scholarly journals First Report of Fusarium Blight on Majesty Palm Caused by Fusarium proliferatum in Italy

Plant Disease ◽  
2003 ◽  
Vol 87 (9) ◽  
pp. 1149-1149 ◽  
Author(s):  
G. Polizzi ◽  
A. Vitale
Keyword(s):  
Fusarium Proliferatum ◽  
Conidial Suspension ◽  
First Report ◽  
Leaf Spots ◽  
Initial Symptoms ◽  
Mt Etna ◽  
Young Leaves ◽  
Pure Cultures ◽  
Severe Infections ◽  
Fusarium Sp

During spring 2002, a new disease of majesty palm (Ravenea rivularis Jumelle & H. Perrier) was observed on young, container-grown plants (3 to 4 years old with five to seven expanded leaves) in a nursery in eastern Sicily. Initial symptoms on the youngest, expanded leaves and especially on the unopened, spear leaves were small, reddish-brown necrotic lesions (2 to 4 mm in diameter) with a yellow halo. In high humidity, lesions increased in size and number, coalescing into large, irregular dead areas. These symptoms developed into blights of the youngest, unopened leaves. As a consequence, infected leaves would dieback and only a few plants recovered from these severe infections. On the surviving plants, reddish-brown necrotic lesions appeared on the rachis. From these lesions, 30 pieces of tissue were cut, surface sterilized (30 s in 1.2% wt/vol of NaOCl), washed with sterile water, and plated on potato dextrose agar supplemented with 1.1 μl/ml of lactic acid (stock 88 to 92%) (A-PDA). Conidia and conidiophores were collected directly from the tissue with a flamed needle and placed on A-PDA. Fusarium sp. was consistently isolated from the necrotic tissue, and after 3 days, single hyphal tips were transferred to pure cultures from which were obtained two single, conidial isolates. These fungal isolates were forwarded to the CABI Bioscience U.K. Centre, Bakeham Lane (Egham), Surrey, U.K., where both isolates were identified as Fusarium proliferatum (T. Matsushima) Nirenberg. A morpho-biometrical characterization was performed on carnation leaf agar with a photoperiod of 10 h. Macroconidia were slender, lightly falcate to almost straight, 3- to 5-septate, and ranged from 37 to 53 × 2.5 to 3 μm (average 44.1 × 2.8 μm). Microconidia, clavate or oval with a truncated base, were formed in chains from mono- or polyphialides. Chlamydospores were absent. Eight 2-year-old seedlings (three to five expanded leaves) of majesty palm had the unopened spear leaves needle-wounded and another eight were unwounded. All were sprayed with a conidial suspension (1.5 × 106 CFU/ml). An equal number of noninoculated plants were used as a control. All plants were covered with polyethylene bags and incubated in a greenhouse at 25 ± 2°C for 72 h. All wounded majesty palms showed brown areas on unopened spear leaves. When natural injures were present, reddish leaf spots appeared as early as 4 days after inoculation. Macroscopic observations revealed the presence of white mycelium on the necrotic areas and reddish spots. Koch's postulates were satisfied by reisolation of the fungus on A-PDA from artificially infected tissues. On the basis of 3 months of field observations in Sicily, spread of Fusarium blight on majesty palm was always greater when plants were injured on the tender and unopened leaves by volcanic cinders from Mt. Etna, which caused bruises on young leaves. The disease does not represent a major threat to nurseries, but it could cause loss in the cultivation of the majesty palm. F. proliferatum was previously recorded in Saudi Arabia as the causal agent of wilt and dieback of date palm (1). To our knowledge, this is the first report of F. proliferatum on palms in Italy and the first outbreak of the disease on majesty palm. Reference: (1)M. Y. Abdalla et al. Plant Dis. 84:321, 2000.

scholarly journals First Report of a Leaf Spot Disease of Bells-of-Ireland (Moluccella laevis) Caused by Cercospora apii in California

Plant Disease ◽  
2003 ◽  
Vol 87 (2) ◽  
pp. 203-203
Author(s):  
S. T. Koike ◽  
S. A. Tjosvold ◽  
J. Z. Groenewald ◽  
P. W. Crous
Keyword(s):  
Leaf Spot ◽  
Sequence Data ◽  
Disease Incidence ◽  
Leaf Spot Disease ◽  
Conidial Suspension ◽  
Internal Transcribed Spacer Region ◽  
First Report ◽  
Spot Disease ◽  
Leaf Spots ◽  
Initial Symptoms

Bells-of-Ireland (Moluccella laevis) (Lamiaceae) is an annual plant that is field planted in coastal California (Santa Cruz County) for commercial cutflower production. In 2001, a new leaf spot disease was found in these commercially grown cutflowers. The disease was most serious in the winter-grown crops in 2001 and 2002, with a few plantings having as much as 100% disease incidence. All other plantings that were surveyed during this time had at least 50% disease. Initial symptoms consisted of gray-green leaf spots. Spots were generally oval in shape, often delimited by the major leaf veins, and later turned tan. Lesions were apparent on both adaxial and abaxial sides of the leaves. A cercosporoid fungus having fasciculate conidiophores, which formed primarily on the abaxial leaf surface, was consistently associated with the spots. Based on morphology and its host, this fungus was initially considered to be Cercospora molucellae Bremer & Petr., which was previously reported on leaves of M. laevis in Turkey (1). However, sequence data obtained from the internal transcribed spacer region (ITS1, ITS2) and the 5.8S gene (STE-U 5110, 5111; GenBank Accession Nos. AY156918 and AY156919) indicated there were no base pair differences between the bells-of-Ireland isolates from California, our own reference isolates of C. apii, as well as GenBank sequences deposited as C. apii. Based on these data, the fungus was subsequently identified as C. apii sensu lato. Pathogenicity was confirmed by spraying a conidial suspension (1.0 × 105 conidia/ml) on leaves of potted bells-of-Ireland plants, incubating the plants in a dew chamber for 24 h, and maintaining them in a greenhouse (23 to 25°C). After 2 weeks, all inoculated plants developed leaf spots that were identical to those observed in the field. C. apii was again associated with all leaf spots. Control plants, which were treated with water, did not develop any symptoms. The test was repeated and the results were similar. To our knowledge this is the first report of C. apii as a pathogen of bells-of-Ireland in California. Reference: (1) C. Chupp. A Monograph of the Fungus Genus Cercospora. Cornell University Press, Ithaca, New York, 1954.

scholarly journals First Report of Crown Rot of Banana Caused by Fusarium porliferatum in Georgia, USA

Plant Disease ◽  
2021 ◽  
Author(s):  
Sumyya Waliullah ◽  
Greg E. Fonsah ◽  
Jason Brock ◽  
Yonggang Li ◽  
Emran Ali
Keyword(s):  
Sequence Similarity ◽  
Morphological Characteristics ◽  
Fusarium Proliferatum ◽  
Crown Rot ◽  
Post Inoculation ◽  
Conidial Suspension ◽  
Banana Fruit ◽  
Single Spore ◽  
First Report ◽  
Initial Symptoms

Crown rot is one of the most damaging disease of banana fruit characterized by rot and necrosis of crown tissues. In severe cases, the disease can spread to the pedicel and banana pulp. Crown rot can be infected by several common fungi, including Lasiodiplodia theobromae, Musicillium theobromae, Colletotrichum musae, and a complex of Fusarium spp. and lead to softening and blackening of tissues (Lassois et al., 2010; Kamel et al., 2016; Triest et al., 2016; Snowdon, 1990). In November 2020, typical crown rot of banana fruits (cv. Pisang Awak, belonging to the tetraploid AABB genome) were observed from UGA Banana Research 12 Plots, Tifton, GA, with incidence rates of 15%. Initial symptoms appeared in the infected crown of green banana fruits. As the infection progressed, the crown tissues became blackened and softened, followed by an internal development of infection affecting the peduncle and the fruit, triggered early ripening of bananas. At last, the development of necrosis on the pedicels and fruits appeared and caused the fingers to fall off. To identify the pathogen, tissue pieces (~0.25 cm2) from the infected crown and pedicles were surface-sterilized in a 10% bleach solution for 1 min, followed by 30 s in 70% EtOH. The disinfected tissues were rinsed in sterile water 3 times and cultured on potato dextrose agar (PDA) amended with 50 µg/ml streptomycin at 25°C in the dark for 5–10 days. Isolates of the pathogen were purified using the single-spore isolation method (Leslie and Summerell 2006). Colonies on PDA produced fluffy aerial mycelium and developed an intense purple pigment when viewed from the underside. A range of colony pigmentation and growth rates were observed among the isolates. The microconidia were ovoid, hyaline, or ellipse in shape. The morphological features of the isolates were identified as Fusarium proliferatum (Leslie and Summerell, 2006). To further identify the isolates, genomic DNA was extracted from a representative isolate. And the internal transcribed spacer (ITS) region, the partial elongation factor (TEF1-α) gene and the β-tubulin gene (TUB2)were amplified and sequenced using the primers ITS1/ITS4 (Yin et al. 2012), EF-1 /EF-2 (O’Donnell et al. 1998) and B-tub1 /B-tub2 (O’Donnell and Cigelnik, 1997), respectively. The amplicons were sequenced and deposited in NCBI (accessions no. MZ292989, MZ293071 for ITS: MZ346602, MZ346603 for TEF1-α and MZ346600 and MZ346601 for B-tub). The ITS, TEF1-α, and B-tub sequences of the isolates showed 100% sequence similarity with Fusarium proliferatum isolates (accessions no. MT560212, LS42312, and LT575130, respectively) using BLASTn in Genbank. For pathogenicity testing, three whole bunched bananas sterilized with 10% bleach solutions and washed by sterilized water, were cut into 5 bananas per brunch. The cut surface of the banana crown was inoculated with conidial suspension (1.0 × 107 cfu/ml) of the pathogen with pipette tips. Equal number of bananas were treated with sterilized water in the same volume as a control. All bananas were sealed in a plastic bag and incubated at 25°C. After 7 days post inoculation, all inoculated bananas showed initial crown rot symptoms while no symptoms were observed on the control bananas. The fungus was re-isolated from the symptomatic tissues of infected bananas and confirmed to be genetically identical to F. proliferatum of the original inoculated strains according to morphological characteristics and molecular identification, fulfilling Koch’s postulates. To the best of our knowledge, this is the first report of F. proliferatum causing crown rot on bananas in Georgia, USA.

scholarly journals First Report of Leaf Spot Caused by Corynespora cassiicola on Viburnum odoratissimum Ker-Gawl. var. awabuki (K. Koch) Zabel ex Rumpl. (sweet viburnum) in China

Plant Disease ◽  
2021 ◽  
Author(s):  
Tianning Zhang ◽  
Huanhuan Liu ◽  
Qingni Song ◽  
Jun Liu ◽  
Qingpei Yang ◽  
...  
Keyword(s):  
Leaf Spot ◽  
Leaf Spot Disease ◽  
Conidial Suspension ◽  
Puncture Wound ◽  
First Report ◽  
Leaf Spots ◽  
Fungal Isolates ◽  
Initial Symptoms ◽  
Viburnum Odoratissimum ◽  
Sweet Viburnum

Sweet viburnum [Viburnum odoratissimum Ker-Gawl. var. awabuki (K. Koch) Zabel ex Rumpl.] belonging to the family Adoxaceae, is a medical and landscape plant, native to Korea (Jeju Island), Taiwan, and Japan (Edita 1988). In June and September 2019, leaf spots were observed on approximately 65% to 80% of sweet viburnum plants in a hedgerow located in Fenghe Xincheng District (28°41'52.9"N 115°52'14.3"E) in Nanchang, China. Initial symptoms of disease appeared as dark brown spots surrounded by red halos (Figure 1 A), which expanded irregularly. Finally, the center of the lesions desiccated and became light-brown, surrounded by a deep-red halos (Figure 1 B). Ten leaf samples with typical symptoms were collected and washed with tap water for about 15 min. The tissue between the healthy and necrotic area (ca. 4 mm × 4 mm) was cut with a sterile scalpel and surface sterilized with 70% alcohol for 45 s, 2% NaClO for 2 min, washed in sterile deionized water three times, dried on sterilized filter paper, then placed in Petri dishes and incubated at 25℃ in the dark. After 3 to 5 days, the hyphal tips from the edges of growing colonies were transferred to fresh PDA dishes. Eventually, 54 fungal isolates were obtained and, of these, 39 isolates were identical in their morphological characteristics. Morphological analysis was performed according with Ellis (1971). The isolate S18, chosen as representative, formed a gray to grayish brown colony with concentric circleson PDA, and a diameter of 8.5 to 9 cm after 7 days incubation at 25℃ (Figure 1 G). Conidia were hyaline, straight or slightly curved, needle shaped, truncate at the base, and acuminate at the tip, with 2 to 6 pseudosepta, 18.90 to 38.38 µm (avg. = 27.51 µm) × 1.64 to 4.50 µm (avg. = 2.60 µm) (n = 36) (Figure 1 H). The genes of fungal isolates (i.e., ITS, tub2 and ACT) were amplified with ITS4/ITS5 for ITS (White, Bruns et al. 1990), Bt2a/Bt2b for tub2 (Glass and Donaldson 1995) and ACT783R/ACT512F for ACT (Carbone and Kohn 1999) and sequenced. The sequences were deposited in GenBank (MW165772 for ITS, MW175900 for ACT and MW168659 for tub2), which showing greater than 99.1% similarity to multiple C. cassiicola accessions, respectively. Pathogenicity tests were performed on healthy leaves in field by inoculating surface-sterilized mature leaves with puncture wound (Figure C) and non-wounded young leaves with 20 µL of a conidial suspension (105 conidia ml-1) (Figure F and G) at 26℃. After 4 to 7 days, all inoculated leaves reproduced similar symptoms as observed initially in the field (Figure 1 C, E and F). To fulfill Koch’s postulates, the fungus was isolated on PDA from the margins of leaf spots on inoculated leaves and confirmed as C. cassiicola by morphological characters and ITS gene sequencing. Previously, C. cassiicola was reported as an endophyte on Viburnum spp. and Viburnum odoratissimum (Alfieri et al. 1994). More recently, C. cassiicola has been reported as a pathogen of many plant species in China, such as kiwifruit (Cui, Gong et al. 2015), American sweetgum (Mao, Zheng et al. 2021), castor bean (Tang, Liu et al. 2020), and holly mangrove (Xie, He et al. 2020). To our knowledge, this is the first report of leaf spot disease on sweet viburnum caused by C. cassiicola in China and the precise identification of the causal agent will be useful for its management.

scholarly journals First Report of Leaf Blight of Basella alba Caused by Alternaria alternata in India

Plant Disease ◽  
2011 ◽  
Vol 95 (11) ◽  
pp. 1476-1476 ◽  
Author(s):  
N. Ravi Sankar ◽  
A. Sreeramulu ◽  
D. Sai Gopal ◽  
G. Bagyanarayana
Keyword(s):  
Alternaria Alternata ◽  
Disease Incidence ◽  
Morphological Characteristics ◽  
Infected Leaf ◽  
Conidial Suspension ◽  
First Report ◽  
Perennial Plant ◽  
Basella Alba ◽  
Leaf Spots ◽  
Severe Infections

Basella alba is a perennial plant of the Basellaceae, native to India, and is distributed widely in the tropics as an ornamental. It is also known as Indian spinach, Ceylon spinach, vine spinach, Malabar spinach or Malabar nightshade and is mostly cultivated as a leafy vegetable or spinach substitute, being rich in vitamin A and C. From 2008 to 2010, severe foliar disease was observed on B. alba in the region of Southern Andhra Pradesh, India. Approximately 75 to 85% of the fields were affected with disease incidence ranging from 70 to 90%. Leaf lesions were elliptical to irregular oval, yellow brown to dark brown, and sometimes concentrically zonate with diffuse margins frequently surrounded by light-colored haloes. Infection often started at the leaf tips and progressed to the base of leaves as symptoms developed. In severe infections, lesions enlarged and coalesced, causing necrosis, wilting, and ultimately death of leaves. Tissues from the margin of infected leaf parts were surface sterilized in 1% sodium hypochlorite for 1 min, plated on potato dextrose agar (PDA), and then incubated at 27°C in the dark for 7 days. Hyphal tips from the margin of each developing colony were subcultured on PDA. Fungal colonies were initially white, becoming olivaceous, and turning brown with age. Conidiophores were brown, short, simple, or sometimes branched. Conidia were obclavate, obpyriform or ellipsoidal with a short conical beak, borne in long chains, branched or unbranched, pale brown to brown, and 18 to 32 μm long and 5 to 14 μm wide at the broadest point. Conidia had three to eight transverse septa and one to two longitudinal septa. On the basis of conidial morphological characteristics, the pathogen was identified as Alternaria alternata (Fr.) Keissler (2). For pathogenicity tests, inoculations were performed on detached, surface sterilized, healthy leaves following the method of Belisario (1). A 5-μl drop of conidial suspension containing 1 × 105 CFU/ml was placed on each leaf and 12 leaves per isolate were used. Leaves were incubated in a growth chamber (90% relative humidity with a 12-h photoperiod). After 7 days, leaf spots that were similar to the original symptoms developed on all inoculated leaves and A. alternata was consistently reisolated from symptomatic leaf tissues on PDA. Control leaves inoculated with sterile distilled water remained asymptomatic. The experiment was performed three times. To our knowledge, this is the first report of A. alternata on B. alba in India. References: (1) A. Belisario et al. Plant Dis. 83:696, 1999. (2) E. G. Simmons. Alternaria: An Identification Manual. The American Phytopathological Society, St. Paul, MN, 2007.

scholarly journals First Report of Fusarium denticulatum from Sweet Potato in Venezuela

Plant Disease ◽  
2003 ◽  
Vol 87 (2) ◽  
pp. 202-202
Author(s):  
M. S. González ◽  
F. Fuenmayor ◽  
F. Godoy ◽  
R. Navas
Keyword(s):  
Sweet Potato ◽  
Ipomoea Batatas ◽  
Germ Plasm ◽  
Apical Cell ◽  
Aerial Mycelium ◽  
Conidial Suspension ◽  
First Report ◽  
Young Leaves ◽  
Pure Cultures ◽  
Leaf Distortion

During 2001and 2002, 53 accessions of sweet potato (Ipomoea batatas L.) from a germ plasm collection maintained in the field at Centro Nacional de Investigaciones Agropecuarias, Maracay, Venezuela, were evaluated for diseases. Sweet potato accessions Catemaco and 2878 were symptomatic for chlorotic leaf distortion with deformation of young leaves and stunted vines. Symptomatic nodes and shoot tips were excised, surface disinfested in 0.5% sodium hypochlorite, cultured on potato dextrose agar (PDA), and incubated at 28°C. Pale pink colonies with white aerial mycelium developed from symptomatic tissues. At 20°C, pure cultures on PDA developed slow-growing, aerial, white-to-pink mycelium. Pigmentation in reverse was light orange. Conidia aggregated in false heads, and orange sporodochia were abundant. Conidiophores in aerial mycelium were prostrate, short, and sometimes branched. Sporodochial conidiophores were branched. Phialides were mostly monophialidic but occasionally polyphialidic and averaged 25.0 × 3.0 µm. Microconidia were abundant, long, oval to allantoid, and 0 to 1 septate. Macroconidia were fusiform to falcate with a beaked apical cell and a footlike basal cell, 3 to 5 sepate, and 38 to 45 × 3.6 to 4.0 µm. Chlamydospores were absent. The fungus was identified as Fusarium denticulatum Nirenberg and O'Donnell (1). Ten 25-cm-long vine-tip cuttings of accessions Catemaco and 2878 were immersed in a conidial suspension (1 × 106 conidia per ml) of F. denticulatum. As a control, vines were immersed in sterile, distilled water. After inoculation, each cutting was planted in a 13-cm plastic pot containing a soil/sand (1:1) mixture. Inoculated plants were covered with plastic bags for 48 h and grown in a greenhouse at temperatures ranging from 30 to 38°C. After 3 months, three inoculated plants of accession Catemaco and two plants of accession 2878 developed purple terminals and moderate interveinal chlorosis. Leaf distortion was not observed. F. denticulatum was recovered from both symptomatic and asymptomatic inoculated plants. To our knowledge, this is the first report of F. denticulatum from sweet potato germ plasm in Venezuela. Dried, pure cultures and slides of the fungus are being deposited in the Albert S. Muller Herbario Micologico (VIA). Reference: (1) H. I. Nirenberg and K. O'Donnell. Mycologia 90:434, 1998.

scholarly journals First Report of Alternaria Leaf Blight on Bupleurum chinense Caused by Alternaria alternata in China

Plant Disease ◽  
2010 ◽  
Vol 94 (7) ◽  
pp. 918-918
Author(s):  
Z. Zhang ◽  
J. H. Wei ◽  
C. M. Yang ◽  
H. Q. Chen ◽  
C. Sui ◽  
...  
Keyword(s):  
Disease Incidence ◽  
Conidial Suspension ◽  
First Report ◽  
High Soil Moisture ◽  
Leaf Spots ◽  
Black Spots ◽  
Initial Symptoms ◽  
Leaf Tissues ◽  
Pathogenicity Tests ◽  
Symptomatic Leaf

Bupleurum chinense DC. (family Umbelliferae) is an important medicinal herb in traditional Chinese medicine and is cultivated as an economically important plant in China (2). From 2006 to 2009, severe foliar disease was observed on B. chinense in Haidian, Changping, and Shunyi districts, Beijing, China. Approximately 75 to 85% of fields were affected with disease incidence ranging from 65 to 90%. Distribution of the disease in affected B. chinense fields was generally associated with high soil moisture, often corresponding to poor drainage. Initial symptoms first appeared on older leaves as irregularly shaped, minute, dark brown-to-black spots, with yellow borders on the edge of the affected leaflet blade. As the disease progressed, the lesions expanded, causing the leaflets to turn brown, shrivel, and die. Isolations performed on potato dextrose agar (PDA) initially resulted in white colonies. After 7 days of incubation at 25°C, the colonies turned gray or brown. Conidia varied in size from 10 × 6 to 40 × 12 μm, appeared brown to dark brown or olive-brown, were short beaked and borne in long chains, oval and bean-shaped with one to six transverse septa and zero to three longitudinal septa. Sequences of the rDNA from the internal transcribed spacer regions 1 and 2 and the 5.8S gene were amplified using primers ITS1 and ITS4, were obtained from three isolates, and comparisons with GenBank showed 100% similarity with A. alternata (Genbank Accession No. AB470912.1). For pathogenicity tests, three isolates were grown on PDA for 14 days. Inoculations were performed on detached, surface-sterilized, and healthy B. chinense leaflets following the method of Belisario (1). A 5-μl drop of conidial suspension containing 1 × 105 CFU/ml was placed on each leaflet and 12 leaves per isolate were used. Leaves were incubated in a growth chamber (80 to 90% relative humidity; 50 to 60 klx/m2 light intensity with a 12-h photoperiod). After 5 days, leaf spots similar to the original symptoms developed on all inoculated leaves and A. alternata was consistently reisolated from symptomatic leaf tissues on PDA. Control leaflets inoculated with sterile water remained asymptomatic. The experiment was performed three times. To our knowledge, this is the first report of A. alternata on B. chinense from China. References: (1) A. Belisario et al. Plant Dis. 83:696, 1999. (2) C. Sui et al. Plant Dis. 93:844, 2009.

scholarly journals First Report of Pilidium concavum on Paeonia suffruticosa in China

Plant Disease ◽  
2010 ◽  
Vol 94 (2) ◽  
pp. 271-271 ◽  
Author(s):  
Y. B. Duan ◽  
Y. B. Kang ◽  
Z. Z. Yu
Keyword(s):  
Aerial Mycelium ◽  
Causal Agent ◽  
Its2 Region ◽  
Paeonia Suffruticosa ◽  
Humid Atmosphere ◽  
First Report ◽  
Leaf Spots ◽  
Initial Symptoms ◽  
Perennial Shrub ◽  
Pure Cultures

Paeonia suffruticosa Andrews, a deciduous perennial shrub, is known for its beautiful and charming flowers. It is regarded as the flower symbol of China and cultivated throughout the country. Since 2006, large, brown necrotic spots have been observed on numerous P. suffruticosa plants in gardens in Luoyang, China. Spots appeared each year and were observed on more than 50% of the plants, sometimes affecting more than half of the leaf. Initial symptoms appeared as small, round, water-soaked lesions in the middle or on the margin of leaves. These areas enlarged up to 1 to 3 cm in diameter and were circular or irregular, brown to dark brown, and pale brown on the margins. In a humid atmosphere, black, sessile, discoid conidiomata developed on the spots and exuded a pink spore mass that turned brown with age. Conidiophores were hyaline, unicellular, cylindrical, and fusiform and 5.0 to 8.0 μm long and 1.4 to 2.0 μm wide. Pure cultures were obtained by plating the spores on potato dextrose agar (PDA) medium. In culture, the fungus produced a gray-to-brown colony with whitish aerial mycelium. The morphology and size of conidia were comparable with previous descriptions of Pilidium concavum (Desm.) Höhn. (1). The ITS1-5.8S-ITS2 region of the isolate was amplified by PCR with primers ITS1 and ITS4 and sequenced. The 472-nt sequence was 100% identical to that of the Pilidium concavum specimen voucher BPI 1107275 (GenBank Accession No. AY487094). To validate Koch's postulates, pathogenicity was tested by inoculating 10 leaves of P. suffruticosa with mycelia plugs from a colony growing on PDA; leaves inoculated with the plugs of PDA medium only served as the control. Leaves were covered with plastic for 24 h to maintain high relative humidity. After 7 days, 100% of the mycelium-inoculated leaves showed symptoms identical to those observed on P. suffruticosa leaves affected in the field, whereas all leaves inoculated with PDA medium only remained free of symptoms. Reisolation of the fungus from leaf lesions confirmed that the causal agent was Pilidium concavum. Thus, we concluded that Pilidium concavum is the causal agent of leaf spots of P. suffruticosa. This disease has been reported to be frequently occurring on P. suffruticosa stems imported from Japan (1), but to our knowledge, this is the first report of Pilidium concavum on P. suffruticosa in China. References: (1) M. E. Palm. Mycologia 83:787, 1991.

scholarly journals First Report of Anthracnose of Alocasia macrorrhiza Caused by Colletotrichum karstii in Guangdong, China

Plant Disease ◽  
2014 ◽  
Vol 98 (5) ◽  
pp. 696-696 ◽  
Author(s):  
Y. He ◽  
C. Shu ◽  
J. Chen ◽  
E. Zhou
Keyword(s):  
Morphological Characteristics ◽  
Pcr Amplification ◽  
Leaf Spot Disease ◽  
Molecular Characteristics ◽  
Conidial Suspension ◽  
Single Spore ◽  
First Report ◽  
Leaf Spots ◽  
Purification Technique ◽  
Initial Symptoms

Alocasia macrorrhiza (L.) Schott. (Araceae), native to South America, is a common, herbaceous perennial ornamental plant in tropical and subtropical areas (1). A severe leaf spot disease was observed on this plant in several places on the campus of authors' university in Guangzhou, Guangdong Province, China, in April 2013. Initial symptoms were water-soaked, dark green leaf spots. These small spots gradually expanded to 6- to 11-mm circular lesions. They were grayish-white in color with a yellow halo and many small, black, concentric dots were observed on them. Microscopic examination revealed that these small dots were acervuli, which were 100 to 300 μm in diameter, developing beneath the epidermis and becoming erumpent with age. By using routine tissue-isolation method and single-spore purification technique, four single-conidial isolates were obtained from each of four diseased leaves. These isolates formed a grayish-white colony with numerous pink spore masses on PDA at 28°C. Their mycelial radial growth rate was about 4.5 mm per day. Conidia were single-celled, hyaline, and cylindrical with an obtuse apex and protruding base; they were 12.7 to 14.2 × 4.8 to 5.9 μm in size. Conidial appressoria were irregular in shape, sepia to dark brown, solitary, and 6.9 to 8.5 × 4.6 to 5.9 μm. These morphological characteristics were consistent with the description of Colletotrichum karstii (2). The sequences of beta-tubulin gene (TUB2) and partial actin gene (ACT) of a representative isolate CAM1 were obtained by PCR amplification with primers BT2a/BT2b and ACT512F/ACT783R, respectively. These sequences were deposited in GenBank under the accession numbers of KF444947 and KF460435. BLAST searches showed a 99% homology with the TUB2 and ACT sequences of C. karstii (JX625209, KC843559). Therefore, the fungus isolated from A. macrorrhiza was identified as C. karstii by morphological and molecular characteristics. Pathogenicity tests were performed on 30-day-old plants of A. macrorrhiza grown in plastic pots (0.8 L) by spraying 15 ml conidial suspension (1 × 106 conidia ml–1) of this fungus onto each plant. The control plants were sprayed only with sterile distilled water. These plants then were placed in an intelligent artificial climate incubator with 12-h photoperiod and 100% relative humidity at 24 ± 1°C. Three replicates, each with five plants, were included in a test, and the test was repeated twice. Seven days after inoculation, the inoculated plants showed necrotic lesions on leaves similar to those observed on the campus, but no symptoms were observed on any non-inoculated controls. The same fungus C. karstii was re-isolated from the infected leaves. Although C. karstii is a well-known anthracnose pathogen on some plants belonging to family Orchidaceae (2), this is the first report of the same pathogen causing anthracnose on A. macrorrhiza in Guangdong, China. References: (1) S. Li et al. PLoS ONE 8(6):e66016, 2013. (2) Y. Yang et al. Cryptogr. Mycol. 32:229, 2011.

scholarly journals First Report of Curvularia aeria on Etlingera linguiformis from Nagaland, India

Plant Disease ◽  
2014 ◽  
Vol 98 (11) ◽  
pp. 1580-1580 ◽  
Author(s):  
C. Kithan ◽  
L. Daiho
Keyword(s):  
Leaf Surface ◽  
Agricultural Research ◽  
Disease Incidence ◽  
Indian Agricultural Research Institute ◽  
Mountain Range ◽  
Pathogenicity Test ◽  
Distilled Water ◽  
Conidial Suspension ◽  
First Report ◽  
Initial Symptoms

Etlingera linguiformis (Roxb.) R.M.Sm. of Zingiberaceae family is an important indigenous medicinal and aromatic plant of Nagaland, India, that grows well in warm climates with loamy soil rich in humus (1). The plant rhizome has medicinal benefits in treating sore throats, stomachache, rheumatism, and respiratory complaints, while its essential oil is used in perfumery. A severe disease incidence of leaf blight was observed on the foliar portion of E. linguiformis at the Patkai mountain range of northeast India in September 2012. Initial symptoms of the disease are small brown water soaked flecks appearing on the upper leaf surface with diameter ranging from 0.5 to 3 cm, which later coalesced to form dark brown lesions with a well-defined border. Lesions often merged to form large necrotic areas, covering more than 90% of the leaf surface, which contributed to plant death. The disease significantly reduces the number of functional leaves. As disease progresses, stems and rhizomes were also affected, reducing quality and yield. The diseased leaf tissues were surface sterilized with 0.2% sodium hypochlorite for 2 min followed by rinsing in sterile distilled water and transferred into potato dextrose agar (PDA) medium. After 3 days, the growing tips of the mycelium were transferred to PDA slants and incubated at 25 ± 2°C until conidia formation. Fungal colonies on PDA were dark gray to dark brown, usually zonate; stromata regularly and abundantly formed in culture. Conidia were straight to curved, ellipsoidal, 3-septate, rarely 4-septate, middle cells broad and darker than other two end cells, middle septum not median, smooth, 18 to 32 × 8 to 16 μm (mean 25.15 × 12.10 μm). Conidiophores were terminal and lateral on hyphae and stromata, simple or branched, straight or flexuous, often geniculate, septate, pale brown to brown, smooth, and up to 800 μm thick (2,3). Pathogen identification was performed by the Indian Type Culture Collection, Division of Plant Pathology, Indian Agricultural Research Institute, New Delhi (ITCC Accession No. 7895.10). Further molecular identity of the pathogen was confirmed as Curvularia aeria by PCR amplification and sequencing of the internal transcribed spacer (ITS) regions of the ribosomal DNA by using primers ITS4 and ITS5 (4). The sequence was submitted to GenBank (Accession No. MTCC11875). BLAST analysis of the fungal sequence showed 100% nucleotide similarity with Cochliobolus lunatus and Curvularia aeria. Pathogenicity tests were performed by spraying with an aqueous conidial suspension (1 × 106 conidia /ml) on leaves of three healthy Etlingera plants. Three plants sprayed with sterile distilled water served as controls. The first foliar lesions developed on leaves 7 days after inoculation and after 10 to 12 days, 80% of the leaves were severely infected. Control plants remained healthy. The inoculated leaves developed similar blight symptoms to those observed on naturally infected leaves. C. aeria was re-isolated from the inoculated leaves, thus fulfilling Koch's postulates. The pathogenicity test was repeated twice. To our knowledge, this is the first report of the presence of C. aeria on E. linguiformis. References: (1) M. H. Arafat et al. Pharm. J. 16:33, 2013. (2) M. B. Ellis. Dematiaceous Hyphomycetes. CMI, Kew, Surrey, UK, 1971. (3) K. J. Martin and P. T. Rygiewicz. BMC Microbiol. 5:28, 2005. (4) C. V. Suberamanian. Proc. Indian Acad. Sci. 38:27, 1955.

scholarly journals First Report of a Septoria sp. on Common Ragweed (Ambrosia artemisiifolia) in Europe

Plant Disease ◽  
1999 ◽  
Vol 83 (7) ◽  
pp. 696-696 ◽  
Author(s):  
Gy. Bohár ◽  
I. Schwarczinger
Keyword(s):  
Ambrosia Artemisiifolia ◽  
Voucher Specimen ◽  
Common Ragweed ◽  
History Museum ◽  
First Report ◽  
Leaf Spots ◽  
Brown Leaf ◽  
Detached Leaves ◽  
Pure Cultures ◽  
Hungarian Natural History Museum

During a survey for potential biocontrol agents of common ragweed (Ambrosia artemisiifolia var. elatior (L.) Descourt) in 1997, plants exhibiting irregular, brown leaf spots were collected repeatedly from six roadside locations in Pest County, Hungary. Many pycnidia developed in the necrotic tissues on detached leaves after 2 days in moist chambers. Pycnidia were globose to slightly flattened, brown, thin walled, 58 to 100 μm in diameter, with a definite ostiole. Conidia were hyaline, filiform with 2 to 3 septa, and 22.0 to 38.0 × 0.7 to 1.3 μm in size. The fungus was isolated on potato dextrose agar and identified as a Septoria sp. To confirm pathogenicity, potted ragweed seedlings were sprayed with a suspension of 5 × 106 conidia per ml from pure cultures of the Septoria sp., placed in a dew chamber for 72 h, and then grown in a greenhouse at 16 to 24°C. After 2 weeks, inoculated plants developed small, brown lesions on leaves and leaf petioles. Three weeks after inoculation, necrotic lesions had enlarged to 1 to 3 mm in diameter with irregular, distinct margins and light brown centers. The lesions on the lower leaves were larger and more numerous than on leaves nearer the tops of the plants. Pycnidia developed on the senescent leaves after 1 month. Infected leaves became completely necrotic and occasionally entire plants died. The pathogen was reisolated from all inoculated plants, thus satisfying Koch's postulates. A voucher specimen was deposited at the Department of Botany of the Hungarian Natural History Museum in Buda-pest (No. BP 92081). Septoria ambrosiae Hemmi et Naito was described on ragweed in Japan (1), but our isolate is morphologically distinct from that species. This is the first report of a Septoria sp. on A. artemisiifolia in Europe. Reference: (1) N. Naito. Mem. Coll. Agric. Kyoto 47:41, 1940.

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