Institut Fresnel, CNRS, Aix Marseille University, Centrale Marseille, Marseille, France.
Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), Gif-sur-Yvette, France.
Biophys J. 2023 Aug 8;122(15):3159-3172. doi: 10.1016/j.bpj.2023.06.020. Epub 2023 Jun 30.
Quantitative phase microscopy (QPM) represents a noninvasive alternative to fluorescence microscopy for cell observation with high contrast and for the quantitative measurement of dry mass (DM) and growth rate at the single-cell level. While DM measurements using QPM have been widely conducted on mammalian cells, bacteria have been less investigated, presumably due to the high resolution and high sensitivity required by their smaller size. This article demonstrates the use of cross-grating wavefront microscopy, a high-resolution and high-sensitivity QPM, for accurate DM measurement and monitoring of single microorganisms (bacteria and archaea). The article covers strategies for overcoming light diffraction and sample focusing, and introduces the concepts of normalized optical volume and optical polarizability (OP) to gain additional information beyond DM. The algorithms for DM, optical volume, and OP measurements are illustrated through two case studies: monitoring DM evolution in a microscale colony-forming unit as a function of temperature, and using OP as a potential species-specific signature.
定量相位显微镜(QPM)代表了一种非侵入性的荧光显微镜替代方法,可用于高对比度的细胞观察,以及在单细胞水平上对干物质(DM)和生长速率进行定量测量。虽然 QPM 已广泛用于哺乳动物细胞的 DM 测量,但对细菌的研究较少,这可能是由于其较小的尺寸需要更高的分辨率和灵敏度。本文展示了用于准确测量 DM 和监测单个微生物(细菌和古菌)的交叉光栅波前显微镜,一种高分辨率和高灵敏度的 QPM。本文涵盖了克服光衍射和样品聚焦的策略,并介绍了归一化光体积和光极化率(OP)的概念,以获得除 DM 之外的额外信息。通过两个案例研究说明了 DM、光学体积和 OP 测量的算法:监测微尺度集落形成单位中 DM 随温度的演变,以及将 OP 用作潜在的种特异性特征。