Literature DB >> 14044954

DIRECT AND INDIRECT FLUORESCENT-ANTIBODY TECHNIQUES FOR THE PSITTACOSIS-LYMPHOGRANULOMA VENEREUM-TRACHOMA GROUP OF AGENTS.

M R ROSS, E K BORMAN.   

Abstract

Ross, Martin R. (Connecticut State Department of Health, Hartford) and Earle K. Borman. Direct and indirect fluorescent-antibody techniques for the psittacosis-lymphogranuloma venereum-trachoma group of agents. J. Bacteriol. 85:851-858. 1963.-Direct and indirect fluorescent-antibody (FA) techniques were developed for the detection of group antigen in infected tissue cultures and the titration of group antibody in human antiserum. The growth of the agent of meningopneumonitis (MP) in mouse embryo lung cell monolayers was followed by infectivity and complement-fixing (CF) antigen titrations, and cytological examination of FA stained cultures. Although infectivity and CF antigen reached a peak at 2 days and remained constant for an additional 3 days, only cells tested 2 to 3 days after infection were suitable for FA staining with labeled anti-MP serum because of excessive artifacts in the older cultures. Fluorescein isothiocyanate-labeled rooster and guinea pig anti-MP serums and human antipsittacosis serums were titrated in direct FA and hemagglutination-inhibition (HI) tests. The rooster conjugate showed brighter staining and higher antibody titers than the guinea pig or human conjugates and was more effective in detecting minimal amounts of virus antigen. FA staining reactions with 1 and 2 units of labeled rooster serum were inhibited by unlabeled rooster serum but clear-cut inhibition with human antipsittacosis serum could not be demonstrated. The indirect FA technique was successfully used for the titration of group antibody in human serum. A comparison of the indirect FA, HI, and CF tests showed the indirect FA technique to be intermediate in sensitivity between the HI and CF tests. None of the three tests showed significant cross reactions with human serums reactive for influenza A and B; parainfluenza 1, 2, and 3; respiratory syncytial virus; Q fever; or the primary atypical pneumonia agent.

Entities:  

Keywords:  CHLAMYDIA; FLUORESCENT ANTIBODY TECHNIC; MIYAGAWANELLA

Mesh:

Substances:

Year:  1963        PMID: 14044954      PMCID: PMC278236          DOI: 10.1128/jb.85.4.851-858.1963

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  15 in total

1.  Species-specific antigens from the cell walls of the agents of meningopneumonitis and feline pneumonitis.

Authors:  H M JENKIN; M R ROSS; J W MOULDER
Journal:  J Immunol       Date:  1961-02       Impact factor: 5.422

2.  Superiority of fluorescein isothiocyanate (Riggs) for fluorescent-antibody technic with a modification of its application.

Authors:  J D MARSHALL; W C EVELAND; C W SMITH
Journal:  Proc Soc Exp Biol Med       Date:  1958 Aug-Sep

3.  Growth of psittacosis virus in tissue culture.

Authors:  J E OFFICER; A BROWN
Journal:  J Infect Dis       Date:  1960 Nov-Dec       Impact factor: 5.226

4.  The isolation and identification of ornithosis infection in turkeys by tissue culture and immunocytochemical staining.

Authors:  P DONALDSON; D E DAVIS; J R WATKINS; S E SULKIN
Journal:  Am J Vet Res       Date:  1958-10       Impact factor: 1.156

5.  Identification by fluorescent antibody of developmental forms of psittacosis virus in tissue culture.

Authors:  S M BUCKLEY; E WHITNEY; F RAPP
Journal:  Proc Soc Exp Biol Med       Date:  1955-10

6.  A passive hemagglutination reaction for psittacosis.

Authors:  A A BENEDICT; E O'BRIEN
Journal:  J Immunol       Date:  1958-02       Impact factor: 5.422

7.  Staining bacterial smears with fluorescent antibody. I. General methods for Malleomyces pseudomallei.

Authors:  M GOLDMAN; M D MOODY; B M THOMASON
Journal:  J Bacteriol       Date:  1956-09       Impact factor: 3.490

8.  Cell wall antigens from members of the psittacosis group of organisms.

Authors:  M R ROSS; H M JENKIN
Journal:  Ann N Y Acad Sci       Date:  1962-03-05       Impact factor: 5.691

9.  A comparative study of the growth cycles of different members of the psittacosis group in different host cells.

Authors:  J LITWIN; J E OFFICER; A BROWN; J W MOULDER
Journal:  J Infect Dis       Date:  1961 Nov-Dec       Impact factor: 5.226

10.  The indirect complement fixation hemagglutination and conglutinating complement absorption tests for viruses of the psittacosis-lymphogranuloma venereum group.

Authors:  M R HILLEMAN; D A HAIG; R J HELMOLD
Journal:  J Immunol       Date:  1951-01       Impact factor: 5.422

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  1 in total

1.  Detection of Chlamydia psittaci by immunofluorescence.

Authors:  V J Lewis; W L Thacker; A F Cacciapuoti
Journal:  Appl Microbiol       Date:  1972-07
  1 in total

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