Lerner P I, Baum G L
Antimicrob Agents Chemother. 1973 Aug;4(2):85-93. doi: 10.1128/AAC.4.2.85.
Variations of inoculum, pH, and composition of the agar assay media each influenced the in vitro susceptibility of Nocardia organisms (30 strains of N. asteroides and 6 strains of N. brasiliensis) to one or more antimicrobial agents incorporated in solid agar and incubated at 37 C for 48 h. Among newer antimicrobial agents, doxycycline, minocycline, and 7-halogenated lincomycin analogues exhibited the most consistent in vitro inhibitory activity; among older agents, viomycin, erythromycin, and streptomycin exhibited more selective in vitro inhibitory activity, but against a significant percentage of strains tested. N. brasiliensis was conspicuously more susceptible to erythromycin and gentamicin and more resistant to viomycin and capreomycin than was N. asteroides. Cycloserine demonstrated no significant in vitro inhibitory activity when assayed in appropriately augmented alanine-free medium. The outstanding feature of this in vitro survey was the marked variation in susceptibility among individual strains of N. asteroides, which variation deserves more careful consideration in future clinical or experimental therapeutic trials.
接种物、pH值以及琼脂检测培养基成分的变化,均对诺卡氏菌属微生物(30株星状诺卡氏菌和6株巴西诺卡氏菌)在体外对添加于固体琼脂中并于37℃孵育48小时的一种或多种抗菌药物的敏感性产生影响。在新型抗菌药物中,强力霉素、米诺环素和7-卤代林可霉素类似物表现出最一致的体外抑制活性;在旧型药物中,紫霉素、红霉素和链霉素表现出更具选择性的体外抑制活性,但针对相当比例的受试菌株。与星状诺卡氏菌相比,巴西诺卡氏菌对红霉素和庆大霉素明显更敏感,而对紫霉素和卷曲霉素更耐药。当在适当添加且不含丙氨酸的培养基中进行检测时,环丝氨酸未表现出明显的体外抑制活性。这项体外研究的突出特点是星状诺卡氏菌各菌株之间敏感性存在显著差异,这种差异在未来的临床或实验性治疗试验中值得更仔细的考虑。