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      Distribution and Relative Abundance of Insect Vectors of Xylella fastidiosa in Olive Groves of the Iberian Peninsula

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          Abstract

          The phytosanitary emergency caused by the spread of Xylella fastidiosa in the Mediterranean has raised demands for a better understanding of the ecology of its presumed and candidate insect vectors. Here, we present the results of a two-year survey carried out in olive groves across southern, eastern and Central Spain and northeastern Portugal. Several sampling methods were tested and compared to select the most appropriate to estimate population levels of potential vectors of X. fastidiosa. The spittlebugs Philaenus spumarius and Neophilaenus campestris (Hemiptera: Aphrophoridae) were the main species associated with olive groves. Both species were widely present on herbaceous ground vegetation within the olive groves; P. spumarius mainly associated with Asteraceae and N. campestris with Poaceae. Due to the patchy distribution of spittlebugs within the olive groves, sweep nets were the most effective and least time-consuming sampling method for the estimation of population size both in the ground cover and tree canopies. Trends in population density showed that spittlebugs can be abundant on ground vegetation but very rare on olive canopies. Spittlebugs disperse in late spring to non-cultivated hosts that act as natural reservoirs. In late fall, adults return to the olive groves for oviposition. However, olive trees may act as transient hosts for spittlebugs and high population densities of these insect vectors should be avoided in areas where X. fastidiosa is present.

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          Scientific Opinion on the risks to plant health posed byXylella fastidiosain the EU territory, with the identification and evaluation of risk reduction options

          (2015)
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            Isolation and pathogenicity of Xylella fastidiosa associated to the olive quick decline syndrome in southern Italy

            In autumn 2013, the presence of Xylella fastidiosa, a xylem-limited Gram-negative bacterium, was detected in olive stands of an area of the Ionian coast of the Salento peninsula (Apulia, southern Italy), that were severely affected by a disease denoted olive quick decline syndrome (OQDS). Studies were carried out for determining the involvement of this bacterium in the genesis of OQDS and of the leaf scorching shown by a number of naturally infected plants other than olive. Isolation in axenic culture was attempted and assays were carried out for determining its pathogenicity to olive, oleander and myrtle-leaf milkwort. The bacterium was readily detected by quantitative polymerase chain reaction (qPCR) in all diseased olive trees sampled in different and geographically separated infection foci, and culturing of 51 isolates, each from a distinct OQDS focus, was accomplished. Needle-inoculation experiments under different environmental conditions proved that the Salentinian isolate De Donno belonging to the subspecies pauca is able to multiply and systemically invade artificially inoculated hosts, reproducing symptoms observed in the field. Bacterial colonization occurred in prick-inoculated olives of all tested cultivars. However, the severity of and timing of symptoms appearance differed with the cultivar, confirming their differential reaction.
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              Transmission ofXylella fastidiosaby naturally infectedPhilaenus spumarius(Hemiptera, Aphrophoridae) to different host plants

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                Author and article information

                Journal
                Insects
                Insects
                insects
                Insects
                MDPI
                2075-4450
                01 December 2018
                December 2018
                : 9
                : 4
                : 175
                Affiliations
                [1 ]Instituto de Ciencias Agrarias, Consejo Superior de Investigaciones Científicas, ICA-CSIC, 28006 Madrid, Spain; mmorentediaz@ 123456gmail.com (M.M.); danielecornara@ 123456gmail.com (D.C.); mariap@ 123456ica.csic.es (M.P.); amoreno@ 123456ica.csic.es (A.M.)
                [2 ]Laboratorio de Producción y Sanidad Vegetal, Junta de Andalucía, 41089 Sevilla, Spain; jmanuel.duran@ 123456juntadeandalucia.es
                [3 ]CITOLIVA, Centro Tecnológico del Olivar y del Aceite, Mengíbar, 23620 Jaen, Spain; ccapiscol@ 123456citoliva.es (C.C.); rtrillo@ 123456citoliva.es (R.T.)
                [4 ]Laboratorio de Producción y Sanidad Vegetal, Junta de Andalucía, 23620 Jaén, Spain; manuelj.ruiz.torres@ 123456juntadeandalucia.es
                [5 ]Instituto de Agricultura Sostenible, Consejo Superior de Investigaciones Científicas, IAS-CSIC, 14004 Córdoba, Spain; cs9carum@ 123456uco.es
                [6 ]Cooperativa Agricola Villena. Ctra. del Puerto, s/n-03400, Villena, 03040 Alicante, Spain; susana.sanjuan@ 123456agricolavillena.com
                [7 ]Instituto Politécnico de Bragança-Campus de Santa Apolónia, 5300-253 Bragança, Portugal; jpereira@ 123456ipb.pt
                Author notes
                [* ]Correspondence: a.fereres@ 123456csic.es ; Tel.: +34-91-745-25-00
                Author information
                https://orcid.org/0000-0001-8258-2291
                https://orcid.org/0000-0002-2260-0600
                https://orcid.org/0000-0001-6012-3270
                Article
                insects-09-00175
                10.3390/insects9040175
                6315892
                30513710
                43e909e8-9eb6-4b3d-a795-0161532e613f
                © 2018 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 02 October 2018
                : 26 November 2018
                Categories
                Article

                philaenus spumarius,neophilaenus campestris,population density,sampling methods,spittlebugs

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