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dc.contributor.authorSmith, Alexis A.
dc.contributor.authorNavasa, Nicolas
dc.contributor.authorYang, Xiuli
dc.contributor.authorWilder, Cara N.
dc.contributor.authorBuyuktanir, Ozlem
dc.contributor.authorMarques, Adriana
dc.contributor.authorPal, Utpal
dc.date.accessioned2020-06-21T13:32:38Z
dc.date.available2020-06-21T13:32:38Z
dc.date.issued2016
dc.identifier.issn1931-3128
dc.identifier.issn1934-6069
dc.identifier.urihttps://doi.org/10.1016/j.chom.2016.06.001
dc.identifier.urihttps://hdl.handle.net/20.500.12712/13240
dc.descriptionYAS, Ozlem BUYUKTANIR/0000-0002-7641-7350; Anguita, Juan/0000-0003-2061-7182; Marques, Adriana/0000-0002-5403-4551en_US
dc.descriptionWOS: 000380707200013en_US
dc.descriptionPubMed: 27374407en_US
dc.description.abstractEvolution of hematophagy in blood-sucking parasites likely involves communication with their hosts. We find that Ixodes ticks are responsive to IFNg acquired in a blood meal from mice infected with the Lyme disease-causing bacteria Borrelia burgdorferi, leading to induction of antimicrobial responses. Ixodes ticks parasitizing B. burgdorferi-infected mice upregulated an I. scapularis Rho-like GTPase (IGTPase). IGTPase knockdown enhanced B. burgdorferi levels in postfed ticks, suggesting this protein controls spirochete survival. Notably, IGTPase was only induced during pathogen acquisition from mice and not upon transmission to naive hosts. Microinjection of ticks with IFNg induced IGTPase, and ticks parasitizing IFNg knockout mice, failed to upregulate IGTPase. Additionally, ticks lacking the transcription factor STAT, which signals downstream of IFNg, did not induce IGTPase. IGTPase expression induced antimicrobial peptides, including Dae2, previously shown to inhibit B. burgdorferi. These results identify an interspecies signaling cascade allowing ticks to detect invading bacteria and mount microbicidal responses.en_US
dc.description.sponsorshipUniversity of Maryland, College Park; National Institute of Allergy and Infectious DiseasesUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Institute of Allergy & Infectious Diseases (NIAID) [AI080615, AI116620]; Ondokuz Mayis UniversityOndokuz Mayis University; Turkish Higher Education CouncilMinistry of National Education - Turkey; Intramural Research Program of the National Institute of Allergy and Infectious DiseaseUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Institute of Allergy & Infectious Diseases (NIAID); European UnionEuropean Union (EU) [602272]en_US
dc.description.sponsorshipWe thank John Anderson, Toru Kariu, Faith Kung, Kavita Sharma, Brian Backstedt, Juraj Koci, and Meghna Thakur for their assistance with this study. We would like to thank Ulrike Munderloh, University of Minnesota, for providing the IDE12 cell line. This work was supported by funding from University of Maryland, College Park, and the National Institute of Allergy and Infectious Diseases Award Number AI080615 and AI116620 (to U.P.). O.B. is supported by funding from Ondokuz Mayis University and Turkish Higher Education Council. A.M. is supported by the Intramural Research Program of the National Institute of Allergy and Infectious Disease. J.A. is funded by the European Union (Grant Agreement number 602272).en_US
dc.language.isoengen_US
dc.publisherCell Pressen_US
dc.relation.isversionof10.1016/j.chom.2016.06.001en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleCross-Species Interferon Signaling Boosts Microbicidal Activity within the Tick Vectoren_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume20en_US
dc.identifier.issue1en_US
dc.identifier.startpage91en_US
dc.identifier.endpage98en_US
dc.relation.journalCell Host & Microbeen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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