Thielaviopsis basicola. [Descriptions of Fungi and Bacteria].

Author(s):  
C. V. Subramanian

Abstract A description is provided for Thielaviopsis basicola. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On a wide host range attacking plants in over fifteen families, primarily belonging to the Leguminosae (groundnut, soyabean, Lespedeza, clover, alfalfa, cowpea, lupin, sunn hemp, bean), Solanaceae (tobacco) and Cucurbitaceae; also from Citrus roots. DISEASES: Causes black root rot in tobacco and many other crops (see above). Recent reports suggest that it may be a serious pathogen on Citrus roots (39: 411; 42: 263, 761). Many species of Nicotiana are susceptible and some are considered resistant or immune (Johnson, 1916, J. agric. Res. 7: 289-300; 50: 248). GEOGRAPHICAL DISTRIBUTION: Africa (S. Africa, Egypt), Asia (Persia, Japan, India, Indonesia); Australasia (Australia, N. Zealand), Europe (Bulgaria, France, Germany, Italy, Netherlands, Norway, Poland, Rumania, Switzerland, U.S.S.R., Yugoslavia), N., C. and S. America. TRANSMISSION: Soil-borne; the pathogen is a soil inhabitant capable of prolonged saprophytic survival in soils.

Author(s):  
B. C. Sutton

Abstract A description is provided for Mycocentrospora acerina. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: A very wide host range (29, 364); parsley, celery, carrot and parsnip are among the most important economically. DISEASE: Pansy leaf spot; celery storage rot; root rot, canker and black crown rot of parsnip; liquorice rot of carrot. GEOGRAPHICAL DISTRIBUTION: Europe (UK, Ireland, Germany, Czechoslovakia, Netherlands, Poland, Rumania, USSR, Denmark); N. America (USA, Canada); Australia, New Zealand. TRANSMISSION By splash dispersed conidia; these are viable for short periods only (26, 133). Survival for longer periods is by infected debris and chlamydospores in the soil (23, 324; 45, 681; 52, 899). Water-borne spread is possible (49, 1526) and transmission on pansy seeds has been demonstrated (51, 422).


Plant Disease ◽  
2008 ◽  
Vol 92 (9) ◽  
pp. 1368-1368 ◽  
Author(s):  
S. T. Koike

In 2005 and 2006, field-grown iceberg lettuce (Lactuca sativa) in California's coastal Salinas Valley (Monterey County) was affected by a previously unreported disease. Symptoms were observed on iceberg lettuce at the post-thin rosette stage (8 to 12 leaves). Plants were stunted and slightly chlorotic. Fine feeder roots had numerous, small (4 to 8 mm long), elongated, dark brown-to-black lesions. Larger secondary roots and taproots lacked lesions. No vascular discoloration was present. Isolations from root lesions consistently resulted in gray fungal colonies that formed catenulate, cylindrical, thin-walled, hyaline endoconidia and catenulate, subrectangular, thick-walled, dark aleuriospores. The fungus was identified as Thielaviopsis basicola (2). Conidial suspensions (5.0 × 105) of eight isolates from iceberg lettuce were used for pathogenicity tests. Iceberg cv. Ponderosa and romaine cv. Winchester were grown for 3 weeks in soilless peat moss rooting mix. Roots of 20 plants per cultivar were washed free of the rooting mix and soaked in conidial suspensions for 5 min. Plants were repotted and grown in a greenhouse. Control plant roots were soaked in sterile distilled water (SDW). After 3 weeks, inoculated iceberg exhibited slight chlorosis in comparison with control plants. Feeder roots of all iceberg plants inoculated with the eight isolates exhibited numerous black lesions and T. basicola was reisolated from these roots. Romaine lettuce, however, did not show any foliar symptoms. Small segments of roots had tan-to-light brown discoloration and T. basicola was occasionally reisolated (approximately 40% recovery). Roots of control iceberg and romaine showed no symptoms. Results were similar when this experiment was repeated. To explore the host range of T. basicola recovered from lettuce, two isolates were prepared and inoculated as described above onto 12 plants each of the following: iceberg lettuce (cv. Ponderosa), bean (cv. Blue Lake), broccoli (cv. Patriot), carrot (cv. Long Imperator #58), celery (cv. Conquistador), cotton (cv. Phy-72 Acala), cucumber (cv. Marketmore 76), green bunching onion (cv. Evergreen Bunching), parsley (cv. Moss Curled), pepper (cv. California Wonder 300 TMR), radish (cv. Champion), spinach (cvs. Bolero and Bossanova), and tomato (cv. Beefsteak). Control plant roots of all cultivars were soaked in SDW. After 4 weeks, only lettuce and bean roots had extensive brown-to-black lesions, from which the pathogen was consistently resiolated. Roots of cotton, pepper, spinach, and tomato had sections of light brown-to-orange discoloration; the pathogen was not consistently recovered from these sections. All other species and the control plants were symptomless. This experiment was repeated with similar results except that inoculated peppers were distinctly stunted compared with control plants. To my knowledge, this is the first report of black root rot caused by T. basicola on lettuce in California. Disease was limited to patches along edges of iceberg lettuce fields; disease incidence in these discrete patches reached as high as 35%. Affected plants continued to grow but remained stunted in relation to unaffected plants and were not harvested. Black root rot of lettuce has been reported in Australia (1); that report also showed that lettuce cultivars vary in susceptibility to T. basicola and isolates from lettuce were highly aggressive on bean but not on many other reported hosts of this pathogen. References: (1) R. G. O'Brien and R. D. Davis. Australas. Plant Pathol. 23:106, 1994. (2) C. V. Subramanian. No. 170 in: Descriptions of Pathogenic Fungi and Bacteria. CMI, Kew, Surrey, UK, 1968.


2017 ◽  
Vol 107 (12) ◽  
pp. 1479-1485 ◽  
Author(s):  
Louisamarie E. Parkinson ◽  
Roger G. Shivas ◽  
Elizabeth K. Dann

Black root rot is a severe disease of young avocado trees in Australia causing black necrotic roots, tree stunting, and leaf drop prior to tree death. Nectriaceous fungi (Nectriaceae, Hypocreales), are commonly isolated from symptomatic roots. This research tested the pathogenicity of 19 isolates from Calonectria, Cylindrocladiella, Dactylonectria, Gliocladiopsis, and Ilyonectria, spp. collected from young avocado trees and other hosts. Glasshouse pathogenicity tests with ‘Reed’ avocado (Persea americana) seedlings confirmed that Calonectria ilicicola is a severe pathogen of avocado, causing stunting, wilting, and seedling death within 5 weeks of inoculation. Isolates of C. ilicicola from peanut, papaya, and custard apple were also shown to be aggressive pathogens of avocado, demonstrating a broad host range. An isolate of a Calonectria sp. from blueberry and avocado isolates of Dactylonectria macrodidyma, D. novozelandica, D. pauciseptata, and D. anthuriicola caused significant root rot but not stunting within 5 to 9 weeks of inoculation. An isolate of an Ilyonectria sp. from grapevine closely related to Ilyonectria liriodendri, and avocado isolates of Cylindrocladiella pseudoinfestans, Gliocladiopsis peggii, and an Ilyonectria sp. were not pathogenic to avocado.


Plant Disease ◽  
2008 ◽  
Vol 92 (10) ◽  
pp. 1394-1399 ◽  
Author(s):  
Warren E. Copes ◽  
Katherine L. Stevenson

A pictorial key was developed and the relationship between disease severity (S) and incidence (I) was examined to aid in the assessment of black root rot of pansy caused by Thielaviopsis basicola. The key consisted of photographs of root segments that represented nine disease severity levels ranging from 1 to 91%. Pansies that had received different fertility treatments, as part of seven separate experiments, were inoculated with T. basicola. Four weeks after inoculation, roots were washed, and incidence and severity of black root rot were visually assessed using a grid-line-intersect method. Disease incidence ranged from 1.3 to 100%, and severity ranged from 0.1 to 21.4% per plant. Four different mathematical models were compared to quantitatively describe the I-S relationship for the combined data from all seven experiments. Although all models provided an adequate fit, the model that is analogous to the Kono-Sugino equation provided the most reliable estimate of severity over the entire range of disease incidence values. The predictive ability and accuracy of this model across data sets was verified by jackknife and cross-validation techniques. We concluded that incidence of black root rot in pansy can be assessed more objectively and with greater precision than disease severity and can be used to provide reliable estimates of disease severity based on derived regression equations that quantify the I-S relationship for black root rot.


1993 ◽  
Vol 42 (5) ◽  
pp. 820-823 ◽  
Author(s):  
L. BØDKER ◽  
N. LEROUL ◽  
V. SMEDEGAARD-PETERSEN

Plant Disease ◽  
1999 ◽  
Vol 83 (4) ◽  
pp. 396-396
Author(s):  
R. J. McGovern ◽  
T. E. Seijo

A bedding plant grower in southwest Florida reported severe losses in potted Catharanthus roseus (Madagascar periwinkle) transplanted on various dates in December 1997. Symptoms included yellowing of lower leaves, defoliation, black root rot, and plant death. Thielaviopsis basicola was consistently isolated from blackened roots on a selective medium (1). A disease survey was conducted during mid March 1998 of 7,500 periwinkle plants in the two cultivar series Pacific (cvs. Punch, Red, and White) and Cooler (cvs. Grape, Icy, Peppermint, Pink, and Raspberry). Black root rot symptoms were observed in 21 to 53% of periwinkles transplanted between 3 and 11 December, and in 0 to 19% of plants transplanted between 21 and 29 December. The two cultivar series did not appear to differ in their susceptibility to T. basicola. The fungus was consistently isolated from symptomatic periwinkle roots, from roots of chlorotic violas (Viola cornuta), and from a potting medium used for early December transplanting. Pathogenicity of isolates of T. basicola from periwinkle, viola, and the contaminated medium was investigated. Inocula were produced by growing the fungus on acidified potato dextrose agar for 18 days. Conidia, chlamydospores, and hyphae of T. basicola were suspended in deionized water (100 ml/95 mm culture plate). One milliliter of inoculum suspensions of each of the three isolates was used to inoculate 12 plants of pansy (Viola × Wittrockiana) cv. Majestic Giant Blue Shade. An equal number of plants served as noninoculated controls. In addition, 5 ml of each isolate suspension was used to inoculate three six-plant replications of periwinkle cv. Pink Cooler. Plants were incubated in a controlled environment chamber at day/night temperatures of 24/22°C with a 12-h photoperiod. After 22 days, moderate to severe root discoloration was produced in pansy by the viola isolate of the fungus, while periwinkle and potting medium isolates produced only minimal discoloration. Chlamydospores typical of T. basicola were observed in the roots of all inoculated pansies, and in the roots of one of 12 non-inoculated controls. After 38 days, periwinkle plants were rated for foliar yellowing (0 = no yellowing, to 3 = severe yellowing) and percent defoliation, and fresh weights of shoots and roots were obtained. T. basicola was recovered on the selective medium from roots of all inoculated plants and from 68% of the noninoculated controls, indicating that secondary spread had occurred. All three isolates of the fungus caused yellowing and defoliation, but only the periwinkle and potting medium isolates significantly reduced both shoot and root weights in periwinkle, compared with control plants. T. basicola has not been previously reported to cause black root rot in C. roseus, and a contaminated potting medium used during early December may have provided initial inocula for the outbreak. The unseasonably cool and rainy weather prevalent during winter 1997 and spring 1998 (“El Niño”) may have also promoted the unusual appearance of the disease. Reference: (1) L. P. Specht and G. J. Griffin. Can. J. Plant Pathol. 7:438, 1985.


Plant Disease ◽  
2020 ◽  
Author(s):  
Liz Beal ◽  
Ian Waghorn ◽  
Joe Perry ◽  
Gerard R G Clover ◽  
Matthew Cromey

Phytophthora root rot (PRR) is a serious disease of horticultural, forest and ornamental plant species caused by species of the oomycete genus Phytophthora. Their wide host range makes choice of resistant plants in management of the disease difficult. We used the Royal Horticultural Society diagnostic dataset of PRR records from U.K. gardens to compare the susceptibility of different host genera to the disease. The dataset was compared with existing reports of plants recorded as notably resistant or notably susceptible to PRR. An index-based approach was used to separate 177 genera of woody plants into three categories: 85 were low-index (<0.10: rarely affected), 34 were medium-index (0.10 – 0.20: sometimes affected) and 58 were high-index (>0.20: frequently affected). Similarly, genera of non-woody plants were separated into: 45 low-index (<0.22), 16 medium-index (0.22 – 0.44) and 18 high-index (>0.44). Taxus was the genus with the highest index, while most genera in the Malvales and Ericales were in the high index group. Most genera in the Myrtales, Fabales and Monocotyledons were low index. Whilst 30 Phytophthora species were recorded in our study, the wide host range spp., P. plurivora, P. cryptogea and P. cinnamomi represented 63% of identifications. Phytophthora plurivora was the most common species on woody plants and P. cryptogea on non-woody plants. These results provide confidence in the use of host resistance as part of the integrated management of PRR.


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