TY - JOUR
T1 - First European Interlaboratory Ring Test Study to Detect DNA of Crayfish and the Crayfish Plague Pathogen From Water Samples
AU - Bohman, Patrik
AU - Andersson, Kristofer
AU - Strand, David A.
AU - Baudry, Thomas
AU - Theissinger, Kathrin
AU - Maguire, Ivana
AU - Aluma, Michael
AU - Aspán, Anna
AU - Bláha, Martin
AU - Bostjancic, Ljudevit Luka
AU - Delaunay, Carine
AU - Diéguez-Uribeondo, Javier
AU - Edsman, Lennart
AU - Ercoli, Fabio
AU - Georges, Jean Yves
AU - Grandjean, Frédéric
AU - Griffin, Bogna
AU - Iso-Touru, Terhi
AU - Jacobsson, Birgitta
AU - Kaldre, Katrin
AU - King, Alex
AU - Kozák, Pavel
AU - Markulin, Lucija
AU - Martínez-Ríos, María
AU - Martín-Torrijos, Laura
AU - Mohammad, Saima
AU - Mojžišová, Michaela
AU - Muha, Teja Petra
AU - Orsén, Ludvig
AU - Persson, John
AU - Pisano, Simone Roberto Rolando
AU - Pukk, Lilian
AU - Rogell, Björn
AU - Ruokonen, Timo J.
AU - Schmidt-Posthaus, Heike
AU - Steiner, Jonas
AU - Söderberg, Linda
AU - Vasemägi, Anti
AU - Zenker, Armin
AU - Petrusek, Adam
N1 - Publisher Copyright:
© 2026 The Author(s). Environmental DNA published by John Wiley & Sons Ltd.
PY - 2026
Y1 - 2026
N2 - In recent years, European countries have intensified efforts to control or limit the spread of invasive freshwater crayfish and the crayfish plague pathogen Aphanomyces astaci, while working to conserve native species such as the noble crayfish (Astacus astacus). Although crayfish shed relatively low amounts of DNA into their environment, environmental DNA (eDNA) approaches have proven effective for detecting their presence. A range of protocols and equipment is currently used in eDNA-based monitoring of freshwater crayfish. To evaluate how methodological variation influences detection accuracy, we conducted the first European interlaboratory ring test using eDNA to detect A. astacus, the invasive signal crayfish Pacifastacus leniusculus, a chronic carrier of A. astaci, and the pathogen itself. The aim is to harmonize monitoring methods for crayfish and disease surveillance across laboratories. Eleven teams from thirteen European countries participated, each using its own equipment and protocols to collect and filter water from indoor tanks and outdoor ponds where the presence of A. astacus and P. leniusculus had been experimentally manipulated, as well as from a natural lake containing a P. leniusculus population. The resulting samples were analyzed in each team's laboratory. Despite methodological differences, all teams successfully detected DNA from both crayfish species in indoor tanks (3–10 crayfish/m3). However, detection accuracy declined in outdoor ponds where crayfish density was an order of magnitude lower (0.32 crayfish/m3). Detection was most variable for A. astaci, likely due to its very low prevalence in the host stock. Our study demonstrates the challenges of achieving consistent eDNA results across laboratories and highlights the importance of interlaboratory comparisons. It also underscores the need to identify sources of variability and error, an essential step toward developing robust and standardized protocols. This multinational intercalibration and exchange of knowledge improved methodology and enhanced reliability in crayfish detection.
AB - In recent years, European countries have intensified efforts to control or limit the spread of invasive freshwater crayfish and the crayfish plague pathogen Aphanomyces astaci, while working to conserve native species such as the noble crayfish (Astacus astacus). Although crayfish shed relatively low amounts of DNA into their environment, environmental DNA (eDNA) approaches have proven effective for detecting their presence. A range of protocols and equipment is currently used in eDNA-based monitoring of freshwater crayfish. To evaluate how methodological variation influences detection accuracy, we conducted the first European interlaboratory ring test using eDNA to detect A. astacus, the invasive signal crayfish Pacifastacus leniusculus, a chronic carrier of A. astaci, and the pathogen itself. The aim is to harmonize monitoring methods for crayfish and disease surveillance across laboratories. Eleven teams from thirteen European countries participated, each using its own equipment and protocols to collect and filter water from indoor tanks and outdoor ponds where the presence of A. astacus and P. leniusculus had been experimentally manipulated, as well as from a natural lake containing a P. leniusculus population. The resulting samples were analyzed in each team's laboratory. Despite methodological differences, all teams successfully detected DNA from both crayfish species in indoor tanks (3–10 crayfish/m3). However, detection accuracy declined in outdoor ponds where crayfish density was an order of magnitude lower (0.32 crayfish/m3). Detection was most variable for A. astaci, likely due to its very low prevalence in the host stock. Our study demonstrates the challenges of achieving consistent eDNA results across laboratories and highlights the importance of interlaboratory comparisons. It also underscores the need to identify sources of variability and error, an essential step toward developing robust and standardized protocols. This multinational intercalibration and exchange of knowledge improved methodology and enhanced reliability in crayfish detection.
UR - https://res.slu.se/id/publ/146025
U2 - 10.1002/edn3.70238
DO - 10.1002/edn3.70238
M3 - Journal article
SN - 2637-4943
VL - 8
JO - Environmental DNA
JF - Environmental DNA
IS - 1
M1 - e70238
ER -