Literature DB >> 8166805

Rapid diagnosis of enterohemorrhagic Escherichia coli O157:H7 directly from fecal specimens using immunofluorescence stain.

C H Park1, D L Hixon, W L Morrison, C B Cook.   

Abstract

Serotype O157:H7 is most frequently encountered among verotoxin-producing Escherichia coli. Most laboratories use MacConkey-sorbitol agar as a screening medium. Presumptive identification of sorbitol-negative colonies is then accomplished by latex agglutination or biochemical tests with serologic confirmation, which requires 18-36 hours for completion. This study attempted to detect E coli O157:H7 directly from stool specimens by direct immunofluorescence (DIF) antibody staining to provide quicker turnaround (< 2 hours). A total of 336 abnormal fecal samples (bloody, watery, semi-liquid, or mucoid) were examined by this method. Results were compared with those of culture. Direct immunofluorescence antibody staining of the direct fecal smear detected all isolates of E coli O157 that were recovered by culture, including nonmotile strains, strains possessing the H7 flagellar antigen, and one strain with a flagellar antigen other than H7. Optimum results were achieved when specimens were pretreated with 5% bleach and centrifugation. No false-negative results were obtained with bleach-pretreated stool samples.

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Year:  1994        PMID: 8166805     DOI: 10.1093/ajcp/101.1.91

Source DB:  PubMed          Journal:  Am J Clin Pathol        ISSN: 0002-9173            Impact factor:   2.493


  9 in total

1.  Production and characterization of monoclonal antibodies specific for the lipopolysaccharide of Escherichia coli O157.

Authors:  R B Westerman; Y He; J E Keen; E T Littledike; J Kwang
Journal:  J Clin Microbiol       Date:  1997-03       Impact factor: 5.948

2.  Rapid Immunoassay for detection of Escherichia coli O157 directly from stool specimens.

Authors:  C H Park; N M Vandel; D L Hixon
Journal:  J Clin Microbiol       Date:  1996-04       Impact factor: 5.948

3.  Isolation of a nonpathogenic strain of Citrobacter sedlakii which expresses Escherichia coli O157 antigen.

Authors:  C H Park; E A Martin; E L White
Journal:  J Clin Microbiol       Date:  1998-05       Impact factor: 5.948

4.  Evaluation of the premier EHEC assay for detection of Shiga toxin-producing Escherichia coli.

Authors:  K S Kehl; P Havens; C E Behnke; D W Acheson
Journal:  J Clin Microbiol       Date:  1997-08       Impact factor: 5.948

Review 5.  Diarrheagenic Escherichia coli.

Authors:  J P Nataro; J B Kaper
Journal:  Clin Microbiol Rev       Date:  1998-01       Impact factor: 26.132

6.  Immunomagnetic-electrochemiluminescent detection of Escherichia coli O157 and Salmonella typhimurium in foods and environmental water samples.

Authors:  H Yu; J G Bruno
Journal:  Appl Environ Microbiol       Date:  1996-02       Impact factor: 4.792

7.  Evaluation of an immunoassay for direct detection of Escherichia coli O157 in stool specimens.

Authors:  B L Dylla; E A Vetter; J G Hughes; F R Cockerill
Journal:  J Clin Microbiol       Date:  1995-01       Impact factor: 5.948

Review 8.  Pathogenesis and diagnosis of Shiga toxin-producing Escherichia coli infections.

Authors:  J C Paton; A W Paton
Journal:  Clin Microbiol Rev       Date:  1998-07       Impact factor: 26.132

9.  Identification of a rough strain of Escherichia coli O157:H7 that produces no detectable O157 antigen.

Authors:  P Feng; R C Sandlin; C H Park; R A Wilson; M Nishibuchi
Journal:  J Clin Microbiol       Date:  1998-08       Impact factor: 5.948

  9 in total

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