Detection, symptomatology and management of aster yellows disease in canola.

2017 ◽  
pp. 233-246 ◽  
Author(s):  
C. Olivier ◽  
T. Dumonceaux ◽  
E. Pérez-López ◽  
T. J. Wist ◽  
B. Elliott ◽  
...  
Keyword(s):  
Aster Yellows

scholarly journals First report of phytoplasmas in the aster yellows group infecting grapevine in Tunisia

2004 ◽  
Vol 53 (4) ◽  
pp. 521-521 ◽  
Author(s):  
S. M'hirsi ◽  
H. Acheche ◽  
S. Fattouch ◽  
G. Boccardo ◽  
M. Marrakchi ◽  
...  
Keyword(s):  
Aster Yellows ◽  
First Report

EFFECT OF FIVE INSECTICIDES ON POPULATIONS OF THE SIX-SPOTTED LEAFHOPPER AND THE INCIDENCE OF ASTER YELLOWS IN CARROTS

1970 ◽  
Vol 50 (2) ◽  
pp. 169-174 ◽  
Author(s):  
R. C. HENNE
Keyword(s):  
Effective Treatment ◽  
Aster Yellows ◽  
Commercial Scale ◽  
Aster Leafhopper ◽  
Insecticide Spray

Five insecticides were evaluated for their ability to control the aster leafhopper, Macrosteles fascifrons (Stål), and to reduce the incidence of aster yellows disease, transmitted by this vector in carrots. Furadan (2,3-dihydro-2,2-dimethyl-7-benzofuranyl methylcarbamate) as a single granular treatment at seeding was as effective in reducing the level of aster yellows disease as five or eight foliar treatments with carbaryl (1-naphthyl N-methylcarbamate) in 1967 and 1968. Oxydemeton-methyl (O,O-dimethyl S-[2-(ethylsulfinyl)-ethyl]phosphorothioate) was comparable with carbaryl in reducing aster leafhopper numbers and incidence of aster yellows disease. Disulfoton (O,O-diethyl S-[2-(ethylthio)ethyl]phosphorodithioate) as a single granular application at seeding was the least effective treatment in this study. Aster yellows incidence in carrots treated with DDT [1,1,1-trichloro-2,2-bis(p-chlorophenyl) ethane] was only slightly lower than with carbaryl in a commercial scale trial. A 5-day insecticide spray schedule was not appreciably more effective than a 10-day schedule.

scholarly journals A New Disease of Cherry Plum Tree with Yellow Leaf Symptoms Associated with a Novel Phytoplasma in the Aster Yellows Group

2014 ◽  
Vol 13 (8) ◽  
pp. 1707-1718 ◽  
Author(s):  
Zheng-nan LI ◽  
Lei ZHANG ◽  
Ye TAO ◽  
Ming CHI ◽  
Yu XIANG ◽  
...  
Keyword(s):  
Yellow Leaf ◽  
New Disease ◽  
Aster Yellows ◽  
Leaf Symptoms ◽  
Plum Tree

scholarly journals Seasonal Patterns of Aster Leafhopper (Hemiptera: Cicadellidae) Abundance and Aster Yellows Phytoplasma Infectivity in Wisconsin Carrot Fields

2013 ◽  
Vol 42 (3) ◽  
pp. 491-502 ◽  
Author(s):  
K. E. Frost ◽  
P. D. Esker ◽  
R. Van Haren ◽  
L. Kotolski ◽  
R. L. Groves
Keyword(s):  
Seasonal Patterns ◽  
Aster Yellows ◽  
Aster Leafhopper ◽  
Aster Yellows Phytoplasma

scholarly journals Molecular Characterization and Classification of Phytoplasmas Associated with Canola Yellows and a New Phytoplasma Strain Associated with Dandelions

Plant Disease ◽  
2001 ◽  
Vol 85 (1) ◽  
pp. 76-79 ◽  
Author(s):  
Keri Wang ◽  
Chuji Hiruki
Keyword(s):  
Fragment Length Polymorphism ◽  
Rflp Analysis ◽  
Universal Primers ◽  
Dna Fragments ◽  
Chain Reaction ◽  
Aster Yellows ◽  
Distinct Subgroup ◽  
16S Ribosomal Dna ◽  
Polymerase Chain

DNA isolated from symptomatic canola (Brassica napus, Brassica rapa) and dandelion (Taraxacum officinale) was used to amplify 16S ribosomal DNA fragments by polymerase chain reaction using two pairs of universal primers P1/P6 and R16F2n/R2. Restriction fragment length polymorphism (RFLP) analysis of the amplified DNA fragments using endonucleases AluI, HhaI, HpaII, MseI, RsaI, and Sau 3AI revealed two distinct types of phytoplasmas in canola with similar symptoms. One had the same RFLP profiles as the phytoplasmas in subgroup 16SrI-A, whereas the other one had RFLP profiles similar to those of phytoplasmas in subgroup 16SrI-B. Phytoplasmas were detected in symptomatic dandelion plants that were collected from canola and alfalfa fields where severe alfalfa witches'-broom occurred. Comparative studies indicated that two different phytoplasmas were associated with the dandelion plants. One was identified as a member of subgroup 16SrI-A, whereas another one was classified as a member of a distinct subgroup in the aster yellows group on the basis of the unique RFLP patterns.

Aster Yellows

2008 ◽  
pp. 323-323
Author(s):  
George Hangay ◽  
Severiano F. Gayubo ◽  
Marjorie A. Hoy ◽  
Marta Goula ◽  
Allen Sanborn ◽  
...  
Keyword(s):  
Aster Yellows

scholarly journals First Report of an Aster Yellows Phytoplasma Associated with Cabbage in Southern Texas

Plant Disease ◽  
2001 ◽  
Vol 85 (4) ◽  
pp. 447-447 ◽  
Author(s):  
I.-M. Lee ◽  
R. A. Dane ◽  
M. C. Black ◽  
Noel Troxclair
Keyword(s):  
16S Rdna ◽  
Nested Pcr ◽  
Restriction Enzymes ◽  
Diagnostic Procedures ◽  
Acid Extraction ◽  
Insect Vector ◽  
Aster Yellows ◽  
First Report ◽  
Pcr Products ◽  
Aster Yellows Phytoplasma

In early spring 2000 carrot crops in southwestern Texas were severely infected by an outbreak of phyllody associated with aster yellows phytoplasma. Cabbage crops that had been planted adjacent to these carrot fields began to display previously unobserved symptoms characteristic of phytoplasma infection. Symptoms included purple discoloration in leaf veins and at the outer edges of leaves on cabbage heads. Proliferation of sprouts also occurred at the base of the stem and between leaf layers of some plants, and sprouts sometimes continued to proliferate on extended stems. About 5% of cabbage plants in the field exhibited these symptoms. Two symptomless and four symptomatic cabbage heads were collected in early April from one cabbage field. Veinal tissues were stripped from each sample and used for total nucleic acid extraction. To obtain specific and sufficient amount of PCR products for analysis, nested PCR was performed by using primer pairs (first with P1/P7 followed by R16F2n/R16R2) (1,2) universal for phytoplasma detection. A specific 16S rDNA fragment (about 1.2 kb) was strongly amplified from the four symptomatic but not from the two asymptomatic samples. The nested PCR products obtained from the four symptomatic samples were then analyzed by restriction fragment length polymorphism (RFLP) using the restriction enzymes MseI, HhaI, and HpaII, and the RFLP patterns were compared to the published patterns of known phytoplasmas (1). The resulting RFLP patterns were identical to those of a phytoplasma belonging to subgroup B of the aster yellows phytoplasma group (16SrI). These RFLP patterns were also evident in putative restriction sites observed in a 1.5 kbp nucleotide sequence of the 16S rDNA. This is the first report of aster yellows phytoplasma associated disease symptoms in cabbage in Texas. The occurrence of cabbage proliferation coincided with the presence of high populations of the insect vector, aster leafhopper. References: (1) I.-M. Lee et al. Int. J. Syst. Bacteriol. 48:1153, 1998. (2) B. Schneider et al. 1995. Molecular and Diagnostic Procedures in Mycoplasmology, Vol. I. Academic Press, San Diego, CA.

scholarly journals Leafhoppers and cixiids in phytoplasma-infected carrot fields: Species composition and potential phytoplasma vectors

2010 ◽  
Vol 25 (4) ◽  
pp. 311-318 ◽  
Author(s):  
Tanja Drobnjakovic ◽  
Pantelija Peric ◽  
Dejan Marcic ◽  
Luca Picciau ◽  
Alberto Alma ◽  
...  
Keyword(s):  
Control Strategies ◽  
Species Level ◽  
Effective Control ◽  
Correct Identification ◽  
Vegetable Crops ◽  
Vegetative Period ◽  
Aster Yellows ◽  
Scaphoideus Titanus ◽  
The Family ◽  
Pcr Rflp

The first molecular analysis of samples collected in southern Backa (Serbia) confirmed the presence of aster yellows (16SrI) and stolbur phytoplasmas (16SrXII) in insects belonging to the family Cicadellidae, as well as in carrot plants where the insects were collected. A correct identification of the phytoplasmas and their vectors is essential to arrange effective control strategies to prevent diseases associated with phytoplasmas from spreading to carrots and other vegetable crops. In order to enhance knowledge about insect vectors of aster yellows and stolbur phytoplasmas in Serbia, Cicadellidae and Cixiidae (Homoptera Auchenorrhyncha), the most common vectors of these phytoplasmas, were monitored in southern Backa during 2008. Adults leaf- and planthoppers were collected and identified at species level using standard entomological methods, and tested for phytoplasma presence by means of PCR/RFLP. A total of 13 insect species of Cicadellidae were identified, as follows: a) three species of the subfamily Agallinae: Anaceratagallia ribauti (Ossiannilsson), Anaceratagallia venosa (Fourcroy), and Anaceratagallia laevis (Ribaut); b) seven species of the subfamily Deltocephalinae: Psammotettix confinis (Dahlbom), Psammotettix striatus (Linnaues) Psammottettix alienus (Dahlbom), Macrosteles sexnotatus (Fall?n), Ophiola decumana (Kontkanen), Errastunus ocellaris Fall?n, and Scaphoideus titanus Ball; c) three species of the subfamily Typhlocibinae: Eupteryx atropunctata (Goeze), Eupteryx mellissae Curtis, Zyginidia pullula (Boheman). Female specimens of the genus Euscelis (Deltocephalinae) were also collected, as well as one species of Reptalus quinquecostatus (Dufour) of the family Cixiidae. Stolbur phytoplasmas were detected in A. laevis, A. ribauti, A. venosa, P. striatus, P. confinis and P. alienus. The species: A. laevis, O. decumana, and P. confinis were AY-infected (subgroup 16SrI-A), while subgroup 16SrI-C was found only in one specimen of P. confinis. Since some aster yellows- and stolbur-infected species of the genera Psammotettix and Anaceratagallia (especially P. confinis and A. laevis) were regularly and commonly found in the infected carrot fields during the whole vegetative period, they could play a significant role in transmitting and spreading these pathogens in natural environment.

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