Soybean target spot (Corynespora cassiicola) has become an important disease in most soybean growing regions in Brazil. The sensitivity of 34 isolates of C. cassiicola to 11 fungicides was evaluated based on mycelial growth inhibition (boscalid, carbendazim, cyproconazole, fluopyram, fluxapyroxad, prothioconazole and thiophanate-methyl) or spore germination inhibition (azoxystrobin, picoxystrobin, pyraclostrobin and trifloxystrobin). In addition, the efficacy of five fungicides to control target spot was tested in four field trials carried out during three crop seasons: 2011/2012, 2012/2013 and 2013/2014. Fungal isolates were collected from soybean plants in several soybean growing areas in Brazil. The effective concentration of each fungicide to inhibit fungal growth or spore germination by 50% (EC₅₀) was calculated for all isolates. Fluxapyroxad and prothioconazole provided the greatest mycelial growth inhibition and pyraclostrobin led to the lowest spore germination percentage, with the lowest EC₅₀ values. At field experiments, cyproconazole and carbendazim showed target spot control ranging from 26% to 29%. On the other hand, fluxapyroxad and prothioconazole prevented an epidemic of the disease by 45% to 55%, respectively. In general, the efficacy of fungicides in the field reflected the in vitro sensitivity averages. Large sensitivity reduction was detected to benzimidazoles (MBC), indicating that this group of fungicides should no longer be used for target spot control. There was a negative and significant correlation (-0.265) between target spot severity and soybean yield. The pathogen showed variability in sensitivity to the fungicide groups carboxamides (SDHI), triazoles (DMI) and strobilurins (QoI), which denotes a high risk of selection for resistance.

Helminthosporium solani populations on potato from the Tulelake area in California frequently have been exposed to thiophanate-methyl but not benomyl. Assessment of three H. solani populations found that 182 of 238 isolates were resistant to both thiophanate-methyl and benomyl and 56 isolates were sensitive to both fungicides. None of the isolates exhibited a differential reaction to the two fungicides. The effective concentrations that reduced growth by 50% for resistant isolates of H. solani were approximately 400 mg/liter for thiophanate- methyl and 35 mg/liter for benomyl. Two point mutations were detected in the β-tubulin gene from H. solani isolates from California; however, only the mutation at the 455-nucleotide position (codon 198) was strongly associated with thiophanate-methyl resistance. This mutation led to a change of glutamic acid to alanine at codon 198. Independent of fungicide resistance, a mutation at the 836-site was detected in all California isolates. A polymerase chain reaction (PCR)-based restriction fragment length polymorphism (RFLP) assay was used to identify thiophanate-methyl resistance in H. solani; resistant isolates exhibited two DNA fragments of 390 and 482 bp, whereas sensitive isolates had three fragments of 62, 390, and 420 bp. Every isolate assigned either as resistant or sensitive by the PCR-based RFLP assay correlated 100% with the results of the assay on fungicide-amended medium.