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Defective Interfering Particles of Poliovirus. IV. Mechanisms of Enrichment

Cole, Charles N. and Baltimore, David (1973) Defective Interfering Particles of Poliovirus. IV. Mechanisms of Enrichment. Journal of Virology, 12 (6). pp. 1414-1426. ISSN 0022-538X. PMCID PMC356783. https://resolver.caltech.edu/CaltechAUTHORS:20120725-095758840

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Abstract

Infection of HeLa cells by mixtures of standard poliovirus and defective, interfering (DI) poliovirus particles leads to a higher ratio of DI particles in the progeny than in the inoculum. The extent of this enrichment could be varied by various manipulations of the co-infected cells. At any time during the infection cycle, virions made within short times after addition of radioactive uridine were hyperenriched in DI particles; this transient hyperenrichment fell to the equilibrium enrichment level within 45 min after uridine addition. A shift of the temperature of infection from 37 to 31 C also led to a hyperenrichment of DI particles and pulse-labeling revealed a superimposed transient hyperenrichment. By contrast, cells continuously infected at 31 C showed a severe decrement in DI particles apparently because poliovirus DI particles behave as cold-sensitive mutants for RNA synthesis. Cycloheximide treatment early in the infection cycle also led to hyperenrichment. Study of the cycloheximide effect showed that the drug acted as if to change the input ratio of standard to DI particles. These effects on enrichment can be explained as aspects of two different phenomena: enrichment due to preferential DI RNA synthesis and enrichment due to preferential encapsidation of DI RNA. Both mechanisms probably play a role in the normal level of enrichment.


Item Type:Article
Related URLs:
URLURL TypeDescription
http://jvi.asm.org/content/12/6/1414.abstractPublisherArticle
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC356783/PubMed CentralArticle
ORCID:
AuthorORCID
Baltimore, David0000-0001-8723-8190
Additional Information:© 1973 American Society for Microbiology. Received for publication 20 August 1973. We thank Donna Smoler for her expert technical assistance and Alice Huang for critical reading of the manuscript. We are grateful to Frensch Niegermeier for inspiration. This investigation was supported by Public Health Service grant AI-08388 from the National Institute of Allergy and Infectious Diseases. D. B. is an American Cancer Society Research professor.
Funders:
Funding AgencyGrant Number
NIHAI-08388
American Cancer SocietyUNSPECIFIED
Issue or Number:6
PubMed Central ID:PMC356783
Record Number:CaltechAUTHORS:20120725-095758840
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20120725-095758840
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:32707
Collection:CaltechAUTHORS
Deposited By:INVALID USER
Deposited On:25 Jul 2012 17:28
Last Modified:03 Oct 2019 04:03

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