First Report of Dothichiza caroliniana Causing Double Spot on Highbush Blueberry in South America

A foliar disease affecting Jewell, Emerald, and O'Neal cultivars of highbush blueberry (Vaccinium corymbosum L.) was observed in commercial plantings in Tucuman, Argentina during February 2007. Typical symptoms were circular leaf spots that were 10 to 15 mm in diameter, light to dark brown with dark reddish borders, and frequently exhibiting a secondary necrotic area around the original spot. The final appearance was a large necrotic area surrounding a pale, smaller spot. On the abaxial leaf surfaces, white mycelia grew from the border of the initial or enlarged spots toward the healthy tissues. Frequently, black pycnidia bearing an amber rubbery cirrhi were observed. Fewer pycnidia were observed on the adaxial leaf lesions. The fungus was isolated by transferring cirrhi from affected leaves onto petri plates containing potato dextrose agar (PDA). Plates were incubated in darkness at 27°C and light brown concentric colonies with an aerial, effuse, white mycelium developed. After 5 days, dark brown cirrhi emerged from pycnidia in culture. Pycnidiospores were obtuse, hyaline, 1-celled (7 × 2 μm), and grew from the base of pycnidia on short conidiophores. Pycnidia were black, conical, obovoid, averaged 110 × 70 μm wide, and were lightly immersed in the mycelium. Pathogenicity tests were performed by spraying a 106 conidia/ml suspension on leaves of nine blueberry plants (cv. Jewell). Plants were incubated in a moist chamber at 25 to 29°C with a 12-h photoperiod. After 5 weeks, all inoculated leaves had foliar symptoms similar to the lesions previously observed in the field. Reisolation of the fungus completed Koch's postulates. Noninoculated leaves did not develop foliar symptoms. Morphological and cultural characteristics of the fungus conformed to the descriptions of Dothichiza caroliniana (Demaree & M.S. Wilcox) reported to cause “double spot” in blueberry (1,2). Symptoms were consistent with those described for double spot disease (2). To our knowledge, this is the first report of D. caroliniana on blueberry in South America. References: (1) J. B. Demaree and M. Wilcox. Phytopathology, 37:490, 1947. (2) R. D. Milholland. Double spot. Page 17 in: Compendium of Blueberry and Cranberry Diseases. F. L. Caruso and D. C. Ramsdell, eds. The American Phytopathological Society, St. Paul, MN 1995.

Download Full-text

First Report of Downy Mildew Caused by Peronospora lamii on Salvia splendens and Salvia coccinea

Plant Disease ◽

10.1094/pdis.2000.84.10.1154b ◽

2000 ◽

Vol 84 (10) ◽

pp. 1154-1154 ◽

Cited By ~ 5

Author(s):

G. E. Holcomb

Keyword(s):

United States ◽

Downy Mildew ◽

Pathogenic Fungi ◽

The United States ◽

Commonwealth Mycological Institute ◽

First Report ◽

Leaf Spots ◽

Salvia Splendens ◽

Leaf Surfaces ◽

Pathogenicity Tests

Angular chlorotic spots were observed on adaxial leaf surfaces of Salvia splendens (scarlet sage cvs. Empire Purple, Empire White, Red Pillar, and Red Hot Sally) and S. coccinea (scarlet or Texas sage cv. Lady in Red) in early May in Baton Rouge area nurseries. Leaf spots sometimes became necrotic and resulted in leaf drop. Abaxial leaf surfaces contained scattered patches of white mycelia with brown spores. Microscopic examination of mycelia revealed irregular dichotomously branched conidiophores with pointed tips and brown oval conidia. Conidiophores averaged 485 × 9 µm and conidia averaged 21 × 18 µm (16 to 26 × 15 to 23 µm) in dimensions. The fungus was identified as Peronospora lamii A. Braun (= P. swinglei Ellis & Everh.) based on these characters and its known occurrence on Salvia spp. and five other genera in the family Lamiaceae (2). Pathogenicity tests were performed by washing conidia from infected leaves into distilled water and mistinoculating S. coccinea cv. Lady in Red and S. splendens cv. Empire Purple with 50,000 spores/ml. Plants were held in a dew chamber at 20°C for 3 days, then moved to a greenhouse where temperatures ranged from 18 to 32°C. Typical angular chlorotic leaf spots developed on inoculated plants within 6 to 8 days and noninoculated plants remained healthy. The fungus did not sporulate under these greenhouse temperatures, but infected leaves that were removed and placed in a moist chamber at 25°C produced conidiophores and brown conidia typical of P. lamii within 2 to 3 days. P. lamii has been reported previously on S. officinalis (3) and S. reflexa (1) in the United States. This is the first report of downy mildew on S. coccinea and S. splendens. Appearance of the disease in retail nurseries that obtained plants from out of state (Arkansas) suggests a widespread occurrence of the disease on these host plants. References: (1) D. F. Farr et al. 1989. Fungi on Plants and Plant Products in the United States. American Phytopathological Society, St. Paul, MN. (2) S. M. Francis. 1981. Peronospora lamii. Descriptions of Pathogenic Fungi and Bacteria No. 688. Commonwealth Mycological Institute, Kew, England. (3) R. T. McMillan and W. R. Graves. Plant Dis. 78:317, 1994.

Download Full-text

First Report of Anthracnose of Velvet Ash Caused by Discula fraxinea in Louisiana

Plant Disease ◽

10.1094/pdis.1998.82.12.1401b ◽

1998 ◽

Vol 82 (12) ◽

pp. 1401-1401 ◽

Cited By ~ 1

Author(s):

G. E. Holcomb

Keyword(s):

Baton Rouge ◽

Potato Dextrose Agar ◽

First Report ◽

Leaf Spots ◽

Fraxinus Velutina ◽

Leaf Surfaces ◽

Ash Trees ◽

Pathogenicity Tests ◽

Chlorotic Leaf ◽

Necrotic Spots

Velvet ash (Fraxinus velutina Torr.), a native tree of the southwestern United States, was commonly planted in Louisiana and other southeastern states until horticulturalists lost interest in the plant due to insect and disease problems. For several years, velvet ash trees in Baton Rouge have exhibited necrotic leaf spots and blotches during March and April. Trees frequently have 10 to 25% foliage infection and those most severely infected may show 50% defoliation. Small hyaline conidia that averaged 9.0 × 3.8 μm were produced in acervuli in necrotic tissue on lower leaf surfaces of affected trees. A fungus that produced similar conidia was consistently isolated from infected leaves and grown on potato dextrose agar. Pathogenicity tests were performed by misting 3 × 106 conidia per ml on leaf surfaces of velvet ash seedlings that were then placed in a dew chamber maintained at 26°C for 48 h. Chlorotic leaf spots developed on inoculated plants in 4 to 6 days at 24°C and were followed by necrotic spots and blotches 4 days later. The fungus was reisolated and identified as Discula fraxinea (Peck) Redlin & Stack (previously known as Gloeosporium aridum Ellis & Holw.) (2). Velvet ash anthracnose was first reported from California in 1949 (1), but this is the first report of its occurrence in Louisiana. References: (1) D. M. Coe and W. W. Wagener. Plant Dis. Rep. 33:232, 1949. (2) S. C. Redlin and R. W. Stack. Mycotaxon 32:175, 1988.

Download Full-text

First report of Armillaria gallica on highbush blueberry (Vaccinium corymbosum) in Italy

Plant Pathology ◽

10.1111/j.1365-3059.2006.01420.x ◽

2006 ◽

Vol 55 (4) ◽

pp. 583-583 ◽

Cited By ~ 2

Author(s):

D. Prodorutti ◽

L. Palmieri ◽

D. Gobbin ◽

I. Pertot

Keyword(s):

Vaccinium Corymbosum ◽

Highbush Blueberry ◽

First Report ◽

Armillaria Gallica

Download Full-text

First Report of Web Blight on Yellow-Sage (Lantana camara) Caused by Rhizoctonia solani in Europe

Plant Disease ◽

10.1094/pdis.2003.87.7.875a ◽

2003 ◽

Vol 87 (7) ◽

pp. 875-875 ◽

Cited By ~ 2

Author(s):

A. Garibaldi ◽

A. Minuto ◽

D. Bertetti ◽

R. Nicoletti ◽

M. L. Gullino

Keyword(s):

United States ◽

Rhizoctonia Solani ◽

The United States ◽

The Philippines ◽

Lantana Camara ◽

First Report ◽

Leaf Spots ◽

Entire Plant ◽

Pathogenicity Tests ◽

Web Blight

Lantana camara is increasingly grown in northern Italy as a potted plant and contributes to the diversification of offerings in the ornamental market. During the spring of 2001, selections of L. camara cuttings growing at a commercial farm located at Albenga (Riviera coast) exhibited tan leaf spots of irregular size and shape. Spots were at first isolated, 4 to 8 mm in diameter, and later coalesced and affected the entire plant. Heavily infected leaves, stems, and branches became blighted and were killed. Infected rooted cuttings also eventually died. Diseased cuttings showed a progressive reduction (to less than 20%) in rooting ability. Isolations from infected leaves and stems on potato dextrose agar (PDA), supplemented with 100 mg/liter of streptomycin sulphate, consistently yielded a fungus with mycelial and cultural characteristics resembling Rhizoctonia solani. The fungal isolates were further characterized as R. solani Kühn AG-4 based on hyphal anastomoses with several AG-4 tester isolates. Pathogenicity tests were performed by placing 5-day-old-fungal mycelial plugs, grown on PDA, at the base of five healthy yellow-sage stems and holding plants in a dew chamber at 18 to 22°C. After 2 days, foliage blight appeared on leaves of inoculated plants, and after 3 days, stems also became infected and entire plants wilted. Five noninoculated plants remained healthy. The fungal pathogen was reisolated from all inoculated plants. R. solani has been observed on L. camara in the United States (1) and the Philippines (2). To our knowledge, this is the first report of R. solani on L. camara in Europe. 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) F. T. Orillo and R. B. Valdez. Philipp. Agric. A. 42:292, 1958.

Download Full-text

First Report of Frog Skin Disease in Cassava (Manihot esculenta) in Venezuela

Plant Disease ◽

10.1094/pdis.2001.85.12.1285d ◽

2001 ◽

Vol 85 (12) ◽

pp. 1285-1285 ◽

Cited By ~ 6

Author(s):

E. I. Chaparro-Martínez ◽

G. Trujillo-Pinto

Keyword(s):

South America ◽

Manihot Esculenta ◽

Enzyme Linked Immunosorbent Assay ◽

Stem Cuttings ◽

Manihot Esculenta Crantz ◽

First Report ◽

Average Temperature ◽

Foliar Symptoms ◽

Viral Particles ◽

Long Stem

Frogskin disease (FSD) is a disease of clonally propagated cassava (Manihot esculenta Crantz) and has been reported to reduce cassava yields significantly in South America (1). FSD is caused by an uncharacterized virus that is restricted to South America. The evidence indicates FSD is transmitted by stem cuttings and graft (3). However, little information is available on its distribution and incidence in Venezuela. Eighty-seven samples with virus-like symptoms were collected with the help of technical staff and producers in cassava-producing states: Amazonas (1 sample), Aragua (7 samples), Barinas (35 samples), Cojedes (8 samples), Monagas (19 samples), and Portuguesa (17 samples). In these states, the average daytime temperature was 26°C, but the average was higher (>28°C) during the dry season. Samples were collected during the rainy season because high temperatures and dry field conditions appeared to suppress symptom expression, while cooler conditions tended to favor symptom development (2). Roots of sampled cassava plants were examined for the presence of FSD. A single 70- to 80-cm-long stem cutting was taken from each plant and subdivided into four pieces. Two pieces were used as rootstocks in graft-inoculation tests with Secundina scions for FSD detection, and two pieces were potted in sterilized soil to be used in other tests. All potted and grafted plants were kept in the Vegetable Virology Laboratory of the Faculty of Agronomy (Universidad Central de Venezuela), at an average temperature of 24°C and 80% relative humidity. FSD-infected plants were identified by mosaic symptoms on Secundina scions and the presence of 80-nm spherical viral particles. Most FSD-infected cultivars expressed only root symptoms. However, in the case of Secundina cvs. MCOL 22 and MCOL 113, foliar symptoms were also detected (1). FSD was found in a simple infection in one cassava sample from Aragua State (14.3% incidence, 1 of 7 samples) and in four cassava samples from Barinas State (11.4% incidence, 4 of 35 samples) associated with Cassava virus X (detected by double-antibody sandwich enzyme-linked immunosorbent assay). To our knowledge, this is the first report of FSD detection in Venezuela. References: (1) E. A. Frison et al. Informe Anual. CIAT, Cali, Colombia, 1995. (2) B. L. Nolt et al. Plant Pathol. 41:384, 1992. (3) Technical Guidelines for the Safe Movement of Cassava Rome. FAO/IBPGR. p. 10-27, 1991.

Download Full-text

First Report of Leaf Spot Caused by Alternaria alternata on Kiwifruit in Italy

Plant Disease ◽

10.1094/pdis.1999.83.5.487d ◽

1999 ◽

Vol 83 (5) ◽

pp. 487-487 ◽

Cited By ~ 3

Author(s):

L. Corazza ◽

L. Luongo ◽

M. Parisi

Keyword(s):

New Zealand ◽

Alternaria Alternata ◽

Leaf Spot ◽

Southern Italy ◽

Morphological Characteristics ◽

Potato Dextrose Agar ◽

First Report ◽

Leaf Spots ◽

Detached Leaves ◽

Pathogenicity Tests

A leaf spot of kiwifruit (Actinidia deliciosa (A. Chev.) C. F. Liang & A. R. Ferg.) leaves was recently observed on plants of the cultivar Hayward in an orchard near Salerno, in southern Italy. The affected plants showed early severe defoliation. The fungus isolated from the infected leaves was identified as Alternaria alternata (Fr.:Fr.) Keissl., based on conidial morphological characteristics. Pathogenicity tests were made by inoculating detached leaves of male pollinator cultivar Tomuri and the female cultivars Hayward and Bruno with a 7-mm disk taken from actively growing cultures of the fungus on potato dextrose agar (PDA). After 14 days, necrotic leaf spots developed and A. alternata was consistently isolated from the inoculated leaves. A. alternata has been observed as a pathogen on leaves and fruits in New Zealand. In the Mediterranean, it has been reported in Israel (2) and in the island of Crete (1). This is the first report of Alternaria leaf spot on kiwifruit in Italy. References: (1) V. A. Bourbos and M. T. Skoudridakis. Petria 7:111, 1997. (2) A. Sive and D. Resnizky. Alon Hanotea 41:409, 1987.

Download Full-text

First Report of Stem and Leaf Anthracnose on Blueberry Caused by Colletotrichum gloeosporioides in China

Plant Disease ◽

10.1094/pdis-11-12-1056-pdn ◽

2013 ◽

Vol 97 (6) ◽

pp. 845-845 ◽

Cited By ~ 1

Author(s):

C. N. Xu ◽

Z. S. Zhou ◽

Y. X. Wu ◽

F. M. Chi ◽

Z. R. Ji ◽

...

Keyword(s):

Colletotrichum Gloeosporioides ◽

Morphological Characteristics ◽

Its Region ◽

Pathogenic Fungi ◽

Molecular Characteristics ◽

First Report ◽

Potted Plants ◽

Leaf Spots ◽

Pathogenicity Tests ◽

Highbush Blueberries

Blueberry (Vaccinium spp.) is becoming increasingly popular in China as a nutritional berry crop. With the expansion of blueberry production, many diseases have become widespread in different regions of China. In August of 2012, stem and leaf spots symptomatic of anthracnose were sporadically observed on highbush blueberries in a field located in Liaoning, China, where approximately 15% of plants were diseased. Symptoms first appeared as yellow to reddish, irregularly-shaped lesions on leaves and stems. The lesions then expanded, becoming dark brown in the center and surrounded by a reddish halo. Leaf and stem tissues (5 × 5 mm) were cut from the lesion margins and surface-disinfected in 70% ethanol for 30 s, followed by three rinses with sterile water before placing on potato dextrose agar (PDA). Plates were incubated at 28°C. Colonies were initially white, becoming grayish-white to gray with yellow spore masses. Conidia were one-celled, hyaline, and cylindrical with rounded ends, measuring 15.0 to 25.0 × 4.0 to 7.5 μm. No teleomorph was observed. The fungus was tentatively identified as Colletotrichum gloeosporioides (PenZ.) PenZ & Sacc. (teleomorph Glomerella cingulata (Stoneman) Spauld. & H. Schrenk) based on morphological characteristics of the colony and conidia (1). Genomic DNA was extracted from isolate XCG1 and the internal transcribed spacer (ITS) region of the ribosomal DNA (ITS1–5.8S-ITS2) was amplified with primer pairs ITS1 and ITS4. BLAST searches showed 99% identity with C. gloeosporioides isolates in GenBank (Accession No. AF272779). The sequence of isolate XCG1 (C. gloeosporioides) was deposited into GenBank (JX878503). Pathogenicity tests were conducted on 2-year-old potted blueberries, cv. Berkeley. Stems and leaves of 10 potted blueberry plants were wounded with a sterilized needle and sprayed with a suspension of 105 conidia per ml of sterilized water. Five healthy potted plants were inoculated with sterilized water as control. Dark brown lesions surrounded by reddish halos developed on all inoculated leaves and stems after 7 days, and the pathogen was reisolated from lesions of 50% of inoculated plants as described above. The colony and conidial morphology were identical to the original isolate XCG1. No symptoms developed on the control plants. The causal agent of anthracnose on blueberry was identified as C. gloeosporioides on the basis of morphological and molecular characteristics, and its pathogenicity was confirmed with Koch's postulates. Worldwide, it has been reported that blueberry anthracnose might be caused by C. acutatum and C. gloeosporioides (2). However, we did not isolate C. acutatum during this study. To our knowledge, this is the first report of stem and leaf anthracnose of blueberry caused by C. gloeosporioides in China. References: (1) J. M. E. Mourde. No 315. CMI Descriptions of Pathogenic Fungi and Bacteria. Kew, Surrey, UK, 1971. (2) N. Verma, et al. Plant Pathol. 55:442, 2006.

Download Full-text

First Report of Anthracnose Caused by Colletotrichum gloeosporioides on Schefflera actinophylla in China

Plant Disease ◽

10.1094/pdis-12-12-1205-pdn ◽

2013 ◽

Vol 97 (7) ◽

pp. 998-998

Author(s):

J. Huang

Keyword(s):

Dna Sequence ◽

Species Complex ◽

Colletotrichum Gloeosporioides ◽

Conidial Suspension ◽

First Report ◽

Leaf Spots ◽

Black Spots ◽

Pathogenicity Tests ◽

Colletotrichum Gloeosporioides Species Complex ◽

And Control

In China, in mild to warm climates, Schefflera actinophylla is commonly grown as a decorative tree in gardens. When mature, it has bright red flowers in inflorescences with up to 20 racemes that develop in summer or early autumn. From 2008 to 2011, lesions were observed on young and mature leaves in several locations in Guangzhou, China. The first symptoms were circular, necrotic areas that usually developed into irregular, dry, brown to reddish brown or black spots. Spots often first appeared at or near the margins of leaves. Reproductive bodies of the pathogen appeared as black specks in leaf spots. Under a 10× magnification, black, needle-like fungal structures (setae) were observed in the centers of spots on the upper leaf surface. A fungus was isolated from the lesion and was identified as Colletotrichum gloeosporioides (Penz.) Penz. & Sacc. based on cultural characteristics and conidial morphology (1). The voucher isolates were deposited in the Institute of Plant Pathology, Zhongkai University of Agriculture and Engineering. C. gloeosporioides is a species complex (2) and there is a degree of unresolved aspects of taxonomy in this species complex. Cultures on potato dextrose agar (PDA) had aerial white mycelium that turned gray to grayish black after 10 days at 25°C and a 12-h photoperiod and produced salmon to orange conidial masses. Brown, 80 to 120 μm long setae were observed in the acervulus. Conidia 14.1 to 18.0 × 4.0 to 6.1 μm in size were hyaline, thin-walled, aseptate, granular inside, clavate to slightly navicular in shape with an obtuse apex and a truncate base. To identify the fungus, a 588-bp segment of the ITS1-5.8S-ITS2 rDNA region was amplified by PCR and sequenced. The DNA sequence was submitted to GenBank as KC207404. A BLAST search of the DNA sequence showed 99% identity with accessions AY266389.1, EF423519.1, and HM575258.1 of C. gloeosporioides. Pathogenicity tests were conducted under greenhouse conditions at 25 ± 2°C. A total of 15 leaves from three 1-year-old S. actinophylla plants were inoculated with mycelial PDA plugs that were placed on 0.5-cm2 leaf wounds and then wrapped with Parafilm. Control leaves were treated similarly except that they were inoculated with PDA plugs without the fungus. No symptoms developed on control leaves after 10 days. Foliar lesions on inoculated leaves closely resembled those observed in the field. C. gloeosporioides was reisolated consistently from inoculated leaves. Pathogenicity was also tested by spraying leaves of potted S. actinophylla plants about 30 cm in height with 10 ml of a conidial suspension (1 × 105 conidia/ml) prepared from 7-day-old PDA cultures grown at 25°C. Leaves sprayed with distilled water were used as controls. Three plants were inoculated in each of two experiments and were incubated at 25°C and 90% relative humidity in a growth chamber. Tiny brown spots started to develop on all inoculated leaves 5 days after inoculation and the progression of symptom development was similar to that observed in the field. Control leaves remained asymptomatic. C. gloeosporioides was reisolated from inoculated leaves. To my knowledge, this is the first report of C. gloeosporioides causing anthracnose on S. actinophylla in China. References: (1) B. C. Sutton. The genus Glomerella and its anamorph Colletotrichum. In: Colletotrichum Biology, Pathology and Control. CAB International, Wallingford, UK, 1992. (2) B. S. Weir et al. The Colletotrichum gloeosporioides species complex. Stud. Mycol. 73:115, 2012.

Download Full-text

First Report of Blueberry Leaf Rust Caused by Thekopsora minima on Vaccinium corymbosum in Michigan

Plant Disease ◽

10.1094/pdis-12-10-0884 ◽

2011 ◽

Vol 95 (6) ◽

pp. 768-768 ◽

Cited By ~ 4

Author(s):

A. M. C. Schilder ◽

T. D. Miles

Keyword(s):

South Africa ◽

New York ◽

Leaf Rust ◽

Vaccinium Corymbosum ◽

Economic Losses ◽

Its2 Region ◽

Highbush Blueberry ◽

Alternate Host ◽

First Report ◽

Growing Seasons

Leaf rust symptoms have been noticed sporadically on northern highbush blueberry plants (Vaccinium corymbosum L.) in Michigan for the past 8 years. In 2009, leaf rust was seen in several cultivated blueberry fields and on greenhouse-grown blueberry plants in southwest Michigan. In 2010, leaf rust was widespread throughout western Michigan and particularly evident in the fall, sometimes resulting in premature defoliation. Cultivars Rubel, Jersey, Elliott, Liberty, and Brigitta were most commonly affected. Both the 2009 and 2010 growing seasons were characterized by above-average precipitation in early to mid-summer. Early symptoms on the adaxial leaf surface consisted of roughly circular yellow spots that later developed brown, necrotic centers. Older lesions were more angular and sometimes surrounded by a purplish border. In the fall, a “green island” effect was sometimes apparent around the lesions. On the abaxial side, numerous yellow-to-orange rust pustules (uredinia) were visible. Uredinia were dome shaped, erumpent, 100 to 400 μm in diameter, clustered, and sometimes coalescing. Urediniospores were broadly obovate with dark yellowish content and measured 19 to 25 × 16 to 20 μm (average 22 × 18 μm, n = 30). Spore walls were hyaline, echinulate, and 1.0 to 1.5 μm thick with obscure germ pores. Uredinia were examined with light and scanning electron microscopy for the presence of conspicuous ostiolar cells characteristic of Naohidemyces vaccinii (Wint.) Sato, Katsuya et Y. Hiratsuka, but none were observed. No telia or teliospores were observed. On the basis of morphology, the pathogen was identified as Thekopsora minima P. Syd. & Syd. (3,4) and a sample was deposited in the U.S. National Fungus Collection (BPI 881107). Genomic DNA was extracted from urediniospores of rust isolates from six different locations, and a 267-bp fragment of the ITS2 region was amplified and sequenced using the primers ITS3 and ITS4 (GenBank Accession No. HQ661383). All sequences were identical to each other and shared 99% identity (232 of 234 bp) with a T. minima isolate from South Africa (GenBank Accession No. GU355675). The alternate host, hemlock (mostly Tsuga canadensis L.) is a common and valuable conifer in the Michigan landscape. Hemlock trees were not examined for the presence of aecia but are assumed to play a role in the epidemiology of the disease in Michigan because leaf rust tends to be more severe near hemlock trees. Pucciniastrum vaccinii (G. Wint.) Jorst. was considered the causal agent of blueberry leaf rust until Sato et al. (1,4) identified three unique species. While T. minima has been reported on black huckleberry (Gaylussacia baccata [Wangenh.] K. Koch) in Michigan (4), to our knowledge, this is the first report of T. minima on highbush blueberry in the state. T. minima has been reported on highbush blueberry in Delaware and New York (4), Japan (2), and South Africa (3). The severity of the outbreak in 2010 warrants further research into economic losses, epidemiology, and management of the disease. References: (1) D. F. Farr and A. Y. Rossman. Fungal Databases. Systematic Botany and Mycology Laboratory, ARS, UDSA. Retrieved from http://nt.ars-grin.gov/fungaldatabases/ , 2010. (2) T. Kobayashi. Page 1227 in: Index of Fungi Inhabiting Woody Plants in Japan. Host, Distribution and Literature. Zenkoku-Noson-Kyoiku Kyokai Publishing Co., Tokyo, 2007. (3) L. Mostert et al. Plant Dis. 94:478, 2010. (4) S. Sato et al. Trans. Mycol. Soc. Jpn. 34:47, 1993.

Download Full-text