scholarly journals Postinfection Biological Control of Oomycete Pathogens of Pea by Burkholderia cepacia AMMDR1

2001 ◽  
Vol 91 (4) ◽  
pp. 383-391 ◽  
Author(s):  
K. Heungens ◽  
J. L. Parke

Burkholderia cepacia AMMDR1 is a biocontrol agent that reduces Pythium damping-off and Aphanomyces root rot severity on peas in the field. We studied the effect of B. cepacia AMMDR1 on post-infection stages in the life cycles of these pathogens, including mycelial colonization of the host, production of oogonia, and production of secondary zoospore inoculum. We used Burkholderia cepacia 1324, a seed and rootcolonizing but antibiosis-deficient Tn5 mutant of B. cepacia AMMDR1, to study mechanisms of biological control other than antibiosis. B. cepacia AMMDR1 significantly reduced Pythium aphanidermatum postinfection colonization and damping-off of pea seeds, even when the bacteria were applied 12 h after zoospore inoculation. B. cepacia AMMDR1 also significantly reduced colonization of taproots by Aphanomyces euteiches mycelium, but only when the bacteria were applied at high population densities at the site of zoospore inoculation. The antibiosisdeficient mutant, B. cepacia 1324, had no effect on mycelial colonization of seeds or roots by Pythium aphanidermatum nor A. euteiches, suggesting that antibiosis is the primary mechanism of biological control. B. cepacia AMMDR1, but not B. cepacia 1324, reduced production of A. euteiches oogonia. This effect occurred even when the population size of B. cepacia AMMDR1 was too small to cause a reduction in lesion length early on in the infection process and may result from in situ antibiotic production. B. cepacia AMMDR1 had no effect on the production of secondary zoospores of A. euteiches from infected roots. The main effects of B. cepacia AMMDR1 on postinfection stages in the life cycles of these pathogens therefore were reductions in mycelial colonization by Pythium aphanidermatum and in formation of oogonia by A. euteiches. No mechanism other than antibiosis could be identified.

2018 ◽  
Vol 101 (2) ◽  
pp. 315-322 ◽  
Author(s):  
Hanan S. Al-Hussini ◽  
Amna Y. Al-Rawahi ◽  
Abdullah A. Al-Marhoon ◽  
Shurooq A. Al-Abri ◽  
Issa H. Al-Mahmooli ◽  
...  

2019 ◽  
Vol 102 (2) ◽  
pp. 305-310 ◽  
Author(s):  
Dhuha Sulaiman Salim Al-Daghari ◽  
Shurooq Abdullah Al-Abri ◽  
Issa Hashil Al-Mahmooli ◽  
Abdullah Mohammed Al-Sadi ◽  
Rethinasamy Velazhahan

1998 ◽  
Vol 64 (10) ◽  
pp. 3939-3947 ◽  
Author(s):  
Yaowei Kang ◽  
Russell Carlson ◽  
Wendy Tharpe ◽  
Mark A. Schell

ABSTRACT Genetic manipulation of fluorescent pseudomonads has provided major insight into their production of antifungal molecules and their role in biological control of plant disease. Burkholderia cepaciaalso produces antifungal activities, but its biological control activity is much less well characterized, in part due to difficulties in applying genetic tools. Here we report genetic and biochemical characterization of a soil isolate of B. cepacia relating to its production of an unusual antibiotic that is very active against a variety of soil fungi. Purification and preliminary structural analyses suggest that this antibiotic (called AFC-BC11) is a novel lipopeptide associated largely with the cell membrane. Analysis of conditions for optimal production of AFC-BC11 indicated stringent environmental regulation of its synthesis. Furthermore, we show that production of AFC-BC11 is largely responsible for the ability ofB. cepacia BC11 to effectively control the damping-off of cotton caused by the fungal pathogen Rhizoctonia solani in a gnotobiotic system. Using Tn5 mutagenesis, we identified, cloned, and characterized a region of the genome of strain BC11 that is required for production of this antifungal metabolite. DNA sequence analysis suggested that this region encodes proteins directly involved in the production of a nonribosomally synthesized lipopeptide.


2019 ◽  
Vol 8 (4) ◽  
pp. 8035-8039

Damping-off is one of the severe diseases caused by soil-borne pathogens notably Pythium sp. the causative agent of this infection in raising tree saplings in forest nurseries. Biological control is an eco-friendly approach in disease management compared to chemical fungicides which in turn affects the soil environment. Biocontrol of Pythium sp. has been emphasized in vegetable nurseries than forest nurseries. The present research work is focused on identification of effective antagonistic organism from forest nursery soils against Pythium aphanidermatum. Bacteria were isolated from various forest soils collected from Boluvampati, Sirumugai and Mettupalayam forest nurseries in Coimbatore district and soil samples were screened for antifungal activity against Pythium aphanidermatum by dual culture technique. Among 245 bacterial isolates, one isolate KUMB1.1 exhibited clear zone of inhibition of 1cm and it was identified by 16S rDNA sequencing as Streptomyces sp. Solvent extraction was performed to isolate an active compound using ethyl acetate, dichloromethane, n-butanol, hexane and chloroform in the ratio 1:1. The antifungal activity of compound was performed by well plate method against Pythium sp. and nbutanol extract exhibited zone of inhibition. The antifungal activity of Streptomyces sp. was tested in a model plant Solanum lycopersicum (Tomato) seeds raised in Pythium aphanidermatum infested soils in seed trays under in vitro conditions. Preemergence and post-emergence disease incidences were observed, and the results exhibited promising efficacy of Streptomyces sp. against the fungal pathogen Pythium aphanidermatum. Seedbed study was carried out in Gmelina arborea seeds, where the seeds are treated with Streptomyces culture broth. In which seed treatment shows 43% increase in germination compared with control.


Plants ◽  
2021 ◽  
Vol 10 (4) ◽  
pp. 788
Author(s):  
Shaban R. M. Sayed ◽  
Shaimaa A. M. Abdelmohsen ◽  
Hani M. A. Abdelzaher ◽  
Mohammed A. Elnaghy ◽  
Ashraf A. Mostafa ◽  
...  

The role of Pythium oligandrum as a biocontrol agent against Pythium aphanidermatum was investigated to avoid the harmful impacts of fungicides. Three isolates of P. oligandrum (MS15, MS19, and MS31) were assessed facing the plant pathogenic P. aphanidermatum the causal agent of Glycine max damping-off. The tested Pythium species were recognized according to their cultural and microscopic characterizations. The identification was confirmed through sequencing of rDNA-ITS regions including the 5.8 S rDNA. The biocontrol agent, P. oligandrum, isolates decreased the mycelial growth of the pathogenic P. aphanidermatum with 71.3%, 67.1%, and 68.7% through mycoparasitism on CMA plates. While the half-strength millipore sterilized filtrates of P. oligandrum isolates degrade the pathogenic mycelial linear growth by 34.1%, 32.5%, and 31.7%, and reduce the mycelial dry weight of the pathogenic P. aphanidermatum by 40.1%, 37.4%, and 36.8%, respectively. Scanning electron microscopy (SEM) of the most effective antagonistic P. oligandrum isolate (MS15) interaction showed coiling, haustorial parts of P. oligandrum to P. aphanidermatum hyphae. Furthermore, P. oligandrum isolates were proven to enhance the germination of Glycine max seedling to 93.3% in damping-off infection using agar pots and promote germination of up to 80% during soil pot assay. On the other hand, P. oligandrum isolates increase the shoot, root lengths, and the number of lateral roots.


Author(s):  
G. M. Waterhouse

Abstract A description is provided for Pythium aphanidermatum. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On a wide range of hosts, often similar to those attacked by P. butleri, but inducing different symptoms, represented in the following families: Amaranthaceae, Amaryllidaceae, Araceae, Basellaceae, Bromeliaceae, Cactaceae, Chenopodiaceae, Compositae, Coniferae, Convolvulaceae, Cruciferae, Cucurbitaceae, Euphorbiaceae, Gramineae, Leguminosae, Linaceae, Malvaceae, Moraceae, Passifloraceae, Rosaceae, Solanaceae, Umbelliferae, Violaceae, Vitaceae, Zingiberaceae. DISEASES: Damping-off of various seedlings; 'cottony-leak' of cucurbit fruit in storage; 'cottony blight' of turf grasses; root and stalk rot of maize. Other hosts: tobacco, sugar-beet, sugar-cane, papaw, pineapple, ginger, bean and cotton. GEOGRAPHICAL DISTRIBUTION: Africa (Central African Republic, Fernando, Ghana, Kenya, Malawi, Mali, Nigeria, Sierra Leone, South Africa, Southern Rhodesia, Sudan, Togo, Zambia); Asia (Ceylon, China, Formosa, India, Indonesia, Israel, Japan, Java, Malaya, Philippines, Sumatra); Australasia & Oceania (Australia, Hawaii, New Caledonia); North America (Canada, Mexico); Central America & West Indies (Antilles, Jamaica, Puerto Rico); South America (Argentina, Brazil, Peru, Venezuela); Europe Austria, Cyprus, Czechoslovakia, Great Britain, Greece, Holland, Italy, Poland, U.S.S.R., Yugoslavia). (CMI Map 309) TRANSMISSION: Soil-borne. Eggplant fruit become infected when blossom end is in contact with soil (5: 465). Readily isolated from soil using fresh potato cubes treated with streptomycin and pimaricin as baits (43, 1519; 43, 46) or seedling papaw roots in soil containing papaw tissue (43, 1720). Also recorded as seed-borne on tomato and cucurbits but doubtful whether seed-transmitted (see Noble et al., An Annotated List of Seed-Borne Diseases, 1958, pp. 23, 25, 124).


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