Shenk T E, Koshelnyk K A, Stollar V
J Virol. 1974 Feb;13(2):439-47. doi: 10.1128/JVI.13.2.439-447.1974.
Cultures of Aedes albopictus cells persistently infected with wild-type Sindbis virus (SV-W) give rise to small plaque-forming mutants which are also temperature sensitive. These mutants, designated SV-C, are neutralized by antiserum produced against SV-W. Mutant ts clones were isolated from SV-C by plaque purification. After serial undiluted passage in BHK or mosquito cells, each of the clones gave rise to ts(+) revertants which, however, remained mutant with respect to plaque morphology. Nineteen of 20 clones derived from SV-C were RNA(+), and one was RNA(-) (SV-C-2). The RNA synthesizing activity, once induced in infected cells by SV-C-2, was stable at the nonpermissive temperature (39.5 C). All clones derived from SV-C were inactivated at 60 C much more quickly than was SV-W. It was not possible to demonstrate complementation between any of the SV-C clones.
持续感染野生型辛德毕斯病毒(SV-W)的白纹伊蚊细胞培养物产生了小斑块形成突变体,这些突变体也是温度敏感型的。这些被命名为SV-C的突变体被针对SV-W产生的抗血清中和。通过噬斑纯化从SV-C中分离出突变体ts克隆。在BHK或蚊细胞中连续未稀释传代后,每个克隆都产生了ts(+)回复体,然而,这些回复体在噬斑形态方面仍然是突变体。从SV-C衍生的20个克隆中有19个是RNA(+),1个是RNA(-)(SV-C-2)。一旦被SV-C-2在感染细胞中诱导,RNA合成活性在非允许温度(39.5℃)下是稳定的。从SV-C衍生的所有克隆在60℃下比SV-W更快失活。不可能证明任何SV-C克隆之间存在互补作用。