Fishbourne Emma, Ludi Anna B, Wilsden Ginette, Hamblin Pip, Statham Bob, Bin-Tarif Abdelghani, Brocchi Emiliana, Grazioli Santina, Dekker Aldo, Eblé Phaedra, King Donald P
The Pirbright Institute, Ash Road, Pirbright, Surrey GU24 0NF, United Kingdom.
The Pirbright Institute, Ash Road, Pirbright, Surrey GU24 0NF, United Kingdom.
Vaccine. 2017 May 9;35(20):2761-2765. doi: 10.1016/j.vaccine.2017.02.047. Epub 2017 Apr 7.
Outbreaks of foot-and-mouth disease (FMD) in North Africa (2013) and the Gulf States (2013) of the Middle East have been caused by a FMD viral lineage (O/ME-SA/Ind-2001) that was before 2013 restricted to the Indian Sub-continent. This study was undertaken to assess the in vivo efficacy of a FMD virus emergency vaccine type O Manisa against heterologous challenge with a representative field virus (O/ALG/3/2014) from this emerging lineage. This widely available vaccine was selected since in vitro vaccine-matching results gave inconclusive results as to whether or not it would be protective. Three groups of five cattle were vaccinated with O Manisa (homologous potency ≥6PD/dose) using study guidelines outlined in the European Pharmacopeia, and challenged at 21days post-vaccination by tongue inoculation. All animals that were vaccinated with the lowest dose (1/16) of vaccine developed generalised FMD, defined as vesicular lesions at the feet. One animal vaccinated with a 1/4 dose of the vaccine also developed generalised disease, as did two animals vaccinated with the full dose of vaccine. These results indicate that the heterologous potency of this high potency O Manisa vaccine was approximately 3.5 PD/dose. These data support the use of the O Manisa vaccine for FMD control in areas where FMDV is endemic e.g. North Africa, and motivate further studies to evaluate other vaccine candidates (or multivalent combinations) that might be potentially used for emergency purposes in FMD-free settings.
2013年北非和中东海湾国家口蹄疫(FMD)疫情是由口蹄疫病毒谱系(O/ME-SA/Ind-2001)引起的,该谱系在2013年之前仅限于印度次大陆。本研究旨在评估O型马尼萨口蹄疫病毒应急疫苗对来自这一新兴谱系的代表性田间病毒(O/ALG/3/2014)进行异源攻击的体内效力。选择这种广泛可用的疫苗是因为体外疫苗匹配结果对于其是否具有保护性尚无定论。按照欧洲药典概述的研究指南,三组每组五头牛接种了O型马尼萨疫苗(同源效力≥6PD/剂量),并在接种疫苗后21天通过舌部接种进行攻击。所有接种最低剂量(1/16)疫苗的动物都出现了全身性口蹄疫,定义为足部出现水疱性病变。一头接种1/4剂量疫苗的动物以及两头接种全剂量疫苗的动物也出现了全身性疾病。这些结果表明,这种高效力的O型马尼萨疫苗的异源效力约为3.5 PD/剂量。这些数据支持在口蹄疫病毒流行地区(如北非)使用O型马尼萨疫苗来控制口蹄疫,并促使进一步开展研究以评估其他可能用于无口蹄疫地区应急目的的候选疫苗(或多价组合疫苗)。