Suppr超能文献

与弗氏志贺氏菌毒力丧失及刚果红结合活性相关的140兆道尔顿质粒的分子改变

Molecular alteration of the 140-megadalton plasmid associated with loss of virulence and Congo red binding activity in Shigella flexneri.

作者信息

Sasakawa C, Kamata K, Sakai T, Murayama S Y, Makino S, Yoshikawa M

出版信息

Infect Immun. 1986 Feb;51(2):470-5. doi: 10.1128/iai.51.2.470-475.1986.

Abstract

A plasmid of about 140 megadaltons has been associated with the invasiveness of Shigella flexneri. Upon subculturing in liquid media of fully virulent isolates of Shigella flexneri 2a YSH6000, which contains only a 230-kilobase-pair (kbp) plasmid in addition to 3.3- and 4.2-kbp cryptic plasmids characteristic to all S. flexneri strains, loss of invasiveness, loss of Congo red binding activity (Pcr), and complete loss of, or a deletion, or even a single-site IS insertion in the plasmid occurred simultaneously. This was ascribed to the fact that, once a noninvasive Pcr- cell has emerged, it overgrows the wild type as a consequence of its selective advantage in artificial media. A deletion map of the 230-kbp plasmid was made by analyzing SalI digests of 39 deletion derivatives plus 1 formed by insertion of an IS1-like element in independently isolated, noninvasive Pcr- mutants. Of 39 deletion derivatives, 16 belonged to a single type, and 6 belonged to another, suggesting deletion hot spots. The deletion map was confirmed and extended by analyzing 359 SalI-generated partial digests of the wild-type plasmid cloned into pBR322. Three copies of IS1-like elements were found on three different SalI fragments by Southern hybridization. Segments required for the Pcr+ phenotype seemed to occur at several different locations in the plasmid. Each of 28 representative Pcr- mutants were negative by the Sereny test. Hence, many, or possibly all, Pcr determinants were required for full virulence.

摘要

一种约140兆道尔顿的质粒与福氏志贺菌的侵袭性有关。在对福氏志贺菌2a YSH6000的完全有毒力分离株进行液体传代培养时,该菌株除了含有所有福氏志贺菌菌株特有的3.3千碱基对(kbp)和4.2 kbp隐蔽质粒外,仅含有一个230 kbp的质粒,侵袭性丧失、刚果红结合活性(Pcr)丧失以及质粒完全缺失、缺失甚至单一位点的插入序列(IS)插入同时发生。这归因于一旦出现非侵袭性Pcr-细胞,由于其在人工培养基中的选择优势,它会超过野生型生长。通过分析39个缺失衍生物的SalI酶切产物以及由插入IS1样元件形成的1个产物,构建了230 kbp质粒的缺失图谱,这些缺失衍生物和插入产物来自独立分离的非侵袭性Pcr-突变体。在39个缺失衍生物中,16个属于单一类型,6个属于另一种类型,提示存在缺失热点。通过分析克隆到pBR322中的野生型质粒的359个SalI产生的部分酶切产物,对缺失图谱进行了确认和扩展。通过Southern杂交在三个不同的SalI片段上发现了三个拷贝的IS1样元件。Pcr+表型所需的片段似乎出现在质粒的几个不同位置。28个代表性Pcr-突变体中的每一个通过Sereny试验均为阴性。因此,许多或可能所有的Pcr决定簇都是完全毒力所必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0baf/262355/b39fa3bceec8/iai00107-0107-a.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验