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Molecular Ecology · 2024 · Vol. 33 · Issue 18 · Wiley
Skin microbiomes provide vital functions, yet knowledge about the drivers and processes structuring their species assemblages is limited—especially for non‐model organisms. In this study, fish skin microbiome was assessed by high throughput sequencing of amplicon sequence variants from metabarcoding of V3–V4 regions in the 16S rRNA gene on fish hosts subjected to the following experimental manipulations: (i) translocation betw...
Frontiers in Marine Science · 2024 · Vol. 10 · Frontiers
Coastal upwelling areas are extraordinarily productive environments where prokaryotic communities, the principal remineralizers of dissolved organic matter (DOM), rapidly respond to phytoplankton bloom and decay dynamics. Nevertheless, the extent of variability of key microbial functions in such dynamic waters remains largely unconstrained. Our metatranscriptomics analyses of 162 marker genes encoding ecologically relevant pro...
Environmental Microbiology · 2023 · Vol. 25 · Issue 9 · Wiley
Cluster 5 picocyanobacteria significantly contribute to primary productivity in aquatic ecosystems. Estuarine populations are highly diverse and consist of many co‐occurring strains, but their physiology remains largely understudied. In this study, we characterized 17 novel estuarine picocyanobacterial strains. Phylogenetic analysis of the 16S rRNA and pigment genes ( cpcB and cpeBA ) uncovered multiple estuarine and freshwate...
Environmental Microbiology · 2023 · Vol. 25 · Issue 3 · Wiley
The distribution of prokaryotic metabolism between maintenance and growth activities has a profound impact on the transformation of carbon substrates to either biomass or CO 2 . Knowledge of key factors influencing prokaryotic maintenance respiration is, however, highly limited. This mesocosm study validated the significance of prokaryotic maintenance respiration by mimicking temperature and nutrients within levels representat...
Limnology and Oceanography · 2022 · Vol. 67 · Issue 1 · Wiley
Human‐induced expansion of oxygen‐deficient zones can have dramatic impacts on marine systems and its resident biota. One example is the formation of the potent neurotoxic methylmercury (MeHg) that is mediated by microbial methylation of inorganic divalent Hg (Hg II ) under oxygen‐deficient conditions. A negative consequence of the expansion of oxygen‐deficient zones could be an increase in MeHg production due to shifts in mic...
Environmental Microbiology · 2021 · Vol. 23 · Issue 8 · Wiley
Summary Climate change is projected to cause increased inflow of terrestrial dissolved organic matter to coastal areas in northerly regions. Estuarine bacterial community will thereby receive larger loads of organic matter and inorganic nutrients available for microbial metabolism. The composition of the bacterial community and its ecological functions may thus be affected. We studied the responses of bacterial community to in...
Environmental Microbiology · 2021 · Vol. 23 · Issue 8 · Wiley
Summary Phage predation constitutes a major mortality factor for bacteria in aquatic ecosystems, and thus, directly impacts nutrient cycling and microbial community dynamics. Yet, the population dynamics of specific phages across time scales from days to months remain largely unexplored, which limits our understanding of their influence on microbial succession. To investigate temporal changes in diversity and abundance of phag...
Environmental Microbiology · 2021 · Vol. 23 · Issue 3 · Wiley
Summary Cobalamin (B12) is an essential cofactor that is exclusively synthesized by some prokaryotes while many prokaryotes and eukaryotes require an external supply of B12. The spatial and temporal availability of B12 is poorly understood in marine ecosystems. Field measurements of B12 along with a large set of ancillary biotic and abiotic factors were obtained during three oceanographic cruises in the NW Iberian Peninsula, c...
Environmental Microbiology · 2019 · Vol. 21 · Issue 4 · Wiley
Summary Thousands of semi‐volatile hydrophobic organic pollutants (OPs) reach open oceans through atmospheric deposition, causing a chronic and ubiquitous pollution by anthropogenic dissolved organic carbon (ADOC). Hydrophobic ADOC accumulates in cellular lipids, inducing harmful effects on marine biota, and can be partially prone to microbial degradation. Unfortunately, their possible effects on microorganisms, key drivers of...
Environmental Microbiology · 2019 · Vol. 21 · Issue 2 · Wiley
Summary The taxonomy of marine and non‐marine organisms rarely overlap, but the mechanisms underlying this distinction are often unknown. Here, we predicted three major ocean‐to‐land transitions in the evolutionary history of Flavobacteriaceae , a family known for polysaccharide and peptide degradation. These unidirectional transitions were associated with repeated losses of marine signature genes and repeated gains of non‐mar...
Environmental Microbiology · 2017 · Vol. 19 · Issue 6 · Wiley
Summary Much of the phenotype of a microorganism consists of its repertoire of metabolisms and how and when its proteins are deployed under different growth conditions. Hence, analyses of protein expression could provide important understanding of how bacteria adapt to different environmental settings. To characterize the flexibility of proteomes of marine bacteria, we investigated protein profiles of three important marine ba...
Environmental Microbiology · 2017 · Vol. 19 · Issue 3 · Wiley
Summary Metapopulation theory developed in terrestrial ecology provides applicable frameworks for interpreting the role of local and regional processes in shaping species distribution patterns. Yet, empirical testing of metapopulation models on microbial communities is essentially lacking. We determined regional bacterioplankton dynamics from monthly transect sampling in the Baltic Sea Proper using 16S rRNA gene sequencing. A...
Environmental Microbiology · 2016 · Vol. 18 · Issue 12 · Wiley
Summary Rhodopsins are light‐driven ion‐pumping membrane proteins found in many organisms and are proposed to be of global importance for oceanic microbial energy generation. Several studies have focused on marine environments, with less exploration of rhodopsins in brackish waters. We investigated microbial rhodopsins in the Baltic Sea using size‐fractionated metagenomic and metatranscriptomic datasets collected along a salin...
Environmental Microbiology · 2015 · Vol. 17 · Issue 7 · Wiley
Summary Multiyear comparisons of bacterioplankton succession reveal that environmental conditions drive community shifts with repeatable patterns between years. However, corresponding insight into bacterioplankton dynamics at a temporal resolution relevant for detailed examination of variation and characteristics of specific populations within years is essentially lacking. During 1 year, we collected 46 samples in the B altic...
Limnology and Oceanography · 2013 · Vol. 58 · Issue 3 · Wiley
Despite representing only a small fraction of the ocean's dissolved organic matter pool, dissolved free amino acids (DFAA) have high turnover rates and are major nitrogen and carbon sources for bacterioplankton. Both phytoplankton and bacterioplankton assimilate and release DFAA, but their consumption and production are difficult to quantify in nature due to their short residence times (min) as dissolved monomers. We segregate...
Environmental Microbiology · 2013 · Vol. 15 · Issue 5 · Wiley
Summary Proteorhodopsin ( PR ), a ubiquitous membrane photoprotein in marine environments, acts as a light‐driven proton pump and can provide energy for bacterial cellular metabolism. However, knowledge of factors that regulate PR gene expression in different bacteria remains strongly limited. Here, experiments with V ibrio sp. AND 4 showed that PR phototrophy promoted survival only in cells from stationary phase and not in ac...
Environmental Microbiology · 2012 · Vol. 14 · Issue 9 · Wiley
Summary The main role of microorganisms in the cycling of the bulk dissolved organic carbon pool in the ocean is well established. Nevertheless, it remains unclear if particular bacteria preferentially utilize specific carbon compounds and whether such compounds have the potential to shape bacterial community composition. Enrichment experiments in the Mediterranean Sea, Baltic Sea and the North Sea (Skagerrak) showed that diff...
Environmental Microbiology · 2010 · Vol. 12 · Issue 11 · Wiley
Summary The suitability of applying empirical conversion factors (eCFs) to determine bacterial biomass production remains unclear because seawater cultures are usually overtaken by phylotypes that are not abundant in situ . While eCFs vary across environments, it has not been tested whether differences in eCFs are driven by changes in bacterial community composition or by in situ environmental conditions. We carried out seawat...
Environmental Microbiology · 2009 · Vol. 11 · Issue 10 · Wiley
Summary We demonstrate here results showing that bottom‐up and top‐down control mechanisms can operate simultaneously and in concert in marine microbial food webs, controlling prokaryote diversity by a combination of viral lysis and substrate limitation. Models in microbial ecology predict that a shift in the type of bacterial growth rate limitation is expected to have a major effect on species composition within the community...
Environmental Microbiology · 2009 · Vol. 11 · Issue 6 · Wiley
Summary Marine bacteria can cause harm to single‐celled and multicellular eukaryotes. However, relatively little is known about the underlying genetic basis for marine bacterial interactions with higher organisms. We examined whole‐genome sequences from a large number of marine bacteria for the prevalence of homologues to virulence genes and pathogenicity islands known from bacteria that are pathogenic to terrestrial animals a...