Resurgence of Cucurbit Downy Mildew in the United States: A Watershed Event for Research and Extension

Plant Disease ◽  
2015 ◽  
Vol 4015 (1) ◽  
pp. 1-14 ◽  
Author(s):  
Gerald J. Holmes ◽  
Peter S. Ojiambo ◽  
Mary K. Hausbeck ◽  
Lina Quesada-Ocampo ◽  
Anthony P. Keinath
Plant Disease ◽  
2015 ◽  
Vol 99 (4) ◽  
pp. 428-441 ◽  
Author(s):  
Gerald J. Holmes ◽  
Peter S. Ojiambo ◽  
Mary K. Hausbeck ◽  
Lina Quesada-Ocampo ◽  
Anthony P. Keinath

In 2004, an outbreak of cucurbit downy mildew (CDM) caused by the oomycete Pseudoperonospora cubensis (Berk. & M. A. Curtis) Rostovzev resulted in an epidemic that stunned the cucumber (Cucumis sativus L.) industry in the eastern United States. The disease affects all major cucurbit crops, including cucumber, muskmelon, squashes, and watermelon. Although the 2004 epidemic began in North Carolina, the cucumber crop from Florida to the northern growing regions in the United States was devastated, resulting in complete crop loss in several areas. Many cucumber fields were abandoned prior to harvest. The rapid spread of the disease coupled with the failure of fungicide control programs surprised growers, crop consultants, and extension specialists. The epidemic raised several fundamental questions about the potential causes for the resurgence of the disease. Some of these questions revolved around whether the epidemic would recur in subsequent years and the possible roles that changes in the host, pathogen, and environment may have played in the epidemic.


2017 ◽  
Vol 107 (3) ◽  
pp. 313-321 ◽  
Author(s):  
Anna Thomas ◽  
Ignazio Carbone ◽  
Yigal Cohen ◽  
Peter S. Ojiambo

During the past two decades, a resurgence of cucurbit downy mildew has occurred around the world, resulting in severe disease epidemics. In the United States, resurgence of the disease occurred in 2004 and several hypotheses, including introduction of a new genetic recombinant or pathotype of the pathogen, have been suggested as potential causes for this resurgence. Occurrence and distribution of mating types of Pseudoperonospora cubensis in the United States were investigated using 40 isolates collected from cucurbits across 11 states from 2005 to 2013. Pairing of unknown isolates with known mating-type tester strains on detached leaves of cantaloupe or cucumber resulted in oospore formation 8 to 10 days after inoculation. Isolates differed in their ability to form oospores across all coinoculation pairings, with oospore numbers ranging from 280 to 1,000 oospores/cm2 of leaf tissue. Oospores were hyaline to golden-yellow, spherical, and approximately 36 μm in diameter. Of the 40 isolates tested, 24 were found to be of the A1 mating type, while 16 were of the A2 mating type. Mating type was significantly (P < 0.0001) associated with host type, whereby all isolates collected from cucumber were of the A1 mating type, while isolates from squash and watermelon were of the A2 mating type. Similarly, mating type was significantly (P = 0.0287) associated with geographical region, where isolates from northern-tier states of Michigan, New Jersey, New York, and Ohio were all A1, while isolates belonging to either A1 or A2 mating type were present in equal proportions in southern-tier states of Alabama, Florida, Georgia, North Carolina, South Carolina, and Texas. Viability assays showed that oospores were viable and, on average, approximately 40% of the oospores produced were viable as determined by the plasmolysis method. This study showed that A1 and A2 mating types of P. cubensis are present and the pathogen could potentially reproduce sexually in cucurbits within the United States. In addition, the production of viable oospores reported in this study suggests that oospores could have an important role in the biology of P. cubensis and could potentially influence the epidemiology of cucurbit downy mildew in the United States.


Author(s):  
Jake Gardner Jones ◽  
Kathryne L. Everts ◽  
Margaret Tuttle McGrath ◽  
Beth K. Gugino

In the United States, fungicides are the primary management option for cucumber growers to protect their crops from Pseudoperonospora cubensis, the causal agent of cucurbit downy mildew. Pathogen resistance to some fungicides can quickly develop with the repeated applications needed to protect yield. In order to determine fungicide efficacy and monitor it over time, bioassays were conducted from 2016-2019 in Delaware, Maryland, Pennsylvania, and New York. Potted cucumber plants were either sprayed with fungicides or not treated, placed next to field-grown plants with cucurbit downy mildew for up to two days, then kept in a greenhouse until symptoms developed. Severity of symptoms or number of lesions on leaves was recorded 6-14 days after exposure started and used to determine fungicide efficacy. Quadris (azoxystrobin) was ineffective in seven of the nine bioassays, while Revus (mandipropamid) was ineffective in six of seven bioassays. Forum (dimethomorph) and Presidio (fluopicolide) were ineffective in three of eight and four of nine bioassays, respectively. The most effective fungicides were Bravo (chlorothalonil), Zing! (zoxamide + chlorothalonil), and Orondis (oxathiapiprolin), all of which consistently suppressed disease severity more than 90% when compared with the untreated control. Previcur Flex (propamocarb hydrochloride) and Ranman (cyazofamid) were also effective in every bioassay.


2020 ◽  
Vol 110 (9) ◽  
pp. 1578-1587 ◽  
Author(s):  
E. C. Wallace ◽  
K. N. D’Arcangelo ◽  
L. M. Quesada-Ocampo

Pseudoperonospora cubensis, the causal agent of cucurbit downy mildew, is an airborne, obligate oomycete pathogen that re-emerged in 2004 and causes foliar disease and yield losses in all major cucurbit crops in the United States. Approximately 60 species in the family Cucurbitaceae have been reported as hosts of P. cubensis. Commercial hosts including cucumber, cantaloupe, pumpkin, squash, and watermelon are grown in North Carolina and many host species occur in the wild as weeds. Little is known about the contribution of wild cucurbits to the yearly epidemic; thus, this study aimed to determine the role of commercial and wild cucurbits in the structuring of P. cubensis populations in North Carolina, a region with high pathogen diversity. Ten microsatellite markers were used to analyze 385 isolates from six commercial and four wild cucurbits from three locations representing different growing regions across North Carolina. Population analyses revealed that wild and commercial cucurbits are hosts of P. cubensis in the United States, that host is the main factor structuring P. cubensis populations, and that P. cubensis has two distinct, host-adapted clades at the cucurbit species level, with clade 1 showing random mating and evidence of recombination and clade 2 showing nonrandom mating and no evidence of recombination. Our findings have implications for disease management because clade-specific factors such as host susceptibility and inoculum availability of each clade by region may influence P. cubensis outbreaks in different commercial cucurbits, timing of fungicide applications, and phenotyping for breeding efforts.


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.


Plant Disease ◽  
1998 ◽  
Vol 82 (5) ◽  
pp. 591-591 ◽  
Author(s):  
S. T. Koike ◽  
P. A. Nolan ◽  
S. A. Tjosvold ◽  
K. L. Robb

In California, hybrid statice (Misty series; Limonium bellidifolium × Limonium latifolium) is grown as a commercial cutflower crop in fields and greenhouses. In 1997, downy mildew was observed on statice plantings in both southern (San Diego County) and central (Monterey and Santa Cruz counties) parts of coastal California. Initial symptoms consisted of light green, irregularly shaped leaf spots that, after a few days, became chlorotic. As disease progressed, chlorotic spots coalesced and turned necrotic, at times resulting in extensive death of leaf tissues. Under favorable conditions, the purple to gray sporulation of the pathogen could be seen on abaxial surfaces of leaves. Conidiophores had main trunks with dichotomous branches and measured 194 to 335 μm in length (mean = 229 μm) from the base to the first branches and 7 to 8 μm across at the widest part. Branch ends were slender with curved tips that measured 5 to 8 μm long. Conidia were ovoid to globose with very short pedicels, and measured 14 to 19 μm × 14 to 17 μm. Conidial surfaces appeared slightly roughened when viewed with a scanning electron microscope. Clearing leaf sections with 10% NaOH (1) revealed the presence of yellow-brown, globose oospores that measured 31 to 47 μm. The pathogen was identified as Peronospora statices (1). Pathogenicity was demonstrated by pressing leaves with abundant sporulation against healthy leaves of test plants (Misty White) and then placing inoculated plants in a humidity chamber. After 10 to 12 days, symptoms similar to those originally observed developed on inoculated plants; after 14 to 16 days, purple fungal growth morphologically similar to the original isolates grew on leaves. Uninoculated control plants did not develop symptoms or signs of downy mildew. This is the first report of downy mildew caused by P. statices on statice in California and the rest of the United States. The disease has also been confirmed on Blue Fantasia (L. bellidifolium × L. perezii). This disease has been reported previously in Italy, The Netherlands, and the United Kingdom (1). Reference: (1) G. S. Hall et al. Eur. J. Plant Pathol. 103:471, 1997.


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.


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 ◽  
2009 ◽  
Vol 93 (2) ◽  
pp. 162-169 ◽  
Author(s):  
X. Li ◽  
X. B. Yang

Ten biological or ecological characteristics of pathogens/diseases were used to quantitatively describe 34 soybean (Glycine max) fungal diseases in the United States. These characteristics included optimal temperatures for disease development, host ranges, characteristics of disease cycle, and the pathogens' survival capacity. Gower's general similarity coefficients for pairs of diseases were determined and used in principal coordinate analysis (PCoA) to project the diseases into a two-dimensional space, in which significant patterns were identified for some of the characteristic variables, e.g., means of pathogen dispersal. Similarity coefficients indicated that soybean rust (Phakopsora pachyrhizi) resembled soybean downy mildew (Peronospora manshurica) and Leptosphaerulina leaf spot (Leptosphaerulina trifolii). Cluster analysis with multiscale bootstrapping identified two major clusters with high significance level (P > 0.95). In a loose cluster (P = 0.86), soybean rust was grouped with brown spot (Septoria glycines), frogeye leaf spot (Cercospora sojina), Phyllosticta leaf spot (Phyllosticta sojicola), purple seed stain (Cercospora kikuchii), downy mildew, and Leptosphaerulina leaf spot. Estimated soybean yield losses in the United States from 1996 to 2005 and the geographical distribution information of the diseases in this cluster implied that the potential geographical distribution range of soybean rust may include most U.S. soybean production regions and that yield losses would be light in the north but moderate in the south if environmental conditions are conducive.


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