[Study on the rapid, secondary-growth mutants of Staphylococcus epidermidis (author's transl)].

C C Tseng
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Abstract

According to colony type, growth rate and development of secondary growth on the proteose-peptone No. 3 mannitol salt agar (PMS) and the nutrient agar (NA) media, Staphylococcus epidermidis may be classified into three groups. Group I includes strains which develop smooth colonies on both media. Group II consists of those which show rapid propagation of entire clones and develop secondary growth on the PMS medium, but grow only smooth colonies on the NA medium, and which may be called reversible mutants. Group III includes thoes which show secondary growth on both PMS and NA as well as other media, which may be called irreversible mutants. One percent proteose-peptone No. 3 and 5--7% NaCl are the essential ingredients for the induction of mutation, and mannitol can enhance it. Except the high sensitivity of the reversible mutants of human origin, the three groups of chicken origin showed similar drug susceptibility to biosynthesis inhibitors of protein and cell wall. On the HI medium, chloramphenicol inhibited secondary growth of irreversible mutants at 25.0 microgram/ml minimal antimutagenesis concentration (MAC), whereas streptomycin, penicillin, erythromycin and oxytetracycline did not at all. The irreversible mutants had higher resistance to biosynthesis inhibitors of DNA or RNA, e.g. mitomycin C (MMC), novobiocin (NOV) and rifampicin (RIF), than the other two groups. On the HI medium, MMC at the MAC of 0.16 microgram/ml, NA at 25.0 microgram/ml and NOV at 2.5 microgram/ml inhibited the secondary growth of irreversible mutants, but RIF did not. To the irreversible mutants, the MIC and MAC of NA on the PMS medium were both higher than those on the HI medium. The MACs of MMC and NOV on the PMS medium were also higher than those on the HI medium, but their geometric mean MIC remained almost unchanged on both media. Because the MACs of MMC (0.31 microgram/ml) and NA (100.0 microgram/ml) to the reversible mutants on the PMS medium were much similar to those of the irreversible mutants, it suggests that both groups had the similar mutation mechanism.

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[表皮葡萄球菌快速、二次生长突变体的研究[作者译]。
根据菌落类型、生长速度和在蛋白酶-蛋白胨3号甘露醇盐琼脂(PMS)和营养琼脂(NA)培养基上的二次生长发育情况,可将表皮葡萄球菌分为三大类。第一类包括在两种培养基上都能形成光滑菌落的菌株。II类突变体是指在PMS培养基上可以快速繁殖并产生二次生长,而在NA培养基上只能生长光滑菌落的突变体。第三组包括那些在PMS和NA以及其他培养基上显示二次生长的突变体,可称为不可逆突变体。1%的蛋白酶-蛋白胨3号和5 ~ 7%的NaCl是诱导突变的必要成分,甘露醇可以增强突变。除了人类来源的可逆突变体具有较高的敏感性外,三组鸡来源的突变体对蛋白质和细胞壁的生物合成抑制剂均表现出相似的药物敏感性。在HI培养基上,在25.0微克/毫升最小抗诱变浓度(MAC)下,氯霉素抑制不可逆突变体的二次生长,而链霉素、青霉素、红霉素和土霉素则完全没有作用。不可逆突变体对DNA或RNA生物合成抑制剂如丝裂霉素C (MMC)、新生物素(NOV)和利福平(RIF)的耐药性高于其他两组。在HI培养基上,MMC的MAC浓度为0.16微克/毫升,NA为25.0微克/毫升,NOV为2.5微克/毫升,对不可逆突变体的二次生长有抑制作用,而RIF则没有作用。对不可逆突变体,NA在PMS培养基上的MIC和MAC均高于HI培养基。MMC和NOV在PMS培养基上的平均MIC也高于HI培养基,但其几何平均MIC在两种培养基上几乎保持不变。在PMS培养基上,MMC(0.31微克/毫升)和NA(100.0微克/毫升)对可逆突变体的MACs与不可逆突变体的MACs非常相似,说明两组突变机制相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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