scholarly journals Severe Outbreak of Downy Mildew Caused by Plasmopara obducens on Impatiens walleriana in Florida

Plant Disease ◽  
2013 ◽  
Vol 97 (5) ◽  
pp. 687-687 ◽  
Author(s):  
A. J. Palmateer ◽  
P. Lopez ◽  
T. E. Seijo ◽  
N. A. R. Peres

Impatiens, Impatiens walleriana Hook.f., are grown as an ornamental crop in greenhouse and shade house production in Florida and other regions of the United States. Downy mildew on impatiens was detected from numerous landscapes (Manatee, Hillsborough, Collier, Hendry, Broward, Palm Beach, and Miami-Dade counties) in the winter of 2012. Incidence reached nearly 100% on many affected landscape plantings. Symptoms initially appeared as yellowing on the lower leaves and were typically vein-delineated, although in some cases the entire leaf was affected. Diseased plants later wilted and infected leaves abscised from the stem. A white, downy growth was apparent on the abaxial leaf surface. Microscopic observation revealed coenocytic mycelium with sporangiophores that were hyaline, thin-walled, and had slightly swollen bases. Branches of sporangiophores were monopodial and formed right angles to the supporting branches. Sporangia were hyaline and obvoid with a single pore on the distal ends that was mostly flat. Sporangia measured 19 to 22.5 × 13 to 17 μm. Oospores were observed in stem and leaf tissue. Leaves of 10 potted impatiens plants, I. walleriana ‘Super Elfin XP Coral’ and ‘Super Elfin XP White,’ were inoculated with a suspension containing 1 × 105 sporangia/ml and sprayed till runoff (approximately 20 ml per plant) with a handheld pressurized Ulva sprayer. Plants were maintained outside in a shade house under 73% shade where the daytime temperatures averaged 24°C and RH averaged 74% and nighttime temperature averaged 18°C with an average of 91% RH. Ten non-inoculated impatiens plants served as controls. After 10 days, symptoms typical of downy mildew occurred on 100% of the inoculated impatiens plants and sporulation was confirmed microscopically. The non-inoculated control plants remained healthy. The 5′ end of the large ribosomal subunit gene (762 bp) from two isolates, one collected in Hillsborough County and one from Miami-Dade County, was amplified by PCR (primers NL1-GCATATCAATAAGCGGAGGAAAAG and NL4-GGTCCGTGTTTCAAGACGG) and sequenced bi-directionally (1,2,3). The consensus sequence from both isolates was identical and it was deposited into GenBank (Accession No. JX217746). Sequence data matched (99% homology) with Plasmopara obducens reported on I. walleriana in Europe and Australia (1,2). To our knowledge, this is the first report of downy mildew on I. walleriana in Florida (4). The disease has made a major impact on impatiens in landscapes throughout Florida and will likely continue to affect future production. References: (1) A. Bulajic et. al. Plant Dis. 95:491, 2011. (2) J. H. Cunnington et. al. Plant Pathol. 57:371, 2008. (3) K. O'Donnell. Curr. Genet. 22:213, 1992. (4) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society, 1989.

Plant Disease ◽  
2004 ◽  
Vol 88 (8) ◽  
pp. 909-909 ◽  
Author(s):  
S. N. Wegulo ◽  
S. T. Koike ◽  
M. Vilchez ◽  
P. Santos

During February 2004, diseased double impatiens (Impatiens walleriana) plants were received from a commercial grower in southern California. The upper surfaces of symptomatic leaves were pale yellow with no distinct lesions. Diseased leaves later wilted, and severely affected leaves abscised from the stem. At the nursery, only double impatiens plants in the Fiesta series were infected, and some cultivars were more heavily infected than others. Disease incidence in cv. Sparkler Hot pink was nearly 100%. The interior of infected leaves was colonized by coenocytic mycelium. A conspicuous white growth was observed only on the underside of leaves. Sporangiophores were hyaline, thin walled, emergent from stomata, and had slightly swollen bases. Sporangiophore branching was distinctly monopodial. Smaller sporangiophore branches were arranged at right angles to the supporting branches, and tips of branches measured 8 to 14 μm long. Sporangia were ovoid and hyaline with a single pore on the distal ends. Distal ends of sporangia were predominantly flat but occasionally had a slight papilla. Short pedicels were present on the attached ends. Sporangia measured 19.4 to 22.2 (-25.0) μm × 13.9 to 16.7 (-19.4) μm. Oospores were not observed in leaf tissue. On the basis of symptoms and morphology of the organism, the pathogen was identified as Plasmopara obducens J. Schröt. Pathogenicity tests were done on double type cvs. Fiesta, Tioga Red, and Tioga Cherry Red and on single type cvs. Cajun Watermelon and Accent Lilac. Plants were spray inoculated with sporangiospore suspensions (1 × 104 sporangiospores per milliliter), incubated for 24 h in a dew chamber (18 to 20°C), and then maintained in a greenhouse (22 to 24°C). Symptoms and signs of downy mildew developed after 12 days only on inoculated cv. Fiesta plants, and the pathogen morphology matched that of the originally observed pathogen. Nontreated control plants did not develop downy mildew. To our knowledge, this is the first report of downy mildew on impatiens in California. P. obducens is one of two causal agents of downy mildew of impatiens (2,4). The other pathogen, Bremiella sphaerosperma, has dichotomous sporangiophore branching and causes lesions with well-defined margins (2,4). In the United States, the disease has been recorded in the eastern and northeastern states and in Indiana, Minnesota, Mississippi, Montana, and Wisconsin (3). In Canada, the disease has been recorded in Manitoba and Quebec (1). References: (1) I. L. Conners. An Annotated Index of Plant Diseases in Canada and Fungi Recorded on Plants in Alaska, Canada, and Greenland. Research Branch, Canada Department of Agriculture, Publication 1251, 1967. (2) O. Constantinescu. Mycologia 83:473, 1991. (3) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society, 1989. (4) G. W. Wilson. Bull. Torrey Bot. Club 34:387, 1907.


Plant Disease ◽  
2009 ◽  
Vol 93 (2) ◽  
pp. 199-199 ◽  
Author(s):  
P. D. Roberts ◽  
R. N. Raid ◽  
P. F. Harmon ◽  
S. A. Jordan ◽  
A. J. Palmateer

Basil is grown as a specialty crop in greenhouse and field production in Florida and other regions of the United States. Downy mildew on basil (Ocimum basilicum) was detected from four production sites (Collier, Hendry, Miami-Dade, and Palm Beach counties) in south Florida in the fall of 2007, and within months, it was also found in west-central north Florida (Hillsborough County). Incidence reached nearly 100% on some of the affected crops and caused complete yield losses on basil grown both in the field for fresh market and potted herbs market. Symptoms developed during transit on basil that appeared symptomless at harvest. Symptoms initially appeared as yellowing on the lower leaves that was typically delineated by the veins, although in some cases the entire leaf area of the leaf surface was affected. A gray, fuzzy growth was apparent on the abaxial leaf surface. Microscopic observation detected dichotomous branching, hyaline sporangiophores (220 to 750 × 4 to 9 μm) bearing single sporangia. Sporangia were light brown, ovoid to slightly ellipsoid, and measured 14 to 15 × 15 to 18 μm. Oospores were not observed. Leaves of potted basil plants and coleus (Solenostemon scutellarioides) were inoculated with a suspension containing 1 × 105 sporangia/ml and sprayed till runoff (approximately 15 ml per plant) with a hand-held pressurized aerosol canister. Plants were covered with a plastic bag for 24 h and maintained in the greenhouse under ambient conditions. Noninoculated plants served as controls. After 7 days, symptoms typical of downy mildew occurred only on the inoculated basil plants and sporulation was confirmed microscopically. The internal transcribed spacer regions of an isolate collected in Hendry County were sequenced bidirectionally. The consensus sequence was deposited into GenBank (Accession No. FJ346561). Sequence data matched (100% homology) with a Peronospora sp. reported on sweet basil in Switzerland (GenBank Accession No. AY884605) and was similar (99% homology) to an isolate (GenBank Accession No. DQ523586) reported on coleus, although inoculation to coleus failed to confirm pathogenicity on this host. The sequence data also distinguished the isolate from P. lamii (87% homology) previously reported to occur on basil. The pathogen was identified as a Peronospora sp. based on morphological characteristics and sequencing homology (1–3). References: (1) L. Belbahri et al. Mycol. Res. 109:1276, 2005. (2) S. Francis. CMI Descriptions of Pathogenic Fungi and Bacteria. No. 688. CMI, Kew, England, 1981. (3) A. McLeod et al. Plant Dis. 90:1115, 2006.


Plant Disease ◽  
2014 ◽  
Vol 98 (5) ◽  
pp. 696-696 ◽  
Author(s):  
J. A. Crouch ◽  
M. P. Ko ◽  
J. M. McKemy

Downy mildew of impatiens (Impatiens walleriana Hook.f.) was first reported from the continental United States in 2004. In 2011 to 2012, severe and widespread outbreaks were documented across the United States mainland, resulting in considerable economic losses. On May 5, 2013, downy mildew disease symptoms were observed from I. walleriana ‘Super Elfin’ at a retail nursery in Mililani, on the Hawai'ian island of Oahu. Throughout May and June 2013, additional sightings of the disease were documented from the islands of Oahu, Kauai, Maui, and Hawai'i from nurseries, home gardens, and botanical park and landscape plantings. Symptoms of infected plants initially showed downward leaf curl, followed by a stippled chlorotic appearance on the adaxial leaf surfaces. Abaxial leaf surfaces were covered with a layer of white mycelia. Affected plants exhibited defoliation, flower drop, and stem rot as the disease progressed. Based on morphological and molecular data, the organism was identified as Plasmopara obducens (J. Schröt.) J. Schröt. Microscopic observation disclosed coenocytic mycelium and hyaline, thin-walled, tree-like (monopodial branches), straight, 94.0 to 300.0 × 3.2 to 10.8 μm sporangiophores. Ovoid, hyaline sporangia measuring 11.0 to 14.6 × 12.2 to 16.2 (average 13.2 × 14.7) μm were borne on sterigma tips of rigid branchlets (8.0 to 15.0 μm) at right angle to the main axis of the sporangiophores (1,3). Molecular identification of the pathogen was conducted by removing hyphae from the surface of three heavily infected leaves using sterile tweezers, then extracting DNA using the QIAGEN Plant DNA kit (QIAGEN, Gaithersburg, MD). The nuclear rDNA internal transcribed spacer was sequenced from each of the three samples bidirectionally from Illustra EXOStar (GE Healthcare, Piscataway, NJ) purified amplicon generated from primers ITS1-O and LR-0R (4). Resultant sequences (GenBank KF366378 to 80) shared 99 to 100% nucleotide identity with P. obducens accession DQ665666 (4). A voucher specimen (BPI892676) was deposited in the U.S. National Fungus Collections, Beltsville, MD. Pathogenicity tests were performed by spraying 6-week-old impatiens plants (I. walleriana var. Super Elfin) grown singly in 4-inch pots with a suspension of 1 × 104 P. obducens sporangia/ml until runoff using a handheld atomizer. Control plants were sprayed with distilled water. The plants were kept in high humidity by covering with black plastic bags for 48 h at 20°C, and then maintained in the greenhouse (night/day temperature of 20/24°C). The first symptoms (downward curling and chlorotic stippling of leaves) and sporulation of the pathogen on under-leaf surfaces of the inoculated plants appeared at 10 days and 21 days after inoculation, respectively. Control plants remained healthy. Morphological features and measurements matched those of the original inoculum, thus fulfilling Koch's postulates. To our knowledge, this is the first report of downy mildew on I. walleriana in Hawai'i (2). The disease appears to be widespread throughout the islands and is likely to cause considerable losses in Hawai'ian landscapes and production settings. References: (1) O. Constantinescu. Mycologia 83:473, 1991. (2) D. F. Farr and A. Y. Rossman. Systematic Mycology and Microbiology Laboratory, ARS, USDA. Retrieved from http://nt.ars-grin.gov/fungaldatabases/ July 16, 2013. (3) P. A. Saccardo. Syllogue Fungorum 7:242, 1888. (4) M. Thines. Fungal Genet Biol 44:199, 2007.


2020 ◽  
Vol 21 (3) ◽  
pp. 214-216
Author(s):  
Margery Daughtrey ◽  
Janna Beckerman ◽  
William J. Davis ◽  
Karen Rane ◽  
Jo Anne Crouch

Two new series of Impatiens walleriana (impatiens) cultivars, Beacon and Imara XDR, were released to commercial growers in the United States in 2019 to 2020. Field trials show these new cultivar series are highly resistant to impatiens downy mildew (IDM). However, neither of these two impatiens series are completely immune to the disease, and preventive fungicide programs are still recommended for use throughout production to maintain plant health. Here we report two destructive outbreaks of IDM from Imara XDR in two commercial production facilities in California, one in 2019 and one in 2020. The disease outbreaks were caused by a known rDNA genotype of Plasmopara destructor (synonym = P. obducens). Modified Koch’s postulates showed that the pathogen could infect and cause disease in both Beacon and Imara XDR plants. Mefenoxam applied by both growers may have been ineffective due to resistance in P. destructor populations, which has been demonstrated on several previous occasions. Given these findings, fungicide programs intended to supplement genetic resistance should not be overly reliant upon application of mefenoxam and should utilize effective materials from different mode of action groups, in rotation. Fungicides to supplement genetic resistance are particularly appropriate in frost-free areas or in any circumstances that provide a potential inoculum source.


Plant Disease ◽  
2013 ◽  
Vol 97 (3) ◽  
pp. 428-428 ◽  
Author(s):  
N. A. Ward ◽  
E. Dixon ◽  
B. Amsden

Impatiens downy mildew (Plasmopara obducens (J. Schröt.) J. Schröt. (syn Peronospora obducens) was first reported in the United States in 2004, but widespread outbreaks were observed throughout North America in 2011 (5). In June 2012, symptoms, including severe defoliation while plants retained upright stems, were observed on approximately 100 landscape impatiens (Impatiens walleriana Hook.f.) in Franklin County in central Kentucky. All plants in the landscape were affected. Plants were primarily defoliated and remaining leaves were stunted, mottled, and chlorotic with edges curled downward; no flowers were present. Under examination with a dissecting microscope, white downy fungal growth was observed. Closer examination confirmed that the growth consisted of colorless sporangiophores that were mainly unbranched, straight, and rigid (1,3). Sporangiophores consisted of apical branches attached at right angles to main axes, ranging from 67.2 to 89.9 μm long (1). Sporangia were ovoid and hyaline, measuring 11.2 to 13.3 μm × 8.2 to 10.7 μm (3). No oospores were observed. Pathogenicity tests were performed by inoculating 20 to 40 leaves on three plants each of the cvs. Dazzler and Super Elfin with suspensions of 1 × 105 sporangiophores per ml in sterile distilled water. Sporangia were obtained by washing infected leaves with sterile distilled water, and inoculations were completed by spraying leaves until runoff. Plants sprayed with sterile water served as controls. Plants were covered with black plastic bags for 48 h and then maintained under fluorescent lights for 10 days at room temperature (22 to 25°C). Sporangiophores were recovered from inoculated plants after 10 days, and morphology matched original inoculum; symptoms included chlorotic, downward curling leaves with sporulation on the undersides. Non-inoculated plants did not develop symptoms after 21 days. Molecular identification of the pathogen was conducted using three leaves from one plant from each cultivar. PCR was conducted by amplifying the large ribosomal subunit DNA using primers NL-1 and NL-4 (2). Amplicons of 762 to 691 bp were produced from diseased plant tissue that contained visible sporangiophores, and the bands were extracted from the gel and purified. Sequence results confirmed 100% similarity to accessions from Florida (GenBank Accession No. JX217746.1) and Ohio (JX142134.1) and 99% similarity to amplicons reported from Serbia (HQ246451.1) and UK (AY587558.1). This is believed to be the first report of downy mildew infecting impatiens in Kentucky. References: (1) O. Constantinescu. Mycologia 83:473, 1991. (2) W. Maier et al. Can. J. Bot 81:12, 2003. (3) P. A. Saccardo. Syllogue Fungorum 7:242, 1888. (4) S. N. Wegulo et al. Plant Dis. 88:909, 2004.


Plant Disease ◽  
2009 ◽  
Vol 93 (12) ◽  
pp. 1349-1349 ◽  
Author(s):  
S. Rooney-Latham ◽  
C. L. Blomquist ◽  
J. Turney

Fenugreek (Trigonella foenum-graecum) is a member of the Fabaceae family and is grown worldwide for culinary and medicinal purposes. The leaves are used as an herb while the seeds are used whole, ground as a spice, or germinated and used as sprouts. In November 2008, a fenugreek plant exhibiting leaf spotting and severe stunting was submitted to the CDFA Plant Pest Diagnostics Laboratory from the Los Angeles County Plant Diagnostic Laboratory. The county had received the sample from a homeowner who reported severe dieback of the fenugreek in his backyard planting. The fenugreek is grown by the resident as an annual and is propagated each year from the previous crop's seed. The seed was originally obtained from a local ethnic grocery store in Lakewood, CA. The homeowner stated that he had noticed symptoms for a number of years and that they seemed especially severe during the winter months. The adaxial surfaces of the leaves exhibited small chlorotic spots often at the leaf margins, while the abaxial surfaces exhibited a grayish violet, felty growth. Conidiophores found on the underside of the leaves branched dichotomously 6 to 10 times and were terminally forked. Conidiophores measured 280 to 525 μm (average 420 μm) with slightly swollen bases (7.5 to 10 μm broad). Conidia were slightly pigmented, oblong to ellipsoid, and measured 23 to 33 × 18 to 23 μm (average 27.8 × 20.3 μm). Globose oospores with verruculose walls measured 30 to 40 μm in diameter (average 36.1 μm) and were found embedded in the leaf tissue of older lesions. The pathogen was identified morphologically as Peronospora trigonellae Gaum. (3). Sequences of a portion of the rDNA, including the internal transcribed spacer regions, were obtained using primers DC6 and ITS6 (1). Sequence data for P. trigonellae had not previously been entered into GenBank and no identity was obtained. Pathogenicity experiments attempted by spraying healthy fenugreek seedlings with conidial suspensions were unsuccessful, presumably because of the age of the inoculum. Since fenugreek is not commercially grown in California, the economic importance of this disease is limited. Although P. trigonellae has been reported on fenugreek in Algeria, India, Pakistan, and the United Kingdom (2–4), to our knowledge, this is the first report of its occurrence in California and the United States. A specimen of P. trigonellae has been deposited in the U.S. National Fungus Collection (BPI 879153). References: (1) D. E. L. Cooke et al. Fungal Genet. Biol. 30:17, 2000. (2) D. F. Farr et al. Fungal Databases. Systematic Mycology and Microbiology Laboratory. Online publication. ARS, USDA, 2009, (3) E. A. Gaumann. Beitr. Kryptogamenflora Schweiz 5:216, 1923. (4) D. R. Jones et al. Plant Pathol. 56:891, 2007.


Plant Disease ◽  
2018 ◽  
Vol 102 (12) ◽  
pp. 2411-2420 ◽  
Author(s):  
Catalina Salgado-Salazar ◽  
Nicholas LeBlanc ◽  
Adnan Ismaiel ◽  
Yazmín Rivera ◽  
Colleen Y. Warfield ◽  
...  

Impatiens downy mildew (IDM) of cultivated Impatiens walleriana has had a significant economic impact on the ornamental horticulture industry in the United States and globally. Although recent IDM outbreaks started in 2003, downy mildews on noncultivated Impatiens species have been documented since the 1880s. To understand the relationship between the pathogen causing recent epidemics and the pathogen historically present in the United States, this work characterized genetic variation among a collection of 1,000 samples on 18 plant hosts. Samples included collections during recent IDM epidemics and historical herbarium specimens. Ten major genotypes were identified from cloned rDNA amplicon sequencing and endpoint SNP genotyping. Three genotypes accounted for >95% of the samples, with only one of these three genotypes found on samples predating recent IDM outbreaks. Based on phylogenetic analysis integrating data from three markers and the presence of individual genotypes on multiple Impatiens species, there was some evidence of pathogen-specific infection of I. noli-tangere, but the distinction between genotypes infecting I. walleriana and I. balsamina was not upheld. Overall, this work provides evidence that the majority of rDNA genotypes recovered from recent IDM epidemics are different from historical U.S. genotypes, and that these genotypes can infect Impatiens spp. other than I. walleriana.


Plant Disease ◽  
2012 ◽  
Vol 96 (1) ◽  
pp. 146-146 ◽  
Author(s):  
A. L. Testen ◽  
J. M. McKemy ◽  
P. A. Backman

Quinoa, Chenopodium quinoa Willd., is an Andean crop prized for its high nutritional value and adaptability to harsh environments. Quinoa is plagued by downy mildew caused by Peronospora variabilis Gäum (formerly Peronospora farinosa f. sp. chenopodii Byford) (1). Quinoa production has spread beyond native Andean ranges and quinoa downy mildew has been reported in India, Canada, and Denmark (1). During the summer of 2011, quinoa trials were established to determine the ability of quinoa to grow under Mid-Atlantic conditions and monitor for regional disease problems. In July, after cool, rainy conditions, downy mildew-like symptoms were observed on quinoa at research plots in Centre and Lancaster counties of Pennsylvania. Symptoms and signs consisted of irregularly shaped areas of foliar chlorosis or pink discoloration accompanied by dense, gray sporulation on both leaf surfaces. Sporangia were tan to gray-brown, semi-ovoid, often with a pedicel, mean length of 31 μm, and mean width of 23 μm. Sporangiophores branched dichotomously, and the terminal branchlets curved and tapered to a point. Orange oospores were present in field samples of leaf tissue. DNA was extracted from infected foliar tissue and sporangial suspensions. A seminested PCR protocol (2) was used to obtain partial internal transcribed spacer (ITS) sequences of six Peronospora isolates. The sequences shared 99% maximum identity to a known P. variabilis accession (FM863721.2) in GenBank. A voucher specimen was deposited into the U.S. National Fungus Collections (BPI 882064). Pathogenicity of each of two strains of P. variabilis was confirmed by inoculating quinoa with sporangia (4). Sporangia were shaken from leaves in sterile distilled water and the suspension was filtered through cheesecloth. A 0.01% Tween solution was added and the suspension diluted to 103 sporangia/ml. With an atomizer, a 10-ml sporangial suspension (or sterile water for noninoculated control plants) was sprayed onto one flat of 18 2-week-old quinoa plants, and relative humidity was increased to saturation using a humidity dome for 24 h. After 1 week, chlorosis and pink discoloration were noted on leaves of inoculated quinoa, and after 18 h of subsequent increased humidity (>95% relative humidity), dense gray sporulation was observed. No symptoms were noted on noninoculated control plants. Sporangia and sporangiophores were examined morphologically and confirmed to be P. variabilis, confirming Koch's postulates. For culture maintenance, 2-week-old quinoa leaves were placed onto a sporangial suspension on top of 1% water agar and maintained in a growth chamber at 20°C with 16 h of light per day. Quinoa downy mildew is seedborne (3) and initial infections may have occurred from oospores in the pericarp, despite intensive processing of consumable quinoa seeds to remove saponins. To our knowledge, this is the first report of quinoa downy mildew in the United States and also the first report of P. variabilis in the United States. References: (1) Y. Choi et al. Mycopathologia 169:403, 2010. (2) D. Cooke et al. Fungal Genet. Biol. 30:17, 2000. (3) S. Danielson et al. Seed Sci. Technol. 32:91, 2004. (4) J. Ochoa et al. Plant Pathol. 48:425, 1999.


Plant Disease ◽  
2014 ◽  
Vol 98 (7) ◽  
pp. 1006-1006 ◽  
Author(s):  
K. N. Conner ◽  
J. Olive ◽  
A. K. Hagan ◽  
L. Zhang ◽  
M. E. Bloodworth

During spring 2012, potted impatiens (Impatiens walleriana Hook.f.) plants with symptoms of a foliar disease were found in several commercial greenhouses in Mobile County, Alabama. Symptomatic leaves were chlorotic with no distinct lesions, and quickly wilted and abscised from erect green stems. In summer 2012 and 2013, numerous landscape impatiens plants with similar symptoms were observed in a large area from Mobile County north to Lee County, Alabama. A downy mildew was observed on the lower surfaces of symptomatic and abscised leaves from all locations. It consisted of hyaline, monopodial sporangiophores and ovoid, hyaline sporangia. Sporangiophores, which emerged from stomata, consisted of apical branches arranged at right angles to the supporting branches; they measured 69 to 90 μm long with individual branches measuring 7 to 14 μm long. Sporangia were borne on the tips of sporangiophore branches and measured 10 to 16.5 × 17 to 22.5 μm. No oospores were observed. In 2013, symptomatic plants were obtained from two separate locations in Alabama (Mobile and Tallapoosa counties). Total genomic DNA was extracted directly from symptomatic plant tissue and the large ribosomal subunit DNA was amplified by PCR using primers NL-1 and NL-4 (1). From both isolates, amplicons of 600 and 775 bp were obtained. DNA from each amplicon of both isolates was purified, sequenced, and the sequences were deposited in GenBank (Accession Nos. KF956518 to 21). The sequences of the 600-bp amplicons were 99% similar to that of I. walleriana (JX142135); the sequences of the 775-bp amplicons were 99% similar to Plasmopara obducens isolates from Florida (JX217746), Ohio (JX142134), Serbia (HQ246451), and the United Kingdom (AY587558). In pathogenicity tests, 10 potted impatiens plants, I. walleriana‘Super Elfin,’ were inoculated with a sporangial suspension (1 × 105 sporangia/ml washed from infected leaves) from the Mobile County isolate, by spraying until runoff. Controls were inoculated with sterile water. Plants were incubated in a moist chamber at 21°C for 48 h and then maintained in a greenhouse at 22 to 25°C until symptom development. All inoculated plants developed symptoms of downy mildew within 10 days. Microscopic examination of the symptomatic tissue revealed sporangiophores and sporangia similar to those observed in naturally infected plants. Control plants showed no symptoms. To our knowledge, this is the first report of downy mildew caused by P. obducens on impatiens in Alabama. This disease has been reported to have a significant economic impact for growers throughout the United States (2,3). Impatiens downy mildew is likely to be a recurring problem in Alabama. References: (1) K. O'Donnell. Curr. Genet. 22:213, 1992. (2) A. Palmateer et al. Plant Dis. 97:687, 2013. (3) S. Wegulo et al. Plant Dis. 88:909, 2004.


HortScience ◽  
2018 ◽  
Vol 53 (7) ◽  
pp. 925-931 ◽  
Author(s):  
Weining Wang ◽  
Yanhong He ◽  
Zhe Cao ◽  
Zhanao Deng

Garden impatiens (Impatiens walleriana), a very important floricultural crop in the United States, has been devastated by impatiens downy mildew (IDM) in recent years. This study was conducted to determine if induced tetraploidy could improve impatiens resistance to downy mildew. Tetraploids were induced by colchicine and confirmed by chromosome counting. Compared with diploids, induced tetraploids showed significant morphological changes, including larger and thicker leaves with larger and fewer stomata; thicker and fewer stems; larger and fewer flowers; and larger pollen grains with higher stainability. In detached leaf and in vivo inoculation assays, tetraploids exhibited improved downy mildew resistance, with lower disease severity, disease incidences, and sporangia densities. Plasmopara obducens, the causal agent of IDM, underwent a similar development process in the leaf tissue of diploids and tetraploids. These results suggest that induced tetraploidy can result in significant changes in impatiens leaf and plant morphology and can increase impatiens resistance to downy mildew to a certain extent.


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