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Antiviral Screening of Multiple Compounds against Ebola Virus.
Dowall, Stuart D; Bewley, Kevin; Watson, Robert J; Vasan, Seshadri S; Ghosh, Chandradhish; Konai, Mohini M; Gausdal, Gro; Lorens, James B; Long, Jason; Barclay, Wendy; Garcia-Dorival, Isabel; Hiscox, Julian; Bosworth, Andrew; Taylor, Irene; Easterbrook, Linda; Pitman, James; Summers, Sian; Chan-Pensley, Jenny; Funnell, Simon; Vipond, Julia; Charlton, Sue; Haldar, Jayanta; Hewson, Roger; Carroll, Miles W.
Afiliação
  • Dowall SD; Public Health England, Porton Down, Salisbury, Wiltshire SP4 0JG, UK. stuart.dowall@phe.gov.uk.
  • Bewley K; Institute of Infection and Global Health, University of Liverpool, Liverpool L69 7BE, UK. stuart.dowall@phe.gov.uk.
  • Watson RJ; Public Health England, Porton Down, Salisbury, Wiltshire SP4 0JG, UK. kevin.bewley@phe.gov.uk.
  • Vasan SS; Public Health England, Porton Down, Salisbury, Wiltshire SP4 0JG, UK. robert.watson@phe.gov.uk.
  • Ghosh C; Public Health England, Porton Down, Salisbury, Wiltshire SP4 0JG, UK. seshadri.vasan@phe.gov.uk.
  • Konai MM; Department of Preventive and Social Medicine, Jawaharlal Institute of Postgraduate Medical Education & Research, Puducherry 605006, India. seshadri.vasan@phe.gov.uk.
  • Gausdal G; Chemical Biology and Medicinal Chemistry Laboratory, New Chemistry Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur, Bengaluru 560064, Karnataka, India. chandradhish@jncasr.ac.in.
  • Lorens JB; Chemical Biology and Medicinal Chemistry Laboratory, New Chemistry Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur, Bengaluru 560064, Karnataka, India. mohinimk@jncasr.ac.in.
  • Long J; BerGenBio, Jonas Lies vei 91, Bergen 5009, Norway. gro.gausdal@bergenbio.com.
  • Barclay W; BerGenBio, Jonas Lies vei 91, Bergen 5009, Norway. jim.lorens@bergenbio.com.
  • Garcia-Dorival I; Imperial College London, St Mary's Campus, London W2 1PG, UK. jason.long08@imperial.ac.uk.
  • Hiscox J; Imperial College London, St Mary's Campus, London W2 1PG, UK. w.barclay@imperial.ac.uk.
  • Bosworth A; Institute of Infection and Global Health, University of Liverpool, Liverpool L69 7BE, UK. g.garcia-dorival@liverpool.ac.uk.
  • Taylor I; Institute of Infection and Global Health, University of Liverpool, Liverpool L69 7BE, UK. julian.hiscox@liverpool.ac.uk.
  • Easterbrook L; NIHR Health Protection Research Unit in Emerging and Zoonotic Infections, UK. julian.hiscox@liverpool.ac.uk.
  • Pitman J; Public Health England, Porton Down, Salisbury, Wiltshire SP4 0JG, UK. andrew.bosworth@phe.gov.uk.
  • Summers S; NIHR Health Protection Research Unit in Emerging and Zoonotic Infections, UK. andrew.bosworth@phe.gov.uk.
  • Chan-Pensley J; Public Health England, Porton Down, Salisbury, Wiltshire SP4 0JG, UK. irene.taylor@phe.gov.uk.
  • Funnell S; Public Health England, Porton Down, Salisbury, Wiltshire SP4 0JG, UK. linda.easterbrook@phe.gov.uk.
  • Vipond J; Public Health England, Porton Down, Salisbury, Wiltshire SP4 0JG, UK. james.pitman@phe.gov.uk.
  • Charlton S; Public Health England, Porton Down, Salisbury, Wiltshire SP4 0JG, UK. sian.summers@phe.gov.uk.
  • Haldar J; Public Health England, Porton Down, Salisbury, Wiltshire SP4 0JG, UK. jenny.chan-pensley@phe.gov.uk.
  • Hewson R; Public Health England, Porton Down, Salisbury, Wiltshire SP4 0JG, UK. simon.funnell@phe.gov.uk.
  • Carroll MW; Public Health England, Porton Down, Salisbury, Wiltshire SP4 0JG, UK. julia.vipond@phe.gov.uk.
Viruses ; 8(11)2016 10 27.
Article em En | MEDLINE | ID: mdl-27801778
In light of the recent outbreak of Ebola virus (EBOV) disease in West Africa, there have been renewed efforts to search for effective antiviral countermeasures. A range of compounds currently available with broad antimicrobial activity have been tested for activity against EBOV. Using live EBOV, eighteen candidate compounds were screened for antiviral activity in vitro. The compounds were selected on a rational basis because their mechanisms of action suggested that they had the potential to disrupt EBOV entry, replication or exit from cells or because they had displayed some antiviral activity against EBOV in previous tests. Nine compounds caused no reduction in viral replication despite cells remaining healthy, so they were excluded from further analysis (zidovudine; didanosine; stavudine; abacavir sulphate; entecavir; JB1a; Aimspro; celgosivir; and castanospermine). A second screen of the remaining compounds and the feasibility of appropriateness for in vivo testing removed six further compounds (ouabain; omeprazole; esomeprazole; Gleevec; D-LANA-14; and Tasigna). The three most promising compounds (17-DMAG; BGB324; and NCK-8) were further screened for in vivo activity in the guinea pig model of EBOV disease. Two of the compounds, BGB324 and NCK-8, showed some effect against lethal infection in vivo at the concentrations tested, which warrants further investigation. Further, these data add to the body of knowledge on the antiviral activities of multiple compounds against EBOV and indicate that the scientific community should invest more effort into the development of novel and specific antiviral compounds to treat Ebola virus disease.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antivirais / Avaliação Pré-Clínica de Medicamentos / Ebolavirus Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antivirais / Avaliação Pré-Clínica de Medicamentos / Ebolavirus Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article