| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1111/NYAS.13213 |
| P698 | PubMed publication ID | 27706829 |
| P50 | author | Michael R. Gillings | Q51470263 |
| P2860 | cites work | After 30 years of study, the bacterial SOS response still surprises us | Q21092806 |
| Pyrosequencing of antibiotic-contaminated river sediments reveals high levels of resistance and gene transfer elements | Q21135543 | ||
| A global perspective on the use, sales, exposure pathways, occurrence, fate and effects of veterinary antibiotics (VAs) in the environment | Q36469502 | ||
| ISCR elements: novel gene-capturing systems of the 21st century? | Q36499667 | ||
| Pervasive selection for and against antibiotic resistance in inhomogeneous multistress environments | Q36528302 | ||
| Evolutionary consequences of antibiotic use for the resistome, mobilome and microbial pangenome | Q36576233 | ||
| Importance of widespread gene transfer agent genes in alpha-proteobacteria. | Q36690543 | ||
| A family of insertion sequences that impacts integrons by specific targeting of gene cassette recombination sites, the IS1111-attC Group | Q36747859 | ||
| Clusters of Antibiotic Resistance Genes Enriched Together Stay Together in Swine Agriculture | Q37123068 | ||
| Progress towards understanding the fate of plasmids in bacterial communities | Q37174799 | ||
| Antibiotics and antibiotic resistance in water environments | Q37183790 | ||
| Host range diversification within the IncP-1 plasmid group. | Q37332245 | ||
| Prokaryotic evolution and the tree of life are two different things | Q37385941 | ||
| Gene cassettes and cassette arrays in mobile resistance integrons. | Q37470852 | ||
| Integrative and Conjugative Elements (ICEs): What They Do and How They Work | Q37529766 | ||
| Conjugative plasmids: vessels of the communal gene pool | Q37538155 | ||
| Call of the wild: antibiotic resistance genes in natural environments | Q37700168 | ||
| Does the wide use of quaternary ammonium compounds enhance the selection and spread of antimicrobial resistance and thus threaten our health? | Q37724848 | ||
| Fate of antibiotics during municipal water recycling treatment processes. | Q37771500 | ||
| Mobility of plasmids. | Q37784107 | ||
| Aquatic systems: maintaining, mixing and mobilising antimicrobial resistance? | Q37860584 | ||
| Gene flow, mobile genetic elements and the recruitment of antibiotic resistance genes into Gram-negative pathogens | Q37868656 | ||
| Combinatorial events of insertion sequences and ICE in Gram-negative bacteria | Q37897646 | ||
| The role of reticulate evolution in creating innovation and complexity | Q21296637 | ||
| Extracellular DNA Required for Bacterial Biofilm Formation | Q22065541 | ||
| Prokaryotes: the unseen majority | Q22066200 | ||
| Genome analysis of multiple pathogenic isolates of Streptococcus agalactiae: implications for the microbial "pan-genome" | Q22066389 | ||
| DNA uptake during bacterial transformation | Q22121988 | ||
| Lateral gene transfer and the nature of bacterial innovation | Q22122396 | ||
| Comparison of 61 sequenced Escherichia coli genomes | Q24614300 | ||
| ACLAME: a CLAssification of Mobile genetic Elements, update 2010 | Q24644500 | ||
| Horizontal gene transfer among genomes: the complexity hypothesis | Q24651300 | ||
| Genomics of bacteria and archaea: the emerging dynamic view of the prokaryotic world | Q24653367 | ||
| Ecology and Evolution of the Human Microbiota: Fire, Farming and Antibiotics | Q26786929 | ||
| Management options for reducing the release of antibiotics and antibiotic resistance genes to the environment | Q26827456 | ||
| Ancient and modern environmental DNA | Q27005869 | ||
| Horizontal gene transfer and the evolution of bacterial and archaeal population structure | Q27006506 | ||
| Antibiotics as a selective driver for conjugation dynamics | Q27313286 | ||
| Antimicrobial-induced DNA damage and genomic instability in microbial pathogens | Q27693195 | ||
| A novel family of potentially mobile DNA elements encoding site-specific gene-integration functions: integrons | Q27976520 | ||
| Pseudomonas aeruginosa Genomic Structure and Diversity | Q28244678 | ||
| A common mechanism of cellular death induced by bactericidal antibiotics | Q28246128 | ||
| Mechanisms of, and barriers to, horizontal gene transfer between bacteria | Q28270244 | ||
| Antibiotic-induced lateral transfer of antibiotic resistance | Q28279661 | ||
| Bacterial genome instability | Q28657639 | ||
| The SOS response controls integron recombination. | Q29346620 | ||
| Prevalence of SOS-mediated control of integron integrase expression as an adaptive trait of chromosomal and mobile integrons. | Q29346731 | ||
| Horizontal gene transfer in prokaryotes: quantification and classification | Q29616017 | ||
| Marine viruses--major players in the global ecosystem | Q29616822 | ||
| Prokaryotic evolution in light of gene transfer | Q29617350 | ||
| Origins and evolution of antibiotic resistance | Q29617791 | ||
| Marine viruses and their biogeochemical and ecological effects | Q30720057 | ||
| Microbial DNA records historical delivery of anthropogenic mercury | Q30968495 | ||
| Genome trees and the tree of life | Q31103613 | ||
| Uncultured soil bacteria are a reservoir of new antibiotic resistance genes | Q33205796 | ||
| The evolution of class 1 integrons and the rise of antibiotic resistance | Q33335636 | ||
| Influence of ciprofloxacin and vancomycin on mutation rate and transposition of IS256 in Staphylococcus aureus | Q43422435 | ||
| SOS response induction by beta-lactams and bacterial defense against antibiotic lethality | Q45016731 | ||
| Intercellular nanotubes mediate bacterial communication. | Q45941890 | ||
| Horizontal gene transfer accelerates genome innovation and evolution. | Q45961682 | ||
| Genomic diversity and evolution within the species Streptococcus agalactiae | Q46626837 | ||
| Metabolic cross-feeding via intercellular nanotubes among bacteria | Q46769311 | ||
| Microbial taxonomy in the post-genomic era: rebuilding from scratch? | Q46795421 | ||
| Present-day mercury resistance transposons are common in bacteria preserved in permafrost grounds since the Upper Pleistocene. | Q47257926 | ||
| Origins of life: born in a watery commune | Q47354744 | ||
| Tn5060 from the Siberian permafrost is most closely related to the ancestor of Tn21 prior to integron acquisition | Q47447843 | ||
| Population genomics: how bacterial species form and why they don't exist | Q47651772 | ||
| The Anthropocene: are humans now overwhelming the great forces of Nature? | Q47715763 | ||
| Integration of horizontally transferred genes into regulatory interaction networks takes many million years | Q47727235 | ||
| Tn5053 family transposons are res site hunters sensing plasmidal res sites occupied by cognate resolvases | Q47931334 | ||
| Tackling antibiotic resistance: the environmental framework | Q48544038 | ||
| Occurrence and characteristics of class 1, 2 and 3 integrons in Escherichia coli, Salmonella and Campylobacter spp. in the Netherlands | Q50073601 | ||
| Plasmids of the same Inc groups in Enterobacteria before and after the medical use of antibiotics | Q50210040 | ||
| Ecology drives a global network of gene exchange connecting the human microbiome. | Q51171065 | ||
| Biased gene transfer in microbial evolution. | Q53085305 | ||
| Sulfonamide resistance: mechanisms and trends. | Q53999423 | ||
| Broad diversity of conjugative plasmids in integron-carrying bacteria from wastewater environments. | Q54340652 | ||
| Is exposure to mercury a driving force for the carriage of antibiotic resistance genes? | Q54388466 | ||
| Adaptive evolution of bacterial metabolic networks by horizontal gene transfer. | Q54474627 | ||
| Horizontal gene transfer depends on gene content of the host. | Q54477925 | ||
| Conjugative plasmids in bacteria of the 'pre-antibiotic' era. | Q54498786 | ||
| Whole-Genome Analysis of Photosynthetic Prokaryotes | Q56680896 | ||
| Ecology and evolution of sex in aphids | Q56814339 | ||
| Co-selection of antibiotic and heavy metal resistance in freshwater bacteria | Q56979506 | ||
| Microbiology of the Anthropocene | Q57007085 | ||
| Cycling of extracellular DNA in the soil environment | Q57070154 | ||
| Antibiotic-Induced Replication Stress Triggers Bacterial Competence by Increasing Gene Dosage near the Origin | Q57825326 | ||
| Diverse aadA gene cassettes on class 1 integrons introduced into soil via spread manure | Q33478785 | ||
| Wastewater bacterial communities bring together broad-host range plasmids, integrons and a wide diversity of uncharacterized gene cassettes | Q33518107 | ||
| Mobile antibiotic resistance encoding elements promote their own diversity | Q33519503 | ||
| Comparative ICE genomics: insights into the evolution of the SXT/R391 family of ICEs | Q33521306 | ||
| Network analyses structure genetic diversity in independent genetic worlds | Q33591742 | ||
| Generation of genic diversity among Streptococcus pneumoniae strains via horizontal gene transfer during a chronic polyclonal pediatric infection | Q33700577 | ||
| Integrons: past, present, and future. | Q33743517 | ||
| Incidence of class 1 integrons in a quaternary ammonium compound-polluted environment | Q33770001 | ||
| Gram-positive bacteria are a major reservoir of Class 1 antibiotic resistance integrons in poultry litter | Q33782927 | ||
| The shared antibiotic resistome of soil bacteria and human pathogens | Q33804392 | ||
| Coral-mucus-associated Vibrio integrons in the Great Barrier Reef: genomic hotspots for environmental adaptation | Q33804889 | ||
| Humans as the world's greatest evolutionary force | Q33954568 | ||
| Phage as agents of lateral gene transfer | Q33967977 | ||
| Incidence of class 1 and 2 integrases in clinical and commensal bacteria from livestock, companion animals, and exotics. | Q33981591 | ||
| Transposons Tn1696 and Tn21 and their integrons In4 and In2 have independent origins | Q33981966 | ||
| The repertoire of ICE in prokaryotes underscores the unity, diversity, and ubiquity of conjugation | Q34005318 | ||
| Plasmid metagenome reveals high levels of antibiotic resistance genes and mobile genetic elements in activated sludge | Q34053442 | ||
| Highways of gene sharing in prokaryotes | Q34063510 | ||
| Complete nucleotide sequence of TOL plasmid pDK1 provides evidence for evolutionary history of IncP-7 catabolic plasmids | Q34119158 | ||
| High Frequency of Horizontal Gene Transfer in the Oceans | Q34142279 | ||
| Ancient horizontal gene transfer | Q34174227 | ||
| Prokaryote genome fluidity: toward a system approach of the mobilome. | Q34238543 | ||
| Evolution of variation in presence and absence of genes in bacterial pathways | Q34240776 | ||
| Genes lost and genes found: evolution of bacterial pathogenesis and symbiosis | Q34250498 | ||
| SOS response promotes horizontal dissemination of antibiotic resistance genes | Q34285480 | ||
| Genome mosaicism and organismal lineages. | Q34316533 | ||
| Shaping bacterial genomes with integrative and conjugative elements | Q34327965 | ||
| Phosphate concentration and the putative sensor kinase protein CckA modulate cell lysis and release of the Rhodobacter capsulatus gene transfer agent | Q34368015 | ||
| Bacterial vesicles in marine ecosystems | Q34396893 | ||
| Bacterial transformation: distribution, shared mechanisms and divergent control | Q34403233 | ||
| Antibiotic-induced SOS response promotes horizontal dissemination of pathogenicity island-encoded virulence factors in staphylococci | Q34409956 | ||
| Pollution from drug manufacturing: review and perspectives | Q34423503 | ||
| Horizontal gene transfer, genome innovation and evolution | Q34447824 | ||
| Switches in bacteriophage lambda development | Q34467169 | ||
| The interconnection between biofilm formation and horizontal gene transfer | Q37996597 | ||
| Are humans increasing bacterial evolvability? | Q37998201 | ||
| The antibiotic resistome | Q38029141 | ||
| Induction of competence for genetic transformation by antibiotics: convergent evolution of stress responses in distant bacterial species lacking SOS? | Q38036489 | ||
| The role of bacterial outer membrane vesicles for intra- and interspecies delivery | Q38066246 | ||
| The role of the natural environment in the emergence of antibiotic resistance in gram-negative bacteria | Q38076545 | ||
| Exploring the costs of horizontal gene transfer. | Q38109292 | ||
| Conjugative and mobilizable genomic islands in bacteria: evolution and diversity. | Q38174149 | ||
| Microbiological effects of sublethal levels of antibiotics. | Q38214805 | ||
| Impact of spontaneous prophage induction on the fitness of bacterial populations and host-microbe interactions | Q38268995 | ||
| Bacterial antimicrobial metal ion resistance. | Q38270762 | ||
| Bacteriophage-mediated spread of bacterial virulence genes. | Q38295446 | ||
| The dualistic nature of integrative and conjugative elements | Q38498279 | ||
| Everyman's Guide to Bacterial Insertion Sequences | Q38536141 | ||
| Horizontal gene transfer: building the web of life. | Q38549036 | ||
| The Tn3-family of Replicative Transposons | Q38583042 | ||
| Aquaculture as yet another environmental gateway to the development and globalisation of antimicrobial resistance | Q38809523 | ||
| Soil-borne reservoirs of antibiotic-resistant bacteria are established following therapeutic treatment of dairy calves. | Q39183682 | ||
| The SOS Response Master Regulator LexA Regulates the Gene Transfer Agent of Rhodobacter capsulatus and Represses Transcription of the Signal Transduction Protein CckA. | Q39256614 | ||
| Genomic islands 1 and 2 play key roles in the evolution of extensively drug-resistant ST235 isolates of Pseudomonas aeruginosa. | Q39879069 | ||
| Source, occurrence and fate of antibiotics in the Italian aquatic environment. | Q39932542 | ||
| Architecture and Characteristics of Bacterial Nanotubes | Q39975579 | ||
| Occurrence and persistence of antibiotic resistance genes in river biofilms after wastewater inputs in small rivers | Q40167129 | ||
| Metagenomic Assembly Reveals Hosts of Antibiotic Resistance Genes and the Shared Resistome in Pig, Chicken, and Human Feces | Q40229288 | ||
| Impacts of reclaimed water irrigation on soil antibiotic resistome in urban parks of Victoria, Australia | Q40342070 | ||
| Antibiotic concentration and antibiotic-resistant bacteria in two shallow urban lakes after stormwater event | Q40351801 | ||
| Sampling the antibiotic resistome | Q40357052 | ||
| Live cell imaging of SOS and prophage dynamics in isogenic bacterial populations | Q40668340 | ||
| Aquaculture changes the profile of antibiotic resistance and mobile genetic element associated genes in Baltic Sea sediments. | Q40755560 | ||
| Minimal selective concentrations of tetracycline in complex aquatic bacterial biofilms. | Q40769264 | ||
| An assay for determining minimal concentrations of antibiotics that drive horizontal transfer of resistance. | Q40820925 | ||
| Differential roles of antimicrobials in the acquisition of drug resistance through activation of the SOS response in Acinetobacter baumannii | Q41036115 | ||
| Homologues of Genetic Transformation DNA Import Genes Are Required for Rhodobacter capsulatus Gene Transfer Agent Recipient Capability Regulated by the Response Regulator CtrA | Q41703108 | ||
| Selection of a multidrug resistance plasmid by sublethal levels of antibiotics and heavy metals | Q41712060 | ||
| Comparative study of class 1 integron and Vibrio cholerae superintegron integrase activities | Q42025330 | ||
| Potential impacts of aquatic pollutants: sub-clinical antibiotic concentrations induce genome changes and promote antibiotic resistance. | Q42057187 | ||
| Evidence for dynamic exchange of qac gene cassettes between class 1 integrons and other integrons in freshwater biofilms | Q42621940 | ||
| Class 1 integrons in benthic bacterial communities: abundance, association with Tn402-like transposition modules and evidence for coselection with heavy-metal resistance. | Q43168574 | ||
| Influence of industrial contamination on mobile genetic elements: class 1 integron abundance and gene cassette structure in aquatic bacterial communities | Q43168810 | ||
| beta-lactam antibiotics induce the SOS response and horizontal transfer of virulence factors in Staphylococcus aureus | Q43259790 | ||
| Exploring the Role of Coliform Bacteria in Class 1 Integron Carriage and Biofilm Formation During Drinking Water Treatment. | Q43347768 | ||
| Correlation between upstream human activities and riverine antibiotic resistance genes | Q43350186 | ||
| Genetic diversity and composition of a plasmid metagenome from a wastewater treatment plant. | Q43362303 | ||
| In 2035, will all bacteria be multiresistant? Yes. | Q43406883 | ||
| Integron prevalence and diversity in manured soil | Q34487960 | ||
| Antibiotic resistance gene abundances associated with waste discharges to the Almendares River near Havana, Cuba | Q34505354 | ||
| Of what use is sex to bacteria? | Q34562948 | ||
| Identification and characterization of integron-mediated antibiotic resistance in the phytopathogen Xanthomonas oryzae pv. oryzae | Q34598331 | ||
| Aeons of distress: an evolutionary perspective on the bacterial SOS response. | Q34691348 | ||
| Directed networks reveal genomic barriers and DNA repair bypasses to lateral gene transfer among prokaryotes | Q34729654 | ||
| Lateral gene transfer challenges principles of microbial systematics. | Q34771047 | ||
| Local mobile gene pools rapidly cross species boundaries to create endemicity within global Vibrio cholerae populations | Q34777542 | ||
| Defining the mobilome | Q34959127 | ||
| Class 1 integrons potentially predating the association with tn402-like transposition genes are present in a sediment microbial community | Q34976781 | ||
| Environmental pollution by antibiotics and by antibiotic resistance determinants | Q34989442 | ||
| When phage, plasmids, and transposons collide: genomic islands, and conjugative- and mobilizable-transposons as a mosaic continuum | Q35013459 | ||
| Diversity and evolution of AbaR genomic resistance islands in Acinetobacter baumannii strains of European clone I. | Q35065744 | ||
| Explaining microbial genomic diversity in light of evolutionary ecology | Q35109746 | ||
| Impacts of anthropogenic activity on the ecology of class 1 integrons and integron-associated genes in the environment | Q35135774 | ||
| What traits are carried on mobile genetic elements, and why? | Q35246646 | ||
| A role for Tn6029 in the evolution of the complex antibiotic resistance gene loci in genomic island 3 in enteroaggregative hemorrhagic Escherichia coli O104:H4. | Q35559889 | ||
| Ancient horizontal gene transfer and the last common ancestors | Q35595309 | ||
| Using the class 1 integron-integrase gene as a proxy for anthropogenic pollution | Q35626365 | ||
| Genomic islands in pathogenic and environmental microorganisms | Q35752419 | ||
| The evolutionary dynamics of integrons in changing environments. | Q35915814 | ||
| The infinitely many genes model for the distributed genome of bacteria. | Q35930255 | ||
| Survival strategies of infectious biofilms | Q36003660 | ||
| Mobile genetic elements are involved in bacterial sociality | Q36105870 | ||
| Studying plasmid horizontal transfer in situ: a critical review | Q36247073 | ||
| The ins and outs of DNA transfer in bacteria. | Q36328634 | ||
| Quorum sensing and DNA release in bacterial biofilms | Q36418307 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | anthropocene | Q26841 |
| horizontal gene transfer | Q83185 | ||
| bacterial evolution | Q115395667 | ||
| P304 | page(s) | 20-36 | |
| P577 | publication date | 2016-10-05 | |
| P1433 | published in | Annals of the New York Academy of Sciences | Q2431664 |
| P1476 | title | Lateral gene transfer, bacterial genome evolution, and the Anthropocene | |
| P478 | volume | 1389 |
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