A set of molecular diagnostics was developed for Monilinia fructicola, caus
al agent of brown rot of stone fruits, capable of sensitive detection of th
e pathogen in planta. Species-specific repetitive sequences were identified
from a partial library of 312 recombinant clones hybridized with total DNA
, followed by subsequent screening for specificity. One hundred isolates, c
omprising 12 fungal species common to California stone fruits, were surveye
d for specificity. Three clones hybridized to 60 geographically diverse M.
fructicola isolates (California, Michigan, Georgia, Oregon, and Australia)
to the exclusion of all other fungi surveyed, including the closely related
M. laxa (n = 12). Two clones were identical and of extrachromosomal origin
(pMF73 and pMF150), whereas the third (pMF210) migrated with uncut DNA. Th
e sensitivity of all three was comparable and capable of detecting 50 pg of
fungal DNA in dot blot hybridizations. Sis species-specific primer pair se
ts were designed. They maintained the same specificity patterns observed in
the initial hybridization surveys and were sensitive enough to detect 50 f
g of fungal DNA template, approximately equivalent to 10 spores. The specie
s-specific clones were capable of detecting the pathogen in planta, specifi
cally from infected plum flowers and nectarine fruit tissue, using both hyb
ridization- and polymerase chain reaction-based methodologies.