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Journal of Insect Science | www.insectscience.org ISSN: 1536-2442<br />

percentage and female fecundity were greater at both<br />

30 and 25 °C and lower at 15 °C. The temperature<br />

threshold (t0) and thermal accumulative effect<br />

(degree-days) were also calculated. The laboratory<br />

studies were confirmed by field applications<br />

examining the relationship between seasonal<br />

temperature and insect populations. The study<br />

demonstrates that T. ricini can, in otherwise unlimited<br />

conditions, persist and increase in number within the<br />

range 20–30 °C. Therefore, the pest is well adapted to<br />

high temperatures and may extend its distribution if the<br />

mean world temperatures increase because of global<br />

warming. Regarding the plant host species, the castor<br />

bean was the preferred host followed by papaya, while<br />

the sweet potato was not preferred. Host plant species<br />

had a significant effect on egg hatching, nymphal<br />

survival, female fecundity and the duration of the life<br />

cycle of T. ricini.<br />

Squash Vein Yellowing Virus, A Novel<br />

Ipomovirus, Isolated from Squash and<br />

Watermelon in Florida<br />

Scott Adkins 1 , Susan E. Webb 2 , Diann Achor 3 ,<br />

Chandrasekar S. Kousik 4 , Pamela D. Roberts 5 , and<br />

Carlye A. Baker 6<br />

1 USDA-ARS, Fort Pierce, FL, USA.<br />

Correspondence: SAdkins@ushrl.ars.usda.gov<br />

2 University of Florida, Gainesville, FL, USA<br />

3 University of Florida, Lake Alfred, FL, USA<br />

4 USDA-ARS, Charleston, SC, USA<br />

5 University of Florida, Immokalee, FL, USA<br />

6 FDACS-DPI, Gainesville, FL, USA<br />

A novel whitefly-transmitted member of the family<br />

Potyviridae was isolated from a squash plant<br />

(Cucurbita pepo) with vein yellowing symptoms in<br />

Florida. The virus, for which the name Squash vein<br />

yellowing virus (SqVYV) is proposed, has flexuous<br />

rod-shaped particles of ~840 nm in length. SqVYV<br />

was transmitted by whiteflies (<strong>Bemisia</strong> tabaci, biotype<br />

B) but was not transmitted by aphids (Myzus persicae).<br />

The experimental host range was limited to species in<br />

the Cucurbitaceae, with the most dramatic symptoms<br />

observed in squash and watermelon, but excluded all<br />

tested species in the Amaranthaceae, Apocynaceae,<br />

Asteraceae, Chenopodiaceae, Fabaceae, Malvaceae<br />

and Solanaceae. Initial greenhouse and field screening<br />

of watermelon germplasm with SqVYV has identified<br />

potential sources of resistance and experiments are in<br />

progress to confirm these preliminary observations.<br />

Infection of squash and watermelon by SqVYV<br />

induced inclusion bodies visible by electron and light<br />

microscopy that were characteristic of members of the<br />

family Potyviridae. Comparison of the SqVYV coat<br />

protein gene and protein sequences with those of<br />

recognized members of the family Potyviridae indicate<br />

that it is a novel member of the genus Ipomovirus. A<br />

limited survey revealed that SqVYV was present over<br />

the five most recent growing seasons in watermelons<br />

suffering from a mature vine decline and fruit rot<br />

observed in southwest and west central Florida.<br />

Inoculation of greenhouse-and field-grown watermelon<br />

plants with SqVYV at different stages of growth was<br />

sufficient to induce these symptoms, suggesting that it<br />

is the likely cause of this disease.<br />

Making a Friend from a Foe: Expressing a<br />

GroEL Gene from the <strong>Whitefly</strong> <strong>Bemisia</strong><br />

tabaci in the Phloem of Tomato Plants<br />

Confers Resistance to Tomato Yellow Leaf<br />

Curl Virus<br />

F. Akad 1 , A. Eybishtz 1 , D. Edelbaum 1 , O. Dar-Issa 2 ,<br />

N. Iraki 2 , and H. Czosnek 1<br />

1 The Otto Warburg Minerva Center for Agricultural Biotechnology<br />

& The Robert H. Smith Institute for Plant Science and Genetics in<br />

Agriculture, The Hebrew University of Jerusalem, Rehovot, Israel.<br />

Correspondence: akad@ufl.edu, czosnek@agri.huji.ac.il<br />

2 UNESCO Biotechnology Center, Bethlehem University,<br />

Bethlehem, West Bank, Palestinian Authority<br />

Breeding for virus resistance in transgenic crop plants<br />

is based on a variety of strategies such as expressing<br />

pathogen-derived genes or on RNA-mediated gene<br />

silencing. The strategy used in the present research is<br />

based on a totally new concept. It takes advantage of<br />

the fact that some, and perhaps all, plant viruses<br />

transmitted by their insect vectors in a circulative<br />

manner interact in the insect haemolymph with GroEL<br />

homologues produced by the vector endosymbiotic<br />

bacteria. It has been suggested that GroEL-virus<br />

interaction could be a mechanism shared by plant<br />

circulative viruses to avoid destruction in the<br />

haemolymph. In this study, we have exploited this<br />

phenomenon to generate transgenic tomato plants<br />

expressing the whitefly GroEL in their phloem. We<br />

expected that once inoculated by their vector,<br />

phloem-limited circulative viruses will be trapped by<br />

GroEL in the plant phloem, thereby inhibiting invasion<br />

of phloem-associated cells and long distance<br />

movement, rendering the plants resistant to the virus.<br />

A gene encoding a GroEL homologue from the<br />

whitefly B. tabaci was cloned in an Agrobacterium<br />

binary vector under the control of an Arabidopsis<br />

phloem-specific promoter, which was used to<br />

transform two tomato genotypes. GroEL was<br />

expressed in the two genotypes, during two<br />

consecutive generations. All the twenty four To<br />

GroEL-transgenic tomato plants obtained (but one and<br />

its progeny) exhibited good levels of resistance to<br />

whitefly-mediated inoculation of TYLCV, exhibiting<br />

mild or no disease symptoms. The transgenic progeny<br />

of the resistant plants expressed GroEL and were as<br />

Journal of Insect Science: Vol. 8 | Article 4 3

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