Rhipicephalus bursa Sialotranscriptomic Response to Blood Feeding and Babesia ovis Infection

Bibliographic Details
Main Author: Antunes, S
Publication Date: 2018
Other Authors: Couto, Joana, Ferrolho, J, Rodrigues, Fábio, Nobre, João, Santos, Ana Sofia, Santos-Silva, Maria Margarida, De La Fuente, José, Domingos, A
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10362/116850
Summary: 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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spelling 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:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-05-22T17:52:42Zoai:run.unl.pt:10362/116850Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T17:23:50.625453Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
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
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