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鼠伤寒沙门氏菌侵袭基因转录激活因子hilA表达增加的突变体的鉴定与表征

Identification and characterization of mutants with increased expression of hilA, the invasion gene transcriptional activator of Salmonella typhimurium.

作者信息

Fahlen T F, Mathur N, Jones B D

机构信息

Department of Microbiology, University of Iowa School of Medicine, 3-330 Bowen Science Bldg., 51 Newton Rd., Iowa City, IA 52242-1109, USA.

出版信息

FEMS Immunol Med Microbiol. 2000 May;28(1):25-35. doi: 10.1111/j.1574-695X.2000.tb01453.x.

Abstract

Induction of invasion gene transcription and expression of the invasive phenotype of Salmonella strains are regulated by environmental conditions. Experimental evidence indicates that oxygen, pH, and osmotic conditions need to closely resemble those of the host intestinal lumen for invasion gene activation. The hilA gene, encoded on Salmonella pathogenicity island 1 (SPI-1), is a transcriptional activator which is required for invasion and whose expression is modulated by oxygen, pH, and osmolarity. Additionally, hilA is regulated by genetic elements encoded on SPI-1 (hilC/sirC/sprA and hilD), as well as by elements which reside outside of SPI-1 (phoP/phoQ and sirA), although how environmental signals modulate hilA is unknown. In an effort to further characterize the Salmonella invasion gene regulon, we have created and preliminarily characterized 18 Tn5 insertions which result in upregulation of a hilA::lacZY fusion. We have classified the mutations based on location and phenotype into three classes. Six class 1 and six class 2 mutants have insertions in SPI-1 near the invasion gene orgA or the invasion gene regulator hilD, respectively. Six class 3 mutants reside outside of SPI-1 in four different loci. The class 2 and 3 mutations induce overexpression of an episomal hilA::lacZY fusion and significantly increase S. typhimurium invasion of HEp-2 cells in a standard invasion assay. These data implicate new regions of SPI-1 as being involved in the regulation of invasion by S. typhimurium and identify new invasion gene regulators located outside of SPI-1.

摘要

沙门氏菌菌株侵袭基因转录的诱导以及侵袭表型的表达受环境条件调控。实验证据表明,氧气、pH值和渗透压条件需与宿主肠腔的条件极为相似才能激活侵袭基因。位于沙门氏菌致病岛1(SPI-1)上的hilA基因是一种转录激活因子,是侵袭所必需的,其表达受氧气、pH值和渗透压调节。此外,hilA受SPI-1上编码的遗传元件(hilC/sirC/sprA和hilD)以及SPI-1之外的元件(phoP/phoQ和sirA)调控,尽管环境信号如何调节hilA尚不清楚。为了进一步表征沙门氏菌侵袭基因调控子,我们构建并初步表征了18个导致hilA::lacZY融合上调的Tn5插入突变体。我们根据位置和表型将这些突变分为三类。6个1类和6个2类突变体分别在侵袭基因orgA或侵袭基因调节因子hilD附近的SPI-1中有插入。6个3类突变体位于SPI-1之外的4个不同位点。2类和3类突变诱导附加型hilA::lacZY融合的过表达,并在标准侵袭试验中显著增加鼠伤寒沙门氏菌对HEp-2细胞的侵袭。这些数据表明SPI-1的新区域参与鼠伤寒沙门氏菌侵袭的调控,并鉴定出位于SPI-1之外的新的侵袭基因调节因子。

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