Literature DB >> 4334291

Heterogeneity of foot-and-mouth disease virus: further studies on plaque formation by two plaque-size variants.

J S Martinsen.   

Abstract

Plaque production by a small-plaque (SP) and large-plaque (LP) variant of foot-and-mouth disease virus, type A, strain 119 (FMDV, A119), was influenced by a number of environmental factors. The SP variant produced plaques on cells of the IB-RS-2 cell line from swine kidney and to a lesser degree on primary cultures of swine kidney cells, but plaque formation was inhibited on primary cultures of bovine kidney (BK) cells unless diethylaminoethyl (DEAE) dextran was added to agar overlays. When DEAE dextran-treated agar overlay was used, the LP variant formed larger plaques on BK cells but not on IB-RS-2 cells. Concentrations of DEAE dextran from 0 to 100 microg/ml greatly enhanced the formation of SP virus plaques on BK cells but had little or no effect on the average size of plaques produced by the LP variant. Higher concentrations of polycation enlarged the plaques formed by both variants. Plaque sizes of the SP and LP variants increased as the concentration of agar or agarose in the overlays decreased. Reducing the concentration of agar to 0.75% facilitated the formation of SP virus plaques, but better plaque production occurred under agarose overlays. The original parent virus consisted predominantly of virus particles that formed small plaques. The rate of neutralization of the parent virus by guinea pig antiserum prepared against the parent virus was faster than antiserum inactivation of a low-passage virus of the same serotype and strain.

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Year:  1972        PMID: 4334291      PMCID: PMC1319651     

Source DB:  PubMed          Journal:  Can J Comp Med        ISSN: 0008-4050


  15 in total

1.  INACTIVATION OF FOOT-AND-MOUTH DISEASE VIRUS BY GLYCIDALDEHYDE.

Authors:  J S MARTINSEN
Journal:  Am J Vet Res       Date:  1964-09       Impact factor: 1.156

2.  APPARENT MODIFICATION OF FOOT-AND-MOUTH DISEASE VIRUS AFTER PROLONGED RESIDENCE IN SURVIVING CELLS.

Authors:  H R SEIBOLD; G E COTTRAL; R E PATTY; P GAILIUNAS
Journal:  Am J Vet Res       Date:  1964-05       Impact factor: 1.156

3.  The comparative titration of foot-and-mouth disease virus inoculated into the tongue and foot pads of guinea pigs.

Authors:  J L HYDE; J H GRAVES
Journal:  Am J Vet Res       Date:  1963-05       Impact factor: 1.156

4.  Large-scale production of bovine kidney cultures for plaque assay of foot-and-mouth disease virus and its ribonucleic acid.

Authors:  H L BACHRACH; J J CALLIS; W R HESS; R E PATTY; C J DE BOER; F E HAMBLET
Journal:  Am J Vet Res       Date:  1962-05       Impact factor: 1.156

5.  [Plaque formation by foot & mouth disease virus].

Authors:  Z DINTER; M SIBALIN
Journal:  Arch Gesamte Virusforsch       Date:  1958

6.  Properties of foot-and-mouth disease virus in tissue culture. I. Changes in plaque morphology and antigenicity following passage in tissue culture.

Authors:  Z DINTER; L PHILIPSON; T WESSLEN
Journal:  Arch Gesamte Virusforsch       Date:  1959

7.  The use of solid carbon dioxide for producing short periods of anesthesia in guinea pigs.

Authors:  J L HYDE
Journal:  Am J Vet Res       Date:  1962-05       Impact factor: 1.156

8.  The behaviour of strains of the virus of foot-and-mouth disease in pig,calf,ox and lamb kidney tissue cultures.

Authors:  R F SELLERS; L M BURT; A CUMMING; D L STEWART
Journal:  Arch Gesamte Virusforsch       Date:  1960

9.  Inhibition of foot-and-mouth disease virus by normal bovine serum.

Authors:  R E Patty
Journal:  Am J Vet Res       Date:  1970-01       Impact factor: 1.156

10.  Effects of chronic residence on size and size distribution of plaques of type A foot-and-mouth disease virus in primary calf kidney cell cultures.

Authors:  E Dougherty; H R Seibold; R E Patty
Journal:  Am J Vet Res       Date:  1968-03       Impact factor: 1.156

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