Exitianus obscurinervis (Hemiptera: Cicadellidae), a New Experimental Vector of Spiroplasma kunkelii

2011 ◽  
Vol 104 (6) ◽  
pp. 1793-1799 ◽  
Author(s):  
E. Carloni ◽  
E. Virla ◽  
S. Paradell ◽  
P. Carpane ◽  
C. Nome ◽  
...  
Keyword(s):  
2003 ◽  
Author(s):  
Charles Thomas Parker ◽  
Dorothea Taylor ◽  
George M Garrity
Keyword(s):  

Author(s):  

Abstract A new distribution map is provided for Spiroplasma kunkelii Whitcomb, Chen et al. Bacteria. Hosts: maize (Zea mays), sweetcorn (Zea mays subsp. mays), teosinte (Zea mexicana) and perennial teosinte (Zea perennis). Information is given on the geographical distribution in North America (Mexico, USA, California, Florida, Louisiana, Michigan, Mississippi, Ohio, Texas), Central America and Caribbean (Belize, El Salvador, Guatemala, Honduras, Jamaica, Nicaragua, Panama), South America (Argentina, Bolivia, Brazil, Mato Grosso do Sul, Minas Gerais, Colombia, Paraguay, Peru, Venezuela).


2006 ◽  
Vol 52 (9) ◽  
pp. 857-867 ◽  
Author(s):  
Ellen L Dally ◽  
Thereza S.L Barros ◽  
Yan Zhao ◽  
ShaoPing Lin ◽  
Bruce A Roe ◽  
...  

Spiroplasma kunkelii (class Mollicutes) is the characteristically helical, wall-less bacterium that causes corn stunt disease. A combination of restriction enzyme analysis, pulsed-field gel electrophoresis (PFGE), and Southern hybridization analysis was used to construct a physical and genetic map of the S. kunkelii CR2-3x chromosome. The order of restriction fragments on the map was determined by analyses of reciprocal endonuclease double digests employing I-CeuI, AscI, ApaI, EagI, SmaI, BssHII, BglI, and SalI; adjacent fragments were identified on two-dimensional pulsed-field electrophoresis gels. The size of the chromosome was estimated at 1550 kb. Oligonucleotide pairs were designed to prime the amplification of 26 S. kunkelii gene sequences in the polymerase chain reaction (PCR). Using PCR amplicons as probes, the locations of 27 S. kunkelii putative single-copy genes were positioned on the map by Southern hybridization analyses of chromosomal fragments separated in PFGE. The nucleotide sequence of the single ribosomal RNA operon was determined and its location mapped to a chromosomal segment bearing recognition sites for SalI, SmaI, EagI, and I-CeuI.Key words: Spiroplasma kunkelii CR2-3x, corn stunt spiroplasma, mollicutes, genome mapping, two-dimensional pulsed-field gel electrophoresis.


2013 ◽  
Vol 106 (4) ◽  
pp. 1574-1581 ◽  
Author(s):  
E. Carloni ◽  
P. Carpane ◽  
S. Paradell ◽  
I. Laguna ◽  
M. P. Giménez Pecci

1993 ◽  
Vol 39 (5) ◽  
pp. 543-547 ◽  
Author(s):  
Elsayed E. Wagih ◽  
Jacqueline Fletcher

A new microtechnique that detects enzyme activity in prokaryotes is described. The technique, designated zymoblot, is based on the immobilization of negatively charged enzymes from an alkaline extract spotted onto a nitrocellulose membrane. The presence of specific enzyme activity in the extract is selectively assayed with a reaction mixture containing the corresponding substrate. The enzyme–substrate reaction produces an insoluble colored product that accumulates at the site. The zymoblot technique offers the advantages of simplicity, sensitivity, reproducibility, speed, and the use of microquantities of reactants. The protein in the spot can be visualized by a technique termed "proteinblot," in which the protein is stained with Coomassie blue. Esterase and tyrosinase were detected by the zymoblot method in six spiroplasmas including four strains of Spiroplasma citri, one of Spiroplasma kunkelii, and one of Spiroplasma melliferum, and two bacteria, Pseudomonas syringae pv. syringae B301D and Escherichia coli K-12. Acid phosphatase, alkaline phosphatase, alanine dehydrogenase, peroxidase, and 6-phosphogluconate dehydrogenase were not detected in any of the spiroplasmas, but were each detected in one or both of the walled bacteria.Key words: spiroplasma, enzyme, protein, zymoblot.


Author(s):  
J. F. Bradbury

Abstract A description is provided for Spiroplasma kunkelii. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: Zea mays is the major natural host. Euchlaena mexicana and E. perennis are known experimental hosts and may be involved in the epidemiology of this disease. Various other plants have been infected by artificial inoculation using leafhopper vectors. e.g. Broad bean and Vinca rosea[Catharanthus roseus] using Euscelidius variegatus (57, 565) but these are probably not natural hosts. DISEASE: Corn/maize stunt. Infected maize is stunted and shows chlorotic stripes and often reddish purple leaf margins (69, 1042). Some plants have been found to be infected but show no symptoms. This is a major disease limiting maize production in tropical lowlands of America. GEOGRAPHICAL DISTRIBUTION: Widespread in tropical lowland America, from Texas in the north to the lowlands of Bolivia in the south (62, 166). Reports include USA: California, Florida (69, 1042), Michigan (Whitcomb et al., 1986); Texas; Mexico (69, 1042); Jamaica (62, 2437); Nicaragua (67, 1283); Peru (66, 3773); Brazil (Paranfi, 65 4390) and possibly Venezuela with very low incidence (57, 133). TRANSMISSION: The principal vector is the leaf hopper Dalbulus maidis but other leaf hoppers, such as Euscelidius variegatus, Dalbulus longulus, Cicadulina and Baldulus spp., have been shown to acquire and transmit the pathogen experimentally (64, 160, 3831; 63, 1748, 5332). No other method of transmission has been found.


2003 ◽  
Author(s):  
Charles Thomas Parker ◽  
Dorothea Taylor ◽  
George M Garrity
Keyword(s):  

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