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通过转座子Tn916插入中断肺炎链球菌3型的荚膜产生。

Interruption of capsule production in Streptococcus pneumonia serotype 3 by insertion of transposon Tn916.

作者信息

Watson D A, Musher D M

机构信息

Infectious Disease Section, Veterans Affairs Medical Center, Houston, Texas 77030.

出版信息

Infect Immun. 1990 Sep;58(9):3135-8. doi: 10.1128/iai.58.9.3135-3138.1990.

Abstract

Transposon Tn916 mutagenesis was used to produce mutant strains of Streptococcus pneumoniae serotype 3 that lacked only a polysaccharide capsule. Southern blotting, DNA-DNA hybridization, and immunochemical analyses demonstrated that the presence of a single copy of Tn916 was sufficient to produce unencapsulation. The 50% lethal dose for such mutants was greater than 5 x 10(7) CFU, as opposed to a 50% lethal dose of 1 CFU for wild-type strains. These experiments outline an effective method for targeting genes in S. pneumoniae by transposon interruption and provide molecular evidence to support the longstanding hypothesis that the capsule is the principal virulence factor in this pathogen.

摘要

转座子Tn916诱变被用于产生仅缺乏多糖荚膜的肺炎链球菌3型突变菌株。Southern印迹法、DNA-DNA杂交和免疫化学分析表明,单个拷贝的Tn916的存在足以导致去荚膜化。此类突变体的半数致死剂量大于5×10⁷CFU,而野生型菌株的半数致死剂量为1CFU。这些实验概述了一种通过转座子插入来靶向肺炎链球菌基因的有效方法,并提供了分子证据来支持长期以来的假说,即荚膜是这种病原体的主要毒力因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07ee/313622/19ad244b7e78/iai00057-0422-a.jpg

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