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Antimicrobial Agents and Chemotherapy, November 2007, p. 4181-4183, Vol. 51, No. 11
0066-4804/07/$08.00+0     doi:10.1128/AAC.00614-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

TEM-158 (CMT-9), a New Member of the CMT-Type Extended-Spectrum ß-Lactamases

Frédéric Robin,^1,2* Julien Delmas,^1,2 Amélie Brebion,¹ Damien Dubois,^1,2 Jean-Michel Constantin,³ and Richard Bonnet^1,2

CHU Clermont-Ferrand, Centre de Biologie, Laboratoire de bactériologie clinique, Clermont-Ferrand F-63003, France,¹ Univ. Clermont 1, UFR Médecine, Laboratoire de bactériologie, EA3844, Clermont-Ferrand F-63001, France,² CHU Clermont-Ferrand, Hôtel-Dieu, Service de Réanimation Adulte, Clermont-Ferrand F-63003, France³

Received 10 May 2007/ Returned for modification 20 July 2007/ Accepted 10 August 2007

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TEM-158 was found to include the substitutions previously observed for TEM-12 and TEM-35. This enzyme presented hydrolytic activity against ceftazidime and a high level of resistance against clavulanate, which can alter its detection. Its discovery highlights the need for accurate detection methods.

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Since the mid-1990s, a new subgroup of TEM ß-lactamases that comprises enzymes harboring both extended-spectrum ß-lactamase (ESBL)-type and inhibitor-resistant TEM (IRT)-type substitutions has emerged. These new ß-lactamases, called complex mutants, were identified in different Enterobacteriaceae species (4, 6-11). They confer different levels of resistance to clavulanic acid and to oxyimino-cephalosporins, depending on the mutations harbored.

Escherichia coli BER1 was isolated from a stool specimen from a patient hospitalized in an intensive care unit of the University Hospital of Clermont-Ferrand, France. This patient had been treated with an amoxicillin-clavulanate combination for an aspiration pneumonia for 10 days. E. coli BER1 harbored a high level of resistance to penicillins and penicillin-clavulanate combinations and was in the intermediate range for ceftazidime. The French double-disk synergy test was negative for E. coli BER1. CLSI MIC testing was not reproducibly positive. A modified double-disk test with a 20-mm interdisk distance was positive between ceftazidime- and amoxicillin-clavulanate-containing disks (Fig. 1).

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FIG. 1. Comparison of the synergy tests performed with a 30-mm interdisk distance (left), following Comité de l'Antibiogramme de la Société Française de Microbiologie recommendations (3), and with a 20-mm interdisk distance (right) for the clinical TEM-158-producing E. coli strain BER1. ATM, aztreonam; CTX, cefotaxime; AMC, amoxicillin-clavulanate; CAZ, ceftazidime; FEP, cefepime. The black arrow indicates a synergy.

E. coli BER1 produced two ß-lactamases, of pI 5.2 and pI 5.4. The genes encoding resistance to ß-lactam antibiotics were transferred by conjugation to rifampin-resistant E. coli C600. A plasmid-content analysis revealed the transfer of an 85-kb plasmid, designated pBER1. The transconjugant E. coli C600 (pBER1) produced only one ß-lactamase, of pI 5.2. TEM-specific PCR experiments were performed with the transconjugant as previously described (8). The nucleic acid sequence of the PCR product revealed a new bla_TEM-type gene called bla_TEM-158. bla_TEM-158 harbored a promoter, P₃. The sequence of bla_TEM-158 showed a pattern of silent mutations identical to that of bla_TEM-1b (5). The novel resulting enzyme, designated TEM-158, combined the mutations of IRT TEM-35 (IRT-4) (Met69Leu and Asn276Asp) and that of ESBL TEM-12 (Arg164Ser) (1, 2). This enzyme is the ninth member of the complex mutant TEM-derived subgroup (4, 6-11). E. coli DH₅ clones producing TEM-158, TEM-12, TEM-35, and TEM-1 were obtained as previously described (8). E. coli BER1, its clone E. coli DH₅ ClBER1, and its transconjugant C600 (pBER1) demonstrated high levels of resistance to penicillins, similar to those of the E. coli clones producing TEM-12 and TEM-35 (2,048 to >2,048 µg/ml) (Table 1). They were also in the intermediate range or resistant to ceftazidime (16 to 32 µg/ml) and to cephalothin (16 to 32 µg/ml). The MICs of cefotaxime, aztreonam, and cefepime were in the susceptible range (0.25 to 4 µg/ml) but higher than those for E. coli DH₅ (<0.06 to 0.12 µg/ml). MICs of cefuroxime, cefoxitin, and imipenem were closely similar to those of E. coli DH₅ (0.25 to 8 µg/ml). Clavulanate and tazobactam did not restore susceptibility to penicillins (128 to 1,024 µg/ml). ClBER1 MICs of penicillin-inhibitor combinations were lower than those of the TEM-35-producing clone (512 to 1,024 versus >2,048 µg/ml) but higher than those of the TEM-12-producing clone (512 to 1,024 versus 2 to 64 µg/ml). The ClBER1 MICs of cephalosporins were closely similar to those of the TEM-12-producing clone (0.25 to 32 µg/ml), but the addition of clavulanate only slightly decreased the MICs of oxyimino-ß-lactams, in contrast to what was observed with E. coli DH₅ (pBK-TEM-12) (0.06 to 8 versus <0.06 to 0.5 µg/ml).

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TABLE 1. MICs of ß-lactam antibiotics for E. coli strainsa

The different enzymes were purified to homogeneity, and their kinetic constants were determined by computerized microacidimetry as previously described (8). TEM-158 harbored 4- to 81-fold lower activity against penicillins than TEM-1, TEM-35, and TEM-12 (Table 2). TEM-158 K_m values for penicillins were closer to those of TEM-1 (K_m values, 24.8 to 142.6 versus 15 to 55 µM) than to those of TEM-35 (K_m values, 140 to 320 µM) and TEM-12 (K_m values, 7 to 15 µM). Overall, the catalytic efficiency of TEM-158 against penicillins was 8- to 129-fold lower than that of TEM-1, TEM-35, or TEM-12. The hydrolytic activity of TEM-158 against cephalothin was 176- to 635-fold lower than that of TEM-1, TEM-35, or TEM-12. However, TEM-158 K_m for this substrate was closer to those of TEM-1 and TEM-12 than to that of TEM-35 (K_m, 170.4 versus 242, 327, and 1,200 µM, respectively). Overall, TEM-158 exhibited low catalytic efficiency against cephalothin, closer to that of TEM-12 and TEM-35 than to that of TEM-1 (k_cat/K_m values, 0.0015, 0.02, 0.04, and 0.7 s^–1·µM^–1). In contrast to TEM-1 and TEM-35, TEM-158 displayed hydrolytic activity against oxyimino-ß-lactams, especially ceftazidime, but its activity was 6- to 132-fold lower than that of the ESBL TEM-12. K_m values for ceftazidime and cefotaxime were similar for TEM-158 and TEM-12. The catalytic efficiency of TEM-158 against oxyimino-ß-lactams was 4- to 75-fold lower than that of TEM-12. Finally, TEM-158 was 100- to 400-fold less susceptible to clavulanic acid and 2- to 4-fold less susceptible to tazobactam than TEM-1 and TEM-12 (Table 3). However, its level of resistance to inhibitor was three- to sevenfold lower than that of the IRT TEM-35.

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TABLE 2. Kinetic parameters of ß-lactamases TEM-158, TEM-12, TEM-35, and TEM-1a

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TABLE 3. IC50s of clavulanic acid and tazobactam for TEM-158, TEM-12, TEM-35, and TEM-1

TEM-158 appears to be close to CMT-type enzymes TEM-121, TEM-125, and TEM-152 (K_cat values, 40, 3.7, and 16 s^–1, respectively), which all are active against ceftazidime, and also had a resistance level to clavulanic acid close to that of an IRT-type enzyme (50% inhibitory concentrations [IC₅₀s], 1, 13.6, and 1 µM, respectively) (7, 8, 10).

Because of its enzymatic characteristics, TEM-158 was difficult to detect as an ESBL. This difficulty was previously observed with other CMT-type ESBLs, especially TEM-125 (7, 8, 10). As with the clinical TEM-125-producing strain TO799, it was not easy to reproducibly detect E. coli BER1 as an ESBL producer when following the American CLSI or the French Comité de l'Antibiogramme de la Société Française de Microbiologie recommendations (8). The presence of Met69Leu, Asn276Asp, and Arg164Ser substitutions in TEM-125 and TEM-158 could explain the closely similar behavior of these enzymes. The discovery of TEM-158 confirms the emergence of this subgroup of atypical ESBLs. The difficulties in detecting these enzymes could be responsible for an underestimation of their number. The observation of a new member of the CMT subgroup, which includes IRT and ESBL properties, highlights the need for an assessment of ESBL detection methods.

Nucleotide sequence accession number. The GenBank accession number for bla_TEM-158 is EF534736.

 
We thank Marlene Jan, Rolande Perroux, and Pamela Chandezon for technical assistance and Sophie Quevillon-Cheruel for providing the modified pET9a plasmid.

This work was supported in part by a grant from Ministère de l'Education Nationale, de l'Enseignement Supérieur et de la Recherche, Paris, France, and a grant from the Centre Hospitalier Régional Universitaire de Clermont-Ferrand, France, and the Ministère de la Santé, de la Famille et des Personnes Handicapées, France (Projet Hospitalier de Recherche Clinique).

 
* Corresponding author. Mailing address: Laboratoire de Bactériologie, Faculté de Médecine, 28 place H. Dunant, 63001 Clermont-Ferrand, France. Phone: (33) 4 73 17 81 50. Fax: (33) 4 73 75 49 22. E-mail: frobin{at}chu-clermontferrand.fr

Published ahead of print on 20 August 2007.

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Antimicrobial Agents and Chemotherapy, November 2007, p. 4181-4183, Vol. 51, No. 11
0066-4804/07/$08.00+0     doi:10.1128/AAC.00614-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

This Article Abstract Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints and Permissions Copyright Information Books from ASM Press MicrobeWorld Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Robin, F. Articles by Bonnet, R. Search for Related Content PubMed PubMed Citation Articles by Robin, F. Articles by Bonnet, R.