Identificador persistente para citar o vincular este elemento:
http://hdl.handle.net/10553/130958
Título: | Molecular insights and antibody response to Dr20/22 in dogs naturally infected with Dirofilaria repens | Autores/as: | Pękacz, Mateusz Basałaj, Katarzyna Młocicki, Daniel Kamaszewski, Maciej Carretón Gómez, Elena Morchón, Rodrigo Wiśniewski, Marcin Zawistowska-Deniziak, Anna |
Clasificación UNESCO: | 310904 Medicina interna 240112 Parasitología animal |
Palabras clave: | Messenger-Rna Brugia-Malayi Fasciola-Hepatica Protein Antigen, et al. |
Fecha de publicación: | 2024 | Publicación seriada: | Scientific Reports | Resumen: | Subcutaneous dirofilariasis, caused by the parasitic nematode Dirofilaria repens, is a growing concern in Europe, affecting both dogs and humans. This study focused on D. repens Dr20/22, a protein encoded by an alt (abundant larval transcript) gene family. While well-documented in L3 larvae of other filariae species, this gene family had not been explored in dirofilariasis. The research involved cloning Dr20/22 cDNA, molecular characterization, and evaluating its potential application in the diagnosis of dirofilariasis. Although Real-Time analysis revealed mRNA expression in both adult worms and microfilariae, the native protein remained undetected in lysates from both developmental stages. This suggests the protein’s specificity for L3 larvae and may be related to a process called SLTS (spliced leader trans-splicing), contributing to stage-specific gene expression. The specificity of the antigen for invasive larvae positions it as a promising early marker for dirofilariasis. However, ELISA tests using sera from infected and uninfected dogs indicated limited diagnostic utility. While further research is required, our findings contribute to a deeper understanding of the molecular and immunological aspects of host-parasite interactions and could offer insights into the parasite's strategies for evading the immune system. | URI: | http://hdl.handle.net/10553/130958 | ISSN: | 2045-2322 | DOI: | 10.1038/s41598-024-63523-9 | Fuente: | Scientific Reports[EISSN 2045-2322],v. 14 (1), (Junio 2024) |
Colección: | Artículos |
Los elementos en ULPGC accedaCRIS están protegidos por derechos de autor con todos los derechos reservados, a menos que se indique lo contrario.