Small molecules from the sea: models for innovative antimicrobial agents

S. Long, D. Resende, P. Pereira-Terra, Â. Inácio, P. M. D. Costa, E. Pinto, A. Kijjoa, M. Pinto, E. Sousa
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Abstract

Antimicrobial resistance is one of the most pressing health issues of our days. The marine environment has proven to be a very rich source of diverse natural products with broad-spectra of biologically activities being a very helpful resource in the search for novel antimicrobial compounds. These structurally distinct molecules are revealing promising biological activities against a very large number of drug-resistant pathogenic bacteria and fungi, catching marine natural products attention in the discovery of new antimicrobial agents. Inspired by antimicrobial lichen xanthones [1] and fungi-derived alkaloids, two series of marine natural products mimics were prepared. The synthesized compounds were evaluated for their antimicrobial activity. Both series produced interesting compounds active against E. faecalis (ATCC 29212 and 29213) and S. aureus (ATCC 29213) with some synthetic alkaloids being active against a MRSA strain. Some revealed a potent fungistatic and fungicidal activity against dermatophytes clinical strains (T. rubrum, M. canis, and E. floccosum). These results highlight the potential of marine natural products as a source of new antimicrobial agents to revert resistance. [1] D. I. S. P. Resende, P. Pereira-Terra, Â. S. Inacio, P. M. Costa, E. Pinto, E. Sousa, M. M. M. Pinto. Lichen Xanthones as Models for New Antifungal Agents. Molecules 2018, 23, 2617; doi:10.3390/molecules23102617 Acknowledgments: This work was partially supported through national funds provided by FCT/MCTES—Foundation for Science and Technology from the Ministry of Science, Technology, and Higher Education (PIDDAC) and the European Regional Development Fund (ERDF) through the COMPETE—Programa Operacional Factores de Competitividade (POFC) programme, under the Strategic Funding UID/Multi/04423/2013, the projects POCI-01-0145-FEDER-028736 and POCI-01-0145-FEDER-016790 (PTDC/MAR-BIO/4694/2014; 3599-PPCDT) in the framework of the programme PT2020, as well as by the project INNOVMAR—Innovation and Sustainability in the Management and Exploitation of Marine Resources (reference NORTE-01-0145-FEDER-000035, within Research Line NOVELMAR), supported by North Portugal Regional Operational Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF). Solida Long thanks Erasmus Mundus Action 2 (LOTUS+, LP15DF0205) for full PhD scholarship. Diana I. S. P. Resende also acknowledge for her grant (NOVELMAR/BPD_2/2016-019) and Patricia Pereira-Terra for her grant (NOVELMAR/BPD/2017/012).
来自海洋的小分子:创新抗菌剂的模型
抗微生物药物耐药性是当今最紧迫的健康问题之一。海洋环境已被证明是多种天然产物的丰富来源,具有广谱的生物活性,是寻找新型抗菌化合物的非常有益的资源。这些结构独特的分子揭示了对大量耐药病原菌和真菌的有希望的生物活性,在发现新的抗菌剂方面引起了海洋天然产物的关注。受抗菌地衣山酮[1]和真菌衍生生物碱的启发,制备了两个系列的海洋天然产物模拟物。对合成的化合物进行了抑菌活性评价。这两个系列都产生了有趣的化合物,对粪肠球菌(ATCC 29212和29213)和金黄色葡萄球菌(ATCC 29213)有活性,一些合成生物碱对MRSA菌株有活性。一些研究显示对皮肤真菌临床菌株(如:rubrum T., M. canis和E.絮凝体)具有有效的抑菌和杀真菌活性。这些结果突出了海洋天然产物作为新的抗菌剂来源的潜力,以恢复耐药性。[1]李志强,王志强,王志强,等。S.伊纳西奥,P. M.科斯塔,E.平托,E.索萨,M. M. M.平托。地衣山酮作为新型抗真菌药物的模型。分子学报,2018,23,2617;doi: 10.3390 / molecules23102617致谢:本研究部分得到了国家科学技术和高等教育部科技基金(PIDDAC)和欧洲区域发展基金(ERDF)通过竞争计划运营要素(POFC)计划提供的国家基金的支持,在战略基金UID/Multi/04423/2013下,项目poci -01-0145-联邦-028736和poci -01-0145-联邦-016790 (PTDC/ mari - bio /4694/2014;3599-PPCDT)在PT2020计划框架内,以及innovmar -海洋资源管理和开发中的创新和可持续性项目(参考文献NORTE-01-0145-联邦-000035,研究线NOVELMAR),由北葡萄牙区域业务计划(NORTE 2020)支持,根据葡萄牙2020伙伴关系协议,通过欧洲区域发展基金(ERDF)。Solida Long感谢Erasmus Mundus Action 2 (LOTUS+, LP15DF0205)全额博士奖学金。Diana I. S. P. Resende和Patricia Pereira-Terra也分别获得了资助(NOVELMAR/BPD/ 2016-019)和资助(NOVELMAR/BPD/2017/012)。
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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