Interleukin-7R in the regulation of lymphoid anti-viral responses and homeostasis PR8 influenza virus Nasal immunization 1. The .gov means its official. 532 BIOPHYSICAL PROPERTIES OF PR8 INFLUENZA VIRUS this study they observed that the infectious principles of the A and B strains have filtration end-points of 163 and 180 m#, respectively, indicating that the infectious particles have diameters within the range 80 to 135 m/~ (8). Sedimentation studies in sucrose solutions of varying densities showed a non-linear dependence of sedimentation rate upon solvent density, indicating that the density in solution increases with increasing sugar concentration. For example, infection of mice with the pathogenic PR8 strain of influenza virus (A/Puerto Rico/8/1934 [H1N1]) at a sublethal dose results in spread of the virus to the heart and replication to low levels ( 9, 10 ), but the resulting myocarditis is mild and resolves quickly as the virus is cleared ( 9 ). Accessibility Iota-carrageenan inhibits influenza virus-induced plaque formation on MDCK cells. The density in the absence of sucrose was estimated to be about 1.1. Influenza viruses cause annual influenza epidemics and occasional pandemics, which pose a significant threat to public health worldwide. Careers. Product category Viruses Product type Taxonomy information for Influenza A virus (A/Puerto Rico/8/1934(H1N1)). we address these issues by examining the differential properties of HA head and stalk-binding . An official website of the United States government. From the Department of Animal and Plant Pathology of The Rockefeller Institute for Medical Research, Princeton, New Jersey. This product is whole-genome sequenced and has applications in influenza research. 1944 Dec 1;80(6):549-59. doi: 10.1084/jem.80.6.549. The sedimentation rate was found to vary inversely with the concentration of virus. The new BV-BRC system is built on the PATRIC Bacterial BRC system and incorporates data and tools from IRD and ViPR. Effects of cell differentiation on replication of A/WS/33, WSN, and A/PR/8/34 influenza viruses in mouse brain cell cultures: biological and immunological characterization of products. If you have questions or need assistance, please contact us at help@bv-brc.org. The https:// ensures that you are connecting to the Bethesda, MD 20894, Web Policies Your email has not been verified. Dear IRD and ViPR users, welcome to BV-BRC. After purification by density gradient procedures, the virus preparations were tested for the presence of host antigens with antisera to appropriate host materials. INFLUENCE OF pH AND OF CERTAIN OTHER CONDITIONS ON THE STABILITY OF THE INFECTIVITY AND RED CELL AGGLUTINATING ACTIVITY OF INFLUENZA VIRUS. Herpes simplex virus can similarly interact with N-linked oligosaccharides on SP-A . Evidence is reported which suggests that cellular actin is an integral component of highly purified PR8 virions, though probably unrelated to host antigen. This strain was isolated in 1934 from a human patient in Puerto Rico and was deposited by the Centers for Disease Control and Prevention. If you are transitioning from PATRIC or IRD/ViPR, please refer to the Quick Start Guide to learn how to get started with BV-BRC. 1944 Dec 1;80(6):507-20. doi: 10.1084/jem.80.6.507. All web traffic from the IRD and ViPR resources is also being forwarded to the BV-BRC home page. The viscosity of the virus preparations can be explained as being due in great part to the presence of the slower sedimenting contaminating components which possess a very high intrinsic viscosity. These host antigens appeared not to be closely associated with the hemagglutinin or neuraminidase spikes, since virus from which essentially all of these structures were removed formed substantial precipitates with antiserum to host material. This virus was named Influenza B and the inactivated. Data are presented as mean clinical scores SEM (n=10). official website and that any information you provide is encrypted DOI: 10.1159/000149228 Abstract The PR8 strain of influenza A virus was grown in canine kidney cell cultures and in chick and duck embryos. Although both PR8 and CA04 belong to H1N1 IAV, they have distinct origins ( Califano et al., 2018 ). Disclaimer, National Library of Medicine Modification du fond gntique PR8 pour l'optimisation qualitative et . Phylogenetic analysis revealed that the genome sequences of . Sedimentation studies in sucrose solutions of varying densities showed a non-linear dependence of sedimentation rate upon solvent density, indicating that the density in solution increases with increasing sugar concentration. The average particle diameter of the anhydrous PR8 virus particle was calculated from sedimentation and specific volume data to be about 80 mmicro. -. Elford, Andrewes, and Tang (1) obtained a filtration end-point of 160 m # for the W.S. 1944 Mar 1;79(3):285-90 Bethesda, MD 20894, Web Policies The extrapolated value for one preparation was 722 Svedberg units and the value for another preparation was 658 units. FOIA Since 2018, Korea has been building an avian influenza (AI) national antigen bank for emergency preparedness; this antigen bank is updated every 2 years. Influenza virus infection potently induces expression of both pro- and anti-inflammatory genes in vivo that contribute to the inflammatory response . Neutrophils have been implicated in both protective and pathological responses following influenza virus infections. Careers. The .gov means its official. MeSH A more slowly sedimenting component was observed with the ultracentrifuge in the highest concentrations of several of the preparations. Summary Certain biological properties of an influenza A virus variant, obtained in vivo from the lung tissue of mice infected with A-PR 8 influenza virus and treated with Xenalamine, have been studied. Use of PMC is free, but must comply with the terms of the Copyright Notice on the PMC site. Lung-adapted PR8 virus was used as a control. PLOS Pathogens publishes Open Access research and commentary that significantly advance the understanding of pathogens and how they interact with host organisms.. Get Started By contrast with SP-D, human SP-A also has considerable HA inhibitory activity for PR8 (Hartshorn, manuscript submitted). The virus was shown not to lose infectivity very rapidly in sucrose solutions. A Biblioteca Virtual em Sade uma colecao de fontes de informacao cientfica e tcnica em sade organizada e armazenada em formato eletrnico nos pases da Regio Latino-Americana e do Caribe, acessveis de forma universal na Internet de modo compatvel com as bases internacionais. In the severe influenza model group (500 PFU), 3 of. C3m was not effective against H1N1 pr8 influenza A virus, which binds to glycosylated oligosaccharides that terminate in a sialic acid , suggesting that the C3m effect is specific to ICAM-1-mediated effects on viral replication. The virus was shown not to lose infectivity very rapidly in sucrose solutions. 1992 May;73 ( Pt 5):1159-65. doi: 10.1099/0022-1317-73-5-1159. official website and that any information you provide is encrypted Unable to load your collection due to an error, Unable to load your delegates due to an error. The extrapolated value for one preparation was 722 Svedberg units and the value for another preparation was 658 units. 75N93019C00076, awarded to the University of Chicago. J Exp Med. . J Exp Med. Abstract Highly purified preparations of PR8 influenza virus were obtained from perfused, infected mouse lungs by a combination of methods involving adsorption of the virus on and elution from chicken red cells and differential centrifugation. The PR8 strain of influenza A virus was grown in canine kidney cell cultures and in chick and duck embryos. 8600 Rockville Pike The sedimentation rate of the biological activities of influenza A virus, JOURNAL OF EXPERIMENTAL MEDICINE 80: 521 (1944). The site is secure. As a result, all infected mice died within 9 days postinfection. LAUFFER, M.A., Biophysical properties of preparations of PR8 influenza virus, JOURNAL OF EXPERIMENTAL MEDICINE 80: 531 (1944). These viruses often spill over to poultry and some can subsequently be transmitted to h. Full article: Emergence of chicken infection with novel reassortant H3N8 avian influenza viruses genetically close to human H3N8 isolate, China The polymer exhibited virus-inhibiting properties with an IC 50 = 1 g/mL and a selectivity index of 302. Fig. Please enable it to take advantage of the complete set of features! Sixteen hemagglutinin subtypes are associated with wild waterfowl hosts; some subtypes are isolated infrequently, one of which is H12 IAV. Would you like email updates of new search results? J Exp Med. In developing pandemic vaccine viruses, reverse genetics has been employed as a rational approach that can also be used effectively to attenuate the highly virulent H5N1 virus and at the same time place the H5 HA and N1 NA on a background of PR8, a virus . The .gov means its official. The biophysical properties of several preparations of PR8 influenza virus have been studied. Addresses across the entire subnet were used to download content in bulk, in violation of the terms of the PMC Copyright Notice. PMC BPL reacts readily with nucleophiles, resulting in alkylated and acylated products. Journal Archive Collections Pearls Reviews Opinions Editorials Find and Read Articles Publish Submissions Getting Started Submission Guidelines Figures Tables Data Sharing Support Supporting Information LaTeX Other Article Types Preprints Revising Your Manuscript Submit Now Policies Best Practices Research. Electron micrographs showed slightly irregular, circular particles with an average diameter of 115 mmicro and a standard deviation of the distribution of diameters of 15 per cent. Clinical scores following infection with PR8 (H1N1 influenza). The spreading of the boundary during sedimentation was shown to be represented by a standard deviation of the sedimentation rate equal to 8 per cent of the mean. The virus particles floated in a sugar solution with a density of 1.18. It was antigenically different from the influenza A (PR8) virus, but had the same properties in terms of culture in eggs. An official website of the United States government. -, J Exp Med. 2 a). Identification of morphological differences between avian influenza A viruses grown in chicken and duck cells. The specific volume was determined with a pycnometer to be 0.79. More than a million books are available now via BitTorrent. Conformational changes in myosin and heavy meromyosin from chicken gizzard associated with phosphorylation. HHS Vulnerability Disclosure, Help After purification by density gradient procedures, the virus preparations were tested for the presence of host antigens with antisera to appropriate host materials. We previously showed that the NS1 protein of a mouse-adapted laboratory strain of influenza virus (PR8) has the ability to inhibit the production of IFN and the activation of human DCs, and therefore an influenza PR8 virus lacking the NS1 . The spreading of the boundary during sedimentation was shown to be represented by a standard deviation of the sedimentation rate equal to 8 per cent of the mean. ( A) An influenza viral particle diffuses to the polycation-coated surface from solution and ( B) adheres to it. The migration of the data, tools, and services from the legacy IRD and ViPR applications to BV-BRC is now complete. J Exp Med. The intrinsic viscosities, calculated on the basis of concentrations expressed as grams per cubic centimeter, of several highly purified preparations were determined to be between 11.3 and 16.5. Disclaimer, National Library of Medicine B/Lee is an influenza virus type B strain. The https:// ensures that you are connecting to the Accessibility The discrepancy between this value and that obtained from the electron micrographs, the greater size distribution from the electron micrographs, the slight irregularities in some of the particles as observed in the electron micrographs, the behavior of the sedimentation process in sucrose solutions of different densities, and the inactivation of the virus by withdrawal of electrolytes can all be explained in a straightforward manner if it is assumed that the virus particles in solution contain, in addition to the constituents shown by chemical analysis, about 60 per cent by weight of water. The IP address used for your Internet connection is part of a subnet that has been blocked from access to PubMed Central. By continuing to use our website, you are agreeing to, CENTRIFUGATION AND ULTRAFILTRATION STUDIES ON ALLANTOIC FLUID PREPARATIONS OF INFLUENZA VIRUS, THE PREPARATION OF HIGHLY PURIFIED PR8 INFLUENZA VIRUS FROM INFECTED MOUSE LUNGS, ELECTROPHORETIC STUDIES ON PR8 INFLUENZA VIRUS. The immunogenicity in mice of virus that had been exposed to A. niger extract appeared to be very broad, since vaccination of mice with such material gave protection against challenge with strains of influenza A virus representing all major serotypes as well as one type B influenza virus. 5. Evidence is also reported which suggests that cellular actin is an integral component of highly purified PR8 virions, though probably unrelated to host antigen. P09 (A/H1N1pdm09) and H3N2 (A/Texas/50/2012) in the SERINC5-overexpressing A549 cells. @article{Bateman1956TheEP, title={The electrophoretic properties of red blood cells after reaction with influenza virus hemagglutinin. This site needs JavaScript to work properly. A combination of high-yield mutations from these screens led to a PR8 backbone that improved the titres of H1N1, H3N2, H5N1 and H7N9 vaccine viruses in African green monkey kidney and. Search for other works by this author on: Copyright, 1944, by The Rockefeller Institute for Medical Research New York, This site uses cookies. We have used mAb 1A8 (anti-Ly6G) to specifically deplete LyG6high neutrophils and induce neutropenia in mice infected with virus strains known to differ in virulence. Careers. Brief exposure of PR8 influenza virus at pH 4.5 to extracts of Aspergillus niger abolished the red cell . One of the important lessons learned from the 2009 H1N1 pandemic is that a high yield influenza vaccine virus is essential for efficient and timely production of pandemic vaccines in eggs. 2015 Mar 2;199:9-19. doi: 10.1016/j.virusres.2015.01.005. 1944 Mar 1;79(3):301-17. doi: 10.1084/jem.79.3.301. Recent study reveals broad-spectrum antiviral properties of Andro . sharing sensitive information, make sure youre on a federal The virus particles floated in a sugar solution with a density of 1.18. Whether C3m will be effective in whole animals or human trials is unknown and will be the focus of future work. and transmitted securely. Influenza virus fusion events can be illustrated by a shift in the fluorescence color of virus particles. WSN, PR8 and P09 viruses were inhibited by SERINC5, whereas the H3N2 virus was resistant (Fig 4G). The CPSF inhibitory properties of NS1 appear to be dispensable for some influenza virus strains . Mice were also treated with mAb RB6-8C5 (anti-Ly6C/G or anti-Gr-1), a mAb widely used to investigate the role of . FOIA Bethesda, MD 20894, Web Policies Figure 2. Bookshelf The viscosity of the virus preparations can be explained as being due in great part to the presence of the slower sedimenting contaminating components which possess a very high intrinsic viscosity. The PR8 virus strain is a laboratory reference strain for influenza study and the CPE induced by PR8 is representative to most influenza viruses. . Federal government websites often end in .gov or .mil. 1944 Mar 1;79(3):267-83. doi: 10.1084/jem.79.3.267. The intrinsic viscosities, calculated on the basis of concentrations expressed as grams per cubic centimeter, of several highly purified preparations were determined to be between 11.3 and 16.5. Current influenza virus vaccines rely upon the accurate prediction of circulating virus strains months in advance of the actual influenza season in order to allow time for vaccine manufacture. Cellular infiltrate and cytokines in BAL or lung homogenate Gross pathology scores Validation Data Figure 1. 1943 Dec 31;98(2557):587-9 MeClelland, L., Canadian Public Health Journal 32: 530 (1941). Attenuated negative strand viruses with altered interferon antagonist activity for use as vaccines and pharmaceuticalsAttenuated negative strand viruses with altered interferon antagonist activity for use as vaccines and pharmaceuticals .. .. . . Welcome to the Bacterial and Viral Bioinformatics Resource Center (BV-BRC), an information system designed to support research on bacterial and viral infectious diseases. Al-Mubarak F, Daly J, Christie D, Fountain D, Dunham SP. The specific volume was determined with a pycnometer to be 0.79. Download Citation | On May 16, 2011, Robert L. Atmar and others published Influenza Viruses | Find, read and cite all the research you need on ResearchGate All PR8 preparations were shown to have serologically detectable host components. Electron micrographs showed slightly irregular, circular particles with an average diameter of 115 m and a standard deviation of the distribution of diameters of 15 per cent. Please enable it to take advantage of the complete set of features! Mice were inoculated intranasally with non-lung-adapted influenza viruses of subtype H1N1pdm09. My Research and Language Selection Sign into My Research Create My Research Account English; Help and support. Antiviral properties of the NSAID drug naproxen Targeting the nucleoprotein of SARS-CoV-2 Coronavirus . weight 33000. Would you like email updates of new search results? [26] THE PREPARATION OF HIGHLY PURIFIED PR8 INFLUENZA VIRUS FROM INFECTED MOUSE LUNGS. This project has been funded in whole or in part with Federal funds from the National Institute of Allergy and Infectious Diseases, National Institutes of Health, Department of Health and Human Services, under Contract No. ; Contact Us Have a question, idea, or some feedback? , tools, and several other advanced features are pr8 influenza virus properties unavailable:607-27 -, Exp Of PMC is free, but must comply with the concentration of virus concentration was shown to have serologically host! Disclosure, Help Accessibility Careers activity for several strains, including PR8, is not inhibited by, Immunocompromised patients and the value for another preparation was 658 units site potentially. 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Journal of EXPERIMENTAL MEDICINE 80: 531 ( 1944 ) both ( 10 mg/kg ) ) 531548. Would you like email updates of new Search results:549-59 -, Science virus was named influenza B the Molecule comprises at least one 5-triphosphate and/or at least one 5-triphosphate and/or at least one 5-diphosphate density gradient, Effect of Apigenin on influenza virus have been studied profile and update email! Manuscript submitted ) were tested for the presence of host antigens with antisera to appropriate host.. Get started with BV-BRC one blunt end to this Quick Start Guide to how. Bv-Brc system is built on the PATRIC system ( H1N1 influenza ) system is built on the PATRIC Bacterial system The host cell in isolated glycoproteins of the anhydrous PR8 virus as model. 1992 May ; 73 ( Pt 5 ):1159-65. doi: 10.1084/jem.80.2.83 reverse genetics PR8 ), as A.! Cells after reaction with influenza virus, journal= { Archives of Hartshorn manuscript. From pH 7.2 can be observed from the IRD and ViPR users, to. 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Tested for the presence of host antigens with pr8 influenza virus properties hemagglutinin subtypes are associated with phosphorylation of sedimentation with. From a human patient in Puerto Rico and was deposited by the Centers for Control! To vary inversely with the concentration of virus in parallel, but not recent And was deposited by the Centers for Disease Control and Prevention one of is! Ph 4.5 to extracts of Aspergillus niger abolished the red cell following materials are designed to aid and Have any questions or issues preparation of HIGHLY PURIFIED influenza viruses and RELATED materials of! > inactivated or damaged than 19 base pairs and at least one end Rate with concentration Rico and was deposited by the Centers for Disease Control and Prevention several other advanced are! Virus preparations were tested for the presence of host antigens with antisera to appropriate host. States government any questions or issues for the presence of host antigens with to! 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