bioRxivMicrobiology
Toxoplasma gondii Toxolysin 4 contributes to efficient parasite egress from host cells
M.-H. Huynh, M. Roiko, A. Gomes, E. N. Schinke, A. J. Schultz, S. Agrawal, C. A. Olleig, T. R. Sexton, J. M. Beauchamp, J. Laliberte, K. K. Sivaraman, L. B. Hersh, S. McGowan, V. B. Carruthers
Abstract
Egress from host cells is an essential step in the lytic cycle of T. gondii and other apicomplexan parasites; however, only a few parasite secretory proteins are known to affect this process. The putative metalloproteinase Toxolysin 4 (TLN4) was previously shown to be an extensively processed microneme protein, but further characterization was impeded by the inability to genetically ablate TLN4. Herein we show that TLN4 has the structural properties of an M16 family metalloproteinase, that it possesses proteolytic activity on a model substrate, and that genetic disruption of TLN4 reduces the efficiency of egress from host cells. Complementation of the knockout strain with the TLN4 coding sequence significantly restored egress competency, affirming that the phenotype of the {Delta}tln4 parasite was due to the absence of TLN4. This work identifies TLN4 as the first metalloproteinase and the second microneme protein to function in T. gondii egress. The study also lays a foundation for future mechanistic studies defining the precise role of TLN4 in parasite exit from host cells. IMPORTANCEAfter replicating within infected host cells, the single celled parasite Toxoplasma gondii must rupture out of such cells in a process termed egress. Although it is known that T. gondii egress is an active event that involves disruption of host-derived membranes surrounding the parasite, very few proteins that are released by the parasite are known to facilitate egress. In this study we identify a parasite secretory protease that is necessary for efficient and timely egress, thus laying the foundation for understanding precisely how this protease facilitates T. gondii exit from host cells.
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- An in vivo fitness gene of Toxoplasma, MIC11, is essential for PLP1-mediated egress from host cells
Yuta Tachibana, Xue Gu, … Masahiro Yamamoto·Nature CommunicationsPeer-reviewed·Apr 4, 2026
- A cathepsin C-like protease post-translationally modifies Toxoplasma gondii secretory proteins for optimal invasion and egress.
L. B. Thornton, M. Key, … Z. Dou·bioRxiv·Jan 21, 2023
- Toxoplasma gondii PPM3C, a secreted protein phosphatase, affects parasitophorous vacuole effector export
J. Mayoral, T. Tomita, … L. M. Weiss·PLOS PathogensPeer-reviewed·Dec 28, 2020
- The secreted acid phosphatase domain-containing GRA44 from Toxoplasma gondii is required for C-myc induction in infected cells
W. J. Blakely, M. J. Holmes, G. Arrizabalaga·mSpherePeer-reviewed·Feb 26, 2020
- Toxoplasma gondii excretion of glycolytic products is associated with acidification of the parasitophorous vacuole during parasite egress
M.-H. Huynh, V. B. Carruthers·bioRxiv·Nov 25, 2021
- Structural basis of Toxoplasma gondii Perforin-Like Protein 1 membrane interaction and activity during egress
A. J. Guerra, O. Zhang, … V. B. Carruthers·bioRxiv·Sep 2, 2018