Amr. Gatehouse et al., TRANSGENIC POTATO PLANTS WITH ENHANCED RESISTANCE TO THE PEACH-POTATOAPHID MYZUS-PERSICAE, Entomologia experimentalis et applicata, 79(3), 1996, pp. 295-307
Potato plants (Solanum tuberosum) cv. Desiree were transformed with th
e genes encoding the proteins bean chitinase (BCH), snowdrop lectin (G
NA) and wheat a-amylase inhibitor (WAI) under the control of the const
itutive CaMV 35S promoter. Transgenic plants with detectable levels of
foreign RNA were then selected for further characterisation with resp
ect to protein expression levels by immunodot blot analysis using poly
clonal antibodies raised against the respective protein. With the exce
ption of WAI, plants expressing high levels of RNA, expressed correspo
ndingly high levels of the foreign protein (1.5-2.0% of the total solu
ble protein). Although high levels of WAI mRNA were detected in some o
f the transformants, the protein could not be detected. On the bases o
f expression levels, two lines, designated PWG6#85 (transformed with t
he double construct WAI/GNA) and PBG6#47 (transformed with the double
construct BCH/GNA), were selected for testing in aphid trials for enha
nced levels of resistance. Both transgenic lines had a marked and sign
ificant effect on fecundity. The number of nymphs produced per female
per day peaked at 4.1 and 4.2 for lines PBG6#47 and PWG6#85 respective
ly, compared to a value of 5.4 on control plants. Total nymphal produc
tion was also significantly lower on either of the transgenic lines co
mpared to control plants (P<0.001) with the differences between the li
nes being only just significant (P= 0.058). On line PBG6#47 there was
a delay in nymphal production of 1.6 days, representing a delay of 15%
, and on line PWG6#85 this was 3.2 days, representing a delay of ca. 3
0%. The intrinsic rates of increase (r(m)) were also significantly low
er on both of the transgenic lines in comparison to that on control pl
ants (P<0.001), however the differences between the lines were not sig
nificant. The potential of using such genes as part of an over all str
ategy for the control of aphid populations is discussed.