Short CommunicationA study of the effects of ‘Candidatus Phytoplasma mali’ on the psyllid Cacopsylla melanoneura (Hemiptera: Psyllidae)
Introduction
Phytoplasmas and their vectors interact in various ways, ranging from the beneficial to the deleterious (Severin, 1946, Beanland et al., 2000). Survival and fecundity are often the main parameters in studies of vector–mollicute interactions (Weintraub and Beanland, 2006). Data concerning changes in the life span and fecundity of vectors are available for a few strains of phytoplasma belonging to the X-disease (‘Candidatus Phytoplasma pruni’) and the aster yellows (‘Ca. P. asteris’) groups, as well as for Spiroplasma spp. (Jensen, 1959, Madden and Nault, 1983, Garcia-Salazar et al., 1991, Ebbert and Nault, 2001).
Phytoplasma infection can make infected plants more suitable hosts for insects, by reducing their chemical defenses or increasing the availability of nutrients. Consequently, infected plants are more attractive to insects (Weintraub and Beanland, 2006). Very little is known about the effects of phytoplasmas on the psyllid genus Cacopsylla (Hemiptera: Psyllidae), which is involved in the transmission of ‘Ca. P. mali’, the etiological agent of apple proliferation (AP) disease. In the apple orchards of the Trentino region, the main vector of the disease is C. picta Förster. However, in recent years, populations of this insect have decreased dramatically (Mattedi et al., 2007). Despite these changes in C. picta populations, the incidence of AP disease has increased.
The full role of C. melanoneura Förster in the spread of ‘Ca. P. mali’ is still unclear (Mattedi et al., 2008), but it has been shown to be an efficient vector of the disease in northwestern Italy (Tedeschi et al., 2002). Despite observed decreases in C. melanoneura populations (Mattedi et al., 2007), large populations can be found in some areas of Trentino, such as Valsugana.
In light of these observations, we chose to focus our attention on C. melanoneura, to better understand the factors that may affect its population dynamics and its role in vectoring the disease. C. melanoneura is a univoltine species. Overwintering adults usually return to apple orchards at the end of January. The new generation of adult insects leaves apple orchards between mid-May and mid-June and overwinters on conifers at high altitudes (Pedrazzoli et al., 2005).
This study investigated the interaction between ‘Ca. P. mali’ and C. melanoneura. In particular, we studied the effects of ‘Ca. P. mali’ on the longevity of overwintered adults, the numbers of eggs laid, the rate of egg hatching and the juvenile survival.
Section snippets
Bioassay
The effect of ‘Ca. P. mali’ on C. melanoneura was studied by evaluating the survival and reproductive performance of overwintered females. As it is not possible to rear C. melanoneura in the laboratory, psyllids were collected from asintomatic apple trees in an orchard in Trentino (northeastern Italy). Sweep netting was used to collect insects at the population peak, which, in 2007, was delayed to late March (due to climatic condition). The proportion of naturally infected individuals in this
Results and discussion
No significant differences were observed between the survival of C. melanoneura adults reared on AP-infected shoots and those reared on healthy shoots (Wilcoxon χ2 = 0.012; df = 1; P = 0.998). The mean and median survival times observed on healthy shoots were 10.00 ± 3.68 and 2.00 days, respectively, whereas the mean and median survival times on AP-infected shoots were 7.70 ± 2.70 and 6.00 days, respectively. On the healthy shoots, a pre-oviposition time of 2.8 ± 0.80 days and an egg-laying period of 24.40 ±
Acknowledgments
The authors thank Dr. A. M. Ciccotti, I. Battocletti and M. Deromedi for the micropropagated plant material and L. Mattedi for suggestions regarding the insects. This research was financed by the Province of Trento.
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