Department of Microbiology, University of Dhaka, Dhaka, 1000, Bangladesh.
Department of Microbiology, BRAC University, Dhaka, Bangladesh.
Sci Rep. 2024 Oct 24;14(1):25236. doi: 10.1038/s41598-024-76669-3.
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.
口蹄疫(FMD)是孟加拉国等以农业为基础的国家的巨大灾难,现有的检测系统限制了血清型的识别和区分。在这项研究中,引入了一种工程平台,该平台结合了血清型特异性 FMDV VP1(结构)、血清型非依赖性 VP2(结构)和 3AB(非结构)蛋白,用于全面检测。VP1 序列通过组合 BAN/TA/Dh-301/2016(血清型 O)、BAN/CH/Sa-304/2016(血清型 A)和 BAN/DH/Sa-318/2016(血清型 Asia1)的序列进行工程化设计。选择流行的病毒基因组构建了共识 3AB 序列。VP1 和 3AB 以及设计的 VP2 序列都进行了密码子使用偏好、稳定 mRNA、二级和三级蛋白质结构的优化。蛋白质在 pET-21a(+)质粒载体中合成,然后转化为大肠杆菌 BL21(DE3),并通过 IPTG 诱导表达。工程蛋白的 Western blot 分析表明,纯化的 VP1 与疫苗接种血清中的抗 VP1 抗体明显结合,而 3AB 和 VP2 分别与感染牛血清中的抗 3AB 和抗 VP2 抗体结合,所有这些抗体均在之前的流行病学调查中收集。此外,斑点杂交证实了膜固定蛋白的有效抗体捕获能力。这种整体诊断平台证明了一种全面的原型诊断试剂盒的合理性,该试剂盒将具有成本效益,并且对血清型特异性和非特异性 FMDV 血清学监测具有高效性。