| Soil pH mediates the balance between stochastic and deterministic assembly of bacteria |
72 |
| Disease-induced assemblage of a plant-beneficial bacterial consortium |
70 |
| Global negative effects of nitrogen deposition on soil microbes |
57 |
| Agricultural intensification reduces microbial network complexity and the abundance of keystone taxa in roots |
55 |
| Distinct patterns and processes of abundant and rare eukaryotic plankton communities following a reservoir cyanobacterial bloom |
51 |
| The consequences of niche and physiological differentiation of archaeal and bacterial ammonia oxidisers for nitrous oxide emissions |
43 |
| Marine probiotics: increasing coral resistance to bleaching through microbiome manipulation |
41 |
| A new widespread subclass of carbonic anhydrase in marine phytoplankton |
41 |
| Expanded diversity of microbial groups that shape the dissimilatory sulfur cycle |
39 |
| Biogeographic patterns of abundant and rare bacterioplankton in three subtropical bays resulting from selective and neutral processes |
38 |
| Bacterial contributions to delignification and lignocellulose degradation in forest soils with metagenomic and quantitative stable isotope probing |
38 |
| Evolutionary trends in host physiology outweigh dietary niche in structuring primate gut microbiomes |
37 |
| High proportions of bacteria and archaea across most biomes remain uncultured |
36 |
| Influence of resistance breeding in common bean on rhizosphere microbiome composition and function |
36 |
| Climate change promotes parasitism in a coral symbiosis |
34 |
| Elevated circulating levels of succinate in human obesity are linked to specific gut microbiota |
33 |
| Contrasting the relative importance of species sorting and dispersal limitation in shaping marine bacterial versus protist communities |
32 |
| Linking the resistome and plasmidome to the microbiome |
32 |
| Comparative genomics sheds light on niche differentiation and the evolutionary history of comammox Nitrospira |
32 |
| Bacterial persistence promotes the evolution of antibiotic resistance by increasing survival and mutation rates |
32 |
| Wastewater treatment plant resistomes are shaped by bacterial composition, genetic exchange, and upregulated expression in the effluent microbiomes |
32 |
| Deposition rates of viruses and bacteria above the atmospheric boundary layer |
31 |
| Specific substrate-driven changes in human faecal microbiota composition contrast with functional redundancy in short-chain fatty acid production |
30 |
| Predicting the structure of soil communities from plant community taxonomy, phylogeny, and traits |
30 |
| Calling from distance: attraction of soil bacteria by plant root volatiles |
30 |
| Linking bacterial community composition to soil salinity along environmental gradients |
30 |
| A methanotrophic archaeon couples anaerobic oxidation of methane to Fe(III) reduction |
30 |
| Gut bacterial and fungal communities of the domesticated silkworm (Bombyx mori) and wild mulberry-feeding relatives |
29 |
| Antiepileptic drug carbamazepine promotes horizontal transfer of plasmid-borne multi-antibiotic resistance genes within and across bacterial genera |
27 |
| Cultivation and genomics of the first freshwater SAR11 (LD12) isolate |
27 |
| Cross-feeding modulates antibiotic tolerance in bacterial communities |
26 |
| Oral microbiome development during childhood: an ecological succession influenced by postnatal factors and associated with tooth decay |
26 |
| Oral microbiota of periodontal health and disease and their changes after nonsurgical periodontal therapy |
26 |
| Photoautotrophic organisms control microbial abundance, diversity, and physiology in different types of biological soil crusts |
25 |
| A strong link between marine microbial community composition and function challenges the idea of functional redundancy |
25 |
| Electrically conductive pili from pilin genes of phylogenetically diverse microorganisms |
25 |
| Microdiversification in genome-streamlined ubiquitous freshwater Actinobacteria |
25 |
| Contrasting effects of ectomycorrhizal fungi on early and late stage decomposition in a boreal forest |
24 |
| Rare symbionts may contribute to the resilience of coral-algal assemblages |
24 |
| Methanotrophy across a natural permafrost thaw environment |
24 |
| Use and abuse of correlation analyses in microbial ecology |
23 |
| Saving seed microbiomes |
23 |
| Polysaccharide utilization loci of North Sea Flavobacteriia as basis for using SusC/D-protein expression for predicting major phytoplankton glycans |
23 |
| Bacterial-derived exopolysaccharides enhance antifungal drug tolerance in a cross-kingdom oral biofilm |
22 |
| Microbial community assembly in wild populations of the fruit fly Drosophila melanogaster |
22 |
| Defining the role of Parasutterella, a previously uncharacterized member of the core gut microbiota |
21 |
| Modeling microbial communities from atrazine contaminated soils promotes the development of biostimulation solutions |
21 |
| The impact of failure: unsuccessful bacterial invasions steer the soil microbial community away from the invader's niche |
21 |
| Geometagenomics illuminates the impact of agriculture on the distribution and prevalence of plant viruses at the ecosystem scale |
21 |
| Clearcutting alters decomposition processes and initiates complex restructuring of fungal communities in soil and tree roots |
20 |
