* El-Deen Abd El-Wahab AS, Abdel-Kader El-Sheikh M, Elnagar S (2011) First record of Frankliniella occidentalis and Impatiens necrotic spot virus in Egypt. Journal of Life Sciences 5, 690-696.
------- Considered to be doubtful as ELISA test only gave a weak reaction.
* Cooper WR, Horton DR, Milickzy E, Wohleb CH, Waters TD (2019) The weed link in zebra chip epidemiology: suitability of non-crop
Solanaceae and Convolvulaceae to potato psyllid and 'Candidatus Liberibacter Solanacearum. American Journal of Potato Research. DOI: 10.1007/s12230-019-09712-z
------- Found to be NOT susceptible in this study.
* Torres GL, Cooper WR, Horton DR, Swisher KD, Garczynski SF, Munyaneza JE, Barcenas NM (2015) Horizontal transmission of 'Candidatus Liberibacter solanacearum' by Bactericera cockerelli (Hemiptera: Triozidae) on Convolvulus and Ipomoea (Solanales: Convolvulaceae). PLOS ONE 10(11), e0142734.
* Goodey JB, Franklin MT, Hooper DJ (1965) T. Goodey's: The Nematode Parasites of Plants Catalogued Under Their Hosts. Commonwealth Agricultural Bureaux, Farnham Royal, Bucks, England. Third edition, 214 pp.
* Parrella G, Gognalons P, Gebre-Selassie K, Vovlas C, Marchoux G (2003) An update of the host range of tomato spotted wilt virus. Journal of Plant Pathology 85(4), 227-264.
------- Confirmed host.
* EFSA (2024) Update of the Xylella spp. host plant database – Systematic literature search up to 31 December 2023. EFSA Journal 22, e8898. https://efsa.onlinelibrary.wiley.com/doi/epdf/10.2903/j.efsa.2024.8898
------- Subspecies unknown.
* Boopathi T (2022) New host plants, natural enemy complex and newly distributed potential areas of exotic spiralling whitefly (Hemiptera: Aleyrodidae) in India. Phytoparasitica 50(2), 335-357.
* Vereijssen J (2020) Ecology and management of Bactericera cockerelli and Candidatus Liberibacter solanacearum in New Zealand. Journal of Integrative Agriculture 19(2), 333–337.
* Zaidi SSEA, Martin DP, Amin I, Farooq M, and Mansoor S (2017) Tomato leaf curl New Delhi virus: a widespread bipartite begomovirus in the territory of monopartite begomoviruses. Molecular Plant Pathology, 18, 901–911. (online supplemental material)
* Longone V, Gonzalez F, Zamorano A, Pino AM, Araya J, Diaz V, Paltrinieri S, Calari A, Bertaccini A, Picciau L, Alma A, Fiore N (2011) Epidemiological aspects of phytoplasmas in Chilean grapevines. Bulletin of Insectology 64 (Supplement), S91-S92.
* Seemüller E (2002) Apple proliferation: Etiology, epidemiology and detection. In: Brunelli A, Canova A (Eds.) Proceedings Giornate Fitopatologiche Vol. 1. Baselga di Piné (TN), 3-6.
* Seemuller E, Garnier M, Schneider B (2002) Mycoplasmas of plants and insects. In: Molecular biology and pathogenicity of mycoplasmas (Eds Razin S & Herrmann R), pp. 91–115. Kluwer Academic Publishers/Plenum Publishers, New York, NY (US). 572 pp.
* Aryan A, Brader G, Mörtel J, Pastar M, Riedle-Bauer M (2014) An abundant ‘Candidatus Phytoplasma solani’ tuf b strain is associated with grapevine, stinging nettle and Hyalesthes obsoletus. European Journal of Plant Pathology 140, 213–227.
* Ember I, Acs Z, Munyaneza JE, Crosslin JM, Kolber M (2011) Survey and molecular detection of phytoplasmas associated with potato in Romania and southern Russia. European Journal of Plant Pathology 130(3), 367-377.
* Kosovac A, Radonjić S, Hrnčić S, Krstić O, Toševski I, Jović J (2016) Molecular tracing of the transmission routes of bois noir in Mediterranean vineyards of Montenegro and experimental evidence for the epidemiological role of Vitex agnus-castus (Lamiaceae) and associated Hyalesthes obsoletus (Cixiidae). Plant Pathology 65, 285–298.
* Mori N, Quaglino F, Tessari F, Pozzebon A, Bulgari D, Casati P, Bianco PA (2014) Investigation on ‘bois noir’epidemiology in north‐eastern Italian vineyards through a multidisciplinary approach. Annals of Applied Biology 166(1), 75-89.
* Quaglino F, Maghradze D, Chkhaidze N, Casati P, Failla O & Bianco PA (2014) First report of 'Candidatus Phytoplasma solani' and 'Ca. P. convolvuli' associated with grapevine bois noir and bindweed yellows, respectively, in Georgia. Plant Disease 98(8), p 1151.
* Quaglino F, Murolo S, Zhao Y, Casati P, Durante G, Wei W, Bianco PA, Romanazzi G, Davis RE (2017) Identification of new -J and -K 16SrXII subgroups and distinct single nucleotide polymorphism genetic lineages among 'Candidatus Phytoplasma solani' strains associated with bois noir in Central Italy. Australasian Plant Pathology 46(1), 31-34.
* Quaglino F, Passera A, Faccincani M, Moussa A, Pozzebon A, Sanna F, Casati P, Bianco PA, Mori N (2021) Molecular and spatial analyses reveal new insights on Bois noir epidemiology in Franciacorta vineyards. Annals of Applied Biology (early view). https://doi.org/10.1111/aab.12694
* Quaglino F, Zhao Y, Casati P, Bulgari D, Bianco PA, Wei W, Davis RE (2013) ‘Candidatus Phytoplasma solani’, a novel taxon associated with stolbur- and bois noir-related diseases of plants. International Journal of Systematic and Evolutionary Microbiology 63, 2879-2894.
* Salem NM, Quaglino F, Abdeen A, Casati P, Bulgari D, Alma A, Bianco PA (2013) First report of 'Candidatus phytoplasma solani' strains associated with grapevine bois noir in Jordan. Plant Disease 97(11), p 1505.
* Orfanidou CG, Dimitriou C, Papayiannis LC, Maliogka VI, Katis NI (2014) Epidemiology and genetic diversity of criniviruses associated with tomato yellows disease in Greece. Virus Research 186, 120–129.
* Adlerz WC (1980) Ecological observations on two leafhoppers that transmit the Pierce’s disease bacteria. Proceedings of the Florida State Horticultural Society 93, 115-120.
------- Adults were observed on this plant.
* Kosovac A, Jakovljević M, Krstić O, Cvrković T, Mitrović M, Toševski I, Jović J (2019) Role of plant-specialized Hyalesthes obsoletus associated with Convolvulus arvensis and Crepis foetida in the transmission of ‘Candidatus Phytoplasma solani’-inflicted bois noir disease of grapevine in Serbia. European Journal of Plant Pathology 153(1), 183-195.
* Janssen D, Ruiz L, Velasco L, Segundo E, Cuadrado IM. (2002) Non-cucurbitaceous weed species shown to be natural hosts of Cucumber vein yellowing virus in south-eastern Spain. Plant Pathology 51(6), 797.
* Papayiannis LC, Kokkinos CD, Alfaro-Fernandez A (2011) Detection, characterization and host range studies of Pepino mosaic virus in Cyprus. European Journal of Plant Pathology 132, 1-7.
* Akel E, Ismail ID, Al-Chaabi S, Fuentes S (2010) New natural weed hosts of Sweet potato feathery mottle virus in Syria. Arab Journal of Plant Protection 28(1), 96-100.
* Ahmad M, Ghaffar A, Rafiq M (2013) Host plants of leaf worm, Spodoptera litura (Fabricius)(Lepidoptera: Noctuidae) in Pakistan. Asian Journal of Agriculture and Biology 1(1), 23-28.
* British Columbia Ministry of Agriculture. Western yellowstriped armyworm (Spodoptera praefica). https://rdno.civicweb.net/document/127358/western-yellowstriped-armyworm.pdf?handle=3CD053B4F8D54F9CBB93F8D6D5572C27
* Ferragut F, Escudero LA (1999) Tetranychus evansi Baker & Pritchard (Acari, Tetranychidae), una nueva araña roja en los cultivos horticolas españoles. Boletin de Sanidad Vegetal, Plagas, 25: 157-164.
* Ferreira MA, Sousa ME (2011) Hosts and Distribution of the Spider Mite Tetranychus evansi (Acari: Tetranychidae) in Portugal. Hale, C., Xxviii International Horticultural Congress on Science and Horticulture for People, Leuven 1, Int Soc Horticultural Science, (917): 133-136.
* Tuttle DM, Baker EW, Sales FM (1977) Spider mites (Tetranychidae: Acarina) of the state of Ceara, Brazil. International Journal of Acarology, 3: 1-8.
* Cultrona M, Bonini N, Pacifico D, Tessitori M (2024) First report of Convolvulus arvensis and Polycarpon tetraphyllum as natural hosts of tomato brown rugose fruit virus. Plant Disease 108(3), 827. https://doi.org/10.1094/PDIS-11-23-2413-PDN
------- Natural host (asymptomatic).
