Sedentary plant-parasitic nematodes are able to induce specialized fee
ding structures in the root system of their host plants by triggering
a series of dramatic cellular responses. These changes presumably are
accompanied by a reprogramming of gene expression. To monitor such cha
nges, a variety of promoter-gusA fusion constructs were introduced int
o Arabidopsis and tobacco. Transgenic plants were analysed histochemic
ally for GUS activity in the nematode feeding structures after infecti
on with either Heterodera schachtii or Meloidogyne incognita. Promoter
s of the Cauliflower Mosaic Virus 35S gene, the bacterial nopaline syn
thase, rooting loci (rol) and T-cyt genes and the plant-derived phenyl
alanine ammonia-lyase I gene, which are highly active in non-infected
roots, were all downregulated in the feeding structures as indicated b
y the strong decrease of GUS activity inside these structures. Less st
ringent down-regulation was observed with chimeric gusA fusion constru
cts harbouring truncated rolB and rolC promoter sequences. Similar obs
ervations were made with transgenic Arabidopsis lines that carried ran
domly integrated promoterless gusA constructs to identify regulatory s
equences in the plant genome. Most of the lines that were selected for
expression in the root vascular cylinder demonstrated local down-regu
lation in feeding structures after infection with H. schachtii. The re
verse pattern of GUS activity, a blue feeding structure amidst unstain
ed root cells, was also found in several lines. However, GUS activity
that was entirely specific for the feeding structures was not observed
. Our data show that the expression of a large number of genes is infl
uenced during the development of the nematode feeding structures.