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Citrus tristeza virus (CTV) is the pathogen causing tristeza diseases in several Rutaceae species and leading to significant economic damage to citrus worldwide. The Ctv locus provides broad spectrum resistance to CTV in Poncirus trifoliata L. Raf. This locus is present also in tolerant and susceptible species, so an epigenetic mechanism of Ctv expression regulation was proposed. Indeed, a difference in plant 24-nt sRNAs distribution corresponding to CTV.20 gene was previously observed in susceptible species following CTV infection. This gene, encoding for a plant virus movement-like protein, was investigated as a candidate gene for CTV susceptibility. Here, we show the presence of differences in methylation status of a specific region of CTV.20 in two susceptible species, sour and sweet orange, following CTV infection. On the contrary, no significant differences were observed in the tolerant Citrange carrizo following the infection. Moreover, a hypermethylation of the whole CTV.20 gene was observed in Citrange carrizo both healthy and infected, and in healthy sour and sweet orange. This preliminary study allows hypothesizing a possible role of methylation in regulation of CTV.20 expression involved in the CTV susceptibility.

The vector-borne bacterial pathogenXylella fastidiosais widely distributed in the Americas; in the last decade it has emerged as a serious threat for agricultural crops, natural environment and landscape in Europe. Following the first EU outbreak in 2013 in southern Italy, associated with a severe disease in olive trees, annual mandatory surveys are now in place in the Member States, leading to the discovery of bacterial outbreaks in different countries. Among the latest findings, an outbreak has been reported in the Italian region of Tuscany, with infections identified in seven different plant species. In this work, we report the isolation and the genetic characterization of isolates associated with this newly discovered outbreak. Multilocus sequence typing approach revealed the occurrence of isolates harbouring a new sequence type, denoted ST87, genetically related to strains of subsp.multiplex, but different from the genotypes of this subspecies previously characterized in Europe. Five cultured strains were successfully recovered from four of the seven host plants, an important achievement for advancing the studies on genomics and pathogenicity of theseisolates and thus assess their potential threat for European agriculture.

The olive quick decline syndrome (OQDS) is a disease that appeared suddenly a few years ago in the province of Lecce (Salento peninsula, southeastern Italy). Among the factors that may be involved in its aetiology, the most relevant is Xylella fastidiosa, a quarantine pathogen of American origin, whose presence in Italy represents its first confirmed record in the European Union. X. fastidiosa is a Gram-negative bacterium that invades the xylem of a wide range of hosts, from which it is acquired by xylem-feeding insect vectors and transferred to other plants. The bacterium multiplies within the plant vessels and occludes them, thus impairing water uptake. Besides olive, the Salentian strain of X. fastidiosa infects in nature a number of woody (almond, cherry) and shrubby (oleander, broom, Acacia saligna, Polygala myrtifolia, Westringia fruticosa, Rosmarinus officinalis, Rhamnus elaternus, Myrtus communis) hosts, with no evidence for grapevines or citrus being hosts. The bacterium was isolated in culture and identified as a genotype of X. fastidiosa subsp. pauca, molecularly identical to an isolate from Costa Rica. Philaenus spumarius (meadow spittlebug), a froghopper quite common in the Salento area where it thrives on olive, was identified as the main vector. Disease eradication and sanitation of infected olives are unfeasible. However, strategies are being enacted for restraining the spread of pathogen and vector(s) within the boundaries of the currently infected zone.

Citrus, one of the most economically important crops, is susceptible to a number of arthropod- and graft-transmissible pathogens. Rapid and reliable methods for detecting multiple pathogens are important for routine diagnosis by reducing time, labour and costs. To this end, primers and TaqMan probes for Citrus psorosis virus (CPsV) and Citrus variegation virus (CVV) detection by singleplex real-time (q) reverse transcription (RT)- PCR were initially designed. Further optimizations included the development of a multiplex (m) RT-qPCR assay to detect simultaneously CPsV, CVV, and Citrus tristeza virus (CTV) in a single reaction. When 10-fold serial dilutions prepared using total RNAs from CPsV- and CVV-infected plants were tested, RT-qPCR assays proved to be 100 and 1000 times more sensitive than conventional RT-PCR, respectively. The target viruses were effectively identified by mRT-qPCR in field-infected clementine and sweet orange trees. The optimized multiplex assay proved to be as sensitive as the singleplex tests, thus providing a valuable alternative tool for detection of these citrus viruses.