Parker Matthew F L, Flavell Robert R, Luu Justin M, Rosenberg Oren S, Ohliger Michael A, Wilson David M
Department of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, California 94158, United States.
Department of Medicine, University of California, San Francisco, San Francisco, California 94158, United States.
ACS Infect Dis. 2020 Jul 10;6(7):1587-1598. doi: 10.1021/acsinfecdis.9b00515. Epub 2020 Jun 9.
This review highlights recent efforts to detect bacteria using engineered small molecules that are processed and incorporated similarly to their natural counterparts. There are both scientific and clinical justifications for these endeavors. The use of detectable, cell-wall targeted chemical probes has elucidated microbial behavior, with several fluorescent labeling methods in widespread laboratory use. Furthermore, many existing efforts including ours, focus on developing new imaging tools to study infection in clinical practice. The bacterial cell wall, a remarkably rich and complex structure, is an outstanding target for bacteria-specific detection. Several cell wall components are found in bacteria but not mammals, especially peptidoglycan, lipopolysaccharide, and teichoic acids. As this review highlights, the development of laboratory tools for fluorescence microscopy has vastly outstripped related positron emission tomography (PET) or single photon emission computed tomography (SPECT) radiotracer development. However, there is great synergy between these chemical strategies, which both employ mimicry of endogenous substrates to incorporate detectable structures. As the field of bacteria-specific imaging grows, it will be important to understand the mechanisms involved in microbial incorporation of radionuclides. Additionally, we will highlight the clinical challenges motivating this imaging effort.
本综述重点介绍了近期利用工程小分子检测细菌的努力,这些小分子的处理和整合方式与其天然对应物相似。这些努力既有科学依据,也有临床依据。使用可检测的、靶向细胞壁的化学探针已经阐明了微生物的行为,有几种荧光标记方法在广泛的实验室中使用。此外,包括我们在内的许多现有努力都集中在开发新的成像工具,以研究临床实践中的感染情况。细菌细胞壁是一个非常丰富和复杂的结构,是细菌特异性检测的一个突出靶点。在细菌中发现了几种细胞壁成分,但在哺乳动物中没有,特别是肽聚糖、脂多糖和磷壁酸。正如本综述所强调的,用于荧光显微镜的实验室工具的发展远远超过了相关的正电子发射断层扫描(PET)或单光子发射计算机断层扫描(SPECT)放射性示踪剂的发展。然而,这些化学策略之间有很大的协同作用,它们都采用模仿内源性底物来整合可检测结构。随着细菌特异性成像领域的发展,了解微生物摄取放射性核素所涉及的机制将很重要。此外,我们将强调推动这种成像努力的临床挑战。