidence suggests that the strain-dependent differences in
cytopathogenicity and neurovirulence result, at least in part, from
variation in the structure of the viral HN glycoprotein which mediates
virion binding to host cells. The proposed experiments are designed to
characterize the structure of the HN glycoprotein and to identify the
functional domains that contribute to mumps virus cytopathogenicity and
neurovirulence. Specifically, three different selection protocols will be
used to isolate mumps virus variants that differ from the parental mumps
virus strain by only minor alterations in the structure of the HN
glycoprotein. The structural alterations will be defined at the level of
the glycoprotein's amino acid sequence for those mumps virus variants that
differ from the parental mumps virus strain in vitro and in vivo biological
effects; in this way, the changes in primary structure that result in a
modification in glycoprotein function and in virus virulence will be
identified. Finally, an attempt will be made to generate polyclonal
antibodies against putative functional domains of the HN glycoprotein by
using as immunogens synthetic peptides with sequence homology to selected
regions of the intact glycoprotein. Anti-peptide antibodies that recognize
the HN glycoprotein in its native configuration will be tested for activity
in in vitro functional assays and for a protective effect in the newborn
hamster model of mumps meningoencephalitis. It is anticipated that the
results of these studies will provide insight into the structure of the
functional domains of the HN glycoprotein and will contribute to the
understanding of the pathogenesis of mumps virus infection of the CNS.
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