Abedon Stephen T
Department of Microbiology, The Ohio State University, Mansfield, OH 44906, USA.
Drugs Drug Candidates. 2023 Sep;2(3):673-688. doi: 10.3390/ddc2030034. Epub 2023 Aug 18.
Bacteriophages (phages) are viruses of bacteria and have been used as antibacterial agents now for over one-hundred years. The primary pharmacodynamics of therapeutic phages can be summed up as follows: phages at a certain concentration can reach bacteria at a certain rate, attach to bacteria that display appropriate receptors on their surfaces, infect, and (ideally) kill those now-adsorbed bacteria. Here, I consider the rate at which phages reach bacteria, during what can be dubbed as an 'extracellular search'. This search is driven by diffusion and can be described by what is known as the phage adsorption rate constant. That constant in turn is thought to be derivable from knowledge of bacterial size, virion diffusion rates, and the likelihood of phage adsorption given this diffusion-driven encounter with a bacterium. Here, I consider only the role of bacterial size in encounter rates. In 1932, Schlesinger hypothesized that bacterial size can be described as a function of cell radius (, or ), as based on the non-phage-based theorizing of Smoluchowski (1917). The surface area of a cell-what is actually encountered-varies however instead as a function . Here, I both provide and review evidence indicating that Schlesinger's assertion seems to have been correct.
噬菌体是细菌病毒,作为抗菌剂已被使用了一百多年。治疗性噬菌体的主要药效学可总结如下:一定浓度的噬菌体能够以一定速率到达细菌,附着在其表面具有合适受体的细菌上,进行感染,并(理想情况下)杀死这些现已吸附的细菌。在此,我考虑在所谓的“细胞外搜索”过程中噬菌体到达细菌的速率。这种搜索由扩散驱动,可以用所谓的噬菌体吸附速率常数来描述。反过来,这个常数被认为可以从细菌大小、病毒体扩散速率以及在这种由扩散驱动的与细菌相遇情况下噬菌体吸附的可能性等知识推导出来。在此,我仅考虑细菌大小在相遇速率中的作用。1932年,施莱辛格假设细菌大小可以描述为细胞半径( ,或 )的函数,这是基于斯莫卢霍夫斯基(1917年)基于非噬菌体的理论。然而,细胞的实际被接触到的表面积却随 函数变化。在此,我既提供又审视证据,表明施莱辛格的断言似乎是正确的。