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鼠疫耶尔森氏菌致病性必需质粒决定因素的遗传分析。

Genetic analysis of essential plasmid determinants of pathogenicity in Yersinia pestis.

作者信息

Portnoy D A, Blank H F, Kingsbury D T, Falkow S

出版信息

J Infect Dis. 1983 Aug;148(2):297-304. doi: 10.1093/infdis/148.2.297.

Abstract

The role of the Yersinia pestis virulence-associated plasmid, pYV019, in the expression of Ca++ dependence, virulence, and the production of the V antigen was investigated. Derivatives of bacteriophage P1 were used to deliver the transposon Tn5 into Y pestis strain EV76. Ca++-independent mutants in which transposon Tn5 had been inserted into plasmid pYV019 were isolated, the resulting plasmids--pYV019::Tn5--were transformed into an Escherichia coli K12 derivative, and the site of insertion of transposon Tn5 was mapped with restriction endonucleases. The plasmids were then transduced by bacteriophage P1 into avirulent strain 195-P1 of Y pestis. The transductants were analyzed for expression of Ca++ dependence, virulence in mice, and the expression of the V antigen. Introduction of plasmid pYV019 with insertions outside of the Ca++ dependence loci restored strain 195-P1 to full virulence, while disruption of plasmid genes associated with Ca++ dependence led to loss of virulence. Using Western blotting analysis and E coli minicells, it was shown that genes specific for the V antigen are plasmid encoded.

摘要

研究了鼠疫耶尔森菌毒力相关质粒pYV019在钙离子依赖性、毒力表达及V抗原产生中的作用。利用噬菌体P1的衍生物将转座子Tn5导入鼠疫耶尔森菌EV76菌株。分离出转座子Tn5插入质粒pYV019的钙离子非依赖性突变体,将所得质粒——pYV019::Tn5——转化到大肠杆菌K12衍生物中,并用限制性核酸内切酶定位转座子Tn5的插入位点。然后用噬菌体P1将这些质粒转导到鼠疫耶尔森菌无毒力菌株195-P1中。分析转导子的钙离子依赖性表达、对小鼠的毒力以及V抗原的表达。导入在钙离子依赖性位点之外有插入片段的质粒pYV019可使菌株195-P1恢复至完全毒力,而破坏与钙离子依赖性相关的质粒基因会导致毒力丧失。通过蛋白质印迹分析和大肠杆菌微小细胞实验表明,V抗原特异性基因是由质粒编码的。

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