Evidence map›Paper›PMID 40579755›Full record

ArticlePest management science2025

Detection of resistance in Phytophthora infestans to the carboxylic acid amide (CAA) fungicides using digital droplet PCR.

Amanpreet Kaur, Ewen Mullins, Steven Kildea

Abstract read
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Article in Pest management science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Amanpreet KaurCrop Research Centre, Carlow, Ireland.
Ewen MullinsCrop Research Centre, Carlow, Ireland.
Steven KildeaCrop Research Centre, Carlow, Ireland.ORCID https://orcid.org/0000-0001-8240-6343

Funding

HORIZON EUROPE Framework ProgrammeTeagasc
6 · The paper itself

Abstract

backgroundPotato late blight caused by Phytophthora infestans remains the greatest biotic threat to potato production globally. In northern Europe to prevent the disease and associated yield losses fungicides are heavily relied upon, with multiple applications required during the potato growing season. Unfortunately, such intensive fungicide usage has the potential to compromise control efficacy as it puts in place immense selective pressure for the emergence and spread of fungicide resistant strains of P. infestans. In recent years this scenario has been realized, with the emergence of strains resistant to the carboxylic acid amide (CAA) fungicides. As resistance to the CAA fungicides in P. infestans has been confirmed to result from changes in the pathogen's cellulose synthase A3 gene (CesA3), specifically at amino acid position 1105, it opens the possibility to develop molecular tools to rapidly monitor populations of the pathogen for the resistance allele.

resultsUsing the Stilla naica® 3-colour system a droplet digital PCR (ddPCR) was successfully developed to simultaneously detect the P. infestans CesA3 gene irrespective of its CAA sensitivity status, and either the CAA wild-type sequence for position 1105 or that conferring the resistant allele G1105S. Using a 'drop-off' in ratio of positive droplets for either the wild-type or G1105S alleles relative to those positive for the general P. infestans CesA3 it was also possible to demonstrate that using the assay other potential alterations known to confer resistance that may occur at this position (e.g. G1105V) can be detected. The assay was validated using DNA extracted from P. infestans cultures or infected leaves preserved on FTA cards.

conclusionsThe assay developed will allow for the accurate and sensitive detection of CAA resistance conferred by alterations at amino acid position 1105 in the CesA3 gene in P. infestans. The capacity to use the assay with multiple DNA sources and potential to adapt the 'drop-off' approach to different ddPCR platforms will ensure its applicability to the wider P. infestans community in monitoring the continued use of CAA-based fungicides for P. infestans management. © 2025 The Author(s). Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

Indexed as

AmidesCarboxylic AcidsDrug Resistance, FungalFungicides, IndustrialPhytophthora infestansPolymerase Chain ReactionGlucosyltransferasesPlant DiseasesSolanum tuberosumAmidesCarboxylic Acidscellulose synthaseFungicides, IndustrialGlucosyltransferasescellulose synthase A3ddPCRlate blightmandipropamid

Identifiers

PMID40579755
PMCPMC12441776

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.