Géosciences Montpellier, University Montpellier 2, CNRS, Montpellier, France.
PLoS One. 2013 Apr 12;8(4):e61663. doi: 10.1371/journal.pone.0061663. Print 2013.
We present a study about AFM imaging of living, moving or self-immobilized bacteria in their genuine physiological liquid medium. No external immobilization protocol, neither chemical nor mechanical, was needed. For the first time, the native gliding movements of Gram-negative Nostoc cyanobacteria upon the surface, at speeds up to 900 µm/h, were studied by AFM. This was possible thanks to an improved combination of a gentle sample preparation process and an AFM procedure based on fast and complete force-distance curves made at every pixel, drastically reducing lateral forces. No limitation in spatial resolution or imaging rate was detected. Gram-positive and non-motile Rhodococcus wratislaviensis bacteria were studied as well. From the approach curves, Young modulus and turgor pressure were measured for both strains at different gliding speeds and are ranging from 20±3 to 105±5 MPa and 40±5 to 310±30 kPa depending on the bacterium and the gliding speed. For Nostoc, spatially limited zones with higher values of stiffness were observed. The related spatial period is much higher than the mean length of Nostoc nodules. This was explained by an inhomogeneous mechanical activation of nodules in the cyanobacterium. We also observed the presence of a soft extra cellular matrix (ECM) around the Nostoc bacterium. Both strains left a track of polymeric slime with variable thicknesses. For Rhodococcus, it is equal to few hundreds of nanometers, likely to promote its adhesion to the sample. While gliding, the Nostoc secretes a slime layer the thickness of which is in the nanometer range and increases with the gliding speed. This result reinforces the hypothesis of a propulsion mechanism based, for Nostoc cyanobacteria, on ejection of slime. These results open a large window on new studies of both dynamical phenomena of practical and fundamental interests such as the formation of biofilms and dynamic properties of bacteria in real physiological conditions.
我们展示了一项关于在其真实生理液体介质中对活的、移动的或自固定的细菌进行原子力显微镜(AFM)成像的研究。不需要外部固定化协议,无论是化学的还是机械的。我们首次通过 AFM 研究了革兰氏阴性念珠藻在表面上以高达 900 µm/h 的速度滑行的固有运动。这得益于一种温和的样品制备过程和一种 AFM 程序的改进组合,该程序基于快速和完全的力-距离曲线在每个像素上进行,大大降低了侧向力。没有检测到空间分辨率或成像率的限制。革兰氏阳性和非运动性的罗德里格斯氏菌也被研究了。从接近曲线中,我们测量了两种菌株在不同滑行速度下的杨氏模量和膨压,其值范围为 20±3 至 105±5 MPa 和 40±5 至 310±30 kPa,具体取决于细菌和滑行速度。对于念珠藻,观察到了具有更高刚度值的空间限制区域。相关的空间周期远高于念珠藻节的平均长度。这可以通过蓝藻中节的不均匀机械激活来解释。我们还观察到在念珠藻周围存在柔软的细胞外基质(ECM)。两种菌株都留下了一层厚度可变的聚合物粘液。对于罗德里格斯氏菌,其厚度约为几百纳米,可能有助于其与样品的粘附。在滑行过程中,念珠藻分泌一层粘液层,其厚度在纳米范围内,并随滑行速度增加而增加。这一结果加强了基于粘液喷射的念珠藻推进机制的假设。这些结果为在实际生理条件下研究生物膜形成和细菌动态特性等具有实际和基础意义的动力学现象提供了广阔的研究窗口。