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dc.contributor.authorTorres, Lorena
dc.contributor.authorAlmazan, Consuelo
dc.contributor.authorAyllon, Nieves
dc.contributor.authorGalindo, Ruth C.
dc.contributor.authorRosario-Cruz, Rodrigo
dc.contributor.authorQuiroz-Romero, Hector
dc.contributor.authorde la Fuente, Jose
dc.date.accessioned2018-11-09T21:10:58Z
dc.date.available2018-11-09T21:10:58Z
dc.date.issued2011-02-10
dc.identifieroksd_torres_functionalgeno_2011-02-10
dc.identifier.citationTorres, L., Almazan, C., Ayllon, N., Galindo, R. C., Rosario-Cruz, R., Quiroz-Romero, H., & de la Fuente, J. (2011). Functional genomics of the horn fly, Haematobia irritans (Linnaeus, 1758). BMC Genomics, 12, Article 105. https://doi.org/10.1186/1471-2164-12-105
dc.identifier.urihttps://hdl.handle.net/11244/302077
dc.description.abstractBackground: The horn fly, Haematobia irritans (Linnaeus, 1758) (Diptera: Muscidae) is one of the most important ectoparasites of pastured cattle. Horn flies infestations reduce cattle weight gain and milk production. Additionally, horn flies are mechanical vectors of different pathogens that cause disease in cattle. The aim of this study was to conduct a functional genomics study in female horn flies using Expressed Sequence Tags (EST) analysis and RNA interference (RNAi).
dc.description.abstractResults: A cDNA library was made from whole abdominal tissues collected from partially fed adult female horn flies. High quality horn fly ESTs (2,160) were sequenced and assembled into 992 unigenes (178 contigs and 814 singlets) representing molecular functions such as serine proteases, cell metabolism, mitochondrial function, transcription and translation, transport, chromatin structure, vitellogenesis, cytoskeleton, DNA replication, cell response to stress and infection, cell proliferation and cell-cell interactions, intracellular trafficking and secretion, and development. Functional analyses were conducted using RNAi for the first time in horn flies. Gene knockdown by RNAi resulted in higher horn fly mortality (protease inhibitor functional group), reduced oviposition (vitellogenin, ferritin and vATPase groups) or both (immune response and 5'-NUC groups) when compared to controls. Silencing of ubiquitination ESTs did not affect horn fly mortality and ovisposition while gene knockdown in the ferritin and vATPse functional groups reduced mortality when compared to controls.
dc.description.abstractConclusions: These results advanced the molecular characterization of this important ectoparasite and suggested candidate protective antigens for the development of vaccines for the control of horn fly infestations.
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dc.languageen_US
dc.publisherBioMed Central
dc.rightsThis material has been previously published. In the Oklahoma State University Library's institutional repository this version is made available through the open access principles and the terms of agreement/consent between the author(s) and the publisher. The permission policy on the use, reproduction or distribution of the material falls under fair use for educational, scholarship, and research purposes. Contact Digital Resources and Discovery Services at lib-dls@okstate.edu or 405-744-9161 for further information.
dc.titleFunctional genomics of the horn fly, Haematobia irritans (Linnaeus, 1758)
osu.filenameoksd_torres_functionalgeno_2011-02-10.pdf
dc.description.peerreviewPeer reviewed
dc.identifier.doi10.1186/1471-2164-12-105
dc.description.departmentVeterinary Pathobiology
dc.type.genreArticle
dc.type.materialText
dc.subject.keywordsserine protease
dc.subject.keywordstick infestation
dc.subject.keywordstick cell
dc.subject.keywordsprotease inhibitor gene
dc.subject.keywordsgene expression silence


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