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Literature DB >> 507639

Preliminary characterization of the particles from productive and abortive infections of L cells by fowl plague virus.

Abstract

Particles produced during the abortive infection of L cells by fowl plague virus (Dobson strain) have been characterized and compared to the infectious particles produced by a mutant of this virus adapted to mammalian cells. The former are of apparently normal morphology but most of them are non-infectious. They have the same RNA/protein ratio as the infectious particles and the same polypeptide composition. They contain also the same RNA segments as those found in infectious particles. Possible reasons for the defectiveness of these particles are discussed.

Entities: Disease Species

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Year: 1979 PMID： 507639

Source DB: PubMed Journal: Ann Microbiol (Paris) ISSN： 0300-5410

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Cited

11 in total

1. Dominant-negative mutants of human MxA protein: domains in the carboxy-terminal moiety are important for oligomerization and antiviral activity.

Authors: A Ponten; C Sick; M Weeber; O Haller; G Kochs
Journal: J Virol Date: 1997-04 Impact factor: 5.103

2. Human MxA protein confers resistance to Semliki Forest virus and inhibits the amplification of a Semliki Forest virus-based replicon in the absence of viral structural proteins.

Authors: H Landis; A Simon-Jödicke; A Klöti; C Di Paolo; J J Schnorr; S Schneider-Schaulies; H P Hefti; J Pavlovic
Journal: J Virol Date: 1998-02 Impact factor: 5.103

Preliminary characterization of the particles from productive and abortive infections of L cells by fowl plague virus.

1. Dominant-negative mutants of human MxA protein: domains in the carboxy-terminal moiety are important for oligomerization and antiviral activity.

2. Human MxA protein confers resistance to Semliki Forest virus and inhibits the amplification of a Semliki Forest virus-based replicon in the absence of viral structural proteins.

3. Resistance to influenza virus and vesicular stomatitis virus conferred by expression of human MxA protein.

4. Dissecting the interferon-induced inhibition of hepatitis C virus replication by using a novel host cell line.

5. Overexpression of the influenza virus polymerase can titrate out inhibition by the murine Mx1 protein.

6. Human and mouse Mx proteins inhibit different steps of the influenza virus multiplication cycle.

7. Inhibition of bunyaviruses, phleboviruses, and hantaviruses by human MxA protein.

8. Influenza A virus strains differ in sensitivity to the antiviral action of Mx-GTPase.

9. Tick-borne thogoto virus infection in mice is inhibited by the orthomyxovirus resistance gene product Mx1.

10. Human MxA protein inhibits tick-borne Thogoto virus but not Dhori virus.