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Published on: June 16, 2011
Capsid protein gene variation among feline calicivirus isolates
T Horimoto1, Y Takeda, K Iwatsuki-Horimoto
1Division of Virology, Institute of Medical Science, University of Tokyo, Japan. horimoto@ims.u-tokyo.ac.jp
Abstract:
We amplified the capsid protein gene fragments of 30 Japanese isolates of feline calicivirus (FCV), including the C, D, and E regions, by reverse transcription-polymerase chain reaction (RT-PCR), followed by direct sequencing. Alignment of the predicted amino acid sequences, together with other published sequences from the isolates obtained in other countries, demonstrated a marked heterogeneity among the isolates, confirming the current definition of hypervariable regions within the capsid protein: these regions give rise to the antigenic variations seen in FCV isolates. Phylogenetic analysis of the nucleotide sequences could not identify significant geographically or temporally separated clusters of FCV isolates, supporting the theory of a single genotype.
Insights
This study analyzed feline calicivirus (FCV) capsid protein gene sequences from Japanese isolates. FCV isolates show significant genetic variation, but phylogenetic analysis suggests a single genotype exists globally.
Area of Science:
- Veterinary Virology
- Molecular Biology
- Immunology
Background:
- Feline calicivirus (FCV) is a highly contagious pathogen causing respiratory and oral disease in cats.
- Antigenic diversity among FCV isolates complicates vaccine development and disease control.
- Understanding the genetic variability of FCV is crucial for effective management strategies.
Purpose of the Study:
- To investigate the genetic diversity of the FCV capsid protein gene in Japanese isolates.
- To compare Japanese FCV isolates with international strains.
- To assess the phylogenetic relationships and potential clustering of FCV isolates.
Main Methods:
- Amplification of capsid protein gene fragments (C, D, E regions) using reverse transcription-polymerase chain reaction (RT-PCR).
- Direct sequencing of amplified gene fragments.
- Alignment and phylogenetic analysis of nucleotide and predicted amino acid sequences.
Main Results:
- Significant heterogeneity was observed in the capsid protein gene sequences among Japanese FCV isolates.
- Hypervariable regions within the capsid protein were confirmed, correlating with antigenic variations.
- Phylogenetic analysis did not reveal distinct geographical or temporal clusters, supporting a single FCV genotype.
Conclusions:
- The FCV capsid protein exhibits marked genetic diversity, primarily in hypervariable regions, leading to antigenic variation.
- Despite regional variations, FCV appears to exist as a single genotype globally.
- Further research into FCV genetic evolution and antigenic drift is warranted for improved diagnostics and vaccines.
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