Rossney A S, Coleman D C, Keane C T
Department of Clinical Microbiology, Sir Patrick Dun Research Laboratory, Trinity College Dublin, St James's Hospital, Ireland.
J Med Microbiol. 1994 Dec;41(6):430-40. doi: 10.1099/00222615-41-6-430.
An antibiogram-resistogram (AR) typing scheme that can simply and rapidly differentiate methicillin-resistant Staphylococcus aureus (MRSA) isolates has been devised. Susceptibility to antibiotics and chemicals was determined by disk diffusion testing. Three disk diffusion methods and three control S. aureus strains were evaluated. A modified Stokes' technique in which S. aureus ATCC 25923 replaced S. aureus NCTC 6571 as the control organism was chosen. Susceptibility patterns against 18 antibiotics and four chemicals were used to determine AR types. AR subtypes were determined with reference to knowledge of the local MRSA population so that plasmid loss would not result in misclassification. AR typing was compared with phage typing and plasmid profiling and found to be more discriminatory than either of these typing methods. Representative isolates of the most frequently occurring AR patterns were further characterised by investigating enterotoxin production, MICs of gentamicin and amikacin, and restriction endonuclease analysis of plasma DNA, to determine whether apparently different strains could have the same AR pattern and to devise confirmatory tests for any such similar patterns. One pattern was shared by two strains but isolates could be differentiated by susceptibility to minocycline. This typing scheme can be used in the diagnostic laboratory and results may be obtained within 24 h.
已设计出一种能简单快速区分耐甲氧西林金黄色葡萄球菌(MRSA)分离株的抗菌谱 - 耐药谱(AR)分型方案。通过纸片扩散试验确定对抗生素和化学物质的敏感性。评估了三种纸片扩散方法和三种对照金黄色葡萄球菌菌株。选择了一种改良的斯托克斯技术,其中用金黄色葡萄球菌ATCC 25923替代金黄色葡萄球菌NCTC 6571作为对照菌株。针对18种抗生素和四种化学物质的药敏模式用于确定AR类型。根据当地MRSA群体的知识确定AR亚型,以免质粒丢失导致错误分类。将AR分型与噬菌体分型和质粒谱分析进行比较,发现其比这两种分型方法中的任何一种都更具鉴别力。通过研究肠毒素产生、庆大霉素和阿米卡星的最低抑菌浓度以及血浆DNA的限制性内切酶分析,对最常见AR模式的代表性分离株进行进一步表征,以确定明显不同的菌株是否可能具有相同的AR模式,并为任何此类相似模式设计确证试验。两种菌株共有一种模式,但分离株可通过对米诺环素的敏感性进行区分。这种分型方案可用于诊断实验室,24小时内即可获得结果。