Root-knot nematode (Meloidogyne spp.) is a destructive pest of sugarbeet (B
eta vulgaris L.) that reduces production in infested areas and is difficult
to manage. Identification of nematode-resistant plants is a time-consuming
process that is subject to genotype-environment interaction. Development o
f resistant cultivars/hybrids is the most effective control. This study was
conducted to establish a rapid and effective screening technique to detect
a large number of sugarbeet genotypes with resistance to Meloidogyne spp.
A nematode-resistant sugarbeet germplasm line, Mi-1 Beta, was previously de
veloped using J2 inoculation and screening procedures. Leaf and cotyledon e
xtractions were used in diagnosis. Phosphoglucomutase (PGM) was found to be
a potentially useful isozyme marker of resistance in Mi-1 Beta and derived
lines in starch gel electrophoresis. Seven banding patterns (four resistan
t and three susceptible) were produced. All susceptible plants shared the b
anding pattern of the resistant strains, except for a single PGM band. If d
emonstrated to be tightly linked to nematode resistance, this novel PGM iso
zyme marker will accelerate breeding sugarbeet with resistance to root-knot
nematode.