Differential inhibitory action of two azoic compounds against arenaviruses

The action of five azo-based compounds against the arenaviruses Junin (JUNV) and Tacaribe (TCRV) was evaluated in vitro by a virus yield inhibition assay in Vero cells and a cell-free virion inactivation assay. The compound 2-azo-(1′-(2′-nitroso)naphthyl)-benzoate (ANNB) was the most effective inhib...

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Autor principal: García, C.C
Otros Autores: Candurra, N.A, Damonte, E.B
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: Elsevier 2003
Acceso en línea:Registro en Scopus
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030 |a IAAGE 
100 1 |a García, C.C. 
245 1 0 |a Differential inhibitory action of two azoic compounds against arenaviruses 
260 |b Elsevier  |c 2003 
270 1 0 |m Damonte, E.B.; Depto. de Quim. Biológica, Universidad de Buenos Aires, Ciudad Universitaria, Piso 4, Buenos Aires 1428, Argentina; email: edamonte@qb.fcen.uba.ar 
506 |2 openaire  |e Política editorial 
504 |a Damonte, E.B., Junin virus (2002) Wiley Encyclopedia of Molecular Medicine, pp. 1844-1846. , T.E. Creighton. New York: Wiley 
504 |a Enria, D.A., Maiztegui, J.I., Antiviral treatment of Argentine hemorrhagic fever (1994) Antiviral Res., 23, pp. 23-31 
504 |a Andrei, G., De Clercq, E., Inhibitory effect of selected antiviral compounds on arenavirus replication in vitro (1990) Antiviral Res., 14, pp. 287-300 
504 |a Candurra, N.A., Maskin, L., Damonte, E.B., Inhibition of arenavirus multiplication in vitro by phenotiazines (1996) Antiviral Res., 31, pp. 149-158 
504 |a Cordo, S.M., Candurra, N.A., Damonte, E.B., Myristic acid analogs are inhibitors of Junin virus replication (1999) Microbes Infect., 1, pp. 609-614 
504 |a Bartolotta, S., García, C.C., Candurra, N.A., Damonte, E.B., Effect of fatty acids on arenavirus replication: Inhibition of virus production by lauric acid (2001) Arch. Virol., 146, pp. 777-790 
504 |a García, C.C., Candurra, N.A., Damonte, E.B., Antiviral and virucidal activities against arenaviruses of zinc-finger active compounds (2000) Antiviral Chem. Chemother., 11, pp. 231-238 
504 |a Martínez Peralta, L.A., Coto, C.E., Weissenbacher, M.C., The Tacaribe complex: Relationship between a pathogenic (Junin) and a nonpathogenic (Tacaribe) arenavirus (1993) The Arenaviridae, , M.S. Salvato. New York: Plenum Press 
504 |a Damonte, E.B., Mersich, S.E., Candurra, N.A., Intracellular processing and transport of Junin virus glycoproteins influences virion infectivity (1994) Virus Res., 34, pp. 317-326 
504 |a Rice, W.G., Turpin, J.A., Huang, M., Azodicarbonamide inhibits HIV-1 replication by targeting the nucleocapsid protein (1997) Nat. Med., 3, pp. 341-345 
504 |a Goebel, F.-D., Hemmer, R., Schmit, J., Phase I/II dose escalation and randomized withdrawal study with add-on azodicarbonamide in patients failing on current antiretroviral therapy (2001) AIDS, 15, pp. 33-45 
504 |a Rice, W.G., Turpin, J.A., Schaeffer, C.A., Evaluation of selected chemotypes in coupled cellular and molecular target-based screens identifies novel HIV-1 zinc finger inhibitors (1996) J. Med. Chem., 39, pp. 3606-3616 
504 |a Rice, W.G., Baker, D.C., Schaeffer, C.A., Inhibition of multiple phases of human immunodeficiency virus type 1 replication by a dithiane compound that attacks the conserved zinc fingers of retroviral nucleocapsid proteins (1997) Antimicrob. Agents Chemother., 41, pp. 419-426 
504 |a Rossio, J.L., Esser, M.T., Suryanarayana, K., Inactivation of human immunodeficiency virus type 1 infectivity with preservation of conformational and functional integrity of virion surface proteins (1998) J. Virol., 72, pp. 7992-8001 
504 |a Turpin, J.A., Terpening, S.J., Schaeffer, C.A., Inhibitors of human immunodeficiency virus type 1 zinc fingers prevent normal processing of Gag precursors and result in the release of noninfectious virus particles (1996) J. Virol., 70, pp. 6180-6189 
504 |a Berthoux, L., Péchoux, C., Darlix, J.L., Multiple effects of an anti-human immunodeficiency virus nucleocapsid inhibitor on virus morphology and replication (1999) J. Virol., 73, pp. 10000-10009 
504 |a Salvato, M.S., Shimomaye, E.M., The completed sequence of lymphocytic chorio-meningitis virus reveals a unique RNA structure and a gene for a zinc finger protein (1989) Virology, 173, pp. 1-10 
504 |a Tortorici, M.A., Ghiringhelli, P.D., Lozano, M.E., Albarino, C.G., Romanowski, V., Zinc-binding properties of Junin virus nucleocapsid protein (2001) J. Gen. Virol., 82, pp. 121-128 
504 |a Garcin, D., Rochat, S., Kolakofsky, D., The Tacaribe arenavirus small zinc finger protein is required for both mRNA synthesis and genome replication (1993) J. Virol., 67, pp. 807-812 
504 |a Salvato, M.S., Molecular biology of the prototype arenavirus, lymphocytic choriomeningitis virus (1993) The Arenaviridae, pp. 133-156. , M.S. Salvato. New York: Plenum Press 
504 |a Lee, K.J., Novella, I.S., Teng, M.N., Oldstone, M.B.A., De la Torre, J.C., NP and L proteins of lymphocytic choriomeningitis virus (LCMV) are sufficient for efficient transcription and replication of LCMV genomic RNA analogs (2000) J. Virol., 74, pp. 3470-3477 
504 |a López, N., Jácamo, R., Franze-Fernández, M.T., Transcription and RNA replication of Tacaribe virus genome and antigenome analogs require N and L proteins: Z protein is an inhibitor of these processes (2001) J. Virol., 75, pp. 12241-12251 
520 3 |a The action of five azo-based compounds against the arenaviruses Junin (JUNV) and Tacaribe (TCRV) was evaluated in vitro by a virus yield inhibition assay in Vero cells and a cell-free virion inactivation assay. The compound 2-azo-(1′-(2′-nitroso)naphthyl)-benzoate (ANNB) was the most effective inhibitor of arenavirus production in Vero cells with EC50 (effective concentration 50%) values in the range 6.5-26.2 μM and without inactivating properties. By contrast, the azodicarbonamide (ADA) was very effective in inactivating both arenaviruses with IC50 (inactivating concentration 50%) values of 7.6 and 5.3 μM against JUNV and TCRV, respectively. The virucidal activity of ADA was time- and temperature-dependent. ANNB had no inhibitory action on virus binding or penetration of target cells and did not affect the synthesis of viral proteins. The most likely event susceptible to ANNB would be the process of intracellular virion assembly. © 2002 Elsevier Science B.V. and International Society of Chemotherapy. All rights reserved.  |l eng 
536 |a Detalles de la financiación: Agencia Nacional de Promoción Científica y Tecnológica 
536 |a Detalles de la financiación: Ministerio de Salud de la Nación, MSAL 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas 
536 |a Detalles de la financiación: Council on Competitive Government 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas 
536 |a Detalles de la financiación: The authors acknowledge the National Cancer Institute, Frederick, USA, for providing the compounds. This work was supported by Consejo Nacional de Investigaciones Cientı́ficas y Técnicas (CONICET), Agencia Nacional de Promoción Cientı́fica y Tecnológica, y Subsecretarı́a de Investigación y Tecnologı́a, Ministerio de Salud, Argentina. EBD is member of the Research Career from CONICET and CCG is fellowship from CONICET. 
593 |a Depto. de Quim. Biológica, Universidad de Buenos Aires, Ciudad Universitaria, Piso 4, Buenos Aires 1428, Argentina 
690 1 0 |a ANTIVIRAL ACTIVITY 
690 1 0 |a ARENAVIRUS 
690 1 0 |a AZOIC COMPOUND 
690 1 0 |a JUNIN VIRUS 
690 1 0 |a TACARIBE VIRUS 
690 1 0 |a VIRION INACTIVATION 
690 1 0 |a 2 AZO[1' (2' NITROSO)NAPHTHYL]BENZOATE 
690 1 0 |a ANTIVIRUS AGENT 
690 1 0 |a AZO COMPOUND 
690 1 0 |a AZOFORMAMIDE 
690 1 0 |a BENZOIC ACID DERIVATIVE 
690 1 0 |a CHEMICAL COMPOUND 
690 1 0 |a UNCLASSIFIED DRUG 
690 1 0 |a UREA DERIVATIVE 
690 1 0 |a VIRUS PROTEIN 
690 1 0 |a ARENAVIRUS 
690 1 0 |a ARTICLE 
690 1 0 |a CHRONOTHERAPY 
690 1 0 |a DRUG ACTIVITY 
690 1 0 |a DRUG EFFICACY 
690 1 0 |a DRUG INHIBITION 
690 1 0 |a DRUG MECHANISM 
690 1 0 |a DRUG SENSITIVITY 
690 1 0 |a EVALUATION 
690 1 0 |a IC 50 
690 1 0 |a IN VITRO STUDY 
690 1 0 |a INHIBITION KINETICS 
690 1 0 |a NONHUMAN 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a PROTEIN SYNTHESIS 
690 1 0 |a TARGET CELL 
690 1 0 |a TEMPERATURE DEPENDENCE 
690 1 0 |a VERO CELL 
690 1 0 |a VIRION 
690 1 0 |a VIRUS ASSEMBLY 
690 1 0 |a VIRUS INFECTION 
700 1 |a Candurra, N.A. 
700 1 |a Damonte, E.B. 
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