Anti-HIV activity of methanolic and aqueous extracts of fifteen materials of beach-cast macroalgae: valorization of underused waste biomass

References

• Ahmadi, A., Zorofchian Moghadamtousi, S., Abubakar, S., & Zandi, K. (2015). Antiviral potential of algae polysaccharides isolated from marine sources: A review. BioMed Research International, 2015, 1–10.
   Google Scholar
• Ahn, M. J., Yoon, K. D., Kim, C. Y., Kim, J. H., Shin, C. G., & Kim, J. (2006). Inhibitory activity on HIV‐1 reverse transcriptase and integrase of a carmalol derivative from a brown alga. Ishige Okamurae. Phytotherapy Research: An International Journal Devoted to Pharmacological and Toxicological Evaluation of Natural Product Derivatives, 20, 711–713.
   Google Scholar
• Ahn, M. J., Yoon, K. D., Kim, C. Y., Min, S. Y., Kim, Y. U., Kim, H. J., … Kim, S. H. (2002). Inhibition of HIV-1 reverse transcriptase and HIV-1 integrase and antiviral activity of Korean seaweed extracts. Journal of Applied Phycology, 14, 325–329.
   Google Scholar
• Ahn, M. J., Yoon, K. D., Min, S. Y., Lee, J. S., Kim, J. H., Kim, T. G., & Kim, J. (2004). Inhibition of HIV-1 reverse transcriptase and protease by phlorotannins from the brown alga Ecklonia cava. Biological & Pharmaceutical Bulletin, 27, 544–547.
   Google Scholar
• Alexandre, K. B., Gray, E. S., Mufhandu, H., McMahon, J. B., Chakauya, E., O’Keefe, B. R., & Morris, L. (2012). The lectins griffithsin, cyanovirin-N and scytovirin inhibit HIV-1 binding to the DC-SIGN receptor and transfer to CD4+ cells. Virology, 423, 175–186.
   Google Scholar
• Amorim, A. M. P. B. (2018). Study of antioxidants, bioactive potential and chemical composition of Chnoospora minima, Dictyopteris plagiogramma, Padina gymnospora, Sargassum cymosum (Ochrophyta) and Codium isthmocladum (Chlorophyta). master dissertation. Institute of Bioscience. University of São Paulo. 122. doi.10.11606/D.41.2019.tde-18022019-091636
   Google Scholar
• Artan, M., Karadeniz, F., Karagozlu, M. Z., Kim, M. M., & Kim, S. K. (2010). Anti-HIV-1 activity of low molecular weight sulfated chitooligosaccharides. Carbohydrate Research, 345, 656–662.
   Google Scholar
• Artan, M., Li, Y., Karadeniz, F., Lee, S. H., Kim, M. M., & Kim, S. K. (2008). Anti-HIV-1 activity of phloroglucinol derivative, 6, 6′-bieckol, from Ecklonia cava. Bioorganic & Medicinal Chemistry, 16, 7921–7926.
   Google Scholar
• Besednova, N. N., Zvyagintseva, T. N., Kuznetsova, T. A., Makarenkova, I. D., Smolina, T. P., Fedyanina, L. N., & Zaporozhets, T. S. (2019). Marine algae metabolites as promising therapeutics for the prevention and treatment of HIV/AIDS. Metabolites, 9, 87.
   Google Scholar
• Bianco, É. M., De Oliveira, S. Q., Rigotto, C., Tonini, M. L., Da rosa guimarães, T., Bittencourt, F., & Martins, C. D. L. (2013). Anti-infective potential of marine invertebrates and seaweeds from the Brazilian coast. Molecules, 18, 5761–5778.
   Google Scholar
• Cavalcanti, D. N., de Oliveira, M. A. R., De-Paula, J. C., Barbosa, L. S., Fogel, T., Pinto, M. A., … Teixeira, V. L. (2011). Variability of a diterpene with potential anti-HIV activity isolated from the Brazilian brown alga Dictyota menstrualis. Journal of Applied Phycology, 23, 873–876.
   Google Scholar
• Cos, P., Vlietinck, A. J., Berghe, D. V., & Maes, L. (2006). Anti-infective potential of natural products: How to develop a stronger in vitro ‘proof-of-concept’. Journal of Ethnopharmacology, 106, 290–302.
   Google Scholar
• Deyab, M., Elkatony, T., & Ward, F. (2016). Qualitative and quantitative analysis of phytochemical studies on brown seaweed. Dictyota dichotoma. International Journal of Engineering Development and Research, 4, 2321–2330.
   Google Scholar
• El Safadi, Y., Vivet-Boudou, V., & Marquet, R. (2007). HIV-1 reverse transcriptase inhibitors. Applied Microbiology and Biotechnology, 75, 723–737.
   Google Scholar
• Fernández, P. V., Arata, P. X., & Ciancia, M. (2014). Polysaccharides from Codium species: Chemical structure and biological activity their role as components of the cell wall. Advances in Botanical Research, 71, 253–278.
   Google Scholar
• Gentile, D., Patamia, V., Scala, A., Sciortino, M. T., Piperno, A., & Rescifina, A. (2020). Putative inhibitors of SARS-CoV-2 main protease from a library of marine natural products: A virtual screening and molecular modeling study. Marine Drugs, 18, 225.
   Google Scholar
• Gómez-Guzmán, M., Rodríguez-Nogales, A., Algieri, F., & Gálvez, J. (2018). Potential role of seaweed polyphenols in cardiovascular-associated disorders. Marine Drugs, 16, 250.
   Google Scholar
• Harb, T. B., Pereira, M. S., Cavalcanti, M. I. L. G., Fujii, M. T., & Chow, F. (2021). Antioxidant activity and related chemical composition of extracts from Brazilian beach-cast marine algae: Opportunities of turning a waste into a resource. Journal of Applied Phycology, 33, 3383–3395.
   Google Scholar
• Huskens, D., & Schols, D. (2012). Algal lectins as potential HIV microbicide candidates. Marine Drugs, 10, 1476–1497.
   Google Scholar
• Jordheim, L. P., Durantel, D., Zoulim, F., & Dumontet, C. (2013). Advances in the development of nucleoside and nucleotide analogues for cancer and viral diseases. Nature Reviews. Drug Discovery, 12, 447–464.
   Google Scholar
• Karaki, N., Sebaaly, C., Chahine, N., Faour, T., Zinchenko, A., Rachid, S., & Kanaan, H. (2013). The antioxidant and anticoagulant activities of polysaccharides isolated from the brown algae Dictyopteris polypodioides growing on the Lebanese coast. Journal of Applied Pharmaceutical Science, 3, 43–51.
   Google Scholar
• Khora, S. S., & Navya, P. (2020). Bioactive polysaccharides from marine macroalgae. Encyclopedia of Marine Biotechnology, 121–145. doi:10.1002/9781119143802.ch6
   Google Scholar
• Kim, S. K., & Karadeniz, F. (2011). Anti-HIV activity of extracts and compounds from marine algae. Advances in Food and Nutrition Research, 64. doi:10.1016/B978-0-12-387669-0.00020-X
   Google Scholar
• Klongklaew, N., Praiboon, J., Tamtin, M., & Srisapoome, P. (2020). Antibacterial and antiviral activities of local Thai green macroalgae crude extracts in pacific white shrimp (Litopenaeus vannamei). Marine Drugs, 18, 140.
   Google Scholar
• Kwon, H. J., Ryu, Y. B., Kim, Y. M., Song, N., Kim, C. Y., Rho, M. C., & Park, S. J. (2013). In vitro antiviral activity of phlorotannins isolated from Ecklonia cava against porcine epidemic diarrhea coronavirus infection and hemagglutination. Bioorganic & Medicinal Chemistry, 21, 4706–4713.
   Google Scholar
• Mattos, B. B., Romanos, M. T. V., Souza, L. M. D., Sassaki, G., & Barreto-Bergter, E. (2011). Glycolipids from macroalgae: Potential biomolecules for marine biotechnology? Revista Brasileira De Farmacognosia, 21, 244–247.
   Google Scholar
• Mendis, E., & Kim, S. K. (2011). Present and future prospects of seaweeds in developing functional foods. Advances in Food and Nutrition Research, 64, 1–15.
   Google Scholar
• Murray, M., Dordevic, A. L., Ryan, L., & Bonham, M. P. (2018). An emerging trend in functional foods for the prevention of cardiovascular disease and diabetes: Marine algal polyphenols. Critical Reviews in Food Science and Nutrition, 58, 1342–1358.
   Google Scholar
• Nunes, N., Ferraz, S., Valente, S., Barreto, M. C., & De Carvalho, M. P. (2017). Biochemical composition, nutritional value, and antioxidant properties of seven seaweed species from the Madeira Archipelago. Journal of Applied Phycology, 29, 2427–2437.
   Google Scholar
• Pina-Pérez, M. C., Rivas, A., Martínez, A., & Rodrigo, D. (2017). Antimicrobial potential of macro and microalgae against pathogenic and spoilage microorganisms in food. Food Chemistry, 235, 34–44.
   Google Scholar
• Premnathan, M., Chandra, K., Bajpai, S. K., & Kathiresan, K. (1992). A survey of some Indian marine plants for antiviral activity. Botanica Marina, 35, 321–324.
   Google Scholar
• Queiroz, K. C. S., Medeiros, V. P., Queiroz, L. S., Abreu, L. R. D., Rocha, H. A. O., Ferreira, C. V., & Leite, E. L. (2008). Inhibition of reverse transcriptase activity of HIV by polysaccharides of brown algae. Biomedicine & Pharmacotherapy, 62, 303–307.
   Google Scholar
• Rodrigues, J. A., Torres, V. M., de Alencar, D. B., Sampaio, A. H., & Farias, W. R. (2009). Extraction and anticoagulant activity of sulfated polysaccharides from the red marine alga. Halymenia Pseudofloresia. Revista Ciência Agronômica, 40, 224.
   Google Scholar
• Rosales-Mendoza, S., García-Silva, I., González-Ortega, O., Sandoval-Vargas, J. M., Malla, A., & Vimolmangkang, S. (2020). The potential of algal biotechnology to produce antiviral compounds and biopharmaceuticals. Molecules, 25, 4049.
   Google Scholar
• Sangtani, R., Ghosh, A., Jha, H. C., Parmar, H. S., & Bala, K. (2020). Potential of algal metabolites for the development of broad-spectrum antiviral therapeutics: Possible implications in COVID-19 therapy. Phytotherapy Research, 35, 2296–2316.
   Google Scholar
• Santos, J. P., Torres, P. B., dos Santos, D. Y., Motta, L. B., & Chow, F. (2019). Seasonal Effects on Antioxidant and anti-HIV Activities of Brazilian Seaweeds. Journal of Applied Phycology, 31, 1333–1341.
   Google Scholar
• Sarafianos, S. G., Marchand, B., Das, K., Himmel, D. M., Parniak, M. A., Hughes, S. H., & Arnold, E. (2009). Structure and function of HIV-1 reverse transcriptase: Molecular mechanisms of polymerization and inhibition. Journal of Molecular Biology, 385, 693–713.
   Google Scholar
• Sato, Y., Hirayama, M., Morimoto, K., Yamamoto, N., Okuyama, S., & Hori, K. (2011). High mannose-binding lectin with preference for the cluster of α1–2-mannose from the green alga Boodlea coacta is a potent entry inhibitor of HIV-1 and influenza viruses. Journal of Biological Chemistry, 286, 19446–19458.
   Google Scholar
• Shi, Q., Wang, A., Lu, Z., Qin, C., Hu, J., & Yin, J. (2017). Overview on the antiviral activities and mechanisms of marine polysaccharides from seaweeds. Carbohydrate Research, 453-454, 1–9.
   Google Scholar
• Singh, R. S., & Walia, A. K. (2018). Lectins from Red Algae and Their Biomedical Potential. Journal of Applied Phycology, 30, 1833–1858.
   Google Scholar
• Snedecor, G. W. (1966). Metodos estadisticos: Aplicacion a la investigacion agricola y biologica (No. C015. 027). Compania Editorial Continental SA.
   Google Scholar
• Spieler, R. (2002). Seaweed compound’s anti-HIV efficacy will be tested in Southern Africa. The Lancet, 359, 1675.
   Google Scholar
• Thuy, T. T. T., Ly, B. M., Van, T. T. T., Van Quang, N., Tu, H. C., Zheng, Y., & Ai, U. (2015). Anti-HIV activity of fucoidans from three brown seaweed species. Carbohydrate Polymers, 115, 122–128.
   Google Scholar
• Torres, M. D., Flórez-Fernández, N., & Domínguez, H. (2019). Integral utilization of red seaweed for bioactive production. Marine Drugs, 17, 314.
   Google Scholar
• Trinchero, J., Ponce, N. M., Córdoba, O. L., Flores, M. L., Pampuro, S., Stortz, C. A., … Turk, G. (2009). Antiretroviral activity of fucoidans extracted from the brown seaweed Adenocystis utricularis. Phytotherapy Research: An International Journal Devoted to Pharmacological and Toxicological Evaluation of Natural Product Derivatives, 23, 707–712.
   Google Scholar
• Turville, S. G., Aravantinou, M., Miller, T., Kenney, J., Teitelbaum, A., Hu, L., & Lifson, J. D. (2008). Efficacy of Carraguard®-based microbicides in vivo despite variable in vitro activity. PloS One, 3, e3162.
   Google Scholar
• Vlietinck, A. J., De Bruyne, T., Apers, S., & Pieters, L. A. (1998). Plant-derived leading compounds for chemotherapy of human immunodeficiency virus (HIV) infection. Planta Medica, 64, 97–109.
   Google Scholar
• Wang, H., Ooi, E. V., & Ang, P. O. (2008). Antiviral activities of extracts from Hong Kong seaweeds. Journal of Zhejiang University. Science. B, 9, 969–976.
   Google Scholar
• Weiner, M. L. (2016). Parameters and pitfalls to consider in the conduct of food additive research, Carrageenan as a case study. Food and Chemical Toxicology, 87, 31–44.
   Google Scholar
• WHO, World Health Organization. (2019). Retrieved from https://www.who.int/hiv/data/en/accessedat15/17/2020
   Google Scholar
• Wittine, K., Saftić, L., Peršurić, Ž., & Kraljević Pavelić, S. (2019). Novel antiretroviral structures from marine organisms. Molecules, 24, 3486.
   Google Scholar
• Witvrouw, M., Este, J. A., Mateu, M. Q., Reymen, D., Andrei, G., Snoeck, R., & De Clercq, E. (1994). Activity of a sulfated polysaccharide extracted from the red seaweed Aghardhiella tenera against human immunodeficiency virus and other enveloped viruses. Antiviral Chemistry & Chemotherapy, 5, 297–303.
   Google Scholar
• Woradulayapinij, W., Soonthornchareonnon, N., & Wiwat, C. (2005). In vitro HIV type 1 reverse transcriptase inhibitory activities of Thai medicinal plants and Canna indica L. rhizomes. Journal of Ethnopharmacology, 101, 84–89.
   Google Scholar
• Yasuhara-Bell, J., & Lu, Y. (2010). Marine compounds and their antiviral activities. Antiviral Research, 86, 231–240.
   Google Scholar
• Yoshie-Stark, Y., Hsieh, Y. P., & Suzuki, T. (2003). Distribution of flavonoids and related compounds from seaweeds in Japan. Journal-Tokyo University of Fisheries, 89, 1–6.
   Google Scholar
• Zaman, S. B., Hussain, M. A., Nye, R., Mehta, V., Mamun, K. T., & Hossain, N. (2017). A review on antibiotic resistance: Alarm bells are ringing. Cureus, 9, 6.
   Google Scholar
• Zeitlin, L., Whaley, K. J., Hegarty, T. A., Moench, T. R., & Cone, R. A. (1997). Tests of vaginal microbicides in the mouse genital herpes model. Contraception, 56, 329–335.
   Google Scholar