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Int J Parasitol ; 43(14): 1133-9, 2013 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-24162076

RESUMEN

We have shown that Fasciola hepatica expresses at least six ß-tubulins in the adult stage of its life cycle, designated F.hep-ß-tub1-6 (Ryan et al., 2008). Here we show that different complements of tubulin isotypes are expressed in different tissues and at different life cycle stages; this information may inform the search for novel anthelmintics. The predominant (as judged by quantitative PCR) isotype transcribed at the adult stage was F.hep-ß-tub1 and immunolocalisation studies revealed that this isotype occurred mainly in mature spermatozoa and vitelline follicles. Quantitative PCR indicated that changes occurred in the transcription levels of ß-tubulin isotypes at certain life cycle stages and may be of importance in the efficacy of benzimidazole-based anthelmintic drugs, but there were no significant differences between the triclabendazole-susceptible Leon isolate and the triclabendazole-resistant Oberon isolate in the transcription levels of each of the isotypes. When three well-characterised isolates with differing susceptibilities to triclabendazole were compared, only one amino acid change resulting from a homozygous coding sequence difference (Gly269Ser) in isotype 4 was observed. However, this change was not predicted to alter the overall structure of the protein. In conclusion, these findings indicate that there is tissue-specific expression of tubulin isotypes in the liver fluke but the development of resistance to triclabendazole is not associated with changes in its presumed target molecule.


Asunto(s)
Fasciola hepatica/crecimiento & desarrollo , Fasciola hepatica/genética , Regulación del Desarrollo de la Expresión Génica , Estadios del Ciclo de Vida , Tubulina (Proteína)/biosíntesis , Tubulina (Proteína)/genética , Animales , Antihelmínticos/farmacología , Bencimidazoles/farmacología , Resistencia a Medicamentos , Fasciola hepatica/efectos de los fármacos , Perfilación de la Expresión Génica , Isoformas de Proteínas/biosíntesis , Isoformas de Proteínas/genética , Reacción en Cadena en Tiempo Real de la Polimerasa , Transcripción Genética , Triclabendazol
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