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用马铃薯根渗出液比较梅尔多拉蓝染色法和孵化试验评估球孢囊线虫属虫卵活力

Comparison of Meldola's Blue Staining and Hatching Assay with Potato Root Diffusate for Assessment of Globodera sp. Egg Viability.

作者信息

Kroese Duncan, Zasada Inga A, Ingham Russell E

机构信息

Oregon State University, Department of Botany and Plant Pathology, Cordley 2082, Corvallis, OR 97331, USA.

出版信息

J Nematol. 2011 Sep;43(3-4):182-6.

Abstract

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.

摘要

用于检测虫卵活力的实验室方法包括用美多拉蓝染色和/或使用马铃薯根浸出液(PRD)进行幼虫(J2)孵化试验。这两种方法尚未在相同条件下进行测试,以直接比较它们对球孢囊线虫虫卵活力的评估。采用两种生物测定策略,对在俄勒冈州发现的一种球孢囊线虫种群的孢囊进行了两种活力评估方法的测试。在策略一中,完整的孢囊首先用美多拉蓝染色(初次染色),然后将虫卵转移至PRD中(二次孵化)。在第二种策略中,完整的孢囊先暴露于PRD中(初次孵化),然后将未孵化的虫卵转移至美多拉蓝中(二次染色)。使用这些实验策略对两组不同的孢囊进行了评估:第1组由温室中在马铃薯上产生的孢囊组成,当暴露于PRD时孵化率较低;第2组由田间采集的孢囊组成,其虫卵在暴露于PRD时孵化率较高。计算了活力百分比,并表示为孵化出的J2幼虫或未染色虫卵的数量/每个孢囊内虫卵的总数。对于田间产生的孢囊,用美多拉蓝进行初次染色和用PRD进行孵化产生的活力估计值相似,平均值分别为74.9%和76.3%。相比之下,对于温室产生的孢囊,这两种方法得出的估计值要低得多且不相等,初次孵化和染色方法分别为32.4%和2.2%。此外,二次暴露于PRD后,来自未染色(有活力)的温室产生的虫卵的J2孵化率为13.7%,而田间产生的虫卵为61.5%。无论孢囊组如何,初次暴露于PRD后仍未孵化的大多数虫卵(>87%)都能用美多拉蓝染色。与PRD孵化试验相比,无论滞育情况如何,用美多拉蓝染色对虫卵活力的评估更为保守。

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