Gallardo Carmina, Mwaengo Dufton M, Macharia Joseph M, Arias Marisa, Taracha Evans A, Soler Alejandro, Okoth Edward, Martín Elena, Kasiti Jackline, Bishop Richard P
Centro de Investigación en Sanidad Animal (CISA-INIA), Ctra Algete el Casar s/n, Valdeolmos, Madrid, 28130, Spain.
Virus Genes. 2009 Feb;38(1):85-95. doi: 10.1007/s11262-008-0293-2. Epub 2008 Nov 14.
Complete sequencing of p54-gene from 67 European, American, and West and East African Swine Fever virus (ASFV) isolates revealed that West African and European ASFV isolates classified within the predominant Genotype I according to partial sequencing of p72 were discriminated into four major sub-types on the basis of their p54 sequences. This highlighted the value of p54 gene sequencing as an additional, intermediate-resolution, molecular epidemiological tool for typing of ASFV viruses. We further evaluated p54-based genotyping, in combination with partial sequences of two other genes, for determining the genetic relationships and origin of viruses responsible for disease outbreaks in Kenya. Animals from Western and central Kenya were confirmed as being infected with ASFV using a p72 gene-based PCR assay, following outbreaks of severe hemorrhagic disease in domestic pigs in 2006 and 2007. Eleven hemadsorbing viruses were isolated in macrophage culture and genotyped using a combination of full-length p54-gene sequencing, partial p72-gene sequencing, and analysis of tetrameric amino acid repeat regions within the variable region of the B602L gene (CVR). The data revealed that these isolates were identical in their p72 and p54 sequence to viruses responsible for ASF outbreaks in Uganda in 2003. There was a minor difference in the number of tetrameric repeats within the B602L sequence of the Kenyan isolates that caused the second Kenyan outbreak in 2007. A practical implication of the genetic similarity of the Kenyan and Ugandan viral isolates is that ASF control requires a regional approach.
对来自欧洲、美洲以及西非和东非的67株猪瘟病毒(ASFV)分离株的p54基因进行全序列分析,结果显示,根据p72基因部分序列被归类为主导基因型I的西非和欧洲ASFV分离株,基于其p54序列可分为四个主要亚型。这凸显了p54基因测序作为一种额外的、中等分辨率的分子流行病学工具,用于ASFV病毒分型的价值。我们进一步评估了基于p54的基因分型,并结合另外两个基因的部分序列,以确定肯尼亚疾病暴发所涉病毒的遗传关系和起源。在2006年和2007年家猪发生严重出血性疾病疫情后,利用基于p72基因的PCR检测方法,确认肯尼亚西部和中部的动物感染了ASFV。在巨噬细胞培养中分离出11株血细胞吸附病毒,并通过全长p54基因测序、p72基因部分测序以及对B602L基因可变区内四聚体氨基酸重复区域(CVR)的分析进行基因分型。数据显示这些分离株的p72和p54序列与2003年乌干达造成非洲猪瘟疫情的病毒相同。在2007年导致肯尼亚第二次疫情暴发的肯尼亚分离株的B602L序列中,四聚体重复的数量存在微小差异。肯尼亚和乌干达病毒分离株遗传相似性的一个实际影响是,非洲猪瘟的防控需要采取区域方法。