An experimental model system to investigate microscale mechanisms behind the soil priming effect

Abstract

The soil priming effect plays an important role in the global carbon cycle. Although well-studied, the mechanisms behind it remain elusive. So far, studies measured the phenomenon at the bulk soil scale, neglecting that it arises from spatially explicit processes that take place at the microscale. Here, we present a novel approach using a microfluidic device to directly assess the response of soil microbes living on a patch of complex substrate to a pulse of easily available substrate. Using time-resolved fluorescence microscopy, we tracked motility, position, shape characteristics and attached biomass of green fluorescent protein expressing Bacillus subtilis cells living on a transparent carboxymethylcellulose substrate patch exposed to a pulse of growth medium with differing concentrations. Assessing CMC decomposition via Congo-Red staining after 42 days of incubations with constant observation, we observed increased decomposition upon addition of enough labile substrate, resembling a priming effect. The pulse triggered a transient increase in bacterial motility, indicating the formation of exploring and growing subpopulations respectively. We observed a concentration-dependent growth response, resulting in different behaviors. High concentrations led to high biomass and decomposition of CMC, however growth was quickly limited, possibly by depletion of necessary nutrients and waste accumulation. Intermediate concentration, however, resulted in a more sustained attached biomass, that showed evidence of spatial self-organization, leading to similar decomposition. We present a novel experimental model system to study the behavior of soil microbes decomposing complex substrate and provide a unique view into the response of such a population to a labile substrate pulse.