Claim · model-written summary
The assay distinguished L412F and L412V mutations using diagnostic bands.
- Taxon
- Botrytis cinerea
Botrytis cinereat0 - Outcome
- detect the nucleotide alterationse0
- Value
- 702 bpe0
Verbatim
e0“A TETRA-primer amplification refractory mutation system polymerase chain reaction (T-ARMS-PCR) was developed to rapidly detect the nucleotide alterations that lead to L412F and L412V mutations, producing a 702 bp band in all isolates, with additional 470 bp (F) or 252 bp (V) fragments”
t0“Botrytis cinerea”
Title
Georgios Sofianos; Athanasios Petmezas; Anastasios Samaras; et al. Pest Management Science 2026. doi:10.1002/ps.70864
Other claims from this paper (9)
- Method / resource The assay detected G408V with MlyI digestion.
- Method / resource Sanger sequencing validated the assay results.
- Observation L412F occurred in 70.2% of resistant isolates from strawberry and tomato.
- Observation L412V occurred in 8.3% of resistant isolates from strawberry and tomato.
- Observation G408V occurred in 4.7% of resistant isolates from strawberry and tomato.
- Observation Sequencing found a low frequency of E407K in Bcmdl1.
- Observation Sequencing indicated additional undefined resistance mechanisms.
- Intervention effect L412F and L412V edited mutants resisted cyprodinil.
- Observation L412F and L412V transformants showed no significant fitness difference from the parental strain.
