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DeRito, C. M.

Publications and source records attributed to DeRito, C. M..

2 recordsLinked to original sources

Phenolic acid-degrading Paraburkholderia prime decomposition in forest soil

Plant-derived phenolic acids are metabolized by soil microorganisms whose activity may enhance the decomposition of soil organic carbon (SOC). We characterized whether phenolic acid-degrading bacteria would enhance SOC mineralization in forest soils when primed with 13C-labeled p-hydroxybenzoic acid (PHB). We further investigated whether PHB-induced priming could explain differences in SOC content among mono-specific tree plantations in a 70-year-old common garden experiment. The activity of Paraburkholderia and Caballeronia dominated PHB degradation in all soils regardless of tree species or soil type. We isolated the principal PHB-degrading phylotype (Paraburkholderia madseniana RP11T), which encoded numerous oxidative enzymes, including secretion signal-bearing laccase, aryl-alcohol oxidase and DyP-type peroxidase, and confirmed its ability to degrade phenolics. The addition of PHB to soil led to significant enrichment (23-fold) of the RP11T phylotype (RP11ASV), as well as enrichment of other phylotypes of Paraburkholderia and Caballeronia. Metabolism of PHB primed significant loss of SOC (3 to 13 {micro}mols C g-1 dry wt soil over 7 days). In contrast, glucose addition reduced SOC mineralization (-3 to -8 {micro}mols C g-1 dry wt soil over 7 days). RP11ASV abundance and the expression of PHB monooxygenase (pobA) correlated with PHB respiration and were inversely proportional to SOC content in the field. We propose that plant-derived phenolics stimulate the activity of phenolic acid-degrading bacteria thereby causing soil priming and SOC loss. We show that Burkholderiaceae dominate soil priming in diverse forest soils and this observation counters the prevailing view that priming phenomena are a generalized non-specific response of community metabolism.

microbiology

Evidence for boundary layer oxygen diffusion limitation as a key driver of asteroid wasting

Sea star wasting disease describes a condition affecting asteroids that resulted in significant Northeastern Pacific population decline following a mass mortality event in 2013. The etiology of sea star wasting is unresolved. We hypothesized that asteroid wasting is a sequela of microbial organic matter remineralization near respiratory surfaces which leads to boundary layer oxygen diffusion limitation (BLODL). Wasting lesions were induced in Pisaster ochraceus by enrichment with a variety of organic matter (OM) sources and by experimentally reduced oxygen conditions. Microbial assemblages inhabiting tissues and at the asteroid-water interface bore signatures of copiotroph proliferation before wasting onset, followed by the proliferation of putatively facultative and strictly anaerobic taxa. These results together illustrate that suboxic conditions at the animal-water interface may be established by heterotrophic bacterial activity in response to organic matter loading. Wasting susceptibility was significantly and positively correlated with rugosity, a key determinant of boundary layer thickness. At a semi-continuously monitored field site (Langley Harbor), wasting predictably occurred at annual peak or decline in phytoplankton biomass over 5 years, suggesting that primary production-derived OM may contribute to BLODL. Finally, wasting individuals from 2013 - 2014 bore stable isotopic signatures reflecting anaerobic processes which suggests that this phenomenon may have affected asteroids during mass mortality. The impacts of BLODL may be more pronounced under higher temperatures due to lower O2 solubility, in more rugose asteroid species due to restricted hydrodynamic flow, and in larger specimens due to their lower surface area to volume ratios which affects diffusive respiratory potential. Moreover, our results demonstrate that marine invertebrate disease may result from heterotrophic microbial activity that occurs adjacent to respiratory tissues, which raises important questions about the etiology of marine diseases in other benthic taxa.

ecology