scholarly journals Avenacin Production in Creeping Bentgrass (Agrostis stolonifera) and Its Influence on the Host Range of Gaeumannomyces graminis

Plant Disease ◽  
2006 ◽  
Vol 90 (1) ◽  
pp. 33-38 ◽  
Author(s):  
S. L. Thomas ◽  
P. Bonello ◽  
P. E. Lipps ◽  
M. J. Boehm

Avenacinase activity has been shown to be a key factor determining the host range of Gaeumannomyces graminis on oats (Avena sativa). G. graminis var. avenae produces avenacinase, which detoxifies the oat root saponin avenacin, enabling it to infect oats. G. graminis var. tritici does not produce avenacinase and is unable to infect oats. G. graminis var. avenae is also reported to incite take-all patch on creeping bentgrass (Agrostis stolonifera). It is unknown whether creeping bentgrass produces avenacin and if the avenacin-avenacinase interaction influences G. graminis pathogenicity on creeping bentgrass. The root extracts of six creeping bentgrass cultivars were analyzed by fluorimetry, thin-layer chromatography, and high performance liquid chromatography for avenacin content. Avenacin was not detected in any creeping bentgrass cultivars, and pathogenicity assays confirmed that both G. graminis var. avenae and G. graminis var. tritici can infect creeping bentgrass and wheat (Triticum aestivum), but only G. graminis var. avenae incited disease on oats. These results are consistent with the root analyses and confirm that avenacinase activity is not required for creeping bentgrass infection by G. graminis.

HortScience ◽  
1999 ◽  
Vol 34 (5) ◽  
pp. 891-892 ◽  
Author(s):  
W.J. Hill ◽  
J.R. Heckman ◽  
B.B. Clarke ◽  
J.A. Murphy

Take-all patch, caused by Gaeumannomyces graminis (Sacc.) Arx. & D. Olivier var. avenae (E.M. Turner) Dennis (Gga), is a disease of creeping bentgrass (Agrostis stolonifera Huds.), which most often is associated with golf courses. Synthesis of ligneous and phenolic compounds by plants requires adequate Mn+2 and Cu+2 nutrition and may be a factor in disease resistance. An experiment was conducted on a creeping bentgrass fairway naturally infested with Gga to determine if foliar applications of Mn+2 (1.02 and 2.04 kg·ha–1 per application) and Cu+2 (0.68 kg·ha–1 per application) would reduce take-all severity. Prior to initiating treatments, soil pH was 6.4 and Mehlich-3 extractable Mn+2 and Cu+2 were 5 mg·kg–1 and 1.7 mg·kg–1, respectively. Manganese and copper sulfate treatments were initiated in July 1995 and foliarly applied every 4 weeks through 1997 with the exception of December, January, and February. Disease incidence was decreased from 20% on untreated turf to 5% with the high rate of MnSO4. For both years, turf treated with the high rate of Mn+2 had less disease than turf receiving the low rate of Mn+2. The application of CuSO4, however, did not influence disease development.


1993 ◽  
Vol 44 (4) ◽  
pp. 745 ◽  
Author(s):  
RF Eastwood ◽  
JF Kollmorgen ◽  
M Hannah

Reactions of 398 accessions of Triticum tawchii to the take-all fungus [Gaeumannomyces graminis var. tritici (Ggt] were assessed. Nineteen accessions were selected for more detailed studies. T. tauschii accessions were identified that had less tissue blackening and more remaining green tissue when challenged by the fungus than the susceptible T. aestivum cv. Condor. However, tissue blackening in the T. tauschii accessions was much greater than that in Avena sativa cv. New Zealand Cape. Synthetic allohexaploid wheats produced from different Triticum turgidum var. durum (genome AABB) accessions and accessions of T. tauschii (genome DD) which had low tissue blackening or high remaining green tissue had more tissue blackening and less remaining green tissue than the T. tauschii parents. The potential of this material for breeding take-all resistant wheats together with experimental methods to minimize the possible confounding effects of seed weight, seed source and genetic effects are discussed.


Plant Disease ◽  
2005 ◽  
Vol 89 (2) ◽  
pp. 204-204 ◽  
Author(s):  
L. P. Tredway

An unknown disease was observed in June 2002 and 2003 on creeping bentgrass (CRB [Agrostis stolonifera L.]) putting greens at The Country Club of Landfall in Wilmington, NC that were established in 2001 with a 1:1 blend of cvs. A-1 and A-4. Soil pH ranged from 7 to 8 at this location because of poor quality irrigation water. Symptoms appeared in circular patches of 0.3 to 1 m in diameter that exhibited signs of wilt followed by chlorosis and orange foliar dieback. The disease was initially diagnosed as take-all patch caused by Gaeumannomyces graminis (Sacc.) Arx & D. Olivier var. avenae (E.M. Turner) Dennis, based on the observation of necrotic roots and crowns that were colonized with dark, ectotrophic hyphae. However, the historical lack of take-all patch occurrence in this region led to the suspicion that G. graminis var. avenae was not involved. Sections of root and crown tissue were surface disinfested in 0.6% NaOCl for 5 min or 1% AgNO3 for 1 min and 5% NaCl for 30 s. Tissue was plated on SMGGT3 (2) or on potato dextrose agar containing 50 mg L-1 of tetracycline, streptomycin, and chloramphenicol. A fungus resembling Magnaporthe poae Landschoot & Jackson was consistently obtained regardless of isolation method. Teleomorph production was conducted on Sachs agar (4) overlaid with autoclaved wheat (Triticum aestivum L.) stem sections. Seven isolates were plated alone or paired with M. poae tester isolates 73-1 or 73-15 (3) and incubated at room temperature under continuous fluorescent illumination. Six isolates produced perithecia and ascospores typical of M. poae (3) when paired with 73-15 but not when plated alone or paired with 73-1; these isolates are, therefore, M. poae mating type ‘a’. Isolate TAP42 did not produce perithecia and remains unidentified. Cone-Tainers (3.8 × 20 cm) containing calcined clay were seeded with ‘A-4’ CRB (9.7 g cm-2) and inoculated 8 weeks later by placing four M. poae-infested rye (Secale cereale L.) grains below the soil surface. Inoculated Cone-Tainers were placed in growth chambers with 12-h day/night cycles at 30/25°C, 35/25°C, or 40/25°C. Field plots (1 m2) of ‘A-4’ CRB in Jackson Springs, NC were inoculated on 19 June 2003 by removing a soil core (1.9 × 10.3 cm) from the center of each plot, adding 25 cm3 of M. poae-infested rye grains, and then capping the hole with sand. Growth chamber and field inoculations were arranged in a randomized complete block with four replications. Eight weeks after inoculation in the growth chamber, isolates TAP35, TAP41, and SCR4 caused significant foliar chlorosis and dieback at 12-h day/night cycles of 30/25°C and 35/25°C, but only TAP41 induced symptoms at 40/25°C. Isolate TAP42 did not induce symptoms at any temperature regimen. Orange patches (10 to 15 cm in diameter) were observed in field plots inoculated with TAP41 on 27 August 2003. No other isolates induced aboveground symptoms. Roots and crowns of plants exhibiting foliar symptoms in the greenhouse and field were necrotic and colonized with ectotrophic hyphae, and M. poae was consistently isolated from this tissue. Although M. poae has been associated with CRB in Florida (1), to our knowledge, this is the first report of summer patch of CRB within the normal zone of adaptation for this turfgrass species. Observation of this disease highlights the need for accurate methods for diagnosis of diseases caused by ectotrophic root-infecting fungi. References: (1) M. L. Elliott. Plant Dis. 77:429, 1993. (2) M. E. Juhnke et al. Plant Dis. 68:233, 1984. (3) P. J. Landschoot and N. Jackson. Mycol. Res. 93:59, 1989. (4) E. S. Lutrell. Phytopathology 48:281, 1958.


2001 ◽  
Vol 84 (4) ◽  
pp. 1232-1241 ◽  
Author(s):  
Xie Peishan ◽  
Yan Yuzhen ◽  
Qian Haoquan ◽  
Lin Qiaoling

Abstract Terpenoid lactones in Ginkgo biloba leaves are the main active constituents and the content of these terpenes is therefore the key factor for evaluating the quality of the leaves, the extract, and its preparations distributed on the market. The precleanup sample solutions were applied onto the silica gel plate modified with sodium acetate solution and developed with a solvent system of toluene–ethyl acetate–acetone–methanol, and a fluorescence chromatogram was generated by means of postchromatographic thermal chemical reaction. Fluorescence scanning was conducted quantitatively. The methodology validation confirmed that it is a practical alternative for routine quality control for ginkgo terpenes and the results are comparable with those obtained by high-performance liquid chromatography (HPLC). On the basis of the method established, a quality survey of the various commercial ginkgo products from different sources was undertaken. The obtained data demonstrated that the fluctuation of the content of individual terpene and/or the total terpenes among replicate samples is so significant as to cast doubts on the consistency of their pharmacological and clinical efficacy.


1999 ◽  
Vol 103 (3) ◽  
pp. 319-327 ◽  
Author(s):  
Gregory T. Bryan ◽  
Eric Labourdette ◽  
Rachel E. Melton ◽  
Paul Nicholson ◽  
Michael J. Daniels ◽  
...  

2016 ◽  
Vol 2016 ◽  
pp. 1-11 ◽  
Author(s):  
Jamuna Senguttuvan ◽  
Paulsamy Subramaniam

The aim of this work was to elucidate the various secondary metabolites such as alkaloids, flavonoids, glycosides, saponins, and terpenoids in the methanolic leaf and root extracts of Hypochaeris radicata, a most important traditional medicinal plant species in Nilgiris, the Western Ghats, India, using high performance thin layer chromatography (HPTLC). This study was carried out using CAMAG HPTLC system equipped with LINOMAT 5 applicator, TLC scanner 3, Reprostar 3, and winCATS 1.3.4 software. A comprehensive assortment of phytoconstituents in methanolic extracts through HPTLC fingerprinting profiles displayed the existence of alkaloids (3 in leaf and 1 in root extract), flavonoids (4 in leaf extract and 5 in root extract), glycosides (1 in leaf extract and 3 in root extract), saponins (1 in root extract), and terpenoids (1 in leaf and root extracts, resp.). The current study overlays boulevard for H. radicata to provide a direction for further exploration in precluding communicable and noncommunicable ailments.


INDIAN DRUGS ◽  
2012 ◽  
Vol 49 (12) ◽  
pp. 44-48
Author(s):  
S Sahoo ◽  
◽  
D Nayak ◽  
G.S Kumar ◽  
S. Jayakumari

The plant Ammania baccifera Linn., commonly known as Jangli mendi, belonging to the family Lythraceae was investigated for its antimicrobial activity against some selected urinary tract (UT) and gastrointestinal tract (GIT) infection causing pathogens and human pathogenic fungi. The ethanolic extract of the whole plant as well as its leaves, stems and roots were screened to evaluate the antibiogram pattern followed by High Performance Thin Layer Chromatography (HPTLC) study. The extracts were then screened for their antibacterial activity against some UTI and GIT infection causing pathogens viz. Staphylococcus aureus MTCC*1430, Enterococcus faecalis MTCC 2729, Escherichia coli MTCC 118, Pseudomonas aeruginosa MTCC 1035, Klebsiella pneumoniae MTCC 109, Proteus mirabilis MTCC 743, Salmonella typhi, Vibrio cholerae and antifungal activity against some human pathogenic fungi viz. Aspergillus niger MTCC 1344, Candida albicans MTCC 3017, Candida tropicalis, Candida krusei by disc diffusion assay method. The minimum inhibitory concentration (MIC) was evaluated by two fold serial dilution assay method. The HPTLC study of the ethanolic extract of whole plant revealed the presence of eight number of components in the chromatogram developed at 254 nm. The ethanolic extract of. whole plant of A. baccifera showed highest antibacterial efficiency followed by leaf, stem and root extracts respectively. However, ethanolic extracts of whole plant and leaves exhibited moderate antifungal potency followed by stem and root extracts, respectively. The results of MIC indicated that the whole plant extract inhibited P. mirabilis, K. pneumoniae, S. typhi and A. niger at a concentration of 62.5 g/ml thus exhibited broad spectrum of inhibition.


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