scholarly journals First Report of Leaf Anthracnose Caused by Colletotrichum tropicale on Oregano (Origanum vulgare) in Mexico

Plant Disease ◽  
2020 ◽  
Vol 104 (6) ◽  
pp. 1855-1855
Author(s):  
S. Ayvar-Serna ◽  
J. F. Díaz-Nájera ◽  
A. Mena-Bahena ◽  
B. E. Ortiz-Montes ◽  
O. G. Alvarado-Gómez ◽  
...  
2021 ◽  
Author(s):  
Olga Sokolova ◽  
Irina Sivicka ◽  
Baiba Krivmane ◽  
Katrīna Kārkliņa

Plant Disease ◽  
2013 ◽  
Vol 97 (8) ◽  
pp. 1119-1119 ◽  
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
P. Pensa ◽  
A. Poli ◽  
M. L. Gullino

Origanum vulgare L., common name oregano, family Labiatae, is grown for its aromatic and medicinal properties and as ornamental. In the fall of 2012, a blight was observed in a farm located near Albenga (northern Italy) on 6% of 30,000 50-day-old plants, grown in trays in a peat/perlite mix. Semicircular, water soaked lesions appeared on leaves and stems, starting from the basal ones. As the disease progressed, blighted leaves turned brown, withered, clung to the shoots, and matted on the surrounding foliage. Eventually, infected plants died. Leaf and stem fragments taken from the margin of the diseased tissues belonging to 10 plants were disinfected for 10 s in 1% NaOCl, rinsed with sterile water, and plated on potato dextrose agar (PDA). A fungus with the morphological characters of Rhizoctonia solani was consistently recovered. Three isolates of R. solani obtained from affected plants were successfully anastomosed with R. solani isolate AG 1 (ATCC 58946). Three pairings were made for each tester strain. The hyphal diameter at the point of anastomosis was reduced, the anastomosis point was obvious, and death of adjacent cells was observed. Results were consistent with other reports on anastomosis reactions (2). Isolates from oregano were paired with R. solani isolates AG 2, 3, 4, 6, 7, or 11 and examined microscopically. Anastomosis was not observed in any of the pairings. Tests were conducted twice. Mycelium of 10-day-old isolates from oregano appeared reddish brown, coarse, and radiate. Numerous dark brown sclerotia, 0.3 to 1.0 mm diameter (average 0.7) developed within 10 days after transfer of mycelia to PDA in 90 mm diameter petri dishes at 21 to 24°C. The descriptions of mycelium and sclerotia were typical for subgroup IB Type 1 (4). The internal transcribed spacer (ITS) region of rDNA was amplified using the primers ITS1/ITS4 and sequenced. BLASTn analysis (1) of the 538 bp showed a 99% homology with the sequence of R. solani FJ746937, confirming the morphological identification of the species. The nucleotide sequence has been assigned the GenBank Accession KC493638. For pathogenicity tests, one of the isolates assigned to the anastomosis group AG-1-IB was tested by placing 9 mm diameter mycelial disks removed from PDA 10-day-old cultures of the fungus on leaves of 90-day-old oregano plants (n = 35). Thirty-five plants inoculated with non-inoculated PDA disks served as controls. Plants were covered with plastic bags and maintained in a growth chamber at 25 ± 1°C with 12 h light/dark. The first symptoms, similar to those observed in the farm, developed 3 days after inoculation. Nine days after the artificial inoculation, 50% of plants were dead. About 10 colonies of R. solani were reisolated from infected leaves of inoculated plants. Control plants remained healthy. The pathogenicity test was carried out twice with similar results. Symptoms caused by R. solani have been recently observed on O. vulgare in Greece (3). This is, to our knowledge, the first report of blight of O. vulgare caused by R. solani in Italy. References: (1) S. F. Altschul et al. Nucleic Acids Res., 25:3389, 1997. (2) D. E. Carling. Grouping in Rhizoctonia solani by hyphal anastomosis reactions. In: Rhizoctonia Species: Taxonomy, Molecular Biology, Ecology, Pathology and Disease control. Kluwer Academic Publishers, The Netherlands, pp. 37-47, 1996. (3) C. D. Holevas et al. Benaki Phytopathol. Inst., Kiphissia, Athens, 19:1-96, 2000. (4) R. T. Sherwood. Phytopathology 59:1924, 1969.


Plant Disease ◽  
2021 ◽  
Author(s):  
Chung-hang Duan ◽  
Guan-ying Chen

Ficus carica L. known as common fig is one of the most profitable fruit crops in Taiwan. Their fruit are harvested for high-priced market. Common fig can be eaten fresh or dried and processed to make different food products. In September 2015, an anthracnose-like disease was widely observed on common fig fruit planted in an orchard in Lukang township (24°04'36" N, 120°27'15" E) in Changhua County, central Taiwan. Symptoms were sunken, water-soaked lesions covered with salmon-colored spore masses and were observed on all stages of fruit, especially when fruit was ripe. Four fungal isolates were collected from four diseased fruit of different plants in the same orchard. Conidia were spread on 2% water agar, and a single conidium was separated by a handmade glass needle. Fungal isolates were grown on potato dextrose agar (PDA) at 24 to 28°C with diffused light. All four strains produced white, aerial, and cottony mycelia covered with abundant salmon-colored conidial masses on PDA. The conidia were hyaline, single celled, round cylindrical on both ends, thin walled, and the contents guttulate. The sizes of conidia were 15.4 (18.5 to 13.1) × 4.73 (5.8 to 3.6) μm [average (max. to min.); length/width ratio = 3.25, n = 40]. DNA was isolated from the representative isolate FC1 and used for amplification of partial sequences of the internal transcribed spacer (ITS), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), actin (ACT), β-tubulin 2 (TUB2), manganese-superoxide dismutase (SOD2), calmodulin (CAL), chitin synthase 1 (CHS-1) (Weir et al. 2012) and the intergenic region of apn2 and MAT1-2-1 gene (ApMat) genes (Sharma et al. 2013). A BLAST search against the NCBI database revealed that FC1 gene sequences [GenBank accession nos. MT192648 (ITS), MT155819 (GAPDH), MT199873 (ACT), MT199874 (TUB2), MT815916 (SOD2), MT815917 (CAL), MW684717 (CHS-1) and MT221652 (ApMat)] displayed 99.1, 98.2, 99.3, 99.6, 99.5, 100.0, 92.8 and 100.0% nucleotide identity to the respective gene sequences of Colletotrichum tropicale CBS 124949 (ICMP18653) (JX010264, JX010007, JX009489, JX010407, JX010329, JX009719, JX009870 and KC790728). Multilocus phylogenetic analysis performed with reference sequences showed that the isolate FC1 clustered with C. tropicale in accordance with BLAST results. A conidial suspension (1 × 106 conidia/mL) prepared from FC1 isolate was inoculated by spraying onto detached, ripe, healthy, non-wounded and surface-disinfected common fig fruit (cv. China, n = 4). Fruit sprayed with sterile water were used as control. Fruit were kept in a moist chamber (greater than 90% relative humidity, 24 to 28°C) for 24 h and then maintained in the lab for additional 5 days. The inoculated fruit developed lesions similar to the disease symptoms in the orchard. No symptom was observed on fruit treated with water. C. tropicale was re-isolated from symptomatic fruits and had similar morphological characteristics to FC1 isolate, thus fulfilling Koch’s postulates. The experiment was repeated once showing similar results. The FC1 isolate of C. tropicale with the identification number BCRC FU31436 has been deposited at Taiwan Bioresource Collection and Research Center. This fungus had previously been found on lotus and mango in Taiwan (Chen and Kirschner 2018; Wu et al. 2020), while the pathogenicity among the isolates from different origins is not yet known. To our knowledge, this is the first report of C. tropicale causing anthracnose on common fig fruit in Taiwan.


2006 ◽  
Vol 7 (1) ◽  
pp. 21
Author(s):  
Carol M. Stiles ◽  
Patricia A. Rayside

Urediniospores were collected separately from rust pustules on oregano (Origanum vulgare) and spearmint (Mentha spicata) plants purchased from retail stores in Gainesville, Alachua Co., FL, in April 2004 and March 2005. Morphological characteristics of the urediniospores from both hosts were consistent with descriptions of Puccinia menthae. Spearmint, peppermint (M. × piperita), oregano (O. vulgare), sweet marjoram (O. majorana), and Greek oregano (Oregano heracleoticum) were inoculated with urediniospore suspensions of each rust isolate in a series of cross-inoculation experiments. Rust developed on oregano, sweet marjoram, and Greek oregano only when inoculated with urediniospores from the oregano plant, and this rust isolate did not infect any of the Mentha spp. tested. Rust developed on spearmint when inoculated with urediniospores from the mint plant, but this isolate did not infect peppermint, oregano, sweet marjoram, or Greek oregano. The two isolates of Puccinia menthae appear to represent different populations, “spearmint rust” and “oregano rust.” This is the first report of P. menthae on oregano in Florida. Accepted for publication 2 March 2006. Published 17 April 2006.


Plant Disease ◽  
2018 ◽  
Vol 102 (10) ◽  
pp. 2030-2030 ◽  
Author(s):  
T. Liu ◽  
D. Chen ◽  
Z. Liu ◽  
J. M. Hou

Plant Disease ◽  
2021 ◽  
Author(s):  
Jackeline Laurentino da Silva ◽  
Walisson Ferreira da Silva da Silva ◽  
Luiz Eduardo Monteiro Lopes ◽  
Maria Jussara dos Santos Silva ◽  
Janaíne Rossane Araújo Silva-Cabral ◽  
...  

Brazil is the world's largest producer and consumer of yellow passion fruit (Passiflora edulis f. flavicarpa), mainly for the manufacture of concentrate and frozen juice as well as for fresh consumption (Faleiro et al. 2005). Between June and July 2018, passion fruit plants with symptoms of anthracnose were observed in commercial planting in the municipality of Coruripe (20 ha), northeastern state of Alagoas, Brazil. Approximately 70% of the plants showed leaves with relatively large, watery, circular spots that affected 30% of the leaf surface. Small fragments taken from the transition region of symptomatic tissue were superficially disinfected in 70% ethanol for 30 s and in 1% NaClO for 1 min, rinsed in sterile distilled water (SDW), dried on filter paper, plated on potato dextrose agar (PDA-Kasvi) incubated at 25°C under white light and 12 h photoperiod, for 3 days. Two isolates were obtained and deposited in the Collection of Phytopathogens at the Universidade Federal de Alagoas (COUFAL0281 and COUFAL0282). To identify the isolates, partial sequences of the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and β-tubulin (TUB2) genes and of the rDNA-ITS (ITS) region were amplified by PCR. The partial sequences were deposited at GenBank (MT299339, MT334694, MT310553, MT299340, MT334695 and MT310554). Based on the BLASTn analysis, sequences of the PCR products showed high nucleotide similarity with sequences of the species C. tropicale (CBS 124949/ex-type and ICMP 18672), for GAPDH (98.94% and 100%), TUB2 (99 and 100%) genes and ITS (100%). This result was also confirmed in the phylogenetic tree of Bayesian Inference assembled with concatenated data (GAPDH, TUB2 and ITS). The colonies of the isolates were white with a white reverse, with dense mycelium, and mean growth rate of 7.54 mm/day, after 7 days on PDA medium at 25° C. Conidia were subcylindrical with rounded ends, hyaline, smooth walls and measured 13.63-20.59μm (= 17.54μm; n= 50) in length and 4.40-7.93 μm (= 5.88 μm; n= 50) in width. Appressoria were melanized, subglobose, irregular and measured 7.44 - 18.57 μm (= 10.04 μm; n= 50) in length and 5.49-10.16 μm (= 7.66 μm; n= 50) in width. These morphological characteristics were consistent with those described for Colletotrichum tropicale E.I. Rojas, S.A. Rehner & Samuels (Rojas et al. 2010). To confirm pathogenicity, 30 µL of a 106 conidia/mL sterile distilled water (SDW) conidia suspension, together with a drop of 20% Tween were deposited on the adaxial surface of passion fruit leaves wounded with a sterile needle, with four repetitions. The control consisted of leaves inoculated only with SDW. The leaves were placed in a plastic Gerbox box with sterilized filter paper moistened with SDW and maintained in a Biochemistry Oxygen Demand (BOD) incubator stove at 25 ºC and photoperiod of 12 h. After 7 days, typical anthracnose symptoms were observed on inoculated leaves. The pathogen was re-isolated and confirmed by morphological characterization, according to Koch's postulates. No symptoms were observed in the negative control. The occurrence of this species has been frequently reported in several other crops grown in northeastern Brazil (Silva et al. 2017; Veloso et al. 2018; Vieira et al. 2018; Costa et al. 2019). Additionally, many of these crops are grown in close proximity to the passion fruit orchards, thus favoring pathogen movement between hosts, probably, due to the anthropic influence, circulation of animals and insects, as well as wind driven rain splashes. However, this is first report of C. tropicale in Passiflora edulis in the world.


2019 ◽  
Vol 86 (1) ◽  
pp. 65-69
Author(s):  
Satoshi Taba ◽  
Kento Fukuchi ◽  
Yuta Tamashiro ◽  
Yasuhiro Tomitaka ◽  
Ken-taro Sekine ◽  
...  

Plant Disease ◽  
2019 ◽  
Vol 103 (3) ◽  
pp. 583-583 ◽  
Author(s):  
J. R. A. Silva-Cabral ◽  
L. R. L. Batista ◽  
J. F. de O. Costa ◽  
M. M. de M. Ferro ◽  
S. J. C. Silva ◽  
...  

Plant Disease ◽  
2014 ◽  
Vol 98 (3) ◽  
pp. 421-421 ◽  
Author(s):  
T. Wang ◽  
W. Zhao ◽  
R.-D. Qi

Celery (Apium graveolens) is an important vegetable in China. In August 2012, about 20 to 70% declining plants with root and basal stem rot were observed in Bengbu, Anhui Province, China. Typical symptoms included large dark brown to black water-soaked lesions near the soil line of stems. As the disease progressed, lesions girdled the stem, and plants became brown, wilted, and eventually died. A Phytophthora-like organism was consistently isolated from symptomatic tissues on a selective medium, P5ARP. Resultant isolates were identified as Phytophthora tentaculata based on their morphological features and rDNA sequence. Sporangia, chlamydospores, hyphal swellings, and oospores were produced on V8 agar. Sporangia were ovoid to pyriform, 28.5 to 52.5 × 21.5 to 40.6 μm, average 35.3 × 29.8 μm, with one or occasionally two papillae. Chlamydospores were spherical, 21.3 to 30.2 μm in diameter, average 25.7 μm. The isolates were homothallic, and one or occasionally two paragynous antheridia were attached to the global oogonia (24 to 39 μm in diameter, average 29.5 μm). The internal transcribed spacer region of rDNA was amplified with primer pair ITS1/ITS4 for one isolate (1), and the sequence (GenBank Accession No. KF501392) showed >99% similarity with those P. tentaculata isolates deposited in GenBank (AJ854302.1). Pathogenicity was confirmed by inoculating Shijihuangqin, a local cultivar of celery, with isolate PT12081. The isolate was cultivated on V8 agar at 25°C for 5 to 7 days to produce sporangia. Five 2-month-old, disease-free celery were drench-inoculated with 10 ml of a suspension of 2 × 104 zoospores/ml, and five control plants per pot were treated with sterile water. There were four pots for each of the inoculated and non-inoculated treatments, and the experiment was repeated twice. All plants were maintained at 25°C for 10 days. Symptoms similar to those observed in the field developed 7 days after inoculation. Ten days later, five plants wilted and two or three died in each pot inoculated with PT12081, but the control plants remained symptomless. P. tentaculata was consistently re-isolated from the symptomatic plants. P. tentaculata has been reported to infect Chrysanthemum spp., Delphinium ajacis, Verbena spp., and Origanum vulgare (2,3). To our knowledge, this is the first report of Phytophthora blight caused by P. tentaculata on celery in China. References: (1) H. Guo et al. Plant Dis. 96:1072, 2012. (2) P. Martini et al. Plant Dis. 93:843, 2009. (3) J. Meng and Y. C. Wang. Plant Dis. 92:1365, 2008.


Sign in / Sign up

Export Citation Format

Share Document