Multiple acquisitions of CTX-M plasmids in the rare D2 genotype of Escherichia coli provide evidence for convergent evolution

被引:32
作者
Deschamps, Catherine [1 ,2 ,3 ]
Clermont, Olivier [1 ,2 ]
Hipeaux, Marie Claire [3 ]
Arlet, Guillaume [4 ,5 ]
Denamur, Erick [1 ,2 ]
Branger, Catherine [1 ,2 ,3 ]
机构
[1] INSERM, U722, Paris, France
[2] Univ Denis Diderot Paris 7, Fac Med, Paris, France
[3] Hop Louis Mourier, AP HP, Serv Microbiol Hyg, F-92701 Colombes, France
[4] Univ Paris 06, EA 2392, Fac Med, Bacteriol Lab, Paris, France
[5] Hop Tenon, AP HP, Serv Bacteriol Hyg, F-75970 Paris, France
来源
MICROBIOLOGY-SGM | 2009年 / 155卷
关键词
SPECTRUM BETA-LACTAMASES; EXTRAINTESTINAL VIRULENCE; QUINOLONE; STRAINS; ENTEROBACTERIACEAE; EXPRESSION; RESISTANCE; DIVERSITY; COMMENSAL; PROFILES;
D O I
10.1099/mic.0.023234-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Over the last decade, CTX-M enzymes have become the most prevalent extended-spectrum beta-lactamases (ESBLs) worldwide, mostly in Escherichia coli, causing a major health problem. An epidemiological relationship has been established between a rare genotype of E coli, the D-2 genotype, and the presence of CTX-M genes. We investigated this striking association by exploring the genetic backgrounds of 18 D-2 genotype CTX-M-producing strains and of the plasmids encoding CTX-M enzymes. The 18 strains had different genetic backgrounds, as assessed by multilocus sequence and 0 typing, and were associated with various plasmids bearing diverse CTX-M genes. The region encompassing the genetic marker of the D-2 genotype (TSPE4.C2) was not correlated with the presence of CTX-M genes. CTX-M-producing D-2 strains had far fewer virulence factors than a control group of 8 non-ESBL-producing D-2 strains, and an inverse relationship was found between the number of co-resistances associated with the CTX-M gene and the number of virulence factors found in the strain. These findings provide evidence for multiple acquisitions of plasmids carrying CTX-M genes in different D-2 genotype strains. They strongly suggest that convergent evolution has occurred, and indicate that there has been selection for the association of a specific genetic background of the strain and the CTX-M gene. This fine-tuning of the relationship between the D-2 genotype and CTX-M genes presumably increases the fitness of the strain, indicating a role for the host cell in the acquisition and dissemination of CTX-M genes.
引用
收藏
页码:1656 / 1668
页数:13
相关论文
共 43 条
[1]   High rate of mobilization for blaCTX-Ms [J].
Barlow, Miriam ;
Reik, Rebecca A. ;
Jacobs, Stephen D. ;
Medina, Monica ;
Meyer, Matthew P. ;
McGowan, John E., Jr. ;
Tenover, Fred C. .
EMERGING INFECTIOUS DISEASES, 2008, 14 (03) :423-428
[2]  
Bettelheim K. A., 1997, P85
[3]  
BETTELHEIM KA, 1997, ESCHERICHIA COLI MEC, P3
[4]   Phylogenetic analysis and prevalence of urosepsis strains of Escherichia coli bearing pathogenicity island-like domains [J].
Bingen-Bidois, M ;
Clermont, O ;
Bonacorsi, S ;
Terki, M ;
Brahimi, N ;
Loukil, C ;
Barraud, D ;
Bingen, E .
INFECTION AND IMMUNITY, 2002, 70 (06) :3216-3226
[5]   Growing group of extended-spectrum β-lactamases:: The CTX-M enzymes [J].
Bonnet, R .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (01) :1-14
[6]  
Boyd EF, 1996, GENETICS, V143, P1091
[7]   Epidemiological typing of extended-spectrum beta-lactamase-producing Klebsiella pneumoniae isolates responsible for five outbreaks in a university hospital [J].
Branger, C ;
Bruneau, B ;
Lesimple, AL ;
Bouvet, PJM ;
Berry, P ;
SevaliGarcia, J ;
LambertZechovsky, N .
JOURNAL OF HOSPITAL INFECTION, 1997, 36 (01) :23-36
[8]   Genetic background of Escherichia coli and extended-spectrum β-lactamase type [J].
Branger, C ;
Zamfir, O ;
Geoffroy, S ;
Laurans, G ;
Arlet, G ;
Thien, HV ;
Gouriou, S ;
Picard, B ;
Denamur, E .
EMERGING INFECTIOUS DISEASES, 2005, 11 (01) :54-61
[9]   The CTX-M β-lactamase pandemic [J].
Canton, Rafael ;
Coque, Teresa M. .
CURRENT OPINION IN MICROBIOLOGY, 2006, 9 (05) :466-475
[10]   Identification of plasmids by PCR-based replicon typing [J].
Carattoli, A ;
Bertini, A ;
Villa, L ;
Falbo, V ;
Hopkins, KL ;
Threlfall, EJ .
JOURNAL OF MICROBIOLOGICAL METHODS, 2005, 63 (03) :219-228