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1.
Rev. Soc. Bras. Med. Trop ; 52: e20180511, 2019. graf
Artículo en Inglés | LILACS | ID: biblio-1003127

RESUMEN

Abstract INTRODUCTION: Insect cell cultures play an essential role in understanding arboviral replication. However, the replicative efficiency of some of these viruses such as dengue (DENV), yellow fever (YFV), and chikungunya (CHIKV) in a new cellular substrate (Lulo) and in the other two recognized cell lines has not been comparatively assessed. METHODS: Vero, C6/36, and Lulo cell lines were infected with DENV, YFV, and CHIKV. The viral progeny was quantified through plaque assays and quantitative reverse transcription-polymerase chain reaction, while for DENV2, the findings were confirmed by immunofluorescence antibody assay. RESULTS: The higher DENV2 titer (from multiplicity of infection 0.001) was obtained on day four post-infection in C6/36 and on day six in Vero cells, while the Lulo cell line was almost impossible to infect under the same conditions. However, C6/36 showed the highest values of viral RNA production compared to Vero cells, while the quantification of the viral RNA in Lulo cells showed high levels of viral genomes, which had no correlation to the infectious viral particles. CONCLUSIONS: C6/36 was the most efficient cell line in the alpha and flavivirus production, followed by Vero cells. Thus, Lulo cells may be a useful substrate to study the mechanisms by which cells evade viral replication.


Asunto(s)
Animales , Replicación Viral/fisiología , Virus de la Fiebre Amarilla/fisiología , Virus Chikungunya/fisiología , Virus del Dengue/fisiología , Insectos/virología , Factores de Tiempo , Células Vero , Chlorocebus aethiops , Cricetinae , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa
2.
Rev. Soc. Bras. Med. Trop ; 47(6): 677-683, Nov-Dec/2014. graf
Artículo en Inglés | LILACS | ID: lil-732989

RESUMEN

Chikungunya virus (CHIKV) and Mayaro virus (MAYV) are emergent arthropod-borne viruses that produce outbreaks of acute febrile illness with arthropathy. Despite their different continental origins, CHIKV and MAYV are closely related and are components of the Semliki Forest Complex of the Alphavirus (Togaviridae). MAYV and, more recently, CHIKV, which are both transmitted by Aedes mosquitoes, have resulted in severe public health problems in the Americas, including Brazil. In this review, we present aspects of the pathogenesis, clinical presentation and treatment of febrile illnesses produced by CHIKV and MAYV. We also discuss the epidemiological aspects and effects related to the prophylaxis of infections by both viruses.


Asunto(s)
Animales , Humanos , Infecciones por Alphavirus/virología , Alphavirus/genética , Enfermedades Transmisibles Emergentes/virología , Américas , Infecciones por Alphavirus/epidemiología , Alphavirus/clasificación , Alphavirus/fisiología , Virus Chikungunya/genética , Virus Chikungunya/fisiología , Enfermedades Transmisibles Emergentes/epidemiología , Insectos Vectores/clasificación , Replicación Viral
3.
Mem. Inst. Oswaldo Cruz ; 104(4): 632-635, July 2009. tab
Artículo en Inglés | LILACS | ID: lil-523732

RESUMEN

Aedes albopictus was responsible for transmission in the first outbreak of chikungunya (CHIK) on La Réunion Island, Indian Ocean, in 2005-2006. The magnitude of the outbreak on this island, which had been free of arboviral diseases for over 30 years, as well as the efficiency of Ae. albopictus as the main vector, raises questions about the maintenance of the CHIK virus (CHIKV) through vertical transmission mechanisms. Few specimens collected from the field as larvae were found to be infected. In this study, Ae. albopictus originating from La Réunion were orally infected with a blood-meal containing 10(8) pfu/mL of the CHIKV epidemic strain (CHIKV 06.21). Eggs from the first and second gonotrophic cycles were collected and raised to the adult stage. The infectious status of the progeny was checked (i) by immunofluorescence on head squashes of individual mosquitoes to detect the presence of viral particles or (ii) by quantitative RT-PCR on mosquito pools to detect viral RNA. We analysed a total of 1,675 specimens from the first gonotrophic cycle and 1,709 from the second gonotrophic cycle without detecting any viral particles or viral RNA. These laboratory results are compared to field records.


Asunto(s)
Animales , Aedes/virología , Virus Chikungunya/patogenicidad , Insectos Vectores/virología , Infecciones por Alphavirus/transmisión , Virus Chikungunya/fisiología , Técnica del Anticuerpo Fluorescente , Océano Índico , Transmisión Vertical de Enfermedad Infecciosa , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , ARN Viral/análisis
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