Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Homologous interference mediated by defective interfering influenza virus derived from a temperature-sensitive mutant of influenza virus. [Ultraviolet radiation]

Journal Article · · J. Virol.; (United States)
OSTI ID:6858844
A temperature-sensitive group II mutant of influenza virus, ts-52, with a presumed defect in viral RNA synthesis, readily produced von Magnus-type defective interfering virus (DI virus) when passed serially (four times) at high multiplicity in MDBK cells. The defective virus (ts-52 DI virus) had a high hemagglutinin and a low infectivity titer, and strongly interfered with the replication of standard infectious viruses (both ts-52 and wild-type ts/sup +/) in co-infected cells. Progeny virus particles produced by co-infection of DI virus and infectious virus were also defective and also had low infectivity, high hemagglutinating activity, and a strong interfering property. Infectious viruses ts/sup +/ and ts-52 were indistinguishable from ts-52 DI viruses by sucrose velocity or density gradient analysis. Additionally, these viruses all possessed similar morphology. However, when the RNA of DI viruses was analyzed by use of polyacrylamide gels containing 6 M urea, there was a reduction in the amount of large RNA species (V1 to V4), and a number of new smaller RNA species (D1 to D6) with molecular weights ranging from 2.9 x 10/sup 5/ to 1.05 x 10/sup 5/ appeared. Since these smaller RNA species (D1 to D6) were absent in some clones of infectious viruses, but were consistently associated with DI viruses and increased during undiluted passages and during co-infection of ts-52 with DI virus, they appeared to be a characteristic of DI viruses. Additionally, the uv target size of interfering activity and infectivity of DI virus indicated that interfering activity was 40 times more resistant to uv irradiation than was infectivity, further implicating small RNA molecules in interference.
Research Organization:
Univ. of California, Los Angeles
OSTI ID:
6858844
Journal Information:
J. Virol.; (United States), Journal Name: J. Virol.; (United States) Vol. 28:1; ISSN JOVIA
Country of Publication:
United States
Language:
English