In this study, virulence properties of L. monocytogenes strains isolated from food and food environments were evaluated. In particular, adhesion and invasion efficiencies were tested in a cell culture model (HeLa). Half of the isolates (9/18) exhibited a high invasion index. In particular, the strain isolated from smoked salmon had the highest invasion index. The remaining isolates showed an intermediate invasion index. All environmental isolates belonged to this group. Finally, no isolates revealed a low invasion index. Regarding intracellular growth, all tested isolates had a replication time between 2 and 6 hours. For this reason, they can be considered virulent. In spite of its capability to invade HeLa cells with a medium/high invasion index, a non-haemolytic rabbit isolate did not show any intracellular growth. In conclusion, differences in invasion efficiency and intracellular growth did not seem strictly related to the origin of the strains. Moreover, invasiveness of an organism is not the only requirement for establishing an infection. Virulence of L. monocytogenes also depends on ability to grow intracellularly and to spread from cell to cell. For these reasons, PCR detection of known virulence genes has the potential to gain additional insight into their pathogenic potential. A comprehensive comparative virulence characterization of different L. monocytogenes strains in studies that include tissue culture models and PCR detection of virulence genes will be necessary to investigate differences in human-pathogenic potentials among the subtypes of this bacterium.

Preliminary notes on invasion and proliferation of foodborne Listeria monocytogenes strains / Conter, Mauro; DI CICCIO, Pierluigi Aldo; Dorio, V; Vergara, A; Zanardi, Emanuela; Ghidini, Sergio; Ianieri, Adriana. - In: ANNALI DELLA FACOLTÀ DI MEDICINA VETERINARIA. UNIVERSITÀ DI PARMA. - ISSN 0393-4802. - VOL. XXVI:(2006), pp. 175-181.

Preliminary notes on invasion and proliferation of foodborne Listeria monocytogenes strains.

CONTER, Mauro;DI CICCIO, Pierluigi Aldo;ZANARDI, Emanuela;GHIDINI, Sergio;IANIERI, Adriana
2006-01-01

Abstract

In this study, virulence properties of L. monocytogenes strains isolated from food and food environments were evaluated. In particular, adhesion and invasion efficiencies were tested in a cell culture model (HeLa). Half of the isolates (9/18) exhibited a high invasion index. In particular, the strain isolated from smoked salmon had the highest invasion index. The remaining isolates showed an intermediate invasion index. All environmental isolates belonged to this group. Finally, no isolates revealed a low invasion index. Regarding intracellular growth, all tested isolates had a replication time between 2 and 6 hours. For this reason, they can be considered virulent. In spite of its capability to invade HeLa cells with a medium/high invasion index, a non-haemolytic rabbit isolate did not show any intracellular growth. In conclusion, differences in invasion efficiency and intracellular growth did not seem strictly related to the origin of the strains. Moreover, invasiveness of an organism is not the only requirement for establishing an infection. Virulence of L. monocytogenes also depends on ability to grow intracellularly and to spread from cell to cell. For these reasons, PCR detection of known virulence genes has the potential to gain additional insight into their pathogenic potential. A comprehensive comparative virulence characterization of different L. monocytogenes strains in studies that include tissue culture models and PCR detection of virulence genes will be necessary to investigate differences in human-pathogenic potentials among the subtypes of this bacterium.
2006
Preliminary notes on invasion and proliferation of foodborne Listeria monocytogenes strains / Conter, Mauro; DI CICCIO, Pierluigi Aldo; Dorio, V; Vergara, A; Zanardi, Emanuela; Ghidini, Sergio; Ianieri, Adriana. - In: ANNALI DELLA FACOLTÀ DI MEDICINA VETERINARIA. UNIVERSITÀ DI PARMA. - ISSN 0393-4802. - VOL. XXVI:(2006), pp. 175-181.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/1659062
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