Literature DB >> 6263946

Highly sensitive assay for Clostridium perfringens enterotoxin that uses inhibition of plating efficiency of Vero cells grown in culture.

J L McDonel, B A McClane.   

Abstract

A highly sensitive and reproducible biological assay for Clostridium perfringens enterotoxin is described that uses Vero (African green monkey kidney) cells grown in tissue cultures. Very small doses of the enterotoxin inhibited the plating efficiency of the cells. This inhibition of plating efficiency could be used to detect as little as 0.1 ng (1 ng/ml) of enterotoxin, and a linear dose-response curve was obtained with 0.5 to 5 ng (5 to 50 ng/ml). A nonlinear, but reproducible, curve was obtained with a dose range from 0.1 to 100 ng (1 to 1,000 ng/ml). A new unit of biological activity, called the plating efficiency unit, was defined as that amount of enterotoxin that caused a 25% inhibition of the plating of 200 cells inoculated into 100 microliters of medium in a microwell culture system. One milligram of highly purified enterotoxin contained about 400,000 plating efficiency units. Additional studies demonstrated that the biological and serological activities of the enterotoxin molecule were not equally labile.

Entities:  

Mesh:

Substances:

Year:  1981        PMID: 6263946      PMCID: PMC273919          DOI: 10.1128/jcm.13.5.940-946.1981

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


  15 in total

1.  Measurement of biological activities of purified and crude enterotoxin of Clostridium perfringens.

Authors:  L Nilo
Journal:  Infect Immun       Date:  1975-08       Impact factor: 3.441

2.  Purification and biochemical properties of Clostridium perfringens type A enterotoxin.

Authors:  R L Stark; C L Duncan
Journal:  Infect Immun       Date:  1972-11       Impact factor: 3.441

3.  Quantitation of Clostridium perfringens type A enterotoxin by electroimmunodiffusion.

Authors:  C L Duncan; E B Somers
Journal:  Appl Microbiol       Date:  1972-11

4.  Rapid detection of Clostridium perfringens enterotoxin by a modified ligated intestinal loop technique in rabbits.

Authors:  A H Hauschild; R Hilsheimer; C G Rogers
Journal:  Can J Microbiol       Date:  1971-11       Impact factor: 2.419

Review 5.  Clostridium perfringens toxins (type A, B, C, D, E).

Authors:  J L McDonel
Journal:  Pharmacol Ther       Date:  1980       Impact factor: 12.310

6.  Biological characteristics of Clostridium perfringens type A enterotoxin.

Authors:  R L Stark; C L Duncan
Journal:  Infect Immun       Date:  1971-08       Impact factor: 3.441

7.  Assay methods for Clostridium perfringens type A enterotoxin.

Authors:  C Genigeorgis; G Sakaguchi; H Riemann
Journal:  Appl Microbiol       Date:  1973-07

8.  In vitro production of Clostridium perfringens enterotoxin and its detection by reversed passive hemagglutination.

Authors:  T Uemura; G Sakaguchi; H P Riemann
Journal:  Appl Microbiol       Date:  1973-09

9.  Response of ligated intestinal loops in chickens to the enterotoxin of Clostridium perfringens.

Authors:  L Niilo
Journal:  Appl Microbiol       Date:  1974-11

10.  Ileal loop fluid accumulation and production of diarrhea in rabbits by cell-free products of Clostridium perfringens.

Authors:  C L Duncan; D H Strong
Journal:  J Bacteriol       Date:  1969-10       Impact factor: 3.490

View more
  3 in total

1.  Rapid detection of Clostridium perfringens type A enterotoxin by enzyme-linked immunosorbent assay.

Authors:  B A McClane; R J Strouse
Journal:  J Clin Microbiol       Date:  1984-02       Impact factor: 5.948

2.  Vero cell assay for rapid detection of Clostridium perfringens enterotoxin.

Authors:  D E Mahony; E Gilliatt; S Dawson; E Stockdale; S H Lee
Journal:  Appl Environ Microbiol       Date:  1989-09       Impact factor: 4.792

3.  Production and characterization of monoclonal antibodies against Clostridium perfringens type A enterotoxin.

Authors:  A P Wnek; R J Strouse; B A McClane
Journal:  Infect Immun       Date:  1985-11       Impact factor: 3.441

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.