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Plasmids are extrachromosomal DNA molecules found in bacteria, archaea, and some eukaryotic microbes like yeast. These small, circular DNA structures typically contain fewer than 30 genes, although some may exist linearly. Plasmids vary in their number within a cell, known as copy number. Single-copy plasmids are present in one copy per cell and multi-copy plasmids are present in multiple copies, reaching over 100 copies per cell.Plasmids usually replicate independently of the chromosomal DNA...
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The lysogenic cycle is a crucial viral replication strategy that allows bacteriophages to persist within host cells without immediately destroying them. This process is primarily observed in temperate phages, such as bacteriophage lambda (λ), which infects Escherichia coli. The cycle allows the viral genome to persist across bacterial generations while keeping host cells viable.Integration of the Viral GenomeUpon infection, bacteriophage lambda attaches to the bacterial surface and injects...
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Bacteriophages, or phages, are viruses that specifically infect bacteria, utilizing their genetic material to hijack host cellular machinery for replication. DNA bacteriophages employ single-stranded DNA (ssDNA) or double-stranded DNA (dsDNA) genomes. These phages exhibit diverse replication strategies and host interactions, influencing their ecological roles and applications in biotechnology and medicine.ssDNA BacteriophagesssDNA phages, with their small genomes, utilize unique strategies to...
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In contrast to the lytic cycle, phages infecting bacteria via the lysogenic cycle do not immediately kill their host cell. Instead, they combine their genome with the host genome, allowing the bacteria to replicate the phage DNA along with the bacterial genome. The incorporated copy of the phage genome is called the prophage. Some prophages can re-activate and enter the lytic cycle. This often occurs in response to a perturbation, such as DNA damage, but can also transpire in the absence of...
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Genomic DNA in Prokaryotes00:46

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The genome of most prokaryotic organisms consists of double-stranded DNA organized into one circular chromosome in a region of cytoplasm called the nucleoid. The chromosome is tightly wound, or supercoiled, for efficient storage. Prokaryotes also contain other circular pieces of DNA called plasmids. These plasmids are smaller than the chromosome and often carry genes that confer adaptive functions, such as antibiotic resistance.
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Quantification of Plasmid-Mediated Antibiotic Resistance in an Experimental Evolution Approach
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Quantification of Plasmid-Mediated Antibiotic Resistance in an Experimental Evolution Approach

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Plasmid carriage can limit bacteria-phage coevolution.

Ellie Harrison1, Julie Truman2, Rosanna Wright3

  • 1Department of Biology, University of York, York YO10 5DD, UK ellie.harrison@york.ac.uk.

Biology Letters
|August 14, 2015
PubMed
Summary
This summary is machine-generated.

Bacterial plasmids, like pQBR103, can limit coevolution with bacteriophages. Plasmid carriage in Pseudomonas fluorescens reduced bacterial phage resistance and phage infectivity, impacting bacterial evolution.

Keywords:
bacteria–phage coevolutionconjugative plasmidmucoid conversion

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High-Resolution Comparison of Bacterial Conjugation Frequencies
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Area of Science:

  • Microbiology
  • Evolutionary Biology
  • Genetics

Background:

  • Bacteria-phage coevolution is a significant driver of bacterial population dynamics.
  • Environmental and genetic factors influence the speed and nature of coevolutionary processes.
  • Large conjugative plasmids can alter bacterial phenotypes and evolutionary trajectories.

Purpose of the Study:

  • To investigate the impact of conjugative plasmid pQBR103 carriage on the coevolution between Pseudomonas fluorescens and its bacteriophage SBW25ϕ2.
  • To determine if plasmid carriage affects the development of phage resistance in bacteria and infectivity in phages.
  • To explore the role of mucoidy in bacterial adaptation during phage-host coevolution in the presence of plasmids.

Main Methods:

  • Experimental evolution of Pseudomonas fluorescens with and without the conjugative plasmid pQBR103 in the presence of bacteriophage SBW25ϕ2.
  • Quantification of bacterial phage resistance and phage infectivity over multiple coevolutionary cycles.
  • Analysis of the costs associated with phage resistance mutations and the frequency of mucoid bacterial phenotypes.

Main Results:

  • Plasmid carriage significantly limited bacteria-phage coevolution, resulting in lower phage resistance in bacteria and reduced infectivity in phages compared to plasmid-free populations.
  • These effects were not attributable to increased costs of phage resistance mutations associated with plasmid carriage.
  • The presence of phages and plasmids led to the evolution of high frequencies of mucoid bacterial colonies, which conferred weak partial resistance to the phage.

Conclusions:

  • Conjugative plasmids can profoundly influence bacteria-phage coevolutionary dynamics.
  • Plasmid carriage can dampen coevolutionary arms races by altering resistance/infectivity levels and promoting alternative resistance strategies like mucoidy.
  • The evolutionary consequences of plasmid carriage extend beyond the direct effects of accessory genes, impacting host-microbe interactions and population evolution.