Nosema ceranae is a widespread obligate intracellular parasite of the ventriculus of many species of honey bee (Apis), including the Western honey bee Apis mellifera, in which it may lead to colony death. It can be controlled in A. mellifera by feeding the antibiotic fumagillin to a colony, though this product is toxic to humans and its use has now been banned in many countries, so in beekeeping, there exists a need for alternative and safe products effective against N. ceranae. Honeybees produce propolis from resinous substances collected from plants and use it to protect their nest from parasites and pathogens; propolis is thought to decrease the microbial load of the hive. We hypothesized that propolis might also reduce N. ceranae infection of individual bees and that they might consume propolis as a form of self-medication. To test these hypotheses, we evaluated the effects of an ethanolic extract of propolis administered orally on the longevity and spore load of experimentally N. ceranae-infected worker bees and also tested whether infected bees were more attracted to, and consumed a greater proportion of, a diet containing propolis in comparison to uninfected bees. Propolis extracts and ethanol (solvent control) increased the lifespan of N. ceranae-infected bees, but only propolis extract significantly reduced spore load. Our propolis extract primarily contained derivatives of caffeic acid, ferulic acid, ellagic acid and quercetin. Choice, scan sampling and food consumption tests did not reveal any preference of N. ceranae-infected bees for commercial candy containing propolis. Our research supports the hypothesis that propolis represents an effective and safe product to control N. ceranae but worker bees seem not to use it to self-medicate when infected with this pathogen.

The effects of different nitrogen fertilization regimes on body size and selected life-history parameters (development time, survival, fecundity and fertility) of the vine mealybug, Planococcus ficus (Signoret) (Hemiptera: Pseudococcidae), were investigated on potted grapevines under laboratory and screenhouse conditions. In both trials, five groups of four grapevines each were supplied with 0, 0.25, 0.5, 1.0 or 2.0 g/l of ammonium nitrate fertilizer for a month and then artificially infested with 200 first-instar vine mealybugs (24 h of age). The concentration of nitrogen on grape leaves was measured during both experiments by a SPAD chlorophyll metre, showing statistical differences among treatments. The nitrogen fertilization significantly affected the investigated P. ficus parameters, providing consistent results in both laboratory and screenhouse trials. The vine mealybug females exhibited higher survival and fecundity, larger body size and lower development time on plants supplied with higher nitrogen fertilization rates. Survival, body size and fecundity of P. ficus were positively correlated with the leaf nitrogen concentration, whereas the development time was negatively correlated. Fertility did not vary significantly among treatments. Our results show that high nitrogen regimes increase the reproductive performance of P. ficus on grapevines and point out the importance of implementing balanced fertilization plans in grapevine IPM programs to reduce population densities and prevent insect outbreaks.

The effect of increasing mating delay on the reproductive performance and population growth rates of the vine mealybug, Planococcus ficus (Signoret) (Hemiptera: Pseudococcidae), was investigated under laboratory conditions. Virgin females were mated at 1, 3, 5, 7, 14, 21 and 28 days after emergence and reproductive and life table parameters were estimated. The pre-oviposition period (number of days between mating and the onset of oviposition) significantly decreased in females mated within 7 days, whereas females mated at older ages showed equivalent pre-oviposition periods (7 days, as shorter delays in mating did not reduce the population growth rates.

DNA extracted from 363 ticks collected in Ethiopia and 9 ticks collected in Chad, Africa were screened by PCR to detect DNA from spotted fever group rickettsiae. Fifteen ticks (4.1%) collected in Ethiopia and one tick (11%) collected in Chad tested positive when PCR targeting the gltA and ompA rickettsial genes was performed. PCR-positive products of the gltA and ompA genes were used for DNA sequencing. Rickettsia africae was detected in 12/118 Amblyomma lepidum and in 1/2 A. variegatum. Also, 2/12 Hyalomma marginatum rufipes collected in Ethiopia and one H. marginatum rufipes collected in Chad were positive for R. aeschlimannii. Our results confirm the previously reported presence of R. africae in Ethiopia and also show the first evidence of R. aeschlimannii in ticks collected in Ethiopia and Chad.

Our findings provide new insights into the mechanisms underlying the pheromone-based control of the vine mealybug and indicate that the reduction of the pest population density is attributable to both a decrease and a delay in female mating. In addition, the population density of vine mealybugs under mating disruption decreased over the years, indicating that consecutive applications of this control strategy would significantly increase the effectiveness of control of the vine mealybug by mating disruption. © 2018 Society of Chemical Industry.