Literature DB >> 3585969

A competitive immunosorbent assay for detection of Pseudomonas pseudomallei exotoxin.

G Ismail, M Noor Embi, O Omar, J C Allen, C J Smith.   

Abstract

The development of monoclonal antibody and enzyme-linked immunosorbent assay (ELISA) techniques has made possible the detection of specific antigens at extremely low concentrations. Diagnosis of recalcitrant diseases such as melioidosis depends upon either early isolation and identification of the causative organism or the identification of a specific marker antigen, Pseudomonas pseudomallei exotoxin, in serum; the latter is better because it allows more rapid and simple diagnosis. A method of detecting exotoxin concentrations of greater than 16 ng/ml by an ELISA based on a monoclonal antitoxin is here described; it is significantly more sensitive than the mouse lethality test (lower threshold 30 micrograms/ml) currently in use and an in-vitro cytotoxicity test (lower threshold 10 micrograms/ml) that we have developed and describe here.

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Year:  1987        PMID: 3585969     DOI: 10.1099/00222615-23-4-353

Source DB:  PubMed          Journal:  J Med Microbiol        ISSN: 0022-2615            Impact factor:   2.472


  4 in total

1.  An ELISA-disc procedure for antibodies toPseudomonas pseudomallei: application for a serological study of melioidosis in an endemic area.

Authors:  N Embi; D Devarajoo; R Mohamed; G Ismail
Journal:  World J Microbiol Biotechnol       Date:  1993-01       Impact factor: 3.312

Review 2.  Melioidosis: epidemiology, pathophysiology, and management.

Authors:  Allen C Cheng; Bart J Currie
Journal:  Clin Microbiol Rev       Date:  2005-04       Impact factor: 26.132

Review 3.  Melioidosis: the tip of the iceberg?

Authors:  D A Dance
Journal:  Clin Microbiol Rev       Date:  1991-01       Impact factor: 26.132

4.  Diagnosis of melioidosis by means of an ELISA detecting antibodies toPseudomonas pseudomallei exotoxin. Preliminary assay evaluation.

Authors:  C J Smith; M Jones; D A Dance; W Chaowagul; N J White
Journal:  World J Microbiol Biotechnol       Date:  1991-01       Impact factor: 3.312

  4 in total

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