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首页> 外文期刊>Biological Control: Theory and Application in Pest Management >Development and verification of SNP arrays to monitor hybridization between two host-associated strains of knotweed psyllid, Aphalara itadori
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Development and verification of SNP arrays to monitor hybridization between two host-associated strains of knotweed psyllid, Aphalara itadori

机译:SNP阵列的开发和验证,以监测虎杖木虱两个寄主相关菌株之间的杂交

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Three species of invasive knotweeds (Fallopia japonica, Fallopia sachalinensis, and Fallopia x bohemica) cause extensive damage to riparian and roadside habitats in North America. Currently, two strains of the psyllid Aphalara itadori are being evaluated for introduction into the United States and Canada for the biological control of these knotweeds following the introduction of A. itadori into the United Kingdom. If approved and released, hybridization between individuals from these two strains is likely and understanding whether barriers to hybridization exist could have an important impact on the sustainability of this biological control program. Here we developed two single nucleotide polymorphism (SNP) arrays and examined their utility for identifying individuals of known pure strains (Hokkaido and Kyushu) and hybrid origins. Using an array of 141 SNPs we correctly identified all individuals to pure and hybrid classes, whereas using a smaller array of 29 SNPs we were able to correctly identify pure line individuals, but not hybrids. (C) 2015 Elsevier Inc. All rights reserved.
机译:三种入侵的虎杖(Fallopia japonica,Falopia sachalinensis和Fallopia x bohemica)对北美的河岸和路边栖息地造成了广泛的破坏。目前,正在评估将两种木虱Aphalara itadori菌株引入美国和加拿大,以便在将A. itadori引入英国后对这些虎杖进行生物防治。如果批准并发布,这两种菌株之间的杂交很可能会发生,了解杂交的障碍是否存在可能对该生物控制计划的可持续性产生重要影响。在这里,我们开发了两个单核苷酸多态性(SNP)阵列,并检查了它们在鉴定已知纯菌株(北海道和九州)和杂种来源的个体中的效用。通过使用141个SNP的阵列,我们可以正确地识别出纯种和杂种类别的所有个体,而使用较小的29个SNP的阵列,我们可以正确地识别纯系个体,而不是杂种。 (C)2015 Elsevier Inc.保留所有权利。

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