Acridones as promising drug candidates against Oropouche virus

被引:4
|
作者
Saivish, Marielena Vogel [1 ]
Menezes, Gabriela de Lima [2 ,3 ]
da Silva, Roosevelt Alves [2 ]
de Assis, Leticia Ribeiro [4 ]
Teixeira, Igor da Silva [1 ]
Fulco, Umberto Laino [3 ]
Avilla, Clarita Maria Secco [1 ,4 ]
Eberle, Raphael Josef [5 ,6 ]
Santos, Igor de Andrade [7 ]
Korostov, Karolina [5 ]
Webber, Mayara Lucia [1 ]
da Silva, Gislaine Celestino Dutra [1 ]
Nogueira, Mauricio Lacerda [1 ]
Jardim, Ana Carolina Gomes [4 ,7 ]
Regasin, Luis Octavio [4 ]
Coronado, Monika Aparecida [5 ]
Pacca, Carolina Colombelli [1 ,4 ]
机构
[1] Fac Med Sao Jose Do Rio Preto, Dept Doencas Dermatol Infecciosas & Parasitarias, Lab Pesquisas Virol, BR-15090000 Sao Jose Do Rio Preto, SP, Brazil
[2] Univ Fed Jatai, Unidade Especial Ciencias Exatas, BR-75801615 Jatai, GO, Brazil
[3] Univ Fed Rio Grande Do Norte, Bioinformat Multidisciplinary Environm, Programa Posgrad Bioinformat, BR-59078400 Natal, RN, Brazil
[4] Sao Paulo State Univ, Inst Biosci Humanities & Exact Sci, BR-15054000 Sao Jose Do Rio Preto, SP, Brazil
[5] Forschungszentrum Julich, Inst Biol Informat Proc IBI Struct Biochem 7, D-52428 Julich, Germany
[6] Heinrich Heine Univ Dusseldorf, Fac Math & Nat Sci, Inst Phys Biol, Univ Str, D-40225 Dusseldorf, Germany
[7] Univ Fed Uberlandia, Inst Biomed Sci, Uberlandia, MG, Brazil
基金
巴西圣保罗研究基金会; 美国国家卫生研究院;
关键词
Oropouche; Endonuclease; Acridone; Drug discovery; Antiviral; CENTRAL-NERVOUS-SYSTEM; STRAND RNA VIRUSES; MOLECULAR-DYNAMICS; HIV-1; REPLICATION; ANTIVIRAL AGENTS; NS3; HELICASE; DERIVATIVES; INHIBITORS; FEVER; IDENTIFICATION;
D O I
10.1016/j.crmicr.2023.100217
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Oropouche virus (OROV) is an emerging vector -borne arbovirus found in South America that causes Oropouche fever, a febrile infection similar to dengue fever. It has a high epidemic potential, causing illness in over 500,000 cases diagnosed since the virus was first discovered in 1955. Currently, the prevention of human viral infection depends on vaccination, but availability for many viruses is limited, and they are classified as neglected viruses. At present, there are no vaccines or antiviral treatments available. An alternative approach to limiting the spread of the virus is to selectively disrupt viral replication mechanisms. Here, we demonstrate the inhibitory effect of acridones, which efficiently inhibited viral replication by 99.9 % in vitro. To evaluate possible mechanisms of action, we conducted tests with dsRNA, an intermediate in virus replication, as well as MD simulations, docking, and binding free energy analysis. The results showed a strong interaction between FAC21 and the OROV endonuclease, which possibly limits the interaction of viral RNA with other proteins. Therefore, our results suggest a dual mechanism of antiviral action, possibly caused by ds-RNA intercalation. In summary, our findings demonstrate that a new generation of antiviral drugs could be developed based on the selective optimization of molecules.
引用
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页数:11
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