Abstract
The double-disk synergy test (DDST) using Mueller-Hinton agar and antibiotic disks with centrally positioned disks of amoxicillin-clavulanate, ampicillin-sulbactam, and piperacillin-tazobactam and, at a center-to-center distance of 25–30 mm, 2–4 disks with 10 various β-lactam antibiotics per one plate was performed in 58 clinical isolates ofStenotrophomonas maltophilia to determine the effectivity of 3 β-lactamase inhibitors. When tested with clavulanate as the central β-lactamase inhibitor synergic action on tested strains was the most frequent with aztreonam (81.0 % of strains), cefoperazone (63.8 %), and cefepime (60.3 %). With sulbactam the synergic action,i.e. DDST positivity, was high in the case of cefoperazone (15.5 %), ampicillin, aztreonam and piperacillin (8.6 % each); with tazobactam it was the most frequent with aztreonam (53.4 %), cefoperazone (44.8 %) and cefepime (37.9 %). No synergy was demonstrated after application of meropenem regardless of the kind of β-lactamase inhibitor used. In 58 strains ofS. maltophilia, 55 different profiles of DDST positivity were found. The results confirm that clavulanate is the most effective inhibitor ofS. maltophilia β-lactamases. The utilization of DDST (performed in the recommended way) for the typization of strainsStenotrophomonas species and for the estimation of potential effectiveness combinations of β-lactams with β-lactamase inhibitors for the therapy of stenotrophomonade infections was suggested.
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Abbreviations
- DDST:
-
double-disk synergy test
- ESBL:
-
extended-spectrum β-lactamases
- β-lac:
-
β-lactamase
- Amp:
-
ampicillin
- Amx:
-
amoxicillin
- Azt:
-
aztreonam
- Cef:
-
cefepime
- Cfa:
-
ceftazidime
- Cfm:
-
cefpirome
- Cfp:
-
cefoperazone
- Cft:
-
ceftriaxone
- Cfx:
-
cefotaxime
- Cla:
-
clavulanate
- Mer:
-
meropenem
- Pip:
-
piperacillin
- Sul:
-
sulbactam
- Taz:
-
tazobactam
References
Blahová J., Králiková K., Krčmery V., Toršova V.: Transferable antibiotic resistance in nosocomialStenotrophomonas maltophilia strain.Diagn.Microbiol.Infect.Dis. 29, 129–132 (1997).
Blahová J., Hupková-Lešická M., Králiková K., Krčmery V.: Extended spectrum β-lactamase reactions inStenotrophomonas maltophilia.Infection 26, 187–188 (1998).
Cantón R., Valdezate S., Sanchez del Saz B., Perez-Vazquez M., Oliver A., Loza E., Baquero F.: Cef and β-lactamase inhibitor combinations against clinical isolates ofStenotrophomonus maltophila.Clin.Microbiol.Infect. 5 (Suppl. 3), 370 (1999).
Denton M., Kerr K.G.: Microbiological and clinical aspects of infection associated withStenotrophomonas maltophilia.Clin.Microbiol.Rev. 11, 57–80 (1998).
Felici A., Amicosante G.: Kinetic analysis of extension of substrate specifity withXanthomonas maltophilia, Aeromonas hydrophila, andBacillus cereus metallo-β-lactamases.Antimicrob.Agents Chemother. 39, 192–199 (1995).
Finkmann W., Altendorf K., Stackebrandt E., Lipski A.: Characterization of N2O-producingXanthomonas-like isolates from biofilters asStenotrophomonas nitritireducens sp nov.,Luteimonas mephitis gen.nov., sp.nov. andPseudoxanthomonas broegbernensis gen.nov., sp.nov.Internat.J.Syst.Evol.Microbiol. 50, 273–282 (2000).
Hejnar P., Chmela Z., Rypka M.: Fatty acid analysis ofStenotrophomonas maltophilia clinical strains showing different susceptibility to antibiotics at 30 and 37°C.Folia Microbiol. 47, 742–746 (2002).
Jarlier V., Nicolas M.H., Fournier G., Philippon A.: Extended broad-spectrum β-lactamases conferring transferable resistance to newer β-lactam agents inEnteropacteriaceae: hospital prevalence and susceptibility patterns.Rev.Infect.Dis. 10, 867–878 (1988).
Kelly M.D., Mortensen J.E., Konkle B.A., Stull T.L.: A plasmid mediating production of a β-lactamase byStenotrophomonas maltophilia.Curr.Ther.Res. 56, 152–162 (1995).
Muñoz Bellido J.L., García-Rodriguez J.A.: Azt-Cla synergy does not mean extended-spectrum β-lactamase inStenotrophomonas maltophilia.J.Antimicrob.Chemother. 41, 493–497 (1998).
Pankuch G.A., Jacobs M.R., Rittenhouse S.F., Appelbaum P.C.: Susceptibilities of 123 strains ofXanthomonas maltophilia to eight β-lactams (including β-lactam-β-lactamase inhibitor combinations) and ciprofloxacin tested by five methods.Antimicrob.Agents Chemother. 38, 2317–2322 (1994).
Paton R., Miles R.S., Amyes S.G.B.: Biochemical properties of inducible β-lactamases produced fromXanthomonas maltophilia.Antimicrob.Agents Chemother. 38, 2143–2149 (1994).
Payne D.J., Cramp R., Bateson J.H., Neall J., Knowles D.: Rapid identification of metallo- and serine β-lactamases.Antimicrob.Agents Chemother. 38, 991–996 (1994).
Pradhananga S.L., Rowling P.J.E., Simpson I.N., Payne D.J.: Sensitivity of L-2 type β-lactamases fromStenotrophomonas maltophilia to serine active site β-lactamase inhibitors.J.Antimicrob.Chemother. 37, 394–396 (1996).
Saino Y., Kobayashi F., Inoue M., Mitsuhashi S.: Purification and properties of inducible penicillin β-lactamase isolated fromPseudomonas maltophilia.Antimicrob.Agents Chemother. 22, 564–570 (1982).
Saino Y., Inoue M., Mitsuhashi S.: Purification and properties of an inducible cephalosporinase fromPseudomonas maltophilia GN 12873.Antimicrob.Agents Chemother. 25, 362–365 (1984).
Townsend R., Winstanley T.G., Spencer R.C.:In vitro susceptibility ofXanthomonas maltophilia to Azt and Cla as a test for the presumptive identification of the species.J.Hosp.Infect. 18, 324–325 (1991).
Valdezate S., Vindel A., Loza E., Baquero F., Cantón R.: Antimicrobial susceptibilities of uniqueStenotrophomonas maltophilia clinical strains.Antimicrob.Agents Chemother. 45, 1581–1584 (2001).
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This work was supported by research project of theMinistry of Education, Youth and Sports of the Czech Republic no. MSM 151100002.
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Hejnar, P., Kolár, M. & Chmela, Z. Double-disk synergy test positivity inStenotrophomonas maltophilia clinical strains. Folia Microbiol 49, 71–74 (2004). https://doi.org/10.1007/BF02931649
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DOI: https://doi.org/10.1007/BF02931649