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MixMate®, incl. 3 tube holders: PCR 96, 0.5 mL, 1.5/2.0 mL, 230 V/50 – 60 Hz

板式搅拌机

Company: Eppendorf
Catalog#: 5353000014
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Isolation of Rice Stripe Virus Preparation from Viruliferous Small Brown Planthoppers and Mechanic Inoculation on Rice
Author:
Date:
2017-11-05
[Abstract]   Tenuiviruses can infect the plants of the family Poaceae, and cause serious loss of crops, particularly rice and maize, in South-Eastern Asian countries. Tenuiviruses usually depend on insect vectors for their transmission and cannot be transmitted between plants through wounds or abrasions. Rice stripe virus (RSV), a typical member of tenuiviruses, is efficiently transmitted by the small brown planthopper Laodelphax striatellus in a persistent-propagative manner to cause rice stripe disease. Here we presented a convenient method, the midrib micro-injection, to mechanically inoculate insect-derived RSV into rice leaves for conducting pathogenicity assay on rice plants. [摘要]  细菌病毒可以感染禾本科植物,并在东南亚国家造成严重的作物损失,特别是稻米和玉米。 病毒通常依靠昆虫载体传播,不能通过伤口或擦伤传播。 水稻条纹病毒(RSV)是典型的tenuiviruses的成员,以持续繁殖的方式被小型褐飞虱灰飞虱高效率地传播,导致水稻条纹病。 在这里,我们提出了一种方便的方法,即中微量注射,以机械方式将昆虫来源的RSV接种到水稻叶中,以对水稻植物进行致病性测定。
【背景】除非通过根据不同的实验细节从1%至90%的完全不同的传输速率进行血管穿刺接种(Louie,1995; Hogenhout等人,2008),否则不能将机器接种到植物中。至于RSV,机械传播通常失败或产生低感染率(Ling,1972)。特别地,从病变植物注射RSV粗提物后,传播率仅为6%(Okuyama and Asuyama,1959)。在这项工作中提到的中微注射方法将RSV传播率提高到17%。虽然机械传播RSV的发生率仍远低于昆虫载体传播(53%),但是我们的方法为持续繁殖的植物病毒的机械接种提供了便利的方法。此外,基于这种方法,可以在受感染的植物宿主中更精确地确定持续增殖植物病毒的复制和基因表达,而不受昆虫即接种剂量和昆虫蛋白质的干扰。

Large-scale Phenotypic Profiling of Gene Deletion Mutants in Candida glabrata
Author:
Date:
2015-07-20
[Abstract]  Here, we describe a method enabling the phenotypic profiling of genome-scale deletion collections of fungal mutants to detect phenotypes for various stress conditions. These stress conditions include among many others antifungal drug susceptibility, temperature-induced and osmotic as well as heavy metal or oxidative stress. The protocol was extensively used to phenotype a collection of gene deletion mutants in the human fungal pathogen Candida glabrata (C. glabrata) (Schwarzmüller et al., 2014). [摘要]  在这里,我们描述了一种使表型分析的基因组规模删除集合的真菌突变体检测表型的各种应力条件的方法。 这些胁迫条件包括许多其它抗真菌药物敏感性,温度诱导和渗透以及重金属或氧化应激。 该方案广泛用于表达人真菌病原体光滑假丝酵母( glabrata )中基因缺失突变体的集合(Schwarzmüller等人 >,2014)。

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