Nested allele-specific PCR primers distinguish genetic groups of Uncinula necator.

Abstract:

:Isolates of the obligately biotrophic fungus Uncinula necator cluster in three distinct genetic groups (groups I, II, and III). We designed PCR primers specific for these groups in order to monitor field populations of U. necator. We used the nucleotide sequences of the gene that encodes eburicol 14alpha-demethylase (CYP51) and of the ribosomal DNA internal transcribed spacer 1 (ITS1), ITS2, and 5. 8S regions. We identified four point mutations (three in CYP51 and one in ITS1) that distinguished groups I and II from group III based on a sample of 132 single-spore isolates originating from Europe, Tunisia, Israel, India, and Australia. We developed a nested allele-specific PCR assay in which the CYP51 point mutations were used to detect and distinguish groups I and II from group III in crude mildewed samples from vineyards. In a preliminary study performed with samples from French vineyards in which isolates belonging to genetic groups I and III were present, we found that a shift from a population composed primarily of group I isolates to a population composed primarily of group III isolates occurred during the grapevine growing season.

journal_name

Appl Environ Microbiol

authors

Délye C,Ronchi V,Laigret F,Corio-Costet MF

doi

10.1128/AEM.65.9.3950-3954.1999

keywords:

subject

Has Abstract

pub_date

1999-09-01 00:00:00

pages

3950-4

issue

9

eissn

0099-2240

issn

1098-5336

journal_volume

65

pub_type

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