一个罕见的σ70变体在大肠杆菌病原菌LF82中建立了独特的基因表达模式。

IF 16.6 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Melissa Arroyo-Mendoza,Alexandra Proctor,Abraham Correa-Medina,Sarah DeWolf,Meghan Wymore Brand,Virginia Rosas,Hernan Lorenzi,Michael J Wannemuehler,Gregory J Phillips,Deborah M Hinton
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引用次数: 0

摘要

LF82 是一种粘附侵袭性大肠杆菌(AIEC)病原体,与克罗恩病(一种病因不明的炎症性肠病)有关。虽然 AIEC 的表型与 "共生 "或致病性大肠杆菌的表型不同,但相关研究却未能发现造成这些差异的遗传特征。我们研究了 LF82 中一个天然但罕见的单核苷酸多态性(SNP),该多态性存在于高度保守的 rpoD 基因中,该基因编码 σ70 [初级 sigma 因子,RNA 聚合酶 (RNAP)]。我们证明,σ70 D445V 会导致与 LF82 表型一致的转录组和表型变化,包括抗生素耐药性和生物膜形成的增加以及蛋氨酸生物合成能力的提高。RNA-seq 分析比较了 σ70 V445 与 σ70 D445,发现在 LF82 和实验室大肠杆菌 K-12 菌株 MG1655 中,σ70 V445 上调了 24 个基因。通过体外转录,我们证明了 σ70 D445V 直接增加了几个上调基因启动子的转录,而 16 bp 的间隔和 -14 G:C 的存在与这种增加有关。D445V 在 RNAP 中的位置表明,它可能会影响 RNAP/间隔物的相互作用。我们的研究首次发现了该病原体的特征性 SNP,并提出了一种未被充分认识的病原体和菌株变异机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A single rare σ70 variant establishes a unique gene expression pattern in the E. coli pathobiont LF82.
LF82, an adherent-invasive Escherichia coli (AIEC) pathobiont, is associated with Crohn's disease, an inflammatory bowel disease of unknown etiology. Although AIEC phenotypes differ from those of 'commensal' or pathogenic E. coli, work has failed to identify genetic features accounting for these differences. We have investigated a natural, but rare, single nucleotide polymorphism (SNP) in LF82 present within the highly conserved rpoD gene, encoding σ70 [primary sigma factor, RNA polymerase (RNAP)]. We demonstrate that σ70 D445V results in transcriptomic and phenotypic changes consistent with LF82 phenotypes, including increased antibiotic resistance and biofilm formation and increased capacity for methionine biosynthesis. RNA-seq analyses comparing σ70 V445 versus σ70 D445 identified 24 genes upregulated by σ70 V445 in both LF82 and the laboratory E. coli K-12 strain MG1655. Using in vitro transcription, we demonstrate that σ70 D445V directly increases transcription from promoters for several of the up-regulated genes and that the presence of a 16 bp spacer and -14 G:C is associated with this increase. The position of D445V within RNAP suggests that it could affect RNAP/spacer interaction. Our work represents the first identification of a distinguishing SNP for this pathobiont and suggests an underrecognized mechanism by which pathobionts and strain variants can emerge.
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来源期刊
Nucleic Acids Research
Nucleic Acids Research 生物-生化与分子生物学
CiteScore
27.10
自引率
4.70%
发文量
1057
审稿时长
2 months
期刊介绍: Nucleic Acids Research (NAR) is a scientific journal that publishes research on various aspects of nucleic acids and proteins involved in nucleic acid metabolism and interactions. It covers areas such as chemistry and synthetic biology, computational biology, gene regulation, chromatin and epigenetics, genome integrity, repair and replication, genomics, molecular biology, nucleic acid enzymes, RNA, and structural biology. The journal also includes a Survey and Summary section for brief reviews. Additionally, each year, the first issue is dedicated to biological databases, and an issue in July focuses on web-based software resources for the biological community. Nucleic Acids Research is indexed by several services including Abstracts on Hygiene and Communicable Diseases, Animal Breeding Abstracts, Agricultural Engineering Abstracts, Agbiotech News and Information, BIOSIS Previews, CAB Abstracts, and EMBASE.
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