Response of Sugarbeet Lines to Isolates of Fusarium oxysporum f. sp. Betae from the United States

2009 ◽  
Vol 46 (1) ◽  
pp. 11-26 ◽  
Author(s):  
L E Hanson ◽  
A L Hill ◽  
B J Jacobsen ◽  
L Panella
Plant Disease ◽  
2022 ◽  
Author(s):  
Roy Davis ◽  
Thomas Isakeit ◽  
Thomas Chappell

Fusarium wilt of cotton, caused by the soilborne fungal pathogen Fusarium oxysporum f. sp. vasinfectum (FOV), occurs in regions of the United States where cotton (Gossypium spp.) is grown. Race 4 of this pathogen (FOV4) is especially aggressive and does not require the co-occurrence of the root knot nematode (Meloidogyne incognita) to infect cotton. Its sudden appearance in far-west Texas in 2016 after many years of being restricted to California is of great concern, as is the threat of its continued spread through the cotton-producing regions of the United States. The aim of this research was to analyze the spatial variability of FOV4 inoculum density in the location where FOV4 is locally emerging, using quantitative and droplet digital polymerase chain reaction (qPCR and ddPCR) methods. Soil samples collected from a field with known FOV4 incidence in Fabens, Texas were analyzed. Appreciable variation in inoculum density was found to occur at spatial scales smaller than the size of plots involved in cultivar trial research, and was spatially autocorrelated (Moran’s I, Z = 17.73, p < 0.0001). These findings indicate that for cultivar trials, accounting for the spatial distribution of inoculum either by directly quantifying it or through the use of densely-distributed “calibration checks” is important to the interpretation of results.


Plant Disease ◽  
1997 ◽  
Vol 81 (9) ◽  
pp. 1077-1081 ◽  
Author(s):  
Reuven Reuveni ◽  
Nativ Dudai ◽  
Eli Putievsky ◽  
W. H. Elmer ◽  
R. L. Wick

Growth chamber evaluation of several cultivars of basil and related herbs examined in the United States revealed that identical cultivars from different sources did not differ in their reactions to artificial inoculation with Fusarium oxysporum f. sp. basilicum. Cultivars differed in susceptibility to the pathogen: “Spicy globe” miniature was the most susceptible, and lemon basil (Ocimum basilicum var. citriodorum), Origanum majorana, and Thymus vulgaris were rated as not susceptible. Twenty isolates of F. oxysporum, originating from stems of diseased basil plants in Israel, were pathogenic on basil in growth chamber and greenhouse tests. Under artificial inoculation, 2 isolates of F. oxysporum f. sp. basilicum from stems were pathogenic to basil but not to 9 species representing Lamiaceae, Cucurbitaceae, Solanaceae, and Compositae indicating the specificity of the pathogen to basil. These isolates were used for additional resistance tests. Ocimum basilicum var. purpurascens (Exotic) and var. citriodorum were rated as not susceptible to the pathogen under artificial inoculation. Resistant germ plasm was identified in several basil plants of a local variety originally introduced from the United States and reselected at Newe Ya'ar. Seeds were planted in the greenhouse in naturally highly infested soil. Symptomless plants that survived in naturally infested soil were the source for F1 seeds of resistant germ plasm, which was confirmed by artificial inoculations with both isolates of the pathogen. Further selection tests to improve resistance were conducted up to the F4 generation in infested soil in the greenhouse. All individuals of the present genetic line remained symptomless, while all individual plants of the original susceptible cultivar defoliated 3 weeks after planting into infested soil, suggesting that the resistance may be a single, dominant gene. The causal organism was reisolated only from the susceptible plants and not from the symptomless resistant plants through all the experiments.


Plant Disease ◽  
2013 ◽  
Vol 97 (9) ◽  
pp. 1200-1206 ◽  
Author(s):  
Kimberly M. Webb ◽  
Austin J. Case ◽  
Mark A. Brick ◽  
Kris Otto ◽  
Howard F. Schwartz

Fusarium oxysporum f. sp. betae causes Fusarium yellows in sugar beet (Beta vulgaris). The F. oxysporum population from sugar beet can be highly variable in virulence and morphology and many isolates are nonpathogenic. Rapid and reliable methods to identify pathogenic isolates from nonpathogenic F. oxysporum generally are unavailable. Little is known about nonpathogenic isolates, including the role they may play in population diversity or virulence to sugar beet. Sugar beet is often grown in rotation with other crops, including dry edible bean (Phaseolus vulgaris) and onion (Allium cepa), with F. oxysporum able to cause disease on all three crops. Thirty-eight F. oxysporum isolates were collected from symptomatic sugar beet throughout the United States to investigate diversity of the F. oxysporum population and the influence of crop rotation on pathogenic variation. These isolates were characterized for pathogenicity to sugar beet, dry edible bean, and onion, as well as vegetative compatibility. Pathogenicity testing indicated that some F. oxysporum isolates from sugar beet may cause disease on onion and dry edible bean. Furthermore, vegetative compatibility testing supported previous reports that F. oxysporum f. sp. betae is polyphyletic and that pathogenic isolates cannot be differentiated from nonpathogenic F. oxysporum using vegetative compatibility.


Plant Disease ◽  
2007 ◽  
Vol 91 (5) ◽  
pp. 639-639 ◽  
Author(s):  
R. C. Ploetz ◽  
A. J. Palmateer ◽  
D. M. Geiser ◽  
J. H. Juba

Roselle, Hibiscus sabdariffa var. sabdariffa, is an annual that is grown primarily for its inflated calyx, which is used for drinks and jellies. It is native from India to Malaysia, but was taken at an early date to Africa and is now widely grown in the tropics and subtropics (2). In late 2005, dying plants were noted by a producer in South Florida. Plants wilted, became chlorotic, and developed generally unthrifty, sparse canopies. Internally, conspicuous vascular discoloration was evident in these plants from the roots into the canopy. After 5 days on one-half-strength potato dextrose agar (PDA), salmon-colored fungal colonies grew almost exclusively from surface-disinfested 5 mm2 pieces of vascular tissue. On banana leaf agar, single-spored strains produced the following microscopic characters of Fusarium oxysporum: copious microconidia on monophialides, infrequent falcate macroconidia, and terminal and intercalary chlamydospores. Partial, elongation factor 1-α (EF1-α) sequences were generated for two of the strains, O-2424 and O-2425, and compared with previously reported sequences for the gene (3). Maximum parsimony analysis of sequences showed that both strains fell in a large, previously described clade of the F. oxysporum complex (FOC) that contained strains from agricultural hosts, as well as human clinical specimens (2; clade 3 in Fig. 4); many of the strains in this clade have identical EF1-α sequences. Strains of F. oxysporum recovered from wilted roselle in Egypt, O-647 and O-648 in the Fusarium Research Center collection, were distantly related to the Florida strains. We are not aware of other strains of F. oxysporum from roselle in other international culture collections. Roselle seedlings were inoculated with O-2424 and O-2425 by placing a mycelial plug (5 mm2, PDA) over a small incision 5 cm above the soil line and then covering the site with Parafilm. Parafilm was removed after 1 week, and plants were incubated under ambient temperatures (20 to 32°C) in full sun for an additional 5 weeks (experiment 1) or 7 weeks (experiment 2). Compared with mock-inoculated (wound + Parafilm) control plants, both O-2424 and O-2425 caused significant (P < 0.05) vascular disease (linear extension of discolored xylem above and below wound site) and wilting (subjective 1 to 5 scale); both isolates were recovered from affected plants. F. oxysporum-induced wilt of roselle has been reported in Nigeria (1) and Malaysia (4) where the subspecific epithet f. sp. rosellae was used for the pathogen. We are not aware of reports of this disease elsewhere. To our knowledge, this is the first report of F. oxysporum-induced wilt of roselle in the United States. Research to determine whether the closely related strains in clade 3 of the FOC are generalist plant pathogens (i.e., not formae speciales) is warranted. References: (1) N. A. Amusa et al. Plant Pathol. J. 4:122, 2005. (2) J. Morton. Pages 81–286 in: Fruits of Warm Climates. Creative Resource Systems, Inc., Winterville, NC, 1987. (3) K. O'Donnell et al. J. Clin. Microbiol. 42:5109, 2004. (4) K. H. Ooi and B. Salleh. Biotropia 12:31, 1999.


Plant Disease ◽  
2011 ◽  
Vol 95 (7) ◽  
pp. 877-877
Author(s):  
A. Garibaldi ◽  
P. Pensa ◽  
D. Bertetti ◽  
A. Poli ◽  
M. L. Gullino

During the summer of 2010, 20% of 7,000 4-month-old plants of apple cactus (Cereus peruvianus monstruosus) showed symptoms of a basal stem rot in a commercial nursery located in Liguria (northern Italy). Affected plants showed yellow orange-to-pale brown color from the crown level to the stem apex and a water-soaked rot was observed on the stem starting from the base. Brown discoloration was observed in the vascular system. Eventually stems bent, plants collapsed and died, and affected tissues dried out. A Fusarium sp. was consistently and readily isolated from symptomatic tissue on Komada selective medium. Isolates were purified and subcultured on potato dextrose agar (PDA). Single-spore cultures on PDA, Spezieller Nährstoffarmer agar (SNA) (3), and carnation leaf-piece agar (CLA) (2) were incubated at 26 ± 1°C (12-h fluorescent light, 12-h dark). On PDA, cultures produced a thick growth of white-to-pink mycelium and pale pink pigments in the agar. On SNA, cultures produced short monophialides with unicellular, ovoid-elliptical microconidia measuring 4.3 to 8.2 × 2.3 to 3.8 (average 6.0 × 2.8) μm. Chlamydospores were abundant, single or paired, terminal and intercalary, rough walled, and 6 to 8 μm in diameter. On CLA, cultures produced orange sporodochia with macroconidia that were 3 to 4 septate, nearly straight with a foot-shaped basal cell and a short apical cell, and measured 31.1 to 51.5 × 4.4 to 3.5 (average 43.2 × 3.8) μm. Such characteristics are typical of Fusarium oxysporum (3). Amplification of the ITS (internal transcribed spacer) of the rDNA using primers ITS1/ITS4 (4) yielded a 498-bp band. Sequencing and BLASTn analysis of this band showed an E-value of 0.0 with F. oxysporum. The nucleotide sequence has been assigned GenBank Accession No. JF422071. To confirm pathogenicity, five 6-month-old healthy plants of C. peruvianus monstruosus were inoculated by dipping roots in a conidial suspension (2.4 × 106 CFU/ml) of F. oxysporum isolated from affected plants. Inoculum was obtained from pure cultures of three single-spore isolates grown for 10 days on casein hydrolysate liquid medium. Roots were not wounded before the inoculation. Plants were transplanted into pots filled with steam-sterilized substrate (sphagnum peat/perlite/pine bark/clay 50:20:20:10). Five noninoculated plants served as a control. Plants were placed in a climatic chamber at 25 ± 1°C (12-h fluorescent light, 12 h-dark). Basal stem rot and vascular discoloration in the crown and stem developed within 30 days on each inoculated plant. Noninoculated plants remained healthy. F. oxysporum was consistently isolated from symptomatic plants. The pathogenicity test was conducted twice. F. oxysporum has been reported on Cereus spp. in the United States (1). To our knowledge, this is the first report of F. oxysporum on C. peruvianus monstruosus in Italy as well as in Europe. Currently, this disease is present in a few nurseries in Liguria. References: (1) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society, St Paul, MN, 1989. (2) N. L. Fisher et al. Phytopathology 72:151, 1982. (3) J. F. Leslie and B. A. Summerell. The Fusarium Laboratory Manual. Blackwell, Ames, IA, 2006. (4) T. J. White et al. PCR Protocols: A Guide to Methods and Applications. M. A. Innis et al., eds. Academic Press, San Diego, 1990.


Plant Disease ◽  
2005 ◽  
Vol 89 (4) ◽  
pp. 432-432 ◽  
Author(s):  
S. A. Gaetán

Canola (Brassica napus) is a developing oleaginous crop grown commercially in Argentina, primarily in the southeastern region of Buenos Aires Province. Since 2002, plants exhibiting symptoms of wilt and xylem discoloration were observed in canola plants in experimental field plots located at the University of Buenos Aires, Buenos Aires, Argentina. Average disease incidence in 5- to 6-month-old canola cultivars developed in different countries was 18% (range = 9 to 27%). Disease symptoms that included yellowing, wilting, stunting, and necrosis of leaf tissue and suppressed root development appeared in irregular-shaped patches following the rows of plants. The first symptom observed was leaf yellowing followed by an irregular, brown necrosis of the leaf margins. Lesions coalesced to form large necrotic areas that led to severe defoliation beginning with the lower leaves. As the disease developed, a pale brown discoloration girdled the stems that progressed from the basal tissues to the apex. Affected plants were stunted and had small pods with no seeds. Diseased plants eventually collapsed and died. From June to July 2003, six samples consisting of five affected plants per sample were randomly collected from experimental field plots. Pieces (1 cm long) of disease basal stem tissue were thoroughly washed, surface sterilized in 1% sodium hypochlorite for 1 min, rinsed in sterile distilled water, blotted dry on sterile Whatman's filter paper, and incubated on potato dextrose agar in the dark at 26°C for 10 days. Ten resulting colonies were examined microscopically and identified as Fusarium oxysporum Schlechtend.:Fr. f. sp. conglutinans (Wollenweb.) W.C. Snyder & H.N.Hans. (3). Pathogenicity tests for three single-spore isolates of the fungus were performed on 6-week-old canola plants of cvs. Impulse, Master, Mistral, Monty, Rivette, and Trooper. Koch's postulates were completed for each isolate by dipping the roots of seedlings in a conidial suspension (2 times; 105 conidia per ml) for 15 min. Plants were repotted in a sterilized soil mix (soil/sand, 2:1). The experiment, which included five inoculated plants and three noninoculated (roots dipped in sterile distilled water) control plants for each cultivar, was conducted in a greenhouse at 23 to 25°C and 75% relative humidity with no supplemental light. Characteristic symptoms, identical to the original observations, developed within 14 days after inoculation on 100% of the inoculated plants for all three isolates. The pathogen was successfully reisolated from internal diseased stem tissue in all instances. Symptoms included stunted seedlings, leaf necrosis, and external stem discoloration. None of the control plants developed disease. The experiment was repeated once with similar results. F. oxysporum f. sp. conglutinans, which has been reported to cause disease in canola in Canada (1) and the United States (2), represents a serious threat to the main canola cultivars grown in Argentina. To our knowledge, this is the first report of canola wilt incited by F. oxysporum f. sp. conglutinans in Argentina. References: (1) D. Bernard et al. Can. Plant Dis. Surv. 81:102, 2001. (2) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society, St. Paul, MN, 1989. (3) P. E. Nelson et al. Fusarium species. An Illustrated Manual for Identification. Pennsylvania State University Press. University Park, PA, 1983.


Plant Disease ◽  
2005 ◽  
Vol 89 (1) ◽  
pp. 108-108 ◽  
Author(s):  
D. S. Egel ◽  
R. Harikrishnan ◽  
R. Martyn

Fusarium oxysporum f. sp. niveum race 1 is uniformly distributed throughout watermelon (Citrullus lanatus (Thunb.) Matsum. & Nakai) growing regions, but F. oxysporum f. sp. niveum race 2 has a limited known distribution in the United States (Texas, Florida, Oklahoma, Maryland, and Delaware) (3,4). Since the spring of 2001, commercial watermelon fields in Knox and Gibson counties in southwestern Indiana have been observed with symptoms of one-sided wilt and vascular discoloration typical of Fusarium wilt. Race 2 of F. oxysporum f. sp. niveum was suspected as the casual agent since the diseased watermelon cultivars are considered resistant to races 0 and 1. Two isolates of F. oxysporum obtained from wilted watermelon plants in two different commercial fields and one isolate obtained from a wilted seedling in a transplant house were compared for pathogenicity in a greenhouse assay. Known isolates of F. oxysporum f. sp. niveum races 0, 1, and 2 were obtained from Don Hopkins (University of Florida, Apopka), Kate Everts (University of Maryland/University of Delaware, Salisbury, MD), and Ray Martyn (Purdue University, West Lafayette, IN), respectively, and were used for comparison. All isolates were grown in shake cultures in a mineral salts liquid medium. (1). After 72 hr, the predominately microconidal suspensions were filtered through cheesecloth and adjusted to 1 × 105 conidia/ml with the aid of a hemacytometer. A concentration of 1 × 105 condia/ml was shown previously to cause the desired disease reaction in the standard cultivars. Seedlings of the differential cvs, Black Diamond (universal susceptible), Charleston Gray (race 0 resistant), and Calhoun Gray (race 0 and 1 resistant) were grown in a 1:1, (v:v) sand/ vermiculite mixture to the first true-leaf stage after which the plants were uprooted and the roots carefully washed prior to root dip inoculation. Subsequent to inoculation, seedlings were planted in a sand/vermiculite/ peat mixture (4:1:1, [v:v:v]) with four seedlings to a 15-cm-diameter pot. The experimental design was a randomized complete block with five replications. Two isolates from the commercial field plants caused an average of 100% wilt on cv. Black Diamond, 95% wilt on cv. Charleston Gray, and 80% wilt on cv. Calhoun Gray, resulting in a designation of race 2. The isolate from a commercial transplant house resulted in 100, 60, and 15% wilt, respectively, on the three standard cultivars resulting in a race 1 designation. The presence of F. oxysporum f. sp. niveum race 2 in Indiana is significant because Indiana currently ranks fifth in the United States in watermelon production and there are no commercially available cultivars that possess resistance to race 2. To our knowledge, this is the first report of F. oxysporum f. sp. niveum race 2 in Indiana and the first report of race 2 from the Midwest region of the United States. Race 2, first described from the United States in 1985 (2), has now been confirmed in six states. References: (1) R. Esposito and A. Fletcher. Arch. Biochem. Biophys. 93:369, 1961. (2) R. Martyn, Plant Dis. 69:1007, 1985. (3) R. Martyn, Plant Dis. 71:233, 1987. (4) X. Zhou and K. Everts. Plant Dis. 87:692, 2003.


Plant Disease ◽  
2009 ◽  
Vol 93 (12) ◽  
pp. 1298-1304 ◽  
Author(s):  
E. A. Holmes ◽  
R. S. Bennett ◽  
D. W. Spurgeon ◽  
P. D. Colyer ◽  
R. M. Davis

Sixty-one isolates of Fusarium oxysporum f. sp. vasinfectum were collected from cotton plants (Gossypium spp.) with symptoms of Fusarium wilt to determine the composition of races present in the southeastern United States. Analysis of partial sequences of the translation elongation factor gene revealed four novel genotypes, as well as the presence of races 3 and 8 for the first time in the United States outside of California. The majority of isolates (16 of 27) sampled from Arkansas were novel genotypes. A subset of isolates representing the novel genotypes was compared with previously described races using sequences from translation elongation factor, phosphate permase, and β-tubulin genes and their pathogenicity on a total of six Upland (Gossypium hirsutum) and Pima (G. barbadense) cotton cultivars. Two of the novel genotypes belonged to a clade containing races 1, 2, 4, 6, and 8 and two shared ancestry with race 3. All new genotypes were pathogenic to at least some of the cotton cultivars tested. The Pima cv. Phytogen 800 was relatively resistant to all genotypes of the pathogen. These results indicate that the population of F. oxysporum f. sp. vasinfectum in the southeastern United States is more diverse than previously recognized.


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