scholarly journals Fusarium Root and Crown Rot: A Disease of Container-Grown Hostas

Plant Disease ◽  
2000 ◽  
Vol 84 (9) ◽  
pp. 980-988 ◽  
Author(s):  
B. Wang ◽  
S. N. Jeffers
Keyword(s):  
South Carolina ◽  
Crown Rot ◽  
Undescribed Species ◽  
Fresh Weight ◽  
Fusarium Spp ◽  
Disease Symptoms ◽  
Leaf Yellowing ◽  
Oat Seeds ◽  
Root And Crown Rot ◽  
Fusarium Sp

A previously unreported disease was observed on 11 cultivars of container-grown hosta plants at five wholesale nurseries in South Carolina between 1997 and 1999. Symptoms included leaf yellowing, plant stunting, rotting of and vascular discoloration in roots, and necrosis in the crowns. Fusarium spp. consistently were isolated from symptomatic hosta plants. Four species were recovered: F. solani, F. oxysporum, F. proliferatum, and an undescribed species designated Fusarium sp.; F. solani and Fusarium sp. were recovered most frequently. To demonstrate pathogenicity, four methods were used to inoculate hosta plants with representative isolates of F. solani, F. oxysporum, and Fusarium sp. Two types of inoculum, colonized oat seeds and conidium suspensions, were used to inoculate wounded and nonwounded plants. Disease symptoms occurred consistently only on hosta plants inoculated by dipping wounded roots and crowns into suspensions of conidia. Symptoms were most severe on plants inoculated with Fusarium sp. and much less severe on plants inoculated with F. solani or F. oxysporum. Disease severity increased and fresh weight of inoculated plants decreased when the concentration of inoculum of Fusarium sp. was increased over the range of 1 × 103 to 1 × 107 conidia per ml. Isolates of Fusarium sp., F. solani, and F. oxysporum varied in virulence when Hosta ‘Francee’ plants were inoculated. This study demonstrated that Fusarium root and crown rot of container-grown hostas is caused primarily by Fusarium sp. but that it also can be caused by F. solani and F. oxysporum. Fusarium sp. appears to be taxonomically distinct from other species, and its identity currently is under investigation.

scholarly journals First report of Fusarium commune causing root and crown rot on maize in Italy

Plant Disease ◽  
2021 ◽  
Author(s):  
Monica Mezzalama ◽  
Vladimiro Guarnaccia ◽  
Ilaria Martino ◽  
Giulia Tabome ◽  
Maria Lodovica GULLINO
Keyword(s):  
Plant Disease ◽  
Tap Water ◽  
Morphological Characteristics ◽  
Plant Diseases ◽  
Crown Rot ◽  
Conidial Suspension ◽  
Fusarium Spp ◽  
First Report ◽  
Root And Crown Rot ◽  
Pathogenicity Tests

Maize (Zea mays L.) is a cereal crop of great economic importance in Italy; production is currently of 62,587,469 t, with an area that covers 628,801 ha, concentrated in northern Italy (ISTAT 2020). Fusarium species are associated with root and crown rot causing failures in crop establishment under high soil moisture. In 2019 maize seedlings collected in a farm located in San Zenone degli Ezzelini (VI, Italy) showed root and crown rot symptoms with browning of the stem tissues, wilting of the seedling, and collapsing due to the rotting tissues at the base of the stem. The incidence of diseased plants was approximately 15%. Seedlings were cleaned thoroughly from soil residues under tap water. Portions (about 3-5 mm) of tissue from roots and crowns of the diseased plants were cut and surface disinfected with a water solution of NaClO at 0.5% for 2 minutes and rinsed in sterile H20. The tissue fragments were plated on Potato Dextrose Agar (PDA) amended with 50 mg/l of streptomycin sulfate and incubated for 48-72 hours at 25oC. Over the 80 tissue fragments plated, 5% were identified as Fusarium verticillioides, 60% as Fusarium spp., 35% developed saprophytes. Fusarium spp. isolates that showed morphological characteristics not belonging to known pathogenic species on maize were selected and used for further investigation while species belonging to F. oxysporum were discarded. Single conidia of the Fusarium spp. colonies were cultured on PDA and Carnation Leaf Agar (CLA) for pathogenicity tests, morphological and molecular identification. The colonies showed white to pink, abundant, densely floccose to fluffy aerial mycelium. Colony reverse showed light violet pigmentation, in rings on PDA. On CLA the isolates produced slightly curved macronidia with 3 septa 28.1 - 65.5 µm long and 2.8-6.3 µm wide (n=50). Microconidia were cylindrical, aseptate, 4.5 -14.0 µm long and 1.5-3.9 µm wide (n=50). Spherical clamydospores were 8.8 ± 2.5 µm size (n=30), produced singly or in pairs on the mycelium, according to the description by Skovgaard et al. (2003) for F. commune. The identity of two single-conidia strains was confirmed by sequence comparison of the translation elongation factor-1α (tef-1α), and RNA polymerase II subunit (rpb2) gene fragments (O’Donnell et al. 2010). BLASTn searches of GenBank, and Fusarium-ID database, using the partial tef-1α (MW419921, MW419922) and rpb2 (MW419923, MW419924) sequences of representative isolate DB19lug07 and DB19lug20, revealed 99% identity for tef-1α and 100% identity to F. commune NRRL 28387(AF246832, AF250560). Pathogenicity tests were carried out by suspending conidia from a 10-days old culture on PDA in sterile H2O to 5×104 CFU/ml. Fifty seeds were immersed in 50 ml of the conidial suspension of each isolate for 24 hours and in sterile water (Koch et al. 2020). The seeds were drained, dried at room temperature, and sown in trays filled with a steamed mix of white peat and perlite, 80:20 v/v, and maintained at 25°C and RH of 80-85% for 14 days with 12 hours photoperiod. Seedlings were extracted from the substrate, washed under tap water, and observed for the presence of root and crown rots like the symptoms observed on the seedlings collected in the field. Control seedlings were healthy and F. commune was reisolated from the symptomatic ones and identified by resequencing of tef-1α gene. F. commune has been already reported on maize (Xi et al. 2019) and other plant species, like soybean (Ellis et al. 2013), sugarcane (Wang et al. 2018), potato (Osawa et al. 2020), indicating that some attention must be paid in crop rotation and residue management strategies. To our knowledge this is the first report of F. commune as a pathogen of maize in Italy. References Ellis M L et al. 2013. Plant Disease, 97, doi: 10.1094/PDIS-07-12-0644-PDN. ISTAT. 2020. http://dati.istat.it/Index.aspx?QueryId=33702. Accessed December 28, 2020. Koch, E. et al. 2020. Journal of Plant Diseases and Protection. 127, 883–893 doi: 10.1007/s41348-020-00350-w O’Donnell K et al. 2010. J. Clin. Microbiol. 48:3708. https://doi.org/10.1128/JCM.00989-10 Osawa H et al. 2020. Journal of General Plant Pathology, doi.org/10.1007/s10327-020-00969-5. Skovgaard K 2003. Mycologia, 95:4, 630-636, DOI: 10.1080/15572536.2004.11833067. Wang J et al. 2018. Plant Disease, 102, doi/10.1094/PDIS-07-17-1011-PDN Xi K et al. 2019. Plant Disease, 103, doi/10.1094/PDIS-09-18-1674-PDN

scholarly journals Effects of Cultural Practices and Temperature on Fusarium Root and Crown Rot of Container-Grown Hostas

Plant Disease ◽  
2002 ◽  
Vol 86 (3) ◽  
pp. 225-231 ◽  
Author(s):  
B. Wang ◽  
S. N. Jeffers
Keyword(s):  
Cultural Practices ◽  
Crown Rot ◽  
Pine Bark ◽  
Disease Development ◽  
Disease Symptoms ◽  
Integrated Strategy ◽  
Different Temperatures ◽  
Conidium Suspension ◽  
Root And Crown Rot ◽  
The Impact

Fusarium root and crown rot of hosta plants grown in containers is caused primarily by Fusarium hostae. In an effort to develop an integrated strategy for managing this disease at nurseries, the effects of wounding, container mix content, watering schedule, and temperature on disease development were investigated. Plants were not wounded or were wounded by severing the roots, severing the roots and making incisions in the crown, or severing the roots and removing a small piece of the crown. Plants were inoculated by dipping roots and crowns into a suspension of conidia from one of two isolates of F. hostae. In addition, some plants were inoculated by wounding crowns with a scalpel dipped in a conidium suspension. Disease development was examined on plants grown at different temperatures (18, 25, or 32°C), grown in different container mixes (100% Canadian sphagnum peat, 100% aged and processed pine bark, or a mixture of 50% peat and 50% bark), and watered on different schedules (which kept the container mix wet, moist, or dry). Significant levels of disease occurred only on plants that were wounded when inoculated. Fusarium root and crown rot was more severe when both the roots and crowns were wounded than when only the roots were wounded. Disease symptoms developed when crowns of plants were wounded with a scalpel infested with conidia, suggesting that contaminated tools used for vegetative propagation may transfer F. hostae. Disease development also was affected significantly by container mix content, watering schedule, and temperature. In separate experiments, disease was most severe on plants grown in 100% aged pine bark, in dry container mix, or at 18 to 25°C. Disease development was significantly less when plants were grown in 100% peat, in wet container mix, or at 32°C. These results suggest that altering or manipulating cultural practices used to produce hostas in containers at nurseries can reduce the impact from Fusarium root and crown rot.

scholarly journals Temperature, Moisture, and Fungicide Effects in Managing Rhizoctonia Root and Crown Rot of Sugar Beet

2010 ◽  
Vol 100 (7) ◽  
pp. 689-697 ◽  
Author(s):  
Melvin D. Bolton ◽  
Lee Panella ◽  
Larry Campbell ◽  
Mohamed F. R. Khan
Keyword(s):  
Sugar Beet ◽  
Disease Incidence ◽  
Environmental Parameters ◽  
Disease Suppression ◽  
Crown Rot ◽  
Disease Development ◽  
Water Control ◽  
Disease Symptoms ◽  
Root And Crown Rot ◽  
Growth Chambers

Rhizoctonia solani AG-2-2 is the causal agent of Rhizoctonia root and crown rot in sugar beet; however, recent increases in disease incidence and severity were grounds to reevaluate this pathosystem. To assess the capacity at which other anastomosis groups (AGs) are able to infect sugar beet, 15 AGs and intraspecific groups (ISGs) were tested for pathogenicity on resistant (‘FC708 CMS’) and susceptible (‘Monohikari’) seedlings and 10-week-old plants. Several AGs and ISGs were pathogenic on seedlings regardless of host resistance but only AG-2-2 IIIB and AG-2-2 IV caused significant disease on 10-week-old plants. Because fungicides need to be applied prior to infection for effective disease control, temperature and moisture parameters were assessed to identify potential thresholds that limit infection. Root and leaf disease indices were used to evaluate disease progression of AG-2-2 IIIB- and AG-2-2 IV-inoculated plants in controlled climate conditions of 7 to 22 growing degree days (GDDs) per day. Root disease ratings were positively correlated with increasing temperature of both ISGs, with maximum disease symptoms occurring at 22 GDDs/day. No disease symptoms were evident from either ISG at 10 GDDs/day but disease symptoms did occur in plants grown in growth chambers set to 11 GDDs/day. Using growth chambers adjusted to 22 GDDs/day, disease was evaluated at 25, 50, 75, and 100% moisture-holding capacity (MHC). Disease symptoms for each ISG were highest in soils with 75 and 100% MHC but disease still occurred at 25% MHC. Isolates were tested for their ability to cause disease at 1, 4, and 8 cm from the plant hypocotyl. Only AG-2-2 IIIB was able to cause disease symptoms at 8 cm during the evaluation period. In all experiments, isolates of AG-2-2 IIIB were found to be more aggressive than AG-2-2 IV. Using environmental parameters that we identified as the most conducive to disease development, azoxystrobin, prothioconazole, pyraclostrobin, difenoconazole/propiconazole, flutolanil, polyoxin D, and a water control were evaluated for their ability to suppress disease development by AG-2-2 IIIB and AG-2-2 IV 17 days after planting. Flutolanil, polyoxin-D, and azoxystrobin provided the highest level of disease suppression. Because R. solani AG-2-2 IIIB and AG-2-2 IV are affected by temperature and moisture, growers may be able to evaluate environmental parameters for optimization of fungicide application.

scholarly journals First Report of Fusarium oxysporum f. sp. radicis-cucumerinum on Cucumber in Spain

Plant Disease ◽  
2001 ◽  
Vol 85 (11) ◽  
pp. 1206-1206 ◽  
Author(s):  
A. Moreno ◽  
A. Alférez ◽  
M. Avilés ◽  
F. Diánez ◽  
R. Blanco ◽  
...  
Keyword(s):  
Fusarium Oxysporum ◽  
Crown Rot ◽  
F1 Hybrid ◽  
Potato Dextrose Broth ◽  
Disease Symptoms ◽  
First Report ◽  
Vascular Discoloration ◽  
Root And Crown Rot ◽  
Three Stages ◽  
Stem Lesions

During December 1999, root and stem rot was observed on greenhouse-grown cucumber (cvs. Albatros, Brunex, Acapulco, and Cerrucho) plants in Almería, Spain, using rock wool cultures. The disease caused severe damage, estimated at a loss of up to 75% of the plants, in the first greenhouse affected; afterward, the disease was found in eight additional greenhouses (14 ha) in 1999 and 2000. Stem lesions extended up to 10 to 12 cm above the crown in mature plants, although no fruit damage was observed. In the advanced stages, abundant development of orange sporodochia was evident on crown and stem lesions, without vascular discoloration. Root, crown, and stem pieces that were placed on potato dextrose agar (PDA) after surface-disinfection with 5% sodium hypochlorite, rinsed, and dried resulted in pure fungal colonies. Based on morphological characteristics of conidia, phialides, and chlamydospores from the isolations, the fungus was identified as Fusarium oxysporum Schlechtend.:Fr. Pathogenicity tests were conducted on cucumber (cvs. Marketmore 76 and Cerrucho [F1 hybrid]), melon (cvs. Amarillo oro, Perlita, Piboule, Tania, and Nipper [F1]), watermelon (cvs. Sugar Baby, Sweet Marvel, Jubilee, and Pata Negra and hybrid Crimson sweet), Cucurbita maxima × Cucurbita moschata, zucchini (cv. Senator), and loofah (Luffa aegyptiaca) at several stages: (i) pregermination; (ii) 1 or 2 true leaves; and (iii) more than 10 true leaves. Five fungal isolates were grown on PDA or shaken potato dextrose broth at 25°C for 8 days. Inoculation was performed in pots (10 seeds or plants of each cultivar or hybrid and isolate) by drenching with 100 ml of a fungal suspension (104 to 106 CFU/ml). Sterile water was applied to noninoculated control plants. Tests were repeated in growth chambers at 25°C (night) and 28°C (day) with a 16-h photoperiod. Fifteen to fifty days after inoculation, cucumber and melon plants at all three stages developed symptoms of root and crown rot in 100% of inoculated plants, with no observed vascular discoloration. Fifty days after inoculation, all three stages of C. maxima × C. moschata and zucchini remained symptomless. Loofah and watermelon germinated poorly or not at all when inoculated at the pregermination stage. Fifteen to fifty days after inoculation, 100% of inoculated cucumber and melon plants developed symptoms. Watermelon plants inoculated at the 10 or more true-leaf stage did not develop disease symptoms. No symptoms developed on noninoculated control plants. F. oxysporum was reisolated from infected roots, crowns, and stems of inoculated plants, confirming Koch's postulates. The main symptoms on cucumber infected by F. oxysporum f. sp. cucumerinum are wilt, yellowing, and vascular discoloration. In contrast, based on inoculation of the host differentials and the resulting disease symptoms found in this study, the fungus was identified as F. oxysporum f. sp. radicis-cucumerinum (1). To our knowledge, this is the first report of F. oxysporum f. sp. radicis-cucumerinum causing root and crown rot in cucumber in Spain. Reference: (1) D. J. Vakalounakis. Plant Dis. 80:313, 1996.

scholarly journals Wilt, Crown, and Root Rot of Common Rose Mallow (Hibiscus moscheutos) Caused by a NovelFusariumsp.

Plant Disease ◽  
2017 ◽  
Vol 101 (2) ◽  
pp. 354-358 ◽  
Author(s):  
S. L. Lupien ◽  
F. M. Dugan ◽  
K. M. Ward ◽  
K. O’Donnell
Keyword(s):  
Rna Polymerase Ii ◽  
Root Rot ◽  
Molecular Phylogenetics ◽  
Phylogenetic Analyses ◽  
Elongation Factor ◽  
Crown Rot ◽  
Root And Crown Rot ◽  
Fusarium Sp ◽  
Crown And Root Rot ◽  
Rot Disease

A new crown and root rot disease of landscape plantings of the malvaceous ornamental common rose mallow (Hibiscus moscheutos) was first detected in Washington State in 2012. The main objectives of this study were to complete Koch’s postulates, document the disease symptoms photographically, and identify the causal agent using multilocus molecular phylogenetics. Results of the pathogenicity experiments demonstrated that the Fusarium sp. could induce vascular wilt and root and crown rot symptoms on H. moscheutos ‘Luna Rose’. Maximum-likelihood and maximum-parsimony phylogenetic analyses of portions of translation elongation factor 1-α and DNA-directed RNA polymerase II largest and second-largest subunit indicated that the Hibiscus pathogen represents a novel, undescribed Fusarium sp. nested within the Fusarium buharicum species complex.

Root and crown rot of strawberry caused by Pythium helicoides and its distribution in strawberry production areas of Japan

2014 ◽  
Vol 80 (5) ◽  
pp. 423-429 ◽  
Author(s):  
Yasushi Ishiguro ◽  
Kayoko Otsubo ◽  
Hideki Watanabe ◽  
Mikihiko Suzuki ◽  
Kiichi Nakayama ◽  
...  
Keyword(s):  
Crown Rot ◽  
Root And Crown Rot ◽  
Pythium Helicoides ◽  
Production Areas

scholarly journals PhytophthoraSpecies Are Common on Nursery Stock Grown for Restoration and Revegetation Purposes in California

Plant Disease ◽  
2019 ◽  
Vol 103 (3) ◽  
pp. 448-455 ◽  
Author(s):  
S. Rooney-Latham ◽  
C. L. Blomquist ◽  
K. L. Kosta ◽  
Y. Y. Gou ◽  
P. W. Woods
Keyword(s):  
North America ◽  
Phytophthora Species ◽  
Molecular Techniques ◽  
Crown Rot ◽  
Native Plant ◽  
Nursery Stock ◽  
Plant Nursery ◽  
Root And Crown Rot ◽  
Symptomatic Tissue ◽  
First Time

Phytophthora tentaculata was detected for the first time in North America in 2012 in a nursery on sticky monkeyflower plant (Diplacus aurantiacus) and again in 2014 on outplanted native plants. At that time, this species was listed as a federally actionable and reportable pathogen by the USDA. As a result of these detections, California native plant nurseries were surveyed to determine the prevalence of Phytophthora species on native plant nursery stock. A total of 402 samples were collected from 26 different native plant nurseries in California between 2014 and 2016. Sampling focused on plants with symptoms of root and crown rot. Symptomatic tissue was collected and tested by immunoassay, culture, and molecular techniques (PCR). Identifications were made using sequences from the internal transcribed spacer (ITS) rDNA region, a portion of the trnM-trnP-trnM, or the atp9-nad9 mitochondrial regions. Phytophthora was confirmed from 149 of the 402 samples (37%), and from plants in 22 different host families. P. tentaculata was the most frequently detected species in our survey, followed by P. cactorum and members of the P. cryptogea complex. Other species include P. cambivora, P. cinnamomi, P. citricola, P. hedraiandra, P. megasperma, P. multivora, P. nicotianae, P. niederhauserii, P. parvispora, P. pini, P. plurivora, and P. riparia. A few Phytophthora sequences generated from mitochondrial regions could not be assigned to a species. Although this survey was limited to a relatively small number of California native plant nurseries, Phytophthora species were detected from three quarters of them (77%). In addition to sticky monkeyflower, P. tentaculata was detected from seven other hosts, expanding the number of associated hosts. During this survey, P. parvispora was detected for the first time in North America from symptomatic crowns and roots of the nonnative Mexican orange blossom (Choisya ternata). Pathogenicity of P. parvispora and P. nicotianae was confirmed on this host. These findings document the widespread occurrence of Phytophthora spp. in native plant nurseries and highlight the potential risks associated with outplanting infested nursery-grown stock into residential gardens and wildlands.

scholarly journals First report of Meloidogyne javanica pathogenic on hybrid lavender (Lavandula ×intermedia) in the United States

Plant Disease ◽  
2021 ◽  
Author(s):  
Samara A. Oliveira ◽  
Daniel M. Dlugos ◽  
Paula Agudelo ◽  
Steven N. Jeffers
Keyword(s):  
South Carolina ◽  
Sandy Loam ◽  
Meloidogyne Javanica ◽  
The United States ◽  
Crown Rot ◽  
Cultivated Plants ◽  
Broad Host Range ◽  
First Report ◽  
Tomato Roots ◽  
The Usa

Root-knot nematodes (RKNs), Meloidogyne spp., are some of the most economically important pathogens of cultivated plants. Meloidogyne javanica is one of the most destructive RKN species and is well known for its broad host range and the severe damage it causes to plant roots (Perry et al. 2009). In Feb 2018, four mature dead and dying hybrid lavender plants (Lavandula ×intermedia ‘Phenomenal’) were collected in Edgefield County, South Carolina, and suspected of having Phytophthora root and crown rot (Dlugos and Jeffers 2018). Greenhouse-grown plants had been transplanted in Dec 2016 and Jan 2017 into a sandy loam soil on a site that had been fallow or in pasture for over 30 years. Some plants began to turn gray and die in summer 2017, and approximately 40% of 1230 plants were symptomatic or dead by Feb 2018. Phytophthora spp. were not isolated from the collected plants but were isolated from plants collected on subsequent visits. Instead, all four plants had small, smooth galls on the roots. Lavender roots were examined microscopically (30-70×), and egg masses of RKNs were observed on the galls. Mature, sedentary RKN females were handpicked from galled roots, and perineal patterns of 10 specimens were examined and identified as M. javanica. Juveniles and eggs were extracted from lavender roots by the method of Coolen and D’herde (1972). To confirm species identification, DNA was extracted from 10 individual juveniles, and a PCR assay was conducted using species-specific primers for M. javanica, Fjav/Rjav (Zijlstra et al. 2000). A single amplicon was produced with the expected size of approximately 720 bp, which confirmed identity as M. javanica. To determine pathogenicity, M. javanica from lavender roots were inoculated onto susceptible tomato plants for multiplication, and severe gall symptoms occurred on tomato roots 60 days later. Nematodes were extracted from tomato roots and inoculated onto healthy, rooted cuttings of ‘Phenomenal’ lavender plants growing in pots of soilless medium in a greenhouse. Plants were inoculated with 0, 1000, 2000, 5000, or 10000 eggs and juveniles of M. javanica. Five single-plant replicates were used for each treatment, and plants were randomized on a greenhouse bench. Plants were assessed 60 days after inoculation, and nematodes were extracted from roots and counted. The reproduction factor was 0, 43.8, 40.9, 9.1, 7.7, and 2.6 for initial nematode populations 0, 1000, 2000, 5000, and 10000, respectively, which confirmed pathogenicity (Hussey and Janssen 2002). Meloidogyne javanica also was recovered in Mar 2018 from galled roots on a ‘Munstead’ (L. angustifolia) lavender plant from Kentucky (provided by the Univ. of Kentucky Plant Disease Diagnostic Laboratories), and an unidentified species of Meloidogyne was isolated in Aug 2020 from a ‘Phenomenal’ plant grown in Florida. COI mtDNA sequences from the SC (MZ542457) and KY (MZ542458) populations were submitted to Genbank. M. javanica previously was found associated with field-grown lavender (hybrid and L. angustifolia) in Brazil, but pathogenicity was not studied (Pauletti and Echeverrigaray 2002). To our knowledge, this is the first report of M. javanica pathogenic to L. ×intermedia in the USA, and the first time RKNs have been proven to be pathogenic to Lavandula spp. following Koch’s Postulates. Further studies are needed to investigate the geographic distribution of M. javanica on lavender and the potential threat this nematode poses to lavender production in the USA.

scholarly journals First Report of Neopestalotiopsis clavispora Causing Root and Crown Rot on Strawberry in Italy

Plant Disease ◽  
2019 ◽  
Vol 103 (11) ◽  
pp. 2959-2959 ◽  
Author(s):  
G. Gilardi ◽  
F. Bergeretti ◽  
M. L. Gullino ◽  
A. Garibaldi
Keyword(s):  
Crown Rot ◽  
First Report ◽  
Root And Crown Rot
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