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dc.contributor.authorVillar, Margarita
dc.contributor.authorLopez, Vladimir
dc.contributor.authorAyllon, Nieves
dc.contributor.authorCabezas-Cruz, Alejandro
dc.contributor.authorLopez, Juan Antonio 
dc.contributor.authorVazquez, Jesus 
dc.contributor.authorAlberdi, Pilar
dc.contributor.authorde la Fuente, Jose
dc.date.accessioned2017-10-30T13:15:40Z
dc.date.available2017-10-30T13:15:40Z
dc.date.issued2016
dc.identifierISI:000383846100001
dc.identifier.citationParasit Vectors. 2016; 9:467
dc.identifier.issn1756-3305
dc.identifier.urihttp://hdl.handle.net/20.500.12105/5203
dc.description.abstractBackground: The intracellular bacteria Anaplasma phagocytophilum are emerging zoonotic pathogens affecting human and animal health, and a good model for the study of tick-host-pathogen interactions. This tick-borne pathogen is transmitted by Ixodes scapularis in the United States where it causes human granulocytic anaplasmosis. Tick midguts and salivary glands play a major role during tick feeding and development, and in pathogen acquisition, multiplication and transmission. Vertebrate host proteins are found in tick midguts after feeding and have been described in the salivary glands of fed and unfed ticks, suggesting a role for these proteins during tick feeding and development. Furthermore, recent results suggested the hypothesis that pathogen infection affects tick metabolic processes to modify host protein digestion and persistence in the tick with possible implications for tick physiology and pathogen life-cycle. Methods: To address this hypothesis, herein we used I. scapularis female ticks fed on uninfected and A. phagocytophilum-infected sheep to characterize host protein content in midguts and salivary glands by proteomic analysis of tick tissues. Results: The results evidenced a clear difference in the host protein content between tick midguts and salivary glands in response to infection suggesting that A. phagocytophilum selectively manipulates the levels of vertebrate host proteins in ticks in a tissue-specific manner to facilitate pathogen infection, multiplication and transmission while preserving tick feeding and development. The mechanisms by which A. phagocytophilum manipulates the levels of vertebrate host proteins are not known, but the results obtained here suggested that it might include the modification of proteolytic pathways. Conclusions: The results of this study provided evidence to support that A. phagocytophilum affect tick proteolytic pathways to selectively manipulate the levels of vertebrate host proteins in a tissue-specific manner to increase tick vector capacity. Investigating the biological relevance of host proteins in tick biology and pathogen infection and the mechanisms used by A. phagocytophilum to manipulate host protein content is essential to advance our knowledge of tick-host-pathogen molecular interactions. These results have implications for the identification of new targets for the development of vaccines for the control of tick-borne diseases.
dc.description.sponsorshipThis research was supported by the Ministerio de Economia y Competitividad (Spain) grant BFU2011-23896 and the European Union (EU) Seventh Framework Programme (FP7) ANTIGONE project number 278976. NA was funded by Ministerio de Economia y Competitividad, Spain. MV was supported by the Research Plan of the University of Castilla - La Mancha, Spain. The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
dc.language.isoeng
dc.publisherBioMed Central (BMC) 
dc.type.hasVersionVoR
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectAnaplasma
dc.subjectTick
dc.subjectIxodes
dc.subjectProteomics
dc.subjectHemoglobin
dc.subjectImmunology
dc.subjectQUANTITATIVE PROTEOMICS
dc.subjectEHRLICHIA-CHAFFEENSIS
dc.subjectGENE-EXPRESSION
dc.subjectSALIVARY-GLANDS
dc.subjectINFECTION
dc.subjectCELLS
dc.subjectINSIGHTS
dc.subjectDISEASE
dc.subjectIDENTIFICATION
dc.subjectARTHROPODS
dc.titleThe intracellular bacterium Anaplasma phagocytophilum selectively manipulates the levels of vertebrate host proteins in the tick vector Ixodes scapularis
dc.typejournal article
dc.rights.licenseAtribución 4.0 Internacional*
dc.identifier.pubmedID27561965
dc.format.volume9
dc.identifier.doi10.1186/s13071-016-1747-3
dc.contributor.funderMinisterio de Economía y Competitividad (España) 
dc.contributor.funderUnión Europea 
dc.contributor.funderRegional Government of Castile-La Mancha (España) 
dc.description.peerreviewed
dc.relation.publisherversionhttps://doi.org/10.1186/s13071-016-1747-3
dc.identifier.journalParasites & Vectors
dc.repisalud.orgCNICCNIC::Grupos de investigación::Proteómica cardiovascular
dc.repisalud.orgCNICCNIC::Unidades técnicas::Proteómica / Metabolómica
dc.repisalud.institucionCNIC
dc.rights.accessRightsopen accesses_ES


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