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oligonucleotide-ligation assay for the differentiation between Cyclospora and Eimeria spp. polymerase chain reaction amplification products

An oligonucleotide-ligation assay (OLA) was developed and compared to a restriction fragment length polymorphism (RFLP) test for distinguishing between 294-bp polymerase chain reaction (PCR) amplification products of the 18S rRNA gene from Cyclospora and Eimeria spp. The PCR/OLA correctly distinguis...

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Bibliographic Details
Published in:Journal of food protection 1999-06, Vol.62 (6), p.682-685
Main Authors: Jinneman, K.C, Wetherington, J.H, Hill, W.E, Omiescinski, C.J, Adams, A.M, Johnson, J.M, Tenge, B.J, Dang, N.L, Wekell, M.M
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Language:English
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Summary:An oligonucleotide-ligation assay (OLA) was developed and compared to a restriction fragment length polymorphism (RFLP) test for distinguishing between 294-bp polymerase chain reaction (PCR) amplification products of the 18S rRNA gene from Cyclospora and Eimeria spp. The PCR/OLA correctly distinguished between three Cyclospora, three E. tenella, and one E. mitis strains and the ratio of positive to negative spectrophotometric absorbance (A(490)) values for each strain ranged from 4.086 to 15.280 (median 9.5). PCR/OLA provides a rapid, reliable, spectrophotometric alternative to PCR/RFLP.
ISSN:0362-028X
1944-9097
DOI:10.4315/0362-028x-62.6.682