2014
DOI: 10.1186/s12917-014-0231-6
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Non-cytotoxic Thymus capitata extracts prevent Bovine herpesvirus-1 infection in cell cultures

Abstract: BackgroundBovine herpes virus type 1 (BHV-1) still causes great economic loss to the livestock industry and trade because there aren’t any available drugs that proved to be fully effective against it. In this study, the cytotoxicity and the antiviral activities of the Thymus capitata extracts were evaluated for the development of new, non toxic and specific anti-herpesvirus drug. Aqueous extracts (AE), ethanolic extracts (EE) and essential oil (EO) of the aerial parts of Thymus capitata were analyzed to determ… Show more

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Cited by 11 publications
(20 citation statements)
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“…Although HSV‐1 and HSV‐2 are structurally and genetically similar, their sensitivity to antiviral compounds may vary depending on the strains and cell type used in antiviral assays as reported for instance in Leary, Wittrock, Sarisky, Weinberg, and Levin (). Similar antiviral results were previously observed against bovine herpesvirus Type 1 infection with EC 50 values of 164, 47.8, and 3.3 μg/ml, respectively (Boubaker‐Elandalousi et al, ). These data indicate a broad spectrum of action of T. capitatus extracts against Herpes viruses.…”
Section: Resultssupporting
confidence: 87%
See 1 more Smart Citation
“…Although HSV‐1 and HSV‐2 are structurally and genetically similar, their sensitivity to antiviral compounds may vary depending on the strains and cell type used in antiviral assays as reported for instance in Leary, Wittrock, Sarisky, Weinberg, and Levin (). Similar antiviral results were previously observed against bovine herpesvirus Type 1 infection with EC 50 values of 164, 47.8, and 3.3 μg/ml, respectively (Boubaker‐Elandalousi et al, ). These data indicate a broad spectrum of action of T. capitatus extracts against Herpes viruses.…”
Section: Resultssupporting
confidence: 87%
“…The ethanolic and aqueous extracts (EE and AE) were prepared as previously described (Boubaker‐Elandalousi et al, ). The essential oil (EO) was prepared by dissolving 100 g of dried plant material in 1 L of distilled water and then submitted to microwave‐assisted hydro‐distillation at 40 °C during 4 hr, in a Clevenger type apparatus.…”
Section: Methodsmentioning
confidence: 99%
“…The relative cell viability rate was determined for each concentration as (OD 450 drug)/(OD 450 control) 9 100. LiCl concentrations below the 50 % cytostatic concentration (CC 50 ) were defined as non-toxic concentrations [19].…”
Section: Cytotoxicity Assaymentioning
confidence: 99%
“…A notable number of studies reviewed in this paper have also tried to detect the exact M-o-A of IS. This was achieved through the time-of-addition (T-o-A) study, which is comprised of assays with different procedures of addition of IS, viral suspension and cell cultures [48,[54][55][56][62][63][64]66,68,69,71,73,74,77,82,87,88,91,92,94,104,106,112]. Based on the highest activity in a certain assay, a conclusion about the exact type of M-o-A can be derived (Fig.…”
Section: Time-of-addition (T-o-a) Studiesmentioning
confidence: 99%