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一种利用小麦抗性基因H13作为模型评估黑森瘿蚊田间种群毒力的新颖、经济的方法。 (双翅目:瘿蚊科)

A Novel, Economical Way to Assess Virulence in Field Populations of Hessian Fly (Diptera: Cecidomyiidae) Utilizing Wheat Resistance Gene H13 as a Model.

作者信息

Johnson Alisha J, Abdel Moniem Hossam E M, Flanders Kathy L, Buntin G David, Reay-Jones Francis P F, Reisig Dominic, Stuart Jeffery J, Subramanyam Subhashree, Shukle Richard H, Schemerhorn Brandon J

机构信息

USDA-ARS, Crop Protection and Pest Control Research Unit, 170 South University St., West Lafayette, IN 47907.

Department of Entomology, Purdue University, 901 South State St., West Lafayette, IN 47907.

出版信息

J Econ Entomol. 2017 Aug 1;110(4):1863-1868. doi: 10.1093/jee/tox129.

Abstract

Mayetiola destructor (Say) is a serious pest of wheat, Triticum aestivum L., in North America, North Africa, and Central Asia. Singly deployed resistance genes in wheat cultivars have provided effective management of Hessian fly populations for >50 yr. Thirty-five H genes have been documented. Defense mediated by the H gene constitutes strong selection on the Hessian fly population, killing 100% of larvae. A mutation in a matching Hessian fly avirulence gene confers virulence to the H gene, leading to survival on the resistant plant. As the frequency of virulence rises in the population, the H gene loses its effectiveness for pest management. Knowing the frequency of virulence in the population is not only important for monitoring but also for decisions about which H gene should be deployed in regional wheat breeding programs. Here, we present a novel assay for detecting virulence in the field. Hessian fly males were collected in Alabama, Georgia, North Carolina, and South Carolina using sticky traps baited with Hessian fly sex pheromone. Utilizing two PCR reactions, diagnostic molecular markers for the six alleles controlling avirulence and virulence to H13 can be scored based on band size. Throughout the southeast, all three avirulence and three virulence alleles can be identified. In South Carolina, the PCR assay was sensitive enough to detect the spread of virulence into two counties previously documented as 100% susceptible to H13. The new assay also indicates that the previous methods overestimated virulence in the field owing to scoring of the plant instead of the insect.

摘要

麦红吸浆虫(Mayetiola destructor (Say))是北美洲、北非和中亚地区小麦(Triticum aestivum L.)的一种严重害虫。在小麦品种中单独部署的抗性基因已对麦红吸浆虫种群进行了50多年的有效管理。已记录了35个H基因。由H基因介导的防御对麦红吸浆虫种群构成了强大的选择压力,可杀死100%的幼虫。匹配的麦红吸浆虫无毒基因发生突变会使H基因产生毒性,导致其在抗性植株上存活。随着种群中毒性频率的上升,H基因失去了对害虫管理的有效性。了解种群中毒性的频率不仅对监测很重要,而且对于决定在区域小麦育种计划中应部署哪个H基因也很重要。在此,我们提出了一种在田间检测毒性的新方法。使用用麦红吸浆虫性信息素诱饵的粘性诱捕器在阿拉巴马州、佐治亚州、北卡罗来纳州和南卡罗来纳州收集麦红吸浆虫雄性。利用两个PCR反应,可以根据条带大小对控制对H13无毒和有毒的六个等位基因的诊断分子标记进行评分。在整个东南部地区,可以识别出所有三个无毒等位基因和三个有毒等位基因。在南卡罗来纳州,PCR检测足够灵敏,能够检测到毒性扩散到之前记录为对H13 100%敏感的两个县。新的检测方法还表明,由于对植物而非昆虫进行评分,以前的方法高估了田间的毒性。

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