Comparative transcriptome analysis of geographically distinct virulent and attenuated Babesia bovis strains reveals similar gene expression changes through attenuation

Autores
Pedroni, Monica J.; Sondgeroth, Kerry S.; Gallego-Lopez, Gina M.; Echaide, Ignacio Eduardo; Lau, Audrey OT
Año de publicación
2013
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Background: Loss of virulence is a phenotypic adaptation commonly seen in prokaryotic and eukaryotic pathogens. This mechanism is not well studied, especially in organisms with multiple host and life cycle stages such as Babesia, a tick-transmitted hemoparasite of humans and animals. B. bovis, which infects cattle, has naturally occurring virulent strains that can be reliably attenuated in vivo. Previous studies suggest the virulence loss mechanism may involve post-genomic modification. We investigated the transcriptome profiles of two geographically distinct B. bovis virulent and attenuated strain pairs to better understand virulence loss and to gain insight into pathogen adaptation strategies. Results: Expression microarray and RNA-sequencing approaches were employed to compare transcriptome profiles of two B. bovis strain pairs, with each pair consisting of a virulent parental and its attenuated derivative strain. Differentially regulated transcripts were identified within each strain pair. These included genes encoding for VESA1, SmORFs, undefined membrane and hypothetical proteins. The majority of individual specific gene transcripts differentially regulated within a strain were not shared between the two strains. There was a disproportionately greater number of ves genes upregulated in the virulent parental strains. When compared with their attenuated derivatives, divergently oriented ves genes were included among the upregulated ves genes in the virulent strains, while none of the upregulated ves genes in the attenuated derivatives were oriented head to head. One gene family whose specific members were consistently and significantly upregulated in expression in both attenuated strains was spherical body protein (SBP) 2 encoding gene where SBP2 truncated copies 7, 9 and 11 transcripts were all upregulated. Conclusions: We conclude that ves heterodimer pair upregulation and overall higher frequency of ves gene expressions in the virulent strains is consistent with the involvement of this gene family in virulence. This is logical given the role of VESA1 proteins in cytoadherence of infected cells to endothelial cells. However, upregulation of some ves genes in the attenuated derivatives suggests that the consequence of upregulation is gene-specific. Furthermore, upregulation of the spherical body protein 2 gene family may play a role in the attenuated phenotype. Exactly how these two gene families may contribute to the loss or gain of virulence is discussed.
EEA Rafaela
Fil: Pedroni, Monica J. Washington State University. College of Veterinary Medicine. Department of Veterinary Microbiology & Pathology. Program of Genomics; Estados Unidos
Fil: Sondgeroth, Kerry S. Washington State University. College of Veterinary Medicine. Department of Veterinary Microbiology & Pathology. Program of Genomics; Estados Unidos
Fil: Gallego-Lopez, Gina M. Washington State University. College of Veterinary Medicine. Department of Veterinary Microbiology & Pathology. Program of Genomics; Estados Unidos
Fil: Echaide, Ignacio Eduardo. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Rafaela. Laboratorio de Inmunología y Parasitología; Argentina
Fil: Lau, Audrey OT. Washington State University. College of Veterinary Medicine. Department of Veterinary Microbiology & Pathology. Program of Genomics; Estados Unidos. Washington State University. College of Veterinary Medicine. Paul G. Allen School for Global Animal Health; Estados Unidos
Fuente
BMC Genomics 14 : 763 (2013)
Materia
Babesia bovis
Genética
Vacuna Viva
Expresión Génica
Secuencia Nucleotídica
Genetics
Live Vaccines
Gene Expression
Nucleotide Sequence
Vacuna Atenuada
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-sa/4.0/
Repositorio
INTA Digital (INTA)
Institución
Instituto Nacional de Tecnología Agropecuaria
OAI Identificador
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oai_identifier_str oai:localhost:20.500.12123/3367
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network_name_str INTA Digital (INTA)
spelling Comparative transcriptome analysis of geographically distinct virulent and attenuated Babesia bovis strains reveals similar gene expression changes through attenuationPedroni, Monica J.Sondgeroth, Kerry S.Gallego-Lopez, Gina M.Echaide, Ignacio EduardoLau, Audrey OTBabesia bovisGenéticaVacuna VivaExpresión GénicaSecuencia NucleotídicaGeneticsLive VaccinesGene ExpressionNucleotide SequenceVacuna AtenuadaBackground: Loss of virulence is a phenotypic adaptation commonly seen in prokaryotic and eukaryotic pathogens. This mechanism is not well studied, especially in organisms with multiple host and life cycle stages such as Babesia, a tick-transmitted hemoparasite of humans and animals. B. bovis, which infects cattle, has naturally occurring virulent strains that can be reliably attenuated in vivo. Previous studies suggest the virulence loss mechanism may involve post-genomic modification. We investigated the transcriptome profiles of two geographically distinct B. bovis virulent and attenuated strain pairs to better understand virulence loss and to gain insight into pathogen adaptation strategies. Results: Expression microarray and RNA-sequencing approaches were employed to compare transcriptome profiles of two B. bovis strain pairs, with each pair consisting of a virulent parental and its attenuated derivative strain. Differentially regulated transcripts were identified within each strain pair. These included genes encoding for VESA1, SmORFs, undefined membrane and hypothetical proteins. The majority of individual specific gene transcripts differentially regulated within a strain were not shared between the two strains. There was a disproportionately greater number of ves genes upregulated in the virulent parental strains. When compared with their attenuated derivatives, divergently oriented ves genes were included among the upregulated ves genes in the virulent strains, while none of the upregulated ves genes in the attenuated derivatives were oriented head to head. One gene family whose specific members were consistently and significantly upregulated in expression in both attenuated strains was spherical body protein (SBP) 2 encoding gene where SBP2 truncated copies 7, 9 and 11 transcripts were all upregulated. Conclusions: We conclude that ves heterodimer pair upregulation and overall higher frequency of ves gene expressions in the virulent strains is consistent with the involvement of this gene family in virulence. This is logical given the role of VESA1 proteins in cytoadherence of infected cells to endothelial cells. However, upregulation of some ves genes in the attenuated derivatives suggests that the consequence of upregulation is gene-specific. Furthermore, upregulation of the spherical body protein 2 gene family may play a role in the attenuated phenotype. Exactly how these two gene families may contribute to the loss or gain of virulence is discussed.EEA RafaelaFil: Pedroni, Monica J. Washington State University. College of Veterinary Medicine. Department of Veterinary Microbiology & Pathology. Program of Genomics; Estados UnidosFil: Sondgeroth, Kerry S. Washington State University. College of Veterinary Medicine. Department of Veterinary Microbiology & Pathology. Program of Genomics; Estados UnidosFil: Gallego-Lopez, Gina M. Washington State University. College of Veterinary Medicine. Department of Veterinary Microbiology & Pathology. Program of Genomics; Estados UnidosFil: Echaide, Ignacio Eduardo. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Rafaela. Laboratorio de Inmunología y Parasitología; ArgentinaFil: Lau, Audrey OT. Washington State University. College of Veterinary Medicine. Department of Veterinary Microbiology & Pathology. Program of Genomics; Estados Unidos. Washington State University. College of Veterinary Medicine. Paul G. Allen School for Global Animal Health; Estados Unidos2018-09-14T16:08:06Z2018-09-14T16:08:06Z2013-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttps://bmcgenomics.biomedcentral.com/articles/10.1186/1471-2164-14-763http://hdl.handle.net/20.500.12123/33671471-2164https://doi.org/10.1186/1471-2164-14-763BMC Genomics 14 : 763 (2013)reponame:INTA Digital (INTA)instname:Instituto Nacional de Tecnología Agropecuariaenginfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)2025-09-29T13:44:26Zoai:localhost:20.500.12123/3367instacron:INTAInstitucionalhttp://repositorio.inta.gob.ar/Organismo científico-tecnológicoNo correspondehttp://repositorio.inta.gob.ar/oai/requesttripaldi.nicolas@inta.gob.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:l2025-09-29 13:44:26.732INTA Digital (INTA) - Instituto Nacional de Tecnología Agropecuariafalse
dc.title.none.fl_str_mv Comparative transcriptome analysis of geographically distinct virulent and attenuated Babesia bovis strains reveals similar gene expression changes through attenuation
title Comparative transcriptome analysis of geographically distinct virulent and attenuated Babesia bovis strains reveals similar gene expression changes through attenuation
spellingShingle Comparative transcriptome analysis of geographically distinct virulent and attenuated Babesia bovis strains reveals similar gene expression changes through attenuation
Pedroni, Monica J.
Babesia bovis
Genética
Vacuna Viva
Expresión Génica
Secuencia Nucleotídica
Genetics
Live Vaccines
Gene Expression
Nucleotide Sequence
Vacuna Atenuada
title_short Comparative transcriptome analysis of geographically distinct virulent and attenuated Babesia bovis strains reveals similar gene expression changes through attenuation
title_full Comparative transcriptome analysis of geographically distinct virulent and attenuated Babesia bovis strains reveals similar gene expression changes through attenuation
title_fullStr Comparative transcriptome analysis of geographically distinct virulent and attenuated Babesia bovis strains reveals similar gene expression changes through attenuation
title_full_unstemmed Comparative transcriptome analysis of geographically distinct virulent and attenuated Babesia bovis strains reveals similar gene expression changes through attenuation
title_sort Comparative transcriptome analysis of geographically distinct virulent and attenuated Babesia bovis strains reveals similar gene expression changes through attenuation
dc.creator.none.fl_str_mv Pedroni, Monica J.
Sondgeroth, Kerry S.
Gallego-Lopez, Gina M.
Echaide, Ignacio Eduardo
Lau, Audrey OT
author Pedroni, Monica J.
author_facet Pedroni, Monica J.
Sondgeroth, Kerry S.
Gallego-Lopez, Gina M.
Echaide, Ignacio Eduardo
Lau, Audrey OT
author_role author
author2 Sondgeroth, Kerry S.
Gallego-Lopez, Gina M.
Echaide, Ignacio Eduardo
Lau, Audrey OT
author2_role author
author
author
author
dc.subject.none.fl_str_mv Babesia bovis
Genética
Vacuna Viva
Expresión Génica
Secuencia Nucleotídica
Genetics
Live Vaccines
Gene Expression
Nucleotide Sequence
Vacuna Atenuada
topic Babesia bovis
Genética
Vacuna Viva
Expresión Génica
Secuencia Nucleotídica
Genetics
Live Vaccines
Gene Expression
Nucleotide Sequence
Vacuna Atenuada
dc.description.none.fl_txt_mv Background: Loss of virulence is a phenotypic adaptation commonly seen in prokaryotic and eukaryotic pathogens. This mechanism is not well studied, especially in organisms with multiple host and life cycle stages such as Babesia, a tick-transmitted hemoparasite of humans and animals. B. bovis, which infects cattle, has naturally occurring virulent strains that can be reliably attenuated in vivo. Previous studies suggest the virulence loss mechanism may involve post-genomic modification. We investigated the transcriptome profiles of two geographically distinct B. bovis virulent and attenuated strain pairs to better understand virulence loss and to gain insight into pathogen adaptation strategies. Results: Expression microarray and RNA-sequencing approaches were employed to compare transcriptome profiles of two B. bovis strain pairs, with each pair consisting of a virulent parental and its attenuated derivative strain. Differentially regulated transcripts were identified within each strain pair. These included genes encoding for VESA1, SmORFs, undefined membrane and hypothetical proteins. The majority of individual specific gene transcripts differentially regulated within a strain were not shared between the two strains. There was a disproportionately greater number of ves genes upregulated in the virulent parental strains. When compared with their attenuated derivatives, divergently oriented ves genes were included among the upregulated ves genes in the virulent strains, while none of the upregulated ves genes in the attenuated derivatives were oriented head to head. One gene family whose specific members were consistently and significantly upregulated in expression in both attenuated strains was spherical body protein (SBP) 2 encoding gene where SBP2 truncated copies 7, 9 and 11 transcripts were all upregulated. Conclusions: We conclude that ves heterodimer pair upregulation and overall higher frequency of ves gene expressions in the virulent strains is consistent with the involvement of this gene family in virulence. This is logical given the role of VESA1 proteins in cytoadherence of infected cells to endothelial cells. However, upregulation of some ves genes in the attenuated derivatives suggests that the consequence of upregulation is gene-specific. Furthermore, upregulation of the spherical body protein 2 gene family may play a role in the attenuated phenotype. Exactly how these two gene families may contribute to the loss or gain of virulence is discussed.
EEA Rafaela
Fil: Pedroni, Monica J. Washington State University. College of Veterinary Medicine. Department of Veterinary Microbiology & Pathology. Program of Genomics; Estados Unidos
Fil: Sondgeroth, Kerry S. Washington State University. College of Veterinary Medicine. Department of Veterinary Microbiology & Pathology. Program of Genomics; Estados Unidos
Fil: Gallego-Lopez, Gina M. Washington State University. College of Veterinary Medicine. Department of Veterinary Microbiology & Pathology. Program of Genomics; Estados Unidos
Fil: Echaide, Ignacio Eduardo. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Rafaela. Laboratorio de Inmunología y Parasitología; Argentina
Fil: Lau, Audrey OT. Washington State University. College of Veterinary Medicine. Department of Veterinary Microbiology & Pathology. Program of Genomics; Estados Unidos. Washington State University. College of Veterinary Medicine. Paul G. Allen School for Global Animal Health; Estados Unidos
description Background: Loss of virulence is a phenotypic adaptation commonly seen in prokaryotic and eukaryotic pathogens. This mechanism is not well studied, especially in organisms with multiple host and life cycle stages such as Babesia, a tick-transmitted hemoparasite of humans and animals. B. bovis, which infects cattle, has naturally occurring virulent strains that can be reliably attenuated in vivo. Previous studies suggest the virulence loss mechanism may involve post-genomic modification. We investigated the transcriptome profiles of two geographically distinct B. bovis virulent and attenuated strain pairs to better understand virulence loss and to gain insight into pathogen adaptation strategies. Results: Expression microarray and RNA-sequencing approaches were employed to compare transcriptome profiles of two B. bovis strain pairs, with each pair consisting of a virulent parental and its attenuated derivative strain. Differentially regulated transcripts were identified within each strain pair. These included genes encoding for VESA1, SmORFs, undefined membrane and hypothetical proteins. The majority of individual specific gene transcripts differentially regulated within a strain were not shared between the two strains. There was a disproportionately greater number of ves genes upregulated in the virulent parental strains. When compared with their attenuated derivatives, divergently oriented ves genes were included among the upregulated ves genes in the virulent strains, while none of the upregulated ves genes in the attenuated derivatives were oriented head to head. One gene family whose specific members were consistently and significantly upregulated in expression in both attenuated strains was spherical body protein (SBP) 2 encoding gene where SBP2 truncated copies 7, 9 and 11 transcripts were all upregulated. Conclusions: We conclude that ves heterodimer pair upregulation and overall higher frequency of ves gene expressions in the virulent strains is consistent with the involvement of this gene family in virulence. This is logical given the role of VESA1 proteins in cytoadherence of infected cells to endothelial cells. However, upregulation of some ves genes in the attenuated derivatives suggests that the consequence of upregulation is gene-specific. Furthermore, upregulation of the spherical body protein 2 gene family may play a role in the attenuated phenotype. Exactly how these two gene families may contribute to the loss or gain of virulence is discussed.
publishDate 2013
dc.date.none.fl_str_mv 2013-11
2018-09-14T16:08:06Z
2018-09-14T16:08:06Z
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv https://bmcgenomics.biomedcentral.com/articles/10.1186/1471-2164-14-763
http://hdl.handle.net/20.500.12123/3367
1471-2164
https://doi.org/10.1186/1471-2164-14-763
url https://bmcgenomics.biomedcentral.com/articles/10.1186/1471-2164-14-763
http://hdl.handle.net/20.500.12123/3367
https://doi.org/10.1186/1471-2164-14-763
identifier_str_mv 1471-2164
dc.language.none.fl_str_mv eng
language eng
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv BMC Genomics 14 : 763 (2013)
reponame:INTA Digital (INTA)
instname:Instituto Nacional de Tecnología Agropecuaria
reponame_str INTA Digital (INTA)
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instname_str Instituto Nacional de Tecnología Agropecuaria
repository.name.fl_str_mv INTA Digital (INTA) - Instituto Nacional de Tecnología Agropecuaria
repository.mail.fl_str_mv tripaldi.nicolas@inta.gob.ar
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