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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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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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Comparative genomic analyses of IncpA1763-KPC plasmids.

Hongchao Chen1, Zhe Zhan2, Xiaoyuan Jiang3

  • 1College of Medicine, First Affiliated Hospital, Zhejiang University, Hangzhou, China.

Journal of Basic Microbiology
|February 8, 2021
PubMed
Summary
This summary is machine-generated.

This study reveals that single IncpA1763-KPC plasmids, though poorly studied, are evolving. Comparative genomics shows their backbone structures vary, with accessory modules driving diversification.

Keywords:
IncpA1763-KPC plasmidsKlebsiella pneumoniaantibiotic resistancemobile elements

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Area of Science:

  • Microbiology
  • Genomics
  • Molecular Biology

Background:

  • Multi-replicon plasmids with IncpA1763-KPC are increasingly reported in Enterobacteriaceae.
  • Single IncpA1763-KPC plasmids are less understood despite their growing prevalence.

Purpose of the Study:

  • To investigate the genomic structure and evolution of single IncpA1763-KPC plasmids.
  • To compare the backbone regions of IncpA1763-KPC plasmids from clinical isolates with previously sequenced plasmids.

Main Methods:

  • High-throughput genome sequencing of two clinical Klebsiella pneumoniae isolates.
  • Linear structural and detailed genomic comparisons of IncpA1763-KPC plasmids.
  • Analysis of backbone regions, maintenance regions, and accessory modules.

Main Results:

  • Plasmids pA1763-KPC and p427113-2 possess complete IncpA1763-KPC backbones.
  • Other IncpA1763-KPC plasmids exhibit deletions or truncations in their backbone regions.
  • Accessory modules, including resistance genes (blaKPC-2, ars, ncr, sil) and insertion sequences, are integrated into plasmid backbones.

Conclusions:

  • Comparative genomics provides insight into the diversification and evolution of IncpA1763-KPC plasmids.
  • Variations in backbone structure and accessory module integration contribute to plasmid evolution.