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SCAR markers for identification of host plant specificity in whitefly, Bemisia tabaci (Genn )

机译:SCAR标记,用于鉴定烟粉虱(烟粉虱)中的寄主植物特异性(Genn)

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摘要

RAPD markers (8 in number) which identified specificity in Bemisia tabaci (Genn ) to a single or two different host plants (out of cotton brinjal tomato soybean and Sida sp a weed) were sequenced Based upon these nucleotide sequences 8 sets of SCAR primers were developed for PCR amplification of the respective SCAR markers from B tabaci genotype holding specificity to a specific host plant During evaluation these primers amplified SCAR markers of expected sizes as per position of primer sequences in the determined sequence for the respective RAPD marker and only from the specific B tabaci genotype Subsequent validation of each of these SCAR markers with 10 individuals from a freshly collected B tabaci population from the respective field of above field crops (and potato) and wildly growing Sida sp plants resulted in correct amplifications with majority of the whitefly individuals (6-8) while the specific SCAR marker was not amplified with a small fraction of B tabaci individuals (2 4) Thus the SCAR markers were found to be true to their identity, whereas failure to amplify the same from minor fraction of the field population could be due to mixed population effect wherein the field population gets mixed with whitefly from alternate source crops and remained undetected The finding that majority of the individuals being detected by respective marker supported the specificity of developed SCAR markers for molecular monitoring of host specific B tabaci individuals and populations besides establishing the existence of host selection of whitefly by the plant host type in nature
机译:鉴定了烟粉虱对一种或两种不同寄主植物(棉花茄子番茄大豆和Sida sp。杂草中)的特异性的RAPD标记(数量为8),基于这些核苷酸序列,对8套SCAR引物进行了测序。开发用于从烟粉虱基因型对特定寄主植物具有特异性的PCR扩增SCAR标记的方法在评估过程中,这些引物根据相应RAPD标记的确定序列中引物序列的位置扩增了预期大小的SCAR标记,并且仅从特定烟粉虱基因型随后用上述田间作物(和马铃薯)和野外生长的Sida sp植物各自田间新鲜收集的烟粉虱种群中的10个个体对这些SCAR标记进行了后续验证,结果导致大多数粉虱个体正确扩增( 6-8),而一小部分烟粉虱个体并未扩增出特异性SCAR标记(2 4)因此,发现SCAR标记符合其真实性,而未能从田间种群的小部分扩增相同的标记可能是由于混合种群效应,其中田间种群与其他来源作物的粉虱混合在一起而未被发现。除了通过自然界中的植物宿主类型确定粉虱寄主选择的存在外,大多数被各自标记物检测到的个体支持了发达的SCAR标记物对宿主特异性烟粉虱个体和种群进行分子监测的特异性。

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