Recent research suggests that a polygeneric immunogen made from the venoms of the most medically important viperid and elapid snakes in sub-Saharan Africa could elicit a broader antibody response in horses compared to the current EchiTAb-plus-ICP antivenom, especially against neurotoxic elapid venoms. To test this, 25 horses that have been regularly immunized to produce this antivenom were reimmunized with an immunogen containing 22 venoms from various snake species from the genera , , , and both spitting and non-spitting . The plasma collected from these horses was processed using the caprylic acid method to produce an industrial-scale freeze-dried antivenom.
View Article and Find Full Text PDFSyst Parasitol
December 2024
During parasitological surveys of marine fishes and zooplankton in localities of the Northwestern Pacific coast of Mexico, 28 Gafftopsail pompano (Trachinotus rhodopus Gill) and 50 mysid crustaceans (Metamysidopsis frankfiersi Hendrickx & Hernández-Payán) we identified to be infected with adults and cystacanths, respectively of an acanthocephalan morphologically corresponding to the genus Rhadinorhynchus Lühe, 1911. DNA sequences of the small (SSU) and large (LSU) subunits of ribosomal DNA, and cytochrome c oxidase subunit 1 (cox 1) from mitochondrial DNA were obtained. Phylogenetic analyses revealed that the newly sequenced individuals in a clade with Rhadinorhynchus sp.
View Article and Find Full Text PDFThe immunization and industrial bleeding of horses are essential stages for producing snake antivenoms. In Costa Rica, the traditional method involves stimulating the antibody response of horses by periodically injecting venoms, collecting hyperimmune plasma over three consecutive bleeding days, and repeating this process every eight weeks. While this method does not cause major physical or hematological issues in horses, the associated stress has not been evaluated.
View Article and Find Full Text PDFSurface-enhanced Raman scattering (SERS) spectroscopy is a versatile molecular fingerprinting technique with rapid signal readout, high aqueous compatibility, and portability. To translate SERS for real-world applications, it is pertinent to overcome inherent challenges, including high sample variability and heterogeneity, matrix effects, and nonlinear SERS signal responses of different analytes in complex (bio)chemical matrices with numerous interfering species. In this perspective, we highlight emerging SERS-based multimodal techniques to address the key roadblocks to improving the sensitivity, specificity, and reliability of (bio)chemical detection, bioimaging, theragnosis, and theragnostic.
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