Surface attachment, promoted by the actomyosin system of Toxoplasma gondii is important for efficient gliding motility and invasion
- Jamie A. Whitelaw†1,
- Fernanda Latorre-Barragan†1,
- Simon Gras1,
- Gurman S. Pall1,
- Jacqueline M. Leung2, 4,
- Aoife Heaslip3,
- Saskia Egarter1,
- Nicole Andenmatten1,
- Shane R. Nelson3,
- David M. Warshaw3,
- Gary E. Ward4 and
- Markus Meissner1Email authorView ORCID ID profile
© The Author(s). 2017
Received: 17 September 2016
Accepted: 10 December 2016
Published: 18 January 2017
Apicomplexan parasites employ a unique form of movement, termed gliding motility, in order to invade the host cell. This movement depends on the parasite’s actomyosin system, which is thought to generate the force during gliding. However, recent evidence questions the exact molecular role of this system, since mutants for core components of the gliding machinery, such as parasite actin or subunits of the MyoA-motor complex (the glideosome), remain motile and invasive, albeit at significantly reduced efficiencies. While compensatory mechanisms and unusual polymerisation kinetics of parasite actin have been evoked to explain these findings, the actomyosin system could also play a role distinct from force production during parasite movement.
In this study, we compared the phenotypes of different mutants for core components of the actomyosin system in Toxoplasma gondii to decipher their exact role during gliding motility and invasion. We found that, while some phenotypes (apicoplast segregation, host cell egress, dense granule motility) appeared early after induction of the act1 knockout and went to completion, a small percentage of the parasites remained capable of motility and invasion well past the point at which actin levels were undetectable. Those act1 conditional knockout (cKO) and mlc1 cKO that continue to move in 3D do so at speeds similar to wildtype parasites. However, these mutants are virtually unable to attach to a collagen-coated substrate under flow conditions, indicating an important role for the actomyosin system of T. gondii in the formation of attachment sites.
We demonstrate that parasite actin is essential during the lytic cycle and cannot be compensated by other molecules. Our data suggest a conventional polymerisation mechanism in vivo that depends on a critical concentration of G-actin. Importantly, we demonstrate that the actomyosin system of the parasite functions in attachment to the surface substrate, and not necessarily as force generator.
KeywordsActin Myosin Motility Attachment Toxoplasma Apicomplexa Host cell invasion Membrane flow
Apicomplexan parasites employ a unique form of movement, termed gliding motility, to disseminate and invade host cells. The current model for gliding motility is centred on the actomyosin system of the parasite in force generation during this process. According to the ‘linear motor’ model, micronemal transmembrane proteins, such as MIC2, are secreted at the apical pole of the parasite and act as force transmitters by interacting with the substrate surface and the actomyosin system, similar to the role of integrins in other motility systems . Accordingly, this model predicts a smooth actomyosin dependent rearwards translocation of the microneme-substrate complex, which results in forward gliding on the substrate or into the host cell . However, recent reverse genetic approaches demonstrated that parasites remain motile in the absence of what were thought to be key components of the motility machinery, including parasite actin [3–6]. In an attempt to reconcile these data, we proposed a novel, hypothetical model based on gelation/solation , where actin/myosin is required for force transmission rather than force production . This model predicts the generation of an osmotic gradient that results in membrane tension and retrograde membrane flow. In order to regulate membrane balance, the parasite then either sheds membrane at the posterior end, as previously observed , and/or recycles the membrane via endocytosis, as suggested for other systems [8, 9].
Many other eukaryotic cells move by crawling, a process powered by the controlled assembly and disassembly of the actin cytoskeleton in proximity to the plasma membrane [10, 11]. While it was previously assumed that the majority of the force for the retraction of the cell rear is powered by myosins, several alternative mechanisms can operate within the cell that also power motility [10, 11]. For example, the motility of Caenorhabditis elegans sperm occurs in the absence of any actin and therefore myosin activity ; instead, force is generated by controlled polymerisation of the major sperm protein. Furthermore, when tumour cells are confined within a microenvironment, motility depends on an osmotic engine and can be independent of actomyosin activity . Finally, migrating cells can employ various migration modes in response to their microenvironment , which allows them to move even in the absence of adhesive coupling . For example, crawling cells, such as Dictyostelium and human leukocytes, can swim efficiently when suspended in a viscous medium [16, 17], demonstrating that adhesion to a solid substrate is not always necessary for movement . It is thus possible that motility can be driven purely by surface membrane flow, which itself results from a secretory-endocytic cycle acting as a fluid drive from the anterior to the posterior end of the cell . In support of membrane flow, many motile cells show a distinct capping activity of surface ligands . Furthermore, surface capping depends on vesicular transport, and both on actin and microtubule function . In good agreement with these observations, numerous modulators of endocytic and secretory trafficking have been demonstrated to be key regulators of cell motility , leading to the hypothesis that membrane transport and retrograde flow during motility are rate-limiting for cell forward translocation .
In the case of apicomplexan parasites, a recent study demonstrated that retrograde membrane flow of malaria sporozoites occurs even at relatively high concentrations of the actin-disrupting drug Cytochalasin D (CD) . Furthermore, biophysical studies on malaria sporozoites have demonstrated the discrete, localised turnover of attachment sites that are not evenly translocated along the surface of the parasite . This involves the formation/disengagement of adhesion sites at the front and rear ends of the zoite, while the sporozoite undergoes a stretching phase. Interestingly, actin is important for the definition and release of the attachment sites , raising the possibility that apicomplexan motility may be similar to amoeboid-like crawling.
In T. gondii, an alternative explanation for the observed phenotypes for mutants of the actomyosin system is the possibility of functional redundancy of actomyosin components . While redundancies cannot be ruled out, in particular for myosins and micronemal proteins [3, 4], even the removal of ostensibly critical structural proteins does not completely block gliding motility or host cell invasion. For example, removal of the gliding-associated protein GAP45 results in the relocation of the remaining MyoA-complex components to the cytosol and severe disruption of the inner membrane complex (IMC), within which the motor complex is normally anchored [3, 25]. While these gap45 conditional knockout (cKO) parasites are completely blocked in host cell egress, they remain motile and can invade host cells . These surprising findings have led to a reassessment of the mechanisms underlying parasite motility and host-cell invasion, as recently reviewed . In fact, not only do the roles of the individual components need to be reanalysed, but also their orientation and organisation within the parasite .
Here, we show that, during motility, the actomyosin system of the parasite functions in attachment to the surface substrate, and may, therefore, act as force transmitter rather than a force generator. We provide evidence that retrograde membrane flow, which may play a role in force generation and motility, does not depend on an intact actomyosin system.
Actin is undetectable within 96 h of removal of act1 in act1 cKO
We previously reported that ACT1 is undetectable in act1 cKO parasites 72 h after rapamycin-induced removal of act1 . A subsequent study suggested that residual actin may, in fact, be present in some of these parasites as long as 5 days after rapamycin treatment . This led us to re-address the question of residual actin levels in the act1 cKO parasites, using additional antibodies and additional controls.
Consistent with other studies, we found that actin levels in wildtype (wt) parasites were somewhat variable (Fig. 1a, b). Similar results were obtained with other housekeeping genes such as myosin light chain 1 (MLC1, Fig. 5a) and aldolase (not shown). Importantly, no overlap of actin levels could be observed between controls and act1 cKO parasites as early as 48 h after rapamycin-induced excision of act1 (Fig. 1a, b). At earlier time points (24–36 h) post induction, significant amounts of ACT1 were still detectable and protein levels were highly variable between vacuoles (Fig. 1a, b). Nevertheless, ACT1 levels were significantly reduced in comparison to control vacuoles. Importantly, 96 h after rapamycin induction, no ACT1 was detectable in YFP+ parasites. Lack of ACT1 detection by IFA correlates well with a recent study suggesting that no F-actin can be formed approximately 48 h after the removal of act1 , the inference being that G-actin levels fall below the critical concentration required for polymerisation.
In good agreement with this result, quantitative immunoblotting of act1 cKO parasites at different time points post-induction demonstrated the loss of all or nearly all of the ACT1 as early as 72 h post induction (Fig. 1c, d), confirming previous results .
In summary, our quantification demonstrates that actin is depleted in the act1 cKO parasites between 72 and 96 h post induction. Based on these observations, assays were performed in a time course up to 96 h after addition of rapamycin to adequately readdress the effects of ACT1 loss.
Loss of actin results in deleterious phenotypes for apicoplast maintenance and host cell egress but not gliding motility and host cell invasion
Next, we analysed the capability of act1 cKO parasites to move by gliding motility and to invade the host cell at different time points after rapamycin induction (Fig. 2e, f). In good agreement with previous results , overall motility and host cell invasion were significantly reduced in the act1 cKO parasites, with less than approximately 25% being motile and capable of invading host cells compared to control parasites (Fig. 2e, f). This phenotype was observed as early as 48 h after rapamycin induction, at a time point when significant amounts of actin were still detectable (Fig. 1). Interestingly, and in striking contrast to the results with apicoplast inheritance and egress, gliding and invasion rates remained constant at 48–96 h post induction, suggesting that once actin levels fall below a critical concentration, these phenotypes are not further affected. The simplest explanation for this result is that apicoplast maintenance and egress are completely dependent on actin, whereas gliding and invasion can occur independent of actin, albeit at significantly reduced efficiencies.
A critical concentration of actin is required to sustain dense granule motility
A recent study demonstrated the essential role of actin and the unconventional myosin F (MyoF) in directed dense granule transport . To assess if potential, residual F-actin in act1 cKO parasites is capable of serving as a track for MyoF-dependent dense granule transport, dense granule motions were tracked at various times after actin excision. In good agreement with the results obtained for apicoplast replication, parasite egress, parasite gliding and invasion, we observed an approximately 50% reduction in the percentage of granules moving in a directed manner from 37% in control to 14% as early as 18 h post excision (Fig. 3a, b). At 36 and 72 h post excision, directed granule motion was completely ablated (Fig. 3b, c) given that the percentage of trajectories in each population was indistinguishable from simulated pure 2D diffusion analysed using the changepoint algorithm (See Methods for details) (Fig. 3b; hashed bars).
The observation of diminished granule movement soon after induction provides further evidence that apicomplexan actin in vivo requires a critical monomer concentration (G-actin) in order to form sufficient F-actin to serve as a substrate for myosin motors such as MyoF. We therefore conclude that act1 cKO parasites are a powerful tool to analyse actin-independent motility and invasion processes.
Conventional actin disrupting drugs are not exclusively specific for Toxoplasma actin
Intriguingly, the phenotypes described above differ significantly from the effects caused by incubating parasites in the presence of drugs used to modulate F-actin turnover, such as CD or Latrunculins. For example, treatment of intracellular parasites with CD results in the formation of huge residual bodies, where organelles such as the apicoplast or secretory organelles accumulate [30, 31], which is not observed in the case of the act1 cKO parasites .
In summary, the experiments presented above demonstrate that, in the absence of actin, less than 25% of parasites remain capable of gliding motility and host cell invasion and establish act1 cKO parasites as a valuable tool for understanding the role of actin in the invasion and gliding mechanisms of T. gondii. The observed phenotype for the act1 cKO parasites is very similar to the phenotype observed for a clonal knockout for myoA . We therefore re-addressed the role of myosins during gliding motility.
Expression levels of MyoC determine its localisation to the IMC in the myoA KO
It was previously suggested that MyoC can compensate for MyoA motor function in myoA KO parasites [3, 39]. In addition, it has been shown that MyoA and MyoC can interact with the same light chain, MLC1, and expression of MyoC from a heterologous promoter demonstrated a certain degree of MyoC association with the parasite pellicle in the absence of MyoA .
While strong expression of MyoC results in efficient relocalisation from the parasite basal end to the periphery of the myoA KO parasites (Fig. 5a, b), as previously reported , expression of MyoC under its own promoter or endogenously-tagged MyoC showed only slight relocalisation, with the majority of the protein being correctly localised to the basal ring of the parasites. This demonstrates that the localisation of MyoC to the IMC is critically dependent on strong expression levels of the protein, which are not reached with native MyoC expression levels in the myoA KO parasite (Fig. 5b). We next analysed propagation of these parasite strains using plaque assays and found that the relative plaque size is larger in myoA KO parasites strongly overexpressing MyoC compared to parasites expressing MyoC under the control of pMyoC (Fig. 5c). This demonstrates that overexpression of MyoC can partially complement the phenotype of the myoA KO parasites (Fig. 5c). Since the localisation of MyoC to the IMC is apparently critical for complementation of the myoA KO parasites, we decided to analyse mlc1 cKO in more detail, given that MLC1 is thought to be required to anchor both MyoA and MyoC to the pellicle [3, 39].
Parasites lacking MLC1 can be maintained in cell culture for several weeks
Next, we were interested in the localisation of MyoA and MyoC in mlc1 cKO parasites. To determine this, we generated two independent lines for colocalization studies, one expressing Ty-tagged MyoA under the control of its endogenous promoter (pMyoA) and another with endogenously Ty-tagged MyoC (Fig. 6d–f). MyoA is completely undetectable at the parasite’s pellicle 72 h after rapamycin-induced excision of mlc1 (Fig. 6d, e), demonstrating that MLC1 is crucial for the localization and stability of MyoA. In contrast, MyoC remains present and shows a normal localization at the basal end of the parasite in the absence of MLC1 (Fig. 6f).
In summary, we have generated and validated important parasite strains that can be used to analyse the role of the actomyosin system during gliding motility and host cell invasion and to investigate alternative mechanisms for these essential processes.
Kinetic analysis of actin and myosin independent motility and invasion
We previously demonstrated that conditional mutants for act1, mlc1 and myoA invade the host cell via the tight junction, demonstrating that these parasites still use an active invasion mechanism and are not passively taken up by the host cell via phagocytosis . However, kinetic analysis of myoA KO parasites demonstrated that both gliding speed and penetration times are significantly reduced, validating a direct function of MyoA during these processes. We were interested how act1 cKO, mlc1 cKO and myoA KO would compare during gliding motility and invasion.
To date, characterisation of gliding motility mainly depends on trail deposition assays, which allow a good estimate of overall motility rates. However, motility rates can be reduced by several factors, such as reduced or increased parasite attachment to the surface, and does not allow a firm conclusion regarding the function of a protein during this process. We speculated that parasites depleted in crucial parts of the actomyosin system should move significantly differently in terms of gliding speed and/or average distance travelled.
Additional file 2: Movie S1. Example of circular gliding motility of RH KillerRed. Time-lapse video microscopy of a RH KillerRed parasite gliding in a circular motion over a FBS-coated Ibidi glass bottom dish. Images were taken at one frame per second in A594 channel, DV Core. Movie is played at 20 frames per second. Movie supports Fig. 7c. (AVI 2799 kb)
Additional file 3: Movie S2. Example of helical gliding motility of RH KillerRed. Time-lapse video microscopy of a RH KillerRed parasite gliding in a helical motion over a FBS-coated Ibidi glass bottom dish. Images were taken at one frame per second in A594 channel, DV Core. Movie is played at 20 frames per second. Movie supports Fig. 7c. (AVI 1877 kb)
Additional file 4: Movie S3. Example of circular gliding motility of mlc1 cKO. Time-lapse video microscopy of a parasite gliding in a circular motion over a FBS-coated Ibidi glass bottom dish. Images were taken at one frame per second in FITC channel, DV Core. Movie is played at 20 frames per second. Movie supports Fig. 7c. (AVI 2960 kb)
Additional file 5: Movie S4. Example of helical gliding motility of mlc1 cKO. Time-lapse video microscopy of a parasite gliding in a helical motion over a FBS-coated Ibidi glass bottom dish. Images were taken at one frame per second in FITC channel, DV Core. Movie is played at 20 frames per second. Movie supports Fig. 7c. (AVI 2047 kb)
Additional file 6: Movie S5. Example of circular gliding motility of act1 cKO. Time-lapse video microscopy of a parasite gliding in a circular motion over a FBS-coated Ibidi glass bottom dish. Images were taken at one frame per second in FITC channel, DV Core. Movie is played at 20 frames per second. Movie supports Fig. 7c. (AVI 1786 kb)
Additional file 7: Movie S6. Example of helical gliding motility of act1 cKO. Time-lapse video microscopy of a parasite gliding in a helical motion over a FBS-coated Ibidi glass bottom dish. Images were taken at one frame per second in FITC channel, DV Core. Movie is played at 20 frames per second. Movie supports Fig. 7c. (AVI 1416 kb)
Additional file 8: Movie S7. Example of fast penetration of act1 cKO. Time-lapse video microscopy of parasite invading an HFF cell. Images were taken at one frame per second in DIC channel, DV Core. Movie is played at 10 frames per second. Movie supports Fig. 7d. (AVI 3363 kb)
Additional file 9: Movie S8. Example of slow penetration of act1 cKO. Time-lapse video microscopy of parasite invading an HFF cell. Images were taken at one frame per second in DIC channel, DV Core. Movie is played at 20 frames per second. Movie supports Fig. 7d. (AVI 1300 kb)
Additional file 10: Movie S9. Example of fast penetration of mlc1 cKO. Time-lapse video microscopy of parasite invading an HFF cell. Images were taken at one frame per second in DIC channel, DV Core. Movie is played at 10 frames per second. Movie supports Fig. 7d. (AVI 2219 kb)
Additional file 11: Movie S10. Example of slow penetration of mlc1 cKO. Time-lapse video microscopy of parasite invading an HFF cell. Images were taken at one frame per second in DIC channel, DV Core. Movie is played at 20 frames per second. Movie supports Fig. 7d. (AVI 2792 kb)
Kinetics of 3D motility: MyoC cannot compensate for the loss of MyoA motor function
The actomyosin system is required for surface attachment
Bead translocation does not depend on the actomyosin system
Apicomplexan parasites are known to translocate beads from the apical to the basal end and such ‘capping activity’ has been directly implicated in the motility of many cell types, including Plasmodium sporozoites . Interestingly, treatment of sporozoites with CD had no significant effect on the speed of retrograde flow, while the force generated at the attached bead was reduced . This could also be explained by the reduced formation of attachment sites, meaning a failure in force transmission rather than production. We therefore wished to analyse if retrograde membrane flow can occur in absence of the actomyosin system.
In this study, we set out to reconcile currently conflicting interpretations regarding the role of the apicomplexan actomyosin system during gliding motility and host cell invasion . While there is no doubt about a critical role of the actomyosin system during motility and invasion, alternative models and mechanisms regarding the exact function of this system have been put forward based on biophysical, reverse genetic and inhibitor studies [3, 21, 22, 26, 38]. Indeed, several observations cannot be easily reconciled with the canonical linear motor model: (1) Biophysical studies on malaria sporozoites demonstrate the discrete, localised turnover of attachment sites that are not evenly translocated along the surface of the parasite . Adhesion sites are formed/disengaged at the front and rear ends of the zoite, while the sporozoite undergoes a stretching phase. Interestingly, actin is important for the definition and release of the attachment sites , raising the possibility that apicomplexan motility is similar to amoeboid-like crawling. (2) Eimeria sporozoites show different types of motility (bending and pivoting). While pivoting appeared substrate- and actin-dependent, bending showed resistance to the actin-disrupting drug Cytochalasin B . (3) A recent study demonstrates that retrograde membrane flow of malaria sporozoites occurs even at relatively high concentrations of the actin-disrupting drug CD . (4) Reverse genetic approaches demonstrated that parasites remain motile in the absence of molecules thought to be key components of the motor machinery, including parasite actin [3–6].
In the case of reverse genetic studies, other groups have suggested that the observed phenotypes are due either to the presence of redundancies within the repertoire of genes involved in motility and invasion  or to an unusually stable actin (encoded by a single copy gene ), which persists many days and parasite generations after gene excision and can polymerize via an unusual isodesmic process that does not require a critical monomer (G-actin) concentration [27, 48]. While isodesmic polymerisation has been demonstrated in vitro, its in vivo relevance is unclear . Previous polymerisation studies used G-actin produced in heterologous protein expression systems. However, a recent study demonstrated that apicomplexan actin is not properly folded when heterologously expressed due to differences in the chaperonin T-complex . Furthermore, a recent study suggests that Toxoplasma actin is capable of forming F-actin structures in vivo that depend on a critical monomer concentration and demonstrates that F-actin is involved in multiple essential processes during intracellular parasite growth such as daughter cell assembly, vacuole organisation and parasite egress . Using a conditional knockout for act1 it was demonstrated that no ACT1 filament formation can occur as early as 48 h after removal of act1 . Finally, although apicomplexans possess actin-like proteins, it is unlikely that they can compensate for ACT1 and form filaments [27, 51]. Here, we performed a careful quantification of actin levels at different time points in the act1 conditional knockout and find that actin is still detectable at 48 h, but fully depleted by 96 h after induction with rapamycin.
In good agreement with previous studies [3, 29], we observed essential roles of actin in apicoplast segregation, host cell egress and dense granule motility upon deletion of act1, while parasite motility and host cell invasion still occur, albeit at significantly reduced levels. Since these findings were in direct conflict with a number of studies that use actin-modulating drugs to probe for actin function, we also performed an analysis of the effects of the actin-disrupting drugs CD, LatA, and LatB, and the actin-stabilising drug Jas on wt and act1 cKO parasites. While the effect of Jas appears to be specific for actin, since treatment of act1 cKO parasites showed no effect of this drug, we find that CD is not uniquely specific for actin, since similar effects on parasite motility can be observed irrespective if wt, act1 cKO or parasites expressing ACT1CDr were analysed. While CD is certainly acting on parasite actin, as indicated by the significant differences between wt and CytDr parasites, we find that concentrations above 0.5 μM CD lead to significant, non-actin-dependent effects on parasite motility, confirming previous studies . In contrast, latA and latB, previously used to analyse the role of apicomplexan actin , appear to have no effect on tachyzoite actin, as noted previously. Together, these data indicate great care should be taken in choosing the correct concentration for actin-modulating drugs, especially when using CD, where an independent, unknown target(s) appears to be present in T. gondii .
Though all myosins are thought to depend on F-actin to function as a motor and, therefore, the act1 cKO likely reflects the cumulative phenotype of all myosins, we were interested in the extent of redundancy between MyoA and MyoC, since previous studies indicated that MyoC can complement a MyoA deficiency [3, 39]. While we confirm that MyoC can partially complement for MyoA function, this complementation appears to depend on overexpression and consequent localisation of MyoC at the IMC. Indeed, our localisation analysis of MyoC in wt and myoA KO parasites demonstrates that, under physiological conditions, no significant relocation of MyoC to the IMC can be detected. In contrast, strong overexpression leads to redistribution of MyoC to the IMC, as described previously . This redistribution appears to be also critical for functional complementation, leading to a higher ratio of motile parasites and host cell invasion. However, MyoC cannot compensate for MyoA function completely, since the parasites overexpressing MyoC remain as slow as uncomplemented myoA KO parasites. These results are also in good agreement with a recent study demonstrating that MyoA is the central myosin involved in host cell invasion and that, in the absence of MyoA, host cell membrane dynamics play an important role in invasion . Importantly, deletion of mlc1 results in a complete loss of the motor complex at the IMC, therefore representing a functional double KO for MyoA and MLC1. This mutant can be kept in cell culture indefinitely when the strong egress phenotype is bypassed by artificially releasing the parasites, followed by enrichment of the population using FACS, demonstrating that MLC1 is not essential for motility and host cell invasion per se. Indeed, mlc1 cKO parasites behave similarly to act1 cKO regarding motility and attachment to the surface.
Together, this analysis suggests a role for the actomyosin system during parasite motility that is distinct from the canonical linear motor model. We hypothesise that, rather than being the force generator during motility, the actomyosin system is instead involved in the regulation of attachment sites that are required to transmit the motility force to the substrate. To address this hypothesis, we used the above mutants to analyse different parameters that are likely crucial for efficient parasite motility such as attachment strength and retrograde membrane flow. We found that most act1 cKO and mlc1 cKO parasites remain immobile. However, those that move do so at speeds similar to wt parasites, albeit with shorter trajectories, suggesting that the actomyosin system is required to initiate and maintain motility. In a 3D environment the motility defects are stronger than in a 2D environment, with most parasites showing a displacement of less than one parasite length (7 μm). In contrast, these mutants are virtually unable to attach, as measured under flow conditions, indicating an important role in the formation of attachment sites, as previously suggested . Unlike the mlc1 cKO and act1 cKO, myoA KO parasites show strong attachment to the surface, but significantly reduced speeds that cannot be compensated by overexpressing MyoC. We interpret these data to indicate that actin is required to form attachment sites, whereas MyoA might be required for the regulated release of these sites, leading to efficient force transmission during motility. A role for myosins in regulating adhesion and thereby traction force has recently been demonstrated . Here, the balance between myosin contraction and adhesion strength determines the frequency of motility initiation . A similar regulation of myosin contraction might occur in the case of apicomplexans in order to initiate motility and failure to do so could result in reduced motility rates. In this scenario, how is the motility and invasive force produced by the parasite? Previous studies implicated the generation of a retrograde membrane flow in parasite motility . Interestingly, the flow itself is relatively resistant to actin-modulating drugs. Here, we modified a bead translocation assay as an indicator of retrograde membrane flow  to analyse the role of ACT1, MLC1 and MyoA in establishing membrane flow. Surprisingly, while fewer beads bind to the surface of the parasite in the absence of these proteins, bead translocation itself appears to be not significantly affected, again indicating a role of the actomyosin system in the formation of attachment sites (in this case for latex beads), but not in bead translocation. Future experiments and tools will be required to carefully address the role of retrograde membrane flow in force production and its exact role, if any, during motility and invasion.
In conclusion, our study demonstrates the importance of the actomyosin system during motility and invasion. It is worth noting that, in physiological settings, this system is absolutely essential for parasite viability. In fact, in vivo experiments with myoA KO parasites demonstrate the complete inability of these parasites to establish an infection or to induce an adaptive immune response (our unpublished results). However, it is important to understand the molecular functions of the components of the gliding and invasion machinery in order to obtain a clear picture of how the individual components of this fascinating system work together to allow the parasite to move, invade into and egress from the host cell.
Cloning DNA constructs
All primers used in this study are listed in Additional file 13: Table S1 and were synthesised from Eurofins (UK).
LoxPact1 CDr geneswap vector
The act1 ORF containing the mutation C408G at the nucleotide level which confers the amino acid mutation of A136G was synthesised by GenScript (USA). Both the original LoxPAct1 geneswap vector  and the synthesised plasmid were digested with XmaI and PacI to replace act1 cDNA.
p5RT70-Ty-MyoC and pMyoC-Ty-MyoC
To generate p5RT70-Ty-MyoC, the myoC ORF was amplified from cDNA using the primers myoC ORF fw/rv. The fragment was cloned via AvrII and PacI into the parental plasmid p5RT70-Ty-KillerRed. To put myoC under its endogenous promotor a 1 kb fragment upstream of the start codon of myoC was amplified from genomic DNA using oligos pmyoC fw/rv and cloned using as template vector p5RT70-Ty-MyoC via KpnI and AvrII.
Endogenous tagged MyoC
This vector was generated by cloning two 5’UTR fragments obtained by amplifying genomic DNA and a fragment of myoC gene using pBSSK + pSag1-Ble-Sag1 as a template vector. Fragment 1, pMyoC, was obtained by amplification of a 1 kb fragment upstream of the start codon of myoC, via HpaI-NotI sites using oligos pmyoC 2 fw/rv. Fragment 2, 5’UTR myoC, was obtained by amplifying a region of approximately 1.5 kb located 1 kb upstream of the myoC start codon. Amplification was done using primers 5’UTR myoC fw/rv and cloned via Kpn1-XhoI. Finally, a 2.2 kb fragment of myoC was amplified using primers myoC gene fw/rv with a Ty-tag included in the forward primer. Subsequently, cloning was performed using enzymes SpeI/NotI.
To express myoA under its endogenous promotor a 2 kb fragment upstream of the start codon of myoA was amplified from genomic DNA using oligos 5’UTR myoA fw/rv and cloned using as template vector p5RT70-Ty-MyoA via KpnI and EcoRI.
Culturing of parasites and host cells
Human foreskin fibroblasts (HFFs) (SRC-1041, ATCC®) were grown on tissue culture-treated plastics and maintained in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% foetal bovine serum, 2 mM L-glutamine and 25 mg/mL gentamycin. Parasites were cultured on HFFs and maintained at 37 °C and 5% CO2. Cultured cells and parasites were regularly screened against mycoplasma contamination using the LookOut® Mycoplasma detection kit (Sigma) and cured with Mycoplasma Removal Agent (Bio-Rad) if necessary.
T. gondii transfection and selection
To generate stable expressing parasites, 1 × 107 of freshly lysed RH ∆hxgprt  or RH-DiCre ∆ku80  parasites were transfected with 20 μg DNA by AMAXA electroporation. Selection was based on mycophenolic acid and xanthine, as described previously , or bleomycin.
Generation and verification of parasite lines
The conditional act1 KOCDr strain (RH-DiCre ∆ku80/endogenous act1::loxPact1 CDr loxP, referred to as loxPAct1 CDr ) was generated by replacing the act1 cassette in the LoxPAct1 geneswap vector  with a synthesised act1 cassette containing the mutation Ala 136 Gly . Integration after transfection was confirmed by PCR using primer sets (1-1’) for act1 ORF (gDNA vs. cDNA), 5’UTR integration and cre-mediated recombination with primer sets (2-2’) and 3’UTR integration (3-3’).
For stabilisation of p5RT70-Ty-MyoC, pMyoC-Ty-MyoC and pMyoA-Ty-MyoA, RH ∆hxgprt and myoA KO parasites were selected using bleomycin. The vector pBSSK + pSag1-Ble-Sag1 was co-transfected with each respective construct in the proportion (2:1), and selection was carried out as described previously .
Inducing conditional knockout lines
act1 cKO and mlc1 cKO were obtained by addition of 50 nM and 100 nM of rapamycin to the parental lines, respectively. Strains were incubated for 4 h at 37 °C and 5% CO2, and cultured as described previously . To increase the population of these lines since they have an egress phenotype, act1 cKO and mlc1 cKO parasite media was swapped for DMEMcomplete supplemented with 2.5% dextran sulphate after 24 h to enrich egress mutants .
Immunofluorescence analysis was carried out as previously described . Briefly, parasites were allowed to invade and replicate in an HFF monolayer grown on glass coverslips. The intracellular parasites were fixed in 4% paraformaldehyde for 20 min at room temperature. Afterwards, coverslips were blocked and permeabilised in 2% BSA and 0.2% Triton X-100 in PBS for 20 min. The staining was performed using the indicated combinations of primary antibodies (Additional file 14: Table S2) for 1 h. Followed by the incubation with secondary AlexaFluor 350, AlexaFluor 488, AlexaFluor 594 or AlexaFluor 633 conjugated antibodies (1:3000, Invitrogen – Molecular Probes) for another 45 min, respectively.
Structured illumination microscope (SIM) imaging
Super-resolution SIM was carried out using an ELYRA PS.1 microscope (Zeiss). Images were acquired using a Plan Apochromat 63×, 1.4 NA oil immersion lens, recorded with a CoolSNAP HQ camera (Photometrics), and analysed using ZEN Black software (Zeiss) and ImageJ software.
Extracellular parasites were pelleted and then resuspended in RIPA buffer (50 mM Tris-HCl pH 8; 150 mM NaCl; 1% Triton X-100; 0.5% sodium deoxycholate; 0.1% SDS; 1 mM EDTA), incubation for 5 min on ice was used to lyse the cells. Afterwards, samples were centrifuged for 60 min at 14,000 rpm at 4 °C and laemmli buffer was added to the supernatant. A total of 5 × 106 parasites were loaded onto an SDS acrylamide gel while, for act1 cKO down-regulation, only 1 × 105 parasites were loaded. Western blotting was performed as described previously  using IRDye680RD or IRDye800RD (Li-Cor) secondary antibodies.
Proteins were detected using the Li-Cor Odyssey and quantified using infrared detection of the protein of interest on Image Studio 5.0 (Li-Cor).
Quantitative immunofluorescence assay (IFA)
Wt and parental LoxP strains were used as controls. For knockout lines, parasites were induced with rapamycin as described previously  and cultured for 24 h on HFFs prior to fixation. An IFA was conducted using the respective primary antibody; TgACT1 (Soldati, 1:100) or TgMLC1 (Soldati, 1:2000) and AlexaFlour 594 (Molecular Probes, 1:3000) as the secondary antibody. Images were obtained using a DeltaVision® Core microscope equipped with a CoolSNAP HQ2 CCD camera and were saved as single red and green channel files. Freeware CellProfiler 2.1.1 software (www.cellprofiler.org) was used to analyse and quantify fluorescence intensities. Greyscale images were imported to the program for analysis. The pipeline was adjusted to detect objects within the range of 5 to 40 pixels. Objects were identified using a global threshold strategy with a three class-Otsu threshold and weighted variances. Under these parameters, we identified in each image YFP-expressing parasites (generated by the DiCre cassette after correct gene excision) and the red coloured region of interest (corresponding to ACT1 and MLC1, respectively). The red signal was quantified on the basis of the total pixel occupied by the YFP expressing objects. The intensity of the red channel was measured for each object and exported to an Excel spreadsheet. The data obtained was filtered manually using area and integrated intensity parameters to include all parasites in a vacuole and exclude clustered vacuoles or random objects. Intensities from 60 vacuoles per time point were quantified and processed to remove the calculated internal background. The background fluorescence of the host cells was calculated using a YFP+ strain that was allowed to replicate under the same conditions as the tested parasites. However, no antibodies were added to the coverslips and, from this, the auto-fluorescence of the host was calculated and plotted as a horizontal dotted line.
Cell fluorescence measurement
An IFA was performed in myoA KO and RH ΔKu80 lines expressing MyoC under different levels (p5RT70-Ty-MyoC, pMyoc-Ty-MyoC and endogenous tagged MyoC). Primary antibody against Ty-tag was used to localise MyoC and DAPI as a DNA marker. Images were obtained using ELYRA PS.1 microscope (Zeiss). All 3D SIM images were collected at the same exposure and resolution parameters. Images were obtained using Zen Black (Zeiss) and analysed using ImageJ. Vacuoles to be analysed were visually identified and traced using the drawing tool. Measurements obtained were area, integrated density and mean grey value. Background measurements were obtained by selecting a portion of the image with no signal. Data was plotted by using the corrected total cell fluorescence (CTCF) which was calculated using the following formula: [CTFC = Integrated density – (Area of selected cell × Mean fluorescence of background readings)] .
Was conducted as described previously . Briefly, 1 × 103 parasites were inoculated on a confluent layer of HFFs and incubated for 5 days, after which the HFFs were washed once with PBS and fixed with ice cold MeOH for 20 min. HFFs were stained with Giemsa with plaque area measured using Fiji software. Mean values of three independent experiments ± standard deviation were determined.
Trail deposition assay
Gliding assays were performed as described before . Briefly, freshly lysed parasites were allowed to glide on FBS-coated glass slides for 30 min before they were fixed with 4% paraformaldehyde (PFA) and stained with α-SAG1 under non-permeabilising conditions. Mean values of three independent experiments ± standard error of the mean (SEM) were determined. Where actin-modulating drugs were used, parasites were pre-incubated for 10 min in the respective concentration before the start of the assay.
For the assay, 5 × 104 freshly lysed parasites were allowed to invade a confluent layer of HFFs for 1 h. Subsequently, five washing steps were performed for removal of extracellular parasites. Cells were then incubated for a further 24 h before fixation with 4% PFA. Afterwards, parasites were stained with the α-IMC1 antibody . The number of vacuoles in 15 fields of view was counted. Mean values of three independent experiments ± SEM were determined.
Egress assays were performed as described previously . Briefly, 5 × 104 parasites were grown on HFF monolayers for 36 h. Media was exchanged for pre-warmed, serum-free DMEM supplemented with 2 μM A23187 (in DMSO) to artificially induce egress. After 5 min, the cells were fixed with 4% PFA and stained with a-SAG1 antibody; 200 vacuoles were counted for their ability to egress out of the host cells. Mean values of three independent assays ± SEM were determined.
Fluorescence activated cell sorting (FACS)
Prior to sorting, mlc1 cKO parasites were scratched, syringed through a 25-G needle and filtered through a 3-μm Millipore filter (Millipore Merck) for purification of the sample. An S3e™ Cell Sorter (Bio-Rad Laboratories, Inc.), equipped with 488, 561 and 640 nm lasers, was used to sort mlc1 cKO/YFP expressing parasites. Parasites were sorted into 5 mL tubes. The temperature for sample loading stage and collection area was set at 37 °C for culturing parasites and at 4 °C for western blot analysis. Before sorting parasites, the equipment was calibrated using ProLine™ universal calibration beads (Bio-Rad Laboratories, Inc.). Gates were adjusted to separate and collect YFP expressing population (mlc1 cKO). For the long-term culturing parasites experiment, sorting was performed in single cell mode in order to obtain the purest population possible. After sorting, parasites were cultured under standard conditions described above. For western blot analysis, sorting was performed in enrichment mode to obtain the highest number of parasites possible.
2D motility assay
Time-lapse video microscopy was used to analyse the kinetics over a 2D surface similarly to as previously described . Briefly, Ibidi μ-dish35mm-high were coated in 100% FBS for 2 h at room temperature. Freshly egressed parasites were added to the dish. Time-lapse videos were taken with a 20× objective at one frame per second using a DeltaVision® Core microscope. Analysis was made using ImageJ wrMTrckr tracking plugin. For analysis, 20 parasites were tracked during both helical and circular trails with the corresponding distance travelled, average and maximum speeds determined. Mean values of three independent experiments ± standard deviation were determined.
Parasites contained in heavily infected HFFs were scratched and passed through a 26-G needle three times to release parasites artificially. Parasites were added to HFFs grown in Ibidi m-Dish35mm-high. Invasion events were observed after approximately 5 min when parasites had settled and penetration time was determined. Time-lapse videos were recorded at 40× objective at a rate of one frame per second using DeltaVision® Core microscope. Invasion events and time were manually tracked and calculated.
3D motility assay
Tachyzoites were prepared and assayed as previously described . Briefly, the rapamycin-induced populations were harvested by syringe release of infected HFF monolayers using a 27-G needle, filtered through a 3-μm Nuclepore filter, and gently centrifuged at 1000 × g for 4 min. The tachyzoite pellet was washed and resuspended at a final concentration of 1–2 × 108 tachyzoites/mL in 3D Motility Media (1× Minimum Essential Medium lacking sodium bicarbonate, 1% (v/v) FBS, 10 mM HEPES pH 7.0 and 10 mM GlutaMAX L-alanyl-L-glutamine dipeptide) supplemented with 0.3 mg/mL Hoechst 33342. The tachyzoite suspension was then mixed with three volumes of 3D Motility Media and three volumes of Matrigel (BD Biosciences, San Jose, CA), pre-chilled on ice. Motility in Matrigel was imaged, tracked and processed using Imaris × 64 v. 7.6.1 software (Bitplane AG, Zurich, Switzerland), as previously described . Three independent biological replicates, each with three technical replicates, were performed. Parameters calculated from 3D motility assays were analysed using two-way ANOVA with Sidak’s multiple comparisons test and with the Kolmogorov–Smirnov test using GraphPad Prism v. 6.01 (La Jolla, CA). Under our imaging conditions, trajectory displacements less than 2 μm (i.e. slightly less than one-third the body length of a parasite (~7 μm)) cannot be distinguished from Brownian motion as measured empirically with heat-killed parasites , and so a cut-off of 2 μm was applied to exclude stationary parasites. Longer displacements were considered parasite-driven and used for more detailed analysis of motility parameters.
Ibidi live cell dishes (29 mm) were coated with 0.1% poly-L-lysine for 30 min and washed with MilliQ water. Fluorescent latex beads (FluoSpheres®, 0.04 μm, Invitrogen) were diluted with 5 μL in 400 μL Hanks Balanced Salt Solution + HEPES (25 mM) (described hereafter as H-H buffer) and sonicated twice for 2 min. After a short spin (10 s, 6000 × g), the supernatant was recovered and left on ice for 30 min before use. Parasites of interest were harvested (by scratch, syringe and filtration). Parasites were pelleted for 5 min at 3000 × g, washed and resuspended in cold 250 μL H-H buffer to achieve 107 parasites/mL. Parasites were then transferred to poly-L-lysine-coated dishes and left on ice for 20 min; 5 μL of diluted beads were added to 250 μL of H-H buffer and added to the parasites. Immediately, the dish was incubated at 37 °C for 15 min. The experiment was stopped by addition of 2 mL of 4% PFA and incubated at 4 °C for 10 min. The PFA was washed gently and parasite nuclei stained with Hoechst 0.01%. For time course, the parasites were fixed at different time points after the addition of the beads. For the drug and buffer assays, parasites were incubated for 10 min in the buffer of interest before their incubation on the coated dish. Bead dilution and the rest of the experiment were also made using the same buffer (Endo Buffer or H-H buffer + 0.5 μM CD).
For each experiment (n), an average of 1000 parasites were analysed. Total numbers of parasites, number of parasites without beads, with beads bound and with beads capped were quantified (e.g. For RH n1, a total of 1615 parasites were counted, within those, 63 were not interacting with the beads, 1062 had beads around them and 490 had capped beads). For each condition, experiments were performed in three independent experiments n = 3. Mean values of each interaction type for three independent experiments ± SEM were determined and compared to RH.
Attachment under fluidic shear stress
LoxP strains were induced to generate KOs as previously described in Egarter et al. . Fresh extracellular parasites (4 × 105 in total, consisting of approximately equal numbers of control and KO) were loaded into collagen IV coated fluidic chambers (Ibidi IB-80192) and allowed to attach at 37 °C for 20 min. PBS was pumped through the chamber using an ‘open loop flow’ microfluidic pump (KD Scientific Legato 200 syringe pump) system, similar to that described previously , to control flow rates and generate fluidic shear stress. In our setup, a flow rate of 1 mL/min achieves 3 dyn/cm2 shear stress at the surface of the channel. Flow at 0.1 mL/min (equivalent to 0.3 dyn/cm2) was used to remove all non-attached parasites. At each fluidic shear stress level, control and mutant parasites were counted from five fields of view per experiment. Parasite count after the 0.1 mL/min wash was taken as 100% of attached parasites. Counts at all other rates of flow were normalised to the 100%. Data collected was analysed using Excel to assess the significance of differences between control and mutants using Student t-test and further analysed using GraphPad Prism v. 6.01 software to display data as trends. Parasites in the chamber were monitored via a Zeiss Axio Vert.A1 microscope setup with a 40× objective combined with an AxioCam ICm1 camera and Zen capture software.
We would like to thank members of the Meissner lab for thoughtful discussions. We would also like to thank Prof. David Sibley (Washington Univeristy, St. Louis), Prof. Dominque Soldati-Favre (University of Geneva), Prof. Artur Scherf (Institut Pasteur, Paris), Dr. Jake Baum (Imperial College, London) and Dr. Maryse Lebrun (University of Montpellier) for generously providing antibodies and parasite strains.
This work was supported by an ERC-Starting grant (ERC-2012-StG 309255-EndoTox) and the Wellcome Trust 087582/Z/08/Z Senior Fellowship for MM, and US Public Health Service grant AI054961 for GEW. The Wellcome Trust Centre for Molecular Parasitology is supported by core funding from the Wellcome Trust (085349). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Availability of data and materials
All data generated or analysed during this study are included in this published article and its supplementary information files, or are available from the authors on reasonable request.
JW and FLB performed experiments analysed results and interpreted data of mutant parasites characterisation; participated in the writing, revision and edition of the manuscript. SG and GSP carried out and analysed retrograde flow and flow chamber experiments respectively. JML set up and analysed 3D motility experiments. AH designed and analysed experiments of dense granules motility. SE and NA generated and analysed the studied mutant lines. GW conceived the 3D motility project, designed the study, analysed results, interpreted data, and drafted and revised the article. SRN and DMW analysed dense granule motility data and revised the article. MM conceived the project, designed the study, analysed results, interpreted data, and wrote the first manuscript. All authors participated in the revision of the manuscripts and approved the final version.
The authors declare no conflict of interest.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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