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分枝杆菌溃疡分枝杆菌大环内酯外毒素(mycolactone)的构效关系研究。

Structure-activity relationship studies on the macrolide exotoxin mycolactone of Mycobacterium ulcerans.

机构信息

Molecular Immunology, Swiss Tropical and Public Health Institute, Basel, Switzerland.

出版信息

PLoS Negl Trop Dis. 2013;7(3):e2143. doi: 10.1371/journal.pntd.0002143. Epub 2013 Mar 28.

DOI:10.1371/journal.pntd.0002143
PMID:23556027
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3610637/
Abstract

BACKGROUND

Mycolactones are a family of polyketide-derived macrolide exotoxins produced by Mycobacterium ulcerans, the causative agent of the chronic necrotizing skin disease Buruli ulcer. The toxin is synthesized by polyketide synthases encoded by the virulence plasmid pMUM. The apoptotic, necrotic and immunosuppressive properties of mycolactones play a central role in the pathogenesis of M. ulcerans.

METHODOLOGY/PRINCIPAL FINDINGS: We have synthesized and tested a series of mycolactone derivatives to conduct structure-activity relationship studies. Flow cytometry, fluorescence microscopy and Alamar Blue-based metabolic assays were used to assess activities of mycolactones on the murine L929 fibroblast cell line. Modifications of the C-linked upper side chain (comprising C12-C20) caused less pronounced changes in cytotoxicity than modifications in the lower C5-O-linked polyunsaturated acyl side chain. A derivative with a truncated lower side chain was unique in having strong inhibitory effects on fibroblast metabolism and cell proliferation at non-cytotoxic concentrations. We also tested whether mycolactones have antimicrobial activity and found no activity against representatives of Gram-positive (Streptococcus pneumoniae) or Gram-negative bacteria (Neisseria meningitis and Escherichia coli), the fungus Saccharomyces cerevisae or the amoeba Dictyostelium discoideum.

CONCLUSION

Highly defined synthetic compounds allowed to unambiguously compare biological activities of mycolactones expressed by different M. ulcerans lineages and may help identifying target structures and triggering pathways.

摘要

背景

类诺卡霉素是由溃疡分枝杆菌(Mycobacterium ulcerans)产生的一类聚酮衍生的大环内酯外毒素,溃疡分枝杆菌是慢性坏死性皮肤病伯氏疏螺旋体溃疡的病原体。毒素由毒性质粒 pMUM 编码的聚酮合酶合成。类诺卡霉素的凋亡、坏死和免疫抑制特性在溃疡分枝杆菌的发病机制中起核心作用。

方法/主要发现: 我们合成并测试了一系列类诺卡霉素衍生物,以进行结构-活性关系研究。使用流式细胞术、荧光显微镜和基于 Alamar Blue 的代谢测定法评估了类诺卡霉素对鼠 L929 成纤维细胞系的活性。C 连接的上侧链(包含 C12-C20)的修饰比 C5-O 连接的多不饱和酰基侧链的修饰引起的细胞毒性变化小。具有截断的下侧链的衍生物具有独特的强抑制作用,可在非细胞毒性浓度下抑制成纤维细胞代谢和增殖。我们还测试了类诺卡霉素是否具有抗菌活性,发现对革兰氏阳性(肺炎链球菌)或革兰氏阴性菌(脑膜炎奈瑟菌和大肠杆菌)、真菌酿酒酵母或变形虫盘基网柄菌没有活性。

结论

高度定义的合成化合物允许明确比较不同溃疡分枝杆菌谱系表达的类诺卡霉素的生物活性,并且可以帮助识别靶结构和触发途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1605/3610637/83b2258e94be/pntd.0002143.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1605/3610637/df078a65bb37/pntd.0002143.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1605/3610637/1f1f6880587c/pntd.0002143.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1605/3610637/c644df6e3fac/pntd.0002143.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1605/3610637/4a217741f5f6/pntd.0002143.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1605/3610637/83b2258e94be/pntd.0002143.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1605/3610637/df078a65bb37/pntd.0002143.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1605/3610637/1f1f6880587c/pntd.0002143.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1605/3610637/c644df6e3fac/pntd.0002143.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1605/3610637/4a217741f5f6/pntd.0002143.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1605/3610637/83b2258e94be/pntd.0002143.g005.jpg

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