May
2001
, Volume
85
, Number
5
Pages
475
-
480
Authors
Thereza S. L.
Barros
,
USDA-ARS, Molecular Plant Pathology Laboratory, Beltsville, MD 20705, and Laboratório de Biologia Molecular, Departamento de Biologia Celular, Universidade de Brasília, Brasília, DF, 70919-970, Brazil
;
Robert E.
Davis
,
USDA-ARS, Molecular Plant Pathology Laboratory, Beltsville, MD 20705
;
Renato O.
Resende
,
Laboratório de Virologia e Microscopia Eletrônica, Departamento de Biologia Celular, Universidade de Brasília, Brasília, DF, 70919-970, Brazil
; and
Ellen L.
Dally
,
USDA-ARS, Molecular Plant Pathology Laboratory, Beltsville, MD 20705
Affiliations
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RelatedArticle
Accepted for publication 16 January 2001.
Abstract
ABSTRACT
Corn stunt disease is a major limiting factor in production of corn (Zea mays) in the Americas. To develop a polymerase chain reaction (PCR) assay specific for detection of the causal agent, Spiroplasma kunkelii, PCR primers were designed on the basis of unique regions of the nucleotide sequence of the S. kunkelii spiralin gene. DNA was amplified in PCRs containing template DNAs derived from laboratory strains of S. kunkelii and from naturally diseased corn plants collected in the field. No DNA amplification was observed in PCRs containing template DNAs derived from other Spiroplasma species tested or from healthy corn or corn infected by maize bushy stunt phytoplasma. The availability of a sensitive and specific PCR for detection and identification of S. kunkelii should facilitate studies of the ecology of this pathogen, as well as its influence in the incidence, spread, and severity of corn stunting diseases.
JnArticleKeywords
Additional keywords:
CSS,
Maize rayado fino virus,
mollicutes
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ArticleCopyright
© 2001 The American Phytopathological Society