dc.creatorGarcia, Gustavo Rocha
dc.creatorGardinassi, Luiz Gustavo
dc.creatorRibeiro, José Marcos
dc.creatorAnatriello, Elen
dc.creatorFerreira, Beatriz Rossetti
dc.creatorMoreira, Higo Nasser Santanna
dc.creatorMafra, Cláudio
dc.creatorMartins, Maria Marlene
dc.creatorSzabó, Matias Pablo Juan
dc.creatorMiranda-Santos, Isabel Kinney Ferreira de
dc.creatorMaruyama, Sandra Regina
dc.date.accessioned2015-01-09T16:54:57Z
dc.date.accessioned2018-07-04T16:58:46Z
dc.date.available2015-01-09T16:54:57Z
dc.date.available2018-07-04T16:58:46Z
dc.date.created2015-01-09T16:54:57Z
dc.date.issued2014
dc.identifierParasites & Vectors. 2014 Sep 08;7(1):430
dc.identifierhttp://www.producao.usp.br/handle/BDPI/47330
dc.identifier10.1186/1756-3305-7-430
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1642995
dc.description.abstractBackground Tick salivary constituents antagonize inflammatory, immune and hemostatic host responses, favoring tick blood feeding and the establishment of tick-borne pathogens in hosts during hematophagy. Amblyomma triste, A. cajennense and A. parvum ticks are very important in veterinary and human health because they are vectors of the etiological agents for several diseases. Insights into the tick salivary components involved in blood feeding are essential to understanding vector-pathogen-host interactions, and transcriptional profiling of salivary glands is a powerful tool to do so. Here, we functionally annotated the sialotranscriptomes of these three Amblyomma species, which allowed comparisons between these and other hematophagous arthropod species. Methods mRNA from the salivary glands of A. triste, A. cajennense and A. parvum ticks fed on different host species were pyrosequenced on a 454-Roche platform to generate four A. triste (nymphs fed on guinea pigs and females fed on dogs) libraries, one A. cajennense (females fed on rabbits) library and one was A. parvum (females fed on dogs) library. Bioinformatic analyses used in-house programs with a customized pipeline employing standard assembly and alignment algorithms, protein databases and protein servers. Results Each library yielded an average of 100,000 reads, which were assembled to obtain contigs of coding sequences (CDSs). The sialotranscriptome analyses of A. triste, A. cajennense and A. parvum ticks produced 11,240, 4,604 and 3,796 CDSs, respectively. These CDSs were classified into over 100 distinct protein families with a wide range of putative functions involved in physiological and blood feeding processes and were catalogued in annotated, hyperlinked spreadsheets. We highlighted the putative transcripts encoding saliva components with critical roles during parasitism, such as anticoagulants, immunosuppressants and anti-inflammatory molecules. The salivary content underwent changes in the abundance and repertoire of many transcripts, which depended on the tick and host species. Conclusions The annotated sialotranscriptomes described herein richly expand the biological knowledge of these three Amblyomma species. These comprehensive databases will be useful for the characterization of salivary proteins and can be applied to control ticks and tick-borne diseases.
dc.languageen
dc.publisherBioMed Central
dc.relationParasites and Vectors
dc.rightsGarcia et al.; licensee BioMed Central Ltd.
dc.rightsopenAccess
dc.subjectTicks
dc.subjectAmblyomma cajennense
dc.subjectAmblyomma parvum
dc.subjectAmblyomma triste
dc.subjectSalivary gland
dc.subjectSaliva
dc.subjectTranscriptome
dc.subjectRNA-seq
dc.titleThe sialotranscriptome of Amblyomma triste, Amblyomma parvum and Amblyomma cajennense ticks, uncovered by 454-based RNA-seq
dc.typeArtículos de revistas


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