Department of Molecular Infection Biology II, Institute of Molecular Infection Biology (IMIB), University of Würzburg, Würzburg, Germany.
SCIGRAPHIX - Scientific Illustrations, Würzburg, Germany.
Nat Commun. 2021 Jul 21;12(1):4433. doi: 10.1038/s41467-021-24689-2.
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.
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。