key: cord-0832911-yeph3ovf
authors: Ben-Amor, Ichrak; Gargouri, Bochra; Attia, Hamadi; Tlili, Khaoula; Kallel, Imen; Musarra-Pizzo, Maria; Sciortino, Maria Teresa; Pennisi, Rosamaria
title: In Vitro Anti-Epstein Barr Virus Activity of Olea europaea L. Leaf Extracts
date: 2021-11-12
journal: Plants (Basel)
DOI: 10.3390/plants10112445
sha: 9654aa775548f11dc07bbdbebcc1ac2baeefdc97
doc_id: 832911
cord_uid: yeph3ovf

Olea europaea L. var. sativa (OESA) preparations are widely used in traditional medicine in the Mediterranean region to prevent and treat different diseases. In this research, olive extracts derived from the leaves of the OESA tree have been screened for antioxidant activity by two methods: the DPPH free radical scavenging assay (DPPH) and the Ferric reducing antioxidant power (FRAP) assay. The DPPH assay showed that OESA possesses a stronger antioxidant activity (84%) at 1 mg/mL while the FRAP method showed a strong metal ion chelating activity (90%) at 1 mg/mL. The low IC(50) values, obtained by two different methods, implies that OESA has a noticeable effect on scavenging free radicals comparable to standards. During EBV infection, the free radicals increased triggering lipid oxidation. Therefore, the monitoring of the secondary lipid peroxidation products was done by measuring malonaldehyde (MDA) and conjugated dienes (DC). The simultaneous treatment of Raji cells with OESA and TPA, as an inductorof the lytic cycle, generated a significant decrease in MDA levels and DC (p < 0.05). Besides, Raji cells simultaneously exposed to TPA and OESA exhibited a percentage of EBV-positive fluorescence cells lower than TPA treated cells (**** p < 0.0001). This suggests that OESA treatment has a protective effect against EBV lytic cycle induction.

The vegetable kingdom has always been an inexhaustible source of resources useful for multiple fields of application. Over the centuries, plants have provided for the basic needs of the human species, starting from food, buildings, clothing manufacturing, and up to medicinal agents for the treatment of diseases [1] . The use of plants to cure several kinds of human diseases has a long history. To date, many medicinal plants are widely studied for their bioactive molecules which have anticancer, antioxidative, anti-inflammatory, and antimicrobial activity. Plants and purified natural products represent a rich resource for novel antiviral drugs [2] [3] [4] [5] [6] . In particular, after the actual pandemic scenario caused by SARS-CoV-2 which represented a severe threat to public health, the scientific community paid more attention to the study of new potential natural antiviral drugs and their antiviral mechanisms. There is, in fact, a large body of literature reporting the antiviral activity of plants and their constituents [7] [8] [9] .

As recently reported, viruses are responsible for several human diseases and novel phytochemicals interact with the viral life cycle, viral entry, replication, assembly, and release [10] [11] [12] [13] . Therefore, natural products are promising candidates for broad application.

percentage of radical scavenging activity. Figure 1 showed that OESA possessed a striking antiradical activity of 84% at 1 mg/mL. Meanwhile, the concentration of the OESA that can scavenge 50% of DPPH free radical in the DPPH free radical scavenging method (IC 50 ) was determined. The lower IC 50 value implies a higher antioxidant activity. OESA has an IC 50 value of 0.1218 mg/mL, similar to the BHT value (IC 50 = 0.09 mg/mL), suggesting its antioxidant efficacy ( Table 1 ). The antioxidant activity of OESA was further confirmed by the FRAP assay that measures the ability of the sample to reduce the Fe 3+ to Fe 2+ . Various concentrations of OESA extracts (0.06 to 1 mg/mL) and ascorbic acid were mixed with FRAP reagents according to the procedure reported before. Given that the FRAP assay is a redox-linked colorimetric reaction, the reduction of ferric ion (Fe 3+ ) to ferrous form (Fe 2+ ) by antioxidants produces an intense blue light revealed as a change in absorption at 593 nm. Like the antioxidant activity of ascorbic acid, the reducing power of OESA increased with increasing concentration to at 1 mg/mL equal to 90%. Besides, the slower concentration of OESA also showed an excellent reducing power (0.25 mg/mL equal to 81.4% and 0.5 mg/mL equal to 87%) ( Figure 2 ). The IC 50 of OESA for the FRAP assays are presented in Table 1 , for OESA the IC 50 was (0.05737 mg/mL) compared with the ascorbic acid value (0.03068 mg/mL).

The antioxidant capacity of OESA was determined according to the DPPH free radical scavenging assay and the Ferric reducing antioxidant power (FRAP) assay. Two standard antioxidants (i.e., BHT and ascorbic acid) were used as the control for the DPPH free radical scavenging assay and FRAP, respectively. The scavenging effect of OESA was calculated as reported in Materials and Methods and the results were expressed as a percentage of radical scavenging activity. Figure 1 showed that OESA possessed a striking antiradical activity of 84% at 1 mg/mL. Meanwhile, the concentration of the OESA that can scavenge 50% of DPPH free radical in the DPPH free radical scavenging method (IC50) was determined. The lower IC50 value implies a higher antioxidant activity. OESA has an IC50 value of 0.1218 mg/mL, similar to the BHT value (IC50 = 0.09 mg/mL), suggesting its antioxidant efficacy (Table 1 ). The antioxidant activity of OESA was further confirmed by the FRAP assay that measures the ability of the sample to reduce the Fe 3+ to Fe 2+ . Various concentrations of OESA extracts (0.06 to 1 mg/mL) and ascorbic acid were mixed with FRAP reagents according to the procedure reported before. Given that the FRAP assay is a redox-linked colorimetric reaction, the reduction of ferric ion (Fe 3+ ) to ferrous form (Fe 2+ ) by antioxidants produces an intense blue light revealed as a change in absorption at 593 nm. Like the antioxidant activity of ascorbic acid, the reducing power of OESA increased with increasing concentration to at 1 mg/mL equal to 90%. Besides, the slower concentration of OESA also showed an excellent reducing power (0.25 mg/mL equal to 81.4% and 0.5 mg/mL equal to 87%) ( Figure 2 ). The IC50 of OESA for the FRAP assays are presented in Table 1 , for OESA the IC50 was (0.05737 mg/mL) compared with the ascorbic acid value (0.03068 mg/mL).

Percentage of radical scavenging capacity for OESA. Aliquots of various concentrations of OESA extracts (0, 0.125, 0.25, 0.5, 1 mg/mL) and standard BHT were mixed with DPPH and incubated in the dark. The antioxidant activity of OESA was measured using a spectrophotometer at 517 nm. Results were expressed as mean inhibition percentage (%) ± standard deviations (n = 3). BHT was used as the reference standard. Figure 1 . Percentage of radical scavenging capacity for OESA. Aliquots of various concentrations of OESA extracts (0, 0.125, 0.25, 0.5, 1 mg/mL) and standard BHT were mixed with DPPH and incubated in the dark. The antioxidant activity of OESA was measured using a spectrophotometer at 517 nm. Results were expressed as mean inhibition percentage (%) ± standard deviations (n = 3). BHT was used as the reference standard. 

The cytotoxic effect of OESA was studied on Raji cell lines by the MTT assay. Then, the cells (6 × 10 4 /well) were cultured in 96-well plates for 48 h, with dilutions of OESA (0.16 mg/mL, 0.31 mg/mL, 0.625 mg/mL, 1.25 mg/mL, 2.5 mg/mL, 5 mg/mL, 10 mg/mL) for 72 h. The percentage of cytotoxicity was calculated as reported in Materials and Methods. Starting from the concentration of 10 mg/mL to 2.5 mg/mL, OESA induced strong cytotoxicity. A moderate effect was detected following 0.625 mg/mL of OESA; conversely, lower concentrations did not shown cytotoxicity. Besides, based on these results, the CC 50 values, indicative of 50% cytotoxic concentration, was 0.8773 mg/mL. Therefore, the 0.31 mg/mL concentration of OESA was selected for further experiments ( Figure 3 ).

Ferric reducing antioxidant power (FRAP) assay of OESA. Various concentrations of OESA extracts (0 to 1 mg/mL) and acid ascorbic were mixed with FRAP reagents. The reduction of ferric ion (Fe 3+ ) to ferrous form (Fe 2+ ) by OESA produces an intense blue light revealed as a change in absorption at 700 nm. Results were expressed as mean inhibition percentage (%) ± standard deviations (n = 3). Ascorbic acid at various concentrations (0 to 1 mg/mL) was used as standard. 

The cytotoxic effect of OESA was studied on Raji cell lines by the MTT assay. Then, the cells (6 × 10 4 /well) were cultured in 96-well plates for 48 h, with dilutions of OESA (0.16 mg/mL, 0.31 mg/mL, 0.625 mg/mL, 1.25 mg/mL, 2.5 mg/mL, 5 mg/mL, 10 mg/mL) for 72 h. The percentage of cytotoxicity was calculated as reported in Materials and Methods. Starting from the concentration of 10 mg/mL to 2.5 mg/mL, OESA induced strong cytotoxicity. A moderate effect was detected following 0.625 mg/mL of OESA; conversely, lower concentrations did not shown cytotoxicity. Besides, based on these results, the CC50 values, indicative of 50% cytotoxic concentration, was 0.8773 mg/mL. Therefore, the 0.31 mg/mL concentration of OESA was selected for further experiments ( Figure 3 ).

Cytotoxicity effect of OESA in Raji cells. Raji cells (6 × 10 4/ well) were exposed to serial dilutions of OESA (0.16 mg/mL, 0.31 mg/mL, 0.625 mg/mL, 1.25 mg/mL, 2.5 mg/mL, 5 mg/mL, 10 mg/mL) for 72 h and further incubated with MTT solution in dark for 4 h. The absorbance was Figure 3 . Cytotoxicity effect of OESA in Raji cells. Raji cells (6 × 10 4/ well) were exposed to serial dilutions of OESA (0.16 mg/mL, 0.31 mg/mL, 0.625 mg/mL, 1.25 mg/mL, 2.5 mg/mL, 5 mg/mL, 10 mg/mL) for 72 h and further incubated with MTT solution in dark for 4 h. The absorbance was measured at 570 nm and the % of cytotoxicity was calculated. Results were expressed as mean ± standard deviations (n = 3).

Lipid peroxidation is a reaction to oxidative degradation of polyunsaturated fatty acids mediated by oxygen-derived free radicals. Several studies reported that EBV lytic cycle induction generates oxidative damages which are involved in the pathogenicity of the EBV [21] [22] [23] . A final product of the polyunsaturated fatty acids peroxidation in the cells during oxidative stress is MDA. To explore lipid peroxidation after induction of the EBV lytic cycle, the levels of MDA were measured on Raji cells treated with TPA and OESA (0.3 mg/mL). The Raji cells were exposed to the minimal and sufficient concentration of TPA (8 nM) able to induce the EBV the lytic cycle. The MDA levels were analyzed after 48 h, which matches with the peak of lytic cycle. Our data show a significant rise in the MDA adduct level in Raji cells after the EBV lytic cycle induction compared to the basal level of MDA. Conversely, the level of lipid peroxidation declined significantly in the OESA treated cells (p < 0.01) (Figure 4 ). OESA (0.3 mg/mL). The Raji cells were exposed to the minimal and sufficient concentration of TPA (8 nM) able to induce the EBV the lytic cycle. The MDA levels were analyzed after 48h, which matches with the peak of lytic cycle. Our data show a significant rise in the MDA adduct level in Raji cells after the EBV lytic cycle induction compared to the basal level of MDA. Conversely, the level of lipid peroxidation declined significantly in the OESA treated cells (p < 0.01) (Figure 4 ). Raji cells were exposed, or not, to TPA (8 nm) and OESA (0.31 mg/mL) simultaneously at a noncytotoxic concentration of 0.3 mg/mL. The levels of MDA produced was evaluated by the determination of thiobarbituric acid reactive substances. The data were expressed in nmol/mg of protein (**: p < 0.01). Results were expressed as mean ± standard deviations (n = 3).

To further confirm the role of OESA as a scavenger of lipid peroxidation, DC levels were measured after the induction of the lytic cycle. DC was produced during the initial stages of lipid oxidation and by breaking down the polyunsaturated fatty acids. Raji cells, untreated or treated with TPA alone or in combination with OESA (0.3 mg/mL). Our data showed a significant reduction in DC levels in Raji cells after EBV lytic cycle induction (p < 0.05) ( Figure 5 ). Raji cells were exposed, or not, to TPA (8 nm) and OESA (0.31 mg/mL) simultaneously at a noncytotoxic concentration of 0.3 mg/mL. The levels of MDA produced was evaluated by the determination of thiobarbituric acid reactive substances. The data were expressed in nmol/mg of protein (**: p < 0.01). Results were expressed as mean ± standard deviations (n = 3).

To further confirm the role of OESA as a scavenger of lipid peroxidation, DC levels were measured after the induction of the lytic cycle. DC was produced during the initial stages of lipid oxidation and by breaking down the polyunsaturated fatty acids. Raji cells, untreated or treated with TPA alone or in combination with OESA (0.3 mg/mL). Our data showed a significant reduction in DC levels in Raji cells after EBV lytic cycle induction (p < 0.05) ( Figure 5 ). Raji cells were exposed, or not, to TPA (8 nm) and OESA (0.31 mg/mL) simultaneously at a noncytotoxic concentration of 0.3 mg/mL. The levels of DC produced were evaluated by measuring the OD at 233 nm (*: p < 0.05). Results were expressed as mean ± standard deviations (n = 3).

To further test the OESA inhibitory activity on the EBV lytic cycle induction, Raji cells were stimulated with TPA, exposed to OESA (0.31 mg/mL), and processed to IFA analysis as reported in Materials and Methods. The OESA inhibitory activity on TPA-activated EBV cells was measured by counting fluorescence cells and was graphically reported as % positive fluorescence cells. HeLa cells (3 × 10 6 ) were cultured in parallel and used as a negative control; on the other hand, Raji cells treated with TPA were employed as a positive control. A protective effect of OESA against the EBV lytic cycle induction in Raji cell lines was observed. Indeed, a statistically significant decrease in the percentage of fluorescence was observed after simultaneous treatment with TPA and OESA (**** p < 0.0001) ( Figure 6 ). Raji cells were exposed, or not, to TPA (8 nm) and OESA (0.31 mg/mL) simultaneously at a noncytotoxic concentration of 0.3 mg/mL. The levels of DC produced were evaluated by measuring the OD at 233 nm (*: p < 0.05). Results were expressed as mean ± standard deviations (n = 3).

To further test the OESA inhibitory activity on the EBV lytic cycle induction, Raji cells were stimulated with TPA, exposed to OESA (0.31 mg/mL), and processed to IFA analysis as reported in Materials and Methods. The OESA inhibitory activity on TPA-activated EBV cells was measured by counting fluorescence cells and was graphically reported as % positive fluorescence cells. HeLa cells (3 × 10 6 ) were cultured in parallel and used as a negative control; on the other hand, Raji cells treated with TPA were employed as a positive control. A protective effect of OESA against the EBV lytic cycle induction in Raji cell lines was observed. Indeed, a statistically significant decrease in the percentage of fluorescence was observed after simultaneous treatment with TPA and OESA (**** p < 0.0001) ( Figure 6 ).

To further test the OESA inhibitory activity on the EBV lytic cycle induction, Raji cells were stimulated with TPA, exposed to OESA (0.31 mg/mL), and processed to IFA analysis as reported in Materials and Methods. The OESA inhibitory activity on TPA-activated EBV cells was measured by counting fluorescence cells and was graphically reported as % positive fluorescence cells. HeLa cells (3 × 10 6 ) were cultured in parallel and used as a negative control; on the other hand, Raji cells treated with TPA were employed as a positive control. A protective effect of OESA against the EBV lytic cycle induction in Raji cell lines was observed. Indeed, a statistically significant decrease in the percentage of fluorescence was observed after simultaneous treatment with TPA and OESA (**** p < 0.0001) ( Figure 6 ). 

Many studies have supported evidence about the pharmacological properties of olive leaves on human health. Indeed, the consumption of olive extracts, commercially widespread in the Mediterranean regions, was strictly associated with a reduced risk of developing diseases due to the capability to exert an antioxidant, hypoglycemic, antihypertensive, antimicrobial, and anti-atherosclerotic activity [24] [25] [26] . Some studies have associated the protective effect to the nature of these compounds constituted by a mixture of phytochemical compounds. The most abundant compound in olive leaves is oleuropein, which has been patented in the treatment of viral infections to formulate antiviral compositions [17, 27] . Recently, there was an increasing interest in the discovery of natural antioxidants taken with the diet in order to compensate for the imbalance between the production and the accumulation of oxygen-reactive species in the human body [28] [29] [30] [31] . This process can negatively damage several cellular structures and trigger human diseases. The detoxicant action of some compounds counteracts the oxidative stress and saturates the overproduction of proton radicals by hydrogen donation. This process, known as radicals scavenging action, is an important neutralizing property of antioxidants and can be measured by several assays. Here, we used the DPPH free radical scavenging assay and the Ferric reducing antioxidant power (FRAP) assay. It was observed that the scavenging effects of OESA on DPPH radicals increased with concentrations ( Figure 1 ). In particular, our results indicate that OESA possesses a stronger antioxidant activity (84%) at 1 mg/mL with an IC 50 = 0.1218 mg/mL (Table 1) , as reported by other studies [32] [33] [34] [35] . Similarly, the antioxidant activity was measured by the FRAP method of OESA extracts. The results of the metal ion chelating activity indicate that OESA has acted. The reduction power of OESA was concentration-dependent ( Figure 2 ). The highest value of reducing power (90%) was at 1 mg/mL with IC 50 = 0.05737 mg/mL (Table 1) . These findings agree with the previous studies. [36, 37] . Moreover, it was demonstrated that the highest antioxidant potential is in the olive leaf Agrielia variety extracts in Greece [38] . The lower IC 50 value, obtained by two different methods, implies that OESA has a noticeable effect on scavenging free radicals comparable to standards, and also exhibits a high antioxidant activity ( Table 1 ). The onset of oxidative stress allows for an excess of hydroxyl radical which can cause a radical chain reaction known as lipid peroxidation. This phenomenon damages cell membranes and lipoproteins and is cytotoxic as well as mutagenic. The free radicals increased production appears to be a feature of EBV infection. The oxidative modifications of lipids, proteins, and DNA were reported on Raji cells after the EBV lytic cycle induction [23] . It was reported that EBV infection triggers oxidative stress, related to MDA increase within cells, which activate the induction of transcription factors, such as STAT3 and NF-κb [39] . Therefore, once that we assessed the antioxidant efficacy of OESA, it was necessary to verify the complete assessment of lipid oxidation which results from EBV infection. The monitoring of lipid peroxidation was done by measuring the secondary lipid peroxidation products, generated by the decomposition of the long-chain polyunsaturated fatty acids, MDA and DC [40] . To evaluate the effective concentration of OESA useful to affect the oxidative process induced by EBV induction, the toxicity assay was performed on Raji cells. Lower concentrations of OESA did not show cytotoxicity (CC 50 = 0.8773 mg/mL) ( Figure 3) . Therefore, the 0.31 mg/mL concentration of OESA was selected for monitoring lipid peroxidation after the EBV induction. As reported previously [21] , we used the nonstressing dose (8 nM) of TPA to induce the EBV lytic cycle, and we detected a low basal level of MDA and DC on Raji cells. The results showed that the TPA-treated cells exhibited maximum MDA production, indicating that this sample undergoes lipid peroxidation as a consequence of the induction of the lytic cycle ( Figure 4) . Otherwise, we observed that the concomitant treatment with TPA and OESA extracts causes a significant decrease in the MDA and DC levels on Raji cells (Figures 4 and 5) . Thus, it was evident that OESA exhibits high antioxidant activity. Our results coincide with the data reported by other studies in which a decrease in MDA levels on gastric mucosa cells treated with Olea europaea L. extracts was described [41] . Indeed, it was reported that the dried leaves of Olea europaea L. were able to maintain the cell membrane integrity and exerted an antilipid peroxidative activity protecting the gastric mucosa This phenomenon was confirmed by the reduction of antigen-antibody immunocomplex reported by IFA assay (Figure 6 ). The results showed that Raji cells simultaneously exposed to TPA and OESA exhibited a percentage of positive fluorescence cells lower than the TPA-treated cells (**** p < 0.0001). This suggests that the OESA treatment has a protective effect against the EBV lytic cycle induction. These results reflect previous studies which reported the antiviral activity of olive leaf extract preparations towards ILTV virus [42] , VHSV virus [43] , HIV-1 [44] , and HSV-1 [45] . Recently, we showed the antiviral effect of OESA against HSV-1. We reported that OESA interferes with the virus attachment to cell receptors, and thus reduces HSV-1 entry and replication on Vero cells [17] . Given that the EBV maintains a lifelong infection, which is persistent and intermittent, and which could be potentially associated with the formation of oxidative stress and trigger inflammatory processes and several diseases [19, 20, 46, 47] , this work suggests the use of OESA in the preventive treatment and deactivation of EBV.

Olive extracts derived from the leaves of the Olea europaea L. var. sativa tree were cultivated and collected during October 2018 from the Sfax region (the southeast of Tunisia). Sfax is one of the biggest coastal cities in Tunisia. It is located in the eastern part of the country. The climate in this area is arid to semiarid with irregular and torrential precipitations [48] . Olive leaves were dried at room temperature, powdered by a mechanical grinder, and macerated overnight in a mixture of water/ethanol (50:50, v/v) under gentle stirring. The hydroethanolic extract was filtered through a cellulose filter, lyophilized, and frozen at −80 • C until use. The extracts were characterized by using LC-DAD-ESI-MS analysis [17] .

The DPPH assay is based on the reduction of the stable radical, DPPH, to the formation of a nonradical form in the presence of hydrogen donating antioxidants. Therefore, the Plants 2021, 10, 2445 8 of 12 antioxidant activity was determined by monitoring the scavenging of the free radical DPPH in presence of the OESA. The DPPH working solution was obtained by mixing the stock solution (200 µL in 1 mL Me OH) with 500 µL of DPPH (0.2 mM), purchased from Merck (Darmstadt, Germany). The final volume was brought to 1 mL with distilled water, shaken vigorously and allowed to reach a steady state at room temperature for 1 h. Aliquots of various concentrations of the OESA extracts (0, 0.125, 0.25, 0.5, 1 mg/mL) and standard antioxidant were mixed with DPPH (0.2 mM) and incubated for 1h in the dark. After 1 h of reaction, the mixtures were poured into an optical glass cuvette and immediately placed in a spectrophotometer. The absorbance was taken at 517 nm using Beckman spectrophotometer (Bichrom Libra S32 (Beckman, Fullerton, CA, USA) [49] . Butylhydroxytoluene (BHT) (SIGMA, St. Louis, MO, USA) was used as a standard antioxidant. The DPPH radical scavenging activity was calculated according to the following equation:

where A0 was the absorbance of the total DPPH (blank, without extract) and A1 was the absorbance of the sample.

The reducing power of OESA was determined according to the Oyaizu method [50] . According to this method, aliquots of various concentrations of the standard and the OLCS extracts (0.06 to 1 mg/mL) were mixed with 1 mL of (pH 6.6) 200 mM phosphate buffer and 1 mL of (1%) potassium ferricyanide (K 3 Fe (CN) 6 ). The mixture was incubated at 50 • C for 20 min. Then, 1 mL of (10%) trichloroacetic acid (TCA) was added to the mixture which was centrifuged at 3000 rpm for 10 min. The upper layer of solution (1.5 mL) was mixed with 1.5 mL of deionized water and 0.1 mL (0.1%) ferric chloride solution (FeCl 3 ). The absorbance was measured at 700 nm in a UV spectrometer. A blank was prepared without adding extract. Ascorbic acid at various concentrations (0 to 1 mg/mL) was used as standard. The reduction of ferric ion (Fe 3+ ) to ferrous form (Fe 2+ ) by OESA produces an intense blue light revealed as a change in absorption at 593 nm related to an antioxidant standard.

The Raji cells (human Burkitt's lymphoma), harboring the latent form of EBV cycle [51] , were obtained from the Institute Pasteur of Tunis. Hela cell line (epithelial cell line derived from cervical cancer) was supplied by ATCC (Manassas, VA, USA). Both cells were employed for cytotoxicity and antioxidant studies. Both cell lines were grown in RPMI 1640 medium (Gibco) supplemented with 10% (v/v) fetal calf serum (FCS) and 2 mM L-glutamine in tissue culture flasks (Nunc). They were passed twice a week and kept at 37 • C in a humidified atmosphere of 95% air and 5% CO 2 .

The MTT (3-(4,5-dimethylthiazolyl-2)-2,5-diphenyltetrazolium bromide) cell proliferation assay is a colorimetric assay for assessing cellular metabolic activity and indirectly serves to assess the cell viability, proliferation, and cytotoxicity This colorimetric assay is based on the reduction of yellow tetrazolium salt (MTT) to purple colored formazan crystals by mitochondrial dehydrogenase. Therefore, it is directly proportional to the number of living and metabolically active cells. Raji cells (6 × 10 4 ) were grown in 96-wells microtiter plates at 37 • C in a 5% CO 2 incubator for 24 h, and after they are exposed to serial dilutions of OESA (0.16, 0.31, 0.625, 1.25, 2.5, 5, 10 mg/mL) for 72 h. Then, 20 µL of MTT solution (5 mg/mL in PBS) (Sigma) were added to each well and the plates were additionally incubated for 4 h at 37 • C in a CO 2 incubator. After incubation, 180 µL of growth medium was removed from each well and replaced with DMSO/methanol (50:50) solution to dissolve the formazan crystals. The plate was shaken on the microtiter plate shaker at room temperature to facilitate the complete solubilization of formazan crystals. The absorbance was measured at 570 nm with a microplate reader (Elx 800 microplate reader) and the % of cytotoxicity was calculated.

For the induction of the lytic cycle, Raji cells (3 × 10 6 /well), were stimulated with 8 nM TPA (12-O-tetradecanoyl-phorbol-13-acetate) (Sigma) for 30 min. Then, the cells were collected [21] and centrifuged for 10 min at 1000 rpm. The pellet was washed once with PBS (1×) and then centrifuged for 10 min at 1000 rpm. The pellet was resuspended in 1 mL of deionized water and lysed by 10 cycles of sonication for 20 s at 37 • C (Sonics, Vibra-Cell).

MDA determination was performed by the thiobarbituric acid reactive species assay. Raji cell lysate (3 × 10 6 /well), previously TPA treated as reported in Section 4.6, were added to 700 µL reagent TBA/TCA (thiobarbituric acid/trichloroacetic acid) (15% trichloroacetic acid, 0.8% TBA, 0.25 N HCl). The mixture was heated at 95 • C for 15 min to form MDA-TBA adduct. This assay measures the MDA bound to proteins. Protein concentration was calculated by using the Protein Assay Kit from Bio-Rad (Marnes-la-Coquette, France) and bovine serum albumin served as the standard [24] . Optical density was measured with a spectrophotometer (Biochrom, Libra S32) (Biocrom Ltd. Waterbeach Cambridge, UK) at 532 nm. Values were compared to a calibration curve of 1,1,3,3-tetraethoxypropane [21] .

Conjugated diene (CD) assay evaluates the lipid oxidation and was determined as described before with some modification [25] . Briefly, 25 µL of Raji cells lysate (3 × 10 6 /well), previously TPA treated as reported in Section 4.6, were extracted with 3 mL of chloroform/methanol (2:1, v/v) solution and centrifuged at 3000 rpm for 15 min. Then, 2 mL of organic phase was transferred into another clear tube dried at 45 • C and dissolved in methanol. The absorbance was measured at 233 nm.

Cells were adjusted to 3 × 10 6 cells/mL and incubated at 37 • C for 48 h. Then, they were treated with TPA [8 nM] and OESA for 30 min, incubated for additional 48 h and centrifuged for 5 min at 1000 rpm. The pellet was incubated with the primary antibody directed against the EBV-VCA (viral capsid antigen) produced previously [21] , diluted 1/500 in PBS (1×) for 20 min at 4 • C. After, the pellet was rinsed briefly in phosphatebuffered saline twice and incubated with fluorescent antihuman IgG for 20 min at 4 • C in the dark. The secondary antibody was decanted, and the cells were washed three times with PBS for 5 min each in the dark. The sample was suspended in PBS, layered on slides, and analyzed using the fluorescence microscope (ZEISS, Axiostar Plus, Landshut, Germany) (magnification, 40×). The negative control consisted of untreated HeLa cells and the positive controls consisted of Raji cells treated TPA. The assay was used to detect the inhibitory activity of EBV lytic cycle induction mediated by OESA.

The statistical analysis was performed with GraphPad Prism 8 software (GraphPad Software, San Diego, CA, USA) and the one-way analysis of variance (ANOVA) was used to compare the different conditions. Results are the mean ± SD of three independent experiments. Half-maximal inhibitory concentration (IC 50 ) values were calculated by using nonlinear regression analysis.

Olive leaf is one of the most common and traditional herbs used among Mediterranean people to cure certain diseases. Accordingly, the analysis of olive leaf extract revealed an antioxidant activity and protection against lipid peroxidation. In addition, the leaves of Oleo europaea cultivated from Sfax showed an antiviral effect against the EBV lytic cycle induction. Oxidative stress during viral replication can play a key role in the development and progression of diseases. Thus, we can conclude that OESA might be used as a natural supplement to fight the oxidative stress and as an adjuvant therapeutic remedy against viral infections. 

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Informed Consent Statement: Not applicable.

The data presented in this study are available in the article.

The authors declare no conflict of interest.