| Literature DB >> 23571092 |
John T Roehrig1, Siritorn Butrapet, Nathan M Liss, Susan L Bennett, Betty E Luy, Thomas Childers, Karen L Boroughs, Janae L Stovall, Amanda E Calvert, Carol D Blair, Claire Y-H Huang.
Abstract
Using an infectious cDNA clone we engineered seven mutations in the putative heparan sulfate- and receptor-binding motifs of the envelope protein of dengue virus serotype 2, strain 16681. Four mutant viruses, KK122/123EE, E202K, G304K, and KKK305/307/310EEE, were recovered following transfection of C6/36 cells. A fifth mutant, KK291/295EE, was recovered from C6/36 cells with a compensatory E295V mutation. All mutants grew in and mediated fusion of virus-infected C6/36 cells, but three of the mutants, KK122/123EE, E202K, G304K, did not grow in Vero cells without further modification. Two Vero cell lethal mutants, KK291/295EV and KKK307/307/310EEE, failed to replicate in DC-SIGN-transformed Raji cells and did not react with monoclonal antibodies known to block DENV attachment to Vero cells. Additionally, both mutants were unable to initiate negative-strand vRNA synthesis in Vero cells by 72h post-infection, suggesting that the replication block occurred prior to virus-mediated membrane fusion. Published by Elsevier Inc.Entities:
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Year: 2013 PMID: 23571092 DOI: 10.1016/j.virol.2013.03.011
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616