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Volume 23, Number 5—May 2017
Letter

CTX-M-27–Producing Escherichia coli of Sequence Type 131 and Clade C1-M27, France

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To the Editor: We read with great interest the Matsumura et al. paper describing extended-spectrum β-lactamase (ESBL) CTX-M-27–producing Escherichia coli of sequence type (ST) 131 clonal group, an emerging clade called C1-M27 (1). ST131 E. coli having blaCTX-M-27 has been described in several countries. We observed an alarming increase of this clonal group in the fecal carriage of children in France (0% in 2010 to 65% in 2015 among ESBL-producing ST131 E. coli) (2).

We wondered whether this clonal group’s expansion in France was attributable to the same clade (C1-M27). For that, we designed primers (M27PP1-B-F, 5′-TTACTCCGACTATGCGTTCAC-3′; M27PP1-B-R, 5′-CAAACTTGCCCCTGATAGCG-3′; amplicon length, 1.5 kb) to amplify the insertion site of the structure comprising the direct repeat and prophage-like genomic island of E. coli PCN033, as previously described (1). PCR was performed on our recently described collection of 39 ESBL-producing ST131 E. coli, including 16 CTX-M-27–producing E. coli: 13 of subgroup O25b with fimH30 allele and 3 of O16 subgroup with fimH41 allele (2). Results showed that 81% (13/16) of the CTX-M-27–producing E. coli ST131 had the M27PP1 structure, similar to strain PCN033, and thus belong to the C1-M27 clade. Therefore, the C1-M27 clade found in Asia and America is also present in Europe in the fecal flora of young children. The 3 isolates belonging to the O16 subgroup with fimH41 lacked M27PP1, suggesting that blaCTX-M-27 might diffuse among non-H30 ST131 E. coli without this prophage-like genomic island. Finally, the non–CTX-M-27–producing ST131 E. coli of our collection were negative for M27PP1 elements.

Our results show that CTX-M-27–producing E. coli ST131 subgroup O25b with fimH30 allele (one third of the ESBL-producing ST131 carriage isolates) isolated from children in France belong to C1-M27 and that CTX-M-27–producing O16 strains display distinct genetic characteristics. Altogether, our data confirm the worldwide distribution of C1-M27 and its high prevalence in children in France.

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André Birgy, Philippe Bidet, Corinne Levy, Elsa Sobral, Robert Cohen, and Stéphane BonacorsiComments to Author 

Author affiliations: Institut National de la Santé et de la Recherche Médicale, Paris, France (A. Birgy, P. Bidet, S. Bonacorsi); Université Paris Diderot, Paris (A. Birgy, P. Bidet, S. Bonacorsi); Hôpital Universitaire Robert-Debré, Paris (A. Birgy, P. Bidet, S. Bonacorsi); Association Clinique Thérapeutique Infantile du Val de Marne, Saint Maur des Fossés, France (C. Levy, E. Sobral, R. Cohen); Groupe de Pathologie Infectieuse Pédiatrique, Paris (C. Levy, R. Cohen); Centre Hospitalier Intercommunal de Créteil, Créteil, France (C. Levy, R. Cohen); Université Paris-Est Créteil, Créteil (C. Levy, R. Cohen)

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References

  1. Matsumura  Y, Pitout  JDD, Gomi  R, Matsuda  T, Noguchi  T, Yamamoto  M, et al. Global Escherichia coli sequence type 131 clade with blaCTX-M-27 gene. Emerg Infect Dis. 2016;22:19007. DOIPubMed
  2. Birgy  A, Levy  C, Bidet  P, Thollot  F, Derkx  V, Béchet  S, et al. ESBL-producing Escherichia coli ST131 versus non-ST131: evolution and risk factors of carriage among French children in the community between 2010 and 2015. J Antimicrob Chemother. 2016;71:294956. DOIPubMed

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Cite This Article

DOI: 10.3201/eid2305.161865

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Table of Contents – Volume 23, Number 5—May 2017

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Stéphane Bonacorsi, Hôpital Robert-Debré, Assistance Publique Hôpitaux de Paris, 48, boulevard Sérurier F75019 Paris, France

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Page created: April 17, 2017
Page updated: April 17, 2017
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