Restricted changes in major surface protein-2 (msp2) transcription after prolonged in vitro passage of Anaplasma

Diana G Scorpio1, Karen Caspersen, Hiroyuki Ogata

  • 1Division of Medical Microbiology, Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA. dscorpio@jhmi.edu

BMC Microbiology
|January 10, 2004
PubMed
Abstract

Insights

Anaplasma phagocytophilum

Area of Science:

  • Microbiology
  • Molecular Biology
  • Bacterial Pathogenesis

Background:

  • Anaplasma phagocytophilum strains exhibit variable Msp2 expression, often linked to immune evasion.
  • Msp2 also functions as an adhesin, but its role in transcriptional changes without immune pressure is unclear.
  • This study investigated Msp2 profiles and transcripts in A. phagocytophilum during in vitro passaging without immune selection.

Purpose of the Study:

  • To determine if Msp2 expression and transcription change in Anaplasma phagocytophilum without immune selective pressures.
  • To explore the functional implications of Msp2 modulation beyond immune evasion.

Main Methods:

  • Immunoblotting using Msp2 monoclonal antibodies to analyze protein profiles.
  • Analysis of msp2 transcript diversity using molecular techniques.
  • Bioinformatic analysis (BLASTN) of msp2 paralogs in the A. phagocytophilum genome.

Main Results:

  • Msp2 protein profiles showed an unchanged dominant band with the appearance of weaker bands over passages.
  • Msp2 transcript diversity evolved, with a decrease in the initial transcript and the emergence of new transcripts.
  • The A. phagocytophilum genome harbors at least 52 msp2 paralogs.

Conclusions:

  • Msp2 expression and transcription are modulated in A. phagocytophilum even without immune selective pressures.
  • Limited msp2 transcript diversity suggests Msp2 selection for specific functions beyond immune evasion.
  • A large genomic reservoir of msp2 paralogs exists, yet expression remains constrained without immune pressure.

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