Literature DB >> 4877497

Use of the antiserum-agar plate technique for specific identification and isolation of Pasteurella pestis.

J M Albizo, M J Surgalla.   

Abstract

Pasteurella pestis colonies were specifically identified on antiserum-agar plates used for primary culture of tissues from experimentally infected guinea pigs. Both selective and nonselective antiserum-agar plates were used to identify P. pestis from guinea pigs kept at 22 C for periods up to 4 days after death from plague. Colonies identified as P. pestis on selective and nonselective antiserum-agar plates, by the appearance of precipitin rings following brief chloroform vapor treatment, remained viable and were subsequently purified on nonselective antiserum-agar plates. Isolates obtained in this manner were uniformly lethal when injected into mice and guinea pigs, and conformed to standard laboratory criteria for P. pestis. P. pestis was identified on selective antiserum-agar plates from the spleens of all guinea pigs killed by the isolates, and from a large majority of the mice. The practical value and confirmative nature of the method were demonstrated.

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Year:  1968        PMID: 4877497      PMCID: PMC547603          DOI: 10.1128/am.16.8.1114-1119.1968

Source DB:  PubMed          Journal:  Appl Microbiol        ISSN: 0003-6919


  8 in total

1.  Pesticins. II. Production of pesticin I and II.

Authors:  R R BRUBAKER; M J SURGALLA
Journal:  J Bacteriol       Date:  1962-09       Impact factor: 3.490

2.  Studies on the nutrition and physiology of Pasteurella pestis. VI. A differential plating medium for the estimation of the mutation rate to avirulence.

Authors:  K HIGUCHI; J L SMITH
Journal:  J Bacteriol       Date:  1961-04       Impact factor: 3.490

3.  Rapid identification of Pasteurella pestis with fluorescent antibody. III. Staining Pasteurella pestis in tissue impression smears.

Authors:  M D MOODY; C C WINTER
Journal:  J Infect Dis       Date:  1959 May-Jun       Impact factor: 5.226

4.  Recommended laboratory methods for the diagnosis of plague.

Authors:  M BALTAZARD; D H DAVIS; R DEVIGNAT; G GIRARD; M A GOHAR; L KARTMAN; K F MEYER; M T PARKER; R POLLITZER; F M PRINCE; S F QUAN; P WAGLE
Journal:  Bull World Health Organ       Date:  1956       Impact factor: 9.408

5.  The pigmentation of Pasteurella pestis on a defined medium containing haemin.

Authors:  T W BURROWS; S JACKSON
Journal:  Br J Exp Pathol       Date:  1956-12

6.  Asymptomatic pharyngeal plague infection in Vietnam.

Authors:  J D Marshall; D V Quy; F L Gibson
Journal:  Am J Trop Med Hyg       Date:  1967-03       Impact factor: 2.345

7.  Specific identification of fraction I-positive Pasteurella pestis colonies on antiserum-agar plates.

Authors:  J M Albizo; M J Surgalla
Journal:  Appl Microbiol       Date:  1968-04

8.  SELECTIVE MEDIA FOR THE ISOLATION OF PASTEURELLA PESTIS.

Authors:  R F KNISELY; L M SWANEY; H FRIEDLANDER
Journal:  J Bacteriol       Date:  1964-08       Impact factor: 3.490

  8 in total
  3 in total

1.  Practical applications of new laboratory methods for plague investigations.

Authors:  M J Surgalla; E D Beesley; J M Albizo
Journal:  Bull World Health Organ       Date:  1970       Impact factor: 9.408

2.  Selective medium for growth of Rhizobium.

Authors:  P H Graham
Journal:  Appl Microbiol       Date:  1969-05

3.  Repression of the virulence of Yersinia pestis by an F' plasmid.

Authors:  R M Zsigray; W D Lawton; M J Surgalla
Journal:  Infect Immun       Date:  1983-02       Impact factor: 3.441

  3 in total

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