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Sequencing analyses and comparison of parainfluenza virus type 4A and 4B NP protein genes

K Kondo1, H Bando, M Kawano

  • 1Department of Microbiology, Mie University School of Medicine, Japan.

Virology
|January 1, 1990
PubMed

Insights

Human parainfluenza viruses 4A and 4B (PIV-4A and PIV-4B) nucleocapsid proteins show high sequence homology. These PIV-4 NPs are closely related to other paramyxoviruses, suggesting a common viral ancestor.

Area of Science:

  • Virology
  • Molecular Biology
  • Genomics

Background:

  • Human parainfluenza viruses (HPIVs) are significant respiratory pathogens.
  • Understanding the genetic diversity and evolutionary relationships of HPIV subtypes is crucial for disease control.
  • Nucleocapsid protein (NP) is a key component of the paramyxovirus genome and plays a vital role in viral replication.

Purpose of the Study:

  • To determine and compare the nucleotide sequences of the nucleocapsid protein (NP) genes of human parainfluenza virus type 4A (PIV-4A) and type 4B (PIV-4B).
  • To analyze the sequence homology between PIV-4A and PIV-4B NP proteins.
  • To investigate the evolutionary relationships of PIV-4 NPs with other members of the Paramyxoviridae family.

Main Methods:

  • Nucleotide sequencing of cDNA copies of PIV-4A and PIV-4B NP mRNA.
  • Bioinformatic analysis of nucleotide and amino acid sequences.
  • Comparative sequence analysis with NP genes from other paramyxoviruses.

Main Results:

  • The PIV-4A NP mRNA contained 1885 nucleotides, encoding a protein of 62,561 Da.
  • PIV-4B NP protein had a similar molecular weight (62,425 Da) and amino acid length.
  • Extensive homologies were found between PIV-4A and PIV-4B NP sequences (87% nucleotide, 93% amino acid).
  • A conserved region of approximately 100 amino acids was identified in NP proteins across nine different paramyxoviruses, including PIV-4s, Newcastle disease virus (NDV), Sendai virus, mumps virus (MuV), PIV-3, BPIV-3, measles virus (MV), and canine distemper virus (CDV).
  • PIV-4 NPs showed closer evolutionary relationships to MuV and NDV than to PIV-3, BPIV-3, or Sendai virus.
  • PIV-4 NPs exhibited slightly higher homology to morbilliviruses (MV, CDV) than to other parainfluenza viruses.

Conclusions:

  • PIV-4A and PIV-4B NP proteins are highly conserved, indicating a close relationship between these two subtypes.
  • The identified conserved region in NP proteins supports the hypothesis of a common ancestor for the studied paramyxoviruses.
  • The phylogenetic analysis suggests distinct evolutionary paths within the Paramyxoviridae family, with PIV-4 NPs occupying a specific position relative to other genera.

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