Dominique C S Evans, Eero J Raittio, Marie B Lund, Rikke L Meyer, Sebastian Schlafer, Mathilde F Kristensen
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引用次数: 0
Abstract
Extracellular DNA (eDNA) is a ubiquitous component of the extracellular matrix of bacterial biofilms, which has been proposed to act as a proton trap. Locally trapped protons will influence the pH of biofilms on the microscale; therefore, we developed a method for correlative imaging of both pH and eDNA microarchitecture in biofilms. We used multispecies dental biofilms inoculated from pooled saliva as a complex biofilm model where it is known that the local pH and matrix composition can vary substantially. We combined correlative imaging of pH and eDNA with analysis of biofilm composition by 16S rRNA sequencing to investigate the association between local pH and abundance of eDNA, and whether biofilm age, sucrose supplementation during biofilm growth, or microbial composition affected this association. Biofilms grown in the presence of sucrose showed significantly lower pH and higher abundance of eDNA than biofilms grown in the absence of sucrose, although pH and the abundance of eDNA were not correlated at the microscale in similarly treated biofilms. The effect was more pronounced in mature four-day old biofilms compared to younger two-day old biofilms. The abundance of streptococci and lactobacilli increased in more acidic biofilms, and we propose that increases in polysaccharides produced in acidogenic and aciduric biofilms are responsible for the increased abundance of eDNA in the biofilm matrix, which points towards complex interactions linking the biofilm matrix composition to dental caries development.
期刊介绍:
The Journal of Microbiological Methods publishes scholarly and original articles, notes and review articles. These articles must include novel and/or state-of-the-art methods, or significant improvements to existing methods. Novel and innovative applications of current methods that are validated and useful will also be published. JMM strives for scholarship, innovation and excellence. This demands scientific rigour, the best available methods and technologies, correctly replicated experiments/tests, the inclusion of proper controls, calibrations, and the correct statistical analysis. The presentation of the data must support the interpretation of the method/approach.
All aspects of microbiology are covered, except virology. These include agricultural microbiology, applied and environmental microbiology, bioassays, bioinformatics, biotechnology, biochemical microbiology, clinical microbiology, diagnostics, food monitoring and quality control microbiology, microbial genetics and genomics, geomicrobiology, microbiome methods regardless of habitat, high through-put sequencing methods and analysis, microbial pathogenesis and host responses, metabolomics, metagenomics, metaproteomics, microbial ecology and diversity, microbial physiology, microbial ultra-structure, microscopic and imaging methods, molecular microbiology, mycology, novel mathematical microbiology and modelling, parasitology, plant-microbe interactions, protein markers/profiles, proteomics, pyrosequencing, public health microbiology, radioisotopes applied to microbiology, robotics applied to microbiological methods,rumen microbiology, microbiological methods for space missions and extreme environments, sampling methods and samplers, soil and sediment microbiology, transcriptomics, veterinary microbiology, sero-diagnostics and typing/identification.