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Genetic manipulation of Fonsecaea pedrosoi using particles bombardment and Agrobacterium mediated transformation

机译:使用颗粒轰击和农杆菌介导转化的Fonsecaea Pedrosoi的遗传操作

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Fonsecaea pedrosoi, a melanized fungal pathogen that causes Chromoblastomycosis, a human disease with a worldwide distribution. Biolistic is a widely used technique for direct delivery of genetic material into intact cells by particles bombardment. Another well-established transformation method is Agrobacterium-mediated transformation (ATMT), which involves the transfer of a T-DNA from the bacterium to the target cells. In F. pedrosoi there are no reports of established protocols for genetic transformation, which require optimization of physical and biological parameters. In this work, intact conidia of F. pedrosoi were particle bombarded and subjected to ATMT. In addition, we proposed hygromycin B, nourseothricin and neomycin as dominant selective markers for F. pedrosoi and vectors were constructed. We tested two parameters for biolistic: the distance of the particles to the target cells and time of cells recovery in nonselective medium. The biolistic efficiency was 37 transformants/mu g of pFpHYG, and 45 transformants/mu g of pAN7.1. Transformants expressing GFP were successfully obtained by biolistic. A co-culture ratio of 10: 1 (bacterium: conidia) and co-incubation time of 72 h yielded the largest number of transformants after ATMT. Southern blot analysis showed the number of foreign DNA insertion into the genome is dependent upon the plasmid used to generate the mutants. This work describes for the first time two efficient methods for genetic modification of Fonsecaea and these results open new avenues to better understand the biology and pathogenicity of the main causal agent of this neglected disease.
机译:Fonsecaea Pedrosoi,一种混合​​的真菌病原体,导致染色体霉菌,具有全球分布的人类疾病。生物化是通过颗粒轰击将遗传物质直接递送到完整细胞中的广泛使用的技术。另一种成熟的转化方法是农杆菌介导的转化(ATMT),其涉及将T-DNA从细菌转移到靶细胞。在F. Pedrosoi中没有报告遗传转化的成立方案,需要优化物理和生物参数。在这项工作中,F. Pedrosoi的完整分泌物是轰击并进行ATMT的粒子。此外,我们提出了潮霉素B,诺尔科膦和新霉素作为F.培养和载体的显性选择性标志物。我们测试了一种抗体的两个参数:颗粒对靶细胞的距离和非选择性培养基中的细胞恢复时间。生物效率为37种转移夹/μg磷乳糊糊剂,45种转移体/μgPan7.1。通过生物化成功地获得表达GFP的转化体。共培养率为10:1(细菌:Catidia)和72小时的共孵育时间,在ATMT之后产生最多的转化体。 Southern印迹分析表明,外来DNA插入到基因组中的数量取决于用于产生突变体的质粒。这项工作描述了第一次有效的Fonsecaea遗传修饰的有效方法,这些结果开放了新的途径,以更好地了解这种被忽视疾病的主要因果剂的生物学和致病性。

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