Evidence for the heritability of resistance to brown root rot of alfalfa, caused byPhoma sclerotioides

2005 ◽  
Vol 27 (1) ◽  
pp. 64-70 ◽  
Author(s):  
C.R. Hollingsworth ◽  
F.A. Gray ◽  
R.W. Groose
Keyword(s):  
Root Rot ◽  
Author(s):  
Tse‐Yen Liu ◽  
Chao‐Han Chen ◽  
Yu‐Liang Yang ◽  
Isheng J. Tsai ◽  
Ying‐Ning Ho ◽  
...  

Plant Disease ◽  
2009 ◽  
Vol 93 (3) ◽  
pp. 317-317 ◽  
Author(s):  
M. J. Wunsch ◽  
R. Kersbergen ◽  
A. U. Tenuta ◽  
M. H. Hall ◽  
G. C. Bergstrom

Brown root rot (BRR), caused by the fungal pathogen Phoma sclerotioides G. Preuss ex Sacc. (synonym Plenodomus meliloti Dearn. & G.B. Sanford), is associated with yield loss of alfalfa (Medicago sativa L.) in regions with severe winters (1). In the spring of 2007, 9 to 69 alfalfa plants were collected from each of five production fields in Maine, 10 fields in Ontario, and nine fields in Pennsylvania. All alfalfa stands existed at least two winters. P. sclerotioides was isolated from alfalfa root and crown lesions from five fields in Maine (Penobscot, Somerset and Waldo counties), seven fields from southwestern (Woodstock and Niagara), south-central (Lindsay and Belleville), and southeastern Ontario (near Ottawa), and four fields in Pennsylvania (Columbia, Crawford, and Jefferson counties; 41.1 to 41.6°N). BRR incidence was 9 to 29% in Maine, 5 to 29% in Ontario, and 8 to 22% in Pennsylvania. In Ontario, some lesions girdled the crown; in three fields in Maine, large pycnidia characteristic of P. sclerotioides were present on alfalfa crowns and overwintered stems. On potato dextrose agar, conidia (5 to 8 × 2 to 3 μm, unicellular, hyaline, and ovoid) and pycnidia (0.33 to 1.15 mm in diameter with multiple beaks) of single-conidium isolates were characteristic of P. sclerotioides (2). Diagnostic PCR (3) of isolates resulted in a single amplicon of expected size (500 bp). The internal transcribed spacer (ITS) 1, 5.8S, and ITS2 of the rDNA were sequenced for 12 representative isolates, and sequences (GenBank Accession Nos. FJ179151 to FJ179162) were 95.5 to 100% identical to P. sclerotioides ATCC isolate 56515 over a 488-bp alignment. Eight months after seeding, potted ‘Vernal’ alfalfa was inoculated (4), kept at 4°C for 8 weeks, 0 to –2°C for 12 weeks, 4°C for 8 weeks, and 10 to 15°C for 7 weeks. Of 108 plants inoculated with the Maine isolates, 35 developed severe cortical lesions and 16 died. Of 18 plants inoculated with the Ontario isolates, 16 developed severe cortical lesions and eight died. Of 18 plants inoculated with a Pennsylvania isolate, 11 developed severe cortical lesions and five died. Lesions were typical of BRR: light to very dark brown, sometimes with a darker border, and often containing abundant pycnidia. Plant mortality was associated with lesions that girdled the root and crown. Of 18 plants in the control treatment, three developed severe cortical lesions and none died. BRR is common in Alberta, Saskatchewan, and Manitoba, but in eastern Canada it has been reported only in Nova Scotia. To our knowledge, this is the first report of BRR in Maine, Ontario, and Pennsylvania and the southernmost report of BRR in eastern North America. References: (1) B. Berkenkamp et al. Can. J. Plant Sci. 71:211, 1991. (2) G. H. Boerema et al. Persoonia 15:431, 1994. (3) R. C. Larsen et al. Plant Dis. 86:928, 2002. (4) M. J. Wunsch et al. Plant Dis. 91:1293, 2007.


2016 ◽  
Vol 5 (1) ◽  
pp. 32
Author(s):  
Supriadi Supriadi ◽  
E.M. Adhia ◽  
D. Wahyuno ◽  
S. Rahayuningsih ◽  
N. Karyani ◽  
...  

Brown root rot disease is a major constraint on cashew plantation in Pekat District, West Nusa Tenggara. Its causal agent has not been characterized. This paper describes efforts to study the pathogen, distribution and loss. Field study was conducted in Pekat District in 2003. Laboratory  experiments to isolate and test the causal agent were conducted in the Indonesian Spices and Medicinal Crops Research Institute, Bogor.  Research results showed that the disease was found widespread in several villages in Pekat District, such as Pekat, Beringin Jaya, Sorinomo, and Nangamiro. Total number of died cashew trees was 1,075 equals to 5,106 kg kernel yield lost, worth Rp20.5 million. Infected trees showed leaf yellowing and defoliation leading to die. The lateral and taproots near collar were encrusted with gravel, earth, and brown mycelia sleeves. The fungus produced arthrospores and brown pigmentation on agar medium containing 0.05% gallic acid. An isolate of the fungus induced typical disease symptoms following inoculation on 5 month-old cashew seedlings. These results indicated that the causal agent of mass decline of cashew in Pekat District is Phellinus noxius. In field, the fungus also infects a barrier tree (Lannea coromandelica [Houtt.] Merr.) (Anacardiaceae), locally known as kedondong pagar or kayu bantenan.


Author(s):  
A. Peerally

Abstract A description is provided for Cylindrocladium clavatum. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: Araucaria angustifolia, Camellia sinensis, Eucalyptus saligna and Pinus. DISEASE: Occasionally associated with Cylindrocladium floridanum[Calonectria kyotensis] and Cylindrocarpon tenue on rotting roots of unthrifty tea bushes in Mauritius. Associated with a root disease of dying 10-15 year old trees of Araucaria angustifolia (Hodges & May, 1972). Roots of such trees are pitch-soaked and copiously exude resin, causing large quantities of soil to stick to the roots, thus resembling in symptomatology the brown root rot caused by Phellinus noxius. Also isolated from the roots of dying trees of several species of Pinus (Hodges & May, 1972). The pine needles on affected trees turn bright yellow, droop and finally turn brick red. Roots were pitch-soaked but resin exudation was slight. Also isolated from seedlings of Eucalyptus saligna (Hodges & May, 1972). GEOGRAPHICAL DISTRIBUTION: Brazil, Mauritius. TRANSMISSION: The pathogen is soil-borne.


1983 ◽  
Vol 102 (2) ◽  
pp. 251-256 ◽  
Author(s):  
N. E. MALATHRAKIS ◽  
G. E. KAPETANAKIS ◽  
D. C. LINARDAKIS
Keyword(s):  
Root Rot ◽  

2008 ◽  
Vol 30 (4) ◽  
pp. 575-580 ◽  
Author(s):  
Claudio M. Oddino ◽  
Adriana D. Marinelli ◽  
Mónica Zuza ◽  
Guillermo J. March

Plant Disease ◽  
2002 ◽  
Vol 86 (9) ◽  
pp. 928-932 ◽  
Author(s):  
R. C. Larsen ◽  
C. R. Hollingsworth ◽  
G. J. Vandemark ◽  
M. A. Gritsenko ◽  
F. A. Gray

A rapid technique for identification and detection of Phoma sclerotioides, the causal agent of brown root rot of alfalfa, has been developed using polymerase chain reaction (PCR). Amplification products obtained from random amplified polymorphic DNA (RAPD) reactions were cloned and sequenced, and two extended primer sets were designed from the resulting data that were used to detect sequence-characterized DNA markers. A single 499-bp DNA amplification product was consistently obtained from primers PSB12499 that was specific for 19 isolates of P.sclerotioides but was not produced from Phoma medicaginis or Phoma betae, or from other soilborne pathogens including Aphanomyces euteiches, Rhizoctonia solani, Fusarium oxysporum, Pythium ultimum, or Phytophthora infestans. A 499-bp amplification product was also produced from root tissue known to be infected with the fungus as verified by microscopic examination. A similar PCR product was obtained from soil samples collected from fields with an established infection of P. sclerotioides on alfalfa. This PCR-based assay enables detection of P. sclerotioides from alfalfa root tissue and in soil samples in a single day, including extraction of DNA, compared with standard methods that require up to 100 days for identification using agar media.


2008 ◽  
Vol 36 (5) ◽  
pp. 483-488 ◽  
Author(s):  
Angelo Garibaldi ◽  
Michele Baudino ◽  
Andrea Minuto ◽  
Maria Lodovica Gullino
Keyword(s):  
Root Rot ◽  

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