A molecular marker for evaluating the pathogenic potential of foodborne Listeria monocytogenes

Christine Jacquet, Michel Doumith, Jeffrey I. Gordon, Paul M.V. Martin, Pascale Cossart, Marc Lecuit

Research output: Contribution to journalArticlepeer-review

205 Scopus citations


Background. Internalin mediates entry of Listeria monocytogenes into some human cultured cell lines and crossing of the intestinal barrier in transgenic mice expressing its receptor, human E-cadherin, in enterocytes. The relevance of these findings for humans is challenged by the observation that some L. monocytogenes isolates express a truncated nonfunctional form of internalin. Methods. We investigated expression of internalin by use of immunoblot assay in 300 clinical strains obtained in France in a single year and a representative set of 150 strains obtained from food products during the same period. Results. Clinical strains expressed full-length internalin far more frequently (288/300 strains [96%]) than did strains recovered from food products (98/150 strains [65%]; odds ratio, 12.73; 95% confidence interval, 6.27-26.34; P < 1 × 10-7). All 61 strains (100%) from pregnancy-related cases, 55 (98%) of 56 strains from patients with central nervous system infections, and 151 (93%) of 162 strains from patients with bacteremia expressed full-length internalin. All 110 strains belonging to serovar 4b, the most frequently implicated serovar in human listeriosis, expressed full-length internalin. Conclusions. This study demonstrates the critical role of internalin in the pathogenesis of human listeriosis. It provides a molecular explanation for the predominance of serovar 4b among clinical strains and supports the usefulness of studying the expression of internalin as a marker of virulence in humans.

Original languageEnglish
Pages (from-to)2094-2100
Number of pages7
JournalJournal of Infectious Diseases
Issue number11
StatePublished - Apr 1 2004


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