Amplified fragment length polymorphism in Elymus elymoides, Elymus multisetus, and other Elymus taxa

2003 ◽  
Vol 81 (8) ◽  
pp. 789-804 ◽  
Author(s):  
Steven R Larson ◽  
Thomas A Jones ◽  
Carrie L McCracken ◽  
Kevin B Jensen

The geographic and phylogenetic significance of amplified fragment length polymorphism within and among 22 Elymus elymoides (Raf.) Swezey subsp. elymoides, 24 E. elymoides subsp. brevifolius (J.G. Sm.) Barkworth, and 13 Elymus multisetus (J.G. Sm.) Burtt-Davy squirreltail accessions was assessed relative to six other North American and three Eurasian Elymus taxa. Elymus elymoides and E. multisetus, comprising Elymus sect. Sitanion (Raf.) Á. Löve, were both monophyletic and closely related compared with other congeners. The monophyly of subsp. elymoides was also supported; subsp. brevifolius, however, was paraphyletic and separated into four genetically distinct groups. Estimates of nucleotide divergence among the five E. elymoides groups range from 0.0194 to 0.0288, with approximately 0.0329 differences per site between E. elymoides and E. multisetus. Corresponding estimates of nucleotide divergence range from 0.0243 to 0.0387 among North American taxa and from 0.0337 to 0.0455 between North American and Eurasian taxa. DNA polymorphism among E. elymoides accessions was correlated with geographic provenance and previously reported quantitative traits. Distinct genetic groups of E. elymoides generally correspond to different geographic regions, whereas divergent E. multisetus and E. elymoides accessions are sympatric. Thus, taxonomic ranks of E. multisetus and E. elymoides were supported and geographic groups within E. elymoides were distinguished.Key words: AFLP, Elymus, nucleotide diversity, squirreltail.




2001 ◽  
Vol 67 (10) ◽  
pp. 4863-4873 ◽  
Author(s):  
Lawrence O. Ticknor ◽  
Anne-Brit Kolstø ◽  
Karen K. Hill ◽  
Paul Keim ◽  
Miriam T. Laker ◽  
...  

ABSTRACT We examined 154 Norwegian B. cereus andB. thuringiensis soil isolates (collected from five different locations), 8 B. cereus and 2B. thuringiensis reference strains, and 2Bacillus anthracis strains by using fluorescent amplified fragment length polymorphism (AFLP). We employed a novel fragment identification approach based on a hierarchical agglomerative clustering routine that identifies fragments in an automated fashion. No method is free of error, and we identified the major sources so that experiments can be designed to minimize its effect. Phylogenetic analysis of the fluorescent AFLP results reveals five genetic groups in these group 1 bacilli. The ATCC reference strains were restricted to two of the genetic groups, clearly not representative of the diversity in these bacteria. Both B. anthracis strains analyzed were closely related and affiliated with a B. cereus milk isolate (ATCC 4342) and a B. cereus human pathogenic strain (periodontitis). Across the entire study, pathogenic strains, including B. anthracis, were more closely related to one another than to the environmental isolates. Eight strains representing the five distinct phylogenetic clusters were further analyzed by comparison of their 16S rRNA gene sequences to confirm the phylogenetic status of these groups. This analysis was consistent with the AFLP analysis, although of much lower resolution. The innovation of automated genotype analysis by using a replicated and statistical approach to fragment identification will allow very large sample analyses in the future.







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