Related Experiment Videos
Antigenic variation of Anaplasma marginale: major surface protein 2 diversity during cyclic transmission between
1Department of Pathobiology, College of Veterinary Medicine, University of Florida, Gainesville, Florida 32611, USA. barbeta@mail.vetmed.ufl.edu
Abstract:
The rickettsial pathogen Anaplasma marginale expresses a variable immunodominant outer membrane protein, major surface protein 2 (MSP2), involved in antigenic variation and long-term persistence of the organism in carrier animals. MSP2 contains a central hypervariable region of about 100 amino acids that encodes immunogenic B-cell epitopes that induce variant-specific antibodies during infection. Previously, we have shown that MSP2 is encoded on a polycistronic mRNA transcript in erythrocyte stages of A. marginale and defined the structure of the genomic expression site for this transcript. In this study, we show that the same expression site is utilized in stages of A. marginale infecting tick salivary glands. We also analyzed the variability of this genomic expression site in Oklahoma strain A. marginale transmitted from in vitro cultures to cattle and between cattle and ticks. The structure of the expression site and flanking regions was conserved except for sequence that encoded the MSP2 hypervariable region. At least three different MSP2 variants were encoded in each A. marginale population. The major sequence variants did not change on passage of A. marginale between culture, acute erythrocyte stage infections, and tick salivary glands but did change during persistent infections of cattle. The variant types found in tick salivary glands most closely resembled those present in bovine blood at the time of acquisition of infection, whether infection was acquired from an acute or from a persistent rickettsemia. These variations in structure of an expression site for a major, immunoprotective outer membrane protein have important implications for vaccine development and for obtaining an improved understanding of the mechanisms of persistence of ehrlichial infections in humans, domestic animals, and reservoir hosts.
Insights
Anaplasma marginale varies its major surface protein 2 (MSP2) expression site, impacting antigenic variation and persistence. This variation is crucial for understanding ehrlichial infections and developing effective vaccines.
Area of Science:
- Veterinary Microbiology
- Molecular Biology
- Immunology
Background:
- Anaplasma marginale, a rickettsial pathogen, causes persistent infections in cattle.
- Major surface protein 2 (MSP2) is critical for A. marginale's antigenic variation and persistence.
- MSP2's hypervariable region contains epitopes inducing variant-specific antibodies.
Purpose of the Study:
- To investigate the genomic expression site of MSP2 in A. marginale infecting tick salivary glands.
- To analyze the variability of the MSP2 expression site in different transmission stages (in vitro, cattle, ticks).
- To understand the implications of MSP2 variation for vaccine development and disease persistence.
Main Methods:
- Analysis of the MSP2 genomic expression site structure in A. marginale.
- Tracking MSP2 variant changes during transmission between culture, cattle, and ticks.
- Comparison of MSP2 variant types in tick salivary glands and bovine blood.
Main Results:
- The MSP2 expression site is conserved in tick salivary glands and cattle.
- Sequence variability in the MSP2 hypervariable region was observed.
- At least three MSP2 variants were encoded per A. marginale population.
- MSP2 variants remained stable during acute infection and tick transmission but changed during persistent cattle infections.
- Tick-borne MSP2 variants matched those in cattle blood at the time of infection acquisition.
Conclusions:
- MSP2 expression site variability contributes to antigenic variation and persistence of A. marginale.
- Understanding MSP2 variation is key for developing vaccines against ehrlichial diseases.
- The findings provide insights into the persistence mechanisms of ehrlichial infections in various hosts.