scholarly journals The infection process of Colletotrichum fuscum on oregano leaves and stems

2021 ◽  
Vol 20 (5) ◽  
pp. 97-106
Author(s):  
Beata Zimowska ◽  
Ewa Dorota Król

Anthracnose, caused by Colletotrichum fuscum, produces regular necrotic spots on oregano leaves and stems, causing severe crop losses. In this study, Koch’s postulates were fulfilled and infection process was investigated using scanning electron microscopy. Leaves and stems of Origanum vulgare were inoculated and incubated at 24°C in wet chambers under high relative humidity. Pathogenicity experiments demonstrated that all tested C. fuscum isolates had infected stems and leaves of oregano. Of all inoculation methods, direct placement of colonized agar plugs on injured epidermis and soaking plant organs in conidial suspension were the most effective. The behavior of the conidia deposited on the oregano leaves was investigated at different time intervals after inoculation: at 12, 18, 32, 48, 67 and 98 h. Conidia produced an appressoria of varying shapes which has been formed at the end of germ tubes of different lengths. Penetration to host tissue through stomata was observed. Acervuli formed on the leaves surface after 98 h after inoculation, typically with sharp pointed setoses.

2012 ◽  
Vol 61 (4) ◽  
pp. 273-279 ◽  
Author(s):  
BEATA ZIMOWSKA

Pathogenicity and ultrastructural investigation of the inoculation of peppermint stems and rhizomes with Phoma strasseri conidia was undertaken using scanning and transmission electron microscopy to examine the host-parasite relationship. Pathogenicity experiments demonstrated that all tested P. strasseri isolates had infected the stems and rhizomes of peppermint. Of all inoculation methods, direct placement of colonized agar plugs on damaged epidermis and soaking stems and rhizomes in conidial suspension were the most effective. The behavior of the conidia deposited on the stems and rhizomes was investigated at different time intervals after inoculation: 6, 16, 24, 36 and 48 h. Conidia produced an appressorium directly at the end of a short germ tube. Appressoria were formed over the cuticle, but never over stomata. Direct penetration to host tissue through the cuticle was observed. The spore and hyphae were covered with a mucilaginous sheath.


Botany ◽  
2011 ◽  
Vol 89 (11) ◽  
pp. 771-777 ◽  
Author(s):  
Ping Zhang ◽  
Guo-zhong Lu ◽  
Xiao-dong Sun ◽  
Wei Zhang ◽  
Bo Qu ◽  
...  

Puccinia xanthii Schwein. f. sp. ambrosiae-trifidae S.W.T. Batra is an obligate parasitic rust fungus of Ambrosia trifida Linn. Field investigations in Liaoning Province, China, showed that it is an effective biocontrol agent of this alien invasive weed. Its infection of the plant was observed by light microscopy combined with Coomassie Brilliant Blue R-250 staining. We report the infection process, including teliospore germination and basidiospore formation on the host leaf surface, penetration of host tissue, and development of fungal hyphae within the host tissue. Fresh teliospores began to germinate from the germ pore within 1 h under suitable conditions and soon produced basidiospores or secondary basidiospores. Basidiospores falling on host leaves germinated from the end of the basidiospore opposite to the apiculus. Appressoria of germ tubes tended to orient along leaf epidermis cell ridges or at junctions near stomata rather than fixing randomly on the leaf surface. These germ tubes grew for short or longer distances before forming appressoria. The rust fungus directly penetrated the host epidermis by infectious pegs rather than through stomata. Within host tissues, the rust fungus formed intraepidermal vesicles, primary hyphae, intracellular hyphae, and M-haustoria. The intricate infectious structures formed by P. xanthii f. sp. ambrosiae-trifidae on or in host tissues suggest that the rust fungus is a suitable organism for researching the interaction between the pathogen and host plant.


1991 ◽  
Vol 69 (8) ◽  
pp. 1865-1871 ◽  
Author(s):  
G. P. Munkvold ◽  
D. Neely

Excised leaves of Quercus rubra were inoculated with suspensions of conidia of Tubakia dryina and the development of the fungus on the leaf tissue was observed by scanning electron and light microscopy. Conidial germination was 2% after 6 h, 53% after 12 h, and 54% after 24 h. Germ tubes formed appressorium-like structures directly on the leaf cuticle or over stomata, or entered stomata directly. Development of conidiomata was first evident 24–72 h after inoculation. Conidiomata first appeared as a small mass of hyphal cells, which then proliferated in a radial fashion, with simultaneous formation of conidia. Conidiogenous cells later ceased to form conidia and became thick walled and pigmented, forming a dark scutellum. Conidiogenous cells continued to proliferate ventrally to the scutellum, producing a ring of conidia embedded in a sticky matrix, surrounding the conidioma. Leaf tissue colonized by the fungus became water soaked, and later turned brown and necrotic. Key words: Actinopelte, leaf spot, oak, pycnothyrium.


Plant Disease ◽  
2000 ◽  
Vol 84 (12) ◽  
pp. 1345-1345 ◽  
Author(s):  
M. C. Rivera ◽  
E. R. Wright ◽  
S. Carballo

Chinese rose (Hibiscus rosa-sinensis L.) is a shrub frequently planted in Argentina. In November 1999, dieback and anthracnose symptoms were detected on stems and leaves of plants cv. Hawaii cultivated in Buenos Aires. Disease prevalence was 50%. Pieces of infected tissues were surface-sterilized for 1 min in 2% NaOCl, plated on potato-dextrose agar and incubated at 24 ± 2°C. The isolate that was consistently recovered from diseased tissues was identified as Colletotrichum gloeosporioides (Penz.) Penz. and Sacc., based on morphological characteristics (1,2). Teleomorph stage was not observed. Inoculation for pathogenicity testing was carried out by spraying a conidial suspension (6.5 × 106 conidia per ml) on plants with previously punctured leaves and pruned stems. Inoculated plants with unwounded tissues, as well as noninoculated controls, were included. Five replications of each treatment were done. Plants were incubated in moist chambers at 24°C. Whitish areas of 0.3 to 0.5 cm diameter surrounded by a purple halo developed on all punctured leaves within 10 days. Stem blight and leaf drop were observed. The center of the lesions was covered by black acervuli 14 days after inoculation. Unwounded and noninoculated controls remained symptomless. The pathogen was reisolated from inoculated leaves, completing Koch's postulates. This is the first report of C. gloeosporioides causing disease on Chinese rose in Argentina. References: (1) J. A. Bailey and M. J. Jeger, eds. 1992. Colletotrichum. CAB International, Surrey, England. (2) B. C. Sutton. 1980. The Coelomycetes. CMI, Kew.


2018 ◽  
Author(s):  
Jianyu Li ◽  
Mengzhu Shi ◽  
Yuechao He ◽  
Jianwei Fu ◽  
Lizhen Zheng

Background. Phyllotreta striolata is a worldwide pest that harms cruciferous vegetables. The use of pathogenic microorganisms to control pests is an important means of biological control. Using pathogenic microorganisms to prevent and control P. striolata has rarely been reported. Methods. In this study, the infection process of a Metarhizium strain highly pathogenic to P. striolata was observed by stereomicroscopyand scanning electron microscopy (SEM). Results.The results showed that the attachment of Metarhizium strain Ma6 to the body surface varied; the conidia distribution was greatest in the tibia of the posterior leg with thick bristles and in the intersegmental abdominal membrane, and the spore distribution occurred least in the smooth and hard portions of the insect’s body. At the start of the infection, Metarhizium strain Ma6 generally grew from the body parts with gaps or connecting spaces such as mouthparts and the thoracic leg base and joints, then the spores germinated with germ tubes and penetration peg, and the penetration peg penetrated the body surface. Ten days after inoculation, the mycelia divided into conidia, and many mycelia and spores covered the entire adult insect’s body. Discussion. Spore germination occurred on the 5th day after inoculation, and many hyphae and spores covered the entire adult insect body within 10 days after inoculation. And the invasion into tissue gaps from the weaker areas is more efficient than intruding from the body hard surface. This may be the reason for the Metarhizium strain Ma6’s high virulence. This study preliminarily clarified the infection ability and invasion approach of a Metarhizium strain against P. striolata, providing evidence for evaluating the strain’s insecticidal effect and application prospect.


2017 ◽  
Vol 9 (1) ◽  
pp. 461-465
Author(s):  
Tanvi Sharma ◽  
Neelam Joshi ◽  
Anu Kalia

This work was aimed to identify the LC50 of the indigenous fungal isolates for controlling L. erysimi infesta-tion in mustard aphid besides to probe the mechanism of action of the local isolates and comparison of the efficacy with the reference culture and commercial formulation ‘Mycojaal’. Three isolates of entomopathogenic fungi Beauveria bassiana were tested for infection on nymph of Lipaphis erysimi Kalt. using scanning electron microscopy (SEM) to record any variation. The SEM revealed adhesion of spores of B.bassiana followed by penetration of L.erysimi nymph surface. It was observed that all Beauveria isolates showed little variation with respect to penetration and adhesion at different time intervals. Further, lethal concentration (LC50) values of B. bassiana isolates against L. erysimi was recorded and was lowest (0.05x107 spores/ml) in B. bassiana MTCC 4495 and highest (0.11.X107 spores/ml) was recorded in native isolate F10 after 120 hours of treatment. The study has established the need for the isolation and evaluation of the indigenous Beauveria isolate. Moreover, it also exhibited the efficacy of the reference and commercially available biocontrol agents.


Plant Disease ◽  
2008 ◽  
Vol 92 (9) ◽  
pp. 1366-1366 ◽  
Author(s):  
T. Kolomiets ◽  
O. Skatenok ◽  
A. Alexandrova ◽  
Z. Mukhina ◽  
T. Matveeva ◽  
...  

In October of 2006, dying Salsola tragus L. (Russian thistle, tumbleweed), family Chenopodiaceae, plants were found along the Azov Sea at Chushka, Russia. Approximately 40 plants in the area were diseased and almost 80% of these were dying. Plants were approximately 1 m tall × 0.5 m wide. Dying plants had irregular, necrotic lesions along the length of the stems. Leaves of these plants were also necrotic. Lesions on stems and leaves were dark brown and usually coalesced. Diseased stems were cut into 3- to 5-mm pieces, disinfested in 70% ethyl alcohol, and then placed onto the surface of potato glucose agar (PGA). Numerous, waxy, subepidermal acervuli with 110 μm long (mean) black setae were observed in all of the lesions after 2 to 3 days. Conidiophores were simple, short, and erect. Conidia were one-celled, hyaline, ovoid to oblong, falcate to straight, and measured 12.9 to 18.0 × 2.8 to 5.5 μm (mean 15.6 × 4.2 μm). Appressoria formed 24 h after placing conidia on a dialysis membrane over 20% V8 juice agar. Appressoria measured 4.0 to 13.9 × 2.4 to 8.8 μm (mean 7.0 × 5.2 μm). These characters conformed to the description of Colletotrichum gloeosporioides (Penz.) Penz. & Sacc. in Penz. (1). A voucher specimen was deposited with the U.S. National Fungus Collections, Beltsville, MD (BPI 878389). Nucleotide sequences for the internal transcribed spacers (ITS 1 and 2) were deposited in GenBank (Accession No. EU530697) and aligned with ITS sequences of two other isolates from S. tragus. There was 100% similarity to each isolate, one from Greece (Accession No. DQ344621) and one from Hungary (Accession No. EU805538). Axenic cultures on PGA were sent to the Foreign Disease-Weed Science Research Unit, USDA, ARS, Fort Detrick, MD for testing in quarantine. Conidia were harvested from 14-day-old cultures grown on 20% V8 juice agar, and healthy stems and leaves of 30-day-old plants of S. tragus (13 plants) were spray inoculated with an aqueous conidial suspension of 1.0 × 106 conidia/ml plus 0.1% v/v polysorbate 20. Another 13 control plants were sprayed with water and surfactant without conidia. Plants were placed in an environmental chamber at 100% humidity for 16 h in the dark at 25°C. After approximately 24 h, all plants were transferred to a greenhouse at 20 to 25°C, 30 to 50% relative humidity, and natural light augmented by 12-h light periods with 500 W sodium vapor lights. Lesions developed on stems of all inoculated plants after 7 days. After 14 days, nine plants were dead and all inoculated plants were dead after 3 weeks. No symptoms developed on control plants. C. gloeosporioides was reisolated from stem pieces of all inoculated plants, and the morphology of the reisolated pathogen was the same as that of the initially isolated pathogen. To our knowledge, this is the first report of anthracnose caused by C. gloeosporioides on S. tragus in Russia. Reference: (1) B. C. Sutton. Page 15 in: Colletotrichum Biology, Pathology and Control. J. A. Bailey and M. J. Jeger, eds. CAB International, Wallingford, UK, 1992.


2000 ◽  
Vol 90 (7) ◽  
pp. 699-709 ◽  
Author(s):  
Bryan A. Bailey ◽  
Patricia C. Apel-Birkhold ◽  
Nichole R. O'Neill ◽  
James Plaskowitz ◽  
Sharon Alavi ◽  
...  

Two pathogenic fungi of opium poppy, Pleospora papaveracea and Dendryphion penicillatum, were isolated from field material in Beltsville, MD. The processes of infection by these two fungi were studied to determine the optimal environmental conditions for infection. Both fungi formed appressoria capable of penetrating directly through the plant epidermal layer. Of the two fungi, P. papaveracea was more aggressive, causing more rapid necrosis. Appressorial formation by P. papaveracea occurred as early as 4 h after application of a conidial suspension to poppy leaves. P. papaveracea formed more appressoria than did D. penicillatum, especially at cool temperatures (7 to 13°C). In greenhouse studies, P. papaveracea caused more damage to opium poppy than did D. penicillatum when applied in 10% unrefined corn oil. In the field, P. papaveracea was more consistent in its effects on opium poppy from a local seed source designated Indian Grocery. P. papaveracea caused higher disease ratings, more stem lesions, and equal or greater yield losses than did D. penicillatum on Indian Grocery. The late-maturing opium poppy variety White Cloud was severely damaged by disease, regardless of formulation or fungal treatment. P. papaveracea was the predominant fungus isolated from poppy seed capsules and the only fungus reisolated from the field the following year. These studies provide a better understanding of the infection process and the differences between these two pathogenic fungi and will be beneficial for the development of the fungi as biological control agents.


Plant Disease ◽  
2013 ◽  
Vol 97 (12) ◽  
pp. 1660-1660
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
A. Poli ◽  
M. L. Gullino

Verbascum nigrum L., common name black mullein, family Scrophulariaceae, is a rustic perennial plant belonging to the native flora in Italy. The plant, which produces bright yellow flowers densely grouped on the tall stem, is used in low-maintenance gardens. During fall 2012, plants grown in mixed planting borders in a garden located in Biella Province (northern Italy) showed extensive foliar disease. Approximately 100 plants were affected by the disease. Early symptoms were small, light brown, necrotic spots on leaves, later reaching 10 mm diameter, with an irregular shape, showing a chlorotic halo. Necrotic areas often coalesced surrounded by yellowing. In some cases, the internal part of the necrotic areas dried with the appearance of holes. The disease progressed from the base to the apex of plants. In some cases, most of leaves turned completely necrotic and plants were severely damaged. Symptomatic tissues were immersed in a solution containing 1% sodium hypochlorite for 2 to 3 s and rinsed with sterile distilled water. Small fragments were excised from the margin of lesions and plated on potato dextrose agar (PDA) medium. Petri dishes were incubated at temperatures ranging between 20 and 25°C under alternating daylight and darkness (12 h light, 12 h dark). A single fungus was consistently isolated and subcultured on malt extract agar (MEA). On MEA, colonies were felty, white cream, and produced dark globose or subglobose pycnidia measuring 68 to 185 × 62 to 177 (average 122 × 113) μm, containing hyaline (light grey in mass), ellipsoid, non-septate conidia measuring 3.1 to 5.7 × 1.5 to 2.7 (average 4.0 × 2.0) μm after 15 days. The internal transcribed spacer (ITS) and D1/D2 regions of rDNA were amplified using the primers ITS1/ITS4 and NL1/NL4, respectively, and then sequenced (GenBank Accession Nos. KC411473 and KF041823). BLAST analysis of both fragments showed 99% homology with the sequences GU237753 and JQ768403 of Phoma novae-verbascicola Aveskamp, Gruyter & Verkley (Basionym: Phyllosticta verbascicola Ellis & Kellerm.). Morphological characteristics of the fungus also were consistent with the descriptions of P. poolensis var. verbascicola (Ellis & Kellerm.) Aa & Boerema (2) (Syn.: P. novae-verbascicola). Pathogenicity tests were performed by spraying a conidial suspension (4 × 104 CFU/ml) obtained from 15-day-old PDA cultures of the fungus onto leaves of three healthy 3-month-old V. nigrum. Three plants inoculated with sterile water served as controls. Plants were maintained in a growth chamber for 5 days at 25 ± 1°C under 70 to 90% relative humidity. The first foliar lesions developed on leaves 2 days after inoculation and after 5 days, 80% of leaves were severely infected. Control plants remained healthy. The organism reisolated on PDA from leaf lesions was identical in morphology to the isolate used for inoculation. The pathogenicity test was carried out twice. Phoma spp. has been reported on Verbascum spp. P. novae-verbascicola has been very recently described (1). To our knowledge, this is the first report of the presence of P. novae-verbascicola on V. nigrum in Italy. At present, the economic importance of this disease is limited, but may become a more significant problem if the cultivation of this species increases. References: (1) M. M. Aveskamp et al. Studies in Mycology, 65: 1, 2010. (2) J. de Gruyter et al. Persoonia 15 (3): 369, 1993.


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