Literature DB >> 6378966

Rapid visual detection of microorganisms in blood culture.

B H Sage, V R Neece.   

Abstract

We describe a method and apparatus for rapid visual detection of microorganisms in blood cultures. In the 30-min procedure, a lysing reagent for the preferential digestion of blood cells and a concentration device which causes 1 ml of lysed specimen to pass through a portion (3 mm2) of a membrane filter (pore size, 0.6 micron) were used. After the material remaining on the filter was Gram stained, the filter was mounted and examined microscopically. The ability to detect microorganisms in blood cultures was determined by spiking seven common blood pathogens into blood cultures prepared from the blood of healthy volunteers. Microorganism concentration in the cultures ranged from 1 to 1,000/ml. All of 34 cultures with at least 100 CFU/ml were detected, 34 of 64 cultures with less than 100 CFU/ml were detected, and 41 of 42 negative controls were correctly reported as negative.

Mesh:

Year:  1984        PMID: 6378966      PMCID: PMC271233          DOI: 10.1128/jcm.20.1.5-8.1984

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


  10 in total

1.  Rapid membrane filtration-epifluorescent microscopy technique for direct enumeration of bacteria in raw milk.

Authors:  G L Pettipher; R Mansell; C H McKinnon; C M Cousins
Journal:  Appl Environ Microbiol       Date:  1980-02       Impact factor: 4.792

2.  Practical aerobic membrane filtration blood culture technique: development of procedure.

Authors:  N M Sullivan; V L Sutter; S M Finegold
Journal:  J Clin Microbiol       Date:  1975-01       Impact factor: 5.948

3.  Automated radiometric detection of bacterial growth in blood cultures.

Authors:  F DeLand; H N Wagner
Journal:  J Lab Clin Med       Date:  1970-03

4.  Evaluation of acridine orange stain for detection of microorganisms in blood cultures.

Authors:  L R McCarthy; J E Senne
Journal:  J Clin Microbiol       Date:  1980-03       Impact factor: 5.948

5.  Blood culture technique based on centrifugation: developmental phase.

Authors:  G L Dorn; J R Haynes; G G Burson
Journal:  J Clin Microbiol       Date:  1976-03       Impact factor: 5.948

6.  Blood-lysing solution nontoxic to pathogenic bacteria.

Authors:  C H Zierdt
Journal:  J Clin Microbiol       Date:  1982-01       Impact factor: 5.948

7.  Detection and quantitation of simulated anaerobic bacteremia by centrifugation and filtration.

Authors:  R E Lamberg; R F Schell; J L LeFrock
Journal:  J Clin Microbiol       Date:  1983-05       Impact factor: 5.948

8.  Rapid automated disgnosis of bacteremia by impedance detection.

Authors:  R L Kagan; W H Schuette; C H Zierdt; J D MacLowry
Journal:  J Clin Microbiol       Date:  1977-01       Impact factor: 5.948

9.  Lysis-filtration blood culture versus conventional blood culture in a bacteremic rabbit model.

Authors:  C H Zierdt; D L Peterson; J C Swan; J D MacLowry
Journal:  J Clin Microbiol       Date:  1982-01       Impact factor: 5.948

10.  Microbiological and clinical evaluation of the isolator lysis-centrifugation blood culture tube.

Authors:  N K Henry; C A McLimans; A J Wright; R L Thompson; W R Wilson; J A Washington
Journal:  J Clin Microbiol       Date:  1983-05       Impact factor: 5.948

  10 in total
  3 in total

1.  Pattern recognition analysis of in vivo enzyme-substrate fluorescence velocities in microorganism detection and identification.

Authors:  A P Snyder; T T Wang; D B Greenberg
Journal:  Appl Environ Microbiol       Date:  1986-05       Impact factor: 4.792

2.  Rapid method for the differentiation of gram-positive and gram-negative bacteria on membrane filters.

Authors:  S Romero; R F Schell; D R Pennell
Journal:  J Clin Microbiol       Date:  1988-07       Impact factor: 5.948

3.  Rapid, colorimetric method for the detection of microorganisms in blood culture.

Authors:  C Wallis; J L Melnick
Journal:  J Clin Microbiol       Date:  1985-04       Impact factor: 5.948

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.