Buffi Matteo, Cailleau Guillaume, Kuhn Thierry, Li Richter Xiang-Yi, Stanley Claire E, Wick Lukas Y, Chain Patrick S, Bindschedler Saskia, Junier Pilar
Laboratory of Microbiology, University of Neuchâtel, Rue Emile-Argand 11, 2000 Neuchâtel, Switzerland.
Laboratory of Eco-Ethology, University of Neuchâtel, Rue Emile-Argand 11, 2000 Neuchâtel, Switzerland.
Microlife. 2023 Oct 18;4:uqad042. doi: 10.1093/femsml/uqad042. eCollection 2023.
This study presents an inexpensive approach for the macro- and microscopic observation of fungal mycelial growth. The 'fungal drops' method allows to investigate the development of a mycelial network in filamentous microorganisms at the colony and hyphal scales. A heterogeneous environment is created by depositing 15-20 µl drops on a hydrophobic surface at a fixed distance. This system is akin to a two-dimensional (2D) soil-like structure in which aqueous-pockets are intermixed with air-filled pores. The fungus (spores or mycelia) is inoculated into one of the drops, from which hyphal growth and exploration take place. Hyphal structures are assessed at different scales using stereoscopic and microscopic imaging. The former allows to evaluate the local response of regions within the colony (modular behaviour), while the latter can be used for fractal dimension analyses to describe the hyphal network architecture. The method was tested with several species to underpin the transferability to multiple species. In addition, two sets of experiments were carried out to demonstrate its use in fungal biology. First, mycelial reorganization of was assessed as a response to patches containing different nutrient concentrations. Second, the effect of interactions with the soil bacterium on habitat colonization by the same fungus was assessed. This method appeared as fast and accessible, allowed for a high level of replication, and complements more complex experimental platforms. Coupled with image analysis, the fungal drops method provides new insights into the study of fungal modularity both macroscopically and at a single-hypha level.
本研究提出了一种用于宏观和微观观察真菌菌丝体生长的低成本方法。“真菌液滴”法可用于研究丝状微生物在菌落和菌丝尺度上菌丝网络的发育情况。通过在疏水表面以固定距离滴加15 - 20微升液滴来创建异质环境。该系统类似于二维(2D)土壤样结构,其中水囊与充满空气的孔隙相互混合。将真菌(孢子或菌丝体)接种到其中一个液滴中,菌丝从该液滴中生长和扩展。使用立体显微镜和显微镜成像在不同尺度上评估菌丝结构。前者可用于评估菌落内区域的局部反应(模块化行为),而后者可用于分形维数分析以描述菌丝网络结构。该方法在多个物种上进行了测试,以证实其对多种物种的适用性。此外,还进行了两组实验以证明其在真菌生物学中的应用。第一,评估了 对含有不同营养浓度斑块的菌丝体重组情况。第二,评估了与土壤细菌 相互作用对同一真菌栖息地定殖的影响。该方法快速且易于操作,允许进行高水平的重复实验,并补充了更复杂的实验平台。结合图像分析,真菌液滴法在宏观和单菌丝水平上为真菌模块化研究提供了新的见解。