The Prospective Use of Brazilian Marine Macroalgae in Schistosomiasis Control

Schistosomiasis is a parasitic disease that affects more than 250 million people. The treatment is limited to praziquantel and the control of the intermediate host with the highly toxic molluscicidal niclosamide. Marine algae are a poorly explored and promising alternative that can provide lead comp...

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Veröffentlicht in:Marine drugs 2021-04, Vol.19 (5), p.234
Hauptverfasser: Stein, Erika M, Tajú, Sara G, Miyasato, Patrícia A, de Freitas, Rafaela P, Tallarico, Lenita de F, Dos Santos, Guilherme S, Luiz, Giovana L F, Rofatto, Henrique K, da Silva, Fábio N V, Colepicolo, Pio, Macedo, Arthur L, Carollo, Carlos A, Nakano, Eliana
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Sprache:eng
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Zusammenfassung:Schistosomiasis is a parasitic disease that affects more than 250 million people. The treatment is limited to praziquantel and the control of the intermediate host with the highly toxic molluscicidal niclosamide. Marine algae are a poorly explored and promising alternative that can provide lead compounds, and the use of multivariate analysis could contribute to quicker discovery. As part of our search for new natural compounds with which to control schistosomiasis, we screened 45 crude extracts obtained from 37 Brazilian seaweed species for their molluscicidal activity against embryos and schistosomicidal activities against . Two sets of extracts were taxonomically grouped for metabolomic analysis. The extracts were analyzed by GC-MS, and the data were subjected to Pattern Hunter and Pearson correlation tests. Overall, 22 species (60%) showed activity in at least one of the two models. Multivariate analysis pointed towards 3 hits against veliger embryos in the set, 5 hits against blastula embryos, and 31 against in the Ochrophyta set. Preliminary annotations suggested some compounds such as triquinane alcohols, prenylated guaianes, dichotomanes, and xenianes. Despite the putative identification, this work presents potential candidates and can guide future isolation and identification.
ISSN:1660-3397
1660-3397
DOI:10.3390/md19050234