Complete Genome Sequence of Foot-and-Mouth Disease Virus Type A Circulating in Bangladesh

Huzzat Ullah1, Mohammad Anwar Siddique1, Munawar Sultana2

  • 1Department of Microbiology, University of Dhaka, Dhaka, Bangladesh.

Genome Announcements
|June 14, 2014
PubMed

Insights

Researchers sequenced a foot-and-mouth disease virus (FMDV) type A strain from Bangladesh. Genetic analysis revealed significant differences in the 5' untranslated region (UTR) and VP1 protein compared to vaccine strains.

Area of Science:

  • Veterinary Virology
  • Molecular Biology
  • Genomics

Background:

  • Foot-and-mouth disease (FMD) is a highly contagious viral disease affecting cloven-hoofed animals.
  • FMDV type A strains pose a significant threat to livestock health and global trade.
  • Understanding genetic variations in circulating FMDV strains is crucial for effective disease control and vaccine development.

Purpose of the Study:

  • To perform a complete genome sequencing of a novel FMDV type A strain isolated in Bangladesh.
  • To identify genetic variations in the sequenced strain compared to existing vaccine strains.
  • To analyze potential implications of these genetic changes on viral properties.

Main Methods:

  • Whole-genome sequencing of the FMDV type A strain (BAN/GA/Sa-197/2013).
  • Bioinformatic analysis to compare the complete genome sequence with reference vaccine strains (e.g., GenBank accession no. HM854025).
  • Identification and characterization of genetic alterations, including nucleotide insertions and amino acid substitutions.

Main Results:

  • The complete genome sequence of the FMDV type A strain BAN/GA/Sa-197/2013 was determined.
  • An 84-nucleotide insertion was identified in the 5'-untranslated region (UTR).
  • A lengthened poly(C) tract and amino acid substitutions in the VP1 region were observed compared to the vaccine strain.

Conclusions:

  • The sequenced FMDV type A strain exhibits distinct genetic features compared to the vaccine strain.
  • These genetic variations, particularly in the 5'-UTR and VP1, may influence viral fitness, antigenicity, or virulence.
  • Further studies are warranted to assess the impact of these genetic differences on FMDV epidemiology and vaccine efficacy in Bangladesh.

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