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Phytophthora capsici is an aggressive pathogen that is distributed worldwide with a broad host range infecting solanaceous, fabaceous, and cueurbitaceous crops. Over the past two decades, increased incidence of Phytophthora blight, particularly in eastern states, has threatened production of many vegetable crops. Cucumis melo L. (honeydew and muskmelon), although especially susceptible to fruit rot, is also highly susceptible to crown rot. Currently, little is known about host resistance to P. capsici in C. melo. To assess crown rot resistance in C. melo seedlings, 308 U.S. PIs, and two commercial cultivars (Athena and Dinero) were grown under greenhouse conditions. Seedlings with three to four true leaves were inoculated with a five-isolate zoospore suspension (1 x 104 zoospores per seedling) at the crown and monitored for 6 weeks. All the susceptible control plants of Athena died within 7 days post-inoculation. The majority of the PIs (281 of 308) were highly susceptible to crown rot and succumbed to the disease rapidly and had less than 20% of the plants survive. Several PIs (PI 181748, PI 182964, and PI 273438) succumbed to crown rot earlier than the susceptible melon cultivars. Eighty-seven PIs selected on the basis of the first screen were re-evaluated and of these PIs, 44 were less susceptible than cultivars Athena and Dinero. Twenty-five of the 87 PIs were evaluated again and of these six PI, greater than 80% of the plants survived in the two evaluations. Disease development was significantly slower on these PIs compared with the susceptible checks. High levels of resistance in S1 plants of P1420180, PI 176936, and PI 176940 were observed, which suggests that development of resistant germplasm for use in breeding programs can be accomplished. Further screening and careful selection within each of these PIs can provide a framework for the development of resistant germplasm for use in breeding programs. [ABSTRACT FROM AUTHOR]

Late blight, caused by Phytophthora infestans, affects tomatoes and potatoes in Florida during the winter-spring crop season. During the 2005 season, severe late blight epidemics were observed in Florida prompting our survey. Isolates from 2005 to 2007 were characterized phenotypically based on growth on three media, mating type, pathogenicity, and sensitivity to metalaxyl and genotypically based on two isozymes, mitochondrial DNA (mtDNA), and genomic profiling using the RG57 probe. Isolates collected in this survey were all A2, mtDNA la, and either 100/100 (2005), or 100/122 (2006/2007) at the Gpi locus, and homozygous 100 at the Pep locus. Novel genotypes infecting tomato in Florida were observed based on the Gpi locus and RG57 genomic profile. We propose US-20 for the collection of clonal isolates recovered during the 2005 season and US-21 for clones recovered during 2006 and 2007. In addition to these novel genotypes recovered from tomato, one isolate was recovered from potato representing the US-8 clonal lineage. The findings of the survey in south Florida and their implications are presented. [ABSTRACT FROM AUTHOR]

Phytophthora capsici and the closely related Phytophthora tropicalis infect different hosts that have documented overlapping geographical distributions. Phytophthora capsici attacks annual vegetable hosts whereas P. tropicalis has been recovered from woody perennial hosts. Our objective was to test whether interspecific hybridization is possible and to characterize the resulting progeny. Crosses were made between P. capsici (LT263) from pumpkin to P. tropicalis from rhododendron (LT232) and to P. tropicalis from Theobroma cacao (LT12). The wild type isolates were analyzed for mitochondrial and nuclear DNA sequence diversity and progeny were tested for mating type (MT), AFLP marker profiles and mitochondrial DNA haplotype (mtDNA type). All oospore progeny from LT263 x LT12 were identical to LT263 whereas progeny from LT263 x LT232 were parental as well as hybrid. Hybrid progeny had either one or the other parent mtDNA type and there was no correlation between MT and mtDNA type. Attempts to generate an F9 population from the hybrids proved unsuccessful while a backcross to the P. capsici parent produced hybrid progeny. These results demonstrate that apomixis might play a significant role in species separation and that hybridization between P. capsici and P. tropicalis is possible beyond the F1 generation. [ABSTRACT FROM AUTHOR]

Species of Phytophthora are ubiquitous in ornamental production resulting in significant crop losses, in Tennessee, national surveys for the sudden oak death pathogen Phytophthora ramorum in 2004 and 2005 led to the isolation of Phytophthora species causing disease in nursery-grown or handled woody ornamentals or both. Isolates recovered were identified to species using direct sequencing of the internal transcribed spacer and examination of morphological characters. Six known species (P. cactorum, P. citricola, P. citrophthora, P. nicotianae, P. palmivora, P. tropicalis) and one newly described species (P.foliorum) were recovered from ericaceous hosts. The most common species recovered were P. citricola and P. citrophthora. Genetic analysis using amplified fragment length polymorphism (AFLP) markers revealed intraspecific genotypic diversity as well as isolates with identical AFLP genotypes from multiple locations across multiple years. This work provides evidence for species and genotypic diversity of Phytophthora recovered in Tennessee as well as insight into the movement of individual genotypes in woody ornamental production. [ABSTRACT FROM AUTHOR]

Each year, large volumes of ornamental and food plant propagative stock are imported into the North America; occasionally, Ralstonia solanacearum is found systemically infecting this plant material. In this study, 107 new R. solanacearum strains were collected over a 10-year period from imported propagative stock and compared with 32 previously characterized R. solanacearum strains using repetitive polymerase chain reaction (rep-PCR) element (BOX, ERIC, and REP) primers. Additional strain comparisons were made by sequencing the endoglucanase and the cytochrome b561 genes. Using rep-PCR primers, populations could be distinguished by biovar and, to a limited extent, country of origin and original host. Similarity coefficients among rep-PCR clusters within biovars were relatively low in many cases, indicating that disease outbreaks over time may have been caused by different clonal populations. Similar population differentiations of R. solanacearum were obtained when comparing strain sequences using either the endoglucanase or cytochrome b561 genes. We found that most of the new biovar I strains of R. solanacearum entering the United States were genetically distinct from the biovar 1 strains currently found infecting vegetable production. These introduced biovar 1 strains also had a broader host range and could infect not only tomato, tobacco, and potato but also anthurium and pothos and cause symptoms on banana. All introductions into North America of race 3, biovar 2 strains in the last few years have been linked to geranium production and appeared to be clonal. [ABSTRACT FROM AUTHOR]