Anti-herpesvirus bovine type 5 activities of extracts obtained from Plocamium brasiliense

Bovine herpesvirus type 5 (BoHV-5) is an important etiologic agent of meningoencephalitis in cattle and has been frequently identified in outbreaks of neurological disease in bovine in the southern hemisphere including Brazil. This study aimed to evaluate the cytotoxic effect and the antiviral properties of extracts obtained from Plocamium brasiliense (Greville) Howe and Taylor in BoHV-5 RJ42/01 replication. The cytotoxic effects were measured in Madin-Darbin bovine kidney cells (MDBK) and cytotoxic concentration (CC50) values have been determined for acyclovir (ACV) (223 mu g +/- 2.0), ethyl acetate extract from P. brasiliense (2,109 mu g +/- 10), hexane extract from P. brasiliense (7.181 mu g +/- 5), dichloromethane extract from P. brasiliense (2.356 mu g +/- 6.5), and hydroalcoholic extract from P. brasiliense (1.408 mu g +/- 5.8). As a first approach to characterize the action of these extracts on BoHV-5 RJ42/01, a virucidal assay activity was performed. A virus suspension containing 1 x 10(5) plaque-forming units (PFU) of the BoHV-5 RJ42/01 was mixed with 600 mu g of extract and acyclovir and kept at room temperature (24 A degrees C) for 3 h. Meanwhile, a control of untreated infected virus was performed in the same conditions. Then, treated virus suspension and untreated control were diluted, and percentage of inhibition of infectivity was determined by plaque assay: ethyl acetate extract (99 %), hexane extract (90 %), dichloromethane extract (99 %), and hydroalcoholic extract (27 %). Acyclovir had a slight virucidal activity on viral particle. The inhibition of attachment was performed in MDBK cells inoculated with 100 PFU of BoHV-5 RJ42/01 in the presence or absence of various concentrations of extracts (0.3, 0.9, and 1.5 mu g mL(-1)). Acyclovir was also assayed at 2.8 and 11.25 mu g mL(-1). The inhibition of adsorption was also tested in MDBK cells treated with the same concentrations of the extracts before virus inoculation. Results: hexane extracts inhibited virus attachment in pre-treated cell 0.9 mu g (55 %) and 1.5 mu g (71 %) and untreated MDBK cell only with 1.5 mu g (63 %). Ethyl acetate extract on cell pre-treated with 0.3 mu g (67 %), 0.9 mu g (81 %), and 1.5 mu g (91 %). Ethyl acetate extract on pre-treated cell 0.3 mu g (67 %), 0.9 mu g (81 %), and 1.5 (91 %) but discrete inhibition on cell untreated. Dichloromethane extract and acyclovir slightly inhibited virus binding on MDBK cell.