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福氏志贺菌和肠聚集性大肠杆菌中重叠pic/set基因座的调控

Regulation of the overlapping pic/set locus in Shigella flexneri and enteroaggregative Escherichia coli.

作者信息

Behrens Martin, Sheikh Jalaluddin, Nataro James P

机构信息

Center for Vaccine Development, Department of Pediatrics, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA.

出版信息

Infect Immun. 2002 Jun;70(6):2915-25. doi: 10.1128/IAI.70.6.2915-2925.2002.

Abstract

Most strains of Shigella flexneri 2a and enteroaggregative Escherichia coli carry a highly conserved chromosomal locus which encodes a 109-kDa secreted mucinase (called Pic) and, on the opposite strand in overlapping fashion, an oligomeric enterotoxin called ShET1, encoded by the setA and setB genes. Here, we characterize the genetic regulation of these overlapping genes. Our data suggest that pic and the setBA loci are transcribed as complementary 4-kb mRNA species. The major pic promoter is maximally activated at 37 degrees C in exponential growth phase. Our data suggest that the setB gene is transcribed from a promoter which lies more than 1.5 kb upstream of the setB structural gene; setA may be transcribed via readthrough of the setB transcript and possibly by its own promoter. The long leader of the setB gene provides a strong silencing effect on setB transcription. The signals which provide relief from setB silencing are not clear, but significant induction is observed in a continuous anaerobic culture of human fecal bacteria, suggesting that some complex characteristics of the human intestine act to lift repression of setB expression. Our studies provide the first insights into the mechanisms affecting expression of this unusual virulence locus.

摘要

大多数福氏志贺菌2a菌株和肠集聚性大肠杆菌携带一个高度保守的染色体位点,该位点编码一种109 kDa的分泌型粘蛋白酶(称为Pic),并且在相反链上以重叠方式编码一种由setA和setB基因编码的寡聚肠毒素,称为ShET1。在此,我们对这些重叠基因的遗传调控进行了表征。我们的数据表明,pic和setBA位点转录为互补的4 kb mRNA种类。主要的pic启动子在指数生长期37℃时被最大程度激活。我们的数据表明,setB基因从位于setB结构基因上游超过1.5 kb的启动子转录;setA可能通过setB转录本的通读以及可能通过其自身的启动子进行转录。setB基因的长前导序列对setB转录具有强烈的沉默作用。解除setB沉默的信号尚不清楚,但在人粪便细菌的连续厌氧培养中观察到显著诱导,这表明人类肠道的一些复杂特征可解除对setB表达的抑制。我们的研究首次深入了解了影响这个不寻常毒力位点表达的机制。

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