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Molecular diagnosis and epidemiology of African swine fever outbreaks in Tanzania.

机译:坦桑尼亚非洲猪瘟疫情的分子诊断与流行病学。

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The objective of this study was to identify specific fingerprints for each African swine fever (ASF) outbreak that occurred in Tanzania from 2001-04. Standard postmortem examination was conducted on all dead pigs in situ: Dar Es Salaam outbreak in 2001 (a total of 13 specimens of lymphoid organs from 3 dead pigs); Arusha outbreak in 2003 (one spleen and 2 lymph nodes from one dead pig); and Kigoma outbreak in 2004 (a total of one, two and three spleen samples from Kasulu, Kibondo and Kigoma districts, respectively). ASF viruses were isolated from samples, confirming the diagnosis of ASF. Specific bands corresponding to the expected 278 bp product size were detected in the samples using the diagnostic primers ASF-1 and ASF-2. Specific bands corresponding to the 478 bp product size were detected in the samples using the epidemiological primers p72U and p72D. Nucleotide sequence data and phylogenetic analysis from the Mbeya and Dar Es Salaam outbreaks revealed that the isolate designated as TAN/1/1 clustered in a group of ASF viruses isolated in Malawi (1978) and Mozambique (1998 and 2001), with 99% homology. The Arusha isolates designated as TAN 2003/1 and TAN 2003/2 clustered with TAN 1/1 isolated in 2001 during the Dar Es Salaam outbreak but belonged to a different genotype. The source of ASFV that caused outbreaks in Arusha was unknown. The ASFV isolates from Kigoma and Kasulu districts designated as TAN 2004/1-4 were 100% homologous. These isolates clustered with ASF from Uganda and Burundi with 100% homology. However, these isolates did not cluster with Tanzanian ASFV isolates. This was the first study to provide a comprehensive insight into the molecular epidemiology of ASF outbreaks in Tanzania..
机译:本研究的目的是识别2001 - 04年坦桑尼亚发生的每种非洲猪瘟(ASF)爆发的特定指纹。标准的后期检查在所有死猪原位进行:2001年达累斯萨拉姆爆发(共有13个死猪的淋巴器官标本); 2003年Arusha爆发(来自一只死猪的脾脏和2个淋巴结); 2004年的Kigoma爆发(共有一,分别为Kibondo和Kigoma地区的一,两和三种脾脏样本)。从样品中分离ASF病毒,证实了ASF的诊断。使用诊断引物ASF-1和ASF-2在样品中检测对应于预期的278bp产品尺寸的特定条带。使用流行病学引物P72U和P72D在样品中检测到对应于478bp产品尺寸的特定条带。来自MBEYA和DAR ES SALAAM爆发的核苷酸序列数据和系统发育分析显示,孤立在马拉维(1978年)和莫桑比克(1998年和2001年)中分离的一组ASF病毒聚集在一组ASF病毒中,患有99%的同源性。在Dar Es Salaam爆发期间,ARUSHA ISOLATE指定为TAN 2003/1和TAN 2003/2与TAN 1/1集聚的TAN 1/1,但属于不同的基因型。在阿鲁沙爆发的ASFV来源未知。来自Kigoma和Kasulu区的ASFV分离物为TAN 2004 / 1-4的含量为100%同源。这些分离物与乌干达和布隆迪的ASF聚集在一起,具有100%同源性。然而,这些隔离物没有与坦桑尼亚ASFV隔离的簇。这是第一次研究坦桑尼亚在ASF爆发的分子流行病学方面的研究。

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