RESUMEN
Bacterial leaf spot of watermelon caused by Pseudomonas syringae has been an emerging disease in the southeastern United States in recent years. Disease outbreaks in Florida were widespread from 2013 to 2014 and resulted in foliar blighting at the early stages of the crop and transplant losses. We conducted a series of field trials at two locations over the course of two years to examine the chemical control options that may be effective in management of this disease, and to investigate the environmental conditions conducive for bacterial leaf spot development. Weekly applications of acibenzolar-S-methyl (ASM) foliar, ASM drip, or copper hydroxide mixed with ethylene bis-dithiocarbamate were effective in reducing the standardized area under the disease progress curve (P < 0.05). Pearson's correlation test demonstrated a negative relationship between the average weekly temperature and disease severity (-0.77, P = 0.0002). When incorporated into a multiple regression model with the square root transformed average weekly rainfall, these two variables accounted for 71% of the variability observed in the weekly disease severity (P < 0.0001). This information should be considered when choosing the planting date for watermelon seedlings as the cool conditions often encountered early in the spring season are conducive for bacterial leaf spot development.
RESUMEN
Polyclonal rabbit antisera were produced to the coat protein of Bean golden mosaic virus Brazil isolate (BGMV), Cabbage leaf curl virus (CabLCV), Tomato yellow leaf curl virus (TYLCV), and Tomato mottle virus (ToMoV), all expressed in Escherichia coli by the pETh expression vector. The expressed coat protein of each virus was purified by sodium dodecyl sulfate-polyacrylamide gel electrophoresis for use as an immunogen. The antisera to BGMV, CabLCV, TYLCV, and ToMoV reacted in indirect (plate-trapping) enzyme-linked immunosorbent assay (ELISA) with extracts from begomovirus-infected tissue. The antisera to BGMV, CabLCV, TYLCV, and ToMoV also reacted specifically with the test begomovirus antigens in leaf imprint blots and Western blots. The CabLCV and TYLCV antisera were used to detect Bean golden yellow mosaic virus antigens by immunogold labeling of thin sections of infected bean tissues. In tissue blot immunoassays, the TYLCV antiserum reacted well with TYLCV antigens but not with ToMoV antigens, while CabLCV antiserum reacted well with ToMoV antigens and weakly with TYLCV antigens. The results indicate that polyclonal antisera prepared to expressed begomovirus coat proteins were useful for the detection of begomoviruses in an array of assays.
RESUMEN
Conspicuous, unusual nuclear inclusions in stained epidermal strips of leaves implicated a virus (designated isolate 2932) as the cause of foliar mosaic in a watermelon plant (Citrullus lanatus) received for analysis from South Florida in 1990. In greenhouse tests, mechanically inoculated plants of Cucurbita pepo (Small Sugar pumpkin and Early Prolific Straightneck squash) and watermelon (Crimson Sweet) developed mosaic or mottle symptoms. Isolate 2932 caused foliar symptoms in 16 cultivars of Cucurbita pepo, including Freedom II and Prelude II, and in six cultivars of watermelon. None of five cultivars of melon (Cucumis melo) or 11 cultivars of cucumber (Cucumis sativus) developed consistent, distinctive symptoms, but all of these cultivars were systemically infected based on back-inoculations to squash. No systemic infection of mechanically inoculated plants of 25 species representing 13 noncucurbitaceous plant families was detected. Crystalline nuclear inclusions, cytoplasmic amorphous inclusions, and cytoplasmic cylindrical inclusions were detected by light and electron microscopy in leaf tissues of infected squash and watermelon. Electron microscopy of squash leaf extracts revealed filamentous particles, and 86% of 159 particles measured ranged from 800 to 890 nm in length. The virus was transmitted in a nonpersistent manner by Myzus persicae from squash to squash in two of three trials. Immunodiffusion tests with polyclonal antisera prepared to partially purified 2932 or its capsid protein showed that the isolate was antigenically different from papaya ringspot virus type W, watermelon mosaic virus 2, and zucchini yellow mosaic virus. In limited testing of field samples of squash and watermelon since 1990, no additional isolates of the 2932 type have been found. The characteristics of isolate 2932 obtained thus far indicate that it is a distinct potyvirus. It is tentatively named watermelon leaf mottle virus to distinguish it from other potyviruses commonly isolated from cucurbits in Florida.