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福氏志贺菌2a的色素沉着丧失与毒力及毒力相关质粒的丧失相关。

Loss of pigmentation in Shigella flexneri 2a is correlated with loss of virulence and virulence-associated plasmid.

作者信息

Maurelli A T, Blackmon B, Curtiss R

出版信息

Infect Immun. 1984 Jan;43(1):397-401. doi: 10.1128/iai.43.1.397-401.1984.

Abstract

In this study, we examined the relationship between the virulence of Shigella flexneri 2a and the ability of strains of S. flexneri 2a to absorb Congo red. Spontaneous nonpigmented (i.e., unable to bind Congo red [Pcr-]) derivatives of a virulent, pigmented (Pcr+) strain of S. flexneri 2a were isolated and assayed for virulence as determined by their ability to invade epithelial cells. All Pcr- mutants examined lost the ability to invade epithelial cells and were thus avirulent. Agarose gel electrophoresis of plasmid DNA from these avirulent, Pcr- mutants showed that the majority of these strains had lost a plasmid band corresponding to a virulence-associated plasmid, pSf2a140. In many of the mutants, concomitant loss of pigmentation, virulence, and pSf2a140 was accompanied by the appearance of a new plasmid, smaller than pSf2a140. We believe these new plasmids to be deletion derivatives of pSf2a140 and that loss of pigmentation and loss of virulence are associated with deletions in pSf2a140. We transduced Pcr- mutants to Pcr+ and isolated transductants which suppressed the Pcr- phenotype. None of the Pcr+ transductants regained the ability to invade epithelial cells. Several suppressors of the Pcr- phenotype were identified as mutations in cell wall biosynthesis. These results support our belief that although pigmentation is usually associated with virulence, genetic determinants unrelated to virulence can also affect the ability of the cell to bind Congo red. Therefore, the ability of S. flexneri 2a to bind Congo red does not necessarily imply the ability to invade epithelial cells. However, loss of ability to bind Congo red is accompanied by loss of virulence.

摘要

在本研究中,我们检测了福氏志贺菌2a的毒力与该菌吸收刚果红能力之间的关系。从一株有毒力、能产生色素(Pcr+)的福氏志贺菌2a菌株中分离出了自发产生的无色素(即无法结合刚果红[Pcr-])衍生物,并通过其侵袭上皮细胞的能力来测定毒力。所有检测的Pcr-突变体均丧失了侵袭上皮细胞的能力,因此无毒力。对这些无毒力的Pcr-突变体的质粒DNA进行琼脂糖凝胶电泳分析表明,这些菌株中的大多数都丢失了一条与毒力相关质粒pSf2a140相对应的质粒条带。在许多突变体中,色素沉着、毒力和pSf2a140的同时丧失伴随着一种新质粒的出现,该新质粒比pSf2a140小。我们认为这些新质粒是pSf2a140的缺失衍生物,并且色素沉着丧失和毒力丧失与pSf2a140中的缺失有关。我们将Pcr-突变体转导为Pcr+,并分离出抑制Pcr-表型的转导子。没有一个Pcr+转导子恢复侵袭上皮细胞的能力。鉴定出几个Pcr-表型的抑制子是细胞壁生物合成中的突变。这些结果支持了我们的观点,即虽然色素沉着通常与毒力相关,但与毒力无关的遗传决定因素也会影响细胞结合刚果红的能力。因此,福氏志贺菌2a结合刚果红的能力并不一定意味着其具有侵袭上皮细胞的能力。然而,结合刚果红能力的丧失伴随着毒力的丧失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4db1/263440/4718ef6e07ad/iai00130-0421-a.jpg

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