Expression of multiple outer membrane protein sequence variants from a single genomic locus of Anaplasma

A F Barbet1, P F M Meeus, M Bélanger

  • 1Department of Pathobiology, College of Veterinary Medicine, University of Florida, PO Box 110880, Gainesville, FL 32611, USA. barbeta@mail.vetmed.ufl.edu

Infection and Immunity
|March 26, 2003
PubMed

Insights

Anaplasma phagocytophilum uses gene conversion to generate diverse outer membrane proteins, similar to Anaplasma marginale. This genetic polymorphism impacts vaccine and diagnostic development for this emerging zoonosis.

Area of Science:

  • Microbiology
  • Immunology
  • Genetics

Background:

  • Anaplasma phagocytophilum causes a serious tick-borne zoonosis in the US and Europe.
  • Persistence in hosts is key for disease transmission, potentially involving outer membrane protein variation.

Purpose of the Study:

  • To investigate the genomic expression site and diversity mechanisms of the major outer membrane protein MSP2(P44) in Anaplasma phagocytophilum.
  • To compare these mechanisms with those of the related Anaplasma marginale.

Main Methods:

  • Defined the genomic expression site for msp2(p44) in A. phagocytophilum.
  • Analyzed msp2(p44) gene polymorphism in various organism populations (in vitro, tick cells, human blood).
  • Examined sequence variations in the expression site and correlated them with mRNA polymorphisms.

Main Results:

  • Identified a genomic expression site for msp2(p44) in A. phagocytophilum.
  • The msp2(p44) gene in this site is polymorphic across all examined organism populations.
  • Culture conditions influenced the predominance of specific msp2(p44) variants.

Conclusions:

  • Anaplasma phagocytophilum likely employs combinatorial gene conversion to generate outer membrane protein diversity, mirroring Anaplasma marginale.
  • This genetic polymorphism has significant implications for developing vaccines and diagnostics against A. phagocytophilum infections.

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