Biancalani, Carola

Bini, L.

Calamai, Silvia

Cerboneschi, Matteo

Tegli, Stefania

English

Florence Research

An International Journal of the Italian Society for Plant PathologyJournal of Plant PathologyFormerly    Rivista di patologia vegetale established in 1892EDIZIONI ETS, Pisa, Italy ISSN 1125-4653Poste Italiane S.p.A. - Spedizione in Abbonamento Postale - D.L. 353/2003 (conv. in L. 27/02/2004 n° 46) art. 1, comma 1 - DCB AREA CENTRO 1/Pisa.Volume 99 (Supplement) October 2017Piacenza, October 4-6, 2017Abstracts of papersXXIII NATIONAL MEETINGOF THE ITALIAN SOCIETY FOR PLANT PATHOLOGY (SIPaV) JPP 99 (supp.).indb   1 22/09/17   10:06Journal of Plant Pathology (2017), 99 (Supplement), Posters S43EVIDENCE FOR THE INVOLVEMENT OF VP37 OF BROAD BEAN WILT VIRUS 1 IN THE INDUCTION OF PLANT SYMPTOMS AND POSTRANSCRIPTIONAL GENE SILENC-ING. C. Carpino1,2, I. Ferriol2, L. Elivira-Gonzalez2, L. Rubio2,3, E. Peri1, S. Davino1, L. Galipienso2,3,4. 1 Department of Agricultural and Forestry Science, University of Palermo, Piazza Marina 61, 90133 Palermo, Italy. 2 Instituto Valenciano de Investigaciones Agrarias (IV-IA), Ctra. CV-315, 46113 Moncada, Valencia, Spain. 3 Euro- Mediter-ranean Institute of Science and Technology (IEMEST), Via Michele Miraglia 20, 90139 Palermo, Italy. 4 Departamento de Biotecnología, Escuela Técnica Superior de Ingeniería Agronómica y del Medio Natu-ral, Universidad Politécnica de Valencia, Camino de Vera s/n, 46022 Valencia, Spain. E-mail: salvatore.davino@unipa.itBroad bean wilt virus 1 (BBWV-1, genus Fabavirus, family Seco-viridae) infects economically important crops (broad bean, pepper, tomato, spinach and ornamental plants) and is worldwide distrib-uted. It is constituted by two positive ssRNA molecules that encode two polyproteins further processed by proteolytic cleavage. RNA-1 encodes proteins necessary for viral replication and expression, whereas RNA-2 encodes a movement protein (MP) and two coat proteins (LCP and SCP). RNA-2 contains an alternative start codon that renders a smaller putative protein (VP37). Until now, BBWV-1 pathogenicity determinants were not identified, and proteins related to symptomatology induction were unknown. In this work BBWV-1 putative VP37 was identified as the main responsible for virus-in-duced symptomatology in Nicotiana benthamiana and broad bean using a BBWV-1 infectious clone and a BBWV-1 mutant. Moreover, VP37 transient expression through a Potato Virus X (PVX) vector caused necrotic lesions in N. benthamiana, indicating that this pro-tein acts as a pathogenicity determinant. Finally, transient expres-sion of VP37 in N. benthamiana 16C, that constitutively expresses the Green Fluorescent Protein (GFP), and a complementation assay with a vector based on Turnip crinkle virus sequence (TCV-sGFP) showed that this protein acts as suppressor of post transcriptional gene silencing (PTGS).Together our results demonstrate that VP37 putative protein is directly involved in the elicitation of BBWV-1 symptomatology in N. benthamiana and broad bean, and that this protein is a symptom determinant and acts as gene silencing suppressor.IDENTIFICATION OF A MULTIDRUG AND TOXIC EXTRU-SION TRANSPORTER INVOLVED IN THE SECRETION OF INDOLE-3-ACETIC ACID AND ITS CONJUGATES IN PSEU-DOMONAS SAVASTANOI. M. Cerboneschi, C. Biancalani, S. Calamai, L. Bini, S. Tegli. Dipartimento di Scienze Produzioni Agroalimentari e dell’Ambiente (DISPAA), Laboratorio di Patologia Vegetale Molecolare, Università degli Studi di Firenze, Via della La-struccia 10, 50019 Sesto Fiorentino (Firenze), Italy. Email: matteo.cerboneschi@unifi.itPseudomonas savastanoi (Psv) is the causal agent of olive and ole-ander knot disease, characterised by hyperplastic galls on the aerial parts, and whose development is dependent on a functional type III secretion system (TTSS) and on the expression of hrp genes. Several phytohormones produced by Psv, i.e. the auxin 3-indole-acetic acid (IAA) and the cytokinin trans-zeatin, are also involved in knot formation. Psv synthesizes IAA from tryptophan, by the se-quential activity of the enzymes IAAM and IAAH encoded by the homonymous genes. In Psv the iaaL gene is also present, coding for an enzyme for conjugation of IAA to lysine to give IAA-Lys. In the genome of the oleander strain Psn23, the iaaM/iaaH operon is lo-cated close to the iaaL gene, which upstream has an ORF encoding a putative multidrug and toxic compound extrusion (MATE) trans-porter (named matE). The IAA-driven inhibition of hrp genes, as well as data from phenotype microarray analysis on ΔiaaM, ΔiaaL and ΔmatE mutants, strongly suggested a functional link existing in Psv between IAA metabolism, TTSS and MATE. Here, through an integrated approach among bioinformatic analysis, structural biol-ogy and site-directed mutagenesis on Psn23 MATE, and HPLC-MS analysis of bacterial auxin production, we found the transporter en-coded by matE contributing to this picture, by mediating IAA and IAA-Lys efflux. This is the first report of a MATE responsible for auxin transport in bacteria. Because of its role on IAA homeostasis in Psv, these findings could also contribute to the development of novel anti-infectives targeting Psv MATE.We gratefully acknowledge EU Commission (project LIFE12 ENV/IT/336 “AFTER Cu”) and Ente Cassa di Risparmio di Firenze (project 2015.0999) for their financial support.INTERFERENCES ON THE DETECTION OF XYLELLA FASTIOSA IN POLYGALA MYRTIFOLIA BY REAL-TIME PCR. V. Chiatti1,2, N. Pucci1, S. Lucchesi1, V. Modesti1, M. Rever-beri2, S. Loreti1. 1 Centro di ricerca per la patologia vegetale (CREA-PAV) via C.G. Bertero 22, 00156 Roma. 2 Dipartimento di Biologia Ambientale, Sapienza Università di Roma. E-mail: stefania.loreti@crea.gov.itXylella fastidiosa (Xf) is a harmful quarantine pathogen that colonizes the xylem vessels of a wide range of host plants. Recently introduced in Europe, it occurred in France on Polygala myrtifo-lia and in Apulia (Southern Italy) on Olea europaea. The disease named “quick decline syndrome of olive” has been associated with the strain CoDiRO, belonging to the subspecies pauca (vari-ant “sequence type 53”). The outbreak on P. myrtifolia was instead caused by the subsp. multiplex. A national research plan has been established, in order to control the disease and perform monitoring activities in pest-free areas. The scope of our studies was to develop and harmonize diagnostic protocols of Xf, mainly on olive – being an economically valuable species – and on P. myrtifolia, which is affected by both the subspecies, and is in evaluation as “spy-indica-tor” plant specie in risky locations to support the early detection of Xf. Two different real-time PCR assays (based on TaqMan™ and EvaGreen™) were used. The overall results proved the assays to be appropriate for testing olive samples. Further investigation was needed for P. myrtifolia, due to ambiguous results obtained with both assays on 38.7% of the samples. To understand the nature of the interference, sequencing of a non specific amplicon obtained by the real-time PCR assay was performed, with no relevant matches found in the BLAST database. The possibility to obtain indeter-minate results by real-time PCR has to be considered when official analyses of P. myrtifolia are performed, to avoid the risk of misin-terpretation of the final results.BIOLOGICAL ACTIVITY OF ALKALI PRE-TREATED ARUNDO DONAX EXTRACT TOWARDS DIFFERENT FILA-MENTOUS FUNGI. S. Cianchetta, M. Nota, S. Galletti. Consiglio per la ricerca in agricoltura e l’analisi dell’economia agraria, Centro di ricerca Agricoltura e Ambiente (CREA-AA), Via di Corticella 133, 40128 Bologna, Italy. E-mail: stefania.galletti@crea.gov.itGiant reed (Arundo donax L.) is considered one of the most promising lignocellulosic species for bioenergy in the Mediterra-nean environment, for its high productivity and low input require-ments. In the framework of the AGROENER project, funded by MiPAAF, a study is undergoing on the possibility of exploiting the biomass as substrate for oleagineous microorganisms, after a delignifying pre-treatment, for the production of 2nd generation biodiesel. The spectrophotometric analysis of an extract, obtained after alkaline pre-treatment of giant reed dry biomass, revealed the JPP 99 (supp.).indb   43 22/09/17   10:06

IDENTIFICATION OF A MULTIDRUG AND TOXIC EXTRUSION TRANSPORTER INVOLVED IN THE SECRETION OF INDOLE-3-ACETIC ACID AND ITS CONJUGATES IN PSEUDOMONAS SAVASTANOI.

https://flore.unifi.it/bitstream/2158/1101578/1/SIPAV2017_JPP_Cerboneschietal_S43.pdf

IDENTIFICATION OF A MULTIDRUG AND TOXIC EXTRUSION TRANSPORTER INVOLVED IN THE SECRETION OF INDOLE-3-ACETIC ACID AND ITS CONJUGATES IN PSEUDOMONAS SAVASTANOI.

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