<b>An anti-dengue and anti-herpetic polysulfated fraction isolated from the coenocytic green seaweed <i>Caulerpa cupressoides</i> inhibits thrombin generation in vitro

• Main Authors: José Ariévilo Gurgel Rodrigues, Ygor Raphael Gomes Eloy, Edfranck de Souza Oliveira Vanderlei, Jéssica Figueiredo Cavalcante, Maria Tereza Villela Romanos, Norma Maria Barros Benevides
• Format: Article
• Language: English
• Published: Universidade Estadual de Maringá 2017-06-01
• Series: Acta Scientiarum : Biological Sciences
• Subjects: Bryopsidales; marine glycans; cytotoxicity; viral infection; thrombin.
• Online Access: http://periodicos.uem.br/ojs/index.php/ActaSciBiolSci/article/view/28081

The antiviral potency of Caulerpa cupressoides (Chlorophyta) sulfated polysaccharidic fractions (Cc-SP1→3) associated with thrombin generation (TG) assay is unknown. This study analyzed the structure of Cc-SP1 and its effects against herpes viruses (HSV-1 and HSV-2), dengue-virus (DENV-1), human-metapneumovirus (HMPV) and adenovirus (AdV) in Vero and mosquito C6/36 cell-lines and as inhibitor of TG in 60-fold diluted human plasma using continuous system. Infrared analysis indicated ulvan containing 11% sulfate, 40.16% total sugars and 6% uronic acid. Procedures of agarose/polyacrylamide gels electrophoresis revealed two major components presenting sulfate and non SPs, with molecular dispersion ranging from 8 to > 100 kDa, respectively, as confirmed by gel permeation chromatography. Cc-SP1 did not cause cytotoxicity up to 1000 μg mL-1 and was more effective inhibitor of DENV-1 (96%, 0.35 μg mL-1) compared with HSV-1 (90%, 27 μg mL-1) and HSV-2 (99.9%, 0.9 μg mL-1) in Vero cell-line, whose selectivity indexes were > 714, > 9.2 and > 131, respectively, but was inactive against HMPV, AdV and C6/36 cell-line using plate reduction assay. Cc-SP1 required concentration 20.8-fold higher of SPs than heparin for abolishes intrinsically TG, but at concentrations so far the anti-HSV-1. Therefore, TG assay provides data to guide studies of Cc-SP1 on anticoagulant/antiviral effects.