Abstract

Studies of unculturable microbes often combine methods, such as 16S rRNA sequencing, metagenomics, and metaproteomics. To apply these techniques to the microbial community inhabiting the surfaces of marine macrophytes, it is advisable to perform a selective DNA and protein isolation prior to the analysis to avoid biases due to the host material being present in high quantities. Two protocols for DNA and protein isolation were adapted for selective extractions of DNA and proteins from epiphytic communities inhabiting the surfaces of two marine macrophytes, the seagrass Cymodocea nodosa and the macroalga Caulerpa cylindracea. Protocols showed an almost complete removal of the epiphytic community regardless of the sampling season, station, settlement, or host species. The obtained DNA was suitable for metagenomic and 16S rRNA sequencing, while isolated proteins could be identified by mass spectrometry. Low presence of host DNA and proteins in the samples indicated a high specificity of the protocols. The procedures are based on universally available laboratory chemicals making the protocols widely applicable. Taken together, the adapted protocols ensure an almost complete removal of the macrophyte epiphytic community. The procedures are selective for microbes inhabiting macrophyte surfaces and provide DNA and proteins applicable in 16S rRNA sequencing, metagenomics, and metaproteomics.

Highlights

  • Surfaces of marine macrophytes are colonized by a diverse microbial community whose structure and function are poorly understood (Egan et al, 2013)

  • To assess the removal efficiency of the DNA and protein isolation procedures, leaves and thalli were examined under a confocal microscope before and after treatments were performed

  • To evaluate whether the obtained DNA is suitable to determine the composition of the microbial community, Illumina sequencing of the V4 region of the 16S rRNA was performed

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Summary

Introduction

Surfaces of marine macrophytes are colonized by a diverse microbial community whose structure and function are poorly understood (Egan et al, 2013). As

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