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来自大肠杆菌O157:H7的志贺毒素2噬菌体933W的序列:志贺毒素作为噬菌体晚期基因产物。

Sequence of Shiga toxin 2 phage 933W from Escherichia coli O157:H7: Shiga toxin as a phage late-gene product.

作者信息

Plunkett G, Rose D J, Durfee T J, Blattner F R

机构信息

Laboratory of Genetics, University of Wisconsin, Madison, Wisconsin 53706, USA.

出版信息

J Bacteriol. 1999 Mar;181(6):1767-78. doi: 10.1128/JB.181.6.1767-1778.1999.

Abstract

Lysogenic bacteriophages are major vehicles for the transfer of genetic information between bacteria, including pathogenicity and/or virulence determinants. In the enteric pathogen Escherichia coli O157:H7, which causes hemorrhagic colitis and hemolytic-uremic syndrome, Shiga toxins 1 and 2 (Stx1 and Stx2) are phage encoded. The sequence and analysis of the Stx2 phage 933W is presented here. We find evidence that the toxin genes are part of a late-phage transcript, suggesting that toxin production may be coupled with, if not dependent upon, phage release during lytic growth. Another phage gene, stk, encodes a product resembling eukaryotic serine/threonine protein kinases. Based on its position in the sequence, Stk may be produced by the prophage in the lysogenic state, and, like the YpkA protein of Yersinia species, it may interfere with the signal transduction pathway of the mammalian host. Three novel tRNA genes present in the phage genome may serve to increase the availability of rare tRNA species associated with efficient expression of pathogenicity determinants: both the Shiga toxin and serine/threonine kinase genes contain rare isoleucine and arginine codons. 933W also has homology to lom, encoding a member of a family of outer membrane proteins associated with virulence by conferring the ability to survive in macrophages, and bor, implicated in serum resistance.

摘要

溶原性噬菌体是细菌之间遗传信息转移的主要载体,包括致病性和/或毒力决定因素。在引起出血性结肠炎和溶血尿毒综合征的肠道病原体大肠杆菌O157:H7中,志贺毒素1和2(Stx1和Stx2)是由噬菌体编码的。本文介绍了Stx2噬菌体933W的序列及分析。我们发现有证据表明毒素基因是晚期噬菌体转录物的一部分,这表明毒素产生可能与裂解生长期间的噬菌体释放相关联,甚至可能依赖于噬菌体释放。另一个噬菌体基因stk编码一种类似于真核丝氨酸/苏氨酸蛋白激酶的产物。基于其在序列中的位置,Stk可能由溶原状态下的原噬菌体产生,并且与耶尔森氏菌属的YpkA蛋白一样,它可能干扰哺乳动物宿主的信号转导途径。噬菌体基因组中存在的三个新的tRNA基因可能有助于增加与致病性决定因素有效表达相关的稀有tRNA种类的可用性:志贺毒素和丝氨酸/苏氨酸激酶基因都含有稀有的异亮氨酸和精氨酸密码子。933W还与lom具有同源性,lom编码一种外膜蛋白家族的成员,该家族通过赋予在巨噬细胞中存活的能力而与毒力相关,并且与bor相关,bor与血清抗性有关。

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