scholarly journals Nigrospora sphaerica Causing Leaf Spot and Twig and Shoot Blight on Blueberry: A New Host of the Pathogen

Plant Disease ◽  
2008 ◽  
Vol 92 (1) ◽  
pp. 171-171 ◽  
Author(s):  
E. R. Wright ◽  
M. Folgado ◽  
M. C. Rivera ◽  
A. Crelier ◽  
P. Vasquez ◽  
...  

Blueberries (Vaccinium corymbosum) have recently become an important alternative crop in different ecological regions of Argentina. In surveys, a new disease characterized by leaf spots and twig and shoot blight has been observed on plants cultivated in Arrecifes, Mercedes, and San Pedro (provinces of Buenos Aires) and Concordia (province of Entre Ríos) since July 2004. Spots initially appear brown, circular, 1 to 2 mm in diameter, and irregularly distributed on the leaves and they eventually coalesce. Fruiting twig and shoot blight developed from the tips toward the base. Affected plants of cvs. O'Neal and Reveille were distributed randomly in the field and with a low incidence (average of 2%). The objective of this work was to identify the causal agent of this disease. Symptomatic plant material was surface disinfested with 0.2% NaOCl for 1 min and 70% ethanol for 1 min, washed once with sterile distilled water, blotted dry with paper towels, and plated on potato dextrose agar. Colonies were initially white, becoming light to dark gray with the onset of sporulation with black, sphaerical to subsphaerical conidia that measured 14 to 19 × 12 to 16 μm. These characteristics agree with published descriptions of Nigrospora sphaerica (Sacc.) Mason (1,4). To evaluate pathogenicity, all leaves, petioles, and stems of seven healthy potted plants of cv. O'Neal were punctured with flamed needles and sprayed with a suspension of 1 × 108 spores of the fungus per milliliter of sterile distilled water. Another seven nonwounded plants were sprayed with the spore suspension. Seven plants similarly injured and seven nonwounded plants were sprayed with sterile distilled water and served as controls. Each plant was covered with a water-sprayed polyethylene bag and maintained in a controlled environment chamber at 20°C with a 12-h photoperiod. The bags were removed after 3 days. All wounded inoculated plants began to show disease symptoms similar to those observed in the field 20 days after inoculation. Controls and nonwounded inoculated plants remained symptomless. The pathogen was reisolated from diseased tissues fulfilling Koch's postulates. N. sphaerica is a well-known saprophyte on many plant species but has been mentioned as pathogen on many hosts (2,3). To our knowledge, this is the first reference of N. sphaerica as a wound pathogen of blueberry. In the field, the fungus would have gained access to the plant through wounds caused by insects or frost after a long-term wetness duration. References: (1) M. B. Ellis. Dematiaceous Hyphomycetes. CMI, Kew, Surrey, UK, 1971. (2) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. American Phytopathological Society, St. Paul, MN, 1989. (3) D. F. Farr et al. Fungal Databases. Systematic Botany and Mycology Laboratory. Online publication. ARS, USDA. 2007. (4) E. W. Mason. Trans. Brit. Mycol. Soc. 12:152, 1927.

Plant Disease ◽  
2011 ◽  
Vol 95 (11) ◽  
pp. 1478-1478 ◽  
Author(s):  
B. A. Pérez ◽  
M. F. Berretta ◽  
E. Carrión ◽  
E. R. Wright

In 2009, a highbush blueberry (Vaccinium corymbosum L. ‘O'Neal’) field located in Rojas, Buenos Aires Province showed 30% of plants with dry or dead branches. Disinfected root pieces were placed on water agar and incubated at 24°C. A fungal colony was obtained and purified by successive transfers of an individual hyphal tip from a sparsely growing colony. Colony color and growth rate were evaluated in potato dextrose agar where the fungus produced white-to-pale pink colonies and grew 3.5 cm after 5 days. The fungus was studied on Spezieller Nährstoffarmer agar (2), carnation leaf-piece agar, and KCl agar where it produced abundant single-celled hyaline microconidia in moderate-length chains and in false heads originated from monophialides and polyphialides. Microconidia measured 6 to 12 × 2 to 3 μm (average 8 × 2.3 μm). On KCl, chains of microconidia and tan-to-light cream sporodochia with 3- to 5-septate, slender, relatively straight macroconidia were easily observed after 4 and 10 days, respectively. Macroconidia measured 38 to 48 × 3.5 to 4 μm (average 43.9 × 3.9 μm). Chlamydospores and sclerotia were not present. Data coincided with the description for Fusarium proliferatum (Matsush.) Niremberg ex Gerlach & Niremberg. The isolate was deposited in the IMYZA Microbial Collection as INTA-IMC 144. The fungus was cultured in 100 ml of Czapek-Dox supplemented with sucrose, peptone, yeast extract, sodium nitrate, and vitamins for 4 days. Genomic DNA was obtained with a DNA extraction kit, PCR amplified with primers ITS1 and ITS4 for the internal transcribed spacer (ITS) region of ribosomal genes, and sequenced. The nucleotide sequence (Accession No JF913468) was compared with GenBank records. The sequence shared 99% identity with Accession No HQ113948 for F. proliferatum. Pathogenicity was confirmed in 1-year-old ‘O'Neal’ plants. A 10-ml suspension (2.4 × 106 conidia/ml in sterile distilled water) was applied to six potted plants grown in sterilized potting mix. Roots were superficially wounded with a needle. Control plants were treated with sterile distilled water. Plants were incubated at 24°C and a 12-h photoperiod. After 90 days, plants showed root rot, leaf chlorosis, and branch necrosis followed by plant death. Control plants remained healthy. F. proliferatum was reisolated from diseased roots of inoculated plants. This fungus was previously cited in Argentina on asparagus (1), corn (1,3), and oat (4). To our knowledge, this is the first report of F. proliferatum as a root pathogen of highbush blueberry in Argentina. References: (1) G. Lori et al. Plant Dis. 82:1405, 1998. (2) H. I. Nirenberg. Releases Fed. Biol. Res. Ctr. Agric. For. (Berlin-Dahlem) 169:1, 1976. (3) D. A. Sampietro et al. Fung. Biol. 114:74, 2010. (4) S. A. Stenglein et al. Plant Dis. 94:783, 2010.


Plant Disease ◽  
2007 ◽  
Vol 91 (5) ◽  
pp. 639-639 ◽  
Author(s):  
P. Vasquez ◽  
J. A. Baldomá ◽  
E. R. Wright ◽  
A. Pérez ◽  
M. Divo de Sesar ◽  
...  

Since 2003, a new field disease has been observed on several cultivars of highbush blueberry (Vaccinium corymbosum L.) in Buenos Aires (Baradero, Colonia Urquiza, Lima, Mercedes, and San Pedro), Entre Ríos (Concordia, Gualeguaychú, and Larroque), and Córdoba (Capilla del Monte and La Cumbre). Infected flowers turned brown to tan with a water-soaked appearance and shriveled up. Blighted flowers typically did not produce fruits; even an entire cluster of berries could be aborted. A chlorotic area, that later became necrotic and turned light brown, developed when leaves were in contact with blighted flowers. A watery rot developed on fruit occasionally before harvest but more generally after harvest. Infected tender green twigs also became blighted, with leaf tissue becoming brown to black. Older twigs and stems were also blighted. Abundant, gray mycelium with conidial masses developed on all affected tissues under moist conditions. Sections of infected leaves, twigs, stems, flowers, and fruits were surfaced sterilized with 0.2% NaOCl, plated on 2% potato dextrose agar (pH 7), and incubated at 22°C. Pure cultures formed a whitish dense mycelial mat and turned gray after 72 h. Conidia were ellipsoid, hyaline, nonseptate, and formed on botryose heads. They ranged from 5.8 to 9 × 8.1 to 13.7 μm (average 8.6 × 10.2 μm). Black, round, and irregular microsclerotia developed on 7-day-old cultures with an average size of 1.1 × 1.7 mm. Morphological characteristics agree with those described for Botrytis cinerea Pers.:Fr (1). Pathogenicity was tested on 10 12-month-old potted blueberry plants cv. O'Neal by spraying a suspension of 1 × 106 conidia per ml of sterile distilled water. Ten plants used as controls were sprayed with sterile distilled water. Each plant was covered with a transparent polyethylene bag for 48 h and incubated at 20 ± 2°C in humid chambers for 15 days. Lesions similar to those observed in the fields developed after 4 days and asexual fructifications developed after 5 days. The same pathogen was reisolated from the lesions, thus completing Koch's postulates. Water-treated plants remained symptomless. To our knowledge, this is the first report of a disease caused by B. cinerea on blueberry in Buenos Aires, Córdoba, and Entre Ríos provinces of Argentina. References: (1) M. V. Ellis and J. M. Waller. Sclerotinia fuckeliana (conidial state: Botrytis cinerea) No. 431 in: Descriptions of Pathogenic Fungi and Bacteria. CMI, Kew, Surrey, UK, 1974.


Plant Disease ◽  
2011 ◽  
Vol 95 (2) ◽  
pp. 219-219 ◽  
Author(s):  
S. Soylu ◽  
S. Dervis ◽  
E. M. Soylu

Chinese wisteria, Wisteria sinensis (Sims) DC., is a woody, twining vine and is commonly cultivated as an ornamental for its foliage and striking, drooping racemes of white, pink, or lavender sweet pea-like flower. Distinct leaf spots were observed in several gardens, retail nurseries, and parks located in Hatay Province since May 2009. The primary infection zones are frequently observed on the leaf margins and apices, brown, up to 2 mm in diameter, and often surrounded by a yellow zone. Foliar symptoms are characterized by grayish, round, semicircular or irregular-shaped, numerous spots (up to 9 mm in diameter) with dark brown borders and the appearance of black, granular structure within the dead leaf tissues. A fungus was consistently isolated from symptomatic tissues on potato dextrose agar (PDA). Fungal colonies were initially white, becoming light to dark gray with the onset of sporulation with black, spherical to subspherical single-celled conidia (15 to 18 × 12 to 15 μm), which were borne on a hyaline vesicle at the tip of the conidiophore. These characteristics agree with published descriptions of Nigrospora sphaerica (Sacc.) E.W. Mason 1927 (1,3). To fulfill Koch's postulates, a conidial suspension (106 conidia per ml) collected from PDA cultures was used to spray inoculate leaves of potted 3-year-old Chinese wisteria plants. Inoculated plants were kept for 48 h in polyethylene bags and maintained in a controlled environment chamber at 20°C with a 12-h photoperiod. The bags were removed after 3 days. In addition, five 3-year-old plants were sprayed with sterile water to serve as controls. After 14 to 20 days, inoculated leaves showed infection symptoms similar to those observed on naturally infected leaves with N. sphaerica. The pathogen was reisolated from the margins of necrotic tissues, but not from the controls. Although N. sphaerica is frequently encountered as a secondary invader or as a saprophyte on many plant species, this fungal agent is also known as a leaf pathogen on several hosts worldwide (2,4). To our knowledge, this is the first report of N. sphaerica as a leaf pathogen of Chinese wisteria in Turkey or worldwide. References: (1) M. B. Ellis. Dematiaceous Hyphomycetes. CMI, Kew, Surrey, UK, 1971. (2) D. F. Farr and A. Y. Rossman. Fungal Databases. Systematic Mycology and Microbiology Laboratory. Online publication. ARS, USDA. Retrieved 28 October from http://nt.ars-grin.gov/fungaldatabases/ , 2010. (3) P. M. Kirk. IMI Descr. Fungi Bact. 106:1056, 1991. (4) E. R. Wright et al. Plant Dis. 92:171, 2008.


Plant Disease ◽  
2004 ◽  
Vol 88 (12) ◽  
pp. 1383-1383 ◽  
Author(s):  
E. R. Wright ◽  
M. C. Rivera ◽  
J. Esperón ◽  
A. Cheheid ◽  
A. Rodríguez Codazzi

Disease symptoms have been observed since October 1997 on highbush blueberry (Vaccinium corymbosum L.) cvs. Georgia Gem, O'Neal, and Sharpblue cultivated in Buenos Aires. Lesions were observed on recently planted, as well as mature plants, in commercial fields. Circular-to-irregular, light brown-to-gray leaf spots with brownish red borders, initially 3 to 7 mm in diameter, enlarged and coalesced. Blight developed on twigs. Reddish circular spots appeared on stems, developing small cankers. Dark sunken lesions were observed on attached ripening berries. During December 2002, postharvest fruit rot was noted. Small pieces of diseased leaves, twigs, stems, and fruits were surface sterilized with 0.2% NaOCl, plated on 2% potato dextrose agar (pH 7), and incubated at 20 ± 3°C. Symptomatic fruits were placed in plastic trays in humid chambers. In all cases, olive mycelium developed after 3 days with septate hyphae and abundant ovoid and obclavate muriformly septate conidia. The isolate obtained from diseased leaves of cv. O'Neal was used to test pathogenicity on micropropagated potted plants of 20-cm height and ripe fruits contained in plastic trays. Both plants and fruits belonged to cv. O'Neal. A suspension of 2 × 105 conidia per ml was sprayed on needle-punctured young stems, fully expanded leaves, and mature fruits. Plants and trays were covered with polyethylene bags and kept at 24 ± 3°C under fluorescent light (12-hr photoperiod). The bags were removed after 72 hr. Symptoms appeared after 3 days on fruits and 8 days on leaves and stems. Controls remained symptomless. The inoculated pathogen was recovered from diseased organs and identified as Alternaria tenuissima (Kunze:Fr.) Wiltshire (1). To our knowledge, this is the first report on the presence of A. tenuissima affecting blueberry crops in Argentina. Reference: (1) E. G. Simmons. Mycotaxon 70:325, 1999.


Plant Disease ◽  
2013 ◽  
Vol 97 (11) ◽  
pp. 1515-1515 ◽  
Author(s):  
E. Kalinowska ◽  
E. Paduch-Cichal ◽  
M. Chodorska

Blueberry scorch virus (BlScV) is a member of the genus Carlavirus and one of the most widespread pathogens of highbush blueberry (Vaccinium corymbosum L.). The virus was first reported in the United States and has been reported in several countries in Europe, including Italy, Germany, the Netherlands, and Poland. Symptoms of scorch disease in highbush blueberry include necrosis of flower blossoms and leaves, shoot blight, and chlorosis. Sometimes BlScV infection is symptomless or limited to single blossoms and shoots, but all highbush blueberry cultivars are susceptible to virus infection. Cranberry (V. macrocarpon L.) and wild black huckleberry (V. membranaceum L.) are known as natural and symptomless hosts of BlScV (1). In June 2012, during the research concerning the occurrence of BlScV in plants outside Vaccinium sp., 15 leaf samples from five elderberry bushes (Sambucus nigra L., family Adoxaceae) were randomly collected from the Lodzkie region in Central Poland and three were positive in double antibody sandwich (DAS)-ELISA using specific antiserum (Agdia Inc., Elkhart, IN). To confirm the presence of the virus, total nucleic acid was extracted from ELISA-positive elderberry samples according to established protocol (T. Malinowski. Proc. 4th Int. EFPP Symposium, 445, 1996) and used in one step reverse transcription PCR. Primers were developed against the published NJ-2, BC-1, and BC-2 sequences of BlScV (GenBank Accession Nos. NC_003499, AY941198, and AY941199, respectively). The forward primer, RDP_1 (5′-ATGGCACTCACATACAGAAGTCC-3′), and the reverse primer, RDP_2 (5′-TGCCTCTTCAATGCACGATGTTC-3′), were used to amplify a 420-bp fragment of the RNA-dependent RNA polymerase gene of the virus. Amplicons of expected size were obtained from three DAS-ELISA-positive samples, while no products were observed for the negative control (DAS-ELISA-negative elderberry tissues). Sequence of one selected PCR product revealed 100, 88, and 87% nucleotide sequence identity and 100, 96, and 96% amino acid sequence identity with BC-2, NJ-2, and BC-1, respectively. BlScV-infected elderberry bushes were asymptomatic. As BlScV is transmitted by aphids in a non-persistent manner, infected elderberry bushes near highbush blueberry plantings may play an important role in virus spread. The potential for BlScV infection of plants outside family Ericaceae should be investigated. To the best of our knowledge, this is the first report of BlScV infecting elderberry. Reference: (1) R. R. Martin et al. Viruses 4:2831, 2012.


2019 ◽  
Vol 109 (12) ◽  
pp. 2055-2063 ◽  
Author(s):  
Francesca Dennert ◽  
Joana Beatrice Meyer ◽  
Daniel Rigling ◽  
Simone Prospero

Intraspecific cryptic invasions may occur when new strains of an invasive species are introduced into an area where this species had already been introduced previously. In plant pathogens, such invasions are not well studied, even if, potentially, they can have severe consequences. Here, we investigated the effects of a potential intraspecific invasion in Europe of Cryphonectria parasitica, the causal agent of chestnut blight. Specifically, we tested the hypotheses that (i) non-European strains are more virulent on Castanea sativa than those already present in Europe because they have never encountered this new host, and (ii) the variation in virulence among strains is higher within native than within introduced populations. In a greenhouse, 2-year-old C. sativa seedlings were inoculated with Cryphonectria parasitica strains from South Korea, the United States, and Switzerland, and lesion development and seedling mortality were recorded weekly. Additionally, growth and sporulation of the strains were measured in vitro on agar medium at 15 and 24°C. Although lesion growth was similar for all strains, seedlings inoculated with strains from South Korea and Switzerland died faster than seedlings inoculated with strains from the United States. Moreover, in vitro strains from South Korea grew faster and produced more spores at both temperatures than the strains from the other two countries. In conclusion, our results did not support the two hypotheses. All strains, regardless of their origin, were found to be highly virulent on the inoculated chestnut seedlings. Nevertheless, current phytosanitary measures to avoid the introduction of new genotypes of C. parasitica into Europe should be further implemented.


2020 ◽  
Vol 7 (Supplement_1) ◽  
pp. S720-S720
Author(s):  
Amy M Beeson ◽  
Grace E Marx ◽  
Amy M Schwartz ◽  
Alison F Hinckley

Abstract Background Lyme disease (LD) is the most common vector-borne disease in the United States and is a significant public health problem. The use of non-standard antibiotic treatment regimens for LD has been associated with adverse effects; however, the overall landscape of treatment has not been described previously. We aimed to describe real-world antibiotic prescribing patterns for LD. Methods We performed a retrospective analysis of the MarketScan commercial claims database of outpatient encounters from 2016-2018 in the United States. We identified all individuals with a visit that included an LD diagnosis code and a prescription within 30 days of the visit for one or more of 12 antibiotics that may be prescribed for LD. We then categorized each individual as having received either standard or non-standard treatment during the two-year period. Standard treatment was defined as treatment with a first, second or third-line antibiotic for LD, for no longer than 30 days, and for no more than two episodes during the study period. Descriptive and multivariable analyses were performed to compare characteristics of people who received standard vs non-standard treatment for LD. Results A total of 84,769 prescriptions met criteria for inclusion, written for 45,926 unique patients. The mean duration of prescriptions was 21.4 days (SD 10.8). Most individuals (84.5%) treated for LD received standard treatment during the study period. Female gender (OR 1.5, p< 0.0001) and age 19-45 (p=0.0003) were significantly associated with being prescribed non-standard LD treatment. Treatment in low-incidence states (OR 2.2 compared to high-incidence states, p< 0.0001) and during non-summer months (OR 2.2, p< 0.0001) was more likely to be non-standard. Age distribution of patients receiving treatment for Lyme disease, by gender and age at first prescription Seasonality of standard versus non-standard treatment of Lyme disease Conclusion In this population of employed, young, and insured patients, young and middle-aged women were at the highest risk of receiving non-standard LD treatment. Treatments prescribed in states with low incidence of LD or during non-summer months were also more likely to be non-standard, a trend which likely reflects misdiagnosis or overtreatment of LD. Future studies are needed to further define prescriber and patient factors associated with non-standard LD treatment and related adverse outcomes. Disclosures All Authors: No reported disclosures


1973 ◽  
Vol 52 (4) ◽  
pp. 680-687 ◽  
Author(s):  
Lewis Menaker ◽  
Juan M. Navia

The specific role of protein deficiency in altering dental caries incidence in rat pups was investigated. A 10% protein supplement given to undernourished rats during development allowed them to overcome weight deficiencies and reversed dental caries to the low incidence found in well-nourished control rats. Caries in undernourished rats supplemented with an isocaloric, proteinfree solution, was as high as that of undernourished rats intubated with distilled water.


2013 ◽  
Vol 53 (1) ◽  
pp. 32-36 ◽  
Author(s):  
Monika Kałużna ◽  
Joanna Puławska ◽  
Beata Meszka

Abstract In 2011, leaf spot disease was observed on the blueberry (Vaccinium corymbosum) cv. Nelson growing on a commercial field located in Central Poland. The disease symptoms could be seen as russet brown, irregular spots. The diameter of the spots was 0.3-0.5 cm, and the spots often coalesced. From these leaf spots, a fluorescent bacterium was repeatedly isolated in almost pure culture. Polymerase chain reaction (PCR) using primers Ps-for and Ps-rev, specific for Pseudomonas spp. confirmed that they belong to this genus. Based on LOPAT tests [levan production from sucrose (L), presence of oxidase (O), pectolytic activity on potato (P), the presence of arginine dihydrolase (A), hypersensitivity reaction on tobacco (T)], 6 isolates were classified to the LOPAT group Ib - group of Pseudomonas syringae subsp. savastanoi and Pseudomonas delphini, and one isolate to group Ia - P. syringae. All isolates caused a hypersensitivity reaction on tobacco plants, and symptoms similar to those under natural conditions, when young leaves of blueberry cv. Nelson were inoculated. Sequence analysis of 16S rRNA and rpoB genes showed the highest similarity of 6 studied strains to the species P. avellanae. Further taxonomic study is necessary to enable definitive classification of these isolates. It is the first time that a bacterial disease caused by the Pseudomonas spp. was observed in Poland.


2005 ◽  
Vol 13 (spe2) ◽  
pp. 1169-1176 ◽  
Author(s):  
Sandra Cristina Pillon ◽  
Beverley O'Brien ◽  
Ketty Aracely Piedra Chavez

The aim was to describe relationships between gender and drug use as well as risk behaviors that may be associated with drug use among first-year students at the University of São Paulo-Ribeirão Preto. The Youth Risk Behavior Survey (YRBS) is an anonymous survey that was used for this descriptive correlational study. It was developed by the Centers for Disease Control and Prevention in the United States. The sample (n=200) included (50%) males and (50%) females. Their ages ranged from 18 to 26 years. Results showed that more female than male students use alcohol and tobacco, but that the probability of heavy consumption is higher among men. There was a low incidence of illicit drug use for both groups. Male students were more likely to drive under the influence of alcohol than female students and more men were involved in violent behaviors such as fights with friends and police. In relation to sexual behavior, male students were likely to have more partners and less protection while under influence of alcohol. It was concluded that gender is associated with recreational drug use, specifically tobacco and alcohol, as well as other risk behaviors in university students.


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