Transgenic hairy roots of soybean [Glycine max (L,) Merrill] induced by Agr
obacterium rhizogenes support the complete life cycle of soybean cyst nemat
ode (SCN, Heterodera glycines Ichinohe) in vitro. However, expression of SC
N resistance in hairy soybean roots has not been investigated. A transgenic
hairy root system would be useful in de,eloping an assay for candidate SCN
resistance genes. The objectives of this study were to characterize transg
ene expression in SCN-infected hairy soybean roots and to evaluate a transg
enic hairy root system for investigations of resistance to SCN. Seedling co
tyledons of the SCN-susceptible cultivars, Agassiz and Parker, and SCN-resi
stant Bell and Faribault were infected with A. rhizogenes strain K599 trans
formed with T-DNA binary vectors containing the, gusA gene fused to promote
rs from either the cauliflower mosaic virus (CaMV 35S), Arabidopsis thalian
a phenylalanine ammonia lyase (PAL), or bean (Phaseolus vulgaris L,) chalco
ne synthase-8 (CNS) genes. Nine days after inoculating transgenic hairy roo
ts with sterile J2 nematodes, CHS-regulated P-glucuronidase (GUS) staining
at infection sites increased in hairy roots of resistant Faribault and decr
eased in susceptible Agassiz. PAL-regulated GUS staining was absent at infe
ction sites in hairy roots of resistant cultivars, but was increased in inf
ection sites in susceptible cultivars, Thirty-fire days after inoculation w
ith SCN, the mean number of cysts formed on hairy roots of the resistant cu
ltivars was about 14% of the mean number of cysts formed on hairy roots of
the susceptible cultivars, indicating that the SCN resistance phenotypes we
re preserved in transgenic hairy roots. These results indicated that the tr
ansgenic hairy soybean root system will be useful for investigating differe
ntial transgene expression during nematode infection and evaluation of cand
idate SCN resistance genes.