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Constant and variable regions of measles virus proteins encoded by the nucleocapsid and phosphoprotein genes derived

K Baczko1, I Pardowitz, B K Rima

  • 1Institute of Virology, University of Würzburg, Germany.

Virology
|September 1, 1992
PubMed

Insights

Analysis of measles virus (MV) genes reveals conserved regions in internal proteins, aiding evolutionary studies. The matrix (M) protein

Area of Science:

  • Virology
  • Molecular Biology
  • Genetics

Background:

  • Measles virus (MV) is a significant human pathogen.
  • Understanding the genetic variability of MV is crucial for tracking its evolution and for developing effective vaccines and therapies.
  • Internal proteins, including Nucleoprotein (N), Phosphoprotein (P), Matrix (M), and others like C and V, play vital roles in the MV life cycle.

Purpose of the Study:

  • To analyze and compare the nucleotide sequences of the N and P genes from two wild-type measles virus strains (JM and CM).
  • To assess the variability within specific regions of MV internal proteins (N, P, C, V, and M).
  • To evaluate the evolutionary relationships between different MV strains based on N, P, and M genes and investigate potential recombination events.

Main Methods:

  • Nucleotide sequence analysis of N and P genes from wild-type measles virus strains JM and CM.
  • Comparative sequence analysis with other known MV strains.
  • Phylogenetic analysis to construct evolutionary trees based on N, P, and M genes.
  • Identification of conserved and variable regions within the analyzed viral proteins.

Main Results:

  • Most variations in the P protein are located in the N-terminus, with conserved middle (residues 201-350) and C-terminal regions.
  • The C protein shows variability primarily in its N-terminal amino acids.
  • The C-terminal residues of the V protein, unique to this protein, exhibit minimal variation across MV strains.
  • Evolutionary trees derived from N, P, and M genes are congruent, suggesting a lack of recombination among these genes in the studied strains.
  • The M protein demonstrates lower variability compared to other genes, indicating that observed changes in M in SSPE and MIBE viruses might be more significant than previously thought.

Conclusions:

  • Specific regions within measles virus internal proteins (P, C, V) exhibit distinct patterns of variability and conservation.
  • The genetic data support the stability of evolutionary relationships based on N, P, and M genes, with no evidence of recombination.
  • The lower variability of the M protein suggests its potential utility as a marker for significant viral evolution or adaptation events, particularly in disease contexts like SSPE and MIBE.

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