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
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.