First report of white rust of Aurinia saxatilis (Alyssum saxatile) caused by Albugo candida in Washington state

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.

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First Report of White Rust of Rocket (Eruca sativa) Caused by Albugo candida in Montenegro

Plant Disease ◽

10.1094/pdis-05-18-0784-pdn ◽

2019 ◽

Vol 103 (1) ◽

pp. 163-163

Author(s):

J. Latinović ◽

N. Latinović ◽

J. Jakše ◽

S. Radišek

Keyword(s):

Eruca Sativa ◽

First Report ◽

Albugo Candida ◽

White Rust

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First Report of White Rust of Lunaria annua Caused by Albugo candida in North America

Plant Health Progress ◽

10.1094/php-2004-0317-01-hn ◽

2004 ◽

Vol 5 (1) ◽

pp. 23

Author(s):

Dean A. Glawe ◽

Jenny R. Glass ◽

Melodie L. Putnam

Keyword(s):

North America ◽

First Report ◽

Albugo Candida ◽

White Rust ◽

Landscape Plant

Lunaria annua, or money plant, is grown as an ornamental landscape plant and is used in dried flower arrangements. This report provides the first documentation of white rust (caused by the fungus Albugo candida) on L. annua in North America, and describes the symptoms and morphology of A. candida useful for identification. Accepted for publication 24 February 2004. Published 17 March 2004.

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First Report of White Rust of Rocket (Eruca sativa) Caused by Albugo candida in South Africa

Plant Disease ◽

10.1094/pdis-09-14-0947-pdn ◽

2015 ◽

Vol 99 (2) ◽

pp. 290-290 ◽

Cited By ~ 1

Author(s):

E. Mangwende ◽

J. B. Kalonji Kabengele ◽

M. Truter ◽

T. A. S. Aveling

Keyword(s):

South Africa ◽

Agricultural Research ◽

Plant Protection ◽

Control Treatment ◽

Eruca Sativa ◽

Voucher Specimen ◽

First Report ◽

Albugo Candida ◽

White Rust ◽

Leaf Surfaces

Garden rocket (Eruca sativa syn.: E. vesicaria subsp. sativa (Mill) Thell.) is an annual plant of the Brassicaceae grown for fresh consumption as a salad vegetable. During winter (May to July) of 2013 and 2014 in South Africa, typical symptoms of white rust were observed in two commercial crops (each ~0.5 ha) of the garden rocket cv. Rucola coltivata in Centurion, Gauteng Province, at 33 and 80% incidence, respectively. Symptomatic leaves were deposited in the National Collection of Fungi, Plant Protection Research Institute, Agricultural Research Council, Pretoria, South Africa (PREM 61073). Early infections appeared as white to cream, blister-like sori on the lower leaf surfaces, and pale yellow lesions on the corresponding upper leaf surfaces. Later stages of infection were characterized by coalescing of lesions into large, irregular, necrotic blotches and development of additional sori on the petioles and stems. Sporangiophores were hyaline, clavate or cylindrical, and measured 24 to 30 × 11 to 14 μm (n = 50). Sporangia developed in basipetal chains and were hyaline, globose or polyangular, and 15 to 20 μm (n = 100). Based on these morphological characters and the host plant, the pathogen was identified as Albugo candida (Pers.) Kunze (2). Genomic DNA was extracted using the DNeasy Plant Mini DNA extraction kit (Qiagen) from sori containing sporangia collected from naturally infected leaves, according to the manufacturer's specifications. The internal transcribed spacer (ITS) region of ribosomonal DNA (rDNA) and the cytochrome c oxidase subunit II (COX2) region were amplified and sequenced (1). The ITS (GenBank Accession No. KM588081) and COX2 (KM588082) sequences confirmed identity of the pathogen as A. candida with 100% homology to the corresponding sequences of several A. candida isolates, including DQ418503 for the ITS sequence and DQ418514 for the COX2 sequence, of a voucher specimen of A. candida on E. sativa (BPI 184870) from Pakistan. Inoculum was prepared by scraping sporangia from infected leaves of the cv. Rucola coltivata collected from the 2014 field and placing the material in sterilized, distilled water (SDW) for 12 h at 5°C to induce zoospore formation. Pathogenicity tests were performed by spraying a suspension of 1 × 105 sporangia/ml onto each of 10 5-week-old rocket seedlings of the cv. Rucola coltivata. Ten additional seedlings were inoculated similarly with SDW to serve as a control treatment. The plants were maintained at 12 to 15°C and 95% RH for 72 h (3) before being moved to a shaded greenhouse at 20 to 24°C and 90% RH. Control plants remained symptomless, whereas white rust symptoms similar to those observed in the original fields developed on leaves of inoculated seedlings 10 to 14 days later, demonstrating that A. candida was the causal agent of the disease on E. sativa. To our knowledge, this is the first report of A. candida infecting garden rocket in South Africa. References: (1) Y.-J. Choi et al. Mol. Phylogenet. Evol. 40:400, 2006. (2) K. Mukerji. Descriptions of Pathogenic Fungi and Bacteria No. 458. CMI, Kew, Surrey, UK, 1975. (3) M. J. Sullivan et al. Plant Dis. 86:753, 2002.

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First Report of Soilborne wheat mosaic virus on Triticum aestivum in Washington State

Plant Health Progress ◽

10.1094/php-2009-1204-01-br ◽

2009 ◽

Vol 10 (1) ◽

pp. 38 ◽

Cited By ~ 3

Author(s):

T. D. Murray ◽

H. R. Pappu ◽

R. W. Smiley

Keyword(s):

Triticum Aestivum ◽

Mosaic Virus ◽

Washington State ◽

First Report

SBWMV was recently also reported from an adjacent county in Oregon. Confirmation of SBWMV in Washington highlights the need for increased awareness of the disease and implementing measures to contain its further spread in the region. Accepted for publication 18 September 2009. Published 4 December 2009.

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First Report of Subanguina radicicola, the Root-Gall Nematode Infecting Poa annua Putting Greens in Washington State

Plant Disease ◽

10.1094/pdis-91-7-0905c ◽

2007 ◽

Vol 91 (7) ◽

pp. 905-905 ◽

Cited By ~ 2

Author(s):

N. A. Mitkowski

Keyword(s):

United States ◽

New York ◽

The United States ◽

Washington State ◽

Poa Annua ◽

Golf Course ◽

Severe Damage ◽

Surrounding Water ◽

Putting Greens ◽

First Report

In the fall of 2006, a golf course in Snoqualmie, WA renovated five putting greens with commercially produced Poa annua L. sod from British Columbia, Canada. Prior to the renovation, the greens had been planted with Agrostis stolonifera L. cv. Providence, which was removed during the renovation. In February of 2007, chlorotic patches were observed on the newly established P. annua greens. When the roots were examined, extensive galling was observed throughout plant roots. Galls were slender and twisted in appearance and less than one millimeter long. Upon dissection of washed galls, hundreds of eggs were exuded into the surrounding water droplet and both mature male and female nematodes were observed. Further morphometric examination of males, females, and juvenile nematodes demonstrated that they were Subanguina radicicola (Greef 1872) Paramanov 1967 (1). Amplification of nematode 18S, ITS1, and 5.8S regions, using previously published primers (2), resulted in a 100% sequence match with the publicly available sequence for S. radicicola, GenBank Accession No. AF396366. Each P. annua plant had an average of six galls (with a range of 1 to 8), primarily located within the top 2 cm of the soil. All five new P. annua putting greens at the golf course were infested with the nematode. Additionally, P. annua from two A. stolonifera cv. Providence greens that had not been renovated was infected, suggesting that the population occurred onsite and was not imported from the Canadian sod. S. radicicola has been identified as causing severe damage in New Brunswick, Canada on P. annua putting greens and in wild P. annua in the northwestern United States, but to our knowledge, this is the first report of the nematode affecting P. annua on a golf course in the United States. References: (1) E. L. Krall. Wheat and grass nematodes: Anguina, Subanguina, and related genera. Pages 721–760 in: Manual of Agricultural Nematology. Marcel Dekker, New York, 1991. (2) N. A. Mitkowski et al. Plant Dis. 86:840, 2002.

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First Report of Grapevine leafroll associated virus-3 in American Vitis spp. Grapevines in Washington State

Plant Disease ◽

10.1094/pd-90-1461a ◽

2006 ◽

Vol 90 (11) ◽

pp. 1461-1461 ◽

Cited By ~ 8

Author(s):

M. J. Soule ◽

K. C. Eastwell ◽

R. A. Naidu

Keyword(s):

New York ◽

Economic Impact ◽

Virus Disease ◽

The United States ◽

Washington State ◽

The State ◽

Enzyme Linked Immunosorbent Assay ◽

Rt Pcr ◽

First Report ◽

Table Grapes

Washington State is the largest producer of juice grapes (Vitis labruscana ‘Concord’ and Vitis labrusca ‘Niagara’) and ranks second in wine grape production in the United States. Grapevine leafroll disease (GLD) is the most wide spread and economically significant virus disease in wine grapes in the state. Previous studies (2) have shown that Grapevine leafroll associated virus-3 (GLRaV-3) is the predominant virus associated with GLD. However, little is known about the incidence and economic impact of GLD on juice and table grapes. Because typical GLD symptoms may not be obvious among these cultivars, the prevalence and economic impact of GLD in Concord and Niagara, the most widely planted cultivars in Washington State, has received little attention from the grape and nursery industries. During the 2005 growing season, 32 samples from three vineyards and one nursery of ‘Concord’ and three samples from one nursery of ‘Niagara’ were collected randomly. Petiole extracts were tested by single-tube reverse transcription-polymerase chain reaction (RT-PCR; 3) with primers LC 1 (5′-CGC TAG GGC TGT GGA AGT ATT-3′) and LC 2 (5′-GTT GTC CCG GGT ACC AGA TAT-3′), specific for the heat shock protein 70 homologue (Hsp70h gene) of GLRaV-3 (GenBank Accession No. AF037268). One ‘Niagara’ nursery sample and eleven ‘Concord’ samples from the three vineyards tested positive for GLRaV-3, producing a single band of the expected size of 546 bp. The ‘Niagara’ and six of the ‘Concord’ RT-PCR products were cloned in pCR2.1 (Invitrogen Corp, Carlsbad, CA) and the sequences (GenBank Accession Nos. DQ780885, DQ780886, DQ780887, DQ780888, DQ780889, DQ780890, and DQ780891) compared with the respective sequence of a New York isolate of GLRaV-3 (GenBank Accession No. AF037268). The analysis revealed that GLRaV-3 isolates from ‘Concord’ and ‘Niagara’ share nucleotide identities of 94 to 98% and amino acid identities and similarities of 97 to 98% with the Hsp70h gene homologue of the New York isolate of GLRaV-3. Additional testing by double-antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) using antibodies specific to GLRaV-3 (BIOREBA AG, Reinach, Switzerland) further confirmed these results in the ‘Niagara’ and two of the ‘Concord’ isolates. GLRaV-3 has previously been reported in labrusca cvs. Concord and Niagara in western New York (4) and Canada (1), but to our knowledge, this is the first report of GLRaV-3 in American grapevine species in the Pacific Northwest. Because wine and juice grapes are widely grown in proximity to each other in Washington State and grape mealybug (Pseudococcus maritimus), the putative vector of GLRaV-3, is present in the state vineyards, further studies will focus on the role of American grapevine species in the epidemiology of GLD. References: (1) D. J. MacKenzie et al. Plant Dis. 80:955, 1996. (2) R. R. Martin et al. Plant Dis. 89:763, 2005. (3) A. Rowhani et al. ICGV, Extended Abstracts, 13:148, 2000. (4) W. F. Wilcox et al. Plant Dis. 82:1062, 1998.

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First Report of Powdery Mildew of Platanus occidentalis caused by Microsphaera platani (Erysiphe platani) in Washington State

Plant Health Progress ◽

10.1094/php-2003-0818-01-hn ◽

2003 ◽

Vol 4 (1) ◽

pp. 33 ◽

Cited By ~ 2

Author(s):

Dean A. Glawe

Keyword(s):

North America ◽

Powdery Mildew ◽

Native Species ◽

Washington State ◽

Eastern North America ◽

First Report ◽

Platanus Occidentalis

American sycamore (Platanus occidentalis L.) is a common native species in eastern North America and is planted widely as a landscape tree in other regions. During a survey of powdery mildew diseases in Washington State, the fungus Microsphaera platani Howe was found on American sycamore trees in Madison Park, Seattle. This report documents the presence of M. platani in Washington State and presents information on the fungus. Accepted for publication 30 July 2003. Published 18 August 2003.

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Sporulation Capacity and Longevity of Puccinia horiana Teliospores in Infected Chrysanthemum Leaves

Plant Health Progress ◽

10.1094/php-2013-0823-01-rs ◽

2013 ◽

Vol 14 (1) ◽

pp. 11 ◽

Cited By ~ 3

Author(s):

Morris R. Bonde ◽

Cristi L. Palmer ◽

Douglas G. Luster ◽

Susan E. Nester ◽

Jason M. Revell ◽

...

Keyword(s):

United States ◽

Fungal Pathogen ◽

Local Environment ◽

The United States ◽

First Report ◽

White Rust ◽

Teliospore Germination ◽

Sporulation Capacity ◽

Leaf Necrosis ◽

Puccinia Horiana

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.

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Mucinous Pleural Effusion in a Dog with a Pulmonary Adenocarcinoma and Carcinomatosis

Journal of the American Animal Hospital Association ◽

10.5326/jaaha-ms-6227 ◽

2015 ◽

Vol 51 (5) ◽

pp. 311-314 ◽

Cited By ~ 2

Author(s):

Melissa Tropf ◽

Rance Sellon ◽

Kathleen Paulson ◽

Danielle Nelson

Keyword(s):

Pleural Effusion ◽

Teaching Hospital ◽

Papillary Adenocarcinoma ◽

Washington State ◽

Postmortem Examination ◽

Pulmonary Adenocarcinoma ◽

Histologic Diagnosis ◽

First Report ◽

Mucin Production ◽

History Of

An 11 yr old castrated male greyhound presented to the Washington State University's Veterinary Teaching Hospital (WSU VTH) for evaluation of a 4 day history of pleural effusion. The pleural effusion had a gelatinous appearance, suggestive of mucus, and was characterized cytologically as a pyogranulomatous exudate with some features suggestive of a carcinoma. Postmortem examination identified a pulmonary mass with evidence of carcinomatosis. Pulmonary papillary adenocarcinoma with carcinomatosis was the histologic diagnosis. Abundant mucin production was present, consistent with a mucinous pulmonary adenocarcinoma. To the authors' knowledge, this is the first report of a mucinous pulmonary adenocarcinoma with mucus pleural effusion in a dog.

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