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Título: | Differential expression analysis for subolesin in Rhipicephalus microplus infected with Anaplasma marginale |
Autor: | Carvajal-de la Fuente, Verónica; Merino, Octavio CSIC ORCID; Tovar-Carman, Erick; Rodríguez-Camarillo, Sergio D.; Lagunes, Rodolfo; Muñoz-Tenería, Fernando A.; Contreras, Marinela CSIC ORCID; Fuente, José de la CSIC ORCID | Palabras clave: | Anaplasma marginale Rhipicephalus microplus Salivary gland Gene expression Subolesin |
Fecha de publicación: | 2018 | Editor: | Springer Nature | Citación: | Experimental and Applied Acarology 76(2): 229-241 (2018) | Resumen: | Rhipicephalus microplus (formerly Boophilus microplus) ticks are potential vectors of several pathogens of livestock especially in tropical and subtropical regions where may have substantial effects on economic development. Among tick-borne pathogens, Anaplasma marginale is considered one of the most important in domestic and wild ruminants worldwide. Different molecular mechanisms have been employed by both ticks and these intracellular pathogens, in order to be able to adapt and survive. Subolesin, originally called 4D8, is an evolutionarily well-preserved protein among ixodid tick species. This new antigen was found to be protective against tick infestations when used as a vaccine, as it has an essential role in tick blood digestion, development and infection of host cells by A. marginale. Recent studies have demonstrated that infection of both tick and vertebrate host cells with this microorganism changed gene expression. Therefore, the main objective of this study was to investigate subolesin expression in uninfected and A. marginale-infected R. microplus salivary glands by real-time reverse transcriptase (RT)-PCR. To analyze the differential expression of the recombinant protein subolesin, the gene was previously expressed from ticks infected with A. marginale. Results from this study revealed that, the expression of subolesin was significantly higher in salivary glands of infected R. microplus in comparison to uninfected ones. | URI: | http://hdl.handle.net/10261/174623 | DOI: | 10.1007/s10493-018-0302-7 | Identificadores: | doi: 10.1007/s10493-018-0302-7 e-issn: 1572-9702 issn: 0168-8162 |
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