scholarly journals First Report of Puccinia coronata var. coronata sensu stricto Infecting Alder Buckthorn in the United States

2017 ◽  
Vol 18 (2) ◽  
pp. 84-86
Author(s):  
Shawn C. Kenaley ◽  
Geoffrey Ecker ◽  
Gary C. Bergstrom
Keyword(s):  
United States ◽  
North America ◽  
Host Range ◽  
Geographic Distribution ◽  
Phylogenetic Analyses ◽  
Rust Fungus ◽  
The United States ◽  
Sensu Stricto ◽  
Puccinia Coronata ◽  
First Report

Field symptoms, host distribution, pathogen morphology, and phylogenetic analyses clearly demonstrated that the rust fungus infecting alder buckthorn in Connecticut is Puccinia coronata var. coronata sensu stricto. To our knowledge, this is the first report and confirmation of P. coronata var. coronata s.s. in the United States. Additional collections from purported aecial and telial hosts of P. coronata var. coronata s.s. are necessary to determine its host range, geographic distribution, and incidence within the United States and elsewhere in North America.

First Report of a 16SrI (Aster Yellows) Group Phytoplasma in Phlox in the United States

2016 ◽  
Vol 17 (3) ◽  
pp. 198-199
Author(s):  
Andrew E. Sathoff ◽  
Deepak Rajendran ◽  
Seth D. Wannemuehler ◽  
Katarina Sweeney ◽  
Fazal Manan ◽  
...  
Keyword(s):  
United States ◽  
North America ◽  
Flowering Time ◽  
Flower Color ◽  
The United States ◽  
Aster Yellows ◽  
First Report ◽  
Color Range ◽  
Small Grains ◽  
Herbaceous Perennial

Phlox are herbaceous perennial ornamentals native to North America grown for their flower color, range in flowering time, scent, and differing forms. Candidatus Phytoplasma asteris, first found to occur in Chinese asters, is spread by aster leafhoppers and in 2001 was reported to be a serious threat to phlox. There have been several reports of Ca. P. asteris in garlic and small grains in Minnesota. This is the first report of Candidatus Phytoplasma asteris in phlox in Minnesota and the United States. Accepted for publication 28 June 2016. Published 6 September 2016.

scholarly journals Common Ancestry of Borrelia burgdorferiSensu Lato Strains from North America and Europe

1999 ◽  
Vol 37 (9) ◽  
pp. 3010-3012 ◽  
Author(s):  
D. Postic ◽  
N. Marti Ras ◽  
R. S. Lane ◽  
P.-F. Humair ◽  
M. M. Wittenbrink ◽  
...  
Keyword(s):  
United States ◽  
North America ◽  
Borrelia Burgdorferi ◽  
North American ◽  
Phylogenetic Analyses ◽  
The United States ◽  
Whole Genome ◽  
Common Ancestry ◽  
Limited Region

Ten atypical European Borrelia burgdorferi sensu lato (Borrelia spp.) strains were genetically characterized, and the diversity was compared to that encountered among relatedBorrelia spp. from North America. Phylogenetic analyses of a limited region of the genome and of the whole genome extend existing knowledge about borrelial diversity reported earlier in Europe and the United States. Our results accord with the evidence that North American and European strains may have a common ancestry.

scholarly journals Trichothecene Genotype of Fusarium graminearum Isolates from Soybean (Glycine max) Seedling and Root Diseases in the United States

Plant Disease ◽  
2014 ◽  
Vol 98 (7) ◽  
pp. 1012-1012 ◽  
Author(s):  
M. L. Ellis ◽  
G. P. Munkvold
Keyword(s):  
United States ◽  
North America ◽  
Fusarium Graminearum ◽  
Root Rot ◽  
Elongation Factor ◽  
Host Shift ◽  
The United States ◽  
Sensu Stricto ◽  
Head Blight ◽  
The Third

Fusarium graminearum is an economically important pathogen that causes Fusarium head blight of wheat, barley, and oat, and Gibberella ear and stalk rot of maize. More recently, F. graminearum was reported as a soybean seedling and root pathogen in North America (1,5), causing seed decay, damping-off, and brown to reddish-brown root rot symptoms. Type B trichothecene mycotoxins are commonly produced by F. graminearum, which can be categorized into three trichothecene genotypes; those that produce 3-acetyldeoxynivalenol (3-ADON), 15-acetyldeoxynivalenol (15-ADON), or nivalenol (NIV). The 15-ADON genotype is dominant in populations from small grains and maize in North America (4), but the 3-ADON genotype has recently been found (4). F. graminearum was known as a pathogen of wheat and maize in North America for over a century before it was reported as a soybean pathogen. Therefore, we hypothesized that recent reports on soybean could be associated with the appearance of the 3-ADON genotype. The objective of this research was to determine the trichothecene genotype of F. graminearum isolates from soybean in the United States. Thirty-eight isolates from soybean were evaluated. Twenty-seven isolates came from a 3-year survey for Fusarium root rot from 2007 to 2009 in Iowa. Other isolates (Ahmad Fakhoury, Southern Illinois University, Carbondale) were collected from soybean seedlings during a multi-state survey in 2012, and included three isolates from Illinois, three from Indiana, and five from Nebraska. Species identification and lineage of F. graminearum were confirmed by sequencing the translation elongation factor gene (EF1-α) using EF-1H and EF-2T primers. A maximum likelihood analysis of the EF1-α, including voucher strains from nine lineages of F. graminearum (2), placed all 38 isolates into lineage 7, F. graminearum sensu stricto (representative GenBank accessions KJ415349 to KJ415352). To determine the trichothecene genotype of each isolate we used three multiplex PCR assays. The first two assays targeted a portion of trichothecene biosynthesis genes Tri3 and Tri12 (4), while the third assay targeted portions of the Tri3, Tri5, and Tri7 genes (3). The PCR for the first two assays was conducted as described by Ward et al. (4) using four sets of primers: 3CON, 3NA, 3D15A, and 3D3A; and 12CON, 12NF, 12-15F, and 12-3F for the Tri3 and Tri12 genes, respectively. The PCR for the third assay was conducted as described by Quarta et al. (3) using the following primers: Tri3F971, Tri3F1325, Tri3R1679, Tri7F340, Tri7R965, 3551H, and 4056H. The amplification products were analyzed by gel electrophoresis. All 38 isolates produced amplicons consistent with the 15-ADON genotype; ~610 and 670 bp for the Tri3 and Tri12 genes, respectively (4), and two amplicons of ~708 and 525 bp for the Tri3/Tri5 genes (3). Our results indicated that the dominant trichothecene genotype among isolates of F. graminearum from soybean is 15-ADON, and the introduction of 3-ADON isolates does not explain the recent host shift of F. graminearum to soybean in North America. To our knowledge, this is the first assessment of trichothecene genotypes in F. graminearum populations from soybean from the United States. References: (1) K. E. Broders et al. Plant Dis. 91:1155, 2007. (2) K. O'Donnell et al. Fungal Gen. Biol. 41:600, 2004. (3) A. Quarta et al. FEMS Microbiol. Lett. 259:7, 2006. (4) T. D. Ward et al. Fungal Gen. Biol. 45:473, 2008. (5) A. G. Zue et al. Can. J. Plant Pathol. 29:35, 2007.

scholarly journals Recent Outbreak of Soybean Sudden Death Syndrome Caused by Fusarium virguliforme and F. tucumaniae in Argentina

Plant Disease ◽  
2004 ◽  
Vol 88 (9) ◽  
pp. 1044-1044 ◽  
Author(s):  
M. Scandiani ◽  
D. Ruberti ◽  
K. O'Donnell ◽  
T. Aoki ◽  
R. Pioli ◽  
...  
Keyword(s):  
United States ◽  
Phylogenetic Analyses ◽  
The United States ◽  
Positive Control ◽  
Koch’S Postulates ◽  
First Report ◽  
Molecular Phylogenetic ◽  
Soil Infestation ◽  
Pathogenicity Tests ◽  
Koch's Postulates

Sudden death syndrome (SDS) of soybean was detected initially in Argentina during 1991-1992 in the Pampas Region and 1992-1993 in the Northwest Region. The first report of the fulfillment of Koch's postulates of SDS caused by Fusarium solani f. sp. glycines in Argentina was published in 2003 (3). Subsequently, analyses have shown that F. solani f. sp. glycines represents several morphologically and phylogenetically distinct species, including F. tucumaniae in Argentina and F. virguliforme in the United States (1). Isolations were made from plants that exhibited typical SDS symptoms (interveinal foliar chlorosis and necrosis leading to defoliation of the leaflets but not the petioles) from fields in Santa Fe and Buenos Aires provinces in 2001, 2002, and 2003. To determine which species are responsible for SDS in Argentina, cultures of eight slow growing isolates that developed bluish pigmentation and produced abundant macroconidia in sporodochia on potato dextrose agar were subjected to morphological and molecular phylogenetic analyses and pathogenicity tests. Morphological analyses demonstrated that three of the isolates were F. virguliforme and five were F. tucumaniae. Isolates of F. tucumaniae produced long and narrow sporodochial conidia while F. virguliforme produced diagnostic comma-shaped conidia. Molecular phylogenetic analyses of DNA sequences from multiple loci confirmed morphology-based identifications and showed that the soybean SDS pathogen in the United States, F. virguliforme, was also present in Argentina. To our knowledge, this is the first report of F. virguliforme in Argentina and of this pathogen outside the United States. Five isolates of F. tucumaniae and three isolates of F. virguliforme were used for pathogenicity tests. F. virguliforme isolate 171 provided by J. Rupe (University of Arkansas, Fayetteville) was used as a positive control. Soybean cultivars Ripley, RA 702, Pioneer 9492RR, Spencer, and A-6445RG were inoculated with each of the isolates tested in a greenhouse assay using soil infestation and toothpick methods (2). All eight isolates produced typical foliar SDS symptoms 15 to 25 days after inoculation. Severity of foliar symptoms averaged 3.3 for F. virguliforme, 2.6 for F. tucumaniae, and 3.3 for the positive control using a disease severity scale in which 1 = no symptoms and 5 = severely infected or dead plants. Under these conditions, F. virguliforme appeared to be more virulent than F tucumaniae. Noninoculated plants remained symptomless. Koch's postulates were confirmed with soybean cultivars RA 702 and A6445RG. Isolates recovered from symptomatic plants inoculated by the soil infestation and toothpick methods were identical to those used to inoculate the plant. Strains were recovered at frequencies of 100 and 60% from plants inoculated by the toothpick and soil infestation methods, respectively. To our knowledge, this is the first report of the fulfillment of Koch's postulates for F. tucumaniae and F. virguliforme in Argentina. References: (1) T. Aoki et al. Mycologia 95:660, 2003. (2) K. W. Roy et al. Plant Dis. 81:1100, 1997 (3) M. Scandiani et al. Plant Dis. 87:447, 2003.

scholarly journals First Report of Leaf Spot Caused by Cercospora bizzozeriana on Lepidium draba in the United States

Plant Disease ◽  
2009 ◽  
Vol 93 (1) ◽  
pp. 108-108 ◽  
Author(s):  
A. J. Caesar ◽  
R. T. Lartey ◽  
D. K. Berner ◽  
T. Souissi
Keyword(s):  
United States ◽  
North America ◽  
Sugar Beet ◽  
Leaf Spot ◽  
The United States ◽  
Initial Report ◽  
Voucher Specimen ◽  
First Report ◽  
Leaf Spots ◽  
Lepidium Draba

The herbaceous perennial Lepidium draba L. is an invasive weed of rangelands and riparian areas in North America and Australia. As of 2002, it had infested 40,500 ha of rangeland in Oregon and large areas in Wyoming and Utah. Little is known of plant pathogens occurring on L. draba, especially in the United States, that could be useful for biological control of the weed. Leaf spots were first noted on a stand of L. draba near Shepherd, MT in 1997. The spots were mostly circular but sometimes irregularly shaped and whitish to pale yellow. The pathogen was erroneously assumed to be Cercospora beticola since its morphological traits closely resembled that species and the area had large fields of sugar beet with heavy Cercospora leaf spot incidence. Diseased leaves of L. draba were collected in 1997 and 2007. Conidia, borne singly on dark gray, unbranched conidiophores produced on dark stromata late in the season, were elongate, hyaline, multiseptate, 38 to 120 × 2 to 6 μm (mostly 38 to 50 × 2 to 5 μm) and had bluntly rounded tips and wider, truncate bases. These characteristics were consistent with the description of C. bizzozeriana Saccardo & Berlese (2). To isolate the fungus, spores were picked from fascicles of conidiophores with a fine-tipped glass rod, suspended in sterile water, and spread on plates of water agar. Germinated spores were transferred to potato dextrose agar (PDA). The ITS1, 5.8S, and ITS2 sequences of this fungus (GenBank Accession No. EU887131) were identical to sequences of an isolate of C. bizzozeriana from Tunisia (GenBank Accession No. DQ370428). However, these sequences were also identical to those of a number of Cercospora spp. in GenBank, including C. beticola. We also compared the actin gene sequences of the Montana isolate of C. bizzozeriana (GenBank Accession No. FJ205397) and an isolate of C. beticola from Montana (GenBank Accession No. AF443281); the sequences were 94.6% similar, an appreciable difference. For pathogenicity tests, cultures were grown on carrot leaf decoction agar. Aqueous suspensions of 104 spores per ml from cultures were sprayed on 6-week-old L. draba plants. Plants were covered with plastic bags and placed on the greenhouse bench at 20 to 25°C for 96 h. Koch's postulates were completed by reisolating the fungus from the circular leaf spots that appeared within 10 days, usually on lower leaves. Spores of C. bizzozeriana were also sprayed on seedlings of sugar beet, collard, mustard, radish, cabbage, and kale under conditions identical to those above. No symptoms occurred. After the discovery of the disease in 1997, plants of L. draba in eastern Montana, Wyoming, and Utah were surveyed from 1998 to 2003 for similar symptoms and signs, but none were found. This, to our knowledge, is the first report of C. bizzozeriana in the United States. The initial report of the fungus in North America was from Manitoba in 1938 (1). It has recently been reported as occurring on L. draba in Tunisia (4) and Russia (3) and is reported as common in Europe (2). A voucher specimen has been deposited with the U.S. National Fungus Collections (BPI No. 878750A). References: (1) G. R. Bisby. The Fungi of Manitoba and Saskatchewan. Natl. Res. Council of Canada, Ottawa, 1938. (2) C. Chupp. A Monograph of the Fungus Genus Cercospora. C. Chupp, Ithaca, NY, 1953. (3) Z. Mukhina et al. Plant Dis. 92:316, 2008. (4) T. Souissi et al. Plant Dis. 89:206, 2005.

scholarly journals bla VIM-7, an Evolutionarily Distinct Metallo-β-Lactamase Gene in a Pseudomonas aeruginosa Isolate from the United States

2004 ◽  
Vol 48 (1) ◽  
pp. 329-332 ◽  
Author(s):  
Mark A. Toleman ◽  
Kenneth Rolston ◽  
Ronald N. Jones ◽  
Timothy R. Walsh
Keyword(s):  
United States ◽  
Pseudomonas Aeruginosa ◽  
North America ◽  
The United States ◽  
Surveillance Program ◽  
First Report ◽  
Antimicrobial Surveillance ◽  
Lactamase Gene

ABSTRACT As part of the CANCER Antimicrobial Surveillance Program in North America, a Pseudomonas aeruginosa isolate, strain 07-406, was shown to possess a metallo-β-lactamase, designated VIM-7. bla VIM-7 is located on a 24-kb plasmid which can be readily transferred into Enterobacteriaceae and other pseudomonads. This is the first report of a mobile metallo-β-lactamase gene, bla VIM-7, being detected within the United States.

The Galium aparine complex in Canada

1975 ◽  
Vol 53 (9) ◽  
pp. 877-893 ◽  
Author(s):  
R. J. Moore
Keyword(s):  
United States ◽  
North America ◽  
Chromosome Number ◽  
The United States ◽  
Sensu Stricto ◽  
Western Canada ◽  
Galium Aparine ◽  
Prairie Provinces

The occurrence in Canada of Galium aparine sensu lato has been studied. It is concluded that two species are present: G. aparine L. sensu stricto (Cleavers) and G. spurium L. (False Cleavers). Although closely related and morphologically similar, these species differ morphologically, cytologically, and physiologically. The chromosome number of collections of G. aparine from Canada and the United States was found to be 2n = 66, that of G. spurium from the prairie provinces of Canada was 2n = 20. The latter species is an introduction from Eurasia and seems to be the more serious weed in fields of grain and rapeseed in western Canada. Galium aparine is believed to be native, as well as introduced from Eurasia, in North America. Galium aparine occurs usually in moist, shaded habitats, whereas G. spurium favors sunnier habitats. Both species have spiny or smooth fruits and these fruit variants have been recognized at various taxonomic levels. In this paper they are reduced to the rank of form.

scholarly journals First Report of the Telial Stage of Japanese Apple Rust on Juniperus chinensis in North America and the Aecial Stage on Malus domestica

Plant Disease ◽  
2010 ◽  
Vol 94 (9) ◽  
pp. 1169-1169
Author(s):  
N. F. Gregory ◽  
J. F. Bischoff ◽  
L. J. Dixon ◽  
R. Ciurlino
Keyword(s):  
United States ◽  
North America ◽  
Malus Domestica ◽  
Large Subunit ◽  
The United States ◽  
Causal Agent ◽  
University Of Delaware ◽  
First Report ◽  
Telial Stage ◽  
Juniperus Chinensis

Following a report in April 2009 of the presence of Gymnosporangium yamadae Miyabae ex G. Yamada on crabapple (Malus toringo Siebold) in Wilmington, DE (2), University of Delaware, State of Delaware, and USDA/APHIS PPQ personnel collaborated to confirm and document the pathogen. G. yamadae is the causal agent of Japanese apple rust. The fungus is known from Asia with an aecial state on economically important Malus species and telial state on Juniperus chinensis. During the April 2009 site visit, ornamental J. chinensis were observed near the original crabapples. On May 7, 2009, telial galls were collected from the ornamental J. chinensis at the Wilmington site. The telia were confirmed to be G. yamadae by morphometric analysis and molecular data. The rDNA large subunit (LSU) sequence derived from the collected telial galls (GenBank Accession No. GU058012) was identical to the eight G. yamadae LSU sequences (GenBank Accession Nos. FJ848760–FJ848765, FJ559373, and FJ559375) reported from Korea by Yun et al. (3). Teliospores were 45 to 54 μm long with pedicels that were wide (7.0 to 8.4 μm) along the full length. The G. yamadae telial gall collected from Wilmington, DE was deposited into the U.S. National Fungus Collection (BPI 879273). Leaves of M. domestica on the University of Delaware farm in Newark were confirmed to have Japanese apple rust on Aug 4, 2009. Identification was made on the morphological presence of unique roestelioid aecia with long cornulated peridia that lacerate along the sides. The aecia differ from those of G. juniperi-virginianae, the causal agent of cedar apple rust, which has aecial peridia that fimbriate to the base and are strongly recurved (1). Following release of a USDA Pest Alert, subsequent samples submitted to USDA/APHIS PPQ indicated widespread incidence of the G. yamadae aecial state in the northeast, including Maryland, Maine, New Hampshire, New Jersey, New York, Pennsylvania, and Rhode Island. Japanese apple rust likely went undetected for several years because of similar symptomatology to cedar apple rust. To our knowledge, this is the first report of the telial stage of G. yamadae in North America and the first report of this pathogen on Malus domestica in the United States. Knowledge of the geographic distribution of G. yamadae is of significance because of the actionable regulatory status of the pathogen and its potential impact on ornamental and fruit growers of Malus spp. in the United States. References: (1) F. D. Kern. A Revised Taxonomic Account of Gymnosporangium. Pennsylvania State University Press, University Park, PA, 1973. (2) H. Y. Yun et al. Plant Dis. 93:430, 2009. (3) H. Y. Yun et al. Mycologia 101:790, 2009.

scholarly journals First Record of Meloidogyne partityla on Pecan in Georgia

Plant Disease ◽  
2002 ◽  
Vol 86 (4) ◽  
pp. 441-441 ◽  
Author(s):  
A. P. Nyczepir ◽  
C. C. Reilly ◽  
B. W. Wood ◽  
S. H. Thomas
Keyword(s):  
United States ◽  
South Africa ◽  
New Mexico ◽  
North America ◽  
Host Range ◽  
Nematode Species ◽  
First Record ◽  
The United States ◽  
Root Knot Nematode ◽  
Narrow Host Range

In July 2000, tree decline was observed in a commercial pecan (Carya illinoensis (Wang.) K. Koch) orchard in Crisp County, GA. Most affected trees exhibited dead branches in the upper canopy, stunted growth, and feeder roots with small galls and associated egg masses typical of root-knot nematode infection. All declining trees that were examined had root systems infected with a Meloidogyne sp. Efforts to culture the nematode on tomato (Lycopersicon esculentum Mill. ‘Rutgers’) were unsuccessful. Identification of the nematode was determined by two laboratory procedures in March 2001. Female nematodes were teased from fresh pecan root galls of declining trees in Georgia, and identified by determining the esterase phenotype from replicate samples of single females compared with standard root-knot nematode species, including a population of M. partityla (3). Galled roots also were sent to New Mexico State University in Las Cruces, where mitochondrial DNA from specimens was extracted and compared with that from standard root-knot nematode species and known populations of M. partityla (2). Specimens had esterase phenotypes and DNA patterns consistent with M. partityla. Esterase phentoypes were inconsistent with M. incognita and M. arenaria, and DNA patterns were inconsistent with M. incognita, M. javanica, and M. hapla. Specimens at both locations were identified as M. partityla Kleynhans (1). To our knowledge, this is the first report of M. partityla from Georgia and the third report of this nematode outside of South Africa. The first and second report of M. partityla from pecan in the United States occurred in Texas and New Mexico in 1996 and 2001, respectively (3,4). Our inability to culture the M. partityla-GA isolate on tomato substantiates previous experience with this nematode in the United States (3) and is not surprising, since this species has a host range limited to the Juglandaceae. Furthermore, M. partityla may be endemic to North America and not South Africa. It is believed this nematode entered South Africa on pecan seedling roots imported from the United States between 1912 and 1940 (1). The unusually narrow host range may explain why M. partityla has gone unrecognized for so long in the United States compared with the more common Meloidogyne spp. (i.e., M. incognita and M. arenaria) with wider host ranges found in pecan orchards. Determining the distribution of M. partityla within the major pecan-growing regions of Georgia and throughout North America is warranted. References: (1) K. P. N. Kleynhans. Phytophylactica 18:103, 1986. (2) T. O. Powers and T. S. Harris. J. Nematol. 25:1, 1993. (3) J. L. Starr et al. J. Nematol. 28:565, 1996. (4) S. H. Thomas et al. Plant Dis. 85:1030, 2001.

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