Literature DB >> 2443531

Intrinsic catalase dot blot immunoassay for identification of Mycobacterium tuberculosis, Mycobacterium avium, and Mycobacterium intracellulare.

L G Wayne1, G A Diaz.   

Abstract

The heat-labile T class of mycobacterial catalase exhibits peroxidase activity with some substrates. Most species of mycobacteria produce T-catalase, which is serologically characterized by a combination of shared epitopes and unique, species-specific epitopes. Antibodies to T-catalases from Mycobacterium tuberculosis, Mycobacterium avium, and Mycobacterium intracellulare have been cross absorbed with T-catalases from heterologous species and applied as dots to nitrocellulose membranes. When these membranes were incubated with crude sonic extracts of 93 strains of mycobacteria that produce sufficient T-catalase, and were then exposed to 3,3'-diaminobenzidine peroxidase substrate, only those extracts made from one of the three species represented yielded a discrete brown dot at the site of the corresponding globulin. The sensitivity of the test was at least 96.5%, and the specificity was in excess of 99.5%.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 2443531      PMCID: PMC269308          DOI: 10.1128/jcm.25.9.1687-1690.1987

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  9 in total

1.  Deoxyribonucleic acid relatedness among species of slowly-growing mycobacteria.

Authors:  I Baess
Journal:  Acta Pathol Microbiol Scand B       Date:  1979-08

2.  Relationship of isoniazid to the metabolism of mycobacteria; catalase and peroxidase.

Authors:  M O TIRUNARAYANAN; W A VISCHER
Journal:  Am Rev Tuberc       Date:  1957-01

3.  A double staining method for differentiating between two classes of mycobacterial catalase in polyacrylamide electrophoresis gels.

Authors:  L G Wayne; G A Diaz
Journal:  Anal Biochem       Date:  1986-08-15       Impact factor: 3.365

4.  Diagnostic probability matrix for identification of slowly growing mycobacteria in clinical laboratories.

Authors:  L G Wayne; M I Krichevsky; D Portyrata; C K Jackson
Journal:  J Clin Microbiol       Date:  1984-10       Impact factor: 5.948

5.  Identification of mycobacteria by specific precipitation of catalase with absorbed sera.

Authors:  L G Wayne; G A Diaz
Journal:  J Clin Microbiol       Date:  1985-05       Impact factor: 5.948

6.  Isolation of nontuberculous mycobacteria in the United States, 1980.

Authors:  R C Good; D E Snider
Journal:  J Infect Dis       Date:  1982-12       Impact factor: 5.226

7.  Enzyme-linked immunoelectrotransfer blot techniques (EITB) for studying the specificities of antigens and antibodies separated by gel electrophoresis.

Authors:  V C Tsang; J M Peralta; A R Simons
Journal:  Methods Enzymol       Date:  1983       Impact factor: 1.600

8.  Deoxyribonucleic acid relationships between different serovars of Mycobacterium avium, Mycobacterium intracellulare and Mycobacterium scrofulaceum.

Authors:  I Baess
Journal:  Acta Pathol Microbiol Immunol Scand B       Date:  1983-06

9.  Serological approaches for the characterization of catalase in tissue-derived mycobacteria.

Authors:  V M Katoch; L G Wayne; G A Diaz
Journal:  Ann Microbiol (Paris)       Date:  1982 Nov-Dec
  9 in total
  3 in total

Review 1.  Agents of newly recognized or infrequently encountered mycobacterial diseases.

Authors:  L G Wayne; H A Sramek
Journal:  Clin Microbiol Rev       Date:  1992-01       Impact factor: 26.132

2.  Detection of a novel catalase in extracts of Mycobacterium avium and Mycobacterium intracellulare.

Authors:  L G Wayne; G A Diaz
Journal:  Infect Immun       Date:  1988-04       Impact factor: 3.441

3.  Comparison of the abilities of Mycobacterium avium and Mycobacterium intracellulare to infect and multiply in cultured human macrophages from normal and human immunodeficiency virus-infected subjects.

Authors:  A J Crowle; E R Ross; D L Cohn; J Gilden; M H May
Journal:  Infect Immun       Date:  1992-09       Impact factor: 3.441

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.