Involvement of cytoskeleton in Junín virus entry

The early events in Junín virus (JUNV) infection are not thoroughly understood. We have previously shown that JUNV enter cells by clathrin-mediated endocytosis. In this report we examine the role of microfilaments and microtubules during early virus infection. Inhibitory effects of drugs affecting m...

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Autor principal: Martinez, M.G
Otros Autores: Cordo, S.M, Candurra, N.A
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2008
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100 1 |a Martinez, M.G. 
245 1 0 |a Involvement of cytoskeleton in Junín virus entry 
260 |c 2008 
270 1 0 |m Candurra, N.A.; Laboratorio de Virología, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Ciudad Universitaria, Pabellon II, Piso 4, 1428 Buenos Aires, Argentina; email: nelica@qb.fcen.uba.ar 
506 |2 openaire  |e Política editorial 
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520 3 |a The early events in Junín virus (JUNV) infection are not thoroughly understood. We have previously shown that JUNV enter cells by clathrin-mediated endocytosis. In this report we examine the role of microfilaments and microtubules during early virus infection. Inhibitory effects of drugs affecting main cytoskeletal components on JUNV entry into Vero cells were analyzed. Drugs that disrupted microfilaments or stabilized microtubules inhibited early steps of virus entry. In contrast, drugs that stabilized microfilaments or depolymerized microtubules were not able to block virus entry very efficiently. Furthermore, real time PCR was performed to detect viral entry and we found more than 10-fold less RNA when microfilaments were depolymerized while a 100-fold diminution was seen when microtubules were stabilized. Taken together our results demonstrate that JUNV relies on an intact actin network during early infection in Vero cells while a dynamic microtubule network is also needed. This represents an important contribution to the characterization of arenavirus multiplication cycle. © 2008 Elsevier B.V. All rights reserved.  |l eng 
536 |a Detalles de la financiación: Agencia Nacional de Promoción Científica y Tecnológica 
536 |a Detalles de la financiación: Universidad de Buenos Aires 
536 |a Detalles de la financiación: This work was supported by grants from, Agencia Nacional de Promoción Científica y Tecnológica (ANPyCT) and Universidad de Buenos Aires (UBA). We are thankful to Dr. A. Sanchez (CDC, Atlanta, GA, USA) for providing JUNV mAbs. M.G.M. is a fellow researcher from UBA and S.M.C. is a fellow researcher from Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). 
593 |a Laboratorio de Virología, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Ciudad Universitaria, Pabellon II, Piso 4, 1428 Buenos Aires, Argentina 
690 1 0 |a ACTIN 
690 1 0 |a CYTOSKELETON 
690 1 0 |a JUNIN VIRUS 
690 1 0 |a TUBULIN 
690 1 0 |a CYTOCHALASIN D 
690 1 0 |a JASPAMIDE 
690 1 0 |a LATRUNCULIN A 
690 1 0 |a NOCODAZOLE 
690 1 0 |a PACLITAXEL 
690 1 0 |a ANIMAL CELL 
690 1 0 |a ARTICLE 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a JUNIN VIRUS 
690 1 0 |a MICROFILAMENT 
690 1 0 |a MICROTUBULE 
690 1 0 |a NONHUMAN 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION 
690 1 0 |a RNA SYNTHESIS 
690 1 0 |a VERO CELL 
690 1 0 |a VIRUS ENTRY 
690 1 0 |a VIRUS INFECTION 
690 1 0 |a ANIMALS 
690 1 0 |a ARENAVIRIDAE INFECTIONS 
690 1 0 |a BICYCLO COMPOUNDS, HETEROCYCLIC 
690 1 0 |a CERCOPITHECUS AETHIOPS 
690 1 0 |a CYTOSKELETON 
690 1 0 |a DEPSIPEPTIDES 
690 1 0 |a HUMANS 
690 1 0 |a JUNIN VIRUS 
690 1 0 |a THIAZOLIDINES 
690 1 0 |a VERO CELLS 
690 1 0 |a VIRUS INTERNALIZATION 
690 1 0 |a ARENAVIRUS 
690 1 0 |a JUNIN VIRUS 
650 1 7 |2 spines  |a VIRUS RNA 
700 1 |a Cordo, S.M. 
700 1 |a Candurra, N.A. 
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