TY - JOUR
T1 - Phenotypic profiling supports that Listeria costaricensis lacks in vitro pathogenicity but exhibits persistence traits
AU - Mata-Salazar, Cristian
AU - Rivas-Solano, Olga
AU - Castro-Gutiérrez, Victor
AU - Huete-Soto, Alejandra
AU - Redondo-Solano, Mauricio
N1 - Publisher Copyright:
© 2026 The Authors.
PY - 2026
Y1 - 2026
N2 - Listeria costaricensis was recently isolated from a food-processing facility. However, its pathogenic potential and persistence capacity remain poorly characterized at the phenotypic level, raising concerns about food safety. Therefore, we assessed its pathogenic potential through phenotypic invasion and adhesion assays in HeLa cells, showing that L. costaricensis cannot invade HeLa cells despite displaying a cell adhesion capacity comparable to that of Listeria monocytogenes and Listeria innocua reference strains. Given the industrial origin of the strain, we further evaluated its susceptibility to commonly used disinfectants by broth microdilution, finding susceptibility to a mixture of quaternary ammonium compounds (MIC < 100 μg/mL), and reduced susceptibility to peracetic acid (MIC > 160 μg/mL) and sodium hypochlorite (MIC > 500 μg/mL). Considering its demonstrated adhesion capacity, we assessed its ability to form biofilms on polystyrene surfaces, reporting a weak biofilm-forming phenotype comparable to other L. monocytogenes strains. Finally, using the VFanalyzer platform we identified on the L. costaricensis genome 28 virulence-associated gene sequences related to regulatory and structural functions, adherence, and an incomplete invasion gene group compared to L. monocytogenes strains. Collectively, these findings phenotypically support the previously proposed non-pathogenic nature of L. costaricensis, while also revealinga level of persistencecomparableto otherL. monocytogenes isolates.
AB - Listeria costaricensis was recently isolated from a food-processing facility. However, its pathogenic potential and persistence capacity remain poorly characterized at the phenotypic level, raising concerns about food safety. Therefore, we assessed its pathogenic potential through phenotypic invasion and adhesion assays in HeLa cells, showing that L. costaricensis cannot invade HeLa cells despite displaying a cell adhesion capacity comparable to that of Listeria monocytogenes and Listeria innocua reference strains. Given the industrial origin of the strain, we further evaluated its susceptibility to commonly used disinfectants by broth microdilution, finding susceptibility to a mixture of quaternary ammonium compounds (MIC < 100 μg/mL), and reduced susceptibility to peracetic acid (MIC > 160 μg/mL) and sodium hypochlorite (MIC > 500 μg/mL). Considering its demonstrated adhesion capacity, we assessed its ability to form biofilms on polystyrene surfaces, reporting a weak biofilm-forming phenotype comparable to other L. monocytogenes strains. Finally, using the VFanalyzer platform we identified on the L. costaricensis genome 28 virulence-associated gene sequences related to regulatory and structural functions, adherence, and an incomplete invasion gene group compared to L. monocytogenes strains. Collectively, these findings phenotypically support the previously proposed non-pathogenic nature of L. costaricensis, while also revealinga level of persistencecomparableto otherL. monocytogenes isolates.
KW - biofilms
KW - cell adhesion
KW - cell invasion
KW - Listeria
KW - sanitizer susceptibility
UR - https://www.scopus.com/pages/publications/105028189287
U2 - 10.1139/cjm-2025-0216
DO - 10.1139/cjm-2025-0216
M3 - Artículo
AN - SCOPUS:105028189287
SN - 0008-4166
VL - 72
SP - 1
EP - 12
JO - Canadian Journal of Microbiology
JF - Canadian Journal of Microbiology
ER -