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Journal of Clinical Microbiology, February 2004, p. 888-890, Vol. 42, No. 2
0095-1137/04/$08.00+0     DOI: 10.1128/JCM.42.2.888-890.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Genetic Analysis of an Ambler Class A Extended-Spectrum Beta-Lactamase from Capnocytophaga ochracea

Anne Jolivet-Gougeon,1* Zohreh Tamanai-Shacoori,2 Laurent Desbordes,1 Nathalie Burggraeve,2 Michel Cormier,1 and Martine Bonnaure-Mallet2

Laboratoire de Microbiologie Pharmaceutique, UPRES-EA 1254, Université de Rennes 1, 35043 Rennes ,1 Equipe de Biologie Buccale, UPRES-EA 1256, UFR Odontologie, Université de Rennes 1, 35000 Rennes, France2

Received 24 June 2003/ Returned for modification 25 August 2003/ Accepted 2 October 2003


   ABSTRACT
Top
 Abstract
Introduction
 References
 
A beta-lactamase gene (cfxA3, 966 bp) was isolated from a beta-lactam-resistant Capnocytophaga ochracea clinical isolate and amplified using primers from the cfxA gene of Bacteroides vulgatus. The MICs of third-generation cephalosporins were much higher than those of the transconjugant Escherichia coli strain. The deduced protein sequence, by comparison with CfxA2 of Prevotella intermedia, had a Y239D substitution and possessed the characteristics of a class A, group 2e beta-lactamase.


   INTRODUCTION
Top
 Abstract
 Introduction
References
 
Capnocytophaga spp. are gram-negative, fusiform, capnophilic bacteria and are part of the normal oral flora in humans. They are found in both immunocompromised and nonimmunocompromised patients (6, 20, 27), are associated with infections of dental origin (11), and can cause various complicated infections (4, 17, 20), including septicemias (7, 14). While clindamycin and amoxicillin-clavulanic acid are the first choices for treating Capnocytophaga infections (19) and the susceptibility of Capnocytophaga spp. to extended-spectrum cephalosporins has been reported to be variable (2, 10), bacteremias in neutropenic patients are often empirically treated with extended-spectrum cephalosporins before the organism has been identified because Capnocytophaga spp. are slow-growing bacteria (19). Beta-lactamase-producing strains are increasingly common (5, 15, 22, 23). It is thus becoming essential to determine which antibiotics are effective against clinical isolates. However, complete characterization of the beta-lactamases has rarely been attempted, except for a plasmid-encoded extended-spectrum TEM-17 beta-lactamase (24). In the beta-lactamase classification scheme of Bush et al. (3), many Bacteroides (CfxA from Bacteroides vulgatus [21]), Prevotella (CfxA2 from Prevotella intermedia [15, 31]), and Capnocytophaga (5, 23) beta-lactamases belong to group 2e, which includes enzymes with significant activity against cephalosporins rather than penicillins. They have acidic pI values and are susceptible to beta-lactamase inhibitors. The occurrence of beta-lactamases in bacteria in the normal flora is a cause of concern about the spread of resistance to extended-spectrum cephalosporins to more pathogenic bacteria. A clinical strain of Capnocytophaga ochracea (E201) was investigated, and a beta-lactamase gene called cfxA3 was cloned and sequenced.

Jolivet-Gougeon et al. (10) reported that some Capnocytophaga strains are highly resistant to broad-spectrum cephalosporins, which makes it important to better understand their resistance mechanisms. Strain E201 was isolated by swabbing the throat of a pediatric cancer patient undergoing chemotherapy at the Department of Pediatric Oncology (Centre Hospitalier Universitaire, Rennes, France) and selected for its ceftazidime resistance. The sample was plated on TBBP agar (Trypticase-blood-bacitracin-polymyxin B) (18), incubated in a 10% CO2 atmosphere for 48 to 72 h, and identified by conventional methods (12, 13, 28, 32).

The MICs of eight beta-lactam antibiotics alone or in combination with a beta-lactamase inhibitor were determined by the agar dilution method as recommended by Rummens et al. (25) and as already described (10). The plates were incubated for 48 h at 37°C in a 10% CO2 atmosphere. Strain E201 produced a beta-lactamase that conferred a high level of resistance to a wide range of beta-lactam antibiotics, including amoxicillin, cefalothin, cefuroxime, ceftazidime, and cefotaxime. Strain E201 remained susceptible to imipenem, cefoxitin, aztreonam, and amoxicillin-clavulanic acid. Intrinsic susceptibility to other beta-lactamase inhibitors (tazobactam and sulbactam) was also observed, as already described (10). MIC determinations showed that strain E201 was resistant to extended-spectrum cephalosporins such as cefotaxime and, more particularly, ceftazidime (Table 1). While the Prevotella strain was susceptible to cefoxitin, the affinity of CfxA2 for cefazolin was about 10-fold greater. Madinier et al. (15) also reported that the resistance of B. vulgatus to cefoxitin might be due to a resistance mechanism other than CfxA production, perhaps a porin mutation.


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  		TABLE 1. MICs of antimicrobial agents for the C. ochracea E201 clinical isolate, transconjugant E. coli TrE201, and E. coli DH5{alpha}

 
Primers cfxA1 plus cfxA4, cfxA5 plus cfxA6, and cfxAZ1 plus cfxAZ2 (Genset SA, Paris, France) were selected from the cfxA sequence of B. vulgatus, (locus BVU38243, GenBank Accession no. U38243) (21) (Table 2) by using primer3.Output software (www-genome.wi.mit.edu/cgi-bin/primer/primer3_www.cgi). The following amplification conditions were used: 94°C for 1 min, 55°C for 1 min, and 72°C for 1 min (35 cycles). Two fragments (580 and 507 bp) were amplified by PCR, and a 966-bp consensus sequence of cfxA3 was determined.


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  		TABLE 2. PCR primers and composite primers from the B. vulgatus cfxA gene sequence

 
For the cloning experiments, total DNA from the C. ochracea E201 cfxA3 gene was amplified with composite primers cfxAZ1 and cfxAZ2 (Table 2), digested with EcoRI and HindIII, ligated in pET-22b+ (the bla gene was replaced by a Kanr gene, which was kindly supplied by Dr. Blanco from the Université de Rennes 1, Rennes, France), and inserted by electroporation into E. coli DH5{alpha}, which harbors the recombinant vector with a 0.970-kb EcoRI-HindIII insert (TrE201 strain).

The sequences of both strands of DNA were determined using a Perkin-Elmer 310 Genetic Analyzer sequencer and assigned GenBank accession no. AF472622 (Banklt 442706). Deduced protein sequences, sequence alignments, and beta-lactamase relatedness were determined using the BLAST similarity search programs of the National Center for Biotechnology Information (NCBI).

Analysis of the nucleotide sequence showed that the gene coding for the C. ochracea beta-lactamase differed from the cfxA gene of B. vulgatus (21) by two amino acid substitutions (K272E and Y239D) and from the cfxA2 gene of P. intermedia (15) by one amino acid substitution (Y239D), according to the numbering scheme of Ambler et al. (1) (Table 3). The cfxA3 gene had the four conserved elements of class A beta-lactamases as per Ambler et al. (1): the Ser-X-X-Lys consensus active-site serine residue at Ser70, the SDN loop at Ser130, Glu166, and the KTG sequence at Lys234. As with the cfxA2 gene (15), the K272E substitution had no significant influence on the catalytic properties of the enzyme with respect to cefoxitin but increased the affinity of CfxA3 for first-generation cephalosporins. The Y239D substitution might not be linked to the extension of the beta-lactamase spectrum to broad-spectrum cephalosporins, especially ceftazidime, because the MICs of both cefotaxime and ceftazidime were in the susceptible range of the E. coli transformant. CfxA had some homology to other beta-lactamases at the active-site serine of Ambler class A beta-lactamases, although it appeared to have diverged significantly, as exemplified by the substitution at position 13 of 25 amino acid residues previously described as being invariant in class A beta-lactamases.


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  		TABLE 3. Nucleotide and amino acid substitution in CfxA, CfxA2, and CfxA3

 
The recombinant Escherichia coli strain harboring the cfxA3 gene was susceptible to ceftazidime and cefotaxime, suggesting a difference in the level of beta-lactamase production, which may be linked to the promoter (33), or alterations in the porins (16). It is also possible that another beta-lactamase with a pI of 5.6, which is close to that of other extended-spectrum beta-lactamases, might be present in the clinical isolate (3, 23). Phylogenetic analyses revealed homologies to other beta-lactamase genes of anaerobic bacteria (NCBI, BLAST N): cfxA of B. vulgatus (locus BVU38243; GenBank accession no. U38243), 99%; cfxA2 of P. intermedia (GenBank accession no. AF118110), 99%; cepA of B. fragilis (GenBank accession no. L13472), 39%; and cblA of B. uniformis (locus BNRCBLAX; GenBank accession no. L08472), 29%. Homologies to extended-spectrum beta-lactamases of aerobic bacilli were also found: TLA-1 of E. coli (GenBank accession no. AF148067), 31%; Per-1 of Pseudomonas aeruginosa (locus PAPER1A; GenBank accession no. Z21957), 30%; and Per-2 of Salmonella enterica serovar Typhimurium (locus STBLAPER2, EMBL accession no. X93314), 32%.

CfxA3 differed from CfxA2 by having an aspartic acid instead of a tyrosine at position 239 and from CfxA by having a glutamic acid instead of a lysine at position 272. The pIs reported for CfxA (B. vulgatus) and CfxA2 (P. intermedia) were 5.8 and 5.4, respectively. Isoelectric focusing experiments with the CfxA3 beta-lactamase revealed only one reactive band with a pI of 5.6 (data not shown). In the beta-lactamase classification scheme of Bush et al. (3), many Capnocytophaga beta-lactamases belong to group 2e, including enzymes that display strong activity against cephalosporins rather than penicillins. They also have acidic pI values and are susceptible to beta-lactamase inhibitors. The Van1 Capnocytophaga beta-lactamase described by Roscoe et al. (23) efficiently hydrolyzes a wide range of beta-lactams, including extended-spectrum cephalosporins. However, their substrate affinities are different despite their closely related MICs and similar pls. Rummens et al. (25) described a cephalosporinase, which was studied by Foweraker et al. (5). It had an isoelectric point of 3.6 (with a minor band at 4.1), conferred resistance to extended-spectrum beta-lactams, and was presumed to be chromosomally encoded. However, a full genetic characterization of the strain has never been performed.

Plasmid DNA from C. ochracea E201 was extracted using the alkaline lysis method of Ish-Horowicz and Burke (9). Plasmids and total DNA were separated on 0.8% agarose gels, transferred to nylon membranes (Amersham), and hybridized with a 510-bp digoxigenin-labeled CfxA3 probe synthesized using the cfxA3 and cfxA4 primers (Table 2) (8) as previously described (26).

Strain E201 contained three plasmids of approximately 3.5, 5, and 9 kb. Specific hybridization experiments with the cfxA3 probe indicated that the cfxA3 gene was located on the 9-kb plasmid, which also carried a mobilizable transposon. Tribble et al. (30) reported the presence of such a transposon in Bacteroides. The spontaneous loss of plasmids during storage made it possible to recover a susceptible phenotype.

Capnocytophaga spp. cause septicemias in compromised hosts with underlying malignancies complicated by severe granulocytopenia. Since multidrug-resistant strains have been described, the importance of detecting beta-lactamase producers is now well established. The occurrence of a gene coding for an extended-spectrum beta-lactamase on a transposable element in a clinical Capnocytophaga strain is potentially a cause for concern about the spread of resistance to extended-spectrum cephalosporins. Additional work is needed to characterize the mobilization genes associated with Capnocytophaga spp. and their spread to other oral bacteria.


   ACKNOWLEDGMENTS
 
We thank Gene Bourgeau and Céline Allaire for their editorial assistance.


   FOOTNOTES
 
* Corresponding author. Mailing address: Laboratoire de Microbiologie Pharmaceutique, UPRES-EA 1254, Université de Rennes 1, 2 avenue du Professeur Léon Bernard 35 043 Rennes, France. Phone: (33) 2 23 23 49 05. Fax: (33) 2 23 23 49 13. E-mail: anne.gougeon{at}univ-rennes1.fr. Back


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Journal of Clinical Microbiology, February 2004, p. 888-890, Vol. 42, No. 2
0095-1137/04/$08.00+0     DOI: 10.1128/JCM.42.2.888-890.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.



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