Prevalence and Severity of Nattrassia mangiferae Root and Stem Rot Pathogen of Cassava in Bénin.

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.

A group I intron in the nuclear small subunit ribosomal DNA of Gaeumannomyces graminis.

The length of the small subunit ribosomal DNA (SSU rDNA) differs among isolates of species and varieties of Gaeumannomyces. The sequence of the 3' region of the SSU rDNA revealed 340-, 365-, and 520-bp insertions for G. graminis varieties avenae, tritici, and graminis, respectively. The intron sequences from varities tritici and avenae were similar, except there was an insert of 23 nucleotides at base 328 from the 5' end of the G. g. var. tritici intron. The G. g. var. graminis intron sequences had 92.4% homology compared with the intron sequences of varieties tritici and avenae. In addition, the intron sequence of variety graminis is larger, having an insert of 155 nucleotides at base 365 of the 5' end of the intron. Little variation in the DNA sequences flanking the introns has been detected among the isolates of Gaeumannomyces that either have or lack an intron. Reverse transcriptase PCR (RT-PCR) indicated the absence of the intron in the mature rRNA. The intron sequence had both a conserved sequence and secondary structural elements classifying it as a group I intron.

First Report of Gray Leaf Spot Caused by Pyricularia grisea on Lolium perenne in Illinois.

Each year from 1991 to 1999, a disease matching the description of gray leaf spot (1) was observed in the central and north central regions of Illinois. Disease severity was low (<10% blight) from 1991 to 1994 and 1999 and was severe (>50% blight in some areas) from 1995 to 1998. The disease was observed on Lolium perenne (perennial ryegrass) golf course fairways and sports fields. Isolations of Pyricularia grisea were made from L. perenne collected from golf courses in Bloomington, Decatur, Kankakee, Pekin, Urbana, and Moline, IL. All isolates were collected from surface-sterilized, symptomatic leaves. Cultures were maintained on one-fifth strength potato-dextrose agar (PDA) and induced to sporulate on full-strength oatmeal agar. All isolates in culture displayed vegetative and conidial characteristics similar to those previously described for P. grisea (1). Twenty-five different L. perenne germ plasms were inoculated with isolate WF9826 (Kankakee) using a suspension of 1 × 105 conidia per milliliter. The 4-week-old lawns (100 plants per 3-cm-diameter cone-tainer) of each ryegrass germ plasm were inoculated by spraying foliage with the conidial suspension until runoff. Inoculated and uninoculated lawns were enclosed in plastic bags and placed in an incubator (16 h light; 28°C) for 7 days. Disease severity was rated using a scale of 0 to 10 (10 = 100% blight). Each treatment was replicated three times, and all experiments were repeated four times. Small blue-gray, water-soaked lesions with dark brown borders were observed on leaves of all inoculated ryegrass germ plasms. Advanced symptoms included blighting of much of the leaves. The mean disease severity rating was 3.8 (range 2 to 7) for all experimental units and all 25 germ plasms. P. grisea was isolated from leaves that were inoculated with WF9826. This is the first report of gray leaf spot of perennial ryegrass caused by P. grisea in Illinois. Reference: (1) P. J. Landschoot et al. Plant Dis. 76:1280, 1992.

Detection of Gaeumannomyces graminis Varieties Using Polymerase Chain Reaction with Variety-Specific Primers.

The polymerase chain reaction (PCR) was used for detection of Gaeumannomyces graminis, the causal agent of take-all disease in wheat, oats, and turfgrass. NS5 and NS6 universal primers amplified the middle region of 18S ribosomal DNA of Gaeumannomyces species and varieties. Primers GGT-RP (5' TGCAATGGCTTCGTGAA 3') and GGA-RP (5' TTTGTGTGTGAC CATAC 3') were developed by sequence analysis of cloned NS5-NS6 fragments. The primer pair NS5:GGT-RP amplified a single 410-bp fragment from isolates of G. graminis var. tritici, a single 300-bp fragment from isolates of G. graminis var. avenae, and no amplification products from isolates of G. graminis var. graminis or other species of Gaeumannomyces. The primer pair NS5:GGA-RP amplified a single 400-bp fragment from isolates of varieties tritici and avenae. Two sets of primer pairs (NS5:GGT-RP and NS5:GGA-RP) were used in PCR reactions to detect and identify the varieties tritici and avenae either colonizing wheat, oats, or grass roots, or in culture. No amplification products were observed using DNA extracted from plants infected with eight other soilborne fungal pathogens or from uninoculated plants.

First Report of Macrophomina phaseolina Causing Pre-harvest Cassava Root Rot in Benin and Nigeria.

In diagnostic surveys conducted in parts of Benin and Nigeria to determine the incidence of pre-harvest cassava root and stem rot during the dry season, Macrophomina phaseolina (Tassi) Goidanich constituted 14.2 and 18.7% of the total fungi (n = 201) associated with cassava root and stem rot from Benin and Nigeria (1). Pathogenicity of M. phaseolina on cassava was tested with cv. Agric. Inocula for pathogenicity tests were prepared by incubating 5-mm-diameter mycelial plugs for each of five isolates (Mp 1 to Mp 5, all collected from Benin) with 500 ml of autoclaved, sterilized, dehusked rice seed for 14 days at 30°C. Five 30-cm-long stem portions per isolate were cut from healthy cassava, surface disinfested in hot water (52°C, 5 min), and planted into 1-liter pots containing autoclaved, sterilized sand mixed with 10 ml of air-dried inoculum. Five plants per isolate similarly treated but not inoculated served as controls. Plants were watered once a week, and maintained in a greenhouse under natural light at 28 to 30°C. Lower leaves of inoculated plants gradually wilted, usually preceded by chlorosis, and brown to black lesions formed on the lower stem portions of some roots. Control plants remained asymptomatic. Plant height and percentage of leaf wilt (determined by counting the number of leaves wilted per plant and dividing by the total number of leaves per plant) were measured on a weekly basis for 8 weeks for each of the control and inoculated plants. At the end of 8 weeks, lesion length on the lower stem was measured. There were significant differences (P < 0.05) in length of the lesions and percentage of leaf wilt induced by the different isolates of M. phaseolina. Isolate Mp 1 induced the longest lesion (7.2 cm), followed by Mp 4 (4.1 cm), Mp 3 and Mp 5 (3.8 cm each), and Mp 2 (1.2 cm). Mp 4 induced the highest percentage of wilted leaves (53%), followed by Mp 1, Mp 3, and Mp 5 (30%), and Mp 2 (10%). All five M. phaseolina isolates (except Mp 3) reduced plant height, compared with control treatments. M. phaseolina was isolated from all infected plants, and the identification was independently confirmed by the International Mycological Institute, Surrey, UK. This is the first report of M. phaseolina causing pre-harvest cassava root rot in Benin and Nigeria. Reference: (1) W. Msikita et. al. Plant Dis. 81:1332, 1997.

Root Growth of Bentgrass and Annual Bluegrass as Influenced by Coinfection with Tylenchorhynchus nudus and Magnaporthe poae.

A study was conducted in growth chambers to examine main factor and interaction effects of Tylenchorhynchus nudus and Magnaporthe poae on creeping bentgrass and annual bluegrass at 24, 28, and 30 C. A 2 x 2 factorial arrangement of treatments was employed with presence and absence of T. nudus and M. poae as factors with each temperature run separately for 14 or 18 days. Tylenchorhynchus nudus decreased bentgrass and annual bluegrass root length at all three temperatures. Magnaporthe poae had no effect on bentgrass root length at 24 C, increased root length at 28 C, and suppressed root growth at 30 C. Magnaporthe poae had no effect on annual bluegrass root length at 24 and 28 C but suppressed root growth at 30 C. A significant interaction between M. poae and T. nudus occurred only on bentgrass at 28 C and 30 C; at these two temperatures, M. poae did not act independently of T. nudus.

Vertical distribution of three nematode genera in a bentgrass putting green in central illinois.

A study was conducted to determine the vertical distribution of Tylenchorhynchus nudus, Criconemella curvata, and Helicotylynchus cornurus in the upper 5 cm of bentgrass (Agrostis palustris cv. Penncross) putting green turf. The effect of fenamiphos on the vertical distribution of these species also was examined. Experimental design was a split-plot in which whole-plots were fenamiphos treated (0.11 kg a.i./100 m(2)) or untreated, and sub-plots were two strata (depths of 0-2.5 crn and 2.5-5.0 cm). Soil samples were collected during the growing season for 2 years after treatment to determine root weight and number of nematodes. Root weight was greater in the upper stratum on all sampling dates in both years. When differences between strata in population density were observed, T. nudus, C. curvata, and H. cornurus were more concentrated in the upper stratum. Vertical distribution of T. nudus, C. curvata, and H. cornurus was similar to the distribution of root weight. The difference in population density of H. cornurus between upper and lower strata was affected by fenamiphos on some dates, whereas differences between strata were unaffected for T. nudus and C. curvata. Double arcsine transformed proportions of the total populations of T. nudus, C. curvata, and H. cornurus in the upper stratum on each sampling date indicated no differences between fenamiphos treated and untreated plots in 1989 or 1990.

Population fluctuations of three nematode genera in putting greens in northern illinois.

Field experiments were conducted in 1989 and 1990 to examine the population fluctuation patterns of Tylenchorhynchus nudus, Criconemella curvata, and Helicotylenchus cornurus in mixed bentgrass and annual bluegrass putting greens on two golf courses near Chicago, Illinois, to determine if fluctuation patterns could be extrapolated to unsampled greens. Fenamiphos-treated and untreated plots were established on seven putting greens on two golf courses. Greens were sampled intensively five times during the growing season, and statistical comparisons of population levels per gram of root were made among dates for each green. Population levels per gram of root changed significantly on all greens in both years for each of the three nematode populations. Within a putting green in either year, population fluctuation patterns in fenamiphos-treated and untreated plots were similar. Population fluctuation patterns were different between years, however. Within a year, population fluctuation patterns among greens showed similarities indicating that carefully monitoring a few locations may allow extrapolation of population fluctuation data to other locations within that year.

Influence of age structure of plant populations on damping-off epidemics.

Germination synchrony may facilitate damping-off epidemics by creating a high density of uniformly susceptible individuals. We tested the hypothesis that synchronous germination causes increased seed and seedling mortality from damping-off in two legume species attacked by the fungal pathogen, Pythium aphanidermatum. Glycine max exhibited rapid, synchronous germination compared to its progenitor, G. soja, and suffered greater mortality from both pre-and postemergent damping-off in controlled environment experiments. However, when mixed-aged populations of G. max were created experimentally by staggering planting times, a significant increase in damping-off mortality occurred. In G. soja, which typically has mixed-aged populations due to asynchronous germination, experimental populations with an even-aged distribution also suffered increased damping-off mortality. Hence, the relationship between population age structure and damping-off mortality was species-specific. We propose that species differences in the duration of individual seedling susceptibility to disbase interact with population age structure to control the cutcome of damping-off epidemics.