Succession of microbial community composition and secondary metabolism during marine biofilm development

Author:

Bech Pernille Kjersgaard1,Jarmusch Scott A1,Rasmussen Jacob Agerbo2,Limborg Morten Tønsberg2,Gram Lone1,Henriksen Nathalie N Suhr Eiris1

Affiliation:

1. Department of Biotechnology and Biomedicine, Technical University of Denmark , Kgs. Lyngby, DK-2800 , Denmark

2. Center for Evolutionary Hologenomics, GLOBE Institute, University of Copenhagen , Copenhagen K, DK-1014 , Denmark

Abstract

Abstract In nature, secondary metabolites mediate interactions between microorganisms residing in complex microbial communities. However, the degree to which community dynamics can be linked to secondary metabolite potential remains largely unknown. In this study, we address the relationship between community succession and secondary metabolism variation. We used 16S and 18S rRNA gene and adenylation domain amplicon sequencing, genome-resolved metagenomics, and untargeted metabolomics to track the taxons, biosynthetic gene clusters, and metabolome dynamics in situ of microorganisms during marine biofilm succession over 113 days. Two phases were identified during the community succession, with a clear shift around Day 29, where the alkaloid secondary metabolites, pseudanes, were also detected. The microbial secondary metabolite potential changed between the phases, and only a few community members, including Myxococotta spp., were responsible for the majority of the biosynthetic gene cluster potential in the early succession phase. In the late phase, bryozoans and benthic copepods were detected, and the microbial nonribosomal peptide potential drastically decreased in association with a reduction in the relative abundance of the prolific secondary metabolite producers. Conclusively, this study provides evidence that the early succession of the marine biofilm community favors prokaryotes with high nonribosomal peptide synthetase potential. In contrast, the late succession is dominated by multicellular eukaryotes and a reduction in bacterial nonribosomal peptide synthetase potential.

Funder

Danish National Research Foundation for the Center for Microbial Secondary Metabolites

Center for Evolutionary Hologenomics

Novo Nordisk Foundation

Publisher

Oxford University Press (OUP)

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