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Antimicrobial Agents and Chemotherapy logoLink to Antimicrobial Agents and Chemotherapy
. 2004 Nov;48(11):4435–4437. doi: 10.1128/AAC.48.11.4435-4437.2004

Community-Onset Disease Caused by Citrobacter freundii Producing a Novel CTX-M β-Lactamase, CTX-M-30, in Canada

Baha Abdalhamid 1, Johann D D Pitout 2, Ellen S Moland 1, Nancy D Hanson 1,*
PMCID: PMC525418  PMID: 15504875

Abstract

Strains of Citrobacter freundii intermediate to cefotaxime but sensitive to ceftazidime were isolated from four different patients in Canada. Sequencing of PCR products by use of CTX-M-specific primers revealed a new combination of four amino acid substitutions. This new gene was designated blaCTX-M-30 and was encoded on a 3-kb plasmid. The pI of CTX-M-30 was 8.0.


Organisms producing CTX-M β-lactamases have been identified throughout the world in Asia, South America, Europe, Canada, and the United States (4, 5, 11, 13, 18). CTX-Ms are class A β-lactamases in which the majority of enzymes are more active against cefotaxime than against ceftazidime (3, 7, 17). The genes encoding blaCTX-Ms show high nucleotide similarity to the chromosomal β-lactamase genes of Kluyvera spp. (2, 10). This study identified a new blaCTX-M gene, blaCTX-M-30, within clinical strains of Citrobacter freundii isolated from patients from communities in Canada.

Five strains of C. freundii intermediate to cefotaxime (CTX) were isolated from the urine samples of four different patients over a 2-month period during 2002. The strains were designated Cf 12, Cf 27, Cf 28, Cf 29, and Cf 30. Strain identification was initially achieved using Vitek (Vitek AMS; BioMérieux Vitek Systems Inc., Hazelwood, Mo.) and API 20E strips (BioMérieux Inc.) and confirmed by 16S rRNA sequencing using a MicroSeq 500 16S rDNA bacterial sequencing kit (Applied Biosystems; Foster City, CA). The resulting sequences were analyzed with MicroSeq analysis software (Applied Biosystems). The 16S rDNA analysis confirmed that the strains were C. freundii.

DNA templates for PCR were prepared as previously described using annealing temperatures of 55°C for primers CTX-M1F (GCAGCACCAGTAAAGTGATGG) and CTX-M1R (GCTGGGTGAAGTAAGTGACC) (accession number X92506) and 46°C to obtain the full-length amplified product by use of primers CTX-M3FLF (CGTCTCTTCCAGAATAAGG) and CTX-M-3FLR (GTTTCCCCATTCCGTTTCCGC) (accession number AF550415) (15). Sequencing using an ABI Prism 3100-Avant genetic analyzer was carried out by automated-cycle sequencing.

The full-length PCR product was cloned into pXL-Topo and transformed into Escherichia coli Top10 (Invitrogen) as recommended by the manufacturer. The resulting transformant was designated tCf 29.

Sequencing data revealed that all strains had identical nucleotide sequences. Computer-generated amino acid analysis using the BLAST program (http://www.ncbi.nlm.nih.gov/BLAST/BLAST.cgi) identified a unique combination of four amino acid substitutions (Thr16Ala, Asn117Asp, Gly242Asp, and Asn289Asp) which had not been previously described. Therefore, this new CTX-M β-lactamase was designated CTX-M-30. The gene blaCTX-M-30 had 11 separate nucleotide changes positioned randomly throughout the gene compared to blaCTX-M-3. Two nucleotide changes resulted in two amino acid substitutions, Thr16Ala and Asn117Asp. In addition, blaCTX-M-30 had seven separate nucleotide changes positioned randomly throughout the gene compared to blaCTX-M-29. Two of these nucleotide changes resulted in two additional amino acid substitutions, Gly242Asp and Asn289Asp. Conjugation and transformation experiments were performed as previously described (4, 9). The gene blaCTX-M-30 was found not to be self-transmissible; therefore, Southern analysis was performed to determine the location of blaCTX-M-30.

Plasmid DNA was extracted by alkaline lysis from strains Cf 12, Cf 27, Cf 28, Cf 29, and Cf 30 as previously described (15), and one-half of each plasmid sample was treated with plasmid-safe DNase (Epicentre Technologies) to remove contaminating chromosomal DNA. The plasmids were separated by electrophoresis in a 0.6% agarose gel. Plasmid profile gels were stained with ethidium bromide (10 mg/ml) and visualized by ultra-violet light with a Kodak EDAS 290 system. Southern analysis was performed as described by the manufacturer (Boehringer Mannheim, Indianapolis, Ind.). The blaCTX-M-30-specific probe was synthesized using PCR by incorporating digoxigenin-11-dUTP into the product by use of primers CTX-M-1F and CTX-M-1 R.

Plasmid profiles revealed that all the clinical strains had the same three plasmids (3, 6, and 16 kb) (data not shown). Southern analysis indicated that blaCTX-M-30 was encoded on a 3-kb plasmid and was not chromosomally encoded (data not shown). The gene blaCTX-M-30 was also detected on the pXL-Topo plasmid transformed into tCf 29.

MICs were determined using broth microdilution and E-tests (AB Biodisk, Solna, Sweden) as recommended by the manufacturers. E. coli ATCC 25922 was used as the quality control strain. Throughout this study, results were interpreted using National Committee for Clinical Laboratory Standards (NCCLS) criteria for broth dilution (12). The presence of an ESBL was evaluated using the modified double disk test (MDDT) (14). Cefotaxime MICs were 32 μg/ml for Cf 29, 16 μg/ml for tCf 29, and 0.12 μg/ml for E. coli Top 10. The ceftazidime MICs were 1 μg/ml for Cf 29, 0.5 μg/ml for tCf 29, and 0.25 μg/ml for E. coli Top 10 (Table 1). The ceftazidime and cefotaxime MICs for E. coli 25922 were within the NCCLS values. All the clinical strains were positive for ESBL production, as determined by the MDDT (14).

TABLE 1.

Antimicrobial susceptibilities

Antibiotic (s) MIC (μg/ml)
C. freundii 29d tCf29e E. coli Top 10
Cefotaximea 32 16 0.12
Cefotaxime and clavulanic acida,c 0.12 0.12 0.12
Cefdinirb 64 32 0.25
Ceftazidimea 1 0.5 0.25
Ceftazidime and clavulanic acida,c 0.25 0.5 0.25
Ceftriaxonea 64 32 0.12
Aztreonama 2 1 0.25
Cefepimea 4 1 ≤0.06
Cefepime and clavulanic acida,c ≤0.03 ≤0.03 ≤0.03
Cefpodoximea 64 32 0.5
Cefpodoxime and clavulanic acida,c 2 0.25 0.5
Cefoxitina ≤4 ≤4 ≤4
Imipenema 0.12 0.12 0.12
Ampicillina >32 >32 2
Amoxicillin and clavulanic acida,c 16 4 4
Piperacillinb >256 >256 2
Piperacillin and tazobactamb,c 1 1 2
a

MICs determined using microbroth according to NCCLS guidelines.

b

MICs determined using E-test.

c

Clavulanate and tazobactam were used at fixed concentrations of 4 μg/ml.

d

The pI(s) of the β-lactamases produced by C. freundii were 5.4, 8.0, and 8.9.

e

The pI of the β-lactamase produced by tCf29 was 8.0.

Sonicates of both Cf 29 and tCf 29 were subjected to analytical isoelectric focusing (IEF) as previously described (1, 16). Analytical IEF revealed the presence of a cefotaxime-hydrolyzing β-lactamase with a pI of 8.0 for both the clinical isolate, Cf 29, and the transformant, tCf 29. This band was inhibited by clavulanic acid but not by cloxacillin. In addition, IEF analysis revealed two additional bands in the clinical strain Cf 29. One band correlated with a pI of 5.4 and was inhibited by clavulanic acid but not cloxacillin. This band most likely represented TEM-1. The other band correlated with a pI of 8.9 and was inhibited by cloxacillin but not by clavulanic acid. This band most likely represented the chromosomal AmpC of C. freundii (data not shown). No bands were detectable when extract from E. coli Top 10 was used.

The relative hydrolysis rates were determined spectrophotometrically by using a 100 μM concentration of each antibiotic, with the exception of ceftazidime, for which the concentration used was 50 μM (15). The enzyme preparations from both Cf 29 and tCf 29 hydrolyzed cefotaxime (Table 2). Considering the hydrolysis rate of cephaloridin as 100%, the relative hydrolysis rates for the enzymes prepared from the clinical strain Cf 29 and the E. coli transformant, tCf 29, were comparable, with the highest level of hydrolysis observed for cefotaxime and no hydrolysis detected for ceftazidime. Interestingly, the AmpC β-lactamase of Cf 29 was not inducible (data not shown) and cefoxitin MICs were ≤4 μg/ml (Table 1); therefore, hydrolysis due to AmpC of any of the β-lactams tested would be negligible. This is reflected by the relative rates of hydrolysis observed for the transformant, tCf29, in which CTX-M-30 was the only β-lactamase present.

TABLE 2.

Relative hydrolysis rates of CTX-M-30

Relative hydrolysis rates (%)
Substrate Cf29a pIs of β-lactamases; 5.4, 8.0, and 8.9 tCf29b, pI of β-lactamase, 8.0
Cephaloridine 100 100
Penicillin 58 59
Cefotaxime 14 19
Ceftazidime NCc NC
Aztreonam NC NC
Cefepime 3.4 5.3
Imipenem NC NC
a

Clinical isolate of C. freundii.

b

E. coli transformant of strain C. freundii 29.

c

NC, not calculated (rates were too low to obtain reliable values).

The plasmid encoding blaCTX-M-30 most likely does not encode the genes required to transfer the plasmid, due to the small size of the plasmid. Self-transmissible plasmids encode tra genes as well as other genes required for transfer which require at least 15 kb of coding region (6, 8). These data, taken together with all the nucleotide changes (both those silent and those leading to amino acid changes), suggest the emergence of a novel CTX-M in Canada and not simply the transfer of established CTX-M genes from other countries.

The worldwide expansion of CTX-M-producing strains is a major concern. Therefore, it is important for clinical microbiologists to use both ceftazidime and cefotaxime for detecting ESBL-producing organisms. The use of ceftazidime alone may result in false-negative detection of organisms producing CTX-M β-lactamases and the unidentified spread of those ESBL producers.

Nucleotide sequence accession number.

The bla-CTX-M-30 gene nucleotide sequence was deposited in the GenBank database with accession number AY292654.

Acknowledgments

We thank Ashfaque Hossain for expert advice on Southern analysis and Mark Reisbig, Daniel Wolter, and Paul Wickman for helpful discussions of the manuscript. We also thank Lorraine Campbell and Philip Le for technical support for MIC and ribosomal analyses.

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