Literature DB >> 1500519

Beta-glucuronidase activities of fecal isolates from healthy swine.

L Jackson1, B E Langlois, K A Dawson.   

Abstract

Research has shown that various percentages of fecal Escherichia coli isolates obtained from healthy subjects may be beta-glucuronidase negative. The ability to detect beta-glucuronidase activity among fecal E. coli isolates from healthy subjects may be affected by assay conditions. A study was conducted in which agar and broth media containing 4-methylumbelliferyl-beta-D-glucuronide (MUG) were used to examine beta-glucuronidase activities of fecal isolates from healthy swine. Rectal swabs were plated on MacConkey agar plus 100 mg of MUG per liter (MAC-MUG) and incubated at 35 degrees C for 24 h. Each of 986 isolates picked from MAC-MUG was inoculated into duplicate tubes of lauryl tryptose broth plus 50 mg of MUG per liter (LT-MUG). One set of tubes was incubated at 35 degrees C and the other set of tubes was incubated at 44.5 degrees C. Gas production and hydrolysis of MUG, indicated by fluorescence when observed with UV light with a wavelength of 360 nm, were determined after incubation for 24 and 48 h. A higher percentage (P less than 0.01) of isolates was MUG positive at 44.5 degrees C than at 35 degrees C after 24 h of incubation in LT-MUG. A higher percentage (P less than 0.01) of isolates was MUG positive after 48 h than after 24 h of incubation at both 35 and 44.5 degrees C. A lower percentage of isolates (P less than 0.05) was observed to be MUG positive on MAC-MUG agar compared with their MUG reactions in LT-MUG at 35 and 44.5 degrees C. Approximately 89% of the isolates identified were beta-glucuronidase-positive E. coli. The largest proportion of MUG-positive E. coli was detected with LT-MUG at 35 degrees C after 48 h of incubation.

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Year:  1992        PMID: 1500519      PMCID: PMC265453          DOI: 10.1128/jcm.30.8.2113-2117.1992

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


  19 in total

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Authors:  S Ratnam; S B March; R Ahmed; G S Bezanson; S Kasatiya
Journal:  J Clin Microbiol       Date:  1988-10       Impact factor: 5.948

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3.  Comparison of beta-glucuronidase-based substrate systems for identification of Escherichia coli.

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4.  beta-Glucuronidase from Escherichia coli as a gene-fusion marker.

Authors:  R A Jefferson; S M Burgess; D Hirsh
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Authors:  J L Pérez; C I Berrocal; L Berrocal
Journal:  J Appl Bacteriol       Date:  1986-12

6.  Laboratory investigation of outbreak of hemorrhagic colitis caused by Escherichia coli O157:H7.

Authors:  C Krishnan; V A Fitzgerald; S J Dakin; R J Behme
Journal:  J Clin Microbiol       Date:  1987-06       Impact factor: 5.948

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Authors:  W Hansen; E Yourassowsky
Journal:  J Clin Microbiol       Date:  1984-12       Impact factor: 5.948

8.  Rapid identification of Enterobacteriaceae. II. Use of a beta-glucuronidase detecting agar medium (PGUA agar) for the identification of E. coli in primary cultures of urine samples.

Authors:  M Kilian; P Bülow
Journal:  Acta Pathol Microbiol Scand B       Date:  1979-10

9.  Fluorogenic assay for rapid detection of Escherichia coli in food.

Authors:  L J Moberg
Journal:  Appl Environ Microbiol       Date:  1985-12       Impact factor: 4.792

10.  COMPARISON OF THE RECOVERY OF ESCHERICHIA COLI FROM FROZEN FOODS AND NUTMEATS BY CONFIRMATORY INCUBATION IN EC MEDIUM AT 44.5 AND 45.5 C.

Authors:  M FISHBEIN; B F SURKIEWICZ
Journal:  Appl Microbiol       Date:  1964-03
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