Ehizibolo D O, Haegeman A, De Vleeschauwer A R, Umoh J U, Kazeem H M, Okolocha E C, Van Borm S, De Clercq K
FMD Laboratory, Viral Research Division, National Veterinary Research Institute (NVRI), Vom, Nigeria.
Department of Veterinary Public Health & Preventive Medicine, Faculty of Veterinary Medicine, Ahmadu Bello University, Zaria, Nigeria.
Transbound Emerg Dis. 2017 Dec;64(6):1979-1990. doi: 10.1111/tbed.12602. Epub 2017 Jan 17.
Control measures for foot and mouth disease (FMD) in Nigeria have not been implemented due to the absence of locally produced vaccines and risk-based analysis resulting from insufficient data on the circulating FMD virus (FMDV) serotypes/strains. In 2013-2015, blood and epithelial samples were collected from reported FMD outbreaks in four states (Kaduna, Kwara, Plateau and Bauchi) in northern Nigeria. FMDV non-structural protein (NSP) seroprevalence for the outbreaks was estimated at 80% (72 of 90) and 70% (131 of 188) post-outbreak. Antibodies against FMDV serotypes O, A, SAT1, SAT2 and SAT3 were detected across the states using solid-phase competitive ELISA. FMDV genome was detected in 99% (73 of 74) of the samples from FMD-affected animals using rRT-PCR, and cytopathic effect was found in cell culture by 59% (44 of 74) of these samples. Three FMDV serotypes O, A and SAT2 were isolated and characterized. The phylogenetic assessments of the virus isolates showed that two topotypes of FMDV serotype O, East Africa-3 (EA-3) and West Africa (WA) topotypes were circulating, as well as FMDV strains belonging to the Africa genotype (G-IV) of serotype A and FMDV SAT2 topotype VII strains. While the serotype O (EA-3) strains from Nigeria were most closely related to a 1999 virus strain from Sudan, the WA strain in Nigeria shares genetic relationship with three 1988 viruses in Niger. The FMDV serotype A strains were closely related to a known virus from Cameroon, and the SAT2 strains were most closely related to virus subtypes in Libya. This study provides evidence of co-occurrence of FMDV serotypes and topotypes in West, Central, East and North Africa, and this has implication for control. The findings help filling the knowledge gap of FMDV dynamics in Nigeria and West Africa subregion to support local and regional development of vaccination-based control plans and international risk assessment.
由于缺乏本地生产的疫苗以及口蹄疫病毒(FMDV)血清型/毒株数据不足导致基于风险的分析缺乏,尼日利亚尚未实施口蹄疫(FMD)控制措施。2013年至2015年期间,从尼日利亚北部四个州(卡杜纳州、夸拉州、高原州和包奇州)报告的口蹄疫疫情中采集了血液和上皮样本。疫情爆发后,口蹄疫病毒非结构蛋白(NSP)血清阳性率估计为80%(90份样本中的72份)和70%(188份样本中的131份)。使用固相竞争ELISA在各州检测到了针对口蹄疫病毒血清型O、A、SAT1、SAT2和SAT3的抗体。使用逆转录实时荧光定量PCR(rRT-PCR)在99%(74份样本中的73份)受口蹄疫影响动物的样本中检测到了口蹄疫病毒基因组,并且在这些样本的59%(74份样本中的44份)细胞培养中发现了细胞病变效应。分离并鉴定了三种口蹄疫病毒血清型O、A和SAT2。对病毒分离株的系统发育评估表明,口蹄疫病毒血清型O的两种拓扑型,即东非-3(EA-3)和西非(WA)拓扑型正在传播,以及属于血清型A非洲基因型(G-IV)的口蹄疫病毒毒株和口蹄疫病毒SAT2拓扑型VII毒株。虽然来自尼日利亚的血清型O(EA-3)毒株与1999年来自苏丹的病毒毒株关系最为密切,但尼日利亚的WA毒株与尼日尔的三种1988年病毒存在遗传关系。口蹄疫病毒血清型A毒株与来自喀麦隆的一种已知病毒关系密切,而SAT2毒株与利比亚的病毒亚型关系最为密切。本研究提供了口蹄疫病毒血清型和拓扑型在西非、中非、东非和北非共同存在的证据,这对控制工作具有重要意义。这些发现有助于填补尼日利亚和西非次区域口蹄疫病毒动态的知识空白,以支持基于疫苗接种的控制计划的地方和区域制定以及国际风险评估。