FB2026_03 , released September 17, 2026
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Klein, J.A., Predeus, A.V., Greissl, A.R., Clark-Herrera, M.M., Cruz, E., Cundiff, J.A., Haeberle, A.L., Howell, M., Lele, A., Robinson, D.J., Westerman, T.L., Wrande, M., Wright, S.J., Green, N.M., Vallance, B.A., McClelland, M., Mejia, A., Goodman, A.G., Elfenbein, J.R., Knodler, L.A. (2024). Pathogenic diversification of the gut commensal Providencia alcalifaciens via acquisition of a second type III secretion system.  Infect. Immun. 92(10): e0031424.
FlyBase ID
FBrf0260655
Publication Type
Research paper
Abstract
Providencia alcalifaciens is a Gram-negative bacterium found in various water and land environments and organisms, including insects and mammals. Some P. alcalifaciens strains encode gene homologs of virulence factors found in pathogenic Enterobacterales members, such as Salmonella enterica serovar Typhimurium and Shigella flexneri. Whether these genes are pathogenic determinants in P. alcalifaciens is not known. In this study, we investigated P. alcalifaciens-host interactions at the cellular level, focusing on the role of two type III secretion systems (T3SS) belonging to the Inv-Mxi/Spa family. T3SS1b is widespread in Providencia spp. and encoded on the chromosome. A large plasmid that is present in a subset of P. alcalifaciens strains, primarily isolated from diarrheal patients, encodes for T3SS1a. We show that P. alcalifaciens 205/92 is internalized into eukaryotic cells, lyses its internalization vacuole, and proliferates in the cytosol. This triggers caspase-4-dependent inflammasome responses in gut epithelial cells. The requirement for the T3SS1a in entry, vacuole lysis, and cytosolic proliferation is host cell type-specific, playing a more prominent role in intestinal epithelial cells than in macrophages or insect cells. In a bovine ligated intestinal loop model, P. alcalifaciens colonizes the intestinal mucosa and induces mild epithelial damage with negligible fluid accumulation in a T3SS1a- and T3SS1b-independent manner. However, T3SS1b was required for the rapid killing of Drosophila melanogaster. We propose that the acquisition of two T3SS has allowed P. alcalifaciens to diversify its host range, from a highly virulent pathogen of insects to an opportunistic gastrointestinal pathogen of animals.
PubMed ID
PubMed Central ID
PMC11477908 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Infect. Immun.
    Title
    Infection and Immunity
    Publication Year
    1970-
    ISBN/ISSN
    0019-9567
    Data From Reference
    Human Disease Models (1)
    Cell Lines (1)