The phytopathogenic mollicute-insect vector interface: a closer look

ABSTRACT Spiroplasma citri, transmitted by phloem-feeding leafhoppers, moves from the gut lumen through the gut wall, hemolymph, and salivary glands and multiplies in insect tissues. Nontransmissible lines were deficient in their ability to cross these barriers. Molecular analysis revealed extensive chromosomal rearrangements between the transmissible and nontransmissible spiroplasma lines including a large chromosomal inversion and deletions of about 10 kb at each inversion border. One open reading frame of the deleted region, cloned from the transmissible strain BR3-3X, encodes an integral membrane protein of 58 kDa that shares limited sequence similarity with major adhesin proteins of two zoopathogenic mycoplasmas. Adhesion of spiroplasmas to cultured leafhopper cells was inhibited by proteases, suggesting that adherence to host cells is mediated by spiroplasma membrane protein(s). A hypothetical model for insect transmission of phytopathogenic mollicutes is presented.     

Ultrasonographic comparison of adhesions induced by two different methods of gastropexy in the dog

Ultrasonography was used to compare adhesions induced by two different methods of gastropexy in 16 dogs. An incisional gastropexy technique was used in eight dogs (group 1) and a 'modified' gastropexy technique in the remaining eight (group 2). The length and thickness of the gastropexy and the peristaltic activity of the stomach were measured ultrasonographically and compared between groups. Measurements for the two groups were taken in the early postoperative interval (two to four days), intermediate postoperative interval (eight to 20 days) and late postoperative interval (57 to 79 days). Both techniques were equally successful in forming permanent adhesions at two months postoperatively and there was no recurrence of gastric dilatation and volvulus. The length and thickness of the gastropexy were similar for both groups at two months postoperatively and there were no surgical complications with either technique. The modified gastropexy provides a technique that can easily be performed by a single surgeon , with no increased operative time or duration of anaesthesia, and with the formation of a permanent adhesion.     

Anti‐microbial Susceptibility for east1+Escherichia coli Isolated from Diarrheic Pigs in Korea

The in vitro susceptibilities of 128 isolates of east1⁺Escherichia coli from pre‐weaned and post‐weaned pigs with diarrhoea were tested with nine commonly used anti‐microbial agents by an agar dilution minimal inhibitory concentration (MIC) procedure according to National Committee for Clinical Laboratory Standards guidelines. For the isolates from pre‐weaned and post‐weaned pigs, most of them were susceptible to low concentrations (MIC₉₀) of tetracycline (4 and 2 μg/ml), ceftiofur (2 and 2 μg/ml), and colistin (4 and 2 μg/ml). Marked resistance was found in others.     

Application of aldicarb in a drip-irrigated cotton field for the control of the Tobacco Whitefly(Bemisia Tabaci)

Cotton was grown in loess soil, in rows 1 m apart, and drip-lines were placed in the center of every second space between rows at a distance of 50 cm from the plants. Aldicarb was applied as granules (containing 15% a.i.) to the field on two dates (mid-June and mid-July) and incorporated into the soil(a) 25 cm from the plants,i.e., equidistant from the plants and the drip-lines, on both sides of the drip-lines; and(b) 50 cm from the plants,i.e., in the center of the spaçe between the rows, near the drip-line. Measurements of mortality ofBemisia tabaci larvae, and of the accumulation of aldicarb from the late (mid-July) treatment showed that best control of the pest and the highest aldicarb residues were obtained with the late treatment. The pest control effectiveness was found to depend on both date and location of aldicarb application. Early treatment (mid-June) was more effective if applied close (25 cm distance) to the plant stems, whereas late treatment (mid-July) was more effective if applied at a distance of 50 cm from the plant stems.     

Sensitivity of Rhizoctonia species to different fungicides

Of 14 fungicides with different modes of action, cyproconazole and tolclofos-methyl were generally inhibitory both in vitro and in vivo against all tested isolates of five Rhizoctonia species belonging to the teleomorphs Thanatephorus cucumeris, Waitea circinata or Ceratobasidium cereale. Triadimenol and carboxin provided considerable variation in activity against different species and isolates, whereas prochloraz was ineffective against all isolates. Imazalil and fenarimol showed moderate control, whereas flusilazole, propiconazole, fenpropimorph and benomyl showed strong activity against R. zeae and R. oryzae, but were much less effective against R. sasakii, R. cerealis and R. solani. Benodanil and iprodione controlled all isolates of R. cerealis and R. solani, but were not very effective against R. zeae and R. oryzae. Pencycuron showed strong activity against R. sasakii and most R. solani isolates, moderate activity against R. zeae, and was ineffective against R. oryzae and R. cerealis.     

RNA‐transfected CD40‐activated B cells as a vaccine strategy in canine malignancies

Introduction: Cell‐based vaccine strategies using dendritic cells as cellular adjuvant have entered phase III trials in humans and have been found to be safe, feasible, and potentially efficacious. Canine patients are generally smaller than adult human patients, which makes production of canine dendritic cell (DC) vaccines problematic, given patient size and the small number of available DC precursors. Here we describe feasibility studies of a novel cell‐based vaccine strategy which uses CD40‐activated B‐cells (CD40‐B) loaded with RNA. This strategy is based on our observations that RNA‐transfected human CD40‐B can drive anti‐tumor T cell responses. One advantage of using CD40‐B cells is the ability to expand this cell population ex vivo, allowing for the numbers of cells required for therapeutic vaccines. Methods: Twenty milliliters of blood were drawn from 6 normal dogs and 5 canine lymphoma patients. Peripheral blood mononuclear cells were separated by Ficoll centrifugation. Culture conditions for B cell activation were optimized using CD40‐ligand, canine IL‐4, and Toll‐like receptor stimulus with CpGoligodinucleotides (ODN). Cyclosporine was added to eliminate peripheral T lymphocytes. Proliferation and activation of CD40‐B cells were demonstrated by CFSE dilution of B cells quantified by flow cytometry. Gene transfer was achieved by mRNA electroporation. Results: Marked in vitro stimulation and proliferation of canine peripheral B cells were achieved with soluble trimeric CD40L, canine IL‐4, and ODN. CD40‐B cells showed dramatic upregulation of MHC class II molecules and CD21 (B‐cell activation marker). After two weeks in culture, cells were negative for CD3 and CD4. Canine CD40‐B cells were efficiently transfected with mRNA, with >60% of CD40‐B expressing green fluorescent protein after GFP mRNA electroporation. Conclusion: RNA‐transfected CD40‐B cells can be efficiently generated from normal and tumor‐bearing dogs. These results provide rationale to test tumor RNA‐transfected CD40‐B as a novel therapeutic approach to treating canine malignancies. Clinical trials in canine lymphoma have been proposed.     

Genetic and phenotypic diversity within the Fusarium graminearum species complex in Norway

European Journal of Plant Pathology - As has been observed in several European countries, the frequency of Fusarium head blight (FHB) caused by members of the Fusarium graminearum species complex...