The following results showed that PeBL1 significantly modified the tomato leaf surface structure to reduce reproduction and deter colonization by M. persicae. Clipboard, Search History, and several other advanced features are temporarily unavailable. In Brussels sprouts, Klaiber et al. Pre-infestation of Tomato Plants by Aphids Modulates Transmission-Acquisition Relationship among Whiteflies, Tomato Yellow Leaf Curl Virus (TYLCV) and Plants. Other aphids that vector poleroviruses include R. padi, Stiobion avenae, and Aphis gossypi. J Gen Virol 80(11):2823–2828, Syller J (1987) The influence of temperature on the transmission of Potato leafroll virus by Myzus persicae Sulz. Effectiveness of oil formulations can vary according to their own physical properties (Zitter and Ozaki, 1978). Donato Gallitelli, ... Giovanni P. Martelli, in Advances in Virus Research, 2012. Myzus persicae . Get the latest public health information from CDC: Beijing 100081, China/The State Key Laboratory for Bio-Pesticides Engineering of Plant Disease Biocontrol and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Science, No. The authors declare that they have no conflict of interest. Myzus persicae) infestation before the whitefly attack. 2000;19:195–216. Jemalong but reduced both of these parameters on N-fixing-deficient mutant dnfl1. Google Scholar, Diener T, Smith D, O’Brien MJ (1972) Potato spindle tuber viroid. Learn more about Institutional subscriptions, Bagnall RH (1977) Resistance to the aphid-borne viruses in the potato. Tobacco necrotic dwarf virus (TNDV) of the genus Enamovirus (family Luteoviridae) causes severe disease symptoms in some tobacco fields in Japan. If the species mainly uses dicots as their host, such as PLRV or Beet western yellows virus (BWYV), the virion instead moves through the midgut. Ryan et al. This provides evidence for the presence of this pest.. Myzus persicae (Sulzer) (Coutin R. / OPIE) New Dis Rep 27:8., Gray S, Gildow FE (2003) Luteovirus-aphid Interactions. Although treatments with alcohol or neutral detergents were not efficient in eliminating infected PLYV from contaminated agricultural tools, the virus is inactivated with 10% sodium hypochlorite, indicating the efficiency of this agent for the treatment of contaminated tools. Virology 48(3):844–846, Article  In laboratory experiments with M. euphorbiae, it was shown that mineral oil treatment induced a lack of attractiveness of the host plant, which lasted at least 24 h, while the feeding behavior on treated plants was modified throughout 1 week posttreatment. White (1971) showed that probably all, at least most, individuals of B. brassicae have wing rudiments and that a prenatal loss of wing-buds in embryos is probably caused by the activity of their maternal CA. Annu Rev Phytopathol 43:117–139, Fox A, Daly M, Nixon T, Brurberg M, Blystad D, Harju V, Skelton A, Adams I (2013) First report of Tomato chlorotic dwarf viroid in tomato in Norway and subsequent eradication. Alterations in the amino acids arginine, aspartate, glutamine, and valine in phloem sap partly explained the effects of eCO2 on aphids. in Slovenia. (2015) studied the performance of R. padi on barley under eCO2. The authors thank the members of the DSMZ Plant Virus Department for generous support and advice on the experimental design. The high stability of the virus particles could also facilitate their dissemination by human actions, which could explain the spreading of virus without a biologic vector (Camarço et al 1996, Lima & Lima 2002, Lima et al 2002, Saraiva et al 2006, Nascimento et al 2010). In additional experiments, these workers have demonstrated that nymph survival was significantly reduced on oil-treated plants, suggesting either a direct toxicity of the treated plant or an indirect effect. Moreover, serial passages of PLRV + TCDVd into host plants and non-host plants showed that TCDVd infections still could be detected in host plants (tomato) even after passage over non-host plants Brassica oleracea (20% compared to 33% only host plant passages). Amino acids essential for aphid growth increased in the phloem sap, so the aphid population increase under eCO2 could be explained in terms of nutrient translocation. Google Scholar, Flores R, Hernández C, Alba AEMd, Daròs J-A, Serio FD (2005) Viroids and viroid-host interactions. (2013a,b) found that eCO2 increased glucosinolate levels without altering primary metabolism and this reduced the performance of the vector species Brevicoryne brassicae (cabbage aphid). Eur J Plant Pathol 110(8):823–831, Verhoeven JTJ, Jansen CCC, Roenhorst JW (2008) First report of pospiviroids infecting ornamentals in the Netherlands: Citrus exocortis viroid in Verbena sp. This indicated that its diminished fitness may be due to poorer plant tissue quality and unfavorable C:N balance rather than due to impaired feeding. (2009, 2010) showed that M. euphorbiae increased its xylem sap consumption on treated plants. Italy is the only Mediterranean country where AV1 presence is documented. The ability of oil sprays to protect against nonpersistent viruses is limited in cases where the crop is under a pressure of large populations of viruliferous aphid vectors. This behavioral response occurred within 24 h of transfer to eCO2 conditions. The extent of damage in the Mediterranean basin is limited. (2013) investigated colonization of three alfalfa (lucerne) (Medicago sativa) cultivars by the aphid vector Acyrthosiphon pisum (pea aphid). doi: 10.1016/j.cropro.2009.01.005. -. Studies on the effect of various oil application methods on the spread of potato virus Y (PVY) and the phytotoxicity they might cause, have shown that control of spread, is largely depended on the concentration of the oil, and to a lesser extent, on its delivery rate (Boiteau and Singh, 1982). Plenum Press, New York, pp 235–258, Chung BN, Canto T, Tenllado F, San Choi K, Joa JH, Ahn JJ, Kim CH, Do KS (2016) The effects of high temperature on infection by Potato virus Y, Potato virus A, and Potato leafroll virus. The virus has been found infecting tomatoes in Italy but not lettuce (Parrella and Crescenzi, 2005). Johnson and Birks (1960) considered all virginoparae of Aphis craccivora to begin development as alates but that development to the apterous form began in the first or second instar. 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