2017
DOI: 10.1002/ps.4761
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Non‐target site SDHI resistance is present as standing genetic variation in field populations of Zymoseptoria tritici

Abstract: BACKGROUNDA new generation of more active succinate dehydrogenase (Sdh) inhibitors (SDHIs) is currently widely used to control Septoria leaf blotch in northwest Europe. Detailed studies were conducted on Zymoseptoria tritici field isolates with reduced sensitivity to fluopyram and isofetamid; SDHIs which have only just or not been introduced for cereal disease control, respectively.RESULTSStrong cross‐resistance between fluopyram and isofetamid, but not with other SDHIs, was confirmed through sensitivity tests… Show more

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Cited by 76 publications
(70 citation statements)
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“…In the current study, four UV mutants were obtained and no mutations in any of the four Sdh genes were detected compared with their parent isolates. The absence of sdh genes mutation has been reported in other fungi . Scalliet et al .…”
Section: Discussionmentioning
confidence: 74%
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“…In the current study, four UV mutants were obtained and no mutations in any of the four Sdh genes were detected compared with their parent isolates. The absence of sdh genes mutation has been reported in other fungi . Scalliet et al .…”
Section: Discussionmentioning
confidence: 74%
“…The absence of sdh genes mutation has been reported in other fungi. 29,32,33 Scalliet et al obtained 452 SDHI-resistant mutants of Z. tritici using a UV mutagenesis approach. The absence of sdh genes mutation was observed in eight mutants (1.8%).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…For example, some newer SDHIs (ex. fluopyram and isofetamid) were reported to show no cross‐resistance with boscalid, an older SDHI fungicide, on some isolates with specific mutation . QoI is also one of the most important classes of fungicides owing to its broad spectrum and effectiveness in disease control.…”
Section: Discussionmentioning
confidence: 99%
“…Resistance management can be achieved by identifying molecules with a novel mode of action (MoA) or by novel adoption of molecules from a known MoA group and previously never used in cereals or by modification of molecules not affected by cross‐resistance to existing analogs. The third approach could be achieved by adjusting chemical structures of molecules to improve interaction with mutated‐target sites …”
Section: Introductionmentioning
confidence: 99%