Price Sarah L, Oakes Robert S, Gonzalez Rodrigo J, Edwards Camilla, Brady Amanda, DeMarco Jennifer K, von Andrian Ulrich H, Jewell Christopher M, Lawrenz Matthew B
Department of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, KY 40202, USA.
Fischell Department of Bioengineering, University of Maryland, College Park, MD 20742, USA.
iScience. 2023 Nov 30;27(1):108600. doi: 10.1016/j.isci.2023.108600. eCollection 2024 Jan 19.
Fleas transmit directly within the dermis of mammals to cause bubonic plague. Syringe-mediated inoculation is widely used to recapitulate bubonic plague and study pathogenesis. However, intradermal needle inoculation is tedious, error prone, and poses a significant safety risk for laboratorians. Microneedle arrays (MNAs) are micron-scale polymeric structures that deliver materials to the dermis, while minimizing the risk of needle sticks. We demonstrated that MNA inoculation is a viable strategy to recapitulate bubonic plague and study bacterial virulence by defining the parameters needed to establish a lethal infection in the mouse model and characterizing the course of infection using live-animal optical imaging. Using MNAs, we also demonstrated that must overcome calprotectin-mediated zinc restriction within the dermis and dermal delivery of an attenuated mutant has vaccine potential. Together, these data demonstrate that MNAs are a safe alternative to study pathogenesis in the laboratory.
跳蚤在哺乳动物真皮内直接传播可引发腺鼠疫。注射器介导接种被广泛用于模拟腺鼠疫并研究发病机制。然而,皮内针刺接种繁琐、易出错,且给实验室工作人员带来重大安全风险。微针阵列(MNAs)是微米级的聚合物结构,可将物质输送到真皮,同时将针刺风险降至最低。我们证明,通过确定在小鼠模型中建立致死性感染所需的参数,并利用活体动物光学成像表征感染过程,微针阵列接种是模拟腺鼠疫和研究细菌毒力的可行策略。使用微针阵列,我们还证明了[此处原文似乎不完整]必须克服真皮内钙卫蛋白介导的锌限制,并且减毒突变体的真皮递送具有疫苗潜力。总之,这些数据表明微针阵列是在实验室研究发病机制的安全替代方法。