Abstract
The sedimentation behavior of influenza virus in dilute solutions of electrolyte was found to be quite variable. At times the virus activity appeared to sediment at a rate comparable with that of particles about 80 to 120 mµ in diameter, at other times at a rate comparable with that of particles about 10 mµ in diameter, and at still other times the bulk of the activity appeared to sediment at a rate comparable with that of the larger particles and the residual activity at a rate comparable with that of the smaller particles. However, in the presence of a sucrose density gradient, the virus activity was always found to sediment with a rate comparable to that of particles about 80 to 120 mµ in diameter; hence it appeared that the variable sedimentation behavior in dilute electrolyte solution was due to convection or mechanical disturbances during centrifugation. About 30 per cent of the high molecular weight protein present in the allantoic fluid of chick embryos infected with the F 12 strain of influenza virus was found to consist of a component having a sedimentation constant of about 30 S, and hence a probable particle diameter of about 10 mµ. The residual protein of high molecular weight was present in the form of a component having a sedimentation constant of about 600 S, and hence a probable particle diameter of about 70 mµ. The proportion of the 30 S component in allantoic fluid of chick embryos infected with the PR8 strain of influenza virus was found to be considerably less. The 600 S and 30 S components of F 12 allantoic fluid were purified and separated by differential centrifugation. The purified preparations of the 600 S component were found to possess a specific virus activity from 100 to over 10,000 times that of the purified preparations of the 30 S component, the difference in activity apparently depending only on the degree of fractionation of the two components. The purified 30 S component was found to sediment normally in the presence of 12 per cent sucrose, whereas the small residual virus activity of such preparations was found to sediment in the presence of a sucrose density gradient with a rate comparable to that of much heavier particles. It is concluded that influenza virus activity is not associated with material having a particle diameter of about 10 mµ, but is associated solely with material having a sedimentation constant of about 600 S and hence a probable particle diameter of about 70 mµ.
Full Text
The Full Text of this article is available as a PDF (992.7 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bauer J. H., Pickels E. G. A HIGH SPEED VACUUM CENTRIFUGE SUITABLE FOR THE STUDY OF FILTERABLE VIRUSES. J Exp Med. 1936 Sep 30;64(4):503–528. doi: 10.1084/jem.64.4.503. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bauer J. H., Pickels E. G. AN IMPROVED AIR-DRIVEN TYPE OF ULTRACENTRIFUGE FOR MOLECULAR SEDIMENTATION. J Exp Med. 1937 Mar 31;65(4):565–586. doi: 10.1084/jem.65.4.565. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chambers L. A., Henle W., Lauffer M. A., Anderson T. F. STUDIES ON THE NATURE OF THE VIRUS OF INFLUENZA : II. THE SIZE OF THE INFECTIOUS UNIT IN INFLUENZA A. J Exp Med. 1943 Mar 1;77(3):265–276. doi: 10.1084/jem.77.3.265. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Henle W., Henle G. INTERFERENCE OF INACTIVE VIRUS WITH THE PROPAGATION OF VIRUS OF INFLUENZA. Science. 1943 Jul 23;98(2534):87–89. doi: 10.1126/science.98.2534.87. [DOI] [PubMed] [Google Scholar]
- Knight C. A. THE STABILITY OF INFLUENZA VIRUS IN THE PRESENCE OF SALTS. J Exp Med. 1944 Mar 1;79(3):285–290. doi: 10.1084/jem.79.3.285. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lauffer M. A., Miller G. L. THE MOUSE INFECTIVITY TITRATION OF INFLUENZA VIRUS. J Exp Med. 1944 Feb 1;79(2):197–203. doi: 10.1084/jem.79.2.197. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miller G. L. A STUDY OF CONDITIONS FOR THE OPTIMUM PRODUCTION OF PR8 INFLUENZA VIRUS IN CHICK EMBRYOS. J Exp Med. 1944 Feb 1;79(2):173–183. doi: 10.1084/jem.79.2.173. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miller G. L., Stanley W. M. QUANTITATIVE ASPECTS OF THE RED BLOOD CELL AGGLUTINATION TEST FOR INFLUENZA VIRUS. J Exp Med. 1944 Feb 1;79(2):185–195. doi: 10.1084/jem.79.2.185. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sharp D. G., Taylor A. R., McLean I. W., Jr, Beard D., Beard J. W., Feller A. E., Dingle J. H. ISOLATION AND CHARACTERIZATION OF INFLUENZA VIRUS B (LEE STRAIN). Science. 1943 Oct 1;98(2544):307–308. doi: 10.1126/science.98.2544.307. [DOI] [PubMed] [Google Scholar]
- Shope R. E. SWINE INFLUENZA : III. FILTRATION EXPERIMENTS AND ETIOLOGY. J Exp Med. 1931 Jul 31;54(3):373–385. doi: 10.1084/jem.54.3.373. [DOI] [PMC free article] [PubMed] [Google Scholar]
