scholarly journals First Report of Dry Rot Caused by Fusarium oxysporum on Rose (Rosa spp.) in Brazil

Plant Disease ◽  
2009 ◽  
Vol 93 (7) ◽  
pp. 766-766
Author(s):  
B. M. Barguil ◽  
F. M. P. Viana ◽  
R. M. Anjos ◽  
J. E. Cardoso

Roses are a high-value niche crop in the higher altitudes of northeastern Brazil. From July of 2007 and throughout 2008, severe stem rot and wilting of rose seedlings were observed in commercial fields in the São Benedito District, Ceará State, Brazil. Although economic losses due to the disease are unknown, it poses a threat to the growing rose industry in that region. Symptoms included leaf yellowing and abscission followed by plant collapse. Symptoms appeared earlier when grafted seedlings were produced during periods of high relative humidity (80 to 98%) and warm temperatures (20 to 31°C). In the laboratory, symptomatic seedlings were rinsed with distilled water, surface sterilized with 0.5% NaOCl, and incubated on PDA at 26 ± 2°C. Fusarium oxysporum was consistently isolated from infected scions and rootstocks. Identification of F. oxysporum was based on colony and conidia morphology obtained from single-spore colonies. Five 4-week-old rose (‘Carola’) seedlings were inoculated with a culture of fungus by spraying the needle-wounded scion with a spore suspension (1 × 105 CFU/ml). The spore suspension was obtained from a 1-week-old PDA culture incubated at 26 ± 2°C. Control seedlings were sprayed with sterile water. Inoculated seedlings were incubated for the first 48 h in a saturated humidity chamber. After 20 days at room temperature, the scion tissue of inoculated seedlings turned necrotic. Two symptomatic seedlings were placed in a saturated humidity chamber for 24 h to determine if fungal sporulation could be observed on the surface of the tissue. After 5 to 7 days, a white mycelium was observed over the necrotic tissue. Seedlings sprayed with sterile water remained symptomless. F. oxysporum was reisolated from symptomatic tissue. An isolate of F. oxyporum (No. 1484) was deposited in the Mycology Collection of Lavras (Minas Gerais State, Brazil). To our knowledge, this is the first report of F. oxysporum causing a disease on rose seedlings in Brazil.

Plant Disease ◽  
2010 ◽  
Vol 94 (12) ◽  
pp. 1509-1509 ◽  
Author(s):  
G. Polizzi ◽  
D. Aiello ◽  
V. Guarnaccia ◽  
A. Vitale ◽  
G. Perrone ◽  
...  

Eremophila spp. (Myoporaceae family), endemic to Australia, are evergreen shrubs or small trees occurring in arid, semi-arid, tropical, or temperate regions. In Europe, Eremophila spp. are grown for their horticultural appeal. During 2009 and 2010, extensive wilting was observed on 2-month to 1-year-old potted plants of Eremophila laanii F. Muell., E. glabra subsp. carnosa Chinnock, and E. maculata (Ker Gawl.) F. Muell. grown in a commercial nursery near Catania (southern Italy). Internally, symptomatic plants had conspicuous vascular discoloration from the crown to the canopy. Diseased crown and stem tissues were surface disinfested for 30 s in 1% NaOCl, rinsed in sterile water, plated on potato dextrose agar (PDA) amended with 100 mg/liter of streptomycin sulfate, and incubated at 25°C. A Fusarium sp. was consistently isolated from affected plant tissues. Colonies with purple mycelia and violet reverse colors developed after 9 days. On carnation leaf agar, single-spore isolates produced microconidia on short monophialides, macroconidia that were three to five septate with a pedicellate base, and solitary and double-celled or aggregated chlamydospores. A PCR assay was conducted on two representative isolates (ITEM 12591 and ITEM 12592) by analyzing sequences of the partial CaM gene (coding calmodulin protein) and benA (coding beta-tubulin protein) using the primers as reported by O'Donnell et al. (1). Calmodulin sequences of ITEM 12951 and ITEM 12952 isolates (GenBank Nos. FR671157 and FR671158) exhibited 99.8 and 99.5% identity with Fusarium oxysporum strain ITEM 2367 (GenBank No. AJ560774), respectively, and had 99.5% homology between them. BenA gene sequences of ITEM 12951 (GenBank No. FR671426) exhibited an identity of 100% to F. oxysporum f. sp. vasinfectum strain CC-612-3 (GenBank No. AY714092.1), and benA gene sequences of ITEM 12952 (GenBank No. FR671427) exhibited an identity of 100% to F. oxysporum f. sp. vasinfectum strain LA 140 (GenBank No. FJ466740.1), whereas the homology between the two strains is 99.5%. Morphological characteristics, as well as CaM and benA sequences, identified the isolates as F. oxysporum Schlechtend:Fr. Pathogenicity tests were performed by placing 1-cm2 plugs of PDA from 9-day-old mycelial cultures near the crown on potted, healthy, 3-month-old cuttings of E. laanii, E. glabra subsp. carnosa, and E. maculata. Twenty plants for each species were inoculated with each isolate. The same number of plants served as noninoculated controls. All plants were enclosed for 4 days in plastic bags and placed in a growth chamber at 24 ± 1°C. Plants were then moved to a greenhouse where temperatures ranged from 23 to 27°C. Symptoms identical to those observed in the nursery developed 20 days after inoculation with both strains. Crown and stem discoloration was detected in all inoculated plants after 45 days. Wilting was detected on 15% of plants. Control plants remained symptomless. F. oxysporum was consistently reisolated from symptomatic tissues and identified as previously above. To our knowledge, this is the first report of F. oxysporum causing disease of Eremophila spp. worldwide. Reference: (1) K. O'Donnell et al. Mycoscience 41:61, 2000.


Plant Disease ◽  
2020 ◽  
Author(s):  
Yue Lian Liu ◽  
Jian Rong Tang ◽  
Yu Han Zhou

Monstera deliciosa Liebm is an ornamental foliage plant (Zhen et al. 2020De Lojo and De Benedetto 2014). In July of 2019, anthracnose lesions were observed on leaves of M. deliciosa cv. Duokong with 20% disease incidence of 100 plants at Guangdong Ocean University campus (21.17N,110.18E), Guangdong Province, China. Initially affected leaves showed chlorotic spots, which coalesced into larger irregular or circular lesions. The centers of spots were gray with a brown border surrounded by a yellow halo (Supplementary figure 1). Twenty diseased leaves were collected for pathogen isolation. Margins of diseased tissue was cut into 2 × 2 mm pieces, surface-disinfected with 75% ethanol for 30 s and 2% sodium hypochlorite (NaOCl) for 60 s, rinsed three times with sterile water before isolation. Potato dextrose agar (PDA) was used to culture pathogens at 28℃ in dark. Successively, pure cultures were obtained by transferring hyphal tips to new PDA plates. Fourteen isolates were obtained from 20 leaves. Three single-spore isolates (PSC-1, PSC-2, and PSC-3) were obtained ,obtained, which were identical in morphology and molecular analysis (ITS). Therefore, the representative isolate PSC-1 was used for further study. The culture of isolate PSC-1 on PDA was initially white and later became cottony, light gray in 4 days, at 28 °C. Conidia were single celled, hyaline, cylindrical, clavate, and measured 13.2 to 18.3 µm × 3.3 to 6.5 µm (n = 30). Appressoria were elliptical or subglobose, dark brown, and ranged from 6.3 to 9.5 µm × 5.7 to 6.5 µm (n = 30). Morphological characteristics of isolate PSC-1 were consistent with the description of Colletotrichum siamense (Prihastuti et al. 2009; Sharma et al. 2013). DNA of the isolate PSC-1 was extracted for PCR sequencing using primers for the rDNA ITS (ITS1/ITS4), GAPDH (GDF1/GDR1), ACT (ACT-512F/ACT-783R), CAL (CL1C/CL2C), and TUB2 (βT2a/βT2b) (Weir et al. 2012). Analysis of the ITS (accession no. MN243535), GAPDH (MN243538), ACT (MN512640), CAL (MT163731), and TUB2 (MN512643) sequences revealed a 97-100% identity with the corresponding ITS (JX010161), GAPDH (JX010002), ACT (FJ907423), CAL (JX009714) and TUB2 (KP703502) sequences of C. siamense in GenBank. A phylogenetic tree was generated based on the concatenated sequences of ITS, GAPDH, ACT, CAL, and TUB2 which clustered the isolate PSC-1 with C. siamense the type strain ICMP 18578 (Supplementary figure 2). Based on morphological characteristics and phylogenetic analysis, the isolate PSC-1 associated with anthracnose of M. deliciosa was identified as C. siamense. Pathogenicity test was performed in a greenhouse at 24 to 30oC with 80% relative humidity. Ten healthy plants of cv. Duokong (3-month-old) were grown in pots with one plant in each pot. Five plants were inoculated by spraying a spore suspension (105 spores ml-1) of the isolate PSC-1 onto leaves until runoff, and five plants were sprayed with sterile water as controls. The test was conducted three times. Anthracnose lesions as earlier were observed on the leaves after two weeks, whereas control plants remained symptomless. The pathogen re-isolated from all inoculated leaves was identical to the isolate PSC-1 by morphology and ITS analysis, but not from control plants. C. gloeosporioides has been reported to cause anthracnose of M. deliciosa (Katakam, et al. 2017). To the best of our knowledge, this is the first report of C. siamense causing anthracnose on M. deliciosa in ChinaC. siamense causes anthracnose on a variety of plant hosts, but not including M. deliciosa (Yanan, et al. 2019). To the best of our knowledge, this is the first report of C. siamense causing anthracnose on M. deliciosa, which provides a basis for focusing on the management of the disease in future.


Plant Disease ◽  
2020 ◽  
Author(s):  
Yi Ming Guan ◽  
Shu Na Zhang ◽  
Ying Ying Ma ◽  
Yue Zhang ◽  
Ya Yu Zhang

Astragalus membranaceus Bunge (Fabaceae) is a perennial medicinal herb widely cultivated in China. In June 2018, root rot was observed on two-year-old A. membranaceus plants in Chaoyangshan town (northeastern China). In a 40-ha field, over 40% of the plants exhibited root rot and the infected area ranged from 10 to 70% of the roots. The roots first exhibited circular or irregular brown, sunken and necrotic lesions, and finally multiple lesions coalesced. The infected root surface was destroyed, showing rusty and dry rot (Fig. 1). Symptoms were concentrated in the main roots (Carlucci et al. 2017). The aboveground parts of infected plants did not initially show symptoms but gradually wilted; 7.6% of the plants died when root decay became severe. Infected roots were not used for processing and were not marketable. Ten infected roots were collected from May to October 2018 from the above location. The diseased root tissue was cut into 25 mm3 pieces, immersed in 1% NaOCl for 2 minutes, rinsed three times with sterile water and placed on water agar in Petri plates. After 15 days of incubation at 20°C, 11 single-spore isolates were obtained. Isolates HQ1 and HQ2 were randomly selected for morphological and molecular identification. Colonies grown for 10 days produced yellow, cottony to felty aerial mycelium on potato dextrose agar. Conidiophores originating laterally or terminally from the mycelium were solitary to loosely aggregated and unbranched or sparsely branched. Macroconidia predominated and were cylindrical, with a tendency to gradually widen towards the tip; 1- to 3-septate; and 20.2 to 31.0 × 3.0 to 6.7 µm (n=100). Microconidia had mostly 0¬- to 1-septate and 8.6 to 16.7 × 1.9 to 5.1 µm (n=100) (Fig. 1). Chlamydospores were rare, but occasional chlamydospore chains were observed. The isolates were tentatively identified as Dactylonectria torresensis (Cabral et al. 2012a). Further confirmation of the two isolates was conducted by DNA sequencing of the internal transcribed spacer (ITS, GenBank accession no. MN558983 and MN558984), β-tubulin (TUB, MN561692 and MN561693), histone 3 (HIS3, MN561694 and MN561695), and translation elongation factor (TEF, MN561696 and MN561697) genes (Cabral et al. 2012b). These sequences had 99 to 100% match with D. torresensis (JF735362 for ITS, JF735492 for TUB, JF735681 for HIS3 and JF735870 for TEF). Phylogenetic trees based on analyses of a concatenated alignment of all loci grouped these isolates into the D. torresensis clade (Fig. 2). The same two isolates were tested for pathogenicity. Healthy two-year-old plants were taken from the field, and their roots were disinfected with 75% alcohol for 3 minutes, rinsed with sterile water three times, immersed in a 1×105/ml spore suspension or sterile water (control) for 10 minutes, transferred to a tray filled with sterile sand and placed in a greenhouse (12 h photoperiod, 25°C). Twelve plants grown in three pots were used for each isolate, and the same number of plants were inoculated as a control. This experiment was repeated three times. After one month, inoculated plant roots showed the same symptoms as those observed in the field, while the controls remained symptomless and no pathogen was recovered. The same fungus was reisolated from all the infected plants and confirmed by sequencing all of the above genes. This is the first report of D. torresensis causing root rot in A. membranaceus in China. The occurrence of this disease poses a threat, and management strategies need to be developed.


Plant Disease ◽  
2011 ◽  
Vol 95 (9) ◽  
pp. 1190-1190 ◽  
Author(s):  
M. Luo ◽  
Z. Y. Dong ◽  
S. Y. Bin ◽  
J. T. Lin

Pomelo (Citrus grandis) is widely cultivated in MeiZhou Guangdong Province of China. In 2008, a disease on pomelo fruit caused significant economic losses by affecting fruit quality. Diseased fruit was collected in December 2008 from MeiZhou Guangdong, surface sterilized in 75% ethanol for 1 min and internal necrotic tissue was transferred to potato dextrose agar (PDA) and incubated at 28°C for 5 days. Three single-spore isolates were obtained from different fruit and identified as Lasiodiplodia theobromae (Pat.) Griffon & Maubl. (synonyms Diplodia natalensis Pole-Evans and Botryodiplodia theobromae Pat.; teleomorph Botryosphaeria rhodina (Cooke) Arx) on the basis of morphological and physiological features. The fungus produced dark brown colonies (initially grayish) on PDA. Young hyphae were hyaline and aseptate, whereas mature hyphae were septate with irregular branches. Cultures of L. theobromae produced globular or irregular pycnidia abundantly on PDA (pH 3.5) at 28°C after 1 month. Mature conidia of L. theobromae were 20 to 26 × 12 to 15.5 μm, subovoid to ellipsoid-ovoid, initially hyaline and nonseptate, remaining hyaline for a long time, and finally becoming dark brown and one septate with melanin deposits on the inner surface of the wall arranged longitudinally giving a striate appearance to the conidia. The internal transcribed spacer (ITS) region of the rDNA was amplified from gDNA using primers ITS1 (5′-TCCGATGGTGAACCTGCGG-3′) and ITS4 (5′-TCCTCCGCTTATTGATATGC-3′) (1). Amplicons were 542 bp long (GenBank Accession No. JF693024) and had 100% nucleotide identity with the corresponding sequence (GenBank Accession No. EU860391) of L. theobromae isolated from a Pinus sp. (2). To satisfy Koch's postulates, six asymptomatic fruit on potted plants were sprayed until runoff with a spore suspension (1 × 106 spores/ml) prepared from 30-day-old cultures of one isolate. Control fruit received water. Plants were covered with sterile wet gauze to maintain high humidity. Fruit spot symptoms similar to those on diseased field fruit appeared after 15 days on all inoculated fruits. L. theobromae was reisolated from all inoculated test fruit. No symptoms were observed on the fruit of control plants. To our knowledge, this is the first report of L. theobromae causing disease on pomelo fruit in China. This pathogen has also been previously reported to be economically important on a number of other hosts by mostly affecting the leaves. References: (1) J. C. Batzer et al. Mycologia 97:1268, 2005. (2) C. A. Pérez et al. Fungal Divers. 41:53,2010.


Plant Disease ◽  
2021 ◽  
Author(s):  
Oliul Hassan ◽  
Taehyun Chang

In South Korea, ovate-leaf atractylodes (OLA) (Atractylodes ovata) is cultivated for herbal medicine. During May to June 2019, a disease with damping off symptoms on OLA seedlings were observed at three farmer fields in Mungyeong, South Korea. Disease incidence was estimated as approximately 20% based on calculating the proportion of symptomatic seedlings in three randomly selected fields. Six randomly selected seedlings (two from each field) showing damping off symptoms were collected. Small pieces (1 cm2) were cut from infected roots, surface-sterilized (1 minute in 0.5% sodium hypochlorite), rinsed twice with sterile water, air-dried and then plated on potato dextrose agar (PDA, Difco, and Becton Dickinson). Hyphal tips were excised and transferred to fresh PDA. Six morphologically similar isolates were obtained from six samples. Seven-day-old colonies, incubated at 25 °C in the dark on PDA, were whitish with light purple mycelia on the upper side and white with light purple at the center on the reverse side. Macroconidia were 3–5 septate, curved, both ends were pointed, and were 19.8–36.62 × 3.3–4.7 µm (n= 30). Microconidia were cylindrical or ellipsoid and 5.5–11.6 × 2.5–3.8 µm (n=30). Chlamydospores were globose and 9.6 –16.3 × 9.4 – 15.0 µm (n=30). The morphological characteristics of present isolates were comparable with that of Fusarium species (Maryani et al. 2019). Genomic DNA was extracted from 4 days old cultures of each isolate of SRRM 4.2, SRRH3, and SRRH5, EF-1α and rpb2 region were amplified using EF792 + EF829, and RPB2-5f2 + RPB2-7cr primer sets, respectively (Carbone and Kohn, 1999; O'Donnell et al. 2010) and sequenced (GenBank accession number: LC569791- LC569793 and LC600806- LC600808). BLAST query against Fusarium loci sampled and multilocus sequence typing database revealed that 99–100% identity to corresponding sequences of the F. oxysporum species complex (strain NRRL 28395 and 26379). Maximum likelihood phylogenetic analysis with MEGA v. 6.0 using the concatenated sequencing data for EF-1α and rpb2 showed that the isolates belonged to F. oxysporum species complex. Each three healthy seedlings with similar sized (big flower sabju) were grown for 20 days in a plastic pot containing autoclaved peat soil was used for pathogenicity tests. Conidial suspensions (106 conidia mL−1) of 20 days old colonies per isolate (two isolates) were prepared in sterile water. Three pots per strain were inoculated either by pouring 50 ml of the conidial suspension or by the same quantity of sterile distilled water as control. After inoculation, all pots were incubated at 25 °C with a 16-hour light/8-hour dark cycle in a growth chamber. This experiment repeated twice. Inoculated seedlings were watered twice a week. Approximately 60% of the inoculated seedlings per strain wilted after 15 days of inoculation and control seedlings remained asymptomatic. Fusarium oxysporum was successfully isolated from infected seedling and identified based on morphology and EF-1α sequences data to confirm Koch’s postulates. Fusarium oxysporum is responsible for damping-off of many plant species, including larch, tomato, melon, bean, banana, cotton, chickpea, and Arabidopsis thaliana (Fourie et al. 2011; Hassan et al.2019). To the best of our knowledge, this is the first report on damping-off of ovate-leaf atractylodes caused by F. oxysporum in South Korea. This finding provides a basis for studying the epidemic and management of the disease.


Plant Disease ◽  
2021 ◽  
Author(s):  
Shipeng Han ◽  
Qing Wang ◽  
Shuo Zhang ◽  
Xi Jin ◽  
Zhi Min Hao ◽  
...  

Angelica dahurica (Fisch. ex Hoffm.) is an abundantly cultivated Chinese herbal medicine plant in China with about 4000 hectares grown, the annual production is up to 24,000 tons. The medicinal part of A. dahurica is its root, and mainly function for treat cold, headache, toothache, rhinitis, diabetes, etc. Besides, A. dahurica is also used as a spice in Asia. In September 2018, brown spot was observed on the leaves of A. dahurica in fields of Anguo City, Hebei Province, China. In the field investigated, the incidence of brown spot disease reached 15%. The infected leaves showed brown spots surrounded with pale yellow edge, resulting in withered of the whole leaf. It seriously endangers the growth of A. dahurica, reducing the yield and quality of medicinal materials, even leading to the death of plants. We isolated the pathogen from 10 leaves with same lesions, the small square leaf pieces of approximately 3 to 5 mm were obtained with the sterile scissors from the junction of infected and healthy tissues, sterilized with sodium hypochlorite (10%) for 1 min followed by washing in sterile water for 3 times, then incubated on potato dextrose agar (PDA) plates at 25°C for 4 days. The culture was transferred to new PDA plates and was cultivated in dark at 25°C for 10 days. A total of 3 species of fungi were isolated, and only one fungus species has been found to be able to cause the original pathological characteristics of A. dahurica leaves through the back-grafting experiment. The mycelium was black and began to sporulate after 8 days on PDA media by single spore separation. Multiple spores joined together to form spores chain. The spores were spindle-shaped, yellow to yellow brown, and size ranged from 45 to 55 × 15 to 20 µm (n=50), with zero to three longitudinal septa and one to five transverse septa. For pathogenicity tests, the spore suspension (3.5×105 spores/mL) were inoculated to healthy plants grown in experimental field, the test was repeated four times, and 10 leaves were inoculated in each repetition, and the sterile water was inoculated as the blank control. Inoculated leaves were covered with transparent plastic bags for 24 h to keep humidity. Nine days later, it was found that there were lesions on the leaves inoculated with the pathogen, and the traits were the same as those in the field, while the controls are healthy. The fungus was consistently isolated from the inoculated leaves. The similar isolates were re-isolated from the inoculated and infected leaves and identified as Alternaria tenuissima by DNA sequencing, fulfilling Koch’s postulates. Fungal genomic DNA was extracted from 7-day-old culture. PCR amplifications were performed using primers ITS1 / ITS4 and TEFF / TEFR respectively (Takahashi et al. 2006, Du 2008). The nucleotide sequence of PCR products, which have been deposited in Genebank under the accession numbers MN153514 and MN735428, showed 99.8%-100% identity with the corresponding sequences of A. tenuissima (MW194297 and MK415954). In order to further identify the pathogen species, we constructed a phylogenetic tree by combining TEF sequence and ITS sequence to distinguish the relationship between the pathogen and other minor species in the genus Alternaria, the isolate was clustered in the Alternaria clade. Therefore, the pathogen was identified as A. tenuissima based on the morphological characteristics and molecular identification. To our knowledge, this is the first report of A. tenuissima causing leaf spot on A. dahurica in China.


Plant Disease ◽  
2009 ◽  
Vol 93 (4) ◽  
pp. 426-426 ◽  
Author(s):  
R.-S. Chen ◽  
W.-L. Wang ◽  
J.-C. Li ◽  
Y.-Y. Wang ◽  
J.-G. Tsay

In March of 2008, a leaf scab disease was observed in a papaya (Carica papaya L.) orchard at Guoshing, 24.03°N, 120.51°E, in Nantou County, Taiwan. Infected papayas developed symptoms of numerous, pale green, water-soaked areas, 0.5 to 1.5 mm. Infected leaves gradually turned white to gray on the upper surface and small, circular swellings were observed on the abaxial surface. Lesions may coalesce to cover more than 50% of the leaf, rendering them to fall prematurely. Lesions on the lower surface of the leaves were covered with olive-gray patches of mycelia and abundant conidia. Pieces (~2 × 2 mm) of diseased leaf tissue from margins of individual lesions were surface disinfected in 1% sodium hypochlorite solution for 1 min, rinsed in sterile water, plated on water agar, and incubated at 25°C. After 4 days, mycelium was isolated and transferred to potato dextrose agar (PDA). Five isolates (Cc-5 to Cc-9) were isolated and identified as Cladosporium cladosporioides (Fresen.) de Vries based on the velvety, olive-brown with almost black reverse colony color and dimensions and color of conidia and conidiophores (1). Conidia formed in long branched chains that readily disarticulate, single celled, elliptical to limoniform, 2 to 9 (4.6) × 2 to 3 (2.2) μm. Conidia were pale-to-olive brown and smooth to verruculose. Ramoconidia were 0 to 1 septate, 6 to 14 (9.4) × 2 to 4 (2.7) μm, smooth or sometimes minutely verruculose. Conidiophores were pale-to-olive brown, macro- and micronemateus, smooth or sometimes verruculose, 68 to 244 (141.7) × 3.2 to 4 (3.9) μm. To confirm the identity of the fungus, the internal transcribed spacer (ITS) 1 and 4 regions and mitochondrial small subunit (mtSSU) rDNA were sequenced (GenBank Accession Nos. EU935608 and FJ362555), which had 99% homology to the ITS and mtSSU rDNA of C. cladosporioides (GenBank Accession Nos. EU497957 and AY291273, respectively). Pathogenicity tests were conducted in the greenhouse at 25°C with natural daylight conditions. Fungal isolate Cc-6 was used; it was grown on PDA for 6 days and a spore suspension was made (106 spores/ml). Three papaya seedlings (cv. Horng-Fe) were sprayed with the spore suspension and covered with plastic bags. Control treatments were sprayed with sterile water. After 2 days, the bags were removed. Symptoms developed on all inoculated seedlings 4 days after inoculation. In all cases, the typical scab symptom, pale green, water-soaked areas on the lower leaf surface, were observed. C. cladosporioides was reisolated from inoculated leaves following the procedure used for the original isolation. Control seedlings developed no symptoms. The five isolates are being maintained at the DBST, NCYU, Taiwan. Previously, papaya scab reported in China was caused by C. cariciolum Corda (2), C. caricinum C. F. Zhang et P. K. Chi (3), and C. cladosporioides (4). To our knowledge, this is the first report of C. cladosporioides causing papaya scab in Taiwan. References: (1) M. B. Ellis. Dematiaceous Hyphomycetes. CMI, Kew, Surrey, England, 1971. (2) H.-H. Peng and Z.-Y. Zhang. J. Yunnan Agric. Univ. 12:23, 1997. (3) C.-F. Zhang. Ph.D. thesis. South China Agricultural University, Guangzhou, P.R.C., 1995. (4) Z. Y. Zhang et al. Flora Fungorum Sinicorum 14:1, 2003.


Plant Disease ◽  
2005 ◽  
Vol 89 (10) ◽  
pp. 1131-1131 ◽  
Author(s):  
L. Eshraghi ◽  
M. P. You ◽  
M. J. Barbetti

Brassica juncea (L.) Czern & Coss (mustard) has potential as a more drought-tolerant oilseed crop than the Brassica napus, and the first two canola-quality B. juncea cultivars will be sown as large strip trials across Australia in 2005. This will allow commercial evaluation of oil and meal quality and for seed multiplication for the commercial release Australia-wide in 2006. Inspection of experimental B. juncea field plantings at Beverley (32°6′30″S, 116°55′22″E), and Wongan Hills (30°50′32″S, 116°43′33″E), Western Australia in September 2004 indicated the occurrence of extensive leaf spotting during B. juncea flowering. Symptoms of this disease included as many as 15 or more grayish white-to-brownish spot lesions per leaf, often with a distinct brown margin. Some elongate grayish stem lesions were also observed as reported earlier for B. napus oilseed rape (1). When affected materials were incubated in moist chambers for 48 h, abundant conidia typical of Pseudocercosporella capsellae (Ellis & Everh.) Deighton were observed that matched the descriptions of conidia given by Deighton (2) and those on B. napus in Western Australia (1). Five single-spore cultures from lesions were grown on water agar (WA) where the colonies characteristically produced purple-pink pigment in the agar after 2 weeks growth in an incubator maintained at 20°C with a 12-h photoperiod (3). Since agar cultures of P. capsellae rarely produce conidia (3), this observation helped with the verification of the cultures. Mycelial inoculum from these cultures was used to inoculate cotyledons of 50 7-day-old plants of B. juncea to satisfy Koch's postulates. Small pieces of mycelia were teased out from the surface of the growing margin of potato dextrose agar (PDA) cultures and inoculated onto both lobes of each cotyledon and plants incubated in a 100% humidity chamber for 48 h within a controlled environment room maintained at 20/15°C (day/night) with a 12-h photoperiod. After 2 weeks, lesions 5 to 8 mm in diameter were observed on the cotyledons. There were no symptoms on control plants that were treated with water only. Lesions on infected cotyledons incubated on moist filter paper for 24 h produced abundant cylindrical conidia showing 2 to 3 septa measuring 42.9 to 71.4 μm long and 2.9 to 3.1 μm wide. Single-spore isolations from these conidia produced typical P. capsellae colonies showing purple-pink pigments in WA, and dark, compacted, and slow-growing colonies with a dentate margin on PDA. White leaf spot caused by P. capsellae is an important disease of crucifers worldwide, but to our knowledge, this is the first report of P. capsellae on B. juncea in Australia. In Western Australia, P. capsellae occurs on B. napus oilseed rape (1) and in 1956, 1984, and 1987, it was recorded on B. rapa, B. oleracea, and B. chinensis, respectively (4), and on the same range of Brassica hosts in other regions of Australia. References: (1) M. J. Barbetti and K. Sivasithamparam. Aust. Plant Pathol.10:43, 1981. (2) F. C. Deighton. Commonw. Mycol. Inst. Mycol. Pap. 133:42, 1973. (3) S. T. Koike. Plant Dis. 80:960, 1996. (4) R. G. Shivas. J. R. Soc. West. Aust. 72:1, 1989.


Plant Disease ◽  
2021 ◽  
Author(s):  
Huifang Zhang ◽  
Ning Kong ◽  
Shida Ji ◽  
Bin Liu ◽  
Zhen Tian ◽  
...  

Populus alba L. × P. berolinensis Dipp. (a hybrid poplar, ‘PaPb poplar’) exhibits fast growth and beautiful tree shape with high drought and cold tolerance, and is widely planted in the cities of Northeast China because of its ornamental and ecological value (Wang et al. 2008). In October 2020, an unknown leaf blight symptom was observed on the seedlings of ‘PaPb poplar’ at Shenyang Agricultural University (41°49′N, 123°34′E) located in Shenyang City, Liaoning Province, China. The disease incidence was 50% in a survey of 200 seedlings on the campus. The typical symptoms were brown-to-black, irregular-shaped lesions (Fig. 1A). To investigate the disease, five symptomatic leaves were collected, and pieces were cut at the margin of diseased and healthy tissue. These pieces were surface sterilized with 2% sodium hypochlorite for 2 min, rinsed three times with sterile distilled water, air dried, placed on potato dextrose agar (PDA) and incubated at 28°C. After 5 days of incubation, three isolates with similar morphological characteristics were observed. Isolate N03 was chosen and used for pathogen identification. The fungal colonies were initially white in color, and later turned gray to black (Fig. 1D). Conidia were single-celled, black, spherical or oblate in shape measuring 9.19 to 12.78 μm × 12.61 to 14.81 μm in diameter (n=40) (Fig. 1E). These were borne on hyaline vesicles at the tip of a conidiophore. Morphologically, the isolate N03 was identified as Nigrospora oryzae (Berk. and Broome) Petch (Wang et al. 2017). The genomic DNA was extracted with a SP Fungal DNA Kit (D5542-01, OMEGA). The internal transcribed spacer (ITS) region, translation elongation factor 1-alpha (TEF1-α), and partial beta-tubulin (TUB) genes were amplified using the primers ITS5/ITS4 (White et al. 1990), EF1-728F/EF-2R (Carbone and Kohn, 1999; O’Donnell et al. 1998), and Bt-2a/Bt-2b (Glass and Donaldson, 1995) primer sets, respectively. The PCR products of ITS, TEF1-α, and TUB were amplified, sequenced, and deposited in GenBank with the following accession numbers MZ148528, MZ182080, and MZ182079, respectively. BLASTn analysis of the ITS, TEF1-α, and TUB sequences had 99.3%, 99.8%, and 99.27% nucleotide identities to MK131325, KY019328, and KY019559, respectively. A phylogenetic tree based on combined ITS, TEF1-α, and TUB sequences was constructed using a Maximum Likelihood method with 1000 bootstraps showing that N03 was grouped with other N. oryzae isolates (Fig. 2). The fungus was identified as N. oryzae based on morphological characteristics and molecular analyses. Koch’s postulates were completed to confirm the pathogenity of N. oryzae on ‘PaPb poplar’. The N03 spore suspension (105 spores/mL) was used to inoculate detached leaves and field leaves in two experiments. The two experiments were repeated three times, respectively. In the detached leaf test, 10 healthy leaves collected from 1-year-old ‘PaPb poplar’ seedlings were inoculated with N03 by spraying with the spore suspension followed by incubation at 28°C on wet filter papers in a petri dish for 7 days. 10 leaves were sprayed with sterile water to save as the controls. For field leaf test, leaves of 5 plants were spray-inoculated with the spore suspension at the 4-week-old growth stage, and an additional 5 plants were sprayed with sterile water. Seven days after inoculation, brown-to-black, irregular-shaped lesions on the margin of leaves were observed on inoculated leaves but not on the controls (Fig. 1B and C). All detached leaves inoculated with N03 were symptomatic. In the field tests, symptom appeared on 20 of the 30 inoculated leaves. N. oryzae was re-isolated from all the inoculated detached leaves and inoculated plants, but not from the controls. N. oryzae is a known pathogen of several hosts, such as Costus speciosus (Koen.) Sm. and Mentha spicata L., but has not been reported on any species of Populus. To our knowledge, this is the first report of leaf blight of ‘PaPb poplar’ caused by N. oryzae in China and the world. This disease could affect growth and development of ‘PaPb poplar’ seedlings, and may cause economic losses in the future. Appropriate strategies should be developed to manage this disease.


Plant Disease ◽  
2013 ◽  
Vol 97 (1) ◽  
pp. 147-147 ◽  
Author(s):  
J. Hrustić ◽  
M. Mihajlović ◽  
B. Tanović ◽  
G. Delibašić ◽  
I. Stanković ◽  
...  

In August 2011, nectarine (Prunus persica (L.) Batsch var. nucipersica (Suckow) C. K. Schneid) fruit originated from Oplenac region with symptoms of fruit rot was collected at a green market in Belgrade. Fruit had large, brown, sunken lesions covered with grayish brown tufts. Symptoms resembled those caused by species of Monilinia including M. laxa, M. fructigena, or M. fructicola (2). In order to isolate the causal organism, small superficial fragments of pericarp were superficially disinfected with commercial bleach and placed on potato dextrose agar (PDA). The majority (32 out of 33) isolates formed rosetted non-sporulating colonies with lobed margins resembling those of M. laxa. However, one isolate (Npgm) produced an abundant, grayish-white colony with even margins and concentric rings of sporogenous mycelium, resembling those described for M. fructicola (2). Conidia were one-celled, hyaline, ellipsoid to lemon shaped, 7.38 to 14.76 × 4.92 to 9.84 μm, and borne in branched monilioid chains. The average daily growth on PDA at 24°C was 10.9 mm. A single-spore isolate of Npgm was identified as M. fructicola based on the morphology of colony and conidia, temperature requirements, and growth rate (2). Morphological identification was confirmed by an amplified product of 535 bp using genomic DNA extracted from the mycelium of pure culture and species-specific PCR for the detection of M. fructicola (2). The ribosomal internal transcribed spacer (ITS) region of rDNA of Npgm was amplified and sequenced using primers ITS1/ITS4. Sequence analysis of ITS region revealed 100% nucleotide identity between the isolate Npgm (GenBank Accession No. JX127303) and 17 isolates of M. fructicola from different parts of the world, including four from Europe (FJ411109, FJ411110, GU967379, JN176564). Pathogenicity of the isolate Npgm was confirmed by inoculating five surface-disinfected mature nectarine and five apple fruits by placing a mycelial plug under the wounded skin of the fruit. Nectarine and apple fruits inoculated with sterile PDA plugs served as a negative controls. After a 3-day incubation at 22°C, inoculated sites developed brown lesions and the pathogen was succesfully reisolated. There were no symptoms on the control nectarine or apple fruits. M. fructicola is commonly present in Asia, North and South America, New Zealand, and Australia, while in the EPPO Region the pathogen is listed as an A2 quarantine organism (3). In Europe, the first discovery of M. fructicola was reported in France and since then, it has been found in Hungary, Switzerland, the Czech Republic, Spain, Slovenia, Italy, Austria, Poland, Romania, Germany, and Slovakia (1). Most recently, M. fructicola was found on stored apple fruits in Serbia (4). To our knowledge, this is the first report of M. fructicola decaying peach fruit in Serbia. These findings suggest that the pathogen is spreading on its principal host plants and causing substantial economic losses in the Serbian fruit production. References: (1) R. Baker et al. European Food Safety Authority. Online publication. www.efsa.europa.eu/efsajournal . EFSA J. 9:2119, 2011. (2) M. J. Côté. Plant Dis. 88:1219, 2004. (3) OEPP/EPPO. EPPO A2 list of pests recommended for regulation as quarantine pests. Version 2009-09. http://www.eppo.org/QUARANTINE/listA2.htm . (4). M. Vasic et al. Plant Dis. 96:456, 2012.


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