Related Experiment Video
Updated: Jun 21, 2026

An In Vitro Enzymatic Assay to Measure Transcription Inhibition by Gallium(III) and H3 5,10,15-tris(pentafluorophenyl)corroles
Published on: March 18, 2015
EFFECTS OF POLYCYCLIC AROMATIC CARCINOGENS ON VIRAL REPLICATION: SIMILARITY TO ACTINOMYCIN D
Abstract:
When incorporated into a nutrient overlay, the carcinogenic hydrocarbons benzo[a]pyrene and 7,12-dimethylbenz[a]anthracene inhibit plaque formation by herpes virus and vaccinia virus, DNA viruses, but not by Sindbis virus, an RNA virus. These carcinogens also decrease herpes and vaccinia virus yields in liquid medium, without affecting Sindbis virus yields. Four structurally related, but noncarcinogenic polycyclic hydrocarbons, namely benzo[e]pyrene, pyrene, benz[a]anthracene and anthracene, have no inhibitory effect on DNA virus replication. Taken together with the known inhibition of interferon production, these effects on virus growth resemble the action of actinomycin D and hence provide evidence for a selective interaction of these carcinogens with DNA.
Insights
Certain carcinogenic hydrocarbons, like benzo[a]pyrene, inhibit DNA virus replication but not RNA virus replication. This suggests these compounds selectively interact with viral DNA, impacting viral growth.
Area of Science:
- Virology
- Molecular Biology
- Toxicology
Background:
- Carcinogenic polycyclic hydrocarbons are known environmental contaminants.
- Some hydrocarbons can interfere with cellular processes.
- The impact of specific hydrocarbons on viral replication is not fully understood.
Purpose of the Study:
- To investigate the effect of carcinogenic hydrocarbons on the replication of DNA and RNA viruses.
- To determine if the observed effects are specific to DNA viruses.
- To explore the mechanism of interaction between these hydrocarbons and viruses.
Main Methods:
- Incorporating carcinogenic hydrocarbons (benzo[a]pyrene, 7,12-dimethylbenz[a]anthracene) into nutrient overlays and liquid media for virus culture.
- Assessing plaque formation and virus yields for herpes virus, vaccinia virus (DNA viruses), and Sindbis virus (RNA virus).
- Testing noncarcinogenic polycyclic hydrocarbons (benzo[e]pyrene, pyrene, benz[a]anthracene, anthracene) for comparison.
Main Results:
- Carcinogenic hydrocarbons inhibited plaque formation and reduced yields of DNA viruses (herpes, vaccinia) but not RNA virus (Sindbis).
- Noncarcinogenic analogs did not affect viral replication.
- The observed effects on viral growth resemble those of actinomycin D.
Conclusions:
- Carcinogenic hydrocarbons selectively inhibit DNA virus replication.
- These findings suggest a specific interaction between carcinogenic hydrocarbons and viral DNA.
- The mechanism may involve interference with DNA-dependent processes, similar to actinomycin D.
Related Concept Videos
DNA Damage can Stall the Cell Cycle
Drugs that Destabilize Microtubules
Combined Effects of Drugs: Synergism
Such synergistic combinations...
Inhibitors of Bacterial DNA Synthesis
Antiviral Nucleoside Inhibitors
Antifungal Agents

