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Attenuation of virulence in an apicomplexan hemoparasite results in reduced genome diversity at the population level
BACKGROUND: Virulence acquisition and loss is a dynamic adaptation of pathogens to thrive in changing milieus. We investigated the mechanisms of virulence loss at the whole genome level using Babesia bovis as a model apicomplexan in which genetically related attenuated parasites can be reliably deri...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166950/ https://www.ncbi.nlm.nih.gov/pubmed/21838895 http://dx.doi.org/10.1186/1471-2164-12-410 |
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author | Lau, Audrey OT Kalyanaraman, Ananth Echaide, Ignacio Palmer, Guy H Bock, Russell Pedroni, Monica J Rameshkumar, Meenakshi Ferreira, Mariano B Fletcher, Taryn I McElwain, Terry F |
author_facet | Lau, Audrey OT Kalyanaraman, Ananth Echaide, Ignacio Palmer, Guy H Bock, Russell Pedroni, Monica J Rameshkumar, Meenakshi Ferreira, Mariano B Fletcher, Taryn I McElwain, Terry F |
author_sort | Lau, Audrey OT |
collection | PubMed |
description | BACKGROUND: Virulence acquisition and loss is a dynamic adaptation of pathogens to thrive in changing milieus. We investigated the mechanisms of virulence loss at the whole genome level using Babesia bovis as a model apicomplexan in which genetically related attenuated parasites can be reliably derived from virulent parental strains in the natural host. We expected virulence loss to be accompanied by consistent changes at the gene level, and that such changes would be shared among attenuated parasites of diverse geographic and genetic background. RESULTS: Surprisingly, while single nucleotide polymorphisms in 14 genes distinguished all attenuated parasites from their virulent parental strains, all non-synonymous changes resulted in no deleterious amino acid modification that could consistently be associated with attenuation (or virulence) in this hemoparasite. Interestingly, however, attenuation significantly reduced the overall population's genome diversity with 81% of base pairs shared among attenuated strains, compared to only 60% of base pairs common among virulent parental parasites. There were significantly fewer genes that were unique to their geographical origins among the attenuated parasites, resulting in a simplified population structure among the attenuated strains. CONCLUSIONS: This simplified structure includes reduced diversity of the variant erythrocyte surface 1 (ves) multigene family repertoire among attenuated parasites when compared to virulent parental strains, possibly suggesting that overall variance in large protein families such as Variant Erythrocyte Surface Antigens has a critical role in expression of the virulence phenotype. In addition, the results suggest that virulence (or attenuation) mechanisms may not be shared among all populations of parasites at the gene level, but instead may reflect expansion or contraction of the population structure in response to shifting milieus. |
format | Online Article Text |
id | pubmed-3166950 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31669502011-09-06 Attenuation of virulence in an apicomplexan hemoparasite results in reduced genome diversity at the population level Lau, Audrey OT Kalyanaraman, Ananth Echaide, Ignacio Palmer, Guy H Bock, Russell Pedroni, Monica J Rameshkumar, Meenakshi Ferreira, Mariano B Fletcher, Taryn I McElwain, Terry F BMC Genomics Research Article BACKGROUND: Virulence acquisition and loss is a dynamic adaptation of pathogens to thrive in changing milieus. We investigated the mechanisms of virulence loss at the whole genome level using Babesia bovis as a model apicomplexan in which genetically related attenuated parasites can be reliably derived from virulent parental strains in the natural host. We expected virulence loss to be accompanied by consistent changes at the gene level, and that such changes would be shared among attenuated parasites of diverse geographic and genetic background. RESULTS: Surprisingly, while single nucleotide polymorphisms in 14 genes distinguished all attenuated parasites from their virulent parental strains, all non-synonymous changes resulted in no deleterious amino acid modification that could consistently be associated with attenuation (or virulence) in this hemoparasite. Interestingly, however, attenuation significantly reduced the overall population's genome diversity with 81% of base pairs shared among attenuated strains, compared to only 60% of base pairs common among virulent parental parasites. There were significantly fewer genes that were unique to their geographical origins among the attenuated parasites, resulting in a simplified population structure among the attenuated strains. CONCLUSIONS: This simplified structure includes reduced diversity of the variant erythrocyte surface 1 (ves) multigene family repertoire among attenuated parasites when compared to virulent parental strains, possibly suggesting that overall variance in large protein families such as Variant Erythrocyte Surface Antigens has a critical role in expression of the virulence phenotype. In addition, the results suggest that virulence (or attenuation) mechanisms may not be shared among all populations of parasites at the gene level, but instead may reflect expansion or contraction of the population structure in response to shifting milieus. BioMed Central 2011-08-12 /pmc/articles/PMC3166950/ /pubmed/21838895 http://dx.doi.org/10.1186/1471-2164-12-410 Text en Copyright ©2011 Lau et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Lau, Audrey OT Kalyanaraman, Ananth Echaide, Ignacio Palmer, Guy H Bock, Russell Pedroni, Monica J Rameshkumar, Meenakshi Ferreira, Mariano B Fletcher, Taryn I McElwain, Terry F Attenuation of virulence in an apicomplexan hemoparasite results in reduced genome diversity at the population level |
title | Attenuation of virulence in an apicomplexan hemoparasite results in reduced genome diversity at the population level |
title_full | Attenuation of virulence in an apicomplexan hemoparasite results in reduced genome diversity at the population level |
title_fullStr | Attenuation of virulence in an apicomplexan hemoparasite results in reduced genome diversity at the population level |
title_full_unstemmed | Attenuation of virulence in an apicomplexan hemoparasite results in reduced genome diversity at the population level |
title_short | Attenuation of virulence in an apicomplexan hemoparasite results in reduced genome diversity at the population level |
title_sort | attenuation of virulence in an apicomplexan hemoparasite results in reduced genome diversity at the population level |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166950/ https://www.ncbi.nlm.nih.gov/pubmed/21838895 http://dx.doi.org/10.1186/1471-2164-12-410 |
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