Abstract
Herpes simplex virus type 2 and simian virus 40 were rapidly inactivated by retinal at micromolar concentrations. Other fat-soluble vitamins, particularly vitamin A derivatives, were also active against herpes simplex virus type 2 and several lipid-containing bacteriophages.
Full text
PDF


Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bradley D. E. The adsorption of the Pseudomonas aeruginosa filamentous bacteriophage Pf to its host. Can J Microbiol. 1973 May;19(5):623–631. doi: 10.1139/m73-103. [DOI] [PubMed] [Google Scholar]
- GIRARDI A. J., SWEET B. H., SLOTNICK V. B., HILLEMAN M. R. Development of tumors in hamsters inoculated in the neonatal period with vacuolating virus, SV-40. Proc Soc Exp Biol Med. 1962 Mar;109:649–660. doi: 10.3181/00379727-109-27298. [DOI] [PubMed] [Google Scholar]
- Olsen R. H., Thomas D. D. Characteristics and purification of PRR1, an RNA phage specific for the broad host range Pseudomonas R1822 drug resistance plasmid. J Virol. 1973 Dec;12(6):1560–1567. doi: 10.1128/jvi.12.6.1560-1567.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Peck G. L., Olsen T. G., Yoder F. W., Strauss J. S., Downing D. T., Pandya M., Butkus D., Arnaud-Battandier J. Prolonged remissions of cystic and conglobate acne with 13-cis-retinoic acid. N Engl J Med. 1979 Feb 15;300(7):329–333. doi: 10.1056/NEJM197902153000701. [DOI] [PubMed] [Google Scholar]
- Rawls W. E., Bacchetti S., Graham F. L. Relation of Herpes simplex viruses to human malignancies. Curr Top Microbiol Immunol. 1977;77:71–95. doi: 10.1007/978-3-642-66740-4_3. [DOI] [PubMed] [Google Scholar]
- Sands J. A., Auperin L. D., Reinhardt A. Enveloped virus inactivation by fatty acid derivatives. Antimicrob Agents Chemother. 1979 Jan;15(1):134–136. doi: 10.1128/aac.15.1.134. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sands J., Auperin D., Snipes W. Extreme sensitivity of enveloped viruses, including herpes simplex, to long-chain unsaturated monoglycerides and alcohols. Antimicrob Agents Chemother. 1979 Jan;15(1):67–73. doi: 10.1128/aac.15.1.67. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schäfer R., Franklin R. M. Structure and synthesis of a lipid-containing bacteriophage. Total reconstitution of bacteriophage PM2 in vitro. Eur J Biochem. 1978 Dec;92(2):589–596. doi: 10.1111/j.1432-1033.1978.tb12781.x. [DOI] [PubMed] [Google Scholar]
- Snipes W., Cupp J., Sands J. A., Keith A., Davis A. Calcium requirement for assemby of the lipid-containing bacteriophage PM2. Biochim Biophys Acta. 1974 Mar 29;339(3):311–322. doi: 10.1016/0005-2736(74)90158-8. [DOI] [PubMed] [Google Scholar]
- Snipes W., Person S., Keith A., Cupp J. Butylated hydroxytoluene inactivated lipid-containing viruses. Science. 1975 Apr 4;188(4183):64–66. doi: 10.1126/science.163494. [DOI] [PubMed] [Google Scholar]
- Snipes W., Person S., Keller G., Taylor W., Keith A. Inactivation of lipid-containing viruses by long-chain alcohols. Antimicrob Agents Chemother. 1977 Jan;11(1):98–104. doi: 10.1128/aac.11.1.98. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sporn M. B., Squire R. A., Brown C. C., Smith J. M., Wenk M. L., Springer S. 13-cis-retinoic acid: inhibition of bladder carcinogenesis in the rat. Science. 1977 Feb 4;195(4277):487–489. doi: 10.1126/science.835006. [DOI] [PubMed] [Google Scholar]
- Strickland S., Mahdavi V. The induction of differentiation in teratocarcinoma stem cells by retinoic acid. Cell. 1978 Oct;15(2):393–403. doi: 10.1016/0092-8674(78)90008-9. [DOI] [PubMed] [Google Scholar]
- Verma A. K., Shapas B. G., Rice H. M., Boutwell R. K. Correlation of the inhibition by retinoids of tumor promoter-induced mouse epidermal ornithine decarboxylase activity and of skin tumor promotion. Cancer Res. 1979 Feb;39(2 Pt 1):419–425. [PubMed] [Google Scholar]
- Yamamoto N., Bister K., zur Hausen H. Retinoic acid inhibition of Epstein-Barr virus induction. Nature. 1979 Apr 5;278(5704):553–554. doi: 10.1038/278553a0. [DOI] [PubMed] [Google Scholar]
