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| Registros recuperados : 64 | |
| 8. |  | MAR, T. B.; LAU, D.; NHANI JUNIOR, A.; SCHONS, J.; YAMAZAKI-LAU, E.; PEREIRA, J. F. Barley and cereal yellow dwarf virus genetic diversity in Brazil. Virus: reviews and research, v. 14, p. 77-78, 2009. Suplemento, ref. 060. Edição dos Resumos do XX National Meeting of Virology, Brasília, DF, nov. 2009.| Biblioteca(s): Embrapa Trigo. |
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| 9. | | MAR, T. B.; LAU, D.; SCHONS, J.; YAMAZAKI-LAU, E.; NHANI JUNIOR, A. Molecular identification based on coat protein sequences of the Barley yellow dwarf virus from Brazil. Scientia Agrícola, Piracicaba, v. 70, n. 6, p. 428-434, Nov./Dec. 2013.| Biblioteca(s): Embrapa Trigo. |
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| 10. | | MAR, T. B.; LAU, D.; NHANI JUNIOR, A.; SCHONS, J.; YAMAZAKI-LAU, E.; PEREIRA, J. F. Diversidade genética do barley e cereal yellow dwarf virus no Brasil. In: MOSTRA DE INICIAÇÃO CIENTÍFICA DA EMBRAPA TRIGO, 5., 2009, Passo Fundo. Resumos... Passo Fundo: Embrapa Trigo, 2009. 1 p. html. (Embrapa Trigo. Documentos online, 115).| Biblioteca(s): Embrapa Trigo. |
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| 12. | | BUENO, P.; LAU, E. Y.; BINNECK, E.; NHANI JUNIOR, A.; SCAGLIUSI, S. M. M. RNA-Seq para análise de genes diferencialmente expressos em micrósporos de trigo. In: MOSTRA DE INICIAÇÃO CIENTÍFICA, 15.; MOSTRA DE PÓS-GRADUAÇÃO DA EMBRAPA TRIGO, 12., 2020, Passo Fundo. Resumos... Brasília, DF: Embrapa, 2021. p. 48.| Biblioteca(s): Embrapa Agricultura Digital; Embrapa Soja. |
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| 13. | | BUENO, P.; LAU, E. Y.; BINNECK, E.; NHANI JUNIOR, A.; SCAGLIUSI, S. M. M. RNA-Seq para análise de genes diferencialmente expressos em micrósporos de trigo. In: MOSTRA DE INICIAÇÃO CIENTÍFICA, 15.; MOSTRA DE PÓS-GRADUAÇÃO DA EMBRAPA TRIGO, 12., 2020, Passo Fundo. Resumos... Brasília, DF: Embrapa, 2021. p. 48.| Biblioteca(s): Embrapa Trigo. |
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| 15. | | MAR, T. B.; LAU, D.; SCHONS, J.; YAMAZAKI-LAU, E.; BRAMMER, S. P.; NHANI JUNIOR, A. Caracterização molecular de isolados virais associados ao nanismo amarelo dos cereais visando à seleção e o desenvolvimento de genótipos de trigo resistentes. In: MOSTRA DE INICIAÇÃO CIENTÍFICA DA EMBRAPA TRIGO, 3., 2007, Passo Fundo. Resumos... Passo Fundo: Embrapa Trigo, 2007. 1 p. html. (Embrapa Trigo. Documentos Online, 82).| Biblioteca(s): Embrapa Trigo. |
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| 16. | | MAR, T. B.; LAU, D.; YAMAZAKI-LAU, E.; SCHONS, J.; NHANI JUNIOR, A. Caracterização molecular de isolados virais do Barley/Cereal Yellow Dwarf Virus (B/CYDV) do Rio Grande do Sul. In: MOSTRA DE INICIAÇÃO CIENTÍFICA DA EMBRAPA TRIGO, 4., 2008, Passo Fundo. Resumos... Passo Fundo: Embrapa Trigo, 2008. 1 p. html. (Embrapa Trigo. Documentos online, 94).| Biblioteca(s): Embrapa Trigo. |
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| 17. | | YAMAZAKI-LAU, E.; LAU, D.; SCHONS, J.; NHANI JUNIOR, A.; BRAMMER, S. P. Caracterização molecular de isolados do vírus do nanismo amarelo do Rio Grande do Sul. In: REUNIÃO DA COMISSÃO BRASILEIRA DE PESQUISA DE TRIGO E TRITICALE, 2., 2008, Passo Fundo. Atas e resumos... Passo Fundo: Comissão Brasileira de Pesquisa de Trigo e Triticale: Embrapa Trigo: Embrapa Transferência de Tecnologia, 2008. 1 p. 1 CD-ROM. Fitopatologia, 6. Área: Fitopatologia.| Biblioteca(s): Embrapa Trigo. |
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| 18. | | BRAMMER, S. P.; SCAGLIUSI, S. M. M.; BONATO, A. L. V.; TORRES, G. A. M.; CONSOLI, L.; NHANI JUNIOR, A. Biotecnologia aplicada à cultura do trigo. In: PIRES, J. L. F.; VARGAS, L.; CUNHA, G. R. da (Ed.). Trigo no Brasil: bases para produção competitiva e sustentável. Passo Fundo: Embrapa Trigo, 2011. Cap. 18, p. 453-488.| Biblioteca(s): Embrapa Trigo. |
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| 19. | | NHANI JUNIOR, A.; PEREIRA, J. F.; FERREIRA, J. R.; BONATO, A. L. V.; MACIEL, J. L. N. Mapping highly informative SSR markers in the genome of Magnaportheoryzae from wheat. Tropical Plant Pathology, Brasília, DF, v. 41, n. 5, p. 331-335, oct. 2016.| Biblioteca(s): Embrapa Trigo. |
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| 20. | | TURCHETTO, C.; GONZÁLES, H. H. S.; FERREIRA, J. R.; TORRES, G. A. M.; CONSOLI, L.; NHANI JUNIOR, A.; BINNECK, E. Prospecção de genes relacionados à interação de Magnaporthe oryzae com trigo. In: MOSTRA DE INICIAÇÃO CIENTÍFICA, 10., MOSTRA DE PÓS-GRADUAÇÃO DA EMBRAPA TRIGO, 7., 2015, Passo Fundo. Resumos... Brasília, DF: Embrapa, 2015. Pós-Graduação. p. 45.| Biblioteca(s): Embrapa Trigo. |
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| Registros recuperados : 64 | |
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Registro Completo
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Biblioteca(s): |
Embrapa Agricultura Digital; Embrapa Gado de Corte. |
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Data corrente: |
28/01/2020 |
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Data da última atualização: |
06/11/2020 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
A - 1 |
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Autoria: |
GIACHETTO, P. F.; CUNHA, R. C.; NHANI JUNIOR, A.; GARCIA, M. V.; FERRO, J. A.; ANDREOTTI, R. |
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Afiliação: |
POLIANA FERNANDA GIACHETTO, CNPTIA; RODRIGO CASQUERO CUNHA, UFPEL; ANTONIO NHANI JUNIOR, CNPTIA; MARCOS VALERIO GARCIA, CNPGC; JESUS APARECIDO FERRO, UNESP; RENATO ANDREOTTI E SILVA, CNPGC. |
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Título: |
Gene expression in the salivary gland of Rhipicephalus (Boophilus) microplus fed on tick-susceptible and tick-resistant hosts. |
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Ano de publicação: |
2020 |
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Fonte/Imprenta: |
Frontiers in Cellular and Infection Microbiology, v. 9, p. 1-15, Jan. 2020. |
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DOI: |
10.3389/fcimb.2019.0047 |
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Idioma: |
Inglês |
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Notas: |
Article 477. |
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Conteúdo: |
The success of cattle tick fixation largely depends on the secretion of substances that alter the immune response of the host. The majority of these substances are expressed by the parasite salivary gland and secreted in tick saliva. It is known that hosts can mount immune responses against ticks and bovine European breeds, and bovine industrial crossbreeds are more susceptible to infestations than are Bos indicus cattle. To identify candidates for the development of novel control strategies for the cattle tick Rhipicephalus (Boophilus) microplus, a salivary gland transcriptome analysis of engorged females fed on susceptible or resistant hosts was performed. Using RNA-Seq, transcriptomes were de novo assembled and produced a total of 235,451 contigs with 93.3% transcriptome completeness. Differential expression analysis identified 137 sequences as differentially expressed genes (DEGs) between ticks raised on tick-susceptible or tick-resistant cattle. DEGs predicted to be secreted proteins include innexins, which are transmembrane proteins that form gap junction channels; the transporters Na+/dicarboxylate, Na+/tricarboxylate, and phosphate transporter and a putative monocarboxylate transporter; a phosphoinositol 4-phosphate adaptor protein; a cysteine-rich protein containing a trypsin inhibitor-like (TIL) domain; a putative defense protein 3 containing a reeler domain; and an F-actin-uncapping protein LRRC16A with a CARMIL_C domain; these genes were upregulated in ticks fed on tick-susceptible cattle. DEGs predicted to be non-secreted proteins included a small heat shock protein and the negative elongation factor B-like, both acting in a coordinated manner to increase HSP transcript levels in the salivary glands of the ticks fed on tick-susceptible cattle; the 26S protease regulatory subunit 6B and another chaperone with similarity to calnexin, also upregulated in ticks fed on tick-susceptible cattle; an EF-hand calcium binding protein and a serine carboxypeptidase (SCP), both involved in the blood coagulation cascade and upregulated in ticks fed on tick-susceptible cattle; and two ribosomal proteins, the 60S acidic ribosomal protein P2 and the 60S ribosomal protein L19. These results help to characterize cattle tick salivary gland gene expression in tick-susceptible and tick-resistant hosts and suggest new putative targets for the control of tick infestations, as those genes involved in the mechanism of stress response during blood feeding. MenosThe success of cattle tick fixation largely depends on the secretion of substances that alter the immune response of the host. The majority of these substances are expressed by the parasite salivary gland and secreted in tick saliva. It is known that hosts can mount immune responses against ticks and bovine European breeds, and bovine industrial crossbreeds are more susceptible to infestations than are Bos indicus cattle. To identify candidates for the development of novel control strategies for the cattle tick Rhipicephalus (Boophilus) microplus, a salivary gland transcriptome analysis of engorged females fed on susceptible or resistant hosts was performed. Using RNA-Seq, transcriptomes were de novo assembled and produced a total of 235,451 contigs with 93.3% transcriptome completeness. Differential expression analysis identified 137 sequences as differentially expressed genes (DEGs) between ticks raised on tick-susceptible or tick-resistant cattle. DEGs predicted to be secreted proteins include innexins, which are transmembrane proteins that form gap junction channels; the transporters Na+/dicarboxylate, Na+/tricarboxylate, and phosphate transporter and a putative monocarboxylate transporter; a phosphoinositol 4-phosphate adaptor protein; a cysteine-rich protein containing a trypsin inhibitor-like (TIL) domain; a putative defense protein 3 containing a reeler domain; and an F-actin-uncapping protein LRRC16A with a CARMIL_C domain; these genes were upregulated in ticks fed ... Mostrar Tudo |
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Palavras-Chave: |
Bioinformática; Cattle tick; Expressão gênica; Host-parasite interaction; RNA-Seq. |
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Thesagro: |
Carrapato; Gado de Corte. |
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Thesaurus NAL: |
Bioinformatics; Cattle; Rhipicephalus microplus; Sialome; Transcriptome. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/215164/1/AP-Gene-expression-in-the-salivary-2020.pdf
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/209727/1/Gene-expression-in-the-salivary.pdf
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Marc: |
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024 7 $a10.3389/fcimb.2019.0047$2DOI
100 1 $aGIACHETTO, P. F.
245 $aGene expression in the salivary gland of Rhipicephalus (Boophilus) microplus fed on tick-susceptible and tick-resistant hosts.$h[electronic resource]
260 $c2020
500 $aArticle 477.
520 $aThe success of cattle tick fixation largely depends on the secretion of substances that alter the immune response of the host. The majority of these substances are expressed by the parasite salivary gland and secreted in tick saliva. It is known that hosts can mount immune responses against ticks and bovine European breeds, and bovine industrial crossbreeds are more susceptible to infestations than are Bos indicus cattle. To identify candidates for the development of novel control strategies for the cattle tick Rhipicephalus (Boophilus) microplus, a salivary gland transcriptome analysis of engorged females fed on susceptible or resistant hosts was performed. Using RNA-Seq, transcriptomes were de novo assembled and produced a total of 235,451 contigs with 93.3% transcriptome completeness. Differential expression analysis identified 137 sequences as differentially expressed genes (DEGs) between ticks raised on tick-susceptible or tick-resistant cattle. DEGs predicted to be secreted proteins include innexins, which are transmembrane proteins that form gap junction channels; the transporters Na+/dicarboxylate, Na+/tricarboxylate, and phosphate transporter and a putative monocarboxylate transporter; a phosphoinositol 4-phosphate adaptor protein; a cysteine-rich protein containing a trypsin inhibitor-like (TIL) domain; a putative defense protein 3 containing a reeler domain; and an F-actin-uncapping protein LRRC16A with a CARMIL_C domain; these genes were upregulated in ticks fed on tick-susceptible cattle. DEGs predicted to be non-secreted proteins included a small heat shock protein and the negative elongation factor B-like, both acting in a coordinated manner to increase HSP transcript levels in the salivary glands of the ticks fed on tick-susceptible cattle; the 26S protease regulatory subunit 6B and another chaperone with similarity to calnexin, also upregulated in ticks fed on tick-susceptible cattle; an EF-hand calcium binding protein and a serine carboxypeptidase (SCP), both involved in the blood coagulation cascade and upregulated in ticks fed on tick-susceptible cattle; and two ribosomal proteins, the 60S acidic ribosomal protein P2 and the 60S ribosomal protein L19. These results help to characterize cattle tick salivary gland gene expression in tick-susceptible and tick-resistant hosts and suggest new putative targets for the control of tick infestations, as those genes involved in the mechanism of stress response during blood feeding.
650 $aBioinformatics
650 $aCattle
650 $aRhipicephalus microplus
650 $aSialome
650 $aTranscriptome
650 $aCarrapato
650 $aGado de Corte
653 $aBioinformática
653 $aCattle tick
653 $aExpressão gênica
653 $aHost-parasite interaction
653 $aRNA-Seq
700 1 $aCUNHA, R. C.
700 1 $aNHANI JUNIOR, A.
700 1 $aGARCIA, M. V.
700 1 $aFERRO, J. A.
700 1 $aANDREOTTI, R.
773 $tFrontiers in Cellular and Infection Microbiology$gv. 9, p. 1-15, Jan. 2020.
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