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[多重耐药金黄色葡萄球菌的药敏研究]

[Study on the drug sensitivity of multiple drug-resistant Staphylococcus aureus].

作者信息

Deguchi K, Fukayama S, Nishimura Y, Yokota N, Tanaka S, Oda S, Matsumoto Y, Ikegami R, Satoh K, Toyonaga Y

出版信息

Jpn J Antibiot. 1985 Aug;38(8):2163-70.

PMID:3852898
Abstract

Of clinically isolated Staphylococcus aureus showing resistance to multiple drugs among penicillins (PCs), cephem antibiotics (CEPs), aminoglycosides (AGs), minocycline (MINO) and fosfomycin (FOM), 64 strains were selected for the determination of MIC. Twenty-one drugs were used for the determination of MIC, with ampicillin (ABPC), cloxacillin (MCIPC), cephalothin (CET), cefazolin (CEZ), cefotiam (CTM), cefuroxime (CXM), cefamandole (CMD), cefotaxime (CTX), ceftizoxime (CZX), cefmenoxime (CMX), cefmetazole (CMZ), cefoxitin (CFX), latamoxef (LMOX), cefotetan (CTT), cefoperazone (CPZ), gentamicin (GM), dibekacin (DKB), tobramycin (TOB), amikacin (AMK), MINO, and FOM. MIC80 of each drug at 10(6) CFU/ml were: ABPC, MCIPC, CEZ, CTM, CXM, CTX, CZX, CMX, CFX, LMOX, CTT, CPZ, GM, DKB and TOB greater than 100 micrograms/ml; CET 50 micrograms/ml; CMD and AMK 25 micrograms/ml; CMZ 12.5 micrograms/ml; FOM 6.25 micrograms/ml; and MINO 0.78 micrograms/ml. The ratio of highly resistant strains with MIC greater than 100 micrograms/ml at 10(6) CFU/ml varied according to drug, and a difference tended to be seen in the degree of influence by resistant factors reflected upon MIC, e.g. drugs for which a high resistance of more than 50% was confirmed were ABPC, CXM, CZX, LMOX and TOB, and 20 approximately 30% MCIPC, CTM, CTX, CMX and CFX. MIC on MCIPC which has a correlation of structural activity with methicillin correlated with cephems (CEPs) resistance to a high degree, but many of the so-called new CEPs showed resistance even to the strains with a low MIC on MCIPC. It was assumed that CEPs resistant strains have multiple drug resistant factors based on the fact that such strains showed multiple drug resistance.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在临床分离出的对多种药物耐药的金黄色葡萄球菌中,这些药物包括青霉素类(PCs)、头孢菌素类抗生素(CEPs)、氨基糖苷类(AGs)、米诺环素(MINO)和磷霉素(FOM),选取64株进行最低抑菌浓度(MIC)测定。使用21种药物进行MIC测定,分别为氨苄西林(ABPC)、氯唑西林(MCIPC)、头孢噻吩(CET)、头孢唑林(CEZ)、头孢替安(CTM)、头孢呋辛(CXM)、头孢孟多(CMD)、头孢噻肟(CTX)、头孢唑肟(CZX)、头孢甲肟(CMX)、头孢美唑(CMZ)、头孢西丁(CFX)、拉氧头孢(LMOX)、头孢替坦(CTT)、头孢哌酮(CPZ)、庆大霉素(GM)、地贝卡星(DKB)、妥布霉素(TOB)、阿米卡星(AMK)、MINO和FOM。每种药物在10⁶CFU/ml时的MIC80为:ABPC、MCIPC、CEZ、CTM、CXM、CTX、CZX、CMX、CFX、LMOX、CTT、CPZ、GM、DKB和TOB大于100微克/毫升;CET为50微克/毫升;CMD和AMK为25微克/毫升;CMZ为12.5微克/毫升;FOM为6.25微克/毫升;MINO为0.78微克/毫升。在10⁶CFU/ml时MIC大于100微克/毫升的高耐药菌株比例因药物而异,并且在MIC所反映的耐药因素影响程度上往往存在差异,例如,确认耐药率超过50%的药物有ABPC、CXM、CZX、LMOX和TOB,以及约20%至30%的MCIPC、CTM、CTX、CMX和CFX。与甲氧西林具有结构活性相关性的MCIPC的MIC与头孢菌素类(CEPs)耐药高度相关,但许多所谓的新型CEPs甚至对MCIPC MIC较低的菌株也显示出耐药性。基于此类菌株表现出多重耐药这一事实,推测CEPs耐药菌株具有多种耐药因素。(摘要截短于250字)

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