| Issues and current standards of controls in microbiome research |
33 |
| Occurrence and abundance of antibiotic resistance genes in agricultural soil receiving dairy manure |
27 |
| Exploring fish microbial communities to mitigate emerging diseases in aquaculture |
23 |
| Identification of phenol- and p-cresol-producing intestinal bacteria by using media supplemented with tyrosine and its metabolites |
23 |
| Planctomycetes in boreal and subarctic wetlands: diversity patterns and potential ecological functions |
19 |
| Sanguina nivaloides and Sanguina aurantia gen. et spp. nov. (Chlorophyta): the taxonomy, phylogeny, biogeography and ecology of two newly recognised algae causing red and orange snow |
17 |
| Dissemination of multi-resistant Gram-negative bacteria into German wastewater and surface waters |
17 |
| Human skin microbiota is a rich source of bacteriocin-producing staphylococci that kill human pathogens |
16 |
| Host blood-meal source has a strong impact on gut microbiota of Aedes aegypti |
16 |
| A critical re-evaluation of multilocus sequence typing (MLST) efforts in Wolbachia |
16 |
| Gut microbial and metabolomic profiles after fecal microbiota transplantation in pediatric ulcerative colitis patients |
15 |
| Alpine soil microbial ecology in a changing world |
14 |
| Antimicrobial resistance and the environment: assessment of advances, gaps and recommendations for agriculture, aquaculture and pharmaceutical manufacturing |
13 |
| Endosymbiont diversity and prevalence in herbivorous spider mite populations in South-Western Europe |
13 |
| Prokaryotic community successions and interactions in marine biofilms: the key role of Flavobacteriia |
12 |
| Water and sanitation: an essential battlefront in the war on antimicrobial resistance |
12 |
| Aeolian dispersal of bacteria in southwest Greenland: their sources, abundance, diversity and physiological states |
12 |
| Host range of antibiotic resistance genes in wastewater treatment plant influent and effluent |
12 |
| Organohalide respiratory chains: composition, topology and key enzymes |
12 |
| Diversity, specificity, co-occurance and hub taxa of the bacterial-fungal pollen microbiome |
12 |
| Primer set 2.0 for highly parallel qPCR array targeting antibiotic resistance genes and mobile genetic elements |
12 |
| Blackening and odorization of urban rivers: a bio-geochemical process |
11 |
| Shift of hindgut microbiota and microbial short chain fatty acids profiles in dairy calves from birth to pre-weaning |
11 |
| Ice algal bloom development on the surface of the Greenland Ice Sheet |
11 |
| The Fe(II)-oxidizing Zetaproteobacteria: historical, ecological and genomic perspectives |
11 |
| Environmental dimensions of antibiotic resistance: assessment of basic science gaps |
11 |
| An Acetobacterium strain isolated with metallic iron as electron donor enhances iron corrosion by a similar mechanism as Sporomusa sphaeroides |
10 |
| The morphology and metabolic potential of the Chloroflexi in full-scale activated sludge wastewater treatment plants |
10 |
| Diversity patterns of microbial eukaryotes mirror those of bacteria in Antarctic cryoconite holes |
10 |
| Arbuscular mycorrhizal fungal communities and global change: an uncertain future |
10 |
| Impact of carbohydrate substrate complexity on the diversity of the human colonic microbiota |
10 |
| Trichoderma atroviride promotes tomato development and alters the root exudation of carbohydrates, which stimulates fungal growth and the biocontrol of the phytopathogen Phytophthora cinnamomi in a tripartite interaction system |
10 |
| A meta-analysis of the bovine gastrointestinal tract microbiota |
10 |
| Microbial nanowires and electroactive biofilms |
10 |
| Dispersal limitation and thermodynamic constraints govern spatial structure of permafrost microbial communities |
9 |
| Bacterial community assemblages in the rhizosphere soil, root endosphere and cyst of soybean cyst nematode-suppressive soil challenged with nematodes |
9 |
| Rhizosphere-enriched microbes as a pool to design synthetic communities for reproducible beneficial outputs |
9 |
| Bacterial biofilm formation on the hyphae of ectomycorrhizal fungi: a widespread ability under controls? |
9 |
| Pathogen suppression by microbial volatile organic compounds in soils |
9 |
| Microbial community structure and microbial networks correspond to nutrient gradients within coastal wetlands of the Laurentian Great Lakes |
9 |
| Microbiomes inhabiting rice roots and rhizosphere |
9 |
| Diversity of fungi and bacteria in species-rich grasslands increases with plant diversity in shoots but not in roots and soil |
9 |
| Bacterial community structure and succession in nests of two megachilid bee genera |
9 |
| Viruses of fungi and oomycetes in the soil environment |
9 |
| Microbial community composition along a 50 000-year lacustrine sediment sequence |
8 |
| Native bacteria promote plant growth under drought stress condition without impacting the rhizomicrobiome |
8 |
| Fungal community composition and diversity vary with soil depth and landscape position in a no-till wheat-based cropping system |
8 |
| Cold adaptation and replicable microbial community development during long-term low-temperature anaerobic digestion treatment of synthetic sewage |
8 |
| Harnessing long-read amplicon sequencing to uncover NRPS and Type I PKS gene sequence diversity in polar desert soils |
8 |
| Biofilm growth and control in cooling water industrial systems |
8 |
