Streptomyces angustmyceticus NR8-2 as a potential microorganism for the biological control of leaf spots of Brassica rapa subsp. pekinensis caused by Colletotrichum sp. and Curvularia lunata

2019 ◽  
Vol 138 ◽  
pp. 104046 ◽  
Author(s):  
Prisana Wonglom ◽  
Nakarin Suwannarach ◽  
Saisamorn Lumyong ◽  
Shin-ichi Ito ◽  
Kenji Matsui ◽  
...  
Plant Disease ◽  
2011 ◽  
Vol 95 (12) ◽  
pp. 1586-1586 ◽  
Author(s):  
D. Berner ◽  
C. Cavin ◽  
Z. Mukhina ◽  
D. Kassanelly

Black swallow-wort, Vincetoxicum nigrum (L.) Moench (= Cynanchum louiseae Kartesz & Gandhi), and pale swallow-wort, V. rossicum (Kleopow) Borhidi (= Cynanchum rossicum (Kleopow) Borhidi), are invasive plants belonging to the family Apocynaceae and are the targets of biological control efforts to control their spread in the United States. In 2010, a disease on a related species, V. scandens Sommier & Levier, was observed in the Krasnodar area of Russia. Disease symptoms were many small, dark red-to-purple leaf spots, approximately 2 to 5 mm in diameter, with white centers. Leaf spots were found on the upper leaf surface. Leaf tips and margins of leaves bearing many of these spots were necrotic. Symptomatic leaves were collected and sent to the BSL-3 containment facility at the Foreign Disease-Weed Science Research Unit (FDWSRU) of the USDA, ARS in Frederick MD. Surface-disinfested symptomatic leaves were incubated at 20 to 25°C in sterile moist chambers. After several days, acervuli and brown setae were observed inside the leaf spots. Pure cultures, designated FDWSRU 10-002, were obtained by transferring spore masses with sterile glass needles onto 20% V8 juice agar. Seeds of V. scandens, collected in Russia, were placed in a freezer at –20°C for 6 weeks and then germinated in sterile petri plates on moist filter paper. The seedlings were then transplanted and grown in a 20°C greenhouse under 12 h of light. Koch's postulates were fulfilled as follows: 2-month-old plants each of V. scandens, V. nigrum, and V. rossicum were inoculated with spores from 2-week-old cultures of isolate 10-002. Plants were inoculated by spraying an aqueous suspension of 106 spores per ml onto each plant until all leaves were wet. Plants were placed in 20 to 24°C dew chambers for 18 h and then placed in a 20°C greenhouse. Two weeks later, diseased leaves with the same symptoms observed in the field were harvested from each species, and the fungus was reisolated from seven of seven inoculated V. scandens plants, one of two V. nigrum plants, and four of four V. rossicum plants. Measurements of fungus fruiting structures were taken from cultures grown on synthetic nutrient-poor agar (SNA) (1). Conidiophores were brown, septate, and branched. Conidia were one-celled, hyaline, smooth walled, ovoid to oblong, falcate, and 20.1 to 26.2 × 1.7 to 3.6 μm (mean ± s.d. = 23.5 ± 1.3 × 2.6 ± 0.4 μm). Lengths of the conidia conformed to the description of Colletotrichum lineola Corda (1), but the conidia were slightly narrower than described. To induce appressoria formation, approximately 104 conidia were placed on sterile dialysis membranes on top of SNA in petri dishes that were wrapped in foil and incubated at 24°C for 24 h. After this time, appressoria were observed with a microscope at ×400 magnification. The appressoria were dark brown, smooth walled, ellipsoidal, and 5.5 to 25.5 × 3.6 to 12.1 μm (mean ± s.d. = 13.4 ± 4.0 × 7.3 ± 2.1 μm), which conformed to the description of appressoria of C. lineola Corda (1). DNA sequences of ITS1, 5.8S, and ITS2 were submitted to GenBank (No. HQ731491), and after BLAST analysis, aligned 100% to 15 previously identified isolates of C. lineola in GenBank. Voucher specimens of the fungus have been deposited in the U.S. National Fungus Collection and were designated as BPI 881105 and BPI 881106. Host range and efficacy tests are planned to determine the suitability of C. lineola for biological control of swallow-worts in the United States. Reference: (1) U. Damm et al. Fungal Divers. 39:45, 2009.


2011 ◽  
Vol 143 (4) ◽  
pp. 399-410 ◽  
Author(s):  
Franck J. Muller ◽  
Lloyd M. Dosdall ◽  
Peter G. Mason ◽  
Ulrich Kuhlmann

AbstractIn Europe, Ceutorhynchus turbatus Schultze and Ceutorhynchus typhae (Herbst) (Coleoptera: Curculionidae) feed on seeds from hoary cress and shepherd's purse (Cardaria draba (L.) Desv. and Capsella bursa-pastoris (L.) Medik.); both plants are invasive in North America. In North America, C. turbatus is a candidate for biological control of hoary cress, C. typhae is adventive, and both are sympatric with cabbage seedpod weevil (Ceutorhynchus obstrictus (Marsham)), an invasive alien pest of canola (Brassica napus L. and Brassica rapa L., Brassicaceae). We investigated host associations among C. turbatus, C. typhae, and their parasitoids in Europe. Of particular interest was host specificity of Trichomalus perfectus (Walker) and Mesopolobus morys (Walker) (Hymenoptera: Pteromalidae), candidates for biological control of C. obstrictus in North America. We found no evidence that T. perfectus attacks C. turbatus or C. typhae; however, M. morys was the most common parasitoid associated with C. turbatus.


Plant Disease ◽  
2004 ◽  
Vol 88 (12) ◽  
pp. 1382-1382 ◽  
Author(s):  
F. M. Eskandari ◽  
D. K. Berner ◽  
J. Kashefi ◽  
L. Strieth

Centaurea solstitialis L. (yellow starthistle [YST]), family Asteraceae, an invasive weed in California and the western United States is targeted for biological control. During the spring of 2004, an epidemic of dying YST plants was found near Kozani, Greece (40°22′07″N, 21°52′35″E, 634 m elevation). Rosettes of YST had small, brown leaf spots on most of the lower leaves. In many cases, these spots coalesced and resulted in necrosis of many of the leaves and death of the rosette. Along the roadside where the disease was found, >100 of the YST plants showed disease symptoms. Diseased plants were collected, air dried, and sent to the quarantine facility of the Foreign Disease-Weed Science Research Unit (FDWSRU), USDA, ARS, Fort Detrick, MD. Diseased leaves were surface disinfested and placed on moist filter paper in petri dishes. Conidiophores and conidia were observed after 48 h. The fungal isolate, DB04-011, was isolated from these diseased leaves. Pathogenicity tests were performed by spray inoculating the foliage of 20 4-week-old YST rosettes with an aqueous suspension of 1 × 106 conidia per ml. Conidia were harvested from 2-week-old cultures grown on modified potato carrot agar (MPCA). Inoculated plants were placed in an environmental chamber at 23°C with 8 h of daily light and continuous dew for 48 h. Inoculated and control plants were moved to a 20°C greenhouse bench and watered twice per day. After 7 days, leaf spots were observed first on lower leaves. After 10–12 days, all inoculated plants showed typical symptoms of the disease. No symptoms developed on control plants. The pathogen, DB04-011, was consistently isolated from symptomatic leaves of all inoculated plants. Disease symptoms were scattered, amphigenous leaf spots in circular to subcircular spots that were 0.2 to 7 mm in diameter and brownish with distinct dark green margins. Intraepidermal stromata, 14 to 77 μm in diameter and pale yellow to brown, were formed within the spots. Conidiophores that arose from the stromata were straight, subcylindrical, simple, 70 to 95 × 2.8 to 4 μm, hyaline, smooth, and continuous or septate with conidial scars that were somewhat thickened, colorless, and refractive. Primary conidia were subcylindrical, slightly obclavate or fusiform, ovoid, 21 to 49 × 5 to 7.5 μm, 0 to 5 septate, hyaline, smooth, had a relatively rounded apex, and the hilum was slightly thickened. Conidial dimensions on MPCA were 11.2 to 39.2 × 4.2 to 7 μm (average 25.5 × 5.5 μm). Koch's postulates were repeated two more times with 20 and 16 plants. On the basis of fungal morphology, the organism was identified as a Cercosporella sp., (1,2; U. Braun and N. Ale-Agha, personal communication). To our knowledge, this is the first report of this genus of fungus parasitizing YST. Results of host range tests will establish if this isolate of Cercosporella has potential as a biological control agent of YST in the United States. A voucher specimen has been deposited with the U.S. National Fungus Collections (BPI 844247). Live cultures are being maintained at FDWSRU and European Biological Control Laboratoryt (EBCL), Greece. References: (1) U. Braun. A Monograph of Cercosporella, Ramularia and Allied Genera (Phytopathogenic Hyphomycetes) Vol. 1. IHW-Verlage, Eching-by-Munich, 1995. (2) U. Braun. A Monograph of Cercosporella, Ramularia and Allied Genera (Phytopathogenic Hyphomycetes) Vol. 2. IHW-Verlage, 1998.


2016 ◽  
Vol 18 (06) ◽  
pp. 1201-1212
Author(s):  
A. Hilal ◽  
Eman El-Argawy ◽  
A. El. Korany ◽  
Taghreed Fekry

Plant Disease ◽  
2016 ◽  
Vol 100 (3) ◽  
pp. 652-652 ◽  
Author(s):  
L. Tong ◽  
L. LongZhou ◽  
H. Jumei ◽  
J. Lan

2002 ◽  
Vol 42 (2) ◽  
pp. 185 ◽  
Author(s):  
P. Bailey ◽  
J-L. Sagliocco ◽  
J. Vitou ◽  
D. Cooke

In South Australia, Reseda lutea is abundant, invading pastures and crops on calcareous soils while in its native Mediterranean range it is uncommon in occurrence and is not reported as a weed of cultivated crops. Its invasive behaviour in South Australia may be attributed to vegetative growth of root fragments spread by cultivation, while propagation by seed is of minor importance. Surveys in Spain, Portugal, Morocco, France, Turkey and Israel indicated that agronomic differences, particularly depth of cultivation and seeding rates of cereals may explain why it is not a crop weed in these countries. Another difference is that plants in the region of origin have an associated fauna not present in Australia. These potential biological control agents include a root-boring weevil, Baris picicornis, flower- and seed-feeding urodontids, Bruchela suturalis and B. rufipes, and a leaf spot pathogen,Cercospora resedae. Baris picicornis was introduced from France and Turkey, under quarantine, to Australia but laboratory specificity-testing demonstrated that it could complete its life cycle on 2 commercially grown cultivars of Brassica rapa (choy sum and Chinese cabbage). Because of this, it is not proposed to release B. picicornis in Australia at present. Bruchela suturalis was also introduced into Australian quarantine from France but attempts to change its annual life cycle to Southern Hemisphere seasons were not successful, and a culture could not be established. Both Baris picicornis and Bruchela spp. remain promising agents, and further work on their introduction is justified by their potential for biological control of R. lutea.


2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Huyly Tann ◽  
Kasem Soytong

<em>Curvularia lunata</em> was isolated from leaf spot of rice var. Sen Pidoa and tested for pathogenicity. <em>Chaetomium cupreum</em> CC3003 expressed antifungal activity against <em>C.</em> <em>lunata</em> in dual culture test. Hexane-crude extract, EtOAc-crude extract and methanol-crude extract from <em>C. cupreum</em> inhibited sporulation of <em>C. lunata</em> with ED50 of 6.41, 0.83 and 7.81 μg/mL, respectively. Pot experiment revealed that plant heights in treated with a spore suspension of <em>C. cupreum</em>, bioformulation of<em> C. cupreum</em>, nano product from <em>C. cupreum</em> and tebuconazole were not significantly different when compared to the inoculated control. Disease reduction compared to the inoculated control from treatment with a spore suspension of Chaetomium, bioformulation of <em>C. cupreum</em>, nano product from <em>C. cupreum</em> and tebuconazole ranged between 41.66% to 58.33%. Field experiment indicated that chemical method was decreased leaf spots infection by 60%, followed by organic method (40%) and GAP methods (40%) , respectively. The chemical and GAP methods were significantly higher in grain weight than the organic method when compared to the non-treated control. This is the first report using <em>C. cupreum</em> to control leaf spot of rice var. Sen Pidoa caused by <em>C. lunata </em>in Cambodia.


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