Antibiotic susceptibility of Stenotrophomonas (Xanthomonas) maltophilia:: Comparative (NCCLS criteria) evaluation of antimicrobial drugs with the agar dilution and the agar disk diffusion (Bauer-Kirby) tests

被引:17
作者
Traub, WH [1 ]
Leonhard, B [1 ]
Bauer, D [1 ]
机构
[1] Univ Saarland, Inst Med Mikrobiol & Hyg, D-66421 Homburg, Germany
关键词
agar dilution test; agar disk diffusion (Bauer-Kirby) test; comparative evaluation; interpretative (NCCLS) criteria; minimal inhibitory concentrations; modified criteria (intermediate susceptibility); susceptibility;
D O I
10.1159/000007111
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ninety-six clinical isolates of Stenotrophomonas maltophilia were examined with the agar dilution method for susceptibility to 19 antimicrobial drugs. Doxycycline, cotrimoxazole, timentin, ofloxacin, fosfomycin, and piperacillin + tazobactam, in that order, inhibited the majority of strains. All isolates were resistant to nitrofurantoin. Concurrent disk susceptibility (Bauer-Kirby method) testing, using currently valid NCCLS interpretative criteria for Pseudomonas aeruginosa, uncovered a significant incidence of very major (category I), major (category II), and minor (categories III and IV) discrepancies for aminoglycosides, cephalosporins, chloramphenicol, and piperacillin + tazobactam and ticarcillin + clavulanic acid. Therefore, new interpretative criteria indicative of intermediate (I) susceptibility of S. maltophilia to these various antibiotics were proposed. In addition, new intermediate susceptibility criteria were proposed for the two beta-lactam-beta-lactamase inhibitor combinations. It was recommended to exclude ciprofloxacin from test batteries against this microorganism due to the wide scatter of minimal inhibitory concentration values and diameters of inhibition zones; the same was true for polymyxin B. It is hoped that the proposed modified, species-specific criteria will improve the clinical utility of laboratory-generated disk antibiograms with respect to the inherently multiple antibiotic-resistant, opportunistic pathogen S. maltophilia.
引用
收藏
页码:164 / 173
页数:10
相关论文
共 71 条
[1]   SUSCEPTIBILITY TO BETA-LACTAM ANTIBIOTICS OF MUTANT STRAINS OF XANTHOMONAS-MALTOPHILIA WITH HIGH-LEVEL AND LOW-LEVEL CONSTITUTIVE EXPRESSION OF L1 AND L2 BETA-LACTAMASES [J].
AKOVA, M ;
BONFIGLIO, G ;
LIVERMORE, DM .
JOURNAL OF MEDICAL MICROBIOLOGY, 1991, 35 (04) :208-213
[2]   Multiple antibiotic resistance in Stenotrophomonas maltophilia [J].
Alonso, A ;
Martinez, JL .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (05) :1140-1142
[3]  
[Anonymous], 1993, M7A3 NCCLS
[4]   TRANSFER OF CEFTAZIDIME AND AZTREONAM RESISTANCE FROM NOSOCOMIAL STRAINS OF XANTHOMONAS (STENOTROPHOMONAS) MALTOPHILIA TO A RECIPIENT STRAIN OF PSEUDOMONAS-AERUGINOSA ML-1008 [J].
BABALOVA, M ;
BLAHOVA, J ;
LESICKAHUPKOVA, M ;
KRCMERY, V ;
KUBONOVA, K .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1995, 14 (10) :925-927
[5]   STENOTROPHOMONAS MALTOPHILIA IN CYSTIC-FIBROSIS PATIENTS [J].
BALLESTERO, S ;
VIRSEDA, I ;
ESCOBAR, H ;
SUAREZ, L ;
BAQUERO, F .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1995, 14 (08) :728-729
[6]  
BARRY AL, 1978, AM J CLIN PATHOL, V70, P909
[7]  
BAUER AW, 1966, AM J CLIN PATHOL, V45, P493
[8]   In vitro activities of beta-lactam-beta-lactamase inhibitor combinations against Stenotrophomonas maltophilia: Correlation between methods for testing inhibitory activity, time-kill curves, and bactericidal activity [J].
Bellido, JLM ;
Criado, SM ;
Garcia, IG ;
Manzanares, MAA ;
Zufiaurre, MNG ;
GarciaRodriguez, JA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (12) :2612-2615
[9]   DNA RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM DIFFERENTIATES CROSSED FROM INDEPENDENT INFECTIONS IN NOSOCOMIAL XANTHOMONAS-MALTOPHILIA BACTEREMIA [J].
BINGEN, EH ;
DENAMUR, E ;
LAMBERTZECHOVSKY, NY ;
BOURDOIS, A ;
MARIANIKURKDJIAN, P ;
CEZARD, JP ;
NAVARRO, J ;
ELION, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1991, 29 (07) :1348-1350
[10]   CLINICAL ISOLATE OF A XANTHOMONAS-MALTOPHILIA STRAIN PRODUCING L-1 DEFICIENT AND L-2-INDUCIBLE BETA-LACTAMASES [J].
BONFIGLIO, G ;
STEFANI, S ;
NICOLETTI, G .
CHEMOTHERAPY, 1995, 41 (02) :121-124