Differences in the biological phenotype of low-yielding (L) and high-yielding (H) variants of swine influenza virus A/NJ/11/76 are associated with their different receptor-binding activity

被引:29
作者
Gambaryan, AS
Matrosovich, MN
Bender, CA
Kilbourne, ED
机构
[1] Russian Acad Med Sci, MP Chumakov Inst Poliomyelitis & Viral Encephalit, Moscow 142782, Russia
[2] Ctr Dis Control & Prevent, Influenza Branch, Atlanta, GA 30333 USA
[3] New York Med Coll, Dept Microbiol & Immunol, Valhalla, NY 10595 USA
关键词
D O I
10.1006/viro.1998.9274
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Low- (L) and high-yielding (H) variants of A/sw/NJ/11/76 influenza virus were compared for their growth properties in embryonated chicken eggs and MDCK cells and for their binding affinity for the membrane fractions prepared from cells of the chicken embryo allantoic membrane, MDCK, and swine tracheal cells, as well as for soluble sialic acid containing macromolecules and monovalent sialosides. We have shown, that during infection in MDCK cells and in eggs, the progeny of the L variant remain predominantly cell associated, in contrast to those of H. As a result, accumulation of the L mutant in allantoic or culture fluid is significantly slowed in comparison with the H variant. Visualization of the infectious foci formed by the viruses in MDCK cell monolayers and on the allantoic membrane revealed that L spreads predominantly from cell to cell, while the spread of H involves release of the virus progeny into solution and its rapid distribution over the cell monolayer via convectional flow of the liquid. In the binding assays, L displayed significantly higher binding affinity than H for cellular membranes, gangliosides, and sialylglycoproteins, however, the affinity of the variants for the monovalent sialic acid compounds was comparable. Unlike H, L bound strongly to dextran sulfate. The data obtained suggest that all distinctions of the L and H biological phenotypes reported previously [Kilbourne, E. D., Taylor, A. H., Whitaker, C. W., Sahai, R., and Caton, A. (1988) Hemagglutinin polymorphism as the basis for low-and high-yield phenotypes of swine influenza virus. Proc. Natl. Acad. Sci USA 85, 7782-7785] could be rationally explained by a more avid binding of the L variant to the surface of target cells, and that this effect is mainly due to enhanced electrostatic interactions. (C) 1998 Academic Press.
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页码:223 / 231
页数:9
相关论文
共 29 条
[1]   ROLE OF SURFACE GLYCOPROTEINS IN INFLUENZA-VIRUS PYROGENICITY [J].
ALLUWAIMI, AM ;
SMITH, H ;
SWEET, C .
JOURNAL OF GENERAL VIROLOGY, 1994, 75 :2835-2840
[2]  
[Anonymous], 1995, BIOL SIALIC ACIDS
[3]   SINGLE AMINO-ACID SUBSTITUTIONS IN THE HEMAGGLUTININ CAN ALTER THE HOST RANGE AND RECEPTOR-BINDING PROPERTIES OF H1-STRAINS OF INFLUENZA-A VIRUS [J].
AYTAY, S ;
SCHULZE, IT .
JOURNAL OF VIROLOGY, 1991, 65 (06) :3022-3028
[4]   HEMAGGLUTININ OF SWINE INFLUENZA-VIRUS - A SINGLE AMINO-ACID CHANGE PLEIOTROPICALLY AFFECTS VIRAL ANTIGENICITY AND REPLICATION [J].
BOTH, GW ;
SHI, CH ;
KILBOURNE, ED .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (22) :6996-7000
[5]   RECEPTOR SPECIFICITY IN HUMAN, AVIAN, AND EQUINE H2 AND H3 INFLUENZA-VIRUS ISOLATES [J].
CONNOR, RJ ;
KAWAOKA, Y ;
WEBSTER, RG ;
PAULSON, JC .
VIROLOGY, 1994, 205 (01) :17-23
[6]   ROLE OF RECEPTOR-BINDING ACTIVITY OF THE VIRAL HEMAGGLUTININ MOLECULE IN THE PRESENTATION OF INFLUENZA-VIRUS ANTIGENS TO HELPER T-CELLS [J].
EISENLOHR, LC ;
GERHARD, W ;
HACKETT, CJ .
JOURNAL OF VIROLOGY, 1987, 61 (05) :1375-1383
[7]  
GAMBARYAN AS, 1992, J VIROL METHODS, V39, P11
[8]   EGG FLUIDS AND CELLS OF THE CHORIOALLANTOIC MEMBRANE OF EMBRYONATED CHICKEN EGGS CAN SELECT DIFFERENT VARIANTS OF INFLUENZA-A (H3N2) VIRUSES [J].
HARDY, CT ;
YOUNG, SA ;
WEBSTER, RG ;
NAEVE, CW ;
OWENS, RJ .
VIROLOGY, 1995, 211 (01) :302-306
[9]   EVIDENCE FOR SIALYL GLYCOCONJUGATES AS RECEPTORS FOR BORDETELLA-BRONCHISEPTICA ON SWINE NASAL-MUCOSA [J].
ISHIKAWA, H ;
ISAYAMA, Y .
INFECTION AND IMMUNITY, 1987, 55 (07) :1607-1609