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. 2016 Dec 10;119(5):869–884. doi: 10.1093/aob/mcw213

Fig. 6.

Fig. 6.

MBSP isolate M3 demonstrates genome-wide diversification based on isolate-specific polymorphisms that are associated with disease symptoms. (A) Maximum likelihood tree of all genomic polymorphic sites among Brazilian MBSP isolates suggests sympatric genetic drift of Piracicaba isolates M3, T14, E10 and R4 rather that diversification by geographic distance compared with G2 and Bouquet, obtained in Guaíra. (B) Allelic polymorphisms in coding regions are associated with specific MBSP isolates with putative effects on disease symptom development. PC1 and PC2 describe >50 % of the symptomatic variation correlated with MBSP genotypes tested. Error bars are one standard error of the mean PC1 and PC2 contribution by each MBSP isolate averaged across all maize genotypes tested. Black dots represent relative PC contribution of polymorphisms in coding sequences from the MBSP isolates.