scholarly journals First Report of White Rust of Spinach Caused by Albugo occidentalis in Italy

Plant Disease ◽  
2021 ◽  
Author(s):  
G. Gilardi ◽  
G. Tabone ◽  
V. Guarnaccia ◽  
M. L. Gullino
Keyword(s):  
2013 ◽  
Vol 14 (1) ◽  
pp. 11 ◽  
Author(s):  
Morris R. Bonde ◽  
Cristi L. Palmer ◽  
Douglas G. Luster ◽  
Susan E. Nester ◽  
Jason M. Revell ◽  
...  

Puccinia horiana Henn., a quarantine-significant fungal pathogen and causal agent of chrysanthemum white rust (CWR), was first discovered in the United States in 1977 and later believed to have been eradicated. Recently, however, the disease has sporadically reappeared in the northeastern US. Possible explanations for the reappearance include survival of the pathogen in the local environment, and reintroduction from other locations. To determine the possibility that the pathogen might be overwintering in the field, we undertook the study described here. Results from the study showed that P. horiana teliospores, imbedded in infected leaves, were capable of sporulating 2 weeks after inoculation, and this capacity continued until the leaf became necrotic and desiccated. This is the first report of the extreme susceptibility of P. horiana teliospores to leaf necrosis and desiccation and suggests that field infections following winter are unlikely to originate from teliospores. Teliospore germination on excised leaves was shown to be inhibited by light. Accepted for publication 3 April 2013. Published 23 August 2013.


Plant Disease ◽  
2011 ◽  
Vol 95 (1) ◽  
pp. 72-72
Author(s):  
I. Camele ◽  
S. M. Mang ◽  
G. L. Rana

Money plant or annual honesty (Lunaria annua L.) is an ornamental landscape plant used in flower beds and borders and also in flower arrangements. It is a biennial plant with large, pointed, oval leaves. Plants of L. annua showing white-to-cream, blister-like lesions on leaves and siliques (2) were found in private gardens where approximately 800 plants of 1,000 (approximately 80 to 90%) that were observed showed symptoms. The disease was also found in two ornamental nurseries, although it was limited to a few mother plants because of extensive fungicide treatments. The gardens and ornamental nurseries were located in Potenza Province (Basilicata Region, southern Italy). Sporangiophores were mostly straight or arched and almost cylindrical with attenuated base and flat or rounded apex and measured 29.2 to 33.4 × 12.8 to 13.4 μm. Sporangia, produced in chains and joined by short connectives, exhibited a spherical or angular shape, were subhyaline, contained vacuoles, and had average maximum and minimum diameters ranging from 15.8 to 18.8 and 14 to 16 μm, respectively. The morphological characteristics closely resembled those reported for Albugo candida (Pers.) Kuntze (3). Sori were collected from naturally and artificially inoculated tissues of L. annua, with the aid of a stereomicroscope, and used to extract genomic DNA via a DNeasy Plant Mini DNA extraction kit (Qiagen, Hilden, Germany) according to the manufacturer's directions. The extracted DNA was used as a template for amplification of the internal transcribed spacer (ITS) region of rDNA with primer pair ITS4/DC6 (1,4) and sequenced. One sequence, GenBank Accession No. GQ328846, matched several sequences of A. candida (Pers). Kuntze (e.g., GenBank Accession Nos. GQ328837, GQ328836, GQ328835, GQ328834, and AF271231), showing 98% identity. Pathogenicity tests were performed and repeated twice. Leaves of 10 healthy seedlings of L. annua were surface cleaned during several washings with distilled water and then spray inoculated with a suspension of 103 sporangia/ml of A. candida. Five healthy seedlings were spray inoculated with the same volume of sterile water and served as controls. Inoculated seedlings were maintained in a moist chamber for 48 h at 20°C before being moved to a shaded glasshouse at 16 to 24°C and 90% relative humidity. White rust symptoms, similar to those observed in natural conditions, appeared on leaves of inoculated seedlings 10 to 14 days later, demonstrating that A. candida was the causal agent of the disease. Control plants remained symptomless. White rust has been reported on L. annua in Europe (Czech Republic, Germany, Poland, and the United Kingdom) and in the northwestern United States (3). To our knowledge, this is the first report of A. candida infecting annual honesty plant in Italy. References: (1) P. Bonants et al. Eur. J. Plant Pathol. 103:345, 1997. (2) D. Choi et al. Mycotaxon 53:261, 1995. (3) D. A. Glawe et al. Online publication. doi:10.1094/PHP-2004-0317-01-HN. Plant Health Progress, 2004. (4) T. J. White et al. Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In: PCR Protocols. A Guide to Methods and Applications. Academic Press, San Diego, CA, 1990.


2015 ◽  
Vol 32 ◽  
pp. 8 ◽  
Author(s):  
S. Sriram ◽  
N.K. Chandran ◽  
Rajiv Kumar ◽  
M. Krishna Reddy
Keyword(s):  

Plant Disease ◽  
2015 ◽  
Vol 99 (9) ◽  
pp. 1279 ◽  
Author(s):  
R. Dheepa ◽  
P. Renukadevi ◽  
S. Vinod Kumar ◽  
S. Nakkeeran

Plant Disease ◽  
2003 ◽  
Vol 87 (5) ◽  
pp. 602-602
Author(s):  
A. P. Keinath ◽  
A. E. Strand ◽  
R. D. Hamilton

Seabeach amaranth (Amaranthus pumilus Raf.), a threatened annual marine plant, is a primary colonizer of the windward side of Atlantic coastal dunes. It serves an important ecological role in dune accumulation and stabilization. Because Hurricane Floyd eliminated all native seabeach amaranth in South Carolina in 1999, experimental reestablishment plantings have been attempted. In August 2000, seabeach amaranth on Dewees and Cape Island in Charleston County, Huntington Beach in Georgetown County, and Otter Island in Colleton County, South Carolina were stunted and senesced prematurely. Leaves on affected plants were only one-half of the normal size and internodes were shortened. Most plants (>90%) at each location were affected. Diseased leaves had small, pale green-to-tan spots above hypophyllous pustules that contained numerous, dry, hyaline, subglobose conidia. Conidia measured 13.5 (10 to 17) × 15.0 (11 to 18) μm. Based on morphological characters and the host, the pathogen was identified as Albugo bliti (Biv.-Bern.) Kuntze (1,2). No oospores were observed. Diseased plants were collected from Dewees and Otter Islands and kept frozen for use as a source of inoculum. Six A. pumilus plants each of six Plant Introductions (PI), 553080 through 553085, that had been grown from seed were sprayed with a suspension of 4.7 × 105 conidia per ml. One plant of each PI was sprayed with sterile distilled water as a noninoculated control. All plants were placed in a humidity chamber for 48 h and then moved to a greenhouse bench. Thirteen days after inoculation, all inoculated plants had pustules of white rust. Diseased plants had a mean of 42 pustules per plant and PI's did not differ in susceptibility. Five of six noninoculated plants also had white rust pustules, but only a mean of 2.3 (range 1 to 5) pustules each. White rust likely appeared on noninoculated plants because plants were spaced closely together in the chamber. Pustules and conidia on inoculated plants were identical to those on plants collected originally. Albugo bliti has been reported on 19 other Amaranthus species (1), but to our knowledge, this is the first report of white rust on seabeach amaranth in the United States. White rust reduced the biomass of infected plants and, hence, their ability to trap sand. White rust was not observed on subsequent plantings in 2001 and 2002 at any location. References: (1) D. F. Farr et al. Fungal Databases. Systematic Botany and Mycology Laboratory, On-line publication. ARS USDA, 2002. (2) G. W. Wilson. Bull. Torrey Bot. Club 34:61, 1907.


Plant Disease ◽  
2003 ◽  
Vol 87 (4) ◽  
pp. 450-450 ◽  
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
D. Bertetti ◽  
M. L. Gullino

Cineraria maritima L. (synonym Senecio cineraria DC.), commonly known as dusty-miller, is grown in Italy for landscape use in parks and gardens. In the spring of 2001, severe outbreaks of a previously unknown disease were observed in commercial farms located in northern Italy. Leaves of infected plants showed several sori on the abaxial surface, progressing to the adaxial surface, and often in the interveinal areas. On the adaxial surface of leaves, chlorotic areas developed and eventually turned brown. Severely infected leaves wilted, but remained attached to the stem. Signs of the fungus were present as whitish and catenulate sporangia emerging from the sori. Sporangia, organized in chains, had an average diameter of 20.5 × 26.5 μm. On the basis of the microscopic observations, the causal agent of the disease was identified as Albugo tragopogonis. Pathogenicity was confirmed by inoculating leaves of healthy C. maritima plants with a sporangial suspension (5 × 102 sporangia per ml) obtained from infected plants. Noninoculated plants served as a control. Plants were kept covered with plastic bags for 72 h and maintained at 15°C. After 10 days, typical symptoms of white rust developed on inoculated plants starting from the basal leaves. Within 30 days, affected leaves were completely wilted. Microscopic examination of sporangia within sori verified the pathogen to be A. tragopogonis. No symptoms developed on the control plants. A. tragopogonis has been reported as the causal agent of white rust on several species belonging to the genus Senecio in the United States (1). In New Zealand, the presence of A. tragopogonis was reported on the genus Cineraria in 1959 (2). To our knowledge, this is the first report of the presence of white rust on Cineraria maritima in Italy. References: (1) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society, St Paul, MN, 1989. (2) J. M. Dingley. N. Z. J. Agric. Res. 2:380, 1959.


Plant Disease ◽  
2019 ◽  
Vol 103 (1) ◽  
pp. 163-163
Author(s):  
J. Latinović ◽  
N. Latinović ◽  
J. Jakše ◽  
S. Radišek

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