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金黄色葡萄球菌中的大环内酯耐药性:大环内酯耐药蛋白合成的诱导

Macrolide resistance in Staphylococcus aureus: induction of macrolide-resistant protein synthesis.

作者信息

Allen N E

出版信息

Antimicrob Agents Chemother. 1977 Apr;11(4):661-8. doi: 10.1128/AAC.11.4.661.

Abstract

Induction of resistance to macrolide-, lincosamide-, and streptogramin B-type antibiotics in Staphylococcus aureus was studied by monitoring the appearance of erythromycin A (EM)-resistant [(14)C]leucine incorporation. Examination of the induction process revealed saturation kinetics and a time course much like that reported for penicillinase in gram-positive bacteria. Induction kinetics in exponentially growing cells were sigmoidal and appeared to reach a maximum and constant rate when growth reached stationary phase. Since the induction of EM-resistant colony-forming ability was complete within 60 min, ribosome modification cannot be limited to a fraction of the population and must occur in essentially every cell. However, EM-resistant growth was expressed in cells where less than half the [(14)C]leucine-incorporating activity was resistant to EM. This suggests that resistance requires that only a threshold level of ribosome modification be exceeded and that, once exceeded, resistance is dominant to sensitivity.

摘要

通过监测对红霉素A(EM)耐药的[¹⁴C]亮氨酸掺入情况,研究了金黄色葡萄球菌对大环内酯类、林可酰胺类和链阳菌素B型抗生素耐药性的诱导。对诱导过程的研究揭示了饱和动力学以及与革兰氏阳性菌中青霉素酶报道情况非常相似的时间进程。指数生长细胞中的诱导动力学呈S形,当生长进入稳定期时似乎达到最大值并保持恒定速率。由于在60分钟内EM耐药菌落形成能力的诱导就已完成,核糖体修饰不可能局限于部分群体,而必定基本上在每个细胞中发生。然而,在[¹⁴C]亮氨酸掺入活性不到一半对EM耐药的细胞中表达出了EM耐药生长。这表明耐药性要求仅超过核糖体修饰的阈值水平,并且一旦超过,耐药性对敏感性占主导。

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本文引用的文献

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Studies on staphylococcal penicillinase.葡萄球菌青霉素酶的研究。
J Gen Microbiol. 1962 Jul;28:461-9. doi: 10.1099/00221287-28-3-461.
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Iodometric assay of penicillinase.青霉素酶的碘量法测定
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