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小 RNA 介导的脂多糖生物合成逐渐调控影响幽门螺杆菌的抗生素耐药性。

Small RNA mediated gradual control of lipopolysaccharide biosynthesis affects antibiotic resistance in Helicobacter pylori.

机构信息

Department of Molecular Infection Biology II, Institute of Molecular Infection Biology (IMIB), University of Würzburg, Würzburg, Germany.

SCIGRAPHIX - Scientific Illustrations, Würzburg, Germany.

出版信息

Nat Commun. 2021 Jul 21;12(1):4433. doi: 10.1038/s41467-021-24689-2.

Abstract

The small, regulatory RNA RepG (Regulator of polymeric G-repeats) regulates the expression of the chemotaxis receptor TlpB in Helicobacter pylori by targeting a variable G-repeat in the tlpB mRNA leader. Here, we show that RepG additionally controls lipopolysaccharide (LPS) phase variation by also modulating the expression of a gene (hp0102) that is co-transcribed with tlpB. The hp0102 gene encodes a glycosyltransferase required for LPS O-chain biosynthesis and in vivo colonization of the mouse stomach. The G-repeat length defines a gradual (rather than ON/OFF) control of LPS biosynthesis by RepG, and leads to gradual resistance to a membrane-targeting antibiotic. Thus, RepG-mediated modulation of LPS structure might impact host immune recognition and antibiotic sensitivity, thereby helping H. pylori to adapt and persist in the host.

摘要

小分子调控 RNA RepG(聚合 G 重复序列的调节剂)通过靶向 tlpB mRNA 前导区中的可变 G 重复序列,调节幽门螺杆菌中趋化性受体 TlpB 的表达。在这里,我们表明 RepG 还通过调节与 tlpB 共转录的基因(hp0102)的表达来控制脂多糖(LPS)的相变异。hp0102 基因编码 LPS O-链生物合成和在体内定植小鼠胃所需的糖基转移酶。G 重复序列的长度通过 RepG 定义了 LPS 生物合成的逐渐(而非开/关)控制,并导致对膜靶向抗生素的逐渐耐药性。因此,RepG 介导的 LPS 结构修饰可能会影响宿主免疫识别和抗生素敏感性,从而帮助幽门螺杆菌适应和在宿主体内存活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6ce/8295292/133786baefcf/41467_2021_24689_Fig1_HTML.jpg

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