Choong Ferdinand X, Sandoval Ruben M, Molitoris Bruce A, Richter-Dahlfors Agneta
Department of Neuroscience, Swedish Medical Nanoscience Center, Karolinska Institutet, Stockholm, Sweden.
Methods Enzymol. 2012;506:35-61. doi: 10.1016/B978-0-12-391856-7.00027-5.
To understand the underlying mechanisms of bacterial infections, researchers have for long addressed the molecular interactions occurring when the bacterium interacts with host target cells. In these studies, primarily based on in vitro systems, molecular details have been revealed along with increased knowledge regarding the general infection process. With the recent advancements in in vivo imaging techniques, we are now in a position to bridge a transition from classical minimalistic in vitro approaches to allow infections to be studied in its native complexity-the live organ. Techniques such as multiphoton microscopy (MPM) allow cellular-level visualization of the dynamic infection process in real time within the living host. Studies in which all interplaying factors, such as the influences of the immune, lymphatic, and vascular systems can be accounted for, are likely to provide new insights to our current understanding of the infection process. MPM imaging becomes extra powerful when combined with advanced surgical procedure, allowing studies of the illusive early hours of infection. In this chapter, our intention is to provide a general view on how to design and carry out intravital imaging of a bacterial infection. While exemplifying this using a spatiotemporally well-controlled uropathogenic Escherichia coli (UPEC) infection in rat kidneys, we hope to provide the reader with general considerations that can be adapted to other bacterial infections in organs other than the kidney.
为了了解细菌感染的潜在机制,长期以来,研究人员一直在探讨细菌与宿主靶细胞相互作用时发生的分子相互作用。在这些主要基于体外系统的研究中,随着对一般感染过程认识的增加,分子细节也得以揭示。随着体内成像技术的最新进展,我们现在能够实现从经典的简约体外方法到在其天然复杂性——活体器官中研究感染的转变。诸如多光子显微镜(MPM)等技术能够在活体宿主内实时对动态感染过程进行细胞水平的可视化观察。考虑到所有相互作用的因素,如免疫、淋巴和血管系统的影响的研究,可能会为我们当前对感染过程的理解提供新的见解。当与先进的外科手术相结合时,MPM成像变得格外强大,从而能够研究难以捉摸的感染早期阶段。在本章中,我们旨在概述如何设计和进行细菌感染的活体成像。我们以大鼠肾脏中时空控制良好的尿路致病性大肠杆菌(UPEC)感染为例,希望为读者提供一些通用的注意事项,这些注意事项可适用于肾脏以外器官的其他细菌感染。