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通过显微注射胚胎细胞质和胚胎匀浆来表征沃尔巴克氏体转染效率。

Characterization of Wolbachia transfection efficiency by using microinjection of embryonic cytoplasm and embryo homogenate.

作者信息

Xi Zhiyong, Dobson Stephen L

机构信息

Department of Entomology, University of Kentucky, S-225 Ag. Science Center North, Lexington, Kentucky 40546, USA.

出版信息

Appl Environ Microbiol. 2005 Jun;71(6):3199-204. doi: 10.1128/AEM.71.6.3199-3204.2005.

Abstract

Wolbachia spp. are intracellular alpha proteobacteria closely related to Rickettsia. The maternally inherited infections occur in a wide range of invertebrates, causing several reproductive abnormalities, including cytoplasmic incompatibility. The artificial transfer of Wolbachia between hosts (transfection) is used both for basic research examining the Wolbachia-host interaction and for applied strategies that use Wolbachia infections to affect harmful insect populations. Commonly employed transfection techniques use embryonic microinjection to transfer Wolbachia-infected embryo cytoplasm or embryo homogenate. Although microinjections of both embryonic cytoplasm and homogenate have been used successfully, their respective transfection efficiencies (rates of establishing stable germ line infections) have not been directly compared. Transfection efficiency may be affected by variation in Wolbachia quantity or quality within the donor embryos and/or the buffer types used in embryo homogenization. Here we have compared Wolbachia bacteria that originate from different embryonic regions for their competencies in establishing stable germ line infections. The following three buffers were compared for their abilities to maintain an appropriate in vitro environment for Wolbachia during homogenization and injection: phosphate-buffered saline, Drosophila Ringer's buffer, and a sucrose-phosphate-glutamate solution (SPG buffer). The results demonstrate that Wolbachia bacteria from both anterior and posterior embryo cytoplasms are competent for establishing infection, although differing survivorships of injected hosts were observed. Buffer comparison shows that embryos homogenized in SPG buffer yielded the highest transfection success. No difference was observed in transfection efficiencies when the posterior cytoplasm transfer and SPG-homogenized embryo techniques were compared. We discuss the results in relation to intra- and interspecific Wolbachia transfection and the future adaptation of the microinjection technique for additional insects.

摘要

沃尔巴克氏体属是与立克次氏体密切相关的细胞内α变形菌。这种母系遗传感染发生在多种无脊椎动物中,会导致多种生殖异常,包括细胞质不相容。在宿主之间人工转移沃尔巴克氏体(转染)既用于研究沃尔巴克氏体与宿主相互作用的基础研究,也用于利用沃尔巴克氏体感染来影响有害昆虫种群的应用策略。常用的转染技术使用胚胎显微注射来转移感染沃尔巴克氏体的胚胎细胞质或胚胎匀浆。虽然胚胎细胞质和匀浆的显微注射都已成功使用,但它们各自的转染效率(建立稳定种系感染的比率)尚未直接比较。转染效率可能受供体胚胎内沃尔巴克氏体数量或质量的变化和/或胚胎匀浆中使用的缓冲液类型的影响。在这里,我们比较了源自不同胚胎区域的沃尔巴克氏体在建立稳定种系感染方面的能力。比较了以下三种缓冲液在匀浆和注射过程中为沃尔巴克氏体维持合适体外环境的能力:磷酸盐缓冲盐水、果蝇林格氏缓冲液和蔗糖 - 磷酸盐 - 谷氨酸溶液(SPG缓冲液)。结果表明,来自胚胎前后部细胞质的沃尔巴克氏体都有能力建立感染,尽管观察到注射宿主的存活情况有所不同。缓冲液比较表明,在SPG缓冲液中匀浆的胚胎产生的转染成功率最高。比较后部细胞质转移和SPG匀浆胚胎技术时,转染效率没有差异。我们讨论了与种内和种间沃尔巴克氏体转染相关的结果以及显微注射技术未来对其他昆虫的适应性。

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