Please use this identifier to cite or link to this item:
http://acervodigital.unesp.br/handle/11449/74531
- Title:
- High Content Screening of a Kinase-Focused Library Reveals Compounds Broadly-Active against Dengue Viruses
- Cruz, Deu John M.
- Koishi, Andrea Cristine
- Taniguchi, Juliana Bosso
- Li, Xiaolan
- Milan Bonotto, Rafaela
- No, Joo Hwan
- Kim, Keum Hyun
- Baek, Sungmin
- Kim, Hee Young
- Windisch, Marc Peter
- Pamplona Mosimann, Ana Luiza
- de Borba, Luana
- Liuzzi, Michel
- Hansen, Michael Adsetts Edberg
- Nunes Duarte dos Santos, Claudia
- Freitas-Junior, Lucio Holanda
- Institut Pasteur Korea
- Fundação Oswaldo Cruz Paraná (ICC/FIOCRUZ-PR)
- Universidade Federal do Paraná (UFPR)
- Universidade Estadual Paulista (UNESP)
- Universidade Feevale
- 1935-2727
- 1935-2735
- Dengue virus is a mosquito-borne flavivirus that has a large impact in global health. It is considered as one of the medically important arboviruses, and developing a preventive or therapeutic solution remains a top priority in the medical and scientific community. Drug discovery programs for potential dengue antivirals have increased dramatically over the last decade, largely in part to the introduction of high-throughput assays. In this study, we have developed an image-based dengue high-throughput/high-content assay (HT/HCA) using an innovative computer vision approach to screen a kinase-focused library for anti-dengue compounds. Using this dengue HT/HCA, we identified a group of compounds with a 4-(1-aminoethyl)-N-methylthiazol-2-amine as a common core structure that inhibits dengue viral infection in a human liver-derived cell line (Huh-7.5 cells). Compounds CND1201, CND1203 and CND1243 exhibited strong antiviral activities against all four dengue serotypes. Plaque reduction and time-of-addition assays suggests that these compounds interfere with the late stage of viral infection cycle. These findings demonstrate that our image-based dengue HT/HCA is a reliable tool that can be used to screen various chemical libraries for potential dengue antiviral candidates. © 2013 Cruz et al.
- 1-Feb-2013
- PLoS Neglected Tropical Diseases, v. 7, n. 2, 2013.
- alpha2a interferon
- chloroquine
- phosphotransferase inhibitor
- ribavirin
- affinity chromatography
- animal cell
- antiviral activity
- Chikungunya alphavirus
- computer model
- computer program
- controlled study
- Dengue virus
- dose response
- drug structure
- genotype
- high throughput screening
- human
- human cell
- nonhuman
- nucleotide sequence
- peptide library
- validation process
- viral disease immunofluorescence assay
- Antiviral Agents
- Cell Line
- Dengue Virus
- Drug Discovery
- Hepatocytes
- High-Throughput Screening Assays
- Humans
- Microbial Sensitivity Tests
- http://dx.doi.org/10.1371/journal.pntd.0002073
- Acesso aberto
- outro
- http://repositorio.unesp.br/handle/11449/74531
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