Rhipicephalus bursa Sialotranscriptomic Response to Blood Feeding and Babesia ovis Infection
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10362/116850 |
Resumo: | Ticks are among the most prevalent blood-feeding arthropods, and they act as vectors and reservoirs for numerous pathogens. Sialotranscriptomic characterizations of tick responses to blood feeding and pathogen infections can offer new insights into the molecular interplay occurring at the tick-host-pathogen interface. In the present study, we aimed to identify and characterize Rhipicephalus bursa salivary gland (SG) genes that were differentially expressed in response to blood feeding and Babesia ovis infection. Our experimental approach consisted of RNA sequencing of SG from three different tick samples, fed-infected, fed-uninfected, and unfed-uninfected, for characterization and inter-comparison. Overall, 7,272 expressed sequence tags (ESTs) were constructed from unfed-uninfected, 13,819 ESTs from fed-uninfected, and 15,292 ESTs from fed-infected ticks. Two catalogs of transcripts that were differentially expressed in response to blood feeding and B. ovis infection were produced. Four genes coding for a putative vitellogenin-3, lachesin, a glycine rich protein, and a secreted cement protein were selected for RNA interference functional studies. A reduction of 92, 65, and 51% was observed in vitellogenin-3, secreted cement, and lachesin mRNA levels in SG, respectively. The vitellogenin-3 knockdown led to increased tick mortality, with 77% of ticks dying post-infestation. The reduction of the secreted cement protein-mRNA levels resulted in 46% of ticks being incapable of correctly attaching to the host and significantly lower female weights post-feeding in comparison to the control group. The lachesin knockdown resulted in a 70% reduction of the levels associated with B. ovis infection in R. bursa SG and 70% mortality. These results improved our understanding of the role of tick SG genes in Babesia infection/proliferation and tick feeding. Moreover, lachesin, vitellogenin-3, and secreted cement proteins were validated as candidate protective antigens for the development of novel tick and tick-borne disease control measures. |
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Rhipicephalus bursa Sialotranscriptomic Response to Blood Feeding and Babesia ovis InfectionIdentification of Candidate Protective AntigensBabesia sppRNA interferenceRhipicephalus bursaSialotranscriptomicsVaccinevector-pathogen interactionsMicrobiologyImmunology and Microbiology(all)Infectious DiseasesSDG 3 - Good Health and Well-beingTicks are among the most prevalent blood-feeding arthropods, and they act as vectors and reservoirs for numerous pathogens. Sialotranscriptomic characterizations of tick responses to blood feeding and pathogen infections can offer new insights into the molecular interplay occurring at the tick-host-pathogen interface. In the present study, we aimed to identify and characterize Rhipicephalus bursa salivary gland (SG) genes that were differentially expressed in response to blood feeding and Babesia ovis infection. Our experimental approach consisted of RNA sequencing of SG from three different tick samples, fed-infected, fed-uninfected, and unfed-uninfected, for characterization and inter-comparison. Overall, 7,272 expressed sequence tags (ESTs) were constructed from unfed-uninfected, 13,819 ESTs from fed-uninfected, and 15,292 ESTs from fed-infected ticks. Two catalogs of transcripts that were differentially expressed in response to blood feeding and B. ovis infection were produced. Four genes coding for a putative vitellogenin-3, lachesin, a glycine rich protein, and a secreted cement protein were selected for RNA interference functional studies. A reduction of 92, 65, and 51% was observed in vitellogenin-3, secreted cement, and lachesin mRNA levels in SG, respectively. The vitellogenin-3 knockdown led to increased tick mortality, with 77% of ticks dying post-infestation. The reduction of the secreted cement protein-mRNA levels resulted in 46% of ticks being incapable of correctly attaching to the host and significantly lower female weights post-feeding in comparison to the control group. The lachesin knockdown resulted in a 70% reduction of the levels associated with B. ovis infection in R. bursa SG and 70% mortality. These results improved our understanding of the role of tick SG genes in Babesia infection/proliferation and tick feeding. Moreover, lachesin, vitellogenin-3, and secreted cement proteins were validated as candidate protective antigens for the development of novel tick and tick-borne disease control measures.Global Health and Tropical Medicine (GHTM)Vector borne diseases and pathogens (VBD)Instituto de Higiene e Medicina Tropical (IHMT)RUNAntunes, SCouto, JoanaFerrolho, JRodrigues, FábioNobre, JoãoSantos, Ana SofiaSantos-Silva, Maria MargaridaDe La Fuente, JoséDomingos, A2021-05-03T22:39:22Z2018-05-042018-05-04T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article17application/pdfhttp://hdl.handle.net/10362/116850eng2235-2988PURE: 6127751https://doi.org/10.3389/fcimb.2018.00116info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-03-11T04:59:38Zoai:run.unl.pt:10362/116850Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:43:19.102753Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Rhipicephalus bursa Sialotranscriptomic Response to Blood Feeding and Babesia ovis Infection Identification of Candidate Protective Antigens |
title |
Rhipicephalus bursa Sialotranscriptomic Response to Blood Feeding and Babesia ovis Infection |
spellingShingle |
Rhipicephalus bursa Sialotranscriptomic Response to Blood Feeding and Babesia ovis Infection Antunes, S Babesia spp RNA interference Rhipicephalus bursa Sialotranscriptomics Vaccine vector-pathogen interactions Microbiology Immunology and Microbiology(all) Infectious Diseases SDG 3 - Good Health and Well-being |
title_short |
Rhipicephalus bursa Sialotranscriptomic Response to Blood Feeding and Babesia ovis Infection |
title_full |
Rhipicephalus bursa Sialotranscriptomic Response to Blood Feeding and Babesia ovis Infection |
title_fullStr |
Rhipicephalus bursa Sialotranscriptomic Response to Blood Feeding and Babesia ovis Infection |
title_full_unstemmed |
Rhipicephalus bursa Sialotranscriptomic Response to Blood Feeding and Babesia ovis Infection |
title_sort |
Rhipicephalus bursa Sialotranscriptomic Response to Blood Feeding and Babesia ovis Infection |
author |
Antunes, S |
author_facet |
Antunes, S Couto, Joana Ferrolho, J Rodrigues, Fábio Nobre, João Santos, Ana Sofia Santos-Silva, Maria Margarida De La Fuente, José Domingos, A |
author_role |
author |
author2 |
Couto, Joana Ferrolho, J Rodrigues, Fábio Nobre, João Santos, Ana Sofia Santos-Silva, Maria Margarida De La Fuente, José Domingos, A |
author2_role |
author author author author author author author author |
dc.contributor.none.fl_str_mv |
Global Health and Tropical Medicine (GHTM) Vector borne diseases and pathogens (VBD) Instituto de Higiene e Medicina Tropical (IHMT) RUN |
dc.contributor.author.fl_str_mv |
Antunes, S Couto, Joana Ferrolho, J Rodrigues, Fábio Nobre, João Santos, Ana Sofia Santos-Silva, Maria Margarida De La Fuente, José Domingos, A |
dc.subject.por.fl_str_mv |
Babesia spp RNA interference Rhipicephalus bursa Sialotranscriptomics Vaccine vector-pathogen interactions Microbiology Immunology and Microbiology(all) Infectious Diseases SDG 3 - Good Health and Well-being |
topic |
Babesia spp RNA interference Rhipicephalus bursa Sialotranscriptomics Vaccine vector-pathogen interactions Microbiology Immunology and Microbiology(all) Infectious Diseases SDG 3 - Good Health and Well-being |
description |
Ticks are among the most prevalent blood-feeding arthropods, and they act as vectors and reservoirs for numerous pathogens. Sialotranscriptomic characterizations of tick responses to blood feeding and pathogen infections can offer new insights into the molecular interplay occurring at the tick-host-pathogen interface. In the present study, we aimed to identify and characterize Rhipicephalus bursa salivary gland (SG) genes that were differentially expressed in response to blood feeding and Babesia ovis infection. Our experimental approach consisted of RNA sequencing of SG from three different tick samples, fed-infected, fed-uninfected, and unfed-uninfected, for characterization and inter-comparison. Overall, 7,272 expressed sequence tags (ESTs) were constructed from unfed-uninfected, 13,819 ESTs from fed-uninfected, and 15,292 ESTs from fed-infected ticks. Two catalogs of transcripts that were differentially expressed in response to blood feeding and B. ovis infection were produced. Four genes coding for a putative vitellogenin-3, lachesin, a glycine rich protein, and a secreted cement protein were selected for RNA interference functional studies. A reduction of 92, 65, and 51% was observed in vitellogenin-3, secreted cement, and lachesin mRNA levels in SG, respectively. The vitellogenin-3 knockdown led to increased tick mortality, with 77% of ticks dying post-infestation. The reduction of the secreted cement protein-mRNA levels resulted in 46% of ticks being incapable of correctly attaching to the host and significantly lower female weights post-feeding in comparison to the control group. The lachesin knockdown resulted in a 70% reduction of the levels associated with B. ovis infection in R. bursa SG and 70% mortality. These results improved our understanding of the role of tick SG genes in Babesia infection/proliferation and tick feeding. Moreover, lachesin, vitellogenin-3, and secreted cement proteins were validated as candidate protective antigens for the development of novel tick and tick-borne disease control measures. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-05-04 2018-05-04T00:00:00Z 2021-05-03T22:39:22Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10362/116850 |
url |
http://hdl.handle.net/10362/116850 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
2235-2988 PURE: 6127751 https://doi.org/10.3389/fcimb.2018.00116 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
17 application/pdf |
dc.source.none.fl_str_mv |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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