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1.
Phytopathology ; 103(2): 129-34, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23013451

ABSTRACT

Corn stunt disease has become a factor limiting maize production in some areas of the Americas in recent years. Although resistant maize genotypes have been developed in the past, this resistance has been unstable over time or in some geographical locations. To better understand disease components that could affect the stability of host resistance, we assessed the genome variability of the etiologic agent, Spiroplasma kunkelii. Isolates were obtained from a number of areas, and characterized molecularly by amplification of several regions of the spiroplasma chromosome and sequencing of specific gene fragments. The degree of polymorphism between isolates of different geographic origins was low, and the level of genomic variability was similar within isolates of different countries. Polymorphism among isolates was found in viral insertions and in the sequence of Skarp, a gene that encodes a membrane protein implicated in attachment to insect cells. The results suggest that the genome composition of this species is highly conserved among isolates. Hence, it is unlikely that the instability of maize resistance is due to generation of new pathotypes of S. kunkelii. Instead, other components of this complex pathosystem could account for the breakdown of resistance.


Subject(s)
Genome, Bacterial/genetics , Plant Diseases/microbiology , Polymorphism, Genetic/genetics , Spiroplasma/genetics , Zea mays/microbiology , Argentina , Bacterial Proteins/genetics , Brazil , Costa Rica , DNA, Bacterial/chemistry , Disease Resistance , Genotype , Geography , Mexico , Phylogeny , Plant Leaves/microbiology , Sequence Analysis, DNA , Spiroplasma/isolation & purification , United States
2.
Curr Microbiol ; 45(5): 334-9, 2002 Nov.
Article in English | MEDLINE | ID: mdl-12232663

ABSTRACT

Metarhizium anisopliae is the best-characterized entomopathogen and is used to control insect pests in sugar cane plantations in Brazil on a commercial scale. We have previously reported the infection of some M. anisopliae strains by dsRNA mycoviruses. Here we describe the purification and characterization of the viruses (MaV-A1, MaV-M5, MaV-RJ) in terms of dsRNA content, capsid proteins, electron microscopy, Western blot, and hybridization patterns. One spontaneous mutant lost some of the high molecular weight dsRNA components and showed significant alterations in colony morphology and spore production, suggesting that viral genes interfere with fungal phenotype. A comparison between dsRNA mycovirus-free and infected M. anisopliae isolates showed that virus-free isolates have increased endochitinase secretion. By comparing the following parameters: the buoyant density in CsCl of the presumed virions; the number and estimated molecular weight of the dsRNA components and the molecular mass of the capsid proteins to other mycoviruses previously described, we suggest the inclusion of MaV-A1 and MaV-M5 in the family Totiviridae and MaV-RJ in the family Partitiviridae.


Subject(s)
Capsid Proteins/metabolism , Chitinases/metabolism , Mitosporic Fungi/enzymology , Mitosporic Fungi/virology , RNA Viruses/growth & development , Antibodies, Viral/blood , Blotting, Western , Brazil , Capsid Proteins/isolation & purification , Microscopy, Electron , Nucleic Acid Hybridization , Pest Control, Biological , RNA Viruses/genetics , RNA Viruses/metabolism , RNA, Viral/chemistry , RNA, Viral/genetics , Reverse Transcriptase Polymerase Chain Reaction
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