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都柏林沙门氏菌天然质粒pSDL2的毒力蛋白(SpvA、-B和-C)的应激诱导

Stress induction of the virulence proteins (SpvA, -B, and -C) from native plasmid pSDL2 of Salmonella dublin.

作者信息

Valone S E, Chikami G K, Miller V L

机构信息

Department of Medicine, University of California, Los Angeles 90024-1736.

出版信息

Infect Immun. 1993 Feb;61(2):705-13. doi: 10.1128/iai.61.2.705-713.1993.

Abstract

The virulence region of the wild-type plasmid pSDL2 contained in Salmonella dublin is highly conserved among plasmids from several nontyphoid Salmonella serotypes and is essential for the development of systemic infection in BALB/c mice. Polyclonal antibodies against three proteins (SpvA, -B, and -C) expressed from a 4.1-kb EcoRI subclone of the plasmid virulence region were generated. These antibodies were used to detect expression of the Spv proteins when S. dublin was grown in vitro under stress-inducing conditions, such as nutrient deprivation and increased temperature, that the bacteria may encounter during the course of infection within the host. Glucose starvation resulted in expression of all three proteins shortly after the lag phase. When the bacteria were grown to the late-log phase without glucose, heat shock strongly induced expression of SpvA but not SpvB or SpvC. The addition of 0.2% glucose to the medium resulted in loss of expression of the proteins until the late-log to stationary phase. Iron limitation or lowered pH induced expression of the proteins during exponential growth even in the presence of glucose. Insertion mutations into the positive regulator gene spvR upstream from spvABC and insertions into spvA and spvC resulted in loss of expression of SpvA, -B, and -C, suggesting a complex regulation of expression. These studies define a variety of environmental conditions that induce expression of the Spv virulence proteins from the wild-type plasmid pSDL2 in S. dublin in vitro.

摘要

都柏林沙门氏菌中含有的野生型质粒pSDL2的毒力区域在几种非伤寒沙门氏菌血清型的质粒中高度保守,并且对于BALB/c小鼠全身性感染的发展至关重要。针对从该质粒毒力区域的一个4.1 kb EcoRI亚克隆表达的三种蛋白质(SpvA、-B和-C)产生了多克隆抗体。这些抗体用于检测都柏林沙门氏菌在体外应激诱导条件下生长时Spv蛋白的表达,这些条件如营养剥夺和温度升高,是细菌在宿主感染过程中可能遇到的。葡萄糖饥饿导致在延迟期后不久所有三种蛋白质都表达。当细菌在没有葡萄糖的情况下生长到对数后期时,热休克强烈诱导SpvA的表达,但不诱导SpvB或SpvC的表达。向培养基中添加0.2%葡萄糖导致蛋白质表达丧失,直到对数后期到稳定期。即使存在葡萄糖,铁限制或降低pH在指数生长期也会诱导蛋白质表达。spvABC上游的正调控基因spvR中的插入突变以及spvA和spvC中的插入导致SpvA、-B和-C的表达丧失,表明表达存在复杂调控。这些研究确定了多种体外诱导都柏林沙门氏菌中野生型质粒pSDL2的Spv毒力蛋白表达的环境条件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dad/302783/3a1497ecbcac/iai00014-0347-a.jpg

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