Sensitivity of an Immunomagnetic-Separation-Based Test for Detecting Escherichia coli O26 in Bovine Feces
The sensitivity of a test for cattle shedding Escherichia coli serogroup O26 was estimated using several fecal pats artificially inoculated at a range of concentrations with different E. coli O26 strains. The test involves the enrichment of fecal microflora in buffered peptone water, the selective c...
Saved in:
Published in | Applied and Environmental Microbiology Vol. 72; no. 11; pp. 7260 - 7263 |
---|---|
Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Washington, DC
American Society for Microbiology
01.11.2006
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | The sensitivity of a test for cattle shedding Escherichia coli serogroup O26 was estimated using several fecal pats artificially inoculated at a range of concentrations with different E. coli O26 strains. The test involves the enrichment of fecal microflora in buffered peptone water, the selective concentration of E. coli O26 using antibody-coated immunomagnetic-separation beads, the identification of E. coli colonies on Chromocult tryptone bile X-glucuronide agar, and confirmation of the serogroup with E. coli serogroup O26-specific antisera using slide agglutination. The effective dose of E. coli O26 for an 80% test sensitivity (ED₈₀) was 1.0 x 10⁴ CFU g⁻¹ feces (95% confidence interval, 4.7 x 10³ to 2.4 x 10⁴). Differences in test sensitivity between different E. coli O26 strains and fecal pats were also observed. Individual estimates of ED₈₀ for each strain and fecal pat combination ranged from 4.2 x 10² to 4.8 x 10⁵ CFU g⁻¹. These results suggest that the test is useful for identifying individuals shedding a large number of E. coli O26 organisms or, if an appropriate number of individuals in a herd are sampled, for identifying affected herds. The study also provides a benchmark estimate of sensitivity that can be used to compare alternative tests for E. coli O26 and a methodological approach that can be applied to tests for other pathogenic members of the Enterobacteriaceae and other sample types. |
---|---|
Bibliography: | http://aem.asm.org/contents-by-date.0.shtml ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Corresponding author. Mailing address: Scottish Agricultural College, Stratherrick Rd., Inverness IV2 4JZ, United Kingdom. Phone: 44 (0) 1463 243030. Fax: 44 (0) 1463 711103. E-mail: malcolm.hall@sac.ac.uk. |
ISSN: | 0099-2240 1098-5336 |
DOI: | 10.1128/AEM.03028-05 |