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Molecular characterization of African swine fever virus from domestic pigs in northern Tanzania during an outbreak in 2013

机译:2013年暴发期间坦桑尼亚北部家猪的非洲猪瘟病毒的分子特征

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摘要

African swine fever (ASF) is an acute, highly contagious and deadly viral hemorrhagic fever of domestic pigs caused by African swine fever virus (ASFV), a double-stranded DNA virus of the family Asfarviridae. In this study, molecular diagnosis and characterization of outbreak ASFV in northern Tanzania, was performed on spleen, lymph node, kidney, and heart samples collected in June and July 2013 from domestic pigs that died during a hemorrhagic disease outbreak. Confirmatory diagnosis of ASF was performed using polymerase chain reaction (PCR) by partial amplification of B646L gene of ASFV encoding the major capsid protein p72 using PPA1/PPA2 primers. PCR using PPA1/PPA2 primers produced an expected PCR product size, confirming ASF outbreak in northern Tanzania. In addition, nucleotide amplification and sequencing, and phylogenetic reconstruction of the variable 3′-end of the B646L gene and complete E183L gene encoding the inner envelope transmembrane protein p54 showed that the 2013 outbreak ASFV from northern Tanzania were 100 % identical and clustered into ASFV B646L (p72) and E183L (p54) genotype X. Furthermore, the tetrameric amino acid repeats within the central variable region (CVR) of the B602L gene coding for the J9L protein had the signature BNBA(BN)5NA with a single novel tetramer NVDI (repeat code N). The results of the present study confirm an ASF outbreak in northern Tanzania in the year 2013 and show that the present outbreak ASFV is closely related to other ASFV from ticks, warthogs, and domestic pigs previously reported from Tanzania.
机译:非洲猪瘟(ASF)是由猪瘟病毒(Asfarviridae家族的双链DNA病毒)引起的家猪的急性,高度传染性和致命性病毒性出血热。在本研究中,对2013年6月和2013年7月从出血性疾病暴发中死亡的家猪收集的脾脏,淋巴结,肾脏和心脏样本进行了坦桑尼亚北部暴发性ASFV的分子诊断和鉴定。使用聚合酶链反应(PCR)通过使用PPA1 / PPA2引物部分扩增编码主要衣壳蛋白p72的ASFV B646L基因进行ASF的确诊。使用PPA1 / PPA2引物的PCR产生了预期的PCR产物大小,证实了坦桑尼亚北部的ASF爆发。此外,对B646L基因的可变3'-端和编码内膜跨膜蛋白p54的完整E183L基因进行核苷酸扩增和测序以及系统发育重建,表明坦桑尼亚北部2013年暴发的ASFV具有100%的同一性并聚集成ASFV B646L(p72)和E183L(p54)基因型X。此外,编码J9L蛋白的B602L基因的中央可变区(CVR)内的四聚氨基酸重复序列具有签名BNBA(BN)5NA和一个新的四聚体NVDI (重复代码N)。本研究的结果证实了2013年坦桑尼亚北部爆发了ASF病毒,并表明目前爆发的ASFV与来自坦桑尼亚的壁虱,疣猪和家猪的其他ASFV密切相关。

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