CEB-Centre of Biological Engineering, LIBRO-Laboratory of Research in Biofilms Rosário Oliveira, University of Minho, Campus de Gualtar, Braga, Portugal.
Front Cell Infect Microbiol. 2020 Nov 11;10:550505. doi: 10.3389/fcimb.2020.550505. eCollection 2020.
Modern medicine is currently facing huge setbacks concerning infection therapeutics as microorganisms are consistently knocking down every antimicrobial wall set before them. The situation becomes more worrying when taking into account that, in both environmental and disease scenarios, microorganisms present themselves as biofilm communities that are often polymicrobial. This comprises a competitive advantage, with interactions between different species altering host responses, antimicrobial effectiveness, microbial pathogenesis and virulence, usually augmenting the severity of the infection and contributing for the recalcitrance towards conventional therapy. and are two opportunistic pathogens often co-isolated from infections, mainly from mucosal tissues like the lung. Despite the billions of years of co-existence, this pair of microorganisms is a great example on how little is known about cross-kingdom interactions, particularly within the context of coinfections. Given the described scenario, this study aimed to collect, curate, and analyze all published experimental information on the molecular basis of and interactions in biofilms, in order to shed light into key mechanisms that may affect infection prognosis, increasing this area of knowledge. Publications were optimally retrieved from PubMed and Web of Science and classified as to their relevance. Data was then systematically and manually curated, analyzed, and further reconstructed as networks. A total of 641 interactions between the two pathogens were annotated, outputting knowledge on important molecular players affecting key virulence mechanisms, such as hyphal growth, and related genes and proteins, constituting potential therapeutic targets for infections related to these bacterial-fungal consortia. Contrasting interactions were also analyzed, and quorum-sensing inhibition approaches were highlighted. All annotated data was made publicly available at www.ceb.uminho.pt/ISCTD, a database already containing similar data for and communication. This will allow researchers to cut on time and effort when studying this particular subject, facilitating the understanding of the basis of the inter-species and inter-kingdom interactions and how it can be modulated to help design alternative and more effective tailored therapies. Finally, data deposition will serve as base for future dataset integration, whose analysis will hopefully give insights into communications in more complex and varied biofilm communities.
现代医学在感染治疗方面正面临巨大挫折,因为微生物不断突破我们为其设置的每一道抗菌防线。考虑到在环境和疾病情况下,微生物都以生物膜群落的形式出现,且往往是多种微生物共存,这种情况就更加令人担忧。这为它们提供了竞争优势,不同物种之间的相互作用改变了宿主的反应、抗菌药物的有效性、微生物的发病机制和毒力,通常会加剧感染的严重程度,并导致对抗生素治疗的耐药性增加。 和 是两种机会性病原体,通常从肺部等粘膜组织的感染中共同分离出来。尽管它们已经共同存在了数十亿年,但这对微生物是一个很好的例子,说明了我们对跨界相互作用知之甚少,特别是在合并感染的背景下。鉴于上述情况,本研究旨在收集、整理和分析所有关于生物膜中 与 相互作用的分子基础的已发表实验信息,以期阐明可能影响感染预后的关键机制,增加这一领域的知识。文献从 PubMed 和 Web of Science 中最佳检索,并根据相关性进行分类。然后对数据进行系统和手动整理、分析,并进一步重建为网络。共注释了这两种病原体之间的 641 种相互作用,输出了影响丝状生长和相关基因和蛋白质等关键毒力机制的重要分子参与者的知识,这些构成了与这些细菌-真菌联合体相关的感染的潜在治疗靶点。还分析了对比相互作用,并强调了群体感应抑制方法。所有注释的数据都在 www.ceb.uminho.pt/ISCTD 上公开可用,该数据库已经包含了 和 通信的类似数据。这将使研究人员在研究这一特定课题时节省时间和精力,有助于理解种间和跨界相互作用的基础以及如何对其进行调节,以帮助设计替代的、更有效的定制疗法。最后,数据的存储将为未来数据集的整合提供基础,其分析有望深入了解更复杂和多样化的生物膜群落中的通讯。