Research Article

Identification of Completely Conserved and Highly Variable Residues in Canine Parvovirus: Large-Scale Genomic Analysis

Volume: 20 Number: 3 December 25, 2025
EN TR

Identification of Completely Conserved and Highly Variable Residues in Canine Parvovirus: Large-Scale Genomic Analysis

Abstract

The viral genome of Canine parvovirus comprises four primary genes: NS1, NS2, VP1, and VP2. NS1 and NS2 are primarily involved in viral replication and the suppression of host intracellular mechanisms, while VP1 and VP2 encode the structural components of the viral capsid. In this study, all available Canine parvovirus sequences deposited in NCBI up to March 20, 2025, were analyzed using MAFFT, Geneious Prime and Swiss Model. For each gene, both completely conserved and highly variable residues were identified, structural modeling was conducted using the consensus data. Our analysis showed that NS1 and NS2 residues were completely conserved at 57.18% and 56.36%, respectively, whereas the rates for VP1 and VP2 were 5.22% and 3.25%. The proportion of highly variable residues was 1.64% for NS1, 4.24% for NS2, 1.92% for VP1, and 2.05% for VP2. Notably, the number of VP1 and VP2 sequences in the dataset was approximately ten times higher than that of NS1 and NS2. Within the VP2 protein, approximately 75% of the highly variable residues were located in the three-fold spikes, which include critical positions such as A297, G300, N426, and T440. At position 426, global strains showed N (CPV-2a) in 43.2%, D (CPV-2b) in 19.1%, and E (CPV-2c) in 37.5% of sequences. Previous studies have also reported K and I substitutions at this site. These findings offer a valuable reference dataset that may support future Canine parvovirus vaccine design and epitope mapping studies.

Keywords

Supporting Institution

The authors declared that they received no financial support for this study.

Project Number

Bulunmamaktadır

Ethical Statement

The study was conducted using NCBI data and did not involve any animal experiments, thus, ethical approval was not required.

Thanks

None

References

  1. 1. Nandi S, Kumar M. Canine parvovirus: current perspective. Indian J Virol. 2010;21(1):31-44.
  2. 2.Carmichael LE. Canine parvovirus type-2-an evolving pathogen of dogs. Ann Med Vet. 1994;138:459-464.
  3. 3.Buonavoglia C, Martella V, Pratelli A, et al. Evidence for evolution of canine parvovirus type 2 in Italy. J Gen Virol. 2001;82:3021-3025.
  4. 4. Zhou H, Cui K, Su X, et al. Overview of recent advances in canine parvovirus research: current status and future perspectives. Microorganisms. 2024;13(1):47.
  5. 5.Parrish CR, Leathers CW, Pearson R, Gorham JR. Comparisons of feline panleukopenia virus, canine parvovirus, raccoon parvovirus, and mink enteritis virus and their pathogenicity for mink and ferrets. Am J Vet Res. 1987;48(10):1429-1435.
  6. 6.Wang X, Hao X, Zhao Y, Xiao X, Li S, Zhou P. Canine parvovirus NS1 induces host translation shutoff by reducing mTOR phosphorylation. J Virol. 2025;99(1):e01463-24.
  7. 7.Li G, Ji S, Zhai X, et al. Evolutionary and genetic analysis of the VP2 gene of canine parvovirus. BMC Genomics. 2017;18:1-13.
  8. 8.Zhou P, Zeng W, Zhang X, Li S. The genetic evolution of canine parvovirus–A new perspective. PLoS One. 2017;12(3):e0175035.9.Miao B, Chen S, Zhang X, et al. T598 and T601 phosphorylation sites of canine parvovirus NS1 are crucial for viral replication and pathogenicity. Vet Microbiol. 2022;264:109301.

Details

Primary Language

English

Subjects

Veterinary Virology, Animal Science, Genetics and Biostatistics

Journal Section

Research Article

Publication Date

December 25, 2025

Submission Date

July 14, 2025

Acceptance Date

October 6, 2025

Published in Issue

Year 2025 Volume: 20 Number: 3

APA
Temizkan, M. C., & Sevinç Temizkan, S. (2025). Identification of Completely Conserved and Highly Variable Residues in Canine Parvovirus: Large-Scale Genomic Analysis. Veterinary Sciences and Practices, 20(3), 133-141. https://doi.org/10.17094/vetsci.1740409
AMA
1.Temizkan MC, Sevinç Temizkan S. Identification of Completely Conserved and Highly Variable Residues in Canine Parvovirus: Large-Scale Genomic Analysis. Veterinary Sciences and Practices. 2025;20(3):133-141. doi:10.17094/vetsci.1740409
Chicago
Temizkan, Mehmet Cevat, and Seçil Sevinç Temizkan. 2025. “Identification of Completely Conserved and Highly Variable Residues in Canine Parvovirus: Large-Scale Genomic Analysis”. Veterinary Sciences and Practices 20 (3): 133-41. https://doi.org/10.17094/vetsci.1740409.
EndNote
Temizkan MC, Sevinç Temizkan S (December 1, 2025) Identification of Completely Conserved and Highly Variable Residues in Canine Parvovirus: Large-Scale Genomic Analysis. Veterinary Sciences and Practices 20 3 133–141.
IEEE
[1]M. C. Temizkan and S. Sevinç Temizkan, “Identification of Completely Conserved and Highly Variable Residues in Canine Parvovirus: Large-Scale Genomic Analysis”, Veterinary Sciences and Practices, vol. 20, no. 3, pp. 133–141, Dec. 2025, doi: 10.17094/vetsci.1740409.
ISNAD
Temizkan, Mehmet Cevat - Sevinç Temizkan, Seçil. “Identification of Completely Conserved and Highly Variable Residues in Canine Parvovirus: Large-Scale Genomic Analysis”. Veterinary Sciences and Practices 20/3 (December 1, 2025): 133-141. https://doi.org/10.17094/vetsci.1740409.
JAMA
1.Temizkan MC, Sevinç Temizkan S. Identification of Completely Conserved and Highly Variable Residues in Canine Parvovirus: Large-Scale Genomic Analysis. Veterinary Sciences and Practices. 2025;20:133–141.
MLA
Temizkan, Mehmet Cevat, and Seçil Sevinç Temizkan. “Identification of Completely Conserved and Highly Variable Residues in Canine Parvovirus: Large-Scale Genomic Analysis”. Veterinary Sciences and Practices, vol. 20, no. 3, Dec. 2025, pp. 133-41, doi:10.17094/vetsci.1740409.
Vancouver
1.Mehmet Cevat Temizkan, Seçil Sevinç Temizkan. Identification of Completely Conserved and Highly Variable Residues in Canine Parvovirus: Large-Scale Genomic Analysis. Veterinary Sciences and Practices. 2025 Dec. 1;20(3):133-41. doi:10.17094/vetsci.1740409

Content of this journal is licensed under a Creative Commons Attribution NonCommercial 4.0 International License

2987230564