TY - JOUR
T1 - Multi-country and intersectoral assessment of cluster congruence between pipelines for genomics surveillance of foodborne pathogens
AU - Mixão, Verónica
AU - Pinto, Miguel
AU - Brendebach, Holger
AU - Sobral, Daniel
AU - Dourado Santos, João
AU - Radomski, Nicolas
AU - Majgaard Uldall, Anne Sophie
AU - Bomba, Arkadiusz
AU - Pietsch, Michael
AU - Bucciacchio, Andrea
AU - de Ruvo, Andrea
AU - Castelli, Pierluigi
AU - Iwan, Ewelina
AU - Simon, Sandra
AU - Coipan, Claudia E.
AU - Linde, Jörg
AU - Petrovska, Liljana
AU - Kaas, Rolf Sommer
AU - Grimstrup Joensen, Katrine
AU - Holtsmark Nielsen, Sofie
AU - Kiil, Kristoffer
AU - Lagesen, Karin
AU - Di Pasquale, Adriano
AU - Gomes, João Paulo
AU - Deneke, Carlus
AU - Tausch, Simon H.
AU - Borges, Vítor
PY - 2025
Y1 - 2025
N2 - Different laboratories employ different Whole-Genome Sequencing (WGS) pipelines for Food and Waterborne disease (FWD) surveillance, casting doubt on the comparability of their results and hindering optimal communication at intersectoral and international levels. Through a collaborative effort involving eleven European institutes spanning the food, animal, and human health sectors, we aimed to assess the inter-pipeline clustering congruence across all resolution levels and perform an in-depth comparative analysis of cluster composition at outbreak level for four important foodborne pathogens: Listeria monocytogenes, Salmonella enterica, Escherichia coli, and Campylobacter jejuni. We found a general concordance between allele-based pipelines for all species, except for C. jejuni, where the different resolution power of allele-based schemas led to marked discrepancies. Still, we identified non-negligible differences in outbreak detection and demonstrated how a threshold flexibilization favors the detection of similar outbreak signals by different laboratories. These results, together with the observation that different traditional typing groups (e.g., serotypes) exhibit a remarkably different genetic diversity, represent valuable information for future outbreak case-definitions and WGS-based nomenclature design. This study reinforces the need, while demonstrating the feasibility, of conducting continuous pipeline comparability assessments, and opens good perspectives for a smoother international and intersectoral cooperation towards an efficient One Health FWD surveillance.
AB - Different laboratories employ different Whole-Genome Sequencing (WGS) pipelines for Food and Waterborne disease (FWD) surveillance, casting doubt on the comparability of their results and hindering optimal communication at intersectoral and international levels. Through a collaborative effort involving eleven European institutes spanning the food, animal, and human health sectors, we aimed to assess the inter-pipeline clustering congruence across all resolution levels and perform an in-depth comparative analysis of cluster composition at outbreak level for four important foodborne pathogens: Listeria monocytogenes, Salmonella enterica, Escherichia coli, and Campylobacter jejuni. We found a general concordance between allele-based pipelines for all species, except for C. jejuni, where the different resolution power of allele-based schemas led to marked discrepancies. Still, we identified non-negligible differences in outbreak detection and demonstrated how a threshold flexibilization favors the detection of similar outbreak signals by different laboratories. These results, together with the observation that different traditional typing groups (e.g., serotypes) exhibit a remarkably different genetic diversity, represent valuable information for future outbreak case-definitions and WGS-based nomenclature design. This study reinforces the need, while demonstrating the feasibility, of conducting continuous pipeline comparability assessments, and opens good perspectives for a smoother international and intersectoral cooperation towards an efficient One Health FWD surveillance.
U2 - 10.1038/s41467-025-59246-8
DO - 10.1038/s41467-025-59246-8
M3 - Journal article
C2 - 40295532
SN - 2041-1723
VL - 16
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 3961
ER -