JVI Figure table search 04
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by McArthur, M. A.
Right arrow Articles by Barrett, A. D. T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by McArthur, M. A.
Right arrow Articles by Barrett, A. D. T.

 Previous Article  |  Next Article 

Journal of Virology, January 2003, p. 1462-1468, Vol. 77, No. 2
0022-538X/03/$08.00+0     DOI: 10.1128/JVI.77.2.1462-1468.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Molecular Characterization of a Hamster Viscerotropic Strain of Yellow Fever Virus

Monica A. McArthur,1,2,3 Miguel T. Suderman,2,3,4 John-Paul Mutebi,2,3,4 Shu-Yuan Xiao,3,4 and Alan D. T. Barrett1,2,3,4*

Departments of Microbiology and Immunology,1 Pathology,4 Sealy Center for Vaccine Development,2 WHO Collaborating Center for Tropical Diseases, The University of Texas Medical Branch, Galveston, Texas 77555-06093

Received 24 July 2002/ Accepted 17 October 2002

A hamster viscerotropic strain of yellow fever (YF) virus has been derived after serial passage of strain Asibi through hamsters. The parental Asibi/hamster p0 virus causes a mild and transient viremia in hamsters with no outward, clinical signs of illness. In contrast, the viscerotropic Asibi/hamster p7 virus causes a robust viremia, severe illness, and death in subadult hamsters. The genome of the hamster viscerotropic Asibi/hamster p7 virus has been sequenced and compared with the parental nonviscerotropic Asibi/hamster p0 virus identifying 14 nucleotide changes encoding only seven amino acid substitutions. The majority of these substitutions (five of seven) fall within the envelope (E) protein at positions Q27H, D28G, D155A, K323R, and K331R. These results support an important role for the E protein in determining YF virus viscerotropism.


* Corresponding author. Mailing address: Department of Pathology, The University of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555-0609. Phone: (409) 772-6662. Fax: (409) 772-2500. E-mail: abarrett{at}utmb.edu.


Journal of Virology, January 2003, p. 1462-1468, Vol. 77, No. 2
0022-538X/03/$08.00+0     DOI: 10.1128/JVI.77.2.1462-1468.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
J. Bacteriol. Mol. Cell. Biol. Microbiol. Mol. Biol. Rev.
Clin. Vaccine Immunol. ALL ASM JOURNALS

Copyright © 2003 by the American Society for Microbiology. All rights reserved.