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Multi-plasmid clash in a bacterial community: plasmid viability depends on the ecological setting of hosts

https://doi.org/10.1101/2021.08.02.454727

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Plasmids and the spread of resistance

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The mating pair formation system of conjugative plasmids—A versatile secretion machinery for transfer of proteins and DNA

inferredcites →https://doi.org/10.1016/j.plasmid.2018.09.009openalex-snapshot

Impact of plasmid interactions with the chromosome and other plasmids on the spread of antibiotic resistance

inferredcites →https://doi.org/10.1016/j.plasmid.2019.03.003openalex-snapshot

The shufflon of IncI1 plasmids is rearranged constantly during different growth conditions

inferredcites →https://doi.org/10.1016/j.tim.2012.04.003openalex-snapshot

Plasmid-mediated horizontal gene transfer is a coevolutionary process

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Conjugative ESBL plasmids differ in their potential to rescue susceptible bacteria via horizontal gene transfer in lethal antibiotic concentrations

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Genome evolution and adaptation in a long-term experiment with Escherichia coli

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Exploiting CRISPR-Cas nucleases to produce sequence-specific antimicrobials

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Persistence and reversal of plasmid-mediated antibiotic resistance

inferredcites →https://doi.org/10.1038/s41467-021-22849-yopenalex-snapshot

Variability of plasmid fitness effects contributes to plasmid persistence in bacterial communities

inferredcites →https://doi.org/10.1038/s41559-017-0243-2openalex-snapshot

Compensatory mutations improve general permissiveness to antibiotic resistance plasmids

inferredcites →https://doi.org/10.1038/s41559-020-1170-1openalex-snapshot

Coevolution of host–plasmid pairs facilitates the emergence of novel multidrug resistance

inferredcites →https://doi.org/10.1038/s41579-018-0031-2openalex-snapshot

Going around in circles: virulence plasmids in enteric pathogens

inferredcites →https://doi.org/10.1073/pnas.1600974113openalex-snapshot

Source–sink plasmid transfer dynamics maintain gene mobility in soil bacterial communities

inferredcites →https://doi.org/10.1073/pnas.82.17.5724openalex-snapshot

An invertible element of DNA controls phase variation of type 1 fimbriae of Escherichia coli.

inferredcites →https://doi.org/10.1080/19490976.2019.1591136openalex-snapshot

Midbiotics: conjugative plasmids for genetic engineering of natural gut flora

inferredcites →https://doi.org/10.1093/genetics/165.4.1641openalex-snapshot

Amelioration of the Cost of Conjugative Plasmid Carriage in Eschericha coli K12

inferredcites →https://doi.org/10.1093/molbev/msw163openalex-snapshot

Survival and Evolution of a Large Multidrug Resistance Plasmid in New Clinical Bacterial Hosts

inferredcites →https://doi.org/10.1098/rsbl.2015.0953openalex-snapshot

Conjugation is necessary for a bacterial plasmid to survive under protozoan predation

inferredcites →https://doi.org/10.1098/rstb.2009.0037openalex-snapshot

Conjugative plasmids: vessels of the communal gene pool

inferredcites →https://doi.org/10.1099/acmi.0.000179openalex-snapshot

Plasmids shape the diverse accessory resistomes of Escherichia coli ST131

inferredcites →https://doi.org/10.1111/j.1574-6976.2009.00168.xopenalex-snapshot

The diversity of conjugative relaxases and its application in plasmid classification

inferredcites →https://doi.org/10.1111/j.1574-6976.2011.00291.xopenalex-snapshot

Identification of bacterial plasmids based on mobility and plasmid population biology

inferredcites →https://doi.org/10.1111/mec.14056openalex-snapshot

Plasmid and clonal interference during post horizontal gene transfer evolution

inferredcites →https://doi.org/10.1111/mmi.13407openalex-snapshot

Evolved plasmid‐host interactions reduce plasmid interference cost

inferredcites →https://doi.org/10.1111/nyas.12696openalex-snapshot

Classification of prokaryotic genetic replicators: between selfishness and altruism

inferredcites →https://doi.org/10.1128/aac.01707-08openalex-snapshot

Resistance Plasmid Families in Enterobacteriaceae

inferredcites →https://doi.org/10.1128/cmr.00088-17openalex-snapshot

Mobile Genetic Elements Associated with Antimicrobial Resistance

inferredcites →https://doi.org/10.1128/iai.74.4.2102-2114.2006openalex-snapshot

An IncI1 Plasmid Contributes to the Adherence of the Atypical EnteroaggregativeEscherichia coliStrain C1096 to Cultured Cells and Abiotic Surfaces

inferredcites →https://doi.org/10.1128/jb.62.3.293-300.1951openalex-snapshot

STUDIES ON LYSOGENESIS I

inferredcites →https://doi.org/10.1128/mbio.02011-17openalex-snapshot

Genomic Analysis of Hospital Plumbing Reveals Diverse Reservoir of Bacterial Plasmids Conferring Carbapenem Resistance

inferredcites →https://doi.org/10.1128/mmbr.00015-09openalex-snapshot

Pathogenomics of the Virulence Plasmids of Escherichia coli

inferredcites →https://doi.org/10.1128/mmbr.00020-10openalex-snapshot

Mobility of Plasmids

inferredcites →https://doi.org/10.1139/cjm-2017-0609openalex-snapshot

Plasmid persistence: costs, benefits, and the plasmid paradox

inferredcites →https://doi.org/10.1155/2012/874153openalex-snapshot

Vehicles, Replicators, and Intercellular Movement of Genetic Information: Evolutionary Dissection of a Bacterial Cell

inferredcites →https://doi.org/10.15252/msb.20209913openalex-snapshot

Conjugation dynamics depend on both the plasmid acquisition cost and the fitness cost

inferredcites →https://doi.org/10.3389/fcimb.2018.00376openalex-snapshot

Bacteriophage Therapy: Clinical Trials and Regulatory Hurdles

inferredcites →https://doi.org/10.3390/antibiotics9060296openalex-snapshot

Beta-Lactam Sensitive Bacteria Can Acquire ESBL-Resistance via Conjugation after Long-Term Exposure to Lethal Antibiotic Concentration

inferredcites →https://doi.org/10.3390/genes11111239openalex-snapshot

Plasmid Transfer by Conjugation in Gram-Negative Bacteria: From the Cellular to the Community Level

inferredcites →https://doi.org/10.3390/nano10112247openalex-snapshot

Adhesion of Escherichia Coli to Nanostructured Surfaces and the Role of Type 1 Fimbriae

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