Lu Qin-Pei, Ye Jing-Jing, Huang Yong-Mei, Liu Di, Liu Li-Fang, Dong Kun, Razumova Elizaveta A, Osterman Ilya A, Sergiev Petr V, Dontsova Olga A, Jia Shu-Han, Huang Da-Lin, Sun Cheng-Hang
Department of Microbial Chemistry, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China.
Beijing Key Laboratory of Antimicrobial Agents, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China.
Antibiotics (Basel). 2019 Nov 27;8(4):236. doi: 10.3390/antibiotics8040236.
Rediscovery of known antibiotics from actinobacteria, especially , has become a bottleneck issue. Nowadays, more specific identification and dereplication could be acquired by a combination of modern analytic techniques with various databases. In this study, 261 actinobacterial strains were isolated from 8 mangrove soil samples by culture-dependent method. A total of 83 strains were selected to evaluate antibacterial activities and mechanisms by disc diffusion method and a unique double fluorescent protein reporter system (pDualrep2), respectively. Thirty-two strains exhibited antagonistic activity against at least one of the "ESKAPE" pathogens. Four strains (B475, B486, B353, and B98) showed strong inhibitory activity against Gram-positive bacteria and induced DNA damage SOS response. One strain (B704) exhibited inhibitory activity against several pathogens and induced attenuation-based translational inhibitors reporter. Seven members of quinoxaline-type antibiotics including quinomycin A, quinomycin monosulfoxide, and other five putative new analogues were found from the culture broth of strain B475 by a combination of anti-MRSA guide, HPTLC, HPLC-UV, and UPLC-UV-HRESIMS/MS analysis, Chemspider searching, and MS/MS-based molecular networking analysis. In conclusion, this study not only demonstrated that mangrove is a rich source of actinobacteria with the potentially new antibiotics but showed rapid dereplication of known antibiotics in the early stage can improve efficiency for the discovery of new antibiotics.
从放线菌中重新发现已知抗生素,尤其是[此处原文缺失具体内容],已成为一个瓶颈问题。如今,通过现代分析技术与各种数据库相结合,可以实现更精确的鉴定和去重复操作。在本研究中,采用依赖培养的方法从8个红树林土壤样本中分离出261株放线菌菌株。总共挑选了83株菌株,分别通过纸片扩散法和独特的双荧光蛋白报告系统(pDualrep2)评估其抗菌活性和作用机制。32株菌株对至少一种“ESKAPE”病原体表现出拮抗活性。4株菌株(B475、B486、B353和B98)对革兰氏阳性菌表现出强烈抑制活性,并诱导DNA损伤SOS反应。1株菌株(B704)对多种病原体表现出抑制活性,并诱导基于衰减的翻译抑制剂报告基因。通过抗MRSA导向、HPTLC、HPLC-UV、UPLC-UV-HRESIMS/MS分析、Chemspider搜索和基于MS/MS的分子网络分析相结合的方法,从菌株B475的培养液中发现了7种喹喔啉类抗生素,包括喹霉素A、喹霉素单亚砜和其他5种推定的新类似物。总之,本研究不仅证明了红树林是放线菌的丰富来源,具有潜在的新型抗生素,而且表明在早期阶段对已知抗生素进行快速去重复操作可以提高新抗生素的发现效率。