Absolute quantification of synthetic microbial communities using a simplified multiplexed ddPCR method
Fatima Ceballos Rodriguez-Conde, Anastasia Fischer, Ryan Mellor, Gary Lye, Duygu DikiciogluABSTRACT
Synthetic microbial communities provide experimentally tractable systems for studying community assembly, stability, and function and for integrating quantitative experiments with mathematical models of community dynamics. These applications require accurate and reproducible absolute quantification of individual community members, yet commonly used methods rely on relative abundance measurements or suffer from amplification bias and limited reproducibility. Here, we present a simplified and scalable multiplexed digital droplet PCR-based workflow for absolute quantification of species abundance in synthetic microbial communities. Using a four-member community composed of
IMPORTANCE
Mechanistic understanding of microbial communities increasingly depends on quantitative data that can be directly compared across experiments and used to parameterize mathematical models. However, simple methods for measuring the absolute abundance of individual species in synthetic microbial communities remain limited. We describe an accessible multiplexed digital droplet polymerase chain reaction workflow that enables direct and reproducible cell quantification in a defined microbial consortium. Unlike methods developed for microbial diagnostics or clinical testing, this approach is optimized for experimental reproducibility and quantitative modeling in well-defined microbial consortia rather than for broad-spectrum detection or regulatory validation. By supporting accurate absolute quantification, this framework strengthens integration between experimental and theoretical studies aimed at explaining how microbial communities are established and maintained.