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A survey of nurseries, greenhouses, and landscapes was conducted from 2006 to 2008 in order to determine the prevalence and diversity of Phytophthora spp. From sites in Iowa, Michigan, Ohio, and, pre-dominantly, Indiana, 121 Phytophthora isolates were obtained from 1,657 host samples spanning 32 host genera. Based on sequence of the internal transcribed spacer (ITS) region of the ribosomal DNA, 11 Phytophthora spp. and two hybrid species were identified. A majority of the isolates were P. citricola (35.9%) or P. citrophthora (27.4%). Six isolates were confirmed as hybrids (four of P. cactorum x hedraiandra and two of P. nicotianae x cactorum) by cloning and sequencing the ITS region. Three P. cactorum x hedraiandra isolates were obtained from the same site, from three Rhododendron spp., which are known hosts to the parental species. The fourth isolate, however, was recovered out of a different location in a Dicentra sp., which is not a known host to either parental species, suggesting an expansion of host range of the hybrid isolate as compared with either parental species. [ABSTRACT FROM AUTHOR]

In November of 2007, 6-inch rooted cuttings of Mandevilla (= Dipladenia) splendens 'Red Riding Hood' were submitted from a greenhouse in Indiana to the Purdue Plant and Pest Diagnostic Lab. Plants exhibited leaf dieback, wilting, and reduced top growth. Microscopic observation revealed no fungal structures within the roots, stems, and leaves; however bacterial streaming was observed from the cut edge of stem and root tissue using ×100 magnification with phase contrast. A Ralstonia solanacearum ImmunoStrip test (Agdia Inc., Elkhart, IN) was used to determine that the samples (roots and stem) were positive for R. solanacearum, the causal agent of southern wilt. A bacterial suspension was prepared from infected tissue and streaked onto King's Medium B (KB). Gram-negative, nonfluorescent, oxidase-positive bacteria were consistently isolated from the diseased tissues and determined as R. solanacearum by BIOLOG (Hayward, CA) carbohydrate utilization. A culture of R. solanacearum and infected plant material were submitted to USDA APHIS PPQ as per select agent protocol. (3) CPHST NPGBL generated pure cultures and together with submitted plant materials they tested positive for R. solanacearum using Agdia ImmunoStrips. Culture and plant material tested positive for R. solanacearum and negative for biovar 2 using the Fegan conventional PCR (1) and the Central Science Lab (CSL, York, UK) real-time PCR (4). Pure cultures were determined to be negative for biovar 2 but positive for biovar 3 using the biovar carbohydrate utilization plate assay (2). On the basis of these results, the bacteria were identified as R. solanacearum biovar 3 and not as the select agent R. solanacearum race 3 biovar 2. Koch's postulates confirmed pathogenicity of the isolated bacteria on tomato, a susceptible host. Three 6-week-old plants were mechanically inoculated with a bacterial suspension of approximately 1 × 10 8 CFU/ml prepared from cultures grown on KB for 2 days at 28°C. Inoculum (0.1ml of bacterial suspension) was injected into stem axils with a 22-gauge hypodermic needle. Three 6-week-old control plants were inoculated with sterile water. Plants were kept at 24°C with supplemental 400W high-pressure sodium light. Within 5 days, all three inoculated plants exhibited wilt symptoms. No symptoms were observed in control plants. Bacteria were reisolated from symptomatic plants on KB medium as described above, and gram negative, nonfluorescent, oxidase-positive bacteria were obtained. Reisolated strains were identical to R. solanacearum using BIOLOG carbohydrate utilization testing, confirming the causal agent of the disease. Personal correspondence with other diagnosticians also confirms the presence of R. solanacearum biovar 3 in Mandevilla in Ohio, Michigan, and Minnesota. To our knowledge, this is the first documented report in the world of R. solanacearum biovar 3 on Mandevilla. References: (1) M. Fegan et al. Page 34 in: Bacterial Wilt Disease Molecular and Ecological Aspects. P. Prior et al., eds. INRA Editions-Springer. Verlag, Germany, 1998. (2) E. R. French et al. Fitopatologia 30:126, 1995. (3) USDA/APHIS/PPQ New Pest Response Guidelines. Ralstonia Solanacearum race3 biovar 2, from http://www.aphis.usda.gov/import_export/plants/manuals/emergency/ downloads/nprg-ralstonia.pdf , retrieved May 2008. (4) S. A. Weller et al. Appl Environ. Microbiol. 7:2853, 2000.

During August 2007 and again in January 2008, compact sweet basil (Ocimum basilicum 'Genovese') plants grown hydroponically in Indiana displayed dark, irregular, stem lesions extending 2 to 3 cm above the interface of the nutrient solution. These necrotic stem lesions (black leg), observed on 20 to 30% of the basil plants caused very weak, brittle stems so that they could not be marketed fresh. Although no wilting was noted, reduced plant height was observed. Similar symptoms of blackleg and poor growth have been reported from Italy on greenhouse-grown basil infected with Microdochium tabacinum (1,2). Diseased plant samples were sent to diagnostic clinics at Purdue University and the University of Massachusetts. Stem samples were surface sterilized and plated on potato dextrose agar (PDA) acidified with 1 ml of 85% lactic acid per liter as well as onto one-quarter-strength PDA. A fungus morphologically consistent with Plectosporium tabacinum (van Beyma) M.E. Palm, W. Gams, & H.I. Nirenberg (synonyms M. tabacinum (von Arx, 1984) and Fusarium tabacinum (Gams & Gerlagh, 1968) (3) was cultured from the basil stems and identified as P. tabacinum by R. Wick. Cultures sent to J. McKemy and J. Bischof (USDA/APHIS/PPQ) and W. Elmer (Connecticut Agricultural Experiment Station) also were identified as P. tabacinum. Amplification of the 323-bp internal transcribed spacer (ITS) region (ITS1, 5.8S rRNA gene, ITS2) and subsequent BLAST alignments of the resulting sequence indicated a 98% match for Plectosphaerella cucumerina (anamorph P. tabacinum) (GenBank Accession No. U17399; MIDI Inc., Newark, DE). Inoculations were performed on basil plants grown in peat-based soilless medium in a greenhouse for 6 weeks. Immediately before inoculation, the roots were washed with tap water to remove the peat-based medium. A single basil plant was placed in each of eight, 125-ml Erlenmeyer flasks. Four flasks were filled with 100 ml of deionized water as negative controls and four were filled with a 1 × 10 6 CFU/ml water suspension of P. tabacinum so that the liquid reached the crown of the basil plant. Basil plants in the Erlenmeyer flasks were incubated on a laboratory bench at 23°C. After 24 h, the solutions in all flasks were discarded and each flask and root system was rinsed three times with deionized water. The plants were then incubated in deionized water on the laboratory bench for four to five additional days. Within 4 days, dark brown-to-black stem lesions similar to those observed originally on basil plants in the hydroponic production greenhouse developed on the plants at the water interface and extended up the stem. Lesions extended a mean of 22 mm above the water level on inoculated plants. Control plants remained symptomless. P. tabacinum was recovered from symptomatic tissue of inoculated plants to complete Koch's postulates. The experiment was repeated several times with similar results. Further evidence of pathogenicity was obtained by stem inoculation of basil plants growing in a soilless medium. These data indicate that P. tabacinum was the causal agent of the symptoms observed on the hydroponic basil. To our knowledge, this is the first report of P. tabacinum causing 'black leg' and reduced growth on basil in the United States and the first report in the world of P. tabacinum on hydroponic basil. References: (1) A. Garibaldi et al. Plant Dis. 81:124.1997. (2) A. Matta. Riv. Patol. Veg. Ser. IV 14:119, 1978. (3) M. Palm et al. Mycologia. 87:397.1995.

In August of 2008, leaves of hybrid corn (Zea mays L.) and popcorn from Pulaski and Jasper counties in northwest Indiana were submitted to the Purdue Plant and Pest Diagnostic Lab with symptoms characteristic of a bacterial disease. Symptomatic leaves had large, tan-to-gray necrotic lesions with dark freckling present within the lesions. Shiny bacterial exudate was present on the surface of many of the lesions. Microscopic observation revealed no fungal structures within the lesions, and bacterial streaming was observed from the cut edge of symptomatic tissue under ×100 magnification with phase contrast. A commercially available ELISA test (Agdia Inc., Elkhart, IN) determined that samples were negative for Pantoea stewartii, the causal agent of Stewart's bacterial leaf blight and wilt. A bacterial suspension was prepared from symptomatic tissue and streaked onto King's B medium and subcultured on semiselective CNS medium (1,2). Axenic, peach-colored colonies present on the CNS medium tested gram positive with a KOH test. Analysis of fatty acid methyl esters (MIDI Inc, Newark, DE) indicated that the strain was very similar (0.611) to Clavibacter michiganensis. Amplification of the 500-bp 16S rRNA region of the bacterial gene and subsequent BLAST alignments of the resulting sequence indicated a 99% match for C. michiganensis subsp. nebraskensis (GenBank Accession Nos. AM410697 and U09763; D16S2 gene bacterial library, version 2.10; MIDI Inc,). Koch's postulates were used to confirm pathogenicity of the isolated bacteria on corn inbred B73. Eighteen plants were mechanically inoculated at growth stage V1 to V2 with a bacterial suspension of approximately 1 × 10 8 CFU/ml prepared from cultures grown on CNS for 10 days at 28°C (2). Inoculum was rubbed onto leaves dusted with Carborundum and 0.1 ml of the bacterial suspension was injected into stems with a hypodermic needle. Nine control plants were inoculated with sterile water. Plants were kept at greenhouse conditions (24°C) with supplemental 400W high-pressure sodium light. Within 5 to 8 days, leaves and stems of all 18 inoculated plants developed water-soaked, necrotic lesions. No symptoms were observed in control plants. Bacteria were reisolated from symptomatic plants on CNS medium as described above, and gram-positive colonies were obtained. Reisolated strains were identical to C. michiganensis subsp. nebraskensis by D16S2 DNA sequence analysis, confirming the causal agent of the disease. Disease incidence in affected fields ranged from 20 to 60% and significant yield loss was reported. This confirmation is of regulatory importance because of potential export restrictions of Indiana-grown seed corn and popcorn to select countries. To our knowledge, this is the first report of Goss's bacterial wilt and leaf blight on corn in Indiana. References: (1) D. C. Gross and A. K. Vidaver. Phytopathology 69:82, 1979. (2) L. M. Shepherd. M.S. thesis. Iowa State University. Ames, 1999.

Pyricularia grisea, the causal agent of gray leaf spot on turfgrass, was isolated from symptomatic perennial ryegrass (Lolium perenne) leaves collected from a golf course in north-central Indiana in August 1999. Gray leaf spot is an emerging threat to stands of perennial ryegrass in the mid-Atlantic and Midwestern United States (1). Symptoms were first evident in taller (6 cm) mown, rough areas surrounding golf course fairways. Field symptoms included diffuse patches (1 to 4 m in diameter) of thin, yellow-tan turf. Within larger affected areas, some of the turf was dead and matted. Close inspection revealed the presence of typical tan-gray lesions with brown margins and fish hook-like distortion of infected leaf blade tips. Incubation of affected turf in a saturated environment at 23°C for 16 h resulted in production of numerous three-celled, pear-shaped conidia characteristic of those produced by P. grisea. A pure culture of the isolate was grown on V8-juice agar in darkness at 29°C. After 10 days, the culture was exposed to continuous light for 4 days at 23°C to induce sporulation. Conidia were washed from the colony surface with sterile distilled water. Two-week-old perennial ryegrass plants in 8-cm-diameter pots were inoculated with the conidial suspension. Typical gray leaf spot symptoms resulted after incubation of inoculated plants at 27°C for 72 h in a saturated atmosphere. Uninoculated control plants exposed to the same environmental conditions remained healthy. This is the first report of gray leaf spot on perennial ryegrass in Indiana. Reference: (1) P. J. Landschoot and B. F. Hoyland. Plant Dis. 76:1280, 1992.