Fana Elliot Mpolokang, Mpoloka Sununguko Wata, Leteane Melvin, Seoke LaToya, Masoba Kelebogile, Mokopasetso Mokganedi, Rapharing Aobakwe, Kabelo Tshephang, Made Patricia, Hyera Joseph
OIE Sub-Saharan Africa Regional Reference Laboratory for Foot-and-Mouth Disease (OIE-SSARRLFMD), Botswana Vaccine Institute, Private Bag 0031, Gaborone, Botswana.
Department of Biological Sciences, Faculty of Science, University of Botswana, Private Bag 00704, Gaborone, Botswana.
Vet Med Int. 2021 Dec 31;2021:7438809. doi: 10.1155/2021/7438809. eCollection 2021.
Foot-and-mouth disease (FMD) virus (FMDv), like other ribonucleic acid (RNA) genome viruses, has a tendency to mutate rapidly. As such, available vaccines may not confer enough cross-protection against incursion of new lineages and sublineages. This paper is a retrospective study to determine the topotypes/lineages that caused previous FMD outbreaks in 6 southern African countries and the efficacy of the current vaccines to protect cattle against them. A total of 453 bovine epithelial tissue samples from 33 FMD outbreaks that occurred in these countries from 2014 to 2018 were investigated for the presence of FMDv. The genetic diversity of the identified Southern African Type (SAT)-FMD viruses was determined by comparing sequences from outbreaks and historical prototype sequences. Of the 453 samples investigated, 176 were positive for four FMDv serotypes. Out of the 176 FMD positive cases there were 105 SAT2 samples, 32 SAT1 samples, 21 SAT3 samples, and 18 serotype O samples. Phylogenetic analysis grouped the SATs VP1 gene sequences into previously observed topotypes in southern Africa. SAT1 viruses were from topotypes I and III, SAT2 viruses belonged to topotypes I, II, III, and IV, and SAT3 viruses were of topotypes I and II. Vaccine matching studies on the field FMDv isolates produced -values greater than or equal to 0.3 for the three SAT serotypes. This suggests that there is no significant antigenic difference between current SAT FMD vaccine strains and the circulating SAT serotypes. Therefore, the vaccines are still fit-purpose for the control FMD in the region. The study did not identify incursion of any new lineages/topotypes of FMD into the sampled southern African countries.
口蹄疫(FMD)病毒(FMDv)与其他核糖核酸(RNA)基因组病毒一样,具有快速变异的倾向。因此,现有的疫苗可能无法提供足够的交叉保护以抵御新谱系和亚谱系的入侵。本文是一项回顾性研究,旨在确定导致南部非洲6个国家先前口蹄疫疫情的拓扑型/谱系,以及当前疫苗保护牛群抵御这些疫情的效力。对2014年至2018年在这些国家发生的33起口蹄疫疫情中采集的453份牛上皮组织样本进行了检测,以确定是否存在FMDv。通过比较疫情序列和历史原型序列,确定了所鉴定的南部非洲型(SAT)-FMD病毒的遗传多样性。在检测的453份样本中,176份对四种FMDv血清型呈阳性。在176例FMD阳性病例中,有105份SAT2样本、32份SAT1样本、21份SAT3样本和18份O型血清样本。系统发育分析将SATs的VP1基因序列归类为南部非洲先前观察到的拓扑型。SAT1病毒来自拓扑型I和III,SAT2病毒属于拓扑型I、II、III和IV,SAT3病毒属于拓扑型I和II。对现场FMDv分离株的疫苗匹配研究显示,三种SAT血清型的 - 值大于或等于0.3。这表明当前的SAT FMD疫苗株与流行的SAT血清型之间没有显著的抗原差异。因此,这些疫苗仍然适用于该地区口蹄疫的防控。该研究未发现任何新的口蹄疫谱系/拓扑型侵入所采样的南部非洲国家。