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Updated: Jun 18, 2026

Tick Microbiome Characterization by Next-Generation 16S rRNA Amplicon Sequencing
Published on: August 25, 2018
Persistence mechanisms in tick-borne diseases
1Department of Infectious Diseases & Pathology, College of Veterinary Medicine, University of Florida, Gainesville, Florida, USA.
Abstract:
The use of new, highly sensitive diagnostic methods has revealed persistent infections to be a common feature of different tick-borne diseases, such as babesiosis, anaplasmosis and heartwater. Antigenic variation can contribute to disease persistence through the continual elaboration of new surface structures, and we know in several instances how this is achieved. Known or suspected mechanisms of persistence in babesial parasites include cytoadhesion and rapid variation of the adhesive ligand in Babesia bovis and genetic diversity in several merozoite stage proteins of different Babesia spp. In Anaplasma, extensive variation in the pfam01617 gene family accompanies cycling of organism levels in chronic infection. One result from the pioneering research at Onderstepoort is the definition of a related polymorphic gene family that is likely involved in immunity against heartwater disease. We are beginning to understand the sizes of the antigenic repertoires and full definition is close, with the possibility of applying simultaneous high-throughput sequencing to the order of 1000 small genomes. We also, for the first time, can consider modifying these genomes and looking at effects on persistence and virulence. However, important biological questions remain unanswered; for example, why we are seeing a new emerging Anaplasma infection of humans and is infection of endothelial cells by Anaplasma significant to persistence in vivo.
Insights
Persistent tick-borne diseases like babesiosis and anaplasmosis are common. Antigenic variation in pathogens, such as Babesia and Anaplasma, allows them to evade immunity and persist.
Area of Science:
- Veterinary Parasitology
- Molecular Biology
- Immunology
Background:
- Highly sensitive diagnostics reveal persistent infections are common in tick-borne diseases (babesiosis, anaplasmosis, heartwater).
- Antigenic variation is a key mechanism enabling pathogen persistence by altering surface structures.
- Previous research identified specific mechanisms in Babesia and Anaplasma, including cytoadhesion, ligand variation, and gene family diversity.
Purpose of the Study:
- To investigate the role of antigenic variation in the persistence of tick-borne diseases.
- To understand the mechanisms of immune evasion employed by Babesia, Anaplasma, and heartwater agents.
- To explore the potential for genomic modification to study pathogen persistence and virulence.
Main Methods:
- Utilizing advanced diagnostic methods to detect persistent infections.
- Analyzing gene families, such as pfam01617 in Anaplasma, associated with chronic infection and immune evasion.
- Applying high-throughput sequencing for comprehensive analysis of pathogen genomes.
- Considering genome modification techniques to assess effects on persistence and virulence.
Main Results:
- Identified a polymorphic gene family in heartwater agents potentially involved in immune evasion.
- Began characterizing the antigenic repertoires of these tick-borne pathogens.
- Advanced understanding of mechanisms contributing to persistence, including cytoadhesion and genetic diversity in Babesia, and gene family variation in Anaplasma.
Conclusions:
- Antigenic variation is a significant factor in the persistence of tick-borne diseases.
- Further research is needed to address emerging infections (e.g., human Anaplasma) and the role of endothelial cell interaction in Anaplasma persistence.
- Genomic approaches offer new possibilities for understanding and potentially manipulating pathogen persistence and virulence.
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