A single rare σ70 variant establishes a unique gene expression pattern in the E. coli pathobiont LF82

Author:

Arroyo-Mendoza Melissa12,Proctor Alexandra2,Correa-Medina Abraham1,DeWolf Sarah2,Brand Meghan Wymore2,Rosas Virginia1,Lorenzi Hernan3,Wannemuehler Michael J2,Phillips Gregory J2,Hinton Deborah M1ORCID

Affiliation:

1. Gene Expression and Regulation Section, Laboratory of Biochemistry and Genetics, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, 8 Center Dr. , Bethesda , MD, USA

2. Department of Veterinary Microbiology and Preventative Medicine, College of Veterinary Medicine, Iowa State University , Ames , IA, USA

3. TriLab Bioinformatics Group, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, 8 Center Dr. , Bethesda , MD, USA

Abstract

Abstract 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.

Funder

National Institutes of Health

Defense Threat Reduction Agency

Publisher

Oxford University Press (OUP)

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