VIEW ARTICLE

Techniques

Detection of Erwinia amylovora by Nested PCR and PCR-Dot-Blot and Reverse-Blot Hybridizations. P. S. McManus, Department of Botany and Plant Pathology and the Pesticide Research Center, Michigan State University, East Lansing 48824-1312; A. L. Jones, Department of Botany and Plant Pathology and the Pesticide Research Center, Michigan State University, East Lansing 48824-1312. Phytopathology 85:618-623. Accepted for publication 28 February 1995. Copyright 1995 The American Phytopathological Society. DOI: 10.1094/Phyto-85-618.

The sensitivity and specificity of four methods based on the polymerase chain reaction (PCR) for detection of Erwinia amylovora were compared. A previously developed single-round PCR assay was used to amplify a specific 1-kb DNA fragment of plasmid pEA29, known to be unique to and conserved in E. amylovora. The ends of the 1-kb single-round PCR product were sequenced, and two new oligonucleotide primers were designed from sequences internal to the original primers and used in nested PCR. These primers directed amplification of a 844-bp fragment from the 1-kb first-round PCR product directly from E. amylovora cells but not from other bacteria associated with apple. Less than one cell of E. amylovora from pure culture was detected with nested PCR—an increase in sensitivity of 1,000-fold compared to single-round PCR. The lower limit of detection of PCR-dot-blot and reverse-blot hybridization methods was approximately 20 cells. Weak positive signals were sometimes produced by bacteria other than E. amylovora in hybridization experiments but only if nonspecific PCR products were visible on ethidium bromide-stained agarose gels. When asymptomatic apple tissue was screened, E. amylovora was detected in 61, 84, and 100% of leaf samples; 0, 66, and 80% of axillary bud samples; and 4, 27, and 75% of mature fruit calyx samples by first-round PCR, PCR-dot-blot hybridization, and nested PCR, respectively. The potential applications of each method are discussed.