PREFERENTIAL SELECTION OF SPECIFIC ROTAVIRUS GENE SEGMENTS IN COINFECTION AND MULTIPLE PASSAGES WITH REASSORTANT VIRUSES AND THEIR PARENTALSTRAIN

Citation
N. Kobayashi et al., PREFERENTIAL SELECTION OF SPECIFIC ROTAVIRUS GENE SEGMENTS IN COINFECTION AND MULTIPLE PASSAGES WITH REASSORTANT VIRUSES AND THEIR PARENTALSTRAIN, Research in virology, 146(5), 1995, pp. 333-342
Citations number
24
Categorie Soggetti
Virology
Journal title
ISSN journal
09232516
Volume
146
Issue
5
Year of publication
1995
Pages
333 - 342
Database
ISI
SICI code
0923-2516(1995)146:5<333:PSOSRG>2.0.ZU;2-8
Abstract
We previously reported non-random selections of human rotavirus (HRV) Wa genes 2 and 5 in reassortant formation between HRV strains Wa and H N126 under selection pressure with neutralizing monoclonal antibodies. In order to study whether or not these genes are preferentially selec ted in the genetic background of a parental strain HN126 in vitro with out selection pressures, coinfection and multiple passage experiments were performed between HN126 and one of three reassortants, C1, C1T an d C1F; C1 possessed genes 2 and 5 derived from Wa and the other genes derived from HN126, while C1T and C1F were single gene reassortants ha ving Wa gene 2 or Wa gene 5 in the genetic background of HN126, respec tively. When MA-104 cells were coinfected with the same infectious uni ts of HN126 and C1, Wa genes 2 and 5 of reassortant C1 became predomin ant within 10 repeated passages, although Wa gene 5 was selected more preferably than Wa gene 2. Similar results were obtained under differe nt experimental conditions in which different doses of parental strain s or different type of cells were used. Also, in coinfections of MA-10 4 cells with HN126 and C1T, or HN126 and C1F, Wa gene 2 or Wa gene 5 b ecame predominant at the sixth passage. Analysis of viral growth curve s indicated that two reassortants, C1 and C1F, replicated to a titre h igher than HN126, while no difference in viral growth was observed bet ween C1T and HN126. These results indicated that in the genetic backgr ound of HN126, Wa gene 5 might provide viruses with a growth advantage compared with its HN126 counterpart, while Wa gene 2 might be prefere ntially selected into reassortant clones through its greater functiona l capacity for assortment during viral replication.