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Characterization of a Chikungunya virus strain isolated from banked patients' sera.
Chalaem, Pattra; Chusri, Sarunyou; Fernandez, Stefan; Chotigeat, Wilaiwan; Anguita, Juan; Pal, Utpal; Promnares, Kamoltip.
Afiliação
  • Chalaem P; Department of Molecular Biotechnology and Bioinformatics, Faculty of Science, Prince of Songkla University, Hatyai, Songkhla, 90112, Thailand.
  • Chusri S; Division of Infectious Disease, Department of Internal Medicine, Faculty of Medicine, Prince of Songkla University, Hatyai, Songkhla, 90112, Thailand.
  • Fernandez S; Department of Virology, Armed Forces Research Institute of Medical Sciences (AFRIMS), Bangkok, Thailand.
  • Chotigeat W; Department of Molecular Biotechnology and Bioinformatics, Faculty of Science, Prince of Songkla University, Hatyai, Songkhla, 90112, Thailand.
  • Anguita J; CIC bioGUNE, 48160, Derio, Bizkaia, Spain.
  • Pal U; Ikerbasque, Basque Foundation for Science, 48011, Bilbao, Bizkaia, Spain.
  • Promnares K; Department of Veterinary Medicine and Virginia-Maryland Regional College of Veterinary Medicine, University of Maryland, College Park, MD, 20742, USA.
Virol J ; 13(1): 150, 2016 09 02.
Article em En | MEDLINE | ID: mdl-27590311
ABSTRACT

BACKGROUND:

Chikungunya virus (CHIKV) is a prevalent mosquito-borne pathogen that is emerging in many parts of the globe causing significant human morbidity. Here, we report the isolation and characterization of an infectious CHIKV from banked serum specimens of suspected patients from the 2009 epidemic in Thailand.

METHODS:

Standard plaque assay was used for CHIKV isolation from the banked serum specimens. Isolated CHIKV was identified base on E1 structural gene sequence. Growth kinetic, infectivity, cell viability and cytokine gene expression throughout CHIKV infection in a permissive cell line, 293T cells, was performed using several approaches, including standard plaque assay, immunofluorescence assay, classical MTT assay, and quantitative real-time PCR. Two tailed Student's t test was used for evaluation statistically significance between the mean values of the groups.

RESULTS:

Based on the E1 structural gene sequence and phylogenetic analysis, we identified the virus as the CHIK/SBY8/10 isolate from Indonesia. Assessment of the growth kinetics, cytopathic effects as well as its ability to induce cellular immune responses suggested that the currently isolated CHIK/SBY8/10 virus is relatively more virulent than a known CHIKV vaccine strain, which also induces more dramatic proinflammatory responses.

CONCLUSIONS:

Our studies further add to the infectivity of a less-studied yet infectious CHIKV isolate as well as underscored the importance and utility of 293T cells as an excellent cell culture model for studying viral growth, CHIKV-induced inflammatory cellular responses and cell death. Together, these studies provide novel information on the CHIKV biology, infectivity and virus-cell interaction, which would help develop novel interventions against the infection.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Plasma / Vírus Chikungunya / Febre de Chikungunya Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Virol J Assunto da revista: VIROLOGIA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Tailândia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Plasma / Vírus Chikungunya / Febre de Chikungunya Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Virol J Assunto da revista: VIROLOGIA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Tailândia