Gene expression analysis of a nasopharynx adapted pneumococcal isolate and a lung adapted pneumococcal isolate in comparison to the wild-type ancestor D39 strain.

  • Thomas Barton (Creator)
  • Angharad E. Green (Creator)
  • Kate C Mellor (Wellcome Sanger Institute) (Creator)
  • Abigail McKnight (St. Jude Children Research Hospital) (Creator)
  • Katharina Bacher (University of Bern) (Creator)
  • Sumit Kumar (Creator)
  • Kyle Newbold (Creator)
  • Oliver Lorenz (Wellcome Sanger Institute) (Creator)
  • Elizabeth Pohler (Creator)
  • Manal S. Monshi (University of Liverpool) (Creator)
  • Adam Bryson (Creator)
  • Felix Dube (University of Cape Town) (Creator)
  • Heather J. Zar (Creator)
  • Mark P. Nicol (University of Western Australia) (Creator)
  • Stephen D. Bentley (Creator)
  • Markus Hilty (Creator)
  • Jason W. Rosch (Creator)
  • Stephanie Lo (Wellcome Sanger Institute, University of Bath, UCL Great Ormond Street Institute of Child Health) (Creator)
  • Daniel Neill (Creator)

Dataset

Description

The gene expression profiles of a nasopharynx adapted pneumococcal isolate C20-3, and a lung adapted pneumococcal isolate P20-10, were compared to the D39N-wild-type ancestor strain. These evolved isolates were from an experimental evolution study with Streptococcus pneumoniae strain D39N in a mouse colonisation model, where we identified mutations arising in pneumococci experimentally adapted to nasopharynx and lung environments- doi.org/10.1093/molbev/msab018 Illumina sequencing of PCR amplicons from the nanB promoter, containing a poly-adenine signature, and from a promoter containing no homopolymer runs was also carried out to quantify mutation rate due to strand slippage
Date made available5 Dec 2024
PublisherNational Center for Biotechnology Information

Keywords

  • S. pneumoniae
  • gene expression
  • promoter
  • evolution

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