Persistent Newcastle Disease Virus Infection in Embryonic Chicken Tracheal Organ Cultures

Author:

Cummiskey J. F.1,Hallum J. V.1,Skinner M. S.1,Leslie G. A.1

Affiliation:

1. Department of Microbiology and Immunology, Tulane University School of Medicine, New Orleans, Louisiana 70112

Abstract

The persistent infection of embryonic chicken tracheal organ cultures with Newcastle disease virus (NDV) is described. Tracheal explants remained morphologically intact and were able to support the replication of NDV for 6 months. Peak titers of released virus occurred at 1 week postinfection, whereas maximal immunofluorescence was not observed until 30 days postinfection. The inoculum titer was not critical, and viral persistence resulted with either of two strains of NDV tested. Serum was not required in the medium for explant viability or to maintain the persistent infection. The presence of a contaminating virus morphologically resembling a leukovirus neither altered the course of infection nor affected the survivability of explants. Although interferon was not detected in the culture medium, persistently infected explants were resistant to heterologous viral challenge, and a similar resistant state could be induced in uninfected explants with exogenous interferon or ultraviolet light-inactivated NDV. No evidence was found to implicate antibody as a regulatory factor in the establishment or maintenance of persistence. The results from electron microscopy and immunofluorescence suggest the cells of the subepithelial connective tissue as the site of NDV persistence.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

Reference25 articles.

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2. Baron S. K. T. Wong C. E. Buckler and F. Dianzani. 1968. Comparative induction of the interferon system by virus statalon and interferon p. 129-145. In G. Rita (ed.) The interferons. An international review. Academic Press Inc. New York.

3. The influence of the route of administration of Newcastle disease virus on host response. III. Immunofluorescent and histopathological studies;Beard C. W.;J. Infect. Dis.,1967

4. Infection of chick embryo tracheal organ cultures with influenza A2 (Hong Kong) virus. I. Cytopathology, histopathology, immunofluorescence, hemadsorption, and titration of the released infectious progeny virus;Blaskovic P.;Arch. Gesamte Virusforsch.,1972

5. Infection of chick embryo tracheal organ cultures with influenza A2 (Hong Kong) virus. II. Electron microscopy;Blaskovic P.;Arch. Gesamte Virusforsch.,1972

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