IngentaConnect Intravenous infection of virulent shigellae causes fulminant hepa...

Authors: Maria Celeste Martino¹; Giacomo Rossi²; Ivan Tattoli¹; Irene Martini¹; Damiana Chiavolini³; Giancarlo Cortese⁴; Gianni Pozzi³; Maria Lina Bernardini¹

Source: Cellular Microbiology, Volume 7, Number 1, January 2005 , pp. 115-127(13)

Publisher: Blackwell Publishing

Abstract:

Summary

Shigella spp. are pathogenic bacteria responsible for bacillary dysentery in humans. The major lesions in colonic mucosa are intense inflammation with apoptosis of macrophages and release of pro-inflammatory cytokines. The study of shigellosis is hindered by the natural resistance of rodents to oral infection with Shigella. Therefore, animal models exploit other routes of infection. Here, we describe a novel murine model in which animals receive shigellae via the caudal vein. Mice infected with 5 × 10⁶ (LD₅₀) virulent shigellae died at 48 h post infection, whereas animals receiving non-invasive mutants survived. The liver is the main target of infection, where shigellae induce microgranuloma formation. In mice infected with invasive bacteria, high frequency of apoptotic cells is observed within hepatic microgranulomas along with significant levels of mRNA for pro-inflammatory cytokines such as IL-1 bgr

, IL-18, IL-12 and IFN- ggr

. Moreover, in the blood of these animals high levels of IL-6 and transaminases are detected. Our results demonstrate the intravenous model is suitable for pathogenicity studies and useful to explore the immune response after Shigella infection.

Document Type: Research article

DOI: 10.1111/j.1462-5822.2004.00441.x

Affiliations: 1: Dipartimento di Biologia Cellulare e dello Sviluppo, Sezione di Scienze Microbiologiche, Università‘La Sapienza’, Via dei Sardi 70, 00185 Roma, Italy. 2: Facoltà di Medicina Veterinaria, Università di Camerino, Matelica, Italy. 3: Dipartimento di Microbiologia, Università di Siena, Italy. 4: Istituto Regina Elena, Roma, Italy.

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Intravenous infection of virulent shigellae causes fulminant hepatitis in mice