Skip to main content
Log in

Isolation and complete genomic sequence analysis of a new Sindbis-like virus

  • Published:
Virologica Sinica

Abstract

The Sindbis-like virus was first discovered in China in 1986. Its complete genomic sequence consists of more than 11 000 bp encoding more than 3 700 amino acids. It contains a 5′ non-transcriptional region (5′-NTR) in a non-structural region, four non-structural proteins (nsP1, nsP2, nsP3, nsP4) regions, capsids in conserved and non-conserved regions and structural E1, E2, E3, 6K regions and a 3′ non-transcriptional region (3′-NTR). The Sindbis-IMB was isolated from the blood of a patient suspected to have encephalitis, and was followed by identification and passage. The virus RNA was extracted from virus supernatant in infected cells and the whole genome was divided into 12 fragments; RT-PCR was then performed to amplify the 12 fragments for complete sequencing. The results showed that the whole genomic sequence of Sindbis-IMB consists of 11 717 bp encoding 3 773 amino acids. Homology comparison with other Sindbis-like isolates demonstrated the highest similarity was the YN87448 with a variation of 1% strain isolated in Yunnan Province and the second highest to the SAAR86 strain with a variation of ∼1.2%. The nucleotide sequence variations were present in non-structural regions, resulting in amino acids K, E, N, R, H, and L in protein sequences in positions 230, 231, 443,781, 1 582, and 1746 in the new isolation respectively. Furthermore, three additional amino acids—glutamic acid, serine and alanine—were noted in nsp4 terminus as compared to the YN87448 isolate.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Dennis A S, Nancy L D, Sheching L, et al. 1996. Complete nucleotide sequence and full-length cDNA clone of S. A. AR86, a South African Alphavirus Related to Sindbis. Virology, 222: 464–469.

    Article  Google Scholar 

  2. Dubuisson J, Shlomo L, Nicolas Rug, et al. 1997. Genetic determinants of Sindbis virus neuroinvasiveness. J Virol, 71: 2636–3646.

    PubMed  CAS  Google Scholar 

  3. Laine M, Luukkainen R, Toivanen A. 2004. Sindbis virus and other alphavirus as cause of human arthritic disease. J Internal Med, 256: 457–471.

    Article  PubMed  CAS  Google Scholar 

  4. Malherbe H S, Cholmley M, Jackson A.L. 1963. Sindbis virus infection in man. South Afr Med J, 37: 547–552.

    CAS  Google Scholar 

  5. Martin P, Richard M K, Oskar R K. 1998. The alphavirus 3′-nontranslated region:size heterogeneity and ar2rangement of repeated sequence elements. Virology, 240(1): 100–110.

    Article  Google Scholar 

  6. Shailly T, Richard W, Janet L S, et al. 2006. Catalytic Core of Alphavirus Nonstructural Protein Nsp4 Possesses Terminal Adenylyltransferase Activity. J Virol, 10: 9962–9969.

    Google Scholar 

  7. Zhou G L, Lian G D, Li L, et al. 1999. Complete nucleotide sequence of the structural region gene of Alphavirus YN87448 strain isolated in China and its relationship to other Sindbis virus. Virologica Sinica, 15: 205–210. (in Chinese).

    CAS  Google Scholar 

  8. Zhou G L, Lian G D, Li L, et al. 1999. Complete nucleotide sequence of the nonstructural gene of Alphavirus YN87448 strain isolated in China and its relationship to other Sindbis virus. Chin J Exp Clin Virol, 13: 314–320. (in Chinese).

    CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Qi-han Li.

Additional information

Foundation items: National Nature Science Founds (30670094 and 30560142)

Equally contributing author

Rights and permissions

Reprints and permissions

About this article

Cite this article

Wang, Jj., Zhang, Hl., Che, Yc. et al. Isolation and complete genomic sequence analysis of a new Sindbis-like virus. Virol. Sin. 23, 31–36 (2008). https://doi.org/10.1007/s12250-008-2891-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12250-008-2891-5

Key words

CLC number

Navigation