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Efficient construction of Haemophilus parasuis mutants based on natural transformation

机译:基于自然转化的高效副猪嗜血杆菌突变体构建

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摘要

Studies on virulence factors and pathogenecity of Haemophilus parasuis have long been hindered by a lack of a consistent system for genetic manipulation. In this study, competence was induced by transferring H. parasuis from rich medium to starvation medium media-IV (M-IV) and iscR gene deficient mutants of H. parasuis were generated efficiently. Transformation frequency varied from 4.1 × 10−5 to 1.1 × 10−8 when using circular plasmid, and increased to about 2- to 31-fold when transformed using linearized plasmid. Allele replacement occurred efficiently in 6 strains, which are transformable using both circular and linearized pTRU, but not in another 2 strains which could only be transformed using linearized plasmid. The iscR mutants were stable for at least 20 passages in vitro. Haemophilus parasuis strains vary extensively in natural transformation efficiency and the method established here allows for transformation of a larger spectrum of strains with an easily accessed plasmid. This provides important tools for genetic manipulation of H. parasuis.
机译:长期以来,由于缺乏一致的基因操作系统,阻碍了副猪嗜血杆菌毒力因子和致病性研究。在这项研究中,通过将副猪嗜血杆菌从丰富培养基转移到饥饿培养基-IV(M-IV)来诱导能力,并有效产生了iscR基因缺陷的副猪嗜血杆菌突变体。使用环状质粒时,转化频率从4.1×10 -5 变化到1.1×10 -8 ,使用线性化质粒转化时,转化频率增加到2-3倍左右。等位基因置换在6个菌株中有效发生,可以同时使用环状和线性pTRU进行转化,而在另2个菌株中则不能,只能使用线性化质粒进行转化。 iscR突变体在体外至少20代稳定。副猪嗜血杆菌菌株的自然转化效率差异很大,此处建立的方法允许使用容易获得的质粒转化更大范围的菌株。这为副猪嗜血杆菌的基因操作提供了重要的工具。

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