{"id":125224,"date":"2021-07-21T08:22:30","date_gmt":"2021-07-21T15:22:30","guid":{"rendered":"https:\/\/lifeboat.com\/blog\/2021\/07\/in-vitro-efficacy-of-artemisinin-based-treatments-against-sars-cov-2"},"modified":"2021-07-21T08:22:30","modified_gmt":"2021-07-21T15:22:30","slug":"in-vitro-efficacy-of-artemisinin-based-treatments-against-sars-cov-2","status":"publish","type":"post","link":"https:\/\/lifeboat.com\/blog\/2021\/07\/in-vitro-efficacy-of-artemisinin-based-treatments-against-sars-cov-2","title":{"rendered":"In vitro efficacy of artemisinin-based treatments against SARS-CoV-2"},"content":{"rendered":"<p><a class=\"aligncenter blog-photo\" href=\"https:\/\/lifeboat.com\/blog.images\/in-vitro-efficacy-of-artemisinin-based-treatments-against-sars-cov-22.jpg\"><\/a><\/p>\n<p><i>Artemisia annua<\/i> plants grown from a cultivated seed line in Kentucky, USA, were extracted using either absolute ethanol or distilled water at 50 \u00b0C for 200 min and analyzed, as described in \u201c<a data-track=\"click\" data-track-label=\"link\" data-track-action=\"section anchor\" href=\"https:\/\/www.nature.com\/articles\/s41598-021-93361-y#Sec11\">Materials and methods<\/a>\u201d and Supplementary Information (Figures <a data-track=\"click\" data-track-label=\"link\" data-track-action=\"supplementary material anchor\" href=\"https:\/\/www.nature.com\/articles\/s41598-021-93361-y#MOESM1\">S1<\/a> and <a data-track=\"click\" data-track-label=\"link\" data-track-action=\"supplementary material anchor\" href=\"https:\/\/www.nature.com\/articles\/s41598-021-93361-y#MOESM1\">S2<\/a>). Solids were removed by filtration and the solvents were evaporated. The extracted materials were dissolved in dimethylsulfoxide (DMSO) (ethanol extract) or a DMSO: water mixture (3:1 for aqueous extract) and filtered (see supporting information for details). Artemisinin (Fig. <a data-track=\"click\" data-track-label=\"link\" data-track-action=\"figure anchor\" href=\"https:\/\/www.nature.com\/articles\/s41598-021-93361-y#Fig1\">1<\/a>, (<b>1<\/b>)) was synthesized and purified following a published procedure or purchased<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 17\" title=\"Horv\u00e1th, Z. et al. Recovery of artemisinin from a complex reaction mixture using continuous chromatography and crystallization. Org. Process Res. Dev. 19624&ndash;634. https:\/\/doi.org\/10.1021\/acs.oprd.5b00048 (2015).\" href=\"https:\/\/www.nature.com\/articles\/s41598-021-93361-y#ref-CR17\" id=\"ref-link-section-d28072e911\">17<\/a><\/sup>, while artesunate (Fig. <a data-track=\"click\" data-track-label=\"link\" data-track-action=\"figure anchor\" href=\"https:\/\/www.nature.com\/articles\/s41598-021-93361-y#Fig1\">1<\/a>, (<b>2<\/b>)) and artemether (Fig. <a data-track=\"click\" data-track-label=\"link\" data-track-action=\"figure anchor\" href=\"https:\/\/www.nature.com\/articles\/s41598-021-93361-y#Fig1\">1<\/a>, (<b>3<\/b>)) were only obtained from commercial sources.<\/p>\n<p>Initial experiments were carried out at FU Berlin, Germany. To initially screen whether extracts and pure artemisinin were active against SARS-CoV-2, their antiviral activity was tested by pretreating VeroE6 cells at different time points during 120 min with selected concentrations of the extracts or compounds prior to infection with the first European SARS-CoV-2 isolated in M\u00fcnchen (SARS-CoV-2\/human\/Germany\/BavPat 1\/2020). The virus-drug mixture was then removed and cells were overlaid with medium containing 1.3% carboxymethylcellulose to prevent virus release into the medium. DMSO was used as a negative control. Plaque numbers were determined either by indirect immunofluorescence using a mixture of antibodies to SARS-CoV N protein<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 18\" title=\"Bussmann, B. M., Reiche, S., Jacob, L. H., Braun, J. M. & Jassoy, C. Antigenic and cellular localization analysis of the severe acute respiratory syndrome coronavirus nucleocapsid protein using monoclonal antibodies. Virus Res. 122119&ndash;126. https:\/\/doi.org\/10.1016\/j.virusres.2006.07.005 (2006).\" href=\"https:\/\/www.nature.com\/articles\/s41598-021-93361-y#ref-CR18\" id=\"ref-link-section-d28072e939\">18<\/a><\/sup> or by staining with crystal violet<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 19\" title=\"von Einem, J., Schumacher, D., O\u2019Callaghan, D. J. & Osterrieder, N. The \u03b1-TIF (VP16) homologue (ETIF) of equine herpesvirus 1 is essential for secondary envelopment and virus egress. J. Virol. 80, 2609&ndash;2620. https:\/\/doi.org\/10.1128\/JVI.80.6.2609-2620.2006 (2006).\" href=\"https:\/\/www.nature.com\/articles\/s41598-021-93361-y#ref-CR19\" id=\"ref-link-section-d28072e943\">19<\/a><\/sup>. The addition of either ethanolic or aqueous <i>A. annua<\/i> extracts prior to virus addition resulted in reduced plaque formation in a concentration dependent manner, while artemisinin exhibited little antiviral activity (Supplemental Tables <a data-track=\"click\" data-track-label=\"link\" data-track-action=\"supplementary material anchor\" href=\"https:\/\/www.nature.com\/articles\/s41598-021-93361-y#MOESM1\">S1 <\/a>\u2013 <a data-track=\"click\" data-track-label=\"link\" data-track-action=\"supplementary material anchor\" href=\"https:\/\/www.nature.com\/articles\/s41598-021-93361-y#MOESM1\">S8<\/a>).<\/p>\n<p>Concentration\u2013response experiments were carried out at Copenhagen University Hospital-Hvidovre. In these experiments the Danish SARS-CoV-2 isolate SARS-CoV-2\/human\/Denmark\/DK-AHH1\/2020 was used employing a 96-well plate based concentration\u2013response antiviral treatment assay, allowing for multiple replicates per concentration, as described in \u201c<a data-track=\"click\" data-track-label=\"link\" data-track-action=\"section anchor\" href=\"https:\/\/www.nature.com\/articles\/s41598-021-93361-y#Sec11\">Materials and methods<\/a>\u201d and Supplementary Information (Figures <a data-track=\"click\" data-track-label=\"link\" data-track-action=\"supplementary material anchor\" href=\"https:\/\/www.nature.com\/articles\/s41598-021-93361-y#MOESM1\">S3<\/a> and <a data-track=\"click\" data-track-label=\"link\" data-track-action=\"supplementary material anchor\" href=\"https:\/\/www.nature.com\/articles\/s41598-021-93361-y#MOESM1\">S4<\/a>)<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 20\" title=\"Ramirez, S. et al. Overcoming culture restriction for SARS-CoV-2 in human cells facilitates the screening of compounds inhibiting viral replication. Antimicrob. Agents Chemother. 65, e0009721. https:\/\/doi.org\/10.1128\/AAC.00097-21 (2021).\" href=\"https:\/\/www.nature.com\/articles\/s41598-021-93361-y#ref-CR20\" id=\"ref-link-section-d28072e977\">20<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 21\" title=\"Gammeltoft, K. A. et al. Hepatitis C Virus Protease Inhibitors Show Differential Efficacy and Interactions with Remdesivir for Treatment of SARS-CoV-2. Antimicrob. Agents Chemother. https:\/\/doi.org\/10.1128\/AAC.02680-20 (2021) (in Press).\" href=\"https:\/\/www.nature.com\/articles\/s41598-021-93361-y#ref-CR21\" id=\"ref-link-section-d28072e980\">21<\/a><\/sup>. Seven replicates were measured at each concentration and a range of concentrations was evaluated to increase data accuracy when compared to the plaque-reduction assay, which was carried out in duplicates. Extracts or compounds were added to VeroE6 cells either 1.5 h prior to (pretreatment (pt)) or 1 h post infection (treatment (t)), respectively, followed by a 2-day incubation of virus with extracts or compounds. Both protocols yielded similar results, with slightly lower median effective concentration (EC<sub>50<\/sub>) values observed for treatment assays.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Artemisia annua plants grown from a cultivated seed line in Kentucky, USA, were extracted using either absolute ethanol or distilled water at 50 \u00b0C for 200 min and analyzed, as described in \u201cMaterials and methods\u201d and Supplementary Information (Figures S1 and S2). Solids were removed by filtration and the solvents were evaporated. The extracted materials [\u2026]<\/p>\n","protected":false},"author":534,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[11,1635],"tags":[],"class_list":["post-125224","post","type-post","status-publish","format-standard","hentry","category-biotech-medical","category-materials"],"_links":{"self":[{"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/posts\/125224","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/users\/534"}],"replies":[{"embeddable":true,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/comments?post=125224"}],"version-history":[{"count":0,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/posts\/125224\/revisions"}],"wp:attachment":[{"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/media?parent=125224"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/categories?post=125224"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/tags?post=125224"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}