scholarly journals Occurrence of Fusarium Wilt Caused by Fusarium oxysporum on Common Sage in Argentina

Plant Disease ◽  
2006 ◽  
Vol 90 (6) ◽  
pp. 833-833
Author(s):  
S. A. Gaetán ◽  
M. Madia

Common sage (Salvia officinalis L.) is being increasingly grown commercially in Argentina for its medicinal properties and as ornamental plants. Although the crop can be produced in greenhouses, most of the crop production is in open fields in Buenos Aires, Córdoba, and Santa Fe provinces. During the last 3 years, common sage has repeatedly shown decline symptoms in several production fields in the southern region of Buenos Aires Province. In the spring of 2004, a serious common sage wilt disease developed under field conditions resulting in as much as 15% loss of plants. The disease, affecting 10-month-old common sage plants, was observed in this region in two commercial fields located at Sierra de la Ventana. Affected plants appeared in irregular patches throughout the rows. Diseased plants exhibited symptoms of chlorosis, wilting, and death. Lower leaves on wilted plants showed gradual yellowing, apical necrosis, and premature defoliation. At advanced stages of the disease, irregular, brown, necrotic areas on the leaves occurred. The necroses on affected leaf parts occasionally expanded and coalesced to form large necrotic lesions that turned the entire leaf brown. Other symptoms included stunting, black streaking on stems, and rotting of roots. Longitudinal sections through stems and roots showed severely necrotic vascular tissue. Pieces taken from stems and roots of diseased plants were plated on potato dextrose agar after surface sterilization with 1% NaOCl for 3 min. The plates were incubated in the dark for 2 days and then kept under 12-h alternations of NUV light/dark for 8 days. On the basis of morphological and cultural characteristics, two fungal colonies were identified as Fusarium oxysporum Schlechtend.:Fr. (1) and used in the following studies. Pathogenicity tests were carried out on 4-month-old healthy common sage plants. Koch's postulates were completed for two isolates by dipping the roots of seedlings in a conidial suspension (2 × 105 conidia/ml) of a single-spore isolate for 25 min. Plants were repotted in a sterilized soil mix (soil/sand, 2:1). The experiment was conducted in a greenhouse at 23 to 25°C and 75% relative humidity with no supplemental light. Within 14 days, all inoculated plants showed typical Fusarium wilt symptoms similar to that observed in the field. Plants exhibited yellowing followed by wilting of foliage, rotting of roots, brown vascular discoloration, and then eventually collapsed. Four weeks postinoculation, 90% of the plants were dead. No symptoms were observed on control plants dipped only in distilled water. The fungus was successfully reisolated from the symptomatic plants, fulfilling Koch's postulates in all instances. F. oxysporum had been previously reported in 1995 to cause a wilt disease in clary sage (Salvia sclarea L.) fields in North Carolina; the disease was detected at seedling stage, reducing plant stand as much as 40 to 50% (2). In Argentina, the pathogen that caused wilt symptoms on common sage had also been observed in 2002 in greenhouses on the outskirts of Buenos Aires, although the disease incidence was low. At this time, the disease could become a limiting factor in common sage production and further information regarding this pathogen within the region is needed. To our knowledge, this is the first report of the occurrence of Fusarium wilt caused by F. oxysporum on commercial S. officinalis in open fields in Argentina. References: (1) P. E. Nelson et al. Fusarium species. An Illustrated Manual for Identification. Pennsylvania State University Press. University Park, PA, 1983. (2) V. P. Subbiah et al. Plant Dis. 80:1080, 1996.

2018 ◽  
Vol 42 (4) ◽  
pp. 599-607
Author(s):  
L Yasmin ◽  
MA Ali ◽  
FN Khan

The efficacy of fungicides in controlling Fusarium wilt of gladiolus was studied at Horticulture Research Centre (HRC), Bangladesh Agricultural Research Institute (BARI), Gazipur during 2010-2012 following RCB design with four replications. Six fungicides such as Bavistin (0.1%), Provax (0.2%), Mancozeb (0.2%), Rovral (0.2%), Chlorax (10%) and Cupravit (0.7%) were evaluated against the Fusarium wilt disease of gladiolus (Fusarium oxysporum f. sp. gladioli) under naturally infested field condition. Bavistin was very effective in reducing the disease incidence and thereby resulting maximum corm germination (99.98%), spike length (73.90 cm), rachis length (43.70 cm), florets spike-1 (12.63), flower sticks plot-1 (38.75) and corm plot-1 (60.23) and cormel yield ha-1 (2.51 t) of gladiolus. Provax and Cupravit were also effective in inhibiting the disease incidence as well as better spike length, rachis length, florets spike-1, no of flower sticks, corm and cormel yield.Bangladesh J. Agril. Res. 42(4): 599-607, December 2017


Plant Disease ◽  
2021 ◽  
Author(s):  
Muhammad Ziaur Rahman ◽  
Khairulmazmi Ahmad ◽  
Yasmeen Siddiqui ◽  
Norsazilawati Saad ◽  
Tan Geok Hun ◽  
...  

Fusarium wilt disease incited by Fusarium oxysporum f. sp. niveum (FON) is the utmost devastating soil-inhabiting fungal pathogen limiting watermelon (Citrullus lanatus) production in Malaysia and globally. The field disease survey of fusarium wilt was carried out during December 2019 and November 2020, in three major production areas (3 farmer fields per location) in Peninsular Malaysia namely, Mersing, Serdang and Kuantan and disease incidence of 30 and 45%, was recorded for each year, respectively. Infected watermelon plants showed symptoms such as vascular discoloration, brown necrotic lesions to the soil line or the crown, one-sided wilt of a plant, or a runner or the whole plant. Infected root and stem tissues, 1-2 cm pieces were surface sterilized with 0.6% NaOCl for 1 minute followed by double washing with sterile water. The disinfected tissues were air-dried and transferred onto semi-selective Komada’s medium (Komada 1975) and incubated for 5 days. The fungal colonies produced were placed on potato dextrose agar (PDA) to attain a pure culture and incubated at 25±2℃ for 15 days. The pure fungal colony was flat, round and light purple in color. Macroconidia were straight to slightly curved, 18.56-42.22 µm in length, 2.69-4.08 µm width, predominantly 3 septate and formed in sporodochia. Microconidia measured 6.16-10.86 µm in length and 2.49-3.83 µm in width, kidney-shaped, aseptate and were formed on short monophialides in false-heads. Chlamydospores were single or in pairs with smooth or rough walls, found both terminally or intercalary. To confirm their pathogenicity, two-week-old watermelon seedlings (cv. NEW BEAUTY) were dipped into spore suspension (1 ˟ 106 spores/ml) of representative isolates of JO20 (Mersing), UPM4 (Serdang) and KU41 (Kuantan) for 30 second and then moved into 10 cm diameter plastic pots containing 300 g sterilized soil mix. Disease symptoms were assessed weekly for one month. Control seedlings were immersed in sterile distilled water before transplanting. The inoculated seedlings showed typical Fusarium wilt symptoms like yellowing, stunted growth, and wilting, which is similar to the farmer field infected plants. However, the seedlings inoculated by sterile distilled water remained asymptomatic. The pathogen was successfully re-isolated from the infected seedlings onto Komada’s medium, fulfilling the Koch’s postulate. For the PCR amplification, primers EF-1 and EF-2 were used to amplify the tef1-α region. A Blastn analysis of the tef1-α sequences of the isolates JO20 (accession nos. MW315902), UPM4 (MW839560) and KU41 (MW839562) showed 100% similarity; with e-value of zero, to the reference sequences of F. oxysporum isolate FJAT-31690 (MN507110) and F. oxysporum f. sp. niveum isolate FON2 790-2 (MN057702). In Fusarium MLST database, isolates JO20, UPM4 and KU41 revealed 100% identity with the reference isolate of NRRL 22518 (accession no. FJ985265). Though isolate FJ985265 belongs to the f. sp. melonis, earlier findings had revealed Fusarium oxysporum f. sp. are naturally polyphyletic and making clusters with diverse groups of the Fusarium oxysporum species complex (O’Donnell et al. 2015). The isolates JO20, UPM4 and KU41 were identified as F. oxysporum f. sp. niveum based on the aligned sequences of tef1-α and molecular phylogenetic exploration by the maximum likelihood method. To the best of our knowledge, this is the first report of F. oxysporum f. sp. niveum as a causative pathogen of Fusarium wilt disease of watermelon in Malaysia. Malaysia enables to export watermelon all-year-round in different countries like Singapore, Hong-Kong, The United Arab Emirates (UAE), and Netherlands. The outburst of this destructive soil-borne fungal pathogen could cause hindrance to watermelon cultivation in Malaysia. Thus, growers need to choice multiple management tactics such as resistant varieties, cultural practices (soil amendments and solarization), grafting, cover crops and fungicide application to control this new pathogen.


2020 ◽  
Vol 31 (3) ◽  
pp. 29-45
Author(s):  
Hazirah Mohd Din ◽  
Osamah Rashed ◽  
Khairulmazmi Ahmad

Fusarium wilt disease is one of the most problematic and destructive disease in cucumber production. The causative agents are Fusarium oxysporum and F. solani. These pathogens are soil borne and transmitted through infested soil and water. A field survey was conducted to study the disease prevalence in the major growing areas of cucumber in Peninsular Malaysia. Field study revealed that the disease was highly prevalence in the field with the disease incidence was in the range of 10%–60%. The morphological properties of F. oxysporum are microconidia (3.8–15.7 μm × 2.9–4.9 μm), macroconidia (14.8–38.5 μm × 2.4–5.7 μm) and number of septate was 1–4. While for F. solani are microconidia (3.39–14.63 μm × 2.36–4.44 μm), macroconidia (7.22–50.46 μm × 2.43–6.14 μm) and number of septate was 1–5. Based on molecular identification had confirmed that the disease is caused by F. oxysporum and F. solani with similarity index of 99%–100% based on internal transcribed spacer (ITS) gene sequences. The pathogenicity test showed that the symptoms of Fusarium wilt disease was firstly appeared as yellowing of old leaves. Progressively, the infected plant will be wilted and finally died. The outputs of this study are highly important to establish an effective disease management programme to reduce disease prevalence and yield loss in the field.


2020 ◽  
Vol 21 (supplemenet 1) ◽  
Author(s):  
K. Vignesh ◽  
K. Rajamohan ◽  
P. Balabaskar ◽  
R. Anandan ◽  
R. Udhayakumar

Tomato is one of the most important, commercial and widely grown vegetable crop in the world. It is affected by several fungal, bacterial and viral diseases. Among these Fusarium wilt caused by the fungus Fusarium oxysporum f.sp. lycopersici causes 30-40% yield loss. A survey was conducted to investigate the incidence and severity of Fusarium wilt incited by Fusarium oxysporum f.sp. lycopersici in ten major tomato growing areas of Krishnagiri district. The occurrence of wilt disease incidence ranged from 18 % to 49% was noticed. Plant showing typical symptoms were taken from 10 fields and identified based on symptom appearance as well as morphological characteristics. The result of the survey revealed that wide range of infection and severity of wilt disease were occurred in the major tomato growing areas in Krishnagiri district. Isolation of the pathogen associated with tomato wilt was made from the diseased tissues in roots and collar region of the plant on the Potato dextrose agar (PDA) medium. Fol3 recorded the maximum wilt incidence followed by Fol4 and the minimum wilt incidence was recorded by Fol6 . The pathogenicity of the fungal pathogen was also proved after artificial inoculation of the tomato seedlings


Plant Disease ◽  
2005 ◽  
Vol 89 (4) ◽  
pp. 432-432 ◽  
Author(s):  
S. A. Gaetán

Canola (Brassica napus) is a developing oleaginous crop grown commercially in Argentina, primarily in the southeastern region of Buenos Aires Province. Since 2002, plants exhibiting symptoms of wilt and xylem discoloration were observed in canola plants in experimental field plots located at the University of Buenos Aires, Buenos Aires, Argentina. Average disease incidence in 5- to 6-month-old canola cultivars developed in different countries was 18% (range = 9 to 27%). Disease symptoms that included yellowing, wilting, stunting, and necrosis of leaf tissue and suppressed root development appeared in irregular-shaped patches following the rows of plants. The first symptom observed was leaf yellowing followed by an irregular, brown necrosis of the leaf margins. Lesions coalesced to form large necrotic areas that led to severe defoliation beginning with the lower leaves. As the disease developed, a pale brown discoloration girdled the stems that progressed from the basal tissues to the apex. Affected plants were stunted and had small pods with no seeds. Diseased plants eventually collapsed and died. From June to July 2003, six samples consisting of five affected plants per sample were randomly collected from experimental field plots. Pieces (1 cm long) of disease basal stem tissue were thoroughly washed, surface sterilized in 1% sodium hypochlorite for 1 min, rinsed in sterile distilled water, blotted dry on sterile Whatman's filter paper, and incubated on potato dextrose agar in the dark at 26°C for 10 days. Ten resulting colonies were examined microscopically and identified as Fusarium oxysporum Schlechtend.:Fr. f. sp. conglutinans (Wollenweb.) W.C. Snyder & H.N.Hans. (3). Pathogenicity tests for three single-spore isolates of the fungus were performed on 6-week-old canola plants of cvs. Impulse, Master, Mistral, Monty, Rivette, and Trooper. Koch's postulates were completed for each isolate by dipping the roots of seedlings in a conidial suspension (2 times; 105 conidia per ml) for 15 min. Plants were repotted in a sterilized soil mix (soil/sand, 2:1). The experiment, which included five inoculated plants and three noninoculated (roots dipped in sterile distilled water) control plants for each cultivar, was conducted in a greenhouse at 23 to 25°C and 75% relative humidity with no supplemental light. Characteristic symptoms, identical to the original observations, developed within 14 days after inoculation on 100% of the inoculated plants for all three isolates. The pathogen was successfully reisolated from internal diseased stem tissue in all instances. Symptoms included stunted seedlings, leaf necrosis, and external stem discoloration. None of the control plants developed disease. The experiment was repeated once with similar results. F. oxysporum f. sp. conglutinans, which has been reported to cause disease in canola in Canada (1) and the United States (2), represents a serious threat to the main canola cultivars grown in Argentina. To our knowledge, this is the first report of canola wilt incited by F. oxysporum f. sp. conglutinans in Argentina. References: (1) D. Bernard et al. Can. Plant Dis. Surv. 81:102, 2001. (2) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society, St. Paul, MN, 1989. (3) P. E. Nelson et al. Fusarium species. An Illustrated Manual for Identification. Pennsylvania State University Press. University Park, PA, 1983.


Plant Disease ◽  
2000 ◽  
Vol 84 (1) ◽  
pp. 100-100 ◽  
Author(s):  
M. C. Rivera ◽  
E. R. Wright

The most important azalea (Rhododendron spp.) growing area in Argentina is located in the outskirts of Buenos Aires. A disease of the azalea flower was detected during surveys conducted during September 1998. Irregular brown spots were uniformly distributed on petals and resulted in a flower blight that did not lead to abscission of petals. Pieces of infected petals were surface-sterilized for 1 min in 2% NaOCl, plated on potato dextrose agar, and incubated at 24 ± 2°C. Pure cultures were identified as Pestalotiopsis guepini (Desmaz.) Steyaert (synamorph P. guepini Desmaz.) based on morphological characteristics (1,2). Inoculation for pathogenicity testing was carried out by spraying a conidial suspension (1 × 106 conidia per ml) on plants with previously punctured petals. Inoculated plants with unwounded flowers, as well as noninoculated controls, were included. Plants were incubated in moist chambers at 24°C. Symptoms appeared on all punctured flowers within 4 to 5 days. Petals were blighted by 9 days after inoculation and were covered with black acervuli by 12 days after inoculation. Unwounded and noninoculated controls remained symptomless. The pathogen was reisolated from inoculated flowers, completing Koch's postulates. Pathogenicity of P. guepini on azalea leaves in Argentina was reported in 1991. This is the first report of P. guepini causing disease on azalea flowers in Argentina. References: (1) J. E. M. Mordue. CMI Descr. Pathog. Fungi Bact. No. 320, 1971. (2) B. C. Sutton. 1980. The Coelomycetes. Commonwealth Mycological Institute, Kew, England.


2018 ◽  
Vol 2018 ◽  
pp. 1-7
Author(s):  
Yigrem Mengist ◽  
Samuel Sahile ◽  
Assefa Sintayehu ◽  
Sanjay Singh

A 2-year experiment was conducted at wilt sick plot infested with natural occurring Fusarium oxysporum f.sp. ciceris at Adet Agricultural Research Center in northwestern Ethiopia with an aim to evaluate effective chickpea varieties and fungicides for the management of chickpea fusarium wilt in order to integrate chickpea varieties and fungicides. Four varieties, namely, Shasho, Arerti, Marye, and local, two fungicides, namely, Apron Star and mancozeb, and untreated local chickpea were used as treatments. Treatments were arranged in a factorial combination in randomized complete block design in three replications. There were significant differences at p<0.05 in the overall mean of fusarium wilt disease incidence, area under disease progress curve %-day, yield and yield components among varieties and fungicides treatments. Data were analyzed using SAS system version 9.2. The results indicated that the maximum disease incidence and area under disease progress curve values 65.62% and 578.5%-day, respectively, were recorded from untreated local chickpea, while the minimum disease incidence and area under disease progress curve values 23.41% and 147%-day, respectively, were recorded from Shasho variety treated with Apron Star. The maximum biomass and grain yield of 6.71 t/ha and 4.6 t/ha, respectively, were recorded from Shasho variety treated with Apron Star while the minimum biomass and grain yield of 0.62 t/ha and 0.21 t/ha, respectively, were recorded from untreated local chickpea. Thus, the experiment results suggested that the variety of Shasho treated with fungicide Apron Star caused significant reduction in chickpea fusarium wilt incidence leading to a corresponding increase in grain yield of chickpea.


Plant Disease ◽  
2014 ◽  
Vol 98 (11) ◽  
pp. 1587-1587 ◽  
Author(s):  
R. J. Zhou ◽  
Y. Yuan ◽  
H. J. Xu ◽  
J. F. Fu ◽  
Y. H. Ou

Common mallow (Malva sylvestris L.) is a perennial medicinal plant in the Malvaceae family, which is native to Asia, Europe, and North Africa. In July 2012, typical symptoms of anthracnose disease, with a disease incidence of ~70%, were observed on common mallow in the Medicinal Herb Garden of Shenyang Pharmaceutical University, Liaoning, China. The fungus mainly infected the stalks and leaves of M. sylvestris. Pinpoint, brownish lesions initially appeared at the flowering stage and the disease spread within the field. The lesions on stems gradually enlarged and became dark brown, elliptical, and slightly concave. Concurrently, acervuli and mucilaginous conidial masses of the pathogen appeared on lesions under moist conditions. Conidia were hyaline, one-celled, cylindrical with both ends rounded, and measured 10.0 to 12.5 × 2.5 to 4.0 μm (mean 11.3 × 3.3 μm). The fungus was isolated from symptomatic tissues. Small pieces from leaves and stems were surface disinfested with 70% ethanol and 1.5% sodium hypochlorite for 1 min, then rinsed three times with sterile distilled water, and cultured on potato dextrose agar (PDA) at 25°C. The colonies on PDA had initially white aerial mycelia, and later became greenish black with regularly whorled rings. To confirm Koch's postulates, five 3-month-old plants of M. sylvestris were inoculated with a conidial suspension (105 conidia/ml) prepared from PDA cultures incubated for 14 days. Five non-inoculated plants served as controls. The plants were maintained in the greenhouse at 22 to 25°C and about 75% relative humidity under natural daylight. Typical symptoms on inoculated plants were reproduced after ~10 to 14 days, whereas control plants remained asymptomatic. The pathogen was successfully recovered from symptomatic tissues and re-identified, completing Koch's postulates. The internal transcribed spacer (ITS) and large subunit -28S (LSU) region of rDNA was amplified with primers ITS1/ITS4 and NL1/NL4, respectively, and sequenced. Phylogenetic trees (ITS and LSU) that were obtained using MEGE3.1 with the neighbor-joining method showed that both of the isolates fall in the Colletotrichum trifolii clade. The representative sequences (ITS and LSU) were deposited in GenBank (Accession Nos. KJ155692 and KJ920935). The fungus isolated from symptomatic tissues was identified as C. trifolii on the basis of morphological, cultural characteristics, and sequence analysis (2). According to previous references, C. orbiculare and C. malvarum on Malvaceae were respectively described in America and Europe (1,3,4). However, the isolate from M. sylvestris significantly differed from those of C. orbiculare and C. malvarum in cultural characteristics and sequence analysis. In this paper, the results showed that M. sylvestris is a new host of C. trifolii. To our knowledge, this is the first report of mallow anthracnose caused by C. trifolii in China. References: (1) J. A. Bailey et al. Phytopathology 86:1076, 1996. (2) U. Damm et al. Fungal Divers. 61:29, 2013. (3) K. Hyde et al. Fungal Divers. 39:147, 2009. (4) L. Tosi et al. Plant Dis. 88:425, 2004.


Plant Disease ◽  
2005 ◽  
Vol 89 (4) ◽  
pp. 435-435 ◽  
Author(s):  
S. A. Gaetán

Canola (Brassica napus) was introduced as an alternative crop to wheat in Argentina. During 2004, typical symptoms of foliar blackleg disease were observed on canola plants in commercial and experimental fields in southern Buenos Aires Province. Average disease incidence was 32% on 2- to 4-month-old plants of canola cvs. Impulse, Master, Mistral, and Teddy. The range of incidence on these cultivars was 21 to 43%. Foliar symptoms were randomly distributed at seedling, rosette, and flowering stages. Symptoms included necrosis and chlorosis of the affected leaf tissue and defoliation. Foliar leaf spots were circular to irregularly oval, 5 to 12 mm in diameter, pale brown in the center, and grayish green at the margin. Small, black pycnidia formed in the center of the adaxial surface of diseased foliage. Under favorable temperature and moisture conditions, lesions enlarged and coalesced. Older lesions appeared chlorotic and desiccated with shredded tissue at the center. A severe defoliation of the lower leaves was observed. As the disease developed, basal stem cankers formed on these plants, although disease incidence in this phase was low. Pieces (0.5 cm long) were taken from leaves and stems of diseased plants, dipped in 70% ethanol, surface sterilized with NaOCl (1%) for 2 min, and rinsed in sterile water. Each segment was blotted dry and placed on potato dextrose agar (PDA). Plates were incubated in the dark at 26°C for 4 days, and then plates were incubated under 12 h of NUV light and 12-h dark for 7 days. Four fungal isolates were obtained. The fungi were examined microscopically and confirmed as Phoma lingam (Tode:Fr.) Desmaz. (Leptosphaeria maculans (Desmaz.) Ces. & De Not) (3,4). P. lingam was the only fungus isolated from the infected tissue. The teleomorph stage was not observed. Koch's postulates were completed for two isolates by spray-inoculating foliage of 3-week-old canola plants of cvs. Impulse, Master, Mistral, and Teddy with a conidial suspension (1 × 106 conidia per ml). The experiment, which included four inoculated plants per isolate and two noninoculated control plants for each cultivar, was performed in a greenhouse at 22 to 24°C and maintained at 75% relative humidity with no supplemental light. Inoculated and control plants were covered with polyethylene bags for 48 h after inoculation. Plants developed small, pale brown lesions on leaves within 11 days for both isolates, and the pathogen was reisolated. Control plants, inoculated only with sterile distilled water, remained symptomless. The experiment was repeated once with similar results. Blackleg is the most important fungal disease affecting canola with a worldwide distribution (1,2). In 1995, the disease was first observed on canola in Argentina in northern Buenos Aires Province, but only in experimental field plots with a low disease incidence. Since that time, it has not been found in other areas where canola is produced. The results emphasize the importance of this pathogen in Argentina, since at the current time most commercial cultivars were susceptible to P. lingam. To our knowledge, this is the first report of an outbreak of P. lingam infection in commercial crops in the main canola-production region in Argentina. References: (1) H. A. Lamey and D. E. Hershman, Plant Dis. 77:1263, 1993. (2) G. A. Petri. Can. Plant Dis. Surv. 65:43, 1985. (3) E. Punithalingham and P. Holliday. No. 331 in: Descriptions of Pathogenic Fungi and Bacteria. CMI Kew, Surrey, UK, 1972. (4) B. C. Sutton. Fungi imperfecti with pycnidia, acervuli and stromata. Pages 386–388 in: The Coelomycetes. CMI, Kew, Surrey, England, 1980.


Plant Disease ◽  
2021 ◽  
Author(s):  
Li Cheng

Konjac (Amorphophallus konjac) is an economically important traditional crop in Fengqing County, Yunnan Province, China. Anthracnose symptoms were observed on this crop in June and July of 2020. The plants developed round, oval, or irregular leaf spots with brown edges and central taupe spots, and exhibited serious defoliation and tree weakness. Disease incidence in affected fields reached up to 35%. Anthracnose caused significant economic losses in konjac production and became a limiting factor of the konjac industry in Fengqing County. To date, no control measures of konjac anthracnose have been reported and tested in China. To determine the causal pathogen, symptomatic leaves were collected and cut into 5 mm2 pieces. The leaf peces were surface sterilized in 70% ethanol for 10 s, followed by treatment with 0.1% mercuric chloride for 3 min and three rinses in sterile distilled water. The tissue pieces were transferred onto potato dextrose agar (PDA) and incubated at 28°C. After 4 days of incubation, hyphal tips from leaf pieces were transferred to new PDA to generate pure cultures. The hyphae were initially white, and then became dark green; red-orange conidial masses were observed on the mycelium plate surface at a growth rate of 13.14 mm/day. The conidia, observed under 400× magnification, were colorless, long-oval to fusiform, one-celled, and 15.4 to 18.2 × 3.3 to 5.9 μm in size. To identify the isolate, the genomic DNA of the pathogen was extracted using the CTAB method. The internal transcribed spacer (ITS) region, glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene, and β-tubulin (TUB) gene were PCR amplified using the ITS1/ITS4, GDF/GDR, and Bt2a/Bt2b primer pairs, respectively (Lee et al. 2020). BLASTn search of the obtained 536 bp ITS fragment (GenBank accession no. MT785772), 229 bp GAPDH sequence (MW187543), and 717 bp TUB sequence (MW187544) revealed a 99.44% to 99.63% sequence homology (100% query cover) with ITS (JQ005152, 99.44%), GADPH (JQ005239, 99.63%), and TUB (JQ005587, 99.60%) sequences of the C. gloeosporioides type strain CBS 112999, respectively. The highest homology with other Colletotrichum species was only 98.16%, including C. siamense, the causal agent of anthracnose in A. paeoniifolius and A. konjac (Prasad et al. 2017; Wu et al. 2020). To complete Koch’s postulates, leaves of 3-month-old konjac plants grown in the field were sprayed with a conidial suspension (106 spores/ml) of the isolate YNFQ-1 (sterile water was used as a negative control). Approximately 5 days after inoculation with YNFQ-1, symptoms similar to those in natural conditions appeared, whereas the negative control plants and fruits inoculated with the sterile water had no disease. The pathogen was re-isolated (strain YNFQ-1) from inoculated leaf tissues, and its identity was confirmed with both morphological and molecular (DNA sequences) tools, thus fulfilling Koch's postulates. The culture properties, morphological characteristics, and molecular identification confirmed the identity of the pathogen as C. gloeosporioides. There have been many reports about anthracnose of Amorphophallus; C. siamense causes anthracnose on A. paeoniifolius in India (Prasad et al. 2017) and A. konjac in Hubei, China (Wu et al. 2020), and C. gloeosporioides causes anthracnose of A. muelleri in Yunnan, China (Yang et al. 2020). To the best of our knowledge, this is the first report of C. gloeosporioides causing anthracnose on A. konjac in Fengqing County, China. The results are expected to have important implications in the diagnosis, control, and future research of anthracnose on A. konjac.


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