Classical biomonitoring techniques have focused primarily on measures linked to various biodiversity metrics and indicator species. Next-generation biomonitoring (NGB) describes a suite of tools and approaches that allow the examination of a broader spectrum of organisational levels - from genes to entire ecosystems. Here, we frame ten key questions that we envisage will drive the field of NGB over the next decade. While not exhaustive, this list covers most of the key challenges facing NGB, and provides the basis of the next steps for research and implementation in this field. These questions have been grouped into current- and outlook-related categories, corresponding to the organization of this paper.
Abstract There has been limited characterisation of bat-borne coronaviruses in Europe. Here, we screened for coronaviruses in 48 faecal samples from 16 of the 17 bat species breeding in the UK, collected through a bat rehabilitation and conservationist network. We recovered nine (two novel) complete genomes across six bat species: four alphacoronaviruses, a MERS-related betacoronavirus, and four closely related sarbecoviruses. We demonstrate that at least one of these sarbecoviruses can bind and use the human ACE2 receptor for infecting human cells, albeit suboptimally. Additionally, the spike proteins of these sarbecoviruses possess an R-A-K-Q motif, which lies only one nucleotide mutation away from a furin cleavage site (FCS) that enhances infectivity in other coronaviruses, including SARS-CoV-2. However, mutating this motif to an FCS does not enable spike cleavage. Overall, while UK sarbecoviruses would require further molecular adaptations to infect humans, their zoonotic risk is unknown and warrants closer surveillance.
The bacterial communities associated with healthy and diseased colonies of the cold-water gorgonian coral Eunicella verrucosa at three sites off the south-west coast of England were compared using denaturing gradient gel electrophoresis (DGGE) and clone libraries. Significant differences in community structure between healthy and diseased samples were discovered, as were differences in the level of disturbance to these communities at each site; this correlated with depth and sediment load. The majority of cloned sequences from healthy coral tissue affiliated with the Gammaproteobacteria. The stability of the bacterial community and dominance of specific genera found across visibly healthy colonies suggest the presence of a specific microbial community. Affiliations included a high proportion of Endozoicomonas sequences, which were most similar to sequences found in tropical corals. This genus has been found in a number of invertebrates and is suggested to have a role in coral health and in the metabolisation of dimethylsulfoniopropionate (DMSP) produced by zooxanthellae. However, screening of colonies for the presence of zooxanthellae produced a negative result. Diseased colonies showed a decrease in affiliated clones and an increase in clones related to potentially harmful/transient microorganisms but no increase in a particular pathogen. This study demonstrates that a better understanding of these bacterial communities, the factors that affect them and their role in coral health and disease will be of critical importance in predicting future threats to temperate gorgonian communities.
Abstract Environmental DNA (eDNA) metabarcoding has been widely employed to describe biological communities in the marine environment and to compare the richness and diversity of sites across large spatial scales. However, fine‐scale temporal eDNA dynamics are poorly understood and the time of eDNA sample collection is rarely reported in publications. Here, we collected surface eDNA samples every 6 h, for 3 days, at two coral reef sites to assess fine‐scale changes in the eukaryotic communities detected. Distinct eukaryotic communities were detected at two sites within the same lagoon. Sampling time was found to have a significant effect on ESV and class richness, both peaking during the 1 p.m. sampling time at both sites. Sampling time also had a significant effect on the detection of eukaryotic taxa, with relative read frequency showing clear diurnal patterns in line with the migratory behavior of planktonic groups. Other groups of organisms showed considerable variation in read frequency, highlighting the dynamic nature of marine eukaryotic communities and potential stochasticity of eDNA detections. For eukaryotic communities, eDNA samples can provide a “snapshot” of contemporary biodiversity and provide information on short‐term community dynamics on hyperdiverse coral reefs. However, our findings add to growing evidence that sampling time should be clearly considered and reported in marine eDNA studies and that multiple samples from the same site are needed to facilitate more robust comparisons across sites.
Spread of SARS-CoV2 by aerosol is considered an important mode of transmission over distances >2 m, particularly indoors.We determined whether SARS-CoV2 could be detected in the air of enclosed/semi-enclosed public spaces.Between March 2021 and December 2021 during the easing of COVID-19 pandemic restrictions after a period of lockdown, we used total suspended and size-segregated particulate matter (PM) samplers for the detection of SARS-CoV2 in hospitals wards and waiting areas, on public transport, in a university campus and in a primary school in West London.We collected 207 samples, of which 20 (9.7%) were positive for SARS-CoV2 using quantitative PCR. Positive samples were collected from hospital patient waiting areas, from hospital wards treating patients with COVID-19 using stationary samplers and from train carriages in London underground using personal samplers. Mean virus concentrations varied between 429 500 copies/m3 in the hospital emergency waiting area and the more frequent 164 000 copies/m3 found in other areas. There were more frequent positive samples from PM samplers in the PM2.5 fractions compared with PM10 and PM1. Culture on Vero cells of all collected samples gave negative results.During a period of partial opening during the COVID-19 pandemic in London, we detected SARS-CoV2 RNA in the air of hospital waiting areas and wards and of London Underground train carriage. More research is needed to determine the transmission potential of SARS-CoV2 detected in the air.
There is growing interest in the potential for combining eDNA and artificial intelligence (machine learning) to detect and evaluate in real time changes in ecosystems at the global scale, in a more sensitive and cost-effective way than current biomonitoring methods. Machine learning might make better use of the eDNA census data that can currently be collected to evaluate the network of ecological interactions that are at the base of the services that ecosystems supply and that we wish to protect. To date, eDNA and machine learning developments have effectively progressed in parallel and in isolation in various spheres of ecosystem monitoring (disease, invasion, conservation, etc. in aerial, terrestrial, and aquatic systems).
The goal of this Research Topic is to explore the range of ongoing activities to build the next generation of biomonitoring tools and in doing so to make researchers in the different spheres aware of the breadth of work being undertaken, and to set a unifying research agenda (the key questions) for the development of global biomonitoring using eDNA and machine learning.
The scope of this Research Topic will be to explore:
1. eDNA approaches currently being used in case study systems from all spheres of monitoring;
2. Theoretical underpinnings of machine learning for biomonitoring;
3. What type of networks do we need to reconstruct for effective monitoring (co-occurrence, trophic, etc);
4. Examples of learning large scale, replicated networks from eDNA in the different spheres;
5. Statistical and analytical approaches to analysing large-scale, highly replicated networks;
6. Technological developments necessary to build a next-generation biomonitoring framework at the global scale;
7. A research agenda paper that develops “10 key questions for eDNA and machine learning in biomonitoring”.
Details for Authors: The Research Topic “A next-generation of global biomonitoring to detect ecosystem change” will publish conceptual, data, case study, technological and synthetic papers on eDNA and machine learning approaches for developing a unified next-generation biomonitoring framework. Paper length conforms to the guidelines of the journal Frontiers in Ecology and Evolution.
Many marine habitats, such as the surface and tissues of marine invertebrates, including corals, harbour diverse populations of microorganisms, which are thought to play a role in the health of their hosts and influence mutualistic and competitive interactions. Investigating the presence and stability of quorum sensing (QS) in these ecosystems may shed light on the roles and control of these bacterial communities. Samples of 13 cnidarian species were screened for the presence and diversity of N-acyl-homoserine lactones (AHLs; a prevalent type of QS molecule) using thin-layer chromatography and an Agrobacterium tumefaciens NTL4 biosensor. Ten of 13 were found to harbour species-specific, conserved AHL profiles. AHLs were confirmed in Anemonia viridis using liquid chromatography tandem mass spectrometry. To assess temporal role and stability, AHLs were investigated in A. viridis from intertidal pools over 16 h. Patterns of AHLs showed conserved profiles except for two mid-chain length AHLs, which increased significantly over the day, peaking at 20:00, but had no correlation with pool chemistry. Denaturing gel electrophoresis of RT-PCR-amplified bacterial 16S rRNA showed the presence of an active bacterial community that changed in composition alongside AHL profiles and contained a number of bands that affiliate with known AHL-producing bacteria. Investigations into the quorum sensing-controlled, species-specific roles of these bacterial communities and how these regulatory circuits are influenced by the coral host and members of the bacterial community are imperative to expand our knowledge of these interactions with respect to the maintenance of coral health.
Abstract How complex microbial communities respond to climatic fluctuations remains an open question. Due to their relatively short generation times and high functional diversity, microbial populations harbor great potential to respond as a community through a combination of strain-level phenotypic plasticity, adaptation, and species sorting. However, the relative importance of these mechanisms remains unclear. We conducted a laboratory experiment to investigate the degree to which bacterial communities can respond to changes in environmental temperature through a combination of phenotypic plasticity and species sorting alone. We grew replicate soil communities from a single location at six temperatures between 4°C and 50°C. We found that phylogenetically- and functionally-distinct communities emerge at each of these temperatures, with K -strategist taxa favoured under cooler conditions, and r -strategist taxa under warmer conditions. We show that this dynamic emergence of distinct communities across a wide range of temperatures (in essence, community-level adaptation), is driven by the resuscitation of latent functional diversity: the parent community harbors multiple strains pre-adapted to different temperatures that are able to “switch on” at their preferred temperature without immigration or adaptation. Our findings suggest that microbial community function in nature is likely to respond rapidly to climatic temperature fluctuations through shifts in species composition by resuscitation of latent functional diversity.
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