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dc.contributor.authorLara, Flávio Alvespt_BR
dc.contributor.authorPohl, Paula Cristianept_BR
dc.contributor.authorGandara, Ana Carolinept_BR
dc.contributor.authorFerreira, Jessica da Silvapt_BR
dc.contributor.authorNascimento-Silva, Maria Clarapt_BR
dc.contributor.authorBechara, Gervásio Henriquept_BR
dc.contributor.authorSorgine, Marcos Henrique Ferreirapt_BR
dc.contributor.authorAlmeida, Igor Correia dept_BR
dc.contributor.authorVaz Junior, Itabajara da Silvapt_BR
dc.contributor.authorOliveira, Pedro Lagerblad dept_BR
dc.date.accessioned2021-07-23T04:41:34Zpt_BR
dc.date.issued2015pt_BR
dc.identifier.issn1932-6203pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/224429pt_BR
dc.description.abstractIn ticks, the digestion of blood occurs intracellularly and proteolytic digestion of hemoglobin takes place in a dedicated type of lysosome, the digest vesicle, followed by transfer of the heme moiety of hemoglobin to a specialized organelle that accumulates large heme aggregates, called hemosomes. In the present work, we studied the uptake of fluorescent metalloporphyrins, used as heme analogs, and amitraz, one of the most regularly used acaricides to control cattle tick infestations, by Rhipicephalus (Boophilus) microplus midgut cells. Both compounds were taken up by midgut cells in vitro and accumulated inside the hemosomes. Transport of both molecules was sensitive to cyclosporine A (CsA), a wellknown inhibitor of ATP binding cassette (ABC) transporters. Rhodamine 123, a fluorescent probe that is also a recognized ABC substrate, was similarly directed to the hemosome in a CsA-sensitive manner. Using an antibody against conserved domain of PgP-1-type ABC transporter, we were able to immunolocalize PgP-1 in the digest vesicle membranes. Comparison between two R. microplus strains that were resistant and susceptible to amitraz revealed that the resistant strain detoxified both amitraz and Sn-Pp IX more efficiently than the susceptible strain, a process that was also sensitive to CsA. A transcript containing an ABC transporter signature exhibited 2.5-fold increased expression in the amitraz-resistant strain when compared with the susceptible strain. RNAi-induced down-regulation of this ABC transporter led to the accumulation of metalloporphyrin in the digestive vacuole, interrupting heme traffic to the hemosome. This evidence further confirms that this transcript codes for a heme transporter. This is the first report of heme transport in a blood-feeding organism. While the primary physiological function of the hemosome is to detoxify heme and attenuate its toxicity, we suggest that the use of this acaricide detoxification pathway by ticks may represent a new molecular mechanism of resistance to pesticides.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofPLOS ONE. San Francisco, CA. Vol. 10, no. 8 (Aug. 2015), e0134779, 20 p.pt_BR
dc.rightsOpen Accessen
dc.subjectEntomologiapt_BR
dc.subjectBiotecnologiapt_BR
dc.subjectRhipicephalus micropluspt_BR
dc.subjectResistência à pesticidapt_BR
dc.titleATP binding cassette transporter mediates both heme and pesticide detoxification in tick midgut cellspt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb000971802pt_BR
dc.type.originEstrangeiropt_BR


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