首页> 美国卫生研究院文献>Journal of Nematology >Comparison of Meldola’s Blue Staining and Hatching Assay with Potato Root Diffusate for Assessment of Globodera sp. Egg Viability
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Comparison of Meldola’s Blue Staining and Hatching Assay with Potato Root Diffusate for Assessment of Globodera sp. Egg Viability

机译:Meldola的蓝色染色和孵化分析与马铃薯根扩散剂的比较用于评估Globodera sp。卵生存力

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摘要

Laboratory-based methods to test egg viability include staining with Meldola’s Blue and/or juvenile (J2) hatching assays using potato root diffusate (PRD). These two methods have not been tested under identical conditions to directly compare their assessments of Globodera egg viability. Using two bioassay strategies, cysts from a Globodera sp. population found in Oregon were subjected to both viability assessment methods. In strategy one, intact cysts were first stained with Meldola’s Blue (primary staining) and eggs were then transferred to PRD (secondary hatching). In the second strategy, intact cysts were exposed to PRD (primary hatching) and then unhatched eggs were transferred to Meldola’s Blue (secondary staining). Two different cohorts of cysts were evaluated using these experimental strategies: cohort 1 was comprised of cysts produced on potato in the greenhouse that exhibited low hatch when exposed to PRD and cohort 2 consisted of field-collected cysts whose eggs yielded significant hatch when exposed to PRD. Percentage viability was calculated and is expressed as the number of hatched J2 or unstained eggs/total number of eggs within a cyst. With field-produced cysts, primary staining with Meldola’s Blue and hatching with PRD produced similar viability estimates, with averages of 74.9% and 76.3%, respectively. In contrast, with greenhouse-produced cysts the two methods yielded much lower and unequal estimates 32.4% to 2.2%, respectively for primary hatching and staining methods. In addition, J2 hatch from unstained (viable) greenhouse-produced eggs was 13.7% after secondary exposure to PRD compared to 61.5% for field-produced eggs. The majority of eggs remaining unhatched after primary exposure to PRD (> 87%) stained with Meldola’s Blue regardless of cyst cohort. Staining with Meldola’s Blue provided a conservative assessment of egg viability compared to hatch assay with PRD regardless of diapause.
机译:以实验室为基础的方法来测试卵的生存能力,包括使用马铃薯根扩散剂(PRD)对Meldola的Blue和/或幼体(J2)孵化试验进行染色。尚未在相同条件下测试这两种方法以直接比较它们对Globodera卵生存力的评估。使用两种生物测定策略,从Globodera sp。获得囊肿。在俄勒冈州发现的人均接受了两种生存能力评估方法。在策略一中,将完整的囊肿首先用Meldola的Blue染色(初步染色),然后将卵转移至PRD(二次孵化)。在第二种策略中,将完整的囊肿暴露于PRD(初次孵化),然后将未孵化的卵转移到Meldola的Blue(二次染色)中。使用这些实验策略对两个不同的囊肿队列进行了评估:第1组由温室中马铃薯上产生的囊肿组成,暴露于PRD时孵化率低;第2组由田间采集的囊肿组成,其卵暴露于PRD时会产生明显的孵化率。计算生存力百分比,并表示为孵出的J2或未染色的卵数/囊肿中卵的总数。对于野外产生的囊肿,用Meldola氏蓝进行的初次染色和用PRD进行的孵化产生的生存力估计值相近,分别为74.9%和76.3%。相比之下,对于温室生产的囊肿,两种方法的初级孵化和染色方法的产率分别低得多和不相等,估计分别为32.4%至2.2%。另外,在二次暴露于PRD后,未染色(可行)温室生产的鸡蛋的J2孵化率为13.7%,而田间生产的鸡蛋为21.5%。初次暴露于PRD后,大多数卵未孵化(> 87%),不论囊肿队列如何,均被Meldola蓝染色。与使用PRD进行孵化测定相比,用Meldola’s Blue染色可对卵生存力进行保守评估,而不论是否滞育。

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