Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2017 Feb 28:6:F1000 Faculty Rev-195.
doi: 10.12688/f1000research.10609.1. eCollection 2017.

Escherichia coli ST131: a multidrug-resistant clone primed for global domination

Affiliations
Review

Escherichia coli ST131: a multidrug-resistant clone primed for global domination

Johann D D Pitout et al. F1000Res. .

Abstract

A single extra-intestinal pathogenic Escherichia coli (ExPEC) clone, named sequence type (ST) 131, is responsible for millions of global antimicrobial-resistant (AMR) infections annually. Population genetics indicate that ST131 consists of different clades (i.e. A, B, and C); however, clade C is the most dominant globally. A ST131 subclade, named C1-M27, is emerging in Japan and has been responsible for the recent increase in AMR ExPEC in that country. The sequential acquisition of several virulence and AMR genes associated with mobile genetic elements during the 1960s to 1980s primed clade C (and its subclades C1 and C2) for success in the 1990s to 2000s. IncF plasmids with F1:A2:B20 and F2:A1:B replicons have shaped the evolution of the C1 and C2 subclades. It is possible that ST131 is a host generalist with different accessory gene profiles. Compensatory mutations within the core genome of this clone have counterbalanced the fitness cost associated with IncF plasmids. ST131 clade C had dramatically changed the population structure of ExPEC, but it still remains unclear which features of this clade resulted in one of the most unprecedented AMR successes of the 2000s.

Keywords: Escherichia coli ST131; ExPEC; antimicrobial-resistant infection.

PubMed Disclaimer

Conflict of interest statement

Competing interests: JDDP has previously received research funds from Merck and Astra Zeneca. RdeV has no competing interests to declare.No competing interests were disclosed.No competing interests were disclosed.

Figures

Figure 1.
Figure 1.. Stepwise evolution of Escherichia coli ST131 clades B, B0, C0, and C.
FQ, fluoroquinolones; GI, genomic islands; Inc, incompatibility; Phi, prophages; ST, sequence types.

References

    1. Pitout JD: Extraintestinal Pathogenic Escherichia coli: A Combination of Virulence with Antibiotic Resistance. Front Microbiol. 2012;3:9. 10.3389/fmicb.2012.00009 - DOI - PMC - PubMed
    1. Pitout JD: Extraintestinal pathogenic Escherichia coli: an update on antimicrobial resistance, laboratory diagnosis and treatment. Expert Rev Anti Infect Ther. 2012;10(10):1165–76. 10.1586/eri.12.110 - DOI - PubMed
    1. World Health Organization: Antimicrobial resistance: global report on surveillance 2014. April 2014 ed, World Heath Organization,2014;257 Reference Source
    1. Pitout JD, Laupland KB: Extended-spectrum beta-lactamase-producing Enterobacteriaceae: an emerging public-health concern. Lancet Infect Dis. 2008;8(3):159–66. 10.1016/S1473-3099(08)70041-0 - DOI - PubMed
    1. Nicolas-Chanoine MH, Bertrand X, Madec JY: Escherichia coli ST131, an intriguing clonal group. Clin Microbiol Rev. 2014;27(3):543–74. 10.1128/CMR.00125-13 - DOI - PMC - PubMed
    2. F1000 Recommendation