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Updated: Jul 29, 2026

Immuno-fluorescence Assay of Leptospiral Surface-exposed Proteins
Published on: July 1, 2011
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
Abstract:
Anaplasma phagocytophilum is the causative agent of an emerging tick-borne zoonosis in the United States and Europe. The organism causes a febrile illness accompanied by other nonspecific symptoms and can be fatal, especially if treatment is delayed. Persistence of A. phagocytophilum within mammalian reservoir hosts is important for ensuring continued disease transmission. In the related organism Anaplasma marginale, persistence is associated with antigenic variation of the immunoprotective outer membrane protein MSP2. Extensive diversity of MSP2 is achieved by combinatorial gene conversion of a genomic expression site by truncated pseudogenes. The major outer membrane protein of A. phagocytophilum, MSP2(P44), is homologous to MSP2 of A. marginale, has a similar organization of conserved and variable regions, and is also encoded by a multigene family containing some truncated gene copies. This suggests that the two organisms could use similar mechanisms to generate diversity in outer membrane proteins from their small genomes. We define here a genomic expression site for MSP2(P44) in A. phagocytophilum. As in A. marginale, the msp2(p44) gene in this expression site is polymorphic in all populations of organisms we have examined, whether organisms are obtained from in vitro culture in human HL-60 cells, from culture in the tick cell line ISE6, or from infected human blood. Changes in culture conditions were found to favor the growth and predominance of certain msp2(p44) variants. Insertions, deletions, and substitutions in the region of the genomic expression site encoding the central hypervariable region matched sequence polymorphisms in msp2(p44) mRNA. These data suggest that, similarly to A. marginale, A. phagocytophilum uses combinatorial mechanisms to generate a large array of outer membrane protein variants. Such gene polymorphism has profound implications for the design of vaccines, diagnostic tests, and therapy.
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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