Fuchs P C, Barry A L, Brown S D
Clinical Microbiology Institute, Tualatin, Oregon 97062, USA.
J Clin Microbiol. 1997 Jan;35(1):125-31. doi: 10.1128/jcm.35.1.125-131.1997.
Two hundred twenty-eight strains of Haemophilus influenzae and 234 strains of Streptococcus pneumoniae were tested by broth microdilution and disk diffusion methods for susceptibility to trimethoprim (TMP) and TMP-sulfamethoxazole (SMX) to evaluate proposed criteria. Data are presented to support the proposed TMP MIC breakpoints of < or = 2.0 micrograms/ml for susceptibility and > or = 4.0 micrograms/ml for resistance for both species and TMP-SMX MIC breakpoints of < or = 2.0-38 micrograms/ml for susceptibility and > or = 4.0-76 micrograms/ml for resistance. Corresponding zone diameter breakpoints for H. influenzae for both drugs are proposed: < or = 10 mm = resistant; > or = 16 mm = susceptible. A 10-laboratory study documented reproducibility of such tests with standard control strains. The following control limits are proposed for tests of H. influenzae ATCC 49247 against TMP; MIC, 0.12 to 0.5 microgram/ml; zone diameter, 27 to 33 mm. The current limits for TMP-SMX were confirmed. For tests of S. pneumoniae ATCC 49619, MICs of TMP were 1.0 to 4.0 micrograms/ml and the current TMP-SMX MIC range was confirmed. Disk susceptibility tests of either drug against pneumococci were not reproducible, and consequently neither quality control limits nor interpretive criteria could be established. Endpoint interpretation and lot-to-lot variability in Mueller-Hinton agars were significant factors leading to interlaboratory variability.
采用肉汤微量稀释法和纸片扩散法对228株流感嗜血杆菌和234株肺炎链球菌进行了甲氧苄啶(TMP)和复方磺胺甲恶唑(TMP-SMX)药敏试验,以评估所提出的标准。提供的数据支持所提出的两种菌的TMP MIC药敏折点:≤2.0微克/毫升为敏感,≥4.0微克/毫升为耐药;TMP-SMX MIC药敏折点:≤2.0-38微克/毫升为敏感,≥4.0-76微克/毫升为耐药。针对两种药物,提出了流感嗜血杆菌相应的抑菌圈直径折点:≤10毫米为耐药;≥16毫米为敏感。一项涉及10个实验室的研究记录了使用标准对照菌株进行此类试验的可重复性。针对流感嗜血杆菌ATCC 49247对TMP的试验,提出了以下对照限度:MIC为0.12至0.5微克/毫升;抑菌圈直径为27至33毫米。TMP-SMX的现行限度得到确认。对于肺炎链球菌ATCC 49619的试验,TMP的MIC为1.0至4.0微克/毫升,现行的TMP-SMX MIC范围得到确认。两种药物对肺炎球菌的纸片药敏试验不可重复,因此无法确定质量控制限度和解释标准。穆勒-欣顿琼脂中的终点判读和批次间差异是导致实验室间差异的重要因素。