Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA, United States of America.
The One Health Microbiome Center, Huck Institutes of the Life Sciences, The Pennsylvania State University, University Park, PA, United States of America.
PLoS One. 2023 Jul 13;18(7):e0287519. doi: 10.1371/journal.pone.0287519. eCollection 2023.
Most animals establish long-term symbiotic associations with bacteria that are critical for normal host physiology. The symbiosis that forms between the Hawaiian squid Euprymna scolopes and the bioluminescent bacterium Vibrio fischeri serves as an important model system for investigating the molecular mechanisms that promote animal-bacterial symbioses. E. scolopes hatch from their eggs uncolonized, which has led to the development of squid-colonization assays that are based on introducing culture-grown V. fischeri cells to freshly hatched juvenile squid. Recent studies have revealed that strains often exhibit large differences in how they establish symbiosis. Therefore, we sought to develop a simplified and reproducible protocol that permits researchers to determine appropriate inoculum levels and provides a platform to standardize the assay across different laboratories. In our protocol, we adapt a method commonly used for evaluating the infectivity of pathogens to quantify the symbiotic capacity of V. fischeri strains. The resulting metric, the symbiotic dose-50 (SD50), estimates the inoculum level that is necessary for a specific V. fischeri strain to establish a light-emitting symbiosis. Relative to other protocols, our method requires 2-5-fold fewer animals. Furthermore, the power analysis presented here suggests that the protocol can detect up to a 3-fold change in the SD50 between different strains.
大多数动物与对其正常生理功能至关重要的细菌建立长期共生关系。夏威夷乌贼 Euprymna scolopes 与发光细菌 Vibrio fischeri 之间形成的共生关系是研究促进动物-细菌共生关系的分子机制的重要模型系统。E. scolopes 从其未定植的卵中孵化出来,这导致了鱿鱼定植测定的发展,该测定基于将培养的 V. fischeri 细胞引入刚孵化的幼年鱿鱼。最近的研究表明,菌株在建立共生关系方面通常表现出很大的差异。因此,我们试图开发一种简化且可重复的方案,使研究人员能够确定适当的接种水平,并为不同实验室的测定提供标准化平台。在我们的方案中,我们采用了一种常用于评估病原体感染力的方法来量化 V. fischeri 菌株的共生能力。由此产生的度量标准,共生剂量 50(SD50),估计了特定 V. fischeri 菌株建立发光共生关系所需的接种水平。与其他方案相比,我们的方法需要的动物数量减少了 2-5 倍。此外,这里提出的功效分析表明,该方案可以检测到不同菌株之间 SD50 的变化高达 3 倍。