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Virology2019; 537; 121-129; doi: 10.1016/j.virol.2019.08.016

Molecular characterization of Equine Infectious Anemia Viruses using targeted sequence enrichment and next generation sequencing.

Abstract: Equine infectious anemia virus (EIAV) is responsible of acute disease episodes characterized by fever, anemia, thrombocytopenia and anorexia in equids. The high mutation rate in EIAV genome limited the number of full genome sequences availability. In the present study, we used the SureSelect target enrichment system with Illumina Next Generation Sequencing to characterize the proviral DNA of Equine Infectious Anemia Virus (EIAV) from asymptomatic horses. This approach allows a direct sequencing of the EIAV whole genome without cloning or amplification steps and we could obtain for the first time the complete genomic DNA sequences of French EIAV strains. We analyzed their phylogenetic relationship and genetic variability by comparison with 17 whole EIAV genome sequences from different parts of the world. The results obtained provide new insights into the molecular detection of EIAV and genetic diversity of European viral strains.
Publication Date: 2019-08-22 PubMed ID: 31493650DOI: 10.1016/j.virol.2019.08.016Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This research focuses on the use of next-generation sequencing techniques to thoroughly characterize the DNA of the Equine Infective Anemia Virus (EIAV) from asymptomatic horses. The article presents the first complete genomic DNA sequences of French EIAV strains, increasing our understanding of the virus’s genetic diversity and aiding in its detection.

Research Methodology

  • The researchers used the SureSelect target enrichment system in combination with Illumina Next Generation Sequencing in their study. These are state-of-the-art technologies that allow scientists to sequence a specific area of interest from the genome, in this case, the EIAV.
  • They applied this methodology to asymptomatic horses. This means that despite being infected with EIAV, these animals did not exhibit apparent clinical symptoms.
  • Unlike traditional methods, this approach eliminates the need for cloning or amplifying DNA sections, leading to a more straightforward and efficient process.
  • The outcome of the research was the extraction and sequencing of the full genomic DNA of French EIAV strains
  • Data Comparison and Analysis

    • After sequencing the complete genomic DNA, the scientists proceeded with a comparative analysis. They measured the genetic variability between the newly obtained French EIAV strains and 17 other EIAV whole genome sequences sourced from various sections of the world.
    • This comparison allowed them to study the genetic diversity of the EIAV strains and facilitated a sort of mapping of the different viral strains.
    • Since EIAV demonstrates a high mutation rate, understanding this genetic diversity is vital to monitor virus evolution, develop accurate diagnostic tools, and propose potential treatments.
    • Research Significance

      • This research significantly contributes to our understanding of the EIAV, specifically European strains. Prior to this, the high mutation rate of EIAV had resulted in limited data on complete virus genome sequences.
      • By providing the comprehensive genomic DNA sequence of French EIAV strains, the study aids in the molecular detection of the virus and potentially optimizes the approach to treatment.
      • Moreover, by comparing the French strains with EIAV genome sequences globally, it paves the way for insight into the global genetic diversity and mutation patterns of this virus, which may have further implications for disease control and prevention.

Cite This Article

APA
Deshiere A, Berthet N, Lecouturier F, Gaudaire D, Hans A. (2019). Molecular characterization of Equine Infectious Anemia Viruses using targeted sequence enrichment and next generation sequencing. Virology, 537, 121-129. https://doi.org/10.1016/j.virol.2019.08.016

Publication

ISSN: 1096-0341
NlmUniqueID: 0110674
Country: United States
Language: English
Volume: 537
Pages: 121-129
PII: S0042-6822(19)30229-6

Researcher Affiliations

Deshiere, Alexandre
  • ANSES- Laboratory for Animal Health in Normandy, Physiopathology and Epidemiology of Equine Diseases Unit, Goustranville, France.
Berthet, Nicolas
  • Institut Pasteur, Unité Environnement et Risques Infectieux, Cellule d'Intervention Biologique d'Urgence, Paris, France; Centre National de Recherche Scientifique (CNRS) UMR3569, Paris, France.
Lecouturier, Fanny
  • ANSES- Laboratory for Animal Health in Normandy, Physiopathology and Epidemiology of Equine Diseases Unit, Goustranville, France.
Gaudaire, Delphine
  • ANSES- Laboratory for Animal Health in Normandy, Physiopathology and Epidemiology of Equine Diseases Unit, Goustranville, France.
Hans, Aymeric
  • ANSES- Laboratory for Animal Health in Normandy, Physiopathology and Epidemiology of Equine Diseases Unit, Goustranville, France. Electronic address: aymeric.hans@anses.fr.

MeSH Terms

  • Animals
  • Asymptomatic Diseases
  • Equine Infectious Anemia / virology
  • France
  • Genetic Variation
  • High-Throughput Nucleotide Sequencing
  • Horses
  • Infectious Anemia Virus, Equine / classification
  • Infectious Anemia Virus, Equine / genetics
  • Infectious Anemia Virus, Equine / isolation & purification
  • Phylogeny
  • Proviruses / classification
  • Proviruses / genetics
  • Proviruses / isolation & purification
  • Whole Genome Sequencing

Citations

This article has been cited 6 times.
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    doi: 10.1038/s41598-021-92315-8pubmed: 34158533google scholar: lookup
  4. Patil AR, Leung MY, Roy S. Identification of Hub Genes in Different Stages of Colorectal Cancer through an Integrated Bioinformatics Approach.. Int J Environ Res Public Health 2021 May 23;18(11).
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  5. Lupulovic D, Savić S, Gaudaire D, Berthet N, Grgić Ž, Matović K, Deshiere A, Hans A. Identification and genetic characterization of equine infectious anemia virus in Western Balkans.. BMC Vet Res 2021 Apr 15;17(1):168.
    doi: 10.1186/s12917-021-02849-2pubmed: 33858420google scholar: lookup
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