Slip and barodiffusion phenomena in slow flows of a gas mixture.

The slip and barodiffusion problems for the slow flows of a gas mixture are investigated on the basis of the linearized moment equations following from the Boltzmann equation. We restrict ourselves to the set of the third-order moment equations and state two general relations (resembling conservation equations) for the moments of the distribution function similar to the conditions used by Loyalka [S. K. Loyalka, Phys. Fluids 14, 2291 (1971)10.1063/1.1693331] in his approximation method (the modified Maxwell method). The expressions for the macroscopic velocities of the gas mixture species, the partial viscous stress tensors, and the reduced heat fluxes for the stationary slow flow of a gas mixture in the semi-infinite space over a plane wall are obtained as a result of the exact solution of the linearized moment equations in the 10- and 13-moment approximations. The general expression for the slip velocity and the simple and accurate expressions for the viscous, thermal, diffusion slip, and baroslip coefficients, which are given in terms of the basic transport coefficients, are derived by using the modified Maxwell method. The solutions of moment equations are also used for investigation of the flow and diffusion of a gas mixture in a channel formed by two infinite parallel plates. A fundamental result is that the barodiffusion factor in the cross-section-averaged expression for the diffusion flux contains contributions associated with the viscous transfer of momentum in the gas mixture and the effect of the Knudsen layer. Our study revealed that the barodiffusion factor is equal to the diffusion slip coefficient (correct to the opposite sign). This result is consistent with the Onsager's reciprocity relations for kinetic coefficients following from nonequilibrium thermodynamics of the discontinuous systems.

Detection of viral antigens by solid phase radioimmunoassay on polyethylene film.

Polyethylene film, without any pretreatment, may serve as a solid phase (SP) for RIA. Viral antigens (HBsAg, and influenza virus) are detected by SP-RIA on the film with a sensitivity of about 2-3 ng/ml or 40-60 pg/assay. The use of polyethylene film allows one to record RIA autographically. The use of micro amounts of reagents and specimens tested is an added advantage. No special equipment is necessary, the method is inexpensive, easy to perform and may be used for mass screening.

Non-equilibrium thermodynamics and kinetic theory of gas mixtures in the presence of interfaces.

A broad range of the boundary value problems of the kinetic theory of gases and gas mixtures is considered based on kinetic theory and non-equilibrium thermodynamics. The interrelation of the kinetic theory and non-equilibrium thermodynamics is discussed. The balance equations at the interface are obtained for the case of the boundary layers with peculiar properties. Procedures for deriving the boundary conditions for slightly rarefied gas mixtures are outlined. The problems of calculating slip coefficients are discussed. The specificity of the kinetic effects in the boundary conditions is shown. A set of general relations related to gas mixture flows in capillaries is deduced. The possibility of non-equilibrium kinetic effects in the form of a paradoxical distribution of non-equilibrium temperature is shown. Methods of non-equilibrium thermodynamics are used to obtain the phenomenological equations describing the thermophoresis and diffusiophoresis of particles and cross phenomena. The growth and evaporation of droplets is considered based on kinetic theory and non-equilibrium thermodynamics.

Prediction of secondary structure, spatial organization and distribution of antigenic determinants for hepatitis A virus proteins.

On the basis of the secondary structure calculations from the known amino acid sequence we came to the conclusion that hepatitis A virus capsid proteins have the typical antiparallel beta-sheet bilayer structure. The predicted secondary structure of the HAV proteins can be well aligned with those of the poliovirus (type 1 Mahoney) and human rhinovirus (type 14). It enabled us to use the X-ray structure of the PV-1M and HRV-14 proteins as a template and then, firstly, to localize the positions of alpha and beta regions in the architecture of the HAV protein molecules and, secondly, to discover the amino acid homologies of the secondary structure regions aligned. The obtained model of the three-dimensional structure for HAV proteins helped us to indicate the exposed regions of the polypeptide chains and to pinpoint the potential neutralizing antigenic sites.

Molecular hybridization study of cells producing oncornaviruses type D.

Five human cell lines producing oncornaviruses type D were studied by the method of molecular hybridization of viral and cellular nucleic acids. Repeated sequences of viral genome equivalents were found in nuclear DNA and numerous copies of viral genome were found in the cytoplasm. The viruses produced by the cell lines were found to be identical or closely related as regards nucleotide sequences of their genomes.

Possible association of oncornavirus type D with some forms of human cancer.

The method of molecular hybridization of nucleic acids of oncornavirus type D produced by HEp2 cells with cellular nucleic acids was applied. No sequences homologous to the viral nucleic acids were found in normal human embryo cells as well as in bovine, porcine, murine, and chicken cells. No such sequences were found in tissues of malignant lymphomas. Sequences homologous to the viral nucleic acids were found in some cancer cells, predominantly in hormone-associated tumors of females.

Immunologic study of antigens and molecular hybridization of nucleic acids from milk of breast cancer patients.

Comparative study has shown that by the gel diffusion assay both anti-HEp-2 virus serum and anti-breast cancer milk ultrasediment serum precipitated an identical antigen in human milk specimens, which was not identical with the group specific antigen of the HEp-2 virus. At the same time tha anti-breast cancer milk serum did not precipitate the HEp-2 virus. However, molecular hybridization experiments revealed nucleotide sequences homologous to nucleic acids of oncornavirus of D-type in milk obtained from breast carcinoma patients as well as in milk of healthy donors.

Radioimmunoassay for major internal structural protein (p21) of the bovine leukemia virus; antibodies detection and viruses identification.

The major internal protein of bovine leukemia virus (BLV p24) was isolated using ion exchange chromatography on phosphocellulose and gel filtration. The specificity of the BLV p24 isolated was checked by both the radioimmunoprecipitation (RIP) and the competitive radioimmunoassay (RIA). No cross reactivity between BLV p25 and the mammalian viruses of type C and D and the retrovirus isolated from human myeloma cells RPMI8226 [8, 17] was detected. The analysis of 429 leukemia-suspected bovine blood sera resulted in the detection of 165 (38.5%) positive and 264 (61.5%) negative blood sera. A correlation of the results of radioimmunoprecipitation reaction of major internal protein p24 and immunodiffusion test on the glycoprotein antigen of BLV was observed.

RNA synthesis in the L cell-SV5 system.

Comparative analysis of the ribonucleoprotein RNA synthesis was performed in two persistently infected L cell systems. In the first (LSV5-I), cells were infected with the cloned standard SV5 virus, in the second (LSV5-II), infecting virus had been enriched with defective interfering particles (DIP). The LSV5(I) system in its 40th-42nd passages was similar to LSV5(II) at the 2nd-3rd passage levels. There was shown that the ribonucleoprotein 3H-RNA synthesized falls into two classes: the minor corresponding to 50S viral RNA and the major revealing predominantly low molecular RNA. The decrease of the synthesis of the heavy viral RNA fraction and the prevalence of the low molecular RNA promoted the limitation of infection, the survival of cells and prolonged the carrier state. The possible correlation between low molecular RNA synthesis and DIP formation in the L cell-SV5 system is discussed.

In vitro studies with the scrapie agent.

Persistent infection with the scrapie agent has been established in L cells. The agent was propagated in homogenates of the cell line designated L-S. The L-S cells showed slower growth rate and morphological changes like pycnosis of nuclei and vacuolization of their cytoplasm. Cytogenetic analysis revealed rearrangement of chromosomes in L-S cells. In the course of passaging the number of cells with the characteristic marker chromosome decreased. Along with this cells were found with deletion of one arm of the marker chromosome. In addition, 3 new marker chromosomes were detected in infected cells, suggesting the influence of the scrapie agent on cytogenetic processes in scrapie-carrier cultures. The infectious activity of nucleic acids isolated from L-S cells was determined in BALB/c mice inoculated with untreated, DNase-treated and pronase-treated nucleic acid preparations. A slightly decreased infectious activity has been noted after DNase and pronase treatments.

Studies on influenza-virus virulence in recombinants between epidemic and vaccine strains.

Influenza virus recombinants between epidemic strains A/Brazil/11/78 (H1N1), A/USSR/382/78 (H3N2) and vaccine strains A/Leningrad/9/46 (H1N1), A/Victoria/35/72/50 (H3N2) have been tested for virulence for humans and albino mice; their genome structure has also been determined. It has been shown that after the replacement of surface antigens of A/Leningrad/9/46 (H1N1) strain by surface antigens of A/Brazil/11/78 (H1N1) or A/USSR/382/78 (H3N2), strains, the virus becomes totally nonpathogenic for mice whereas its virulence for humans is enhanced. The combination in recombinant X/28 (H1N1) of haemagglutinin and neuraminidase of A/Brazil/11/78 (H1N1) virus and othercomponents of A/Leningrad/9/46 virus determines its high affinity to the epithelium of the upper respiratory tract of humans, as well as its marked virulence for seronegative volunteers. Genetic mechanisms of influenza virus virulence and the involvement of surface proteins in its specific manifestations are discussed. It has been shown that pathogenic properties and the affinity of the virus to particular tissues are determined by different genes and their reasortment can result in the appearance of essentially new properties in recombinants.

Molecular and biological properties of a variant of avian influenza A/Seal/Massachusetts/1/80 (H7N7) virus that is pathogenic for mice.

A/Seal/Mass/80 influenza virus has been shown to be closely related antigenically and genetically to avian influenza H7N7 viruses, however, the virus does not replicate efficiently in avian species but does replicate in most mammals, except mice (Hinshaw et al., Infect. Immun., 34, 351-361, 1981). In order to develop a model defining the molecular changes that occur during acquisition of virulence, the A/Seal/Mass/80 virus was adapted to growth in mouse lungs. The adaptation was accompanied by changes in a number of properties of the haemagglutinin as well as by changes in other genes of the virus as determined by RNA: RNA hybridization.

Radioimmunoassay of type D oncovirus from continuous J-96 cells.

Radioimmunoassay of J-96 virus and an extract of J-96 cells in the homologous and heterologous systems aimed at detecting antigenic determinants of p25 of Mason-Pfizer virus, as well as group-specific and interspecies antigenic determinants p30 of Rauscher leukaemia virus demonstrated that (1) J-96 virus contains a major internal protein immunologically identical with p25 protein of Mason-Pfizer virus based on the antigenic determinants detectable by the radioimmunoassay used; and (2) no interspecies antigenic determinants characteristic of the major internal protein of mammalian type C viruses were detectable in the J-96 virus or the J-96 cell extract.

Persistent SV5 virus infection in continuous cell cultures.

A continuous line of guinea pig kidney cells (CGPK/H) and a continuous line of mouse fibroblasts (L/H) spontaneously infected with parainfluenza virus SV5 were found. These cultures showed no enhanced cell degeneration or symplast formation, nor was haemagglutinin accumulation or infectious virus demonstrated in them. However, regular reproduction of ribonucleoprotein (RNP) characteristic of parainfluenza viruses, morphologically complete virions and antigens producing antibody to SV5 virus were found in the cells. Focal haemadsorption neutralized by antiserum to SV5 virus was also demonstrated. The infection persisted in the cell populations for over 2 years (the observation period) under standard conditions of cell dispersion and subcultivation.

Comparative studies on biological properties and genome composition of influenza virus recombinants.

Some biological properties and the genome composition of antigenic recombinants obtained by crossing of human and animal influenza viruses were studied. Analysis of the recombinants has shown that upon heating of virions in vitro thermostability of the haemagglutinin (HA) does not necessarily correlate with the properties of parent HA; apparently it depended not only on the properties of the HA itself, but also on the peculiarities of other virion proteins. All recombinants obtained by crossing of pathogenic and apathogenic for mice parents either had a reduced pathogenicity for mice or were apathogenic. In some instances, reduction or loss of pathogenicity was observed in recombinants which inherited only one gene from the apathogenic parent; however, the data obtained suggest that pathogenicity involves functions of a number of genes. Human and animal influenza virus strains under study proved to be capable of replication in human embryo tracheal and kidney organ cultures. The degree of reproduction of the recombinants was either lower or higher as compared to the parent strains.

[Integration and transfection of an arbovirus by mammalian cells]. / Integratsiia i transfektsiia arbovirusa kletkami mlekopitaiushchikh.

A system: L cells chronically infected with Sindbis virus was studied. Unlike acute infection wherein the mature virions are produced, the chronically infected tissue culture produces subviral structures-infectious ribonucleoproteins. Molecular hybridization experiments revealed the integration of the viral genome (DNA-transcript) into the cellular genome. Transfection experiments showed the possibility to induce the synthesis of the virus in sensitive cells treated with DNA from the chronically infected cells.

[Expression of gag gene of human immunodeficiency virus in recombinant vaccinia virus]. / Ekspressiia gena gag virusa immunodefitsita cheloveka v sostave rekombinantnogo virusa ospovaktsiny.

A fragment of HTLV-IIIB gag-gene, coding for the first 441 amino acids of the p53 gag-precursor was expressed in the recombinant vaccinia virus, vC5. Two HIV specific proteins were detected by western blot in CV-1 cells infected with vC5. Their relative molecular masses were 50 and 35 Kd, pointing out that the first of the proteins is a full length expression product of the cloned sequence, while the second one is a result of processing or abortive translation. Possibilities of using such a strain as a vaccine or in Western blot conformation test are discussed.

[Properties of monoclonal antibodies interacting with determinants of hepatitis B virus surface antigen]. / Svoistva monoklonal'nykh antitel, vzaimodeistvuiushchikh s determinantami poverkhnostnogo antigena virusa gepatita B.

Fourteen hybridoma clones have been isolated producing the monoclonal antibodies to the surface antigen of the hepatitis B virus (HBsAg). Monoclonal antibodies have been shown to react in high titres with HBsAg in the reactions of PHA, PH and ELISA. The specificity of monoclonal antibodies to two antigenic determinants has been found by the competitive solid phase ELISA technique. Monoclonal antibodies from nine clones react with one determinant while monoclonal antibodies from the rest five clones react with the other nonoverlapping determinant.

[Detection of genomic RNA of the hepatitis A virus in clinical samples using the blot hybridization method]. / Detektsiia genomnoi RNK virusa gepatita A v klinicheskikh obraztsakh s pomoshch'iu metoda tochechno gibridizatsii.

The synthetic oligonucleotide sequence 3'CTCCTCGTACTTTA-5' complementing hepatitis A virus RNA was compared with cDNA probes in identification of viral genomic RNA. The clinical materials from patients in the 1-2 weeks of jaundice were screened. High specificity of the technique was demonstrated. Possibility of clinical using of the blot hybridization technique is discussed.

[Activity of virion RNA-polymerase in influenza A and B virus variants with different pathogenicities for mice]. / Aktivnost' virionnoi RNK-polimerazy u variantov virusa grippa A i B, razlichaiushchikhsia po priznaku patogennosti dlia myshei.

RNA polymerase activities in parental strains of influenza A and B viruses nonpathogenic for mice and their pathogenic variants have been studied. The parental strains are A/seal/Massachusetts 1/80, A/USSR 05/81, A/Philippines 2/82, B/Singapore 222/79. The RNA polymerase activity has been also studied in recombinant strains obtained by crossing various parental strains, one of which is pathogenic for mice (AR/PR 8/34), and having different degrees of pathogenicity. The nonpathogenic viruses had low transcriptase activity. RNA polymerase activity in pathogenic variants is shown to be 1.5-3 times higher than that in the parental strains. All the recombinants, whatever their pathogenicity, had approximately the same transcriptase activities which were 1.5-2 times higher than those registered in parental nonpathogenic strains.