Root rot pathogens were found through diagnostic surveys in all departments (regions) of Bénin, West Africa, to affect 86 to 100% and 96 to 100% of cassava fields during the dry and rainy seasons, respectively. Disease incidence in individual fields ranged between 0 and 53%, and averaged 16 to 27% per department. Nattrassia mangiferae was consistently the most frequently isolated root rot pathogen (56% in the dry season and 22 to 52% in the rainy season). Pathogenicity of N. mangiferae was confirmed on four cultivars of cassava using stem cuttings and storage roots. For all four cultivars, N. mangiferae significantly reduced the number of roots. Lesions (3 to 15 cm long) formed on the lower stem portion of all inoculated plants, whereas control plants remained symptom free. On storage roots, the disease profile was similar to that formed on stem cuttings. Other root rot pathogens detected during the dry season were Macrophomina phaseolina (14.2%), Fusarium spp. (11.8%), Botryodiplodia theobromae (7.7%), and Pythium spp. (2.9%). During the rainy season, Fusarium spp. were the second most commonly isolated root rot pathogens in three departments (Atlantique, Borgou, and Mono). In Oueme and Zou, B. theobromae was the second most isolated root rot pathogen (ranging between 24 and 28%) during the rainy season. During the same season, Pythium spp. were pronounced in Borgou (18%), followed by Mono (11%), Atlantique (9%), Atacora (8%), Oueme (5%), and Zou (6%). Results of the study are discussed with a view to creating awareness of the destructive power of N. mangiferae, a hitherto poorly recognized root rot pathogen of cassava in Bénin and West Africa in general.
Four tronchuda (Brassica oleracea var. tronchuda Bailey) cultivars were tested for their ability to regenerate in vitro on Murashige & Skoog (MS) medium supplemented with 3 different combinations of ~t-naphthaleneacetic acid (NAA) and 6-benzylaminopurine (BAP). Explants were either axillary bud-free whole cotyledons or hypocotyls from 7-day-old darkgrown seedlings. The ability to regenerate varied by cultivars, explants and the concentration of growth regulators. Hypocotyl explants of all 4 cultivars, and cotyledon explants of 2 cultivars, developed plantlets within 4 weeks. Hypocotyl explants produced more shoots than cotyledons. Cotyledon explants produced more roots than hypocotyls. Best shoot regeneration was on MS medium supplemented with 2 mg 1 i BAP and 0.1 mg 1-1 NAA. 'Portuguesa' produced the most shoots. Some regenerants varied in leaf shape and pbyllotaxy.
During part of the dry season in 1996 (November to December), surveys were made for incidence of root and stem rot in 99 fields of cassava (Manihot esculenta Crantz) randomly selected between latitudes 6°36′N and 7°49′N in Benin (79 fields) and Nigeria (20 fields). Root rot was observed in 65 fields in Benin and 15 fields in Nigeria. Disease incidence ranged from 0 to 54%. A total of 201 samples of wilted and/or dead plants were collected for laboratory analysis. Infected root and stem portions (0.5 to 1 cm) were cut out, surface disinfested (10 min) in 10% bleach (0.6% sodium hypochlorite), rinsed in sterilized distilled water, and cultured on potato dextrose agar acidified to pH 4.5 with 0.4% (vol/vol) lactic acid. Cultures were incubated at 25°C, under 12-h day length provided by cool-white fluorescent lamps. After 1 week, mycelia, conidiophores, and conidia were observed at ×30 to ×40 magnification under a compound microscope. Out of the 169 symptomatic samples collected from Benin, nine fungal genera were isolated: Aspergillus spp. (1% of fungi observed), Botryodiplodia theobromae Pat (7.7%), Fusarium spp. (11.8%), Macrophomina phaseolina (Tassi) Goidanich (14.2%), Nattrassia mangiferae (Syd. & P. Syd.) B. Sutton & Dyko (56.2%), Penicillium spp. (0.6%), Pythium spp. (2.9%), Rhizopus spp. (1.7%), and Trichoderma spp. (2.4%). One percent of the fungi isolated did not sporulate in culture and were not identified. Out of the 32 samples collected from Nigeria, four fungal genera were identified: N. mangiferae (40.6%), B. theobromae (28.1%), M. phaseolina (18.7%), and Fusarium spp. (12.5%). Since N. mangiferae was isolated with the highest frequency, its pathogenicity was tested on cassava (cultivars Agric, Ben 86052, Dessa 88, Tchukunochi, and TMS 30572). Two weeks prior to the experiment, inocula for pathogenicity tests were prepared by incubating 5-mm-diameter mycelial plugs of N. mangiferae with 500 ml of autoclaved rice seed for 10 days at 25°C, followed by air drying in a laminar flow hood for 2 days. Five 30-cm-long stem portions were cut from healthy plants of each cassava cultivar, surface disinfested in hot water (52°C, 5 min), and transplanted into sterilized (autoclaved, 1 h) sand in 1-liter pots to which 10 ml of the N. mangiferae-colonized rice inoculum had been added. There were five control stems for each cultivar, similarly treated, but not inoculated. Plants were maintained in a greenhouse under natural light at 28 to 30°C. Thirty days after planting, plant height, lesion length, and number of shoots and roots were recorded. For all five cultivars, N. mangiferae significantly (P < 0.05) reduced plant height and number of shoots and roots, compared with control plants. Lesions (3 to 15 cm long) formed on the lower stem portions of all inoculated plants, resulting in variable degrees of wilting of the infected plants. Two of the cultivars (Agric and Ben 86052) died 3 weeks after planting. Control plants remained asymptomatic. N. mangiferae was consistently reisolated from infected plants, and the identification was independently confirmed by the International Mycological Institute, Surrey, UK. Scytalidium sp., a synamorphic state of N. mangiferae (2), was reported to cause up to 85% cassava root yield loss in South America (1). This is the first report of N. mangiferae causing cassava root and stem rot in West Africa. References: (1) Anonymous. Annu. Rep. Cassava Prog., CIAT Working Doc. No. 116:97, 1992. (2) B. C. Sutton and B. J. Dyko. Mycol. Res. 93:466, 1989.
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