Onyango Maria G, Beebe Nigel W, Gopurenko David, Bellis Glenn, Nicholas Adrian, Ogugo Moses, Djikeng Appolinaire, Kemp Steve, Walker Peter J, Duchemin Jean-Bernard
CSIRO Health & Biosecurity Australian Animal Health Laboratory, 5 Portalington Road, Geelong, Victoria, 3220, Australia.
School of Medicine, Deakin University, 75 Pidgons Road, Waurn Ponds, Victoria, 3216, Australia.
Vet Res. 2015 Sep 25;46:108. doi: 10.1186/s13567-015-0250-8.
Bluetongue virus (BTV) is a major pathogen of ruminants that is transmitted by biting midges (Culicoides spp.). Australian BTV serotypes have origins in Asia and are distributed across the continent into two distinct episystems, one in the north and another in the east. Culicoides brevitarsis is the major vector of BTV in Australia and is distributed across the entire geographic range of the virus. Here, we describe the isolation and use of DNA microsatellites and gauge their ability to determine population genetic connectivity of C. brevitarsis within Australia and with countries to the north. Eleven DNA microsatellite markers were isolated using a novel genomic enrichment method and identified as useful for genetic analyses of sampled populations in Australia, northern Papua New Guinea (PNG) and Timor-Leste. Significant (P < 0.05) population genetic subdivision was observed between all paired regions, though the highest levels of genetic sub-division involved pair-wise tests with PNG (PNG vs. Australia (FST = 0.120) and PNG vs. Timor-Leste (FST = 0.095)). Analysis of multi-locus allelic distributions using STRUCTURE identified a most probable two-cluster population model, which separated PNG specimens from a cluster containing specimens from Timor-Leste and Australia. The source of incursions of this species in Australia is more likely to be Timor-Leste than PNG. Future incursions of BTV positive C. brevitarsis into Australia may be genetically identified to their source populations using these microsatellite loci. The vector's panmictic genetic structure within Australia cannot explain the differential geographic distribution of BTV serotypes.
蓝舌病病毒(BTV)是反刍动物的主要病原体,通过吸血蠓(库蠓属)传播。澳大利亚的BTV血清型起源于亚洲,分布于整个大陆,形成两个不同的流行系统,一个在北部,另一个在东部。短角库蠓是澳大利亚BTV的主要传播媒介,分布在该病毒的整个地理范围内。在此,我们描述了DNA微卫星的分离和应用,并评估它们确定澳大利亚境内以及与北部国家的短角库蠓种群遗传连通性的能力。使用一种新的基因组富集方法分离出11个DNA微卫星标记,并确定其对澳大利亚、巴布亚新几内亚(PNG)北部和东帝汶采样种群的遗传分析有用。在所有配对区域之间均观察到显著(P < 0.05)的种群遗传细分,尽管最高水平的遗传细分涉及与PNG的成对测试(PNG与澳大利亚(FST = 0.120)以及PNG与东帝汶(FST = 0.095))。使用STRUCTURE对多位点等位基因分布进行分析,确定了一个最可能的两簇种群模型,该模型将PNG标本与包含东帝汶和澳大利亚标本的簇分开。该物种在澳大利亚的入侵来源更可能是东帝汶而非PNG。未来BTV阳性的短角库蠓入侵澳大利亚时,可利用这些微卫星位点从基因上确定其来源种群。该传播媒介在澳大利亚境内的随机交配遗传结构无法解释BTV血清型的不同地理分布。