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Published on: May 18, 2016
The immunization-induced antibody response to the Anaplasma marginale major surface protein 2 and its association
Susan M Noh1, Yan Zhuang, James E Futse
1Animal Disease Research Unit, Agricultural Research Service, U.S. Department of Agriculture, Pullman, WA 99164-7030, USA. snoh@vetmed.wsu.edu <snoh@vetmed.wsu.edu>
Abstract:
Many vector-borne pathogens evade clearance via rapid variation in their immunogenic surface expressed proteins. This is exemplified by Anaplasma marginale, a tick-borne bacterial pathogen that generates major surface protein 2 (Msp2) variants to provide for immune escape and allow long-term pathogen persistence. In contrast to persistence following infection, immunization with a surface protein complex, which includes Msp2, induces a response that prevents infection upon challenge. We hypothesized that the immune response induced by immunization altered the anti-Msp2 antibody repertoire as compared to that induced during infection, shifting the immune response toward conserved and thus broadly protective epitopes. The antibody response to the conserved (CR) and hypervariable (HVR) regions encoded by the full set of msp2 variant alleles was determined for immunized animals prior to challenge and non-immunized, infected animals. While both groups of animals had a similar antibody repertoire in terms of breath and magnitude, the titers to the Msp2 CR were strongly correlated (p<0.005) with control of bacteremia only in the infected animals. Among the immunized animals, there was no correlation between the breadth or magnitude of the anti-Msp2 antibody response and either complete protection from infection or control of bacteremia. This is consistent with separate immunologic mechanisms being responsible for control of bacteremia in infected animals as compared to immunized animals and suggests that conserved outer membrane proteins other than Msp2 are responsible for the complete clearance observed following challenge of vaccinees.
Insights
Anaplasma marginale evades immune clearance through major surface protein 2 (Msp2) variation. Immunization, unlike infection, shifted antibody responses, suggesting other proteins confer protection against this tick-borne pathogen.
Area of Science:
- Veterinary immunology
- Pathogen immune evasion
- Bacterial surface protein variation
Background:
- Vector-borne pathogens like Anaplasma marginale use surface protein variation for immune escape.
- Major surface protein 2 (Msp2) variants enable pathogen persistence.
- Immunization with Msp2-containing complexes prevents infection, unlike natural infection.
Purpose of the Study:
- To investigate if immunization alters the anti-Msp2 antibody repertoire compared to natural infection.
- To determine if immunization shifts immune responses towards conserved Msp2 epitopes for broader protection.
Main Methods:
- Determined antibody response to conserved (CR) and hypervariable (HVR) regions of Msp2 variants.
- Analyzed antibody repertoires in immunized and infected animals.
- Correlated antibody titers with control of bacteremia and protection from infection.
Main Results:
- Both immunized and infected animals showed similar antibody repertoire breadth and magnitude.
- Anti-Msp2 CR antibody titers correlated with bacteremia control only in infected animals.
- No correlation found between anti-Msp2 antibodies and protection/bacteremia control in immunized animals.
Conclusions:
- Distinct immunologic mechanisms control bacteremia in infected versus immunized animals.
- Conserved outer membrane proteins, other than Msp2, likely mediate complete clearance in vaccinated animals.
- Msp2 variation is a key immune evasion strategy for Anaplasma marginale persistence.
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