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作为抗生素发现重点的人类微生物组:显示出针对……的活性

The Human Microbiome as a Focus of Antibiotic Discovery: Displays Activity Against .

作者信息

Aho Ellen L, Ogle Jenie M, Finck Anna M

机构信息

Department of Biology, Concordia College, Moorhead, MN, United States.

出版信息

Front Microbiol. 2020 Dec 3;11:577762. doi: 10.3389/fmicb.2020.577762. eCollection 2020.

Abstract

infections are a serious global health problem. This organism has developed disturbing levels of antibiotic resistance, resulting in the need for new approaches to prevent and treat gonorrhea. The genus also includes several members of the human microbiome that live in close association with an array of microbial partners in a variety of niches. We designed an undergraduate antibiotic discovery project to examine a panel of nonpathogenic species for their ability to produce antimicrobial secondary metabolites. Five strains belonging to the species group displayed activity against other in delayed antagonism assays; three of these were active against . The antimicrobial compound secreted by NRL 9300 remained active in the presence of catalase, trypsin, and HEPES buffer, and effectively inhibited a DNA uptake mutant of . Antimicrobial activity was also retained in an ethyl acetate extract of plate grown NRL 9300. These data suggest produces an antimicrobial secondary metabolite that is distinct from previously described antigonococcal agents. This work also serves as a demonstration project that could easily be adapted to studying other members of the human microbiome in undergraduate settings. We offer the perspective that both introductory and more advanced course-based and apprentice-style antibiotic discovery projects focused on the microbiome have the potential to enrich undergraduate curricula and we describe transferrable techniques and strategies to facilitate project design.

摘要

感染是一个严重的全球健康问题。这种微生物已产生了令人不安的抗生素耐药水平,因此需要新的方法来预防和治疗淋病。该属还包括人类微生物组的几个成员,它们与各种生态位中的一系列微生物伙伴密切相关。我们设计了一个本科抗生素发现项目,以检测一组非致病性物种产生抗微生物次级代谢产物的能力。在延迟拮抗试验中,属于该物种组的五个菌株对其他菌株表现出活性;其中三个对淋病奈瑟菌有活性。NRL 9300菌株分泌的抗微生物化合物在过氧化氢酶、胰蛋白酶和HEPES缓冲液存在的情况下仍保持活性,并有效抑制淋病奈瑟菌的一个DNA摄取突变体。平板培养的NRL 9300菌株的乙酸乙酯提取物也保留了抗微生物活性。这些数据表明该菌株产生了一种不同于先前描述的抗淋病奈瑟菌药物的抗微生物次级代谢产物。这项工作还作为一个示范项目,可以很容易地适用于本科阶段对人类微生物组其他成员的研究。我们认为,专注于微生物组的基础入门和更高级的基于课程及学徒式抗生素发现项目都有潜力丰富本科课程,并且我们描述了可转移的技术和策略以促进项目设计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8d/7744932/d34a82b40c31/fmicb-11-577762-g001.jpg

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