Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
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
_version_ 1782211212888506368
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
work_keys_str_mv AT lauaudreyot attenuationofvirulenceinanapicomplexanhemoparasiteresultsinreducedgenomediversityatthepopulationlevel
AT kalyanaramanananth attenuationofvirulenceinanapicomplexanhemoparasiteresultsinreducedgenomediversityatthepopulationlevel
AT echaideignacio attenuationofvirulenceinanapicomplexanhemoparasiteresultsinreducedgenomediversityatthepopulationlevel
AT palmerguyh attenuationofvirulenceinanapicomplexanhemoparasiteresultsinreducedgenomediversityatthepopulationlevel
AT bockrussell attenuationofvirulenceinanapicomplexanhemoparasiteresultsinreducedgenomediversityatthepopulationlevel
AT pedronimonicaj attenuationofvirulenceinanapicomplexanhemoparasiteresultsinreducedgenomediversityatthepopulationlevel
AT rameshkumarmeenakshi attenuationofvirulenceinanapicomplexanhemoparasiteresultsinreducedgenomediversityatthepopulationlevel
AT ferreiramarianob attenuationofvirulenceinanapicomplexanhemoparasiteresultsinreducedgenomediversityatthepopulationlevel
AT fletchertaryni attenuationofvirulenceinanapicomplexanhemoparasiteresultsinreducedgenomediversityatthepopulationlevel
AT mcelwainterryf attenuationofvirulenceinanapicomplexanhemoparasiteresultsinreducedgenomediversityatthepopulationlevel