Division of Advanced Materials, Instituto Potosino de Investigación Científica y Tecnológica, Camino a la Presa San José 2055, 78216 San Luis Potosí, Mexico.
Division of Advanced Materials, Instituto Potosino de Investigación Científica y Tecnológica, Camino a la Presa San José 2055, 78216 San Luis Potosí, Mexico.
Fungal Genet Biol. 2021 May;150:103549. doi: 10.1016/j.fgb.2021.103549. Epub 2021 Mar 4.
The evaluation of morphology is fundamental to comprehend how fungi grow, develop, and interact with the environment. Although fungal growth has been extensively studied associated to two-dimensional geometries, lack of appropriate experimental tools has limited exploration of the complex three-dimensional (3D) structures exhibited by mycelia in more general contexts. In this paper, we report the construction of a light-sheet fluorescence microscope (LSFM) capable of performing time-lapse visualization of 3D biological structures (4D microscopy), and the use of this instrument to follow the dynamics of fungal growth. LSFM uses scanning of selective plane illumination and digital reconstruction to provide 3D images of the specimen. We describe the optical, electronic, and computational means to implement two-color LSFM, and provide detailed procedures for aligning and testing the setup. We successfully demonstrate use of both autofluorescence and specific tagging to image Trichoderma atroviride and Neurospora crassa strains growing in liquid media, over extended times (12 h) and volumes (400 × 1500 × 800 μm) at single-hypha resolution. The excellent image contrast provided by LSFM enables us to visualize the dynamics of mycelial architecture, interactions among hyphae, and measure rates of 3D apical extension. Altogether, our work shows a powerful imaging tool to perform 3D morphological analysis of fungi, from hyphae to mycelium.
形态评估对于理解真菌的生长、发育以及与环境的相互作用至关重要。尽管真菌的生长已经在二维几何形状方面得到了广泛研究,但缺乏适当的实验工具限制了对菌丝在更广泛背景下所表现出的复杂三维(3D)结构的探索。在本文中,我们报告了一种构建能够对 3D 生物结构进行延时可视化(4D 显微镜)的光片荧光显微镜(LSFM)的方法,并利用该仪器来跟踪真菌生长的动态。LSFM 通过选择性平面照明的扫描和数字重建来提供标本的 3D 图像。我们描述了实现双色 LSFM 的光学、电子和计算手段,并提供了对齐和测试设置的详细步骤。我们成功地展示了使用自发荧光和特定标记对在液体培养基中生长的深绿木霉和粗糙脉孢菌菌株进行成像的方法,在单根菌丝分辨率下,能够对长达约 12 小时和体积约 400×1500×800μm 的样本进行扩展时间和体积的成像。LSFM 提供的优异图像对比度使我们能够可视化菌丝体结构的动态、菌丝之间的相互作用,并测量 3D 顶端延伸的速率。总的来说,我们的工作展示了一种强大的成像工具,可用于对真菌进行 3D 形态分析,从菌丝到菌丝体。