scholarly journals Leaf spots of calibrachoa caused by Nigrospora oryzae

2020 ◽  
Vol 26 (4) ◽  
pp. 591-597
Author(s):  
Nicolás Pablo Borrelli ◽  
Santiago Stancanelli ◽  
Mirta Leonor Papone ◽  
María Virginia Moreno ◽  
Sebastián Stenglein ◽  
...  

Abstract Calibrachoa hybrida (calibrachoa, million bells) is a flowering ornamental with increasing importance due to the existence of many successful cultivars for growing indoors in containers and planting in the garden and landscape. The outstanding characteristic is a profuse flowering and intense colour. In October 2019, a fungal isolate was obtained from basal calibrachoa leaves with irregular brown leaf spots, in plants cultivated in Buenos Aires, Argentina. The aim of the present study was to identify the cause of the disease in this ornamental genus, to expand knowledge about prevalent pathologies. The isolate was identified using morphological and molecular markers, and the pathogenicity tests were fulfilled. This paper reports that Nigrospora oryzae is pathogenic to calibrachoa, which seems to be the first record of this leaf spot disease in the world.

Plant Disease ◽  
2013 ◽  
Vol 97 (9) ◽  
pp. 1256-1256 ◽  
Author(s):  
L. F. Zhai ◽  
J. Liu ◽  
M. X. Zhang ◽  
N. Hong ◽  
G. P. Wang ◽  
...  

Aloe vera L. var Chinese (Haw) Berg is a popular ornamental plant cultivated worldwide, whose extracts are used in cosmetics and medicine. Aloe plants are commonly affected by leaf spot disease caused by Alternaria alternata in Pakistan, India, and the United States (1). An outbreak of Alternaria leaf spot recently threatened aloe gel production and the value of ornamental commerce in Louisiana (1). During the summer of 2011, leaf spot symptoms were observed on A. vera plants growing in several greenhouses and ornamental gardens in Wuhan, Hubei Province, China. In two of the greenhouses, disease incidence reached 50 to 60%. The initial symptoms included chlorotic and brown spots that expanded to 2 to 4 mm in diameter and became darker with age. Lesions also developed on the tips of 30 to 50% of the leaves per plant. In severe infections, the lesions coalesced causing the entire leaf to become blighted and die. In September of 2012 and February of 2013, 10 symptomatic A. vera leaves were collected randomly from two greenhouses and gardens in Wuhan. A fungus was consistently recovered from approximately 80% of the tissue samples using conventional sterile protocols, and cultured on potato dextrose agar (PDA). The colonies were initially white, becoming grey to black, wool-like, and growing aerial mycelium covering the entire petri dish (9 cm in diameter) plate within 5 days when maintained in the dark at 25°C. The conidia were brown or black, spherical to subspherical, single celled (9 to 13 μm long × 11 to 15 μm wide), borne on hyaline vesicles at the tip of conidiophores. The conidiophores were short and rarely branched. These colonies were identified as Nigrospora oryzae based on the described morphological characteristics of N. oryzae (2). Genomic DNA was extracted from a representative isolate, LH-1, and the internal transcribed spacer region was amplified using primer pair ITS1/ITS4 (3). A 553-bp amplicon was obtained and sequenced. The resulting nucleotide sequence (GenBank Accession No. KC519728) had a high similarity of 99% to that of strain AHC-1 of N. oryzae (JQ864579). Pathogenicity tests for strain LH-1 were conducted in triplicate by placing agar pieces (5 mm in diameter) containing 5-day-old cultures on A. vera leaves. Four discs were placed on each punctured surface of each leaf. Noncolonized PDA agar pieces were inoculated as controls. Leaves were placed in moist chambers at 25°C with a 12-h photoperiod. After 3 days, the inoculated leaves showed symptoms similar to those observed in the greenhouses. N. oryzae was reisolated from these spots on the inoculated leaves. No visible symptoms developed on the control leaves. The pathogenicity tests were performed twice with the same results. Based on the results, N. oryzae was determined as a pathogen responsible for the leaf spots disease on A. vera. N. oryzae has been described as a leaf pathogen on fig (Ficus religiosa), cotton (Gossypium hirsutum) and Kentucky bluegrass (Poa pratensis) (4), and to our knowledge, this is the first report of N. oryae causing leaf spot disease on A. vera worldwide. References: (1) W. L. da Silva and R. Singh. Plant Dis. 86:1379, 2012. (2) M. B. Ellis. Dematiaceous Hyphomycetes, CAB, Kew, Surrey, England, 1971. (3) T. J. White et al. PCR Protocols: A Guide to Methods and Applications. Academic Press, San Diego, 1990. (4) L. X. Zhang et al. Plant Dis. 96:1379, 2012.


2017 ◽  
Vol 57 (37) ◽  
pp. 473
Author(s):  
José Matias Rusconi ◽  
Maria Fernanda Achinelly ◽  
Nora Beatriz Camino

Thelastomatidae is one of the largest families parasitizing insects, within the order Oxyurida. In this work we reported parasitism in nymphs and adults of Neocurtilla claraziana by two different thelastomatid species as a part of a field survey on agricultural pests. Nymphs and adults of this insect were isolated from grasslands of Buenos Aires State, Argentina using a tensio-active solution. The nematode species Gryllophila skrjabini Sergiev, 1923 and Cephalobellus magalhaesi Schwenk, 1926 are briefly described and measurements are given. Both nematodes are reported for the first time in Argentina with C. magalhaesi being the second isolation of this species in the world. Neocurtilla clarziana is a new host record for G. skrjabini.


Plant Disease ◽  
2010 ◽  
Vol 94 (2) ◽  
pp. 274-274 ◽  
Author(s):  
G. Polizzi ◽  
D. Aiello ◽  
G. Parlavecchio ◽  
A. Vitale ◽  
F. Nigro

Dwarf willow myrtle (Agonis flexuosa (Willd.) Sweet) cv. Nana, an evergreen ornamental shrub belonging to the Myrtaceae, is grown in Italy as an ornamental potted plant. In November 2008, a widespread new leaf spot disease was noticed on ~80% of 5,000 6-month-old potted plants. Plants were obtained from cuttings and produced by a commercial nursery in Catania Province. Symptomatic leaves showed minute, reddish brown spots that enlarged (3 to 5 mm in diameter) and then darkened, presenting a necrotic center defined by a dark purple halo. Leaf spots were surface disinfested with 0.8% NaOCl and plated on potato dextrose agar. Twenty isolates of the fungus that was consistently isolated from the spots were selected and cultured for 8 days at 25°C on carnation leaf agar (CLA). Macroconidiophores consisted of a stipe, a penicillate arrangement of fertile branches, and stipe extension terminating in an obpyriform to ellipsoidal vesicle (6 to 10 μm in diameter). Cylindrical conidia were rounded at both ends, straight, one-septate, and ranged from 44 to 60 × 4 to 5 μm. The fungus was tentatively identified as Cylindrocladium pauciramosum based on these morphological characteristics (2). All single-conidium isolates were mated with tester strains of Calonectria pauciramosa C. L. Schoch & Crous, telomorph of C. pauciramosum, on CLA and produced fertile perithecia (4). Perithecia were solitary or in groups, orange to red-brown, subglobose to ovoid, and ranged from 280 to 400 μm long × 180 to 290 μm in diameter. Further confirmation of species was obtained by amplification and sequencing of the intergenic spacer (IGS) region of rDNA, using M13 Forward (-20) and M13 Reverse primers. On the basis of the complete IGS sequence, two primer sets (218F/218R and 106F/106R) were designed and successfully used in a nested-PCR protocol for the detection of C. pauciramosum from tissues of infected plants (3). On the basis of the combination of morphological characters, mating type, and molecular data, the isolates were identified as C. pauciramosum C.L. Schoch & Crous. One representative isolate (DISTEF-Af1) was deposited at Centraalbureau voor Schimmelcultures open fungi collection (Fungal Biodiversity Centre, Utrecht, the Netherlands; CBS 124659). Pathogenicity tests were performed by adding sterile water to CLA cultures of C. pauciramosum from a single-conidium isolate (DISTEF-Af1) and spraying the resulting spore suspension (105 conidia per ml) on the leaf surface of 20 6-month-old A. flexuosa cv. Nana potted plants. The same number of plants served as noninoculated controls. Following inoculation, plants were kept in plastic bags in a growth chamber at 25 ± 1°C. All inoculated plants developed circular, brown leaf spots identical to those observed in the nursery 5 to 7 days after inoculation. Control plants remained symptomless. C. pauciramosum was always reisolated from the infected plants and identified as previously described. Leaf spotting in seedlings of A. flexuosa was previously associated with infections by C. scoparium in Australia (1). To our knowledge, this is the first record in the world of leaf spots caused by C. pauciramosum on A. flexuosa. References: (1) A. L. Bertus. Agric. Gaz. N. S. W. 87:22, 1976. (2) P. W. Crous. Taxonomy and Pathology of Cylindrocladium (Calonectria) and Allied Genera. The American Phytopathological Society, St. Paul MN, 2002. (3) F. Nigro et al. J. Plant Pathol. 88:S22, 2006. (4) G. Polizzi and P. W. Crous. Eur. J. Plant Pathol. 105:407, 1999.


Plant Disease ◽  
2001 ◽  
Vol 85 (9) ◽  
pp. 1028-1028 ◽  
Author(s):  
A. Karakaya

Circular to irregular brown leaf spots, 0.2 to 1.5 cm in diameter, were commonly observed on kiwifruit (Actinidia deliciosa) cv. Hayward plants in the Artvin-Arhavi region of northeastern Turkey. Leaf spots sometimes covered large portions of infected leaves, giving them a blighted appearance. Fruit symptoms consisted of brown, sunken, shriveled areas that were 0.5 to 3 cm in diameter. A fungus, later identified as a Pestalotiopsis sp. (1), was consistently isolated from diseased tissues. Pathogenicity tests were performed on 2-year-old kiwifruit plants and mature fruits at 18/22°C (day/night). A spore suspension (1 × 106 conidia per ml) was sprayed on leaves of 2-year-old kiwifruit plants. Agar pieces, 3 mm in diameter, from 10-day-old cultures also were applied to the leaves. Controls were treated with water and agar alone. Plants were covered with plastic bags for 3 days to ensure high humidity. After 2 weeks, disease symptoms were observed on inoculated leaves. Pestalotiopsis sp. was consistently isolated from these regions. Agar pieces from 10-day-old cultures were placed in small wounds made on the surfaces of mature, surface-disinfested fruits. Controls were treated with agar pieces alone. Softening of tissues next to the wound was observed 1 week after inoculation. Pestalotiopsis sp. was isolated from these areas. No symptoms were observed on noninoculated leaves or fruits. It was concluded that this disease is caused by Pestalotiopsis sp. This is the first report of its occurrence in Turkey. Reference: (1) T. R. Nag Raj. Coelomycetous anamorphs with appendage bearing conidia. Mycologue Publications, Ontario, Canada, 1993.


2021 ◽  
Vol 24 (2) ◽  
pp. 141-148
Author(s):  
Julieta De Pasqua ◽  
Federico Agnolin ◽  
Alexis M. Aranciaga Rolando ◽  
Sergio Bogan ◽  
Diego Gambetta

Carcharocles megalodon is considered a macropredatory shark that inhabited the seas around the world from middle Miocene to late Pliocene. In Argentina, it has only been formally recorded at two localities. Here, we report the first record for this taxon in the Buenos Aires Province. This occurrence is based on an isolated tooth recovered on the beach at the Punta Médanos locality, which lacks clear stratigraphic context. Based on the regional geology, the specimen probably came from Pliocene beds. Its size indicates that it probably belongs to a juvenile individual. Keywords: Carcharocles megalodon, macropredatory shark, fossil teeth, Mar de Ajó.


Plant Disease ◽  
2011 ◽  
Vol 95 (6) ◽  
pp. 771-771 ◽  
Author(s):  
Q. Bai ◽  
Y. Xie ◽  
J. Gao ◽  
B. Lu ◽  
W. Wang ◽  
...  

Fraxinella, Dictamnus dasycarpus Turcz (Rutaceae), is a perennial herbal plant and mainly distributed in Eurasia and North America. It is often used to treat jaundice, cough, rheumatism, and other diseases and is extensively cultivated in the northeast and northwest of China (3). In June 2009, a severe foliar disease was observed on D. dasycarpus in medicinal plantations in Antu, China. The disease occurred on 100% of the plants and at least 25% of the surface was affected. In the early stages of disease development, symptoms were visible on the top and bottom of infected leaves as small brown spots. Subsequently, these spots became elliptical to irregularly shaped, with beige or grayish white centers and dark brown margins. Within the spots, numerous, dark brown or black, subglobose or ostiolate pycnidia measuring 152 to 367 μm in diameter were observed. Fungal isolates were obtained from the infected leaves on potato dextrose agar (PDA) medium, with conidia that were aseptate or one-septate and ellipsoidal or reniform, measuring approximately 4.7 to 12.6 × 2.1 to 4.5 μm. On the basis of these characteristics, the fungus was identified as a Phoma sp. Four well-sporulating isolates, designated as DdPh-1, DdPh-2, DdPh-3, and DdPh-4, were selected for further studies. The morphological and cultural characteristics of these four isolates were studied as described by Boerema et al. and the fungus was identified as Phoma dictamnicola Boerema et al. (1). The internal transcribed spacer (ITS) region of the nuclear rDNA was amplified and sequenced using primers ITS4/ITS5 (2). All four of the ITS sequences were identical (GenBank Accession No. FR681861) and were 99% identical to P. dictamnicola strains CBS507.91 (Accession No. GU237877) and KACC42445 (Accession No. EF600960). Pathogenicity tests were performed by spraying the leaves of healthy D. dasycarpus plants with a conidial suspension (1 × 106 conidia/ml). Five plants were inoculated with each isolate (DdPh-1, DdPh-2, DdPh-3, and DdPh-4) and five plants were mock inoculated with sterile water. The plants were covered with plastic bags and kept in a greenhouse at 20 to 25° for 72 h. After 9 to 13 days, all inoculated plants showed characteristic symptoms as previously described, while the control plants remained healthy. The fungus was reisolated from the leaf spots of inoculated plants. Currently, the economic importance of this disease is limited, but it may become a more significant problem in production of D. dasycarpus with the cultivation area increasing. The fungus was found in the Netherlands and Korea, but to our knowledge, this is the first report of P. dictamnicola on D. dasycarpus in China. References: (1) G. H. Boerema et al. Phoma Identificatión Manual: Differentiation of Specific and Infra-Specific Taxa in Culture. CABI Publishing. Wallingford, U.K., 2004. (2) D. E. L. Cooke et al. Mycol. Res. 101:667, 1997. (3) S. S. Jiang et al. Biosci. Biotechnol. Biochem. 72:660, 2008.


Plant Disease ◽  
2002 ◽  
Vol 86 (4) ◽  
pp. 440-440 ◽  
Author(s):  
H. B. Lee ◽  
C.-J. Kim

A zonate leaf spot disease on a wild bean variety, Vigna vexillata L. var. tsusimensis Mat., occurred in the patch fields and foothills of Chungnam and Kyonggi districts in Korea during late September, October, and early November of 1999 to 2001. The zonate lesions were particularly prevalent in October following periods of heavy dew accumulation. Initial symptoms were small, circular lesions with darkbrown marginal rings that later developed into large spots with characteristic target-shaped rings. The spots were gray to bright or blackish brown, progressed rapidly, and sometimes fused together to form lesions of up to 20 mm in diameter. Sporophores on the natural host were generally hypophyllous but sometimes amphigenous, abundant on large spots, fewer on small spots, solitary, erect, easily detachable, and up to 864 μm long. The upper portion of the sporophore is considered an individual conidium and consisted of a pyramidal head that was fusiform to ventricose and cristulate, 495 to 534 μm long, and 210 to 290 μm wide at the broadest point. Branches within the pyramidal head were short and compact, and dichotomously or trichotomously branched. The central axis within the conidium was hyaline, broad, septate, tapering toward an acute apex, and sometimes constricted at the basal septum. Conidiophores were 272 to 330 μm long and up to 24 μm wide. The fungus was identified as Cristulariella moricola (Hino) Redhead based on morphological characteristics (1,2). The fungus was isolated from Vigna leaf spots, placed on 2% water agar or potato dextrose agar (PDA), and maintained on PDA amended with 2% Vigna leaf extract. For pathogenicity tests, 4- to 5-week-old leaves of V. vexillata var. tsusimensis were surface-sterilized in 1% NaOCl. Agar disks (approximately 10 mm diameter) containing mycelia of the fungus were placed on the upper leaf surface. The inoculated plants (two leaflets per plant × 2) were then sprayed with distilled water, covered with premoistened polyethylene bags, and incubated at 15 to 25°C. Within 5 days, small leaf spots appeared that were similar to those originally observed on all inoculated leaflets. Uninoculated control leaves exposed to the same environmental conditions remained healthy. C. moricola was consistently reisolated from the infected leaves. The hyphomycete fungus C. moricola has been known to cause a bull's eye or zonate leaf spot and defoliation on woody and annual plants, including at least 73 host species and 36 families distributed in the central and eastern United States and Japan (1). In Asia, the occurrence of Cristulariella spp. on several hosts has been reported only in Taiwan and Japan (3,4). No species in the genus has ever been reported from Korea. To our knowledge, V. vexillata var. tsusimensis represents a previously unreported host for C. moricola. References: (1) M. C. Niedbalski et al. Mycologia 75:988, 1983. (2) S. A. Redhead. Mycologia 71:1248, 1979. (3). H. J. Su and S. C. Leu. Plant Dis. 67:915, 1983. (4) T. Yokoyama and K. Tubaki. Trans. Mycol. Soc. Jpn. 15:189, 1974.


Plant Disease ◽  
2015 ◽  
Vol 99 (3) ◽  
pp. 415-415 ◽  
Author(s):  
M. O. Jibrin ◽  
S. Timilsina ◽  
N. Potnis ◽  
G. V. Minsavage ◽  
K. C. Shenge ◽  
...  

Bacterial spot (BS) is an important disease of tomato in Nigeria (2). Although a xanthomonad was isolated from tomato in Nigeria and characterized using phenotypic and pathogenicity tests, the bacterium was not characterized genetically to confirm the species. To determine the species associated with BS, leaves were collected in fields in northwestern Nigeria from tomato plants showing typical BS symptoms, which consisted of dark, irregular-shaped brown leaf spots that coalesced, resulting in a blighted appearance. Isolations from individual lesions were made on nutrient agar (NA). Yellow, mucoid colonies typical of Xanthomonas were isolated from 14 lesions and all were determined to be amylolytic (3). To determine the races of these strains, bacterial suspensions of the tomato strains, derived from 24-h cultures grown on NA at 28°C, were adjusted to 108 CFU/ml and infiltrated into leaves of tomato and pepper differential genotypes (5). The tomato strains elicited hypersensitive reactions (HRs) on the four pepper differential lines and an HR on the tomato genotype FL 216, which contains the R gene Xv3, but elicited susceptible reactions on the tomato genotypes Hawaii 7998 and Bonny Best. These reactions are typical of X. perforans tomato race 3 strains (5). Multilocus sequence analysis (MLSA) of six housekeeping genes (fusA, lacF, gyrB, gltA, gapA, and lepA) was used to further analyze four representative strains (1) (GenBank Accession Nos. KJ938581 to KJ938584, KJ938588 to KJ938591, KJ938595 to KJ938598, KJ938602 to KJ938605, KJ938629 to KJ938632, and KJ938636 to KJ938639, respectively). A partial sequence of hrpB2 was also made since the four Xanthomonas species associated with BS can be differentiated based on sequence divergence of this gene (3) (KJ938609 to KJ938621 and KJ938628). The housekeeping gene sequences were aligned along with other Xanthomonas sequences imported from the National Center for Biotechnology Information (NCBI) database ( www.ncbi.nlm.nih.gov ) using the MUSCLE tool from MEGA software, 5.2.2. Maximum likelihood phylogenetic trees constructed for the six housekeeping gene sequences individually and in concatenation revealed that the strains grouped most closely with the X. euvesicatoria reference strain 85-10 but more distantly to X. perforans. The hrpB2 sequence, which is highly conserved for each Xanthomonas species pathogenic on tomato (4), was sequenced from the tomato strains. These sequences were identical to the hrpB2 sequence from X. perforans strains but different from X. euvesicatoria. Although BS is common in Nigeria, to our knowledge, this represents a unique group of X. euvesicatoria strains from tomato that are identical to X. perforans based on pathogenic reactions on tomato and pepper and hrpB2 sequence identity but are more closely related to X. euvesicatoria based on the six housekeeping gene sequences. References: (1) N. F. Almeida et al. Phytopathology 100:208, 2010. (2) E. U. Opara and F. J. Odibo. J. Mol. Genet. 1:35, 2009. (3) J. B. Jones et al. Syst. Appl. Microbiol. 27:755, 2004. (4) A. Obradovic et al. Eur. J. Plant Pathol. 88:736, 2004. (5) R. E. Stall et al. Annu. Rev. Phytopathol. 47:265, 2009.


Plant Disease ◽  
2020 ◽  
pp. PDIS-12-18-2181
Author(s):  
X.-D. Sun ◽  
X.-L. Cai ◽  
Q.-Q. Pang ◽  
M. Zhou ◽  
W. Zhang ◽  
...  

Plant Disease ◽  
1999 ◽  
Vol 83 (7) ◽  
pp. 694-694 ◽  
Author(s):  
S. T. Koike ◽  
D. M. Henderson ◽  
S. A. Tjosvold ◽  
E. G. Simmons

Saponaria (Saponaria vaccaria [= Vaccaria hispanica]) is a Caryophyllaceae plant that is grown commercially in California as a cut flower. In 1998, a leaf spot disease devastated the commercially grown saponaria in coastal California. The entire saponaria crop was completely unmarketable because of extensive leaf spotting. Symptoms consisted of circular, brown, necrotic leaf spots with diameters up to 8 mm and concentric zones of lighter and darker tissue. Chlorotic borders developed around the spots. Conidia from leaves were obclavate, usually had 7 transverse and 1 to 4 longitudinal septa, and narrowed gradually toward the apex into a blunt-tipped, unbranched beak cell. The spore body measured 69 to 90 (to 119) × 17 to 21 (to 25) μm, with the distinctive beak cell 17 to 53 μm long. Conidia formed short chains on host tissue. The fungus was identified as Alternaria saponariae (Peck) Neergaard (2). For pathogenicity tests, six representative isolates were grown on V8 juice agar under fluorescent tube lighting. Potted saponaria were sprayed with either conidial concentrations (1 × 10e5 conidia per ml) or water. Plants were incubated in a chamber with a humidifier for 48 h and then maintained in a greenhouse (23 to 25°C). After 14 days, leaf spots similar to the original symptoms developed on all inoculated plants, and the pathogen was reisolated. Plants sprayed with water were symptomless. The experiment was repeated and the results were similar. Using the same isolates and method, we inoculated carnation (Dianthus caryophyllus), sweet William (Dianthus barbatus), and saponaria. However, disease developed only on saponaria. While A. saponariae on saponaria was reported previously in California (1), this is the first report to characterize the pathogen and document that isolates are pathogenic on saponaria but not on other commercial Caryophyllaceae hosts. References: (1) K. F. Baker and L. H. Davis. Plant Dis. Rep. 34:403, 1950. (2) P. Neergaard. Aarsberet. J. E. Ohlsens Enkes Plantepat. Lab. No. 3, 1938.


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