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Genetic characterization of Chikungunya virus 2009 isolates from South India.
Sarangan, Gopalsamy; Nayar, Seema A; Mani, Monika; Sundarrajan, Sudharsana; Sankar, Sathish; Palani, Gunasekaran; Selvaraj, Gracy Fathima; Damodharan, Jayachandran; Muthumani, Karuppaiah; Srikanth, Padma.
Afiliação
  • Sarangan G; Department of Microbiology, Sri Ramachandra Medical College and Research Institute, Chennai, India.
  • Nayar SA; Department of Microbiology, Trivandrum Medical College, Trivandrum, India.
  • Mani M; Department of Microbiology, Sri Ramachandra Medical College and Research Institute, Chennai, India.
  • Sundarrajan S; Department of Biotechnology, Vellore Institute of Technology, Vellore, India.
  • Sankar S; Sri Sakthi Amma Institute of Biomedical Research Sri Narayani Hospital and Research Centre, Sripuram, India.
  • Palani G; Department of Virology, King Institute of Preventive Medicine, India.
  • Selvaraj GF; Department of Virology, King Institute of Preventive Medicine, India.
  • Damodharan J; Saveetha Institute of Medical and Technical Sciences, Chennai, India.
  • Muthumani K; The Wistar Institute, Philadelphia, USA.
  • Srikanth P; Department of Microbiology, Sri Ramachandra Medical College and Research Institute, Chennai, India.
Bioinformation ; 14(3): 106-112, 2018.
Article em En | MEDLINE | ID: mdl-29785069
ABSTRACT
Chikungunya Virus (CHIKV) is a single stranded positive sense enveloped RNA virus. Re-emergence of CHIKV caused a massive outbreak with severe clinical manifestation affecting multiple organs. The genetic diversity of CHIKV, which caused recurring outbreaks in India, was studied. Blood samples were collected from suspected human cases of CHIKV infection in Chennai, Tamil Nadu and three Northern districts of Kerala in Southern India during the CHIKV outbreak in 2009. A partial E2 gene segment was amplified by RT-PCR. Among 119 samples 37 samples were positive for CHIKV by RT-PCR. Phylogenetic analysis revealed that the isolated sequences belonged to Indian Ocean Lineage (IOL) of ECSA genotype. The mutational analysis revealed the presence of substitutions such as S299N, T312M, A344T, S375T, V386G, W339R and S375P in the current study. In addition, a novel mutation V386G was observed in all the sequences. Two isolates found with unique substitutions W339R and S375P are reported. The structural analysis of the wild type and mutant proteins revealed that the structural changes are accompanied by modification in the intraprotein interactions.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Idioma: En Revista: Bioinformation Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Idioma: En Revista: Bioinformation Ano de publicação: 2018 Tipo de documento: Article