Light quality affects in vitro adventitious rooting and ex vitro performance of cherry rootstock Colt

The effect of light quality on in vitro rooting of cherry rootstock “Colt” was studied to evaluate adventitious root development, ex vitro acclimatization and plant growth performance. Adventitious rooting was dependent on the light quality to which the microcutting were exposed. Highest number of roots per microcuttings was recorded under dichromatic light (blue + red). This response could be ascribed to the control of a strong synergistic interaction between phytochromes and blue light photoreceptors. Red light was more effective on root elongation than blue light. In this response a strong synergistic interaction between phytochromes and blue light photoreceptors was suggested. The effect of light quality on the number of root/explant affected the plant during acclimation, scoring the highest level of plant survival in the blue-, red- and blue + red-exposed plantlets. The light quality effect was also observed under greenhouse culture conditions, as shown by growth parameters at the end of six months in plants growth. No specific role was observed for the photoequilibrium of phytochrome. The results reported in this work show that plantlets exposed to different light quality, during the in vitro rooting phase, retain the light quality effects in the subsequent plant acclimatization and greenhouse plant growth phase.     

Nutritional (Fe-Mn) interactions in ‘Big Top’ peach plants as influenced by the rootstock and by the soil CaCO3 concentration

Manganese (Mn) toxicity in plants is often not a clearly identifiable disorder and it can interfere with the absorption, translocation, and utilization of other elements such as Ca, Mg, Fe, and P. Soil conditions, management factors, and the use of different genotypes of rootstock can determine the degree of Mn toxicity and of interaction with other elements in the orchard. Five plants of the cultivar ‘Big Top’® grafted onto itself, onto plum rootstock ‘Mr.S.2/5’ and onto hybrid peach x almond rootstock ‘GF677’ were grown in 25-L containers under three treatments, 0, 20, 30% concentration of total lime, obtained by mixing powdered CaCO₃ to a sandy soil. Plants were fertilized with manure and a solid fertilizer early in April and irrigated in summer periodically with water rich in manganese. After just 28 d, active lime caused a decrease of chlorophyll SPAD index especially in plants grafted on itself, while those grafted on the tolerant ‘GF677’ rootstock behaved better than those grafted on ‘Mr.S.2/5.’ From June to September, irrigation caused increases in soil Mn concentration and Mn concentration in control plants. This caused first a serious defoliation in Big Top / Big Top plants and then a re-greening of cultivar grafted onto ‘Mr.S.2/5’ and ‘GF677,’ probably due to the interaction between iron and manganese at high pH. In particular the 20% CaCO₃ addition to the soil preserved the plants of cultivar grafted onto ‘Mr.S.2/5’ from Mn toxicity, as shown by their high chlorophyll content and growth and lower Mn leaf concentrations. Plants grafted onto ‘GF677’ rootstock showed the best behaviour under 30% CaCO₃ treatment associated to higher Fe(III)-reducing capacity and photosynthetic activity. Rootstocks and soil conditions (lime and waterlogging) influenced mineral status and growth of the peach cultivar ‘Big Top,’ particularly by interacting together and modifying Fe-Mn availability.     

In vitro study of the replication capacity of the RGNNV and the SJNNV betanodavirus genotypes and their natural reassortants in response to temperature

Betanodaviruses are the causative agents of viral nervous necrosis and affect a broad range of fish species worldwide. Their bi-segmented genome is composed of the RNA1 and the RNA2 molecules encoding the viral polymerase and the coat protein, respectively. In southern Europe the presence of the RGNNV and the SJNNV genotypes, and the RGNNV/SJNNV and RGNNV/SJNNV reassortants has been documented. Several studies have reported a correlation between water temperature and disease onset. To explore the replication efficiency of betanodaviruses with different genomes in relation to temperature and to understand the role of genetic reassortment on viral phenotype, RGNNV, SJNNV, RGNNV/SJNNV and RGNNV/SJNNV field isolates were fully sequenced, and growth curves generated in vitro at four different temperatures (15, 20, 25, 30 °C) were developed for each isolate. The data obtained, corroborated by statistical analysis, demonstrated that viral titres of diverse betanodavirus genotypes varied significantly in relation to the incubation temperature of the culture. In particular, at 30 °C betanodaviruses under investigation presented different phenotypes, and viruses containing the RNA1 of the RGNNV genotype showed the best replication efficiency. Laboratory results demonstrated that viruses clustering within the same genotype based on the polymerase gene, possess similar growth kinetics in response to temperature, thus highlighting the key role of RNA1 in controlling viral replication at different environmental conditions. The results generated might have practical implications for the inference of viral phenotype according to genetic features and may contribute to a better understanding of betanodavirus ecology.     

Characterisation of Oil-Degrading Bacteria Isolated from Bilge Water

During an initial screening in samples of bilge water, four bacterial strains capable to oil degrade have been isolated. Two strains, named isolates BW-1 and BW-2, were clustered with Acinetobacter genus (a similarity of 100% and 99%, respectively) and two strains, named isolates BW-3 and BW-4 were related to Rhodococcus genus (a similarity of 99% and 98%, respectively). During growth (8?days) in M9 medium with Arabian Light Crude Oil (1%, w/v), measures of microbial abundance, surface tension, emulsification index (E ₂₄) and oil degradation, were carried out. During cultivation, isolates BW-1 and BW-2 are good biosurfactant producers and about 80% of crude oil is degraded. Also, isolates BW-3 and BW-4 show, during cultivation, production of biosurfactant but only 40% of total oil is degraded. Data obtained give important results in order to utilise these isolate native bilge waste microorganisms in the studies/process of bioremediation.     

West Nile Virus in North‐Eastern Italy, 2011: Entomological and Equine IgM‐Based Surveillance to Detect Active Virus Circulation

Since 2008, West Nile Virus (WNV) has expanded its range in several Italian regions, and its yearly recurrence suggests the virus may have become endemic in some areas. In 2011, a new plan based also on the detection of IgM antibodies was implemented in the north‐eastern Italian regions of Veneto and Friuli Venezia Giulia, aiming to early detect WNV infections in areas where the virus had already circulated during the previous summers, and in adjacent zones. From July to November 2011, 1880 sera from 521 equine premises were screened by a commercial IgM capture ELISA. Mosquitoes were captured by CDC‐CO₂ traps at 61 locations in the two regions. Collected mosquitoes were identified, pooled by species/date/location and examined by real‐time RT‐PCR and sequencing. Passive surveillance was carried out on clinically affected horses and non‐migratory wild birds found dead. IgM sero‐positive equines were detected in 19 holdings, five in the area with WNV circulation (AWC) and 14 in the surveillance area (SA); 10 more horse premises tested positive to further serological controls within 4 km of the positive holdings. A total of 85 398 mosquitoes of 15 species were collected and 2732 pools examined. Five Culex pipiens pools tested positive for the presence of WNV. Passive surveillance on non‐migratory wild birds allowed detection of the virus only in one found dead collared dove (Streptopelia decaocto), of 82 birds sampled. The WNV belonged to the lineage 2, which had been isolated for the first time in Italy earlier in 2011. By the first week of October, nine human cases had been confirmed in the same area. The implementation of a protocol combining IgM screening of horses with surveillance on mosquito vectors proved to be valuable for early detecting WNV circulation.