TCID | Name | Domain | Kingdom/Phylum | Protein(s) |
---|---|---|---|---|
1.C.75.1.1 | The Serratia pore-forming hemolysin/toxin of 1608 aas, ShlA. ShlA expression allows Serratia to trigger a Ca2+ signal that reshapes cytoskeleton dynamics and ends up pushing the Serratia-containing vacuoles out of the cell in an exocytic-like process (Di Venanzio et al. 2016). Thus, pore-forming toxins can allow bacteria to exit without compromising host cell integrity. ShlA triggers cadherin cleavage by promoting calcium influx which activates ADAM10 for proteolysis (Reboud et al. 2017). | Bacteria |
Pseudomonadota | ShlA of Serratia marcescens (P15320) |
1.C.75.1.2 | Haemolysin of 3456 aas. Hemagglutinin repeat-containing protein. | Bacteria |
Pseudomonadota | Haemolysin of Enterobacter agglomerans (Erwinia herbicola) (Pantoea agglomerans) |
1.C.75.1.3 | Two-partner secretion system hemagglutinin TpsA2 of 2521 aas | Bacteria |
Pseudomonadota | Haemagglutinin of Pseudomonas aeruginosa |
1.C.75.1.4 | Filamentous hemagglutinin protein of 1599 aas. It is a two-partner secretion exoprotein, HrpA. | Bacteria |
Pseudomonadota | Filamentous hemagglutinin of Neisseria meningitidis |
1.C.75.1.5 | Haemolysin XhlA of 1470 aas with 1 N-terminal TMS (Cowles and Goodrich-Blair 2005). | Bacteria |
Pseudomonadota | XhlA of Xenorhabdus nematophila (Achromobacter nematophilus) |
1.C.75.1.6 | Exotoxin, ChlA of 1628 aas (Brumbach et al. 2007). | Bacteria |
Pseudomonadota | |
1.C.75.1.7 | Filamentous haemagglutinin family outer membrane protein of 2818 aas. | Bacteria |
Pseudomonadota | Haemagglutinin of Burkholderia ambifaria |
1.C.75.1.8 | Cytopathogenic toxin, CptA, of 1991 aas and an N-terminal signal TMS. Sneathia amnii is a poorly characterized emerging pathogen that has been implicated in amnionitis and urethritis. Gentile et al. 2020 found that S. amnii damages fetal membranes, and they identified and purified the cytotoxic exotoxin, CptA, that lyses human red blood cells and damages cells from fetal membranes. It binds to red blood cell membranes and forms pores with a diameter of 2.0-3.0 nanometers, resulting in osmolysis. There is an association between Sneathia vaginalis and preterm birth (O'Brien et al. 2023). The Gram-negative anaerobe produces a large exotoxin, the cytopathogenic toxin A (CptA), that forms pores in human epithelial cells and red blood cells. In silico analysis predicts that a large amino-terminal region of the protein is globular and separated from the carboxy-terminal tandem repeats by a disordered region. O'Brien et al. 2023 found that a recombinant protein consisting of the predicted structured amino-terminal portion of CptA and devoid of the repeat region was sufficient to permeabilize epithelial cells and red blood cells. The repeat region was capable of binding to epithelial cells but did not permeabilize them or lyse red blood cells. CptA is the only S. vaginalis virulence factor that has been examined mechanistically (O'Brien et al. 2023). | Bacteria |
Fusobacteriota | CptA of Sneathia amnii |