Use este identificador para citar ou linkar para este item: http://www.alice.cnptia.embrapa.br/alice/handle/doc/1154064
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Campo DCValorIdioma
dc.contributor.authorMOREIRA, V. J. V.
dc.contributor.authorPINHEIRO, D. H.
dc.contributor.authorLOURENCO, I. T.
dc.contributor.authorBASSO, M. F.
dc.contributor.authorLISEI-DE-SA, M. E.
dc.contributor.authorSILVA, M. C. M. da
dc.contributor.authorDANCHIN, E. G. J.
dc.contributor.authorGUIMARAES, P. M.
dc.contributor.authorGRYNBERG, P.
dc.contributor.authorBRASILEIRO, A. C. M.
dc.contributor.authorMACEDO, L. L. P. de
dc.contributor.authorMORGANTE, C. V.
dc.contributor.authorENGLER, J. de A.
dc.contributor.authorSA, M. F. G. de
dc.date.accessioned2024-04-06T07:24:58Z-
dc.date.available2024-04-06T07:24:58Z-
dc.date.created2023-05-29
dc.date.issued2024
dc.identifier.citationJournal of Pest Science, v. 97, p. 411-427, 2024.
dc.identifier.urihttp://www.alice.cnptia.embrapa.br/alice/handle/doc/1154064-
dc.descriptionMeloidogyne incognita is one of the most important plant-parasitic nematodes (PPNs) causing severe crop losses worldwide. Plants have evolved complex defense mechanisms to respond to PPNs attacks. Conversely, PPNs have evolved infection mechanisms that involve the secretion of effector proteins into host plants to suppress immune responses and facilitate para- sitism. Therefore, effector genes are attractive targets for the genetic improvement of plant resistance to M. incognita. In this study, we functionally characterized the Minc16803 (Minc3s00746g16803) putative effector gene to evaluate its role during plant-nematode interactions. First, we found that the Minc16803 gene is expressed in all nematode life stages and encodes a protein with an N-terminal signal peptide for secretion, a motif characteristic of effector proteins and with the absence of transmembrane domain. In addition, our data demonstrated that transgenic Arabidopsis thaliana lines overexpressing a Minc16803-dsRNA efficiently downregulated the Minc16803 transcripts in infecting nematodes. Furthermore, transgenic lines were significantly less susceptible to M. incognita compared to wild-type control plants. The number of galls per plant was reduced by up to 84%, while the number of egg masses per plant decreased by up to 93.3%. Moreover, galls and feed- ing sites in the roots of transgenic lines were smaller than those in the control plants. Histological analysis revealed giant cells without cytoplasm, disordered neighboring cells, and malformed maturing nematodes in transgenic galls. Curiously, numerous hatching ppJ2 juveniles were often observed near the female body within the transgenic root tissues before egg mass extrusion. All findings strongly suggest that Minc16803 gene is a promising target to engineer agricultural crops for M. incognita resistance through host-induced gene silencing.
dc.language.isoeng
dc.rightsopenAccess
dc.subjectHost-induced gene silencing
dc.subjectDsRNA
dc.subjectPlant-nematode interactions
dc.subjectRoot-knot nematode
dc.subjectNematoide das galhas
dc.subjectInterações planta-nematóide
dc.titleIn planta RNAi targeting Meloidogyne incognita Minc16803 gene perturbs nematode parasitism and reduces plant susceptibility.
dc.typeArtigo de periódico
dc.subject.thesagroPlanta
dc.subject.thesagroParasito de Planta
dc.subject.thesagroNematóide
dc.subject.thesagroMeloidogyne Incognita
dc.subject.nalthesaurusNematode biology
dc.subject.nalthesaurusNematode control
dc.subject.nalthesaurusPlant parasitic nematodes
dc.description.notesNa publicação: Isabela Tristan Lourenço-Tessutti; Maria C. M. Silva; Leonardo L. P. Macedo; Maria Fatima Grossi-de-Sa.
riaa.ainfo.id1154064
riaa.ainfo.lastupdate2024-04-05
dc.identifier.doihttps://doi.org/10.1007/s10340-023-01623-7
dc.contributor.institutionVALDEIR JUNIO VAZ MOREIRA, Biotechnology Center, PPGBCM, UFRGS; DANIELE HELOÍSA PINHEIRO, National Institute of Science and Technology; ISABELA TRISTAN LOURENCO TESSUTTI, Cenargen; MARCOS FERNANDO BASSO, National Institute of Science and Technology; MARIA E. LISEI-DE-SA, National Institute of Science and Technology; MARIA CRISTINA MATTAR DA SILVA, Cenargen; ETIENNE G. J. DANCHIN, National Institute of Science and Technology; PATRICIA MESSEMBERG GUIMARAES, Cenargen; PRISCILA GRYNBERG, Cenargen; ANA CRISTINA MIRANDA BRASILEIRO, Cenargen; LEONARDO LIMA PEPINO DE MACEDO, Cenargen; CAROLINA VIANNA MORGANTE, CPATSA; JANICE DE ALMEIDA ENGLER, National Institute of Science and Technology; MARIA FATIMA GROSSI DE SA, Cenargen.
Aparece nas coleções:Artigo em periódico indexado (CPATSA)

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