Bacterial diseases of potatoes: from classical phytobacteriology to molecular pathogenicity

Various bacterial pathogens attack potato plants and tubers. These pathogens includeErwinia, Corynebacterium (Clavibacter), Psuedomonas andStreptomyces. Over the past few years there have been significant advances in the molecular biological analysis of several of these pathogens and this is now helping us to understand the major aspects of virulence mechanisms. However, to date, such information is not sufficiently useful to allow us to intervene rationally in these potato diseases, except by the standard practises of good husbandry.     

Characterisation of energy-dependent efflux of imazalil and fenarimol in isolates of Penicillium italicum with a low,medium and high degree of resistance to DMI-fungicides

Differential accumulation of [¹⁴C]imazalil and [¹⁴C]fenarimol by germlings of wild-type and DMI-resistant isolates ofPenicillium italicum was studied at various pH values. At pH 7 and 8 the low-resistant isolate E_300–3 accumulated 22% and 35%, respectively, less imazalil than the wild-type isolate W₅. Imazalil accumulation at pH 5 and 6 was similar. Isolate E_300–3 also accumulated less fenarimol as compared with the wild-type isolate. This difference was much more obvious than for imazalil and was observed at all pH values tested. Differences in accumulation of both imazalil and fenarimol between low (E_300–3), medium (H₁₇) and high resistant (I₃₃) isolates were not observed. These results suggest that decreased accumulation of DMIs is responsible for a low level of resistance only and that additional mechanisms of resistance might operate in isolates with a medium and high degree of resistance. With all isolates fenarimol accumulation was energy-dependent. This was not obvious for imazalil.The wild-type and DMI-resistant isolates had a similar plasma membrane potential as determined with the probe [¹⁴C]tetraphenylphosphonium bromide ([¹⁴C]TPP⁺). Various test compounds, among which ATPase inhibitors, ionophoric antibiotics and calmodulin antagonists, affected the accumulation of [¹⁴C]TPP⁺, [¹⁴C]imazalil and [¹⁴C]fenarimol. No obvious correlation between the effects of the test compounds on accumulation levels of the fungicides and [¹⁴C]TPP⁺ could be observed. These results indicate that the plasma membrane potential does not mediate the efflux of DMI fungicides byP. italicum.     

New predators for biocontrol under glass

Several species ofOrius are under investigation in the UK, Europe and North America for the biological control of thrips, especially western flower thrips(Frankliniella occidentalis). The available species are briefly compared and findings on effectiveness and oviposition ofO. laevigatus are reported.     

Interactions among herbivores,microbial insecticides and crop plants

Knowledge of the interactions among lepidopterous insects, microbial insecticides and plants is either lacking or incomplete. In some of the interactions, plant allelochemicals antagonized the insecticidal activity of the microbe by means of feeding reduction. In others, microbe activity was enhanced either by causing insect toxicity or by a potentiation of the crystal protein. Nutritional evaluations of the interactions amongHeliothis virescens. Bacillus thuringiensis crystal protein and tannin showed that microbe toxicity in the larva was antagonized by this phytochemical.     

Nutritional stress in ficea sitchensis plantations in coastal British columbia: The effects of gaultheria shallon and declining site fertility

Examples of nutritional stress in conifer seedlings caused by competing ericaceous species (e.g. Calluna and Kalmia), have been reported in several parts of the world. Nutritional stress (primarily N deficiency) has been reported in Sitka spruce (Picea sitchensis) plantations growing in association with an ericaceous species, salal (Gaultheria shallon), in coastal British Columbia. Nutritional interference by salal was investigated on a chronosequence of sites up to 10 yr after clearcutting and slashburning. No direct evidence for an allelopathic contribution to the N stress was obtained. However, the rapid accumulation of salal fine roots and rhizomes, and the nutrients contained therein, provides a partial explanation for the observed stress symptoms. Soil analyses and seedling bioassays demonstrated a reduction in fertility in the period 8 to 10 yr after clearcutting and slashburning in comparison to the period 2 to 4 yr, which is believed to impose further nutritional stress on Sitka spruce. It is concluded that the nutritional stress in these Sitka spruce plantations is caused by a combination of (1) salal competition for nutrients and their subsequent immobilization in salal biomass, and (2) declining site fertility caused by the termination of the flush of nutrients (the assert period) that occurs in the immediate post-clearcutting and slashburning period. Sustaining good growth of plantations under such circumstances will require site nutrient management as well as vegetation management.