Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
1996-7-23
pubmed:abstractText
The dengue type 4 virus (DEN4) genome contains a 384-nucleotide (nt) 3' noncoding sequence in which the last 81 nt, predicted to form a secondary structure, are thought to be essential for virus replication. Immediately upstream of the secondary structure, short RNA sequences that are conserved among mosquito-borne flaviviruses have been identified. A series of deletions that range from 30 to 262 nt were introduced into this upstream region of full-length DEN4 cDNA to create viable deletion mutants, some of which might prove to be useful for inclusion in a live attenuated virus vaccine. When studied by an infectious-center assay, most full-length RNA transcripts of the deletion constructs exhibited reduced infectivity when transfected into simian LLC-MK2 cells compared with the full-length RNA transcripts of wild-type parental virus. Deletion mutations that extended as far as the 5' boundary of the 3' noncoding region and whose 3' boundary did not extend beyond the last 113 nt of the 3' end were viable. With the exception of mutant 3'd 303-183, which contained a deletion of nt 303 to 183 from the 3' terminus, deletion mutants produced plaques that appeared late on simian LLC-MK2 cells or exhibited a small-plaque morphology on mosquito C6/36 cells compared with the wild-type virus. These mutants also replicated less efficiently and attained a lower titer in LLC-MK2 cells than parental wild-type virus. Significantly, mutant 3'd 303-183 grew to a high titer and was least restricted in growth. Mutant 3'd 303-183 and four other moderately to severely restricted mutants were selected for evaluation of infectivity and immunogenicity in rhesus monkeys. There was a suggestion that occurrence and duration of viremia were reduced for some of the deletion mutants compared with the wild-type virus. However, more convincing evidence for attenuation of some of the mutants was provided by an analysis of antibody response to infection. Mutant 3'd 303-183 induced an antibody response equivalent to that stimulated by wild-type virus, whereas other mutants induced low to moderate levels of antibodies, as measured by radioimmunoprecipitation and virus neutralization. The immunogenicity of these 3' DEN4 deletion mutants in monkeys appeared to correlate with their efficiency of growth in simian LLC-MK2 cells. One or more mutants described in this paper may prove to be useful for immunization of humans against disease caused by dengue virus.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-13559592, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-13644196, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-1433509, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-1433515, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-14361897, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-1438242, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-14888958, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-14903434, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-1772972, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-1975159, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-2052593, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-2174669, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-2319643, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-2389825, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-2828633, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-2959795, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-3011975, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-3016981, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-3022479, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-3171230, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-3496985, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-3727403, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-4023707, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-409682, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-6376649, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-6476216, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-7871753, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-7995984, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-8388482, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-8418788, http://linkedlifedata.com/resource/pubmed/commentcorrection/8648730-8648761
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0022-538X
pubmed:author
pubmed:issnType
Print
pubmed:volume
70
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3930-7
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1996
pubmed:articleTitle
Dengue type 4 virus mutants containing deletions in the 3' noncoding region of the RNA genome: analysis of growth restriction in cell culture and altered viremia pattern and immunogenicity in rhesus monkeys.
pubmed:affiliation
Molecular Viral Biology Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't