Genus-specific detection of salmonellae in equine feces by use of the polymerase chain reaction

Noah D. Cohen From the Departments of Large Animal Medicine & Surgery (Cohen, Wallis) and Pathobiology (Neibergs, Simpson, McGrude, Hargis), College of Veterinary Medicine, Texas A&M University, College Station, TX 77843.

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Holly L. Neibergs From the Departments of Large Animal Medicine & Surgery (Cohen, Wallis) and Pathobiology (Neibergs, Simpson, McGrude, Hargis), College of Veterinary Medicine, Texas A&M University, College Station, TX 77843.

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Deeann E. Wallis From the Departments of Large Animal Medicine & Surgery (Cohen, Wallis) and Pathobiology (Neibergs, Simpson, McGrude, Hargis), College of Veterinary Medicine, Texas A&M University, College Station, TX 77843.

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R. Bruce Simpson From the Departments of Large Animal Medicine & Surgery (Cohen, Wallis) and Pathobiology (Neibergs, Simpson, McGrude, Hargis), College of Veterinary Medicine, Texas A&M University, College Station, TX 77843.

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Edward D. McGruder From the Departments of Large Animal Medicine & Surgery (Cohen, Wallis) and Pathobiology (Neibergs, Simpson, McGrude, Hargis), College of Veterinary Medicine, Texas A&M University, College Station, TX 77843.

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B. M. Hargis From the Departments of Large Animal Medicine & Surgery (Cohen, Wallis) and Pathobiology (Neibergs, Simpson, McGrude, Hargis), College of Veterinary Medicine, Texas A&M University, College Station, TX 77843.

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Summary

Members of the genus Salmonella were identified in feces from horses, using the polymerase chain reaction (pcr) and genus-specific oligonucleotide primers. Feces from healthy horses were determined to be culture-negative for Salmonella spp. Fecal samples were inoculated with known numbers of colony-forming units (cfu) of S anatum, S derby, S enteritidis, S heidelberg, S newport, and S typhimurium. The dna was extracted from fecal samples and amplified by pcr, using genus-specific primers. Sensitivity of the assay extended to 103 cfu of Salmonella sp/g of feces; sensitivity of microbiologic culture with enrichment extended to 102 cfu of Salmonella sp/g of feces. Feces that were not inoculated with Salmonella spp were negative by the pcr. Detection of salmonellae in feces was possible, using the pcr, within 10 to 12 hours from the time of submission of samples.

Summary

Members of the genus Salmonella were identified in feces from horses, using the polymerase chain reaction (pcr) and genus-specific oligonucleotide primers. Feces from healthy horses were determined to be culture-negative for Salmonella spp. Fecal samples were inoculated with known numbers of colony-forming units (cfu) of S anatum, S derby, S enteritidis, S heidelberg, S newport, and S typhimurium. The dna was extracted from fecal samples and amplified by pcr, using genus-specific primers. Sensitivity of the assay extended to 103 cfu of Salmonella sp/g of feces; sensitivity of microbiologic culture with enrichment extended to 102 cfu of Salmonella sp/g of feces. Feces that were not inoculated with Salmonella spp were negative by the pcr. Detection of salmonellae in feces was possible, using the pcr, within 10 to 12 hours from the time of submission of samples.

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