AI Article Synopsis

  • Foot-and-mouth disease (FMD) significantly impacts agriculture in countries like Bangladesh, with current detection systems struggling to differentiate between virus serotypes.
  • This study presents a new diagnostic platform using engineered proteins (VP1, VP2, and 3AB) that can effectively identify both serotype-specific and serotype-independent FMD viruses by utilizing optimized genetic sequences.
  • The diagnostic kit shows promising results through various tests, demonstrating its potential as a cost-effective and efficient tool for FMD sero-surveillance in affected regions.

Article Abstract

Foot-and-mouth disease (FMD) is a great havoc in agri-business-based countries like Bangladesh, for which existing detection system limits the identification and differentiation of serotypes. In this study, an engineered platform was introduced incorporating serotype-specific FMDV VP1 (structural), serotype-independent VP2 (structural) and 3AB (non-structural) proteins for holistic detection. VP1 sequences were engineered combining sequences of BAN/TA/Dh-301/2016 (serotype O), BAN/CH/Sa-304/2016 (serotype A) and BAN/DH/Sa-318/2016 (serotype Asia1). Consensus 3AB sequence was constructed from the selected prevalent viral genomes. Both VP1 and 3AB along with designed VP2 sequences were optimized for codon usage bias, stable mRNA, secondary and tertiary protein structure. Proteins were synthesized in pET-21a ( +) plasmid vector followed by transformation of Escherichia coli BL21(DE3) and IPTG-induced- expression. The western blot analysis of engineered proteins showed that purified VP1 prominently bound to anti-VP1 antibodies in vaccinated sera, whereas 3AB and VP2 bound anti-3AB and anti-VP2 antibodies, respectively from infected cattle sera, all previously collected during epidemiological investigation. Furthermore, dot blot hybridization confirmed efficient antibody capture ability of the membrane-immobilized proteins. This holistic diagnostic platform justifies a comprehensive prototype diagnostic kit that would be cost-effective and efficient for serotype specific and non-specific FMDV sero-surveillance.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11502911PMC
http://dx.doi.org/10.1038/s41598-024-76669-3DOI Listing

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