Department of Embryology, Carnegie Institution for Science.
Department of Embryology, Carnegie Institution for Science; Department of Biology, Johns Hopkins University;
J Vis Exp. 2023 Jan 13(191). doi: 10.3791/64298.
The intestines of animals are colonized by commensal microbes, which impact host development, health, and behavior. Precise quantification of colonization is essential for studying the complex interactions between host and microbe both to validate the microbial composition and study its effects. Drosophila melanogaster, which has a low native microbial diversity and is economical to rear with defined microbial composition, has emerged as a model organism for studying the gut microbiome. Analyzing the microbiome of an individual organism requires identification of which microbial species are present and quantification of their absolute abundance. This article presents a method for the analysis of a large number of individual fly microbiomes. The flies are prepared in 96-well plates, enabling the handling of a large number of samples at once. Microbial abundance is quantified by plating up to 96 whole fly homogenates on a single agar plate in an array of spots and then counting the colony forming units (CFUs) that grow in each spot. This plating system is paired with an automated CFU quantification platform, which incorporates photography of the plates, differentiation of fluorescent colonies, and automated counting of the colonies using an ImageJ plugin. Advantages are that (i) this method is sensitive enough to detect differences between treatments, (ii) the spot plating method is as accurate as traditional plating methods, and (iii) the automated counting process is accurate and faster than manual counting. The workflow presented here enables high-throughput quantification of CFUs in a large number of replicates and can be applied to other microbiology study systems including in vitro and other small animal models.
动物的肠道中定植着共生微生物,这些微生物会影响宿主的发育、健康和行为。精确量化定植对于研究宿主与微生物之间的复杂相互作用至关重要,既可以验证微生物组成,也可以研究其影响。黑腹果蝇具有较低的天然微生物多样性,并且可以用定义明确的微生物组成进行经济地饲养,因此已成为研究肠道微生物组的模式生物。分析单个生物体的微生物组需要确定存在哪些微生物物种,并对其绝对丰度进行量化。本文介绍了一种分析大量个体蝇微生物组的方法。将蝇准备在 96 孔板中,能够一次性处理大量样本。通过在单个琼脂平板上的阵列点中接种多达 96 个完整蝇匀浆,从而定量微生物丰度,并计算每个点中生长的菌落形成单位(CFU)的数量。该平板系统与自动化 CFU 定量平台相结合,该平台整合了平板摄影、荧光菌落的区分以及使用 ImageJ 插件自动对菌落进行计数。该方法的优点在于:(i)该方法足够灵敏,可以检测处理之间的差异;(ii)点板法与传统平板法一样准确;(iii)自动化计数过程比手动计数更准确、更快。这里提出的工作流程可以在大量重复中实现 CFU 的高通量定量,并且可以应用于其他微生物学研究系统,包括体外和其他小动物模型。