Plasmids shape the diverse accessory resistomes of Escherichia coli ST131. Issue 1 (18th January 2021)

• Record Type: Journal Article
• Authors: Decano, Arun Gonzales; Tran, Nghia; Al-Foori, Hawriya; Al-Awadi, Buthaina; Campbell, Leigh; Ellison, Kevin; Mirabueno, Louisse Paolo; Nelson, Maddy; Power, Shane; Smith, Genevieve; Smyth, Cian; Vance, Zoe; Woods, Caitriona; Rahm, Alexander; Downing, Tim
• Is Part Of: Access microbiology. Volume 3:Issue 1(2021)
• Publication Date: 2021-01-18
• Subjects: Escherichia coli -- evolution -- fimbrial -- Genome -- infection -- plasmid -- ST131; Microbiology -- Periodicals; 579
• DOI: 10.1099/acmi.0.000179
• Languages: English
• ISSNs: 2516-8290

Abstract

Abstract : The human gut microbiome includes beneficial, commensal and pathogenic bacteria that possess antimicrobial resistance (AMR) genes and exchange these predominantly through conjugative plasmids. Escherichia coli is a significant component of the gastrointestinal microbiome and is typically non-pathogenic in this niche. In contrast, extra-intestinal pathogenic E. coli (ExPEC) including ST131 may occupy other environments like the urinary tract or bloodstream where they express genes enabling AMR and host cell adhesion like type 1 fimbriae. The extent to which commensal E. coli and uropathogenic ExPEC ST131 share AMR genes remains understudied at a genomic level, and we examined this here using a preterm infant resistome. We found that individual ST131 had small differences in AMR gene content relative to a larger shared resistome. Comparisons with a range of plasmids common in ST131 showed that AMR gene composition was driven by conjugation, recombination and mobile genetic elements. Plasmid pEK499 had extended regions in most ST131 Clade C isolates, and it had evidence of a co-evolutionary signal based on protein-level interactions with chromosomal gene products, as did pEK204 that had a type IV fimbrial pil operon. ST131 possessed extensive diversity of selective type 1, type IV, P and F17-like fimbriae genes that was highest in subclade C2. The structure and composition of AMR genes, plasmids and fimbriae vary widely in ST131 Clade C and this may mediate pathogenicity and infection outcomes.