Genetic impairment of parasite myosin motors uncovers the contribution of host cell membrane dynamics to Toxoplasma invasion forces

Background The several-micrometer-sized Toxoplasma gondii protozoan parasite invades virtually any type of nucleated cell from a warm-blooded animal within seconds. Toxoplasma initiates the formation of a tight ring-like junction bridging its apical pole with the host cell membrane. The parasite then actively moves through the junction into a host cell plasma membrane invagination that delineates a nascent vacuole. Recent high resolution imaging and kinematics analysis showed that the host cell cortical actin dynamics occurs at the site of entry while gene silencing approaches allowed motor-deficient parasites to be generated, and suggested that the host cell could contribute energetically to invasion. In this study we further investigate this possibility by analyzing the behavior of parasites genetically impaired in different motor components, and discuss how the uncovered mechanisms illuminate our current understanding of the invasion process by motor-competent parasites. Results By simultaneously tracking host cell membrane and cortex dynamics at the site of interaction with myosin A-deficient Toxoplasma, the junction assembly step could be decoupled from the engagement of the Toxoplasma invasive force. Kinematics combined with functional analysis revealed that myosin A-deficient Toxoplasma had a distinct host cell-dependent mode of entry when compared to wild-type or myosin B/C-deficient Toxoplasma. Following the junction assembly step, the host cell formed actin-driven membrane protrusions that surrounded the myosin A-deficient mutant and drove it through the junction into a typical vacuole. However, this parasite-entry mode appeared suboptimal, with about 40 % abortive events for which the host cell membrane expansions failed to cover the parasite body and instead could apply deleterious compressive forces on the apical pole of the zoite. Conclusions This study not only clarifies the key contribution of T. gondii tachyzoite myosin A to the invasive force, but it also highlights a new mode of entry for intracellular microbes that shares early features of macropinocytosis. Given the harmful potential of the host cell compressive forces, we propose to consider host cell invasion by zoites as a balanced combination between host cell membrane dynamics and the Toxoplasma motor function. In this light, evolutionary shaping of myosin A with fast motor activity could have contributed to optimize the invasive potential of Toxoplasma tachyzoites and thereby their fitness. Electronic supplementary material The online version of this article (doi:10.1186/s12915-016-0316-8) contains supplementary material, which is available to authorized users.


Background
Non-professional phagocytes such as epithelial, endothelial, and fibroblast cells provide intracellular niches to a plethora of single-celled invasive microbes. The proliferation of these intracellular microbes including nonparasitic and parasitic prokaryotes or eukaryotes can cause diseases with devastating sociological or economic impact on livestock and humans. A common mechanism among the sequences that set intracellular niches for microbes is the remodeling of both the host cell lipid bilayer and the cortical cytoskeleton. This rearrangement provides the membrane and drives the force required to engulf the microbe within subcellular compartments. Most bacteria enter non-phagocytic cells within a few minutes by either "discreet zippering" phagocytosis or "conspicuous triggering" macropinocytosis, although this oversimplified categorization has been questioned [1]. The general concept distinguishes (1) the restrained host cell membrane protrusions firmly adhering to and extending like a zipper around the bacteria surface to form a tight-fitting phagosome from (2) the diffuse host cell membrane ruffles emerging at the vicinity of the bacteria once triggered by the first wave of bacterial effectors, and further shaping spacious macropinosomes/phagosomes [2,3]. Once sealed, these subcellular compartments acquire and lose endocytic markers, thereby creating a microenvironment that bacteria have to control or escape [4]. In contrast, a group of flagellated protozoan parasites clustered in the Apicomplexa phylum has evolved a distinct strategy to colonize their host cells that relies upon both their own driving force and their ability to avoid the host cell endocytic pathway once internalized within vacuoles. Early studies on major members of this phylum, specifically Toxoplasma gondii and Plasmodium spp., have highlighted the lack of host cell contribution when the parasite invasive stages, also called zoites, actively invade their respective host cells in a process completed within a few seconds [5][6][7][8]. Invasion starts with the insertion in the host cell plasma membrane (PM), by the zoite, of a multi-subunit complex (identified as the apical major antigen 1 (AMA1)-rhoptry neck (RON) complex and possibly enlarged with the recently discovered claudin-like apicomplexa microneme protein (CLAMP) [9]. This macromolecular complex connects the two cells by forming a circular tight junction (TJ) [10][11][12][13] that will act as a door of entry. The zoite then tracts itself into a PM invagination that arises below the TJ [14] and then evolves as a nonfusogenic parasitophorous vacuole (PV) that will support zoite growth and multiplication [15]. Our recent kinematic analysis has allowed tracking of the RON complex during its secretion and assembly into the PM and its establishment of a traction bridge with the host PM and its associated cortical actin lattice [16,17]. In this scheme, the invasive force is thought to be provided by the single-headed unconventional myosin A (MyoA) of the apicomplexan-specific myosin class XIV [8,18,19]. Accordingly, the general expectation was that MyoA-deficient T. gondii parasites would lose their ability to enter the host cells and would not be viable. Yet, using a conditional recombination system, it was possible to maintain MyoA-lacking (ΔMyoA) parasites in vitro [13,20]. It was then proposed that another class XIV myosin, namely myosin C (MyoC), a spliced variant of the single gene encoding MyoB and MyoC isoforms, would compensate for MyoA loss of function [21]. On the other hand, mutants for additional components of the motor complex including actin -which cannot be compensated by paralogs being encoded by a single copy genewere also engineered and have led to the proposal of alternative mechanisms for zoite motility and cell invasion based on zoite hydrodynamic forces [20] but which need to be validated. However, it has not been investigated so far whether a contribution from the host cell could potentially account for the residual invasiveness of MyoA-deficient Toxoplasma. Yet, phagocytosis-mediated uptake of live zoites into phagocytes followed within a few minutes by egress from the early phagosome into a second vacuole, namely the PV, has already been reported for motor-competent virulent [5] and avirulent [22] tachyzoites. We therefore decided to reevaluate the role of T. gondii zoite motors during invasion by applying high resolution live and fixed imaging in conjunction with functional assays to compare how motor-competent and MyoA-or MyoB/C-deficient tachyzoites access a growth-compatible PV in nonphagocytic cells. Together, our data undoubtedly position the MyoA motor at the center of the Toxoplasma tachyzoite invasive force. Further, this study reveals that MyoAdeficient zoites enter host cells by a yet undescribed process that shares only initial features with macropinocytosis. This in-depth analysis of how motor-impaired Toxoplasma interact with mammalian cells to either succeed or fail at entering them calls for a new Toxoplasma-host cell invasion paradigm based on a balanced contribution between zoite motor engagement and host cell membrane/cortex dynamics.

Results
MyoA-deficient tachyzoites enter their non-phagocytic host cells with a significantly slower kinetics than MyoA + tachyzoites T. gondii tachyzoites deficient for MyoA motor have been genetically engineered using the diCre-lox site-specific recombination system [23]. The parental line expressed a loxP-flanked sequence of MyoA in fusion with the Ty epitope tag (lox-MyoA) that ensured constitutive MyoA synthesis, while the mutant line (ΔMyoA) did not produce MyoA proteins as illustrated with in situ staining with anti-Ty antibodies (Fig. 1a). The duration of the entry process by tachyzoites from these two strains in a variety of non-phagocytic cells including fibroblastic, epithelial, endothelial, and osteoblastic cells was measured. While the time range was restricted for lox-MyoA (n = 235) with values rarely above 60 s (average time x = 29.8 s), it significantly increased for ΔMyoA tachyzoites (n = 300) with kinetic values between 64-1413 s and an average time of x = 267 s. In addition, we included another MyoA + strain that was deficient in MyoB/C (characterized in [20]) (ΔMyoB/C, n = 216) and confirmed a kinetic profile significantly similar to lox-MyoA tachyzoites with an average time of entry of x = 31.2 s (Fig. 1b), thus strongly suggesting that MyoA could play a specific key function during host cell entry.
Real-time tracking of the host cell PM and cortical actin demonstrates that MyoA-but not MyoB/C-deficient tachyzoites are pushed into host cells through actinpowered PM protrusions that encircle the zoite body To investigate whether ΔMyoA tachyzoites used a distinct method of entry that would explain the slower kinetics when compared to MyoA + tachyzoites, we compared the behavior of MyoA + (n = 451) and MyoA-deficient (n = 396) parasites in contact with cells that expressed genetically encoded fluorescent markers for the PM and the nascent PV and/or for the cortical actin cytoskeleton (listed in Methods). Similarly to MyoA + tachyzoites, ΔMyoA mutants extruded their apical conoid and made a polarized contact with the host cell PM as depicted in Fig. 2 (white arrowheads; additional movie files show this in real time (see Additional files 1-4)), but they then followed a different path. In HeLa cells expressing the CAAX-mCherry (CAAX-mC) PM reporter, lox-MyoA (= MyoA + ) or ΔMyoB/C (= MyoA + ) tachyzoites entered the nascent PVs through static or capped TJs (Fig. 2a, blue trajectories; additional movie file shows these trajectories in real time (see Additional file 5)) as described for motor-competent tachyzoites [17]. In contrast, the apex of ΔMyoA tachyzoites appeared tightly enwrapped within a tight collar or a glove of host cell PM protrusions we will refer to as "PM ruffles" (Fig. 2b, white arrows). In both HeLa (Fig. 2b) and U2OS (Fig. 2c) cells expressing either the CAAX-mC or the platelet-derived growth factor receptor trans-membrane domain (PDGFRTM)-green fluorescent protein (GFP) fusion proteins as PM markers, the PM ruffles were seen to protrude and stretch over the tachyzoite mid-region to eventually fold over the zoite (Fig. 2c, yellow arrows; additional movie files show this detail in real time (see Additional files 1-3)). Additional file 6: Figure S1 depicts invasion assays related to the actual actin dynamics of the PM ruffles. This is discussed in detail in a later section. PM encircling of the zoite was associated with forward displacement of the latter into the host cell (Fig. 2b, black arrows), while thereafter PM protrusions withdrew (Fig. 2c, yellow arrowheads). The sequences also revealed that once PM ruffles emerged, tachyzoites were typically pushed backward a few micrometers, suggesting that a force arose underneath the contact point. Remarkably, the PM could supply enough material to envelop two parasites that remained jointed by their posterior ends by residual material derived from the mother cell (i.e., the residual body) and which represented a volume of about 450-600 μm 3 (an additional movie file shows this in real time (see Additional file 4)). Finally, to analyze the detailed structure of the PM protrusions that formed around the ΔMyoA zoites and to compare with the process induced by lox-MyoA tachyzoites, we used scanning electron microscopy (SEM). While we visualized thin and spatially restricted PM protrusions around the  apex of MyoA + attached and invading tachyzoites (Fig. 2d, e, white arrowheads), we observed a much more pronounced and PM glove-like protrusion covering the first third of the ΔMyoA zoite (Fig. 2f, white arrowheads) and expanding over its body (Fig. 2 g, white arrowheads) in full agreement with the dynamic imaging of mutant zoite internalization. Because cortical actin dynamics orchestrates a number of PM remodeling processes including phagocytosis and macropinocytosis [2,24], we next investigated whether host cell actin polymerization was associated with the entry of MyoA-deficient zoites using cells transiently expressing the F-actin binding LifeAct peptide in fusion with GFP [25]. In U2OS cells, F-actin was detected in thick fibers throughout the cells but also in thinner structures formed at and elongated from the site of intimate contact between the two cells ( Fig. 2 h, green arrows) before collapsing behind the internalized zoite ( Fig. 2 h, green arrowhead; additional movie files show these details in real time (see Additional files 7 and 8)). Finally, coexpression of a fluorescent PM reporter and LifeAct-GFP in the host cell revealed the spatiotemporal coincidence of the PM (Fig. 2i, yellow arrows and arrowhead, see zoomed area) and F-actin dynamics during zoite internalization (Fig. 2i, green arrows and arrowhead; an additional movie file shows these details in real time (see Additional file 9)). All this information indicates that actin polymerization stretched and pushed the PM outwards over the zoite, thereby supporting the idea that the force directing ΔMyoA parasites originates from the host cell actin assembly.
Host cell PM ruffles force ΔMyoA tachyzoites to pass through the TJ into a primary PV which traffics in the cytoplasm and allows subsequent Toxoplasma development Since uptake of tachyzoites through a transient phagosome has been reported [5,22], it was pertinent to analyze in detail the fate of the ΔMyoA parasites once enwrapped within PM ruffles. Monitoring host cell PM dynamics allowed us to distinguish the outward collar of ruffles from a single PM invagination that hinted at a nascent PV membrane. PM invagination was detectable before ruffles expanded around the zoite and was next seen to enlarge while the zoite moved forward (Fig. 3a, red thin and thick arrows; an additional movie file shows this detail in real time (see Additional file 10)). Importantly, the signal intensity for both PM and G/F-actin markers was significantly higher for the PM ruffles than for the PM invagination (Fig. 3b, transections 1 and 2 and corresponding signal profiles). These acute observations substantiate the view of the tachyzoite being passively driven into a PM-derived PV that arose at the site of contact (see cartoon Fig. 3c). We next showed that neither escape from the primary PV nor folding of a secondary PV was required for ΔMyoA zoite survival and growth by monitoring vacuole-containing ΔMyoA mutants up to 5 h post-internalization ( Fig. 3d; an additional movie file shows this detail in real time (see Additional file 11), n = 29 observations). Finally, to confirm that ΔMyoA parasites assemble a typical TJ, we applied high resolution laser scanning microscopy on samples stained for the TJ marker rhoptry neck protein (RON) 4 [10] as well as for host cell F-actin and actinassociated proteins in epithelial, fibroblastic, and endothelial cells. Not only was a typical ring-shaped RON-positive TJ (Fig. 4a, red arrows) observed in agreement with what was reported in [20], but it was surrounded by a densely packed belt of host cell F-actin (Fig. 4a, green arrows). Apart from F-actin (Fig. 4b, green arrows) the actinnucleating factors, i.e., actin-related proteins 2 and 3 (Arp2/3) complex and cortactin ( Fig. 4c-e), were largely co-recruited at the TJ site, thereby arguing for a host cell actin turnover during ΔMyoA Toxoplasma entry.
The unique mode of ΔMyoA zoite entry relies on host cell actin polymerization but not on late effectors of macropinocytosis, consistent with the absence of macropinosome formation Since host cell F-actin was dynamically visualized in the expanding PM protrusions enwrapping ΔMyoA zoites, (See figure on previous page.) Fig. 2 Real-time tracking of the host cell PM and cortical actin demonstrate that MyoA-but not MyoC-deficient tachyzoites are pushed into host cells through actin-powered PM protrusions. a-c, h, i Time lapses showing differential interference contrast (DIC) and fluorescent characteristic sequences of interaction between (a) ΔMyoC (n = 216) or (b, c, h, i) ΔMyoA (n = 300) tachyzoites and (a, b) HeLa cells that stably express the PM targeting domain CAAX-mCherry (CAAX-mC) or (c, h, i) U2OS cells. c U2OS cells transiently express the PM reporter PDGF trans-membrane domain (PDGFTM) coupled to GFP or (h) the F-actin binding peptide LifeAct coupled to GFP (LifeAct-GFP), or (i) transiently co-express the PDGFTM PM marker coupled to mCherry (mC) and LifeAct, coupled to GFP. Note the extruded position of the conoid prior to the contact with the host cell PM (a-c, i; white arrowheads) and the forward displacement of the tachyzoite (a, b, h; black arrows). a Trajectories (blue lines) of the constriction site (i.e., the TJ) with time reveal that ΔMyoB/C tachyzoites enter their host cells using a typical static or capped TJ scenario. In contrast, tracking of the PM (b, c, i) and cortical F-actin (h, i) dynamics reveals progressive encircling of the ΔMyoA tachyzoites by PM ruffles that are supported by F-actin (yellow and green arrows, respectively). Note that retraction of the PM ruffles together with F-actin disassembly follow zoite internalization as indicated with yellow and green arrowheads, respectively. i Right frame shows the overlap between PM and actin remodeling for the zoomed frame of the time lapse showing half in-half out zoite labeled with a white star. All scale bars: 5 μm. d-g SEM micrographs showing (d) RH-MyoA + , (e) lox-MyoA (MyoA + ), (f, g) ΔMyoA (MyoA -) interacting with host cells. Note (d, e) the host cell spatially restricted "glove-like" PM protrusions around the zoite apex (white arrowheads) and (f, g) the thin host cell PM long sheath that constrains a third of the zoite and expands over its body. Scale bars: 1 μm (d, f, g) and 2 μm (e) we next interrogated how interfering with host cell actin dynamics affected the rate of ΔMyoA zoite entry. To this end, we exposed U2OS and spontaneously arising retinal pigment epithelial (ARPE-19) cells to a cocktail of cell-permeant actin poisons that quickly arrests actin dynamics and myosin II-based reorganization but preserves the existing steady-state actin organization, in contrast to most actin inhibitors described so far. The cocktail acts a Note the concomitant development of (i) a PM invagination that remains almost F-actin-negative and that starts at the constriction site (thick red arrows) to eventually surround the internalized parasite and (ii) an outer basket of PM projections (thin red arrows) enriched in F-actin (green arrows). b Overlay between the three layers of the zoite "half in-half out" (top frame) and the pseudocolored image for each fluorescent signal at the same time point (bottom frames). Two transections covering the extracellular (1) and intracellular (2) regions of the parasites allowed us to retrieve signal intensity profiles and show that F-actin is mainly associated with the outer ruffles encircling the extracellular region of the zoite. c Schematic sequence of interaction events leading to progressive enwrapping of the ΔMyoA parasite by host cell actin-driven PM ruffles that push the zoite through the TJ. d Note that the zoite internalized through the wrapping process further develops in the primary vacuole over the 5-h post-entry videorecording. Scale bar: 5 μm through the concerted activities of jasplakinolide, latrunculin B, and Y27632 (JLY): it is effective within seconds for periods longer than 10-15 min after drug removal [26]. These unique features gave us the opportunity to selectively block host cell actin turnover in fetal calf serum (FCS)-starved U2OS and ARPE-19 cells independently of Toxoplasma.
We observed an acute drop in the ΔMyoA rate of internalization to less than 2 % (n infected U2OS cells = 273/17,001) in serum-starved U2OS cells treated with JLY compared to 27.7 % (n infected U2OS cells = 6514/ 23,503) when cells were incubated with the dimethyl sulfoxide (DMSO) vehicle alone ( Fig. 5a; an additional file shows this assay (see Additional file 6: Figure S1a)). We did not notice any significant cytotoxic effect of the JLY by measuring the rate of live (i.e., calcein-positive) and dead (i.e., calcein-negative) cells during a period of 2 h following the JLY treatment (n cells = 460 to 720 cells for each measure; this assay is shown in Additional file 6: Figure S1b). In addition we observed that 2 h post-treatment, the rate of ΔMyoA tachyzoites was restored to more than 80 % of the control (see Additional file 6: Figure S1c). A similar decrease in internalization was obtained when ARPE-19 cells were exposed to JLY under the same experimental conditions as for U2OS cells (Fig. 5b). In the same line, when cells were pretreated only with jasplakinolide, which blocks actin turnover by promoting the incorporation of all cytoplasmic free actin into filaments [27,28], about a threefold decrease was observed (n infected U2OS cells = 1953/ 23,240; 8.4 %) ( Fig. 5a; Additional file 6: Figure S1a shows this assay). Moreover, since myosin II also participates in the disassembly of the actin network, we used either blebbistatin, which directly inhibits myosin II activity [29], or the Rho-associated protein kinase (ROCK) inhibitor Y27632 [30], which blocks upstream myosin II activators, or a combination of the two drugs. Because each compound is soluble under different conditions and both are rapidly reversible, we used different control populations and did not wash the drug out when adding ΔMyoA to the pre-treated FCS-starved cells. However, intracellular mutant tachyzoites were found even at a significantly higher rate than for the respective host cell control population when myosin II activity was inhibited (for Y27632, n infected U2OS cells = 5218/12,968; 42 % versus control = 11310/42,629; 26. 5 % and for blebbistatin, n = 8475/20,755; 40.8 % versus control = 6514/23,503; 27.7 %), and an additive effect was actually obtained ( Fig. 5a; Additional file 6: Figure S1a). These data indicate that host cell myosin II contractile activity was not required for the folding of membrane projections that translocated Toxoplasma into a nascent vacuole. Interestingly, myosin II as well as phosphoinositide 3-kinase (PI3K) have often been reported to control late steps of both Samples were fixed and processed for double or triple immunofluorescence staining with (a) anti-RON4 antibodies (red) and phalloidin (green); note the RONpositive TJ (red arrows), (b, c, e) anti-P30 antibodies (blue) prior to permeabilization to selectively label surface-exposed antigens, and (b) phalloidin (green) or (c) anti-Arp2/3 antibodies (green) after cell permeabilization. Note the spectacular co-enrichment of F-actin and the Arp2/3 complex that surrounded the TJ ring or area (green arrows), (d) anti-cortactin antibodies to localize the regulatory Arp2/3-nucleating factor (cortactin, red) and its target (the Arp2/3 complex, green), and (e) anti-Arp 2/3 antibodies (red) and phalloidin (green). Note the co-localization of F-actin and the actin nucleating machinery (Arp2/3 and cortactin) at the TJ (green and red arrows). All scale bars: 5 μm constitutive (in dendritic cells) and regulated macropinocytosis or even phagocytosis [31] coinciding with ruffle closure or subsequent cup sealing [32][33][34][35][36]. In line with these observations, we found that pre-treatment of both U2OS and ARPE-19 cells with the irreversible PI3K inhibitor wortmannin had no effect on the rate of ΔMyoA parasite entry regardless of the drug concentration (n infected U2OS cells = 3282/11,358; 28.9 %) (Fig. 5a, b; Additional file 6: Figure S1a). In the control, uptake of the macropinocytosis tracer Alexa 594-coupled 10-kDa dextran (Dx) was nullified by all treatments (JLY, blebbistatin, and wortmannin). We also observed that the space delineated by the PM invagination around the entering ΔMyoA mutants was negative for the macropinocytosis tracer (n = 0 for >200 intracellular ΔMyoA tachyzoites analyzed). Collectively these data suggested that the route of ΔMyoA parasite entry was not macropinocytosis (Fig. 5c). We further interrogated whether a specific marker of young typical PVs such as the rhoptry protein (ROP) 2, which is thought to be secreted during invasion [37], could be associated with the process of ΔMyoA zoite entry. We systematically found ROP2 decorating the inner PM invagination that encircled the apical part of the ΔMyoA zoite, thus before complete internalization had occurred, an early and yet not documented timing for ROP2 secretion (Fig. 5c,d; an additional movie file shows this distribution (see Additional file 12)). A threedimensional (3D) reconstruction based on image stacks suggested that the ROP2 nascent vacuole was not intimately associated with the Dx-positive compartment (i.e., endosomes and macropinosomes) (Fig. 5c, d, bottom panels; Additional file 12). In sum, these findings reinforce the live imaging data and demonstrate that ΔMyoA tachyzoites enter a typical PV. Note that addition of epidermal growth factor (EGF) at the time when Toxoplasma mutants establish contact with host cells had only a slight positive effect on parasite entry in ARPE-19 epithelial cells that elicit many ruffles in response to EGF and had no specific effect on U2OS (Fig. 5a). All these data fit well with the view that upstream of the PM remodeling, the sequences of RON release and TJ formation remain limiting steps of the entry process. Additionally these data (1) confirm that Toxoplasma was not internalized in a potentially harmful macropinosome but in a typical vacuole and (2) demonstrate that the force produced by host cell actin assembly drives PM protrusions.
Long-lasting compressive forces applied by the host cell ruffles on the zoite apex induce critical hydrostatic pressure leading to Toxoplasma irreversible membrane damage A marked constriction of the zoite body was typically observed when ΔMyoA tachyzoites enter retinal ARPE-19 and kidney PtK1 epithelial cells (Fig. 6a, b; black arrowheads; an additional movie file shows this detail (see Additional file 13)). This constriction was exacerbated when PM ruffles persistently encaged the zoite apex without being able to progress past the TJ site, as shown in endothelial HBMEC and epithelial HeLa cells (Fig. 6c, d): in these situations, the parasite body appeared almost split into two parts from the segment of constriction (Fig. 6c, black arrowheads; an additional movie file shows this detail (see Additional file 14)). Irregular PM protrusions failed to surround tachyzoites whose apex seemed squeezed within active actin-driven protrusions (Fig. 6d, outlined arrows). Accordingly, the parasites frequently rounded up and formed a large membrane bleb (Fig. 6d, e; pink triangles) accompanied by cytoplasmic vacuolization (Fig. 6d, e; white triangles; additional movie files show these events (see Additional files 15-17)). Further, SEM analysis documented the very tight compression on the zoite anterior region trapped in the PM protrusions (Fig. 6f, arrowhead) and the swelling of the extracellular posterior part that is likely to result from the PM-driven compressive forces (Fig. 6f, white arrows) we visualized by live cell imaging. Note that this damage was concomitant with the disengagement of the zoite apex from the host cell PM, thus implying that the tight interaction between the two cells had been ruptured. The whole sequence is schematized in Fig. 6 g and accounts for about half of the internalization failures (n = 105/196) (Fig. 6 h).
Interestingly, an impressive rearward thrust of the tachyzoite when apically engaged in the PM invagination could also be observed when PM ruffles failed to enwrap the zoite body. These vigorous movements were imposed by a several-micrometer-sized host cell PM dynamic stretch or tube supported by F-actin that we visualized using three different PM reporters (Fig. 7a-c, white arrows; additional movie files show this detail in real time (see Additional files [18][19][20]) and the LifeAct actin reporter (Fig. 7d; an additional movie file shows this detail (see Additional file 21)), respectively, until it retracted, further releasing tachyzoites with structural alterations (Fig. 7a, pink triangles). Even when the deformation was discrete, a short pulse of medium fluid flow was sufficient to wash the tachyzoite off the cell, thereby confirming that the attachment of the zoite to the PM had been disrupted ( Fig. 7c; additional movie file shows this detail (see Additional file 20)). Next, static fluorescent imaging with anti-RON4 antibodies and phalloidin confirmed (1) that a TJ had initially formed (Fig. 8a) and (2) that host cell actin-myosin contractility was likely to contribute to PM tube formation and dynamics. Indeed a prominent accumulation of F-actin (Fig. 8a, b) together with the Arp2/3 complex (Fig. 8c) were seen to culminate at the tube base together with the myosin II motor (Fig. 8b), suggesting that a second process of PM dynamics might be coupled to the emergence of compressive PM ruffles. Remarkably, SEM images capturing the host cell responses to ΔMyoA tachyzoites showed an impressively large PM tube ahead of the zoite, in particular at its base (Fig. 8d, white open arrows), the apex of the latter still being maintained by the PM folds (Fig. 8d, white arrowhead).

Discussion
Until recently, the force driving the entry of Toxoplasma tachyzoites into non-professional phagocytes was thought to exclusively rely on the functional interplay between parasite F-actin and myosin motors while the host cell remained essentially passive [5,6]. This study alters this view by reporting that tachyzoites devoid of MyoA motor can still access a typical PV following their polarized contact with the target cell due to an active contribution of the latter. This work also highlights the need to assess in depth the contribution of host cell membrane dynamics to the highspeed process of wild-type Toxoplasma entry into cells.
Host cell actin-based forces promote the formation of PM protrusions that drive a fraction of the ΔMyoA tachyzoite population into a typical PV through a process with unique features In the absence of the MyoA motor, we found that tachyzoites can rely on local host cell PM protrusions that fold over the distal part of the zoite body and apply forces eventually moving the tachyzoite through a TJ into the nascent PV. Such observations explain the in vitro viability of the ΔMyoA mutant. Because of the drastic reduction in the rate of internalized ΔMyoA parasites when host cells are chemically impaired in actin polymerizing/depolymerizing machineries, we conclude that host cell actin turnover is necessary to internalize these mutants. In line with this requirement, dynamic tracking of the PM/PV and of actin cytoskeleton remodeling revealed a selective accumulation of F-actin underneath the TJ and within the PM projections wrapping around the zoite. While Toxoplasma survival is expected to be prevented if the PM projections sealed into a macropinosome-like compartment that would rapidly integrate the endocytic pathway [36], ΔMyoA parasites were indeed not found within macropinosomes. Furthermore, the lack of effect of inhibitors directed against the PI3K or against myosin II and ROCK, all known to target late effectors required for macropinosome or phagosome closure [32,33,[38][39][40][41], allowed us to propose a novel strategy used by Toxoplasma tachyzoites to enter cells that shares initial but not late features with macropinocytosis.

TJ assembly in the host cell PM/cortex associates with PM/cortex dynamic remodeling
The MyoA-deficient Toxoplasma is the first mutant providing the unique opportunity to uncouple TJ insertion into the host cell PM from zoite motor activity. In the absence of MyoA, we found that the early steps of invasion, before mobilization of motor activity, i.e., rhoptry secretion and/or TJ folding, were associated with confined host cell PM ruffle-like protrusions. The flattening out of PM reservoirs is now universally recognized as an actin assembly-driven mechanism regulated by membrane tension to adjust cell shape and properties [42,43]. Insertion of hydrophobic proteins in the PM can act as wedges known to create local changes in curvature in tight interplay with actin rearrangements [44]. Interestingly, further characterization of several host actin regulatory factors that have been identified as required during cell invasion using high throughput RNA interference screening should enable one to shed light on the host cell cortex remodeling during Toxoplasma entry [45]. Therefore, we propose that the PM protrusions emerging around ΔMyoA mutants result from the local change of PM tension occurring upon insertion of the RON complex. In addition the local dismantling of the host cell cortical actin meshwork following secretion of the actin-severing rhoptry protein toxofilin at the onset of entry [46] is likely to contribute to a shift in membrane tension. Future engineering of a double MyoA-toxofilin knock out Toxoplasma would help to precisely decipher whether toxofilin activity can not only (1) fuel the TJ anchoring response as we proposed in, but also (2) be involved in more complex changes in PM dynamics including those promoting ruffle-like protrusions. If we hypothesize that TJ induces PM remodeling, we could expect the PM responses to be limited when the TJ remains transient as occurs with motor-functional tachyzoites, whereas these changes should be exacerbated in time and nature when tachyzoites have no MyoA motor to engage generation of traction forces at the TJ. Note that several Fig. 8 A PM tunnel folds when the ΔMyoA tachyzoite is attached to the cell surface through a TJ and is supported by a cap of newly assembled F-actin enriched in myosin II. a-c Laser scan confocal micrographs of ΔMyoA zoites in contact with HFF and HBMEC cells. Samples were fixed and processed for double or triple immunofluorescence staining with (a), anti-RON4 antibodies (red) and phalloidin (green): note the RON-positive TJ (red arrow) and the F-actin cup underneath the zoite (green arrow); (b, c), anti-P30 antibodies (blue) prior to permeabilization to selectively label surface-exposed antigens and with (b) anti-myosin II antibodies (red) and phalloidin (green) or (c) anti-Arp2/3 antibodies after cell permeabilization: note the accumulation of myosin II (b, red arrows) and F-actin (b, green arrows) at the bases of PM tubes while F-actin and the Arp2/3 complex also spread throughout the PM tube (c, red arrows). All scale bars: 5 μm. d Scanning electron micrograph of a ΔMyoA tachyzoite interacting with an ARPE-19 cell; note the impressive several micrometer-sized thin host cell PM tube-like protrusion indicated with white arrows into which the apical end of the parasite is embedded (white arrowhead). Scale bar: 1 μm SEM micrographs have documented protrusions around the apex of motor-competent zoites in endothelial and leukocyte cells [47,48], neutrophils included [49] during what was thought to be active invasion. Importantly, while neutrophils are prototypic cells for PM unwrinkling and tube-like protrusions [50,51], our SEM analysis revealed that fibroblasts also formed small PM ruffles around the apex of motor-competent parasites, thus reinforcing the concept of a general early and transient local response from the host cell PM and cortex when the TJ builds up regardless of subsequent motor engagement. SEM also strongly supported a key contribution of PM remodeling during internalization of MyoA-deficient zoites. It is worth mentioning the recent biophysical model of plasmodial merozoite invasion of the erythrocyte that assumes a modification of PM curvature triggered by the TJ insertion in the red blood cell and proposes this shift to account for the early enwrapping of the zoite [52]. The triggers underlying changes in PM might be even more diverse, as a pioneer study using optical tweezers showed that randomly attached merozoites, i.e., those that have not released RONs, were already able to induce red blood cell deformation [53]. In this framework, analyzing if and how MyoA-deficient Plasmodium merozoites triggered sufficient changes in the red blood cell PM and underlying cytoskeletal cortex to be successfully enwrapped will certainly be informative.

Multiple and intertwined PM responses following TJ assembly can lead to either successful or failed internalization events
The membrane dynamics that operates at the TJ site includes not only the PM outer protrusions but also a tightfitting inner PM invagination that surrounded the apex of the mutant zoite ahead from the TJ. The dynamics of the two processes worked in tandem as they concomitantly formed, retracted, and withdrew. Quantitative analysis of the video sequences revealed that when PM ruffles could not stretch enough over the zoite body, they instead trapped the zoite into the PM infolding to eventually cause a huge membrane bleb in the zoite. These observations suggest that PM outer protrusions apply compressive forces on the apex of the zoite that can harm the zoite. In support of this view is the increased rate of internalization (i.e., decrease in the rate of failed events) when host cell contractile activities are inhibited. In addition, in some abortive events, a tube of PM several micrometers long that spun and dragged the parasite formed underneath the TJ being enriched in F-actin and associated actin proteins, in particular myosin II. In that setting the zoite stayed engaged in the PM inner tight invagination and showed a RON2positive ring that suggested a TJ had formed. Collectively these data point to a complex interplay between effector and regulatory factors of the host cell actomyosin-driven contractile activities to promote folding of the PM tube.

Conclusions
This study positions T. gondii tachyzoite MyoA as a central provider of parasite invasive force and highlights a previously unseen mode of entry for intracellular microbes, relying on host cell membrane dynamics following zoite tight polarized contact. It provides a precise explanation for the marked reduction in invasiveness for ΔMyoA tachyzoites. Future structural and functional studies are necessary to understand how the RON complex insertion dictates the fast remodeling of the PM and how its tension/stretching properties are changed and appropriate curvatures promoted to allow (1) PV folding and (2) ruffles/tube assembly and dynamics. An interesting candidate is the CLAMP, appropriately localized to the cell zoite TJ throughout invasion, as published in the course of the reviewing process by the team of Lourido [9]. Finally, given the harmfulness of the host cell PM remodeling on the MyoA-deficient zoite, we propose to consider host cell invasion as the competitive contribution of both a Toxoplasma motor function and a complex host cell membrane dynamics. The shaping of MyoA during evolution, with a low affinity for ADP [54] that correlates with fast motor activity, may have contributed to optimize the invasive potential of Toxoplasma tachyzoites and thereby their fitness.

Transient expression of PM and actin fluorescent reporters
In addition to the PM reporters that were stably expressed in HeLa cells (see above), we used transient expression of additional host cell PM and actin markers. U2OS and HeLa cells were routinely transfected separately or in pair combination with various constructs. The list of constructs included pDisplay TM plasmid encoding the PDGFR trans-membrane domain (Life Technologies, Thermo Fisher, Waltham, MA, USA) in fusion with GFP (gift from V. Heussler, Institut Cell Biology, Bern (CH), Bern, Switzerland) or in fusion with mCherry (mC) (homemade), p CMV mCherry-actin (gift of V. Delorme-Walker, Scripps, La Jolla, CA, USA), and p CMV LifeAct-TagGFP2 (Ibidi, Biovalley, Nanterre, France).

Videomicroscopy, confocal microscopy, and image acquisition
Parasites were collected within a few hours following spontaneous egress from the HFF monolayers and washed in Hanks' Balanced Salt Solution (HBSS) supplemented with 1 % FCS (HBSS-FCS). Time-lapse video microscopy was conducted in Chamlide chambers (LCI Corp., Seoul, Korea) installed on an Eclipse Ti inverted confocal microscope (Nikon France Instruments, Champigny sur Marne, France) with a temperature-and CO 2 -controlled stage and chamber (LCI Corp., Seoul, Korea), equipped with a CoolSNAP HQ2 camera (Photometrics, Roper Scientific, Lisses, France) and a CSU X1 Yokogawa spinning disk (Roper Scientific, Lisses, France), three lasers (with excitation wavelength λ 491, 561, and 642 nm), and three dichroic mirrors. The microscope was piloted using Metamorph software (Universal Imaging Corporation, Roper Scientific, Lisses, France), and images of parasitecell interaction were acquired with settings including 1 or 2 frames/s for up to 40 min, and 1 frame/30 s for up to 6 h when assessing the viability of internalized parasites. Depending on the experiment, one to two laser wavelengths were used sequentially for each time point to monitor separately or simultaneously the dynamics of PM and actin fluorescent reporters. When needed, the chamber was perfused with syringe-pumped HBSS-FCS medium for 1 min at a medium flow rate of about 20-30 μL/min. Confocal imaging was performed on the same device using the three lasers with sections ranging from 0.250-0.3 μm.

Image analysis
Image stacks for every event of interest were prepared and annotated with time, bar scale, and arrows with Metamorph software from the raw image data file. Next ImageJ software (Rasband, W.S., ImageJ, US National Institutes of Health, Bethesda, MD, USA, http://imagej. nih.gov/ij/, 1997-2014) was used to add some additional labels on the time lapses, movies, and maximal projections from confocal z stacks. In some video sequences, the "Manual tracking" plug-in was used to track in time the spatial xy positions of the parasite's constriction site [17].

Immunofluorescence labeling of ΔMyoA tachyzoites interacting with host cells
We analyzed the modalities of interaction between ΔMyoA parasites and a variety of epithelial, fibroblastic, endothelial, and osteosarcoma cells that were grown in complete medium at 70-90 % confluency on poly-L-lysine-coated glass coverslips. Cell monolayers were washed with HBSS-FCS, and newly released ΔMyoA parasites were rapidly centrifuged (1.5 min, 250 g) on top of the monolayers to synchronize the contact between the two partner cells. Samples were next incubated for 10-20 min under culture conditions before paraformaldehyde (PFA) fixation (2 % in phosphate-buffered saline (PBS), 30 min, room temperature (RT)). Free aldehydes were quenched in NH 4 Cl (50 mM, 10 min), and cells were incubated in blocking buffer (2 % bovine serum albumin in PBS, 30 min, RT), then with anti-P30 antibodies (20 min, RT) (Novocastra, Nanterre, France) followed by Alexa Fluor® conjugated anti-mouse antibodies (30 min, RT) (Molecular Probes, Life Technologies, St Aubin, France). Samples were next permeabilized with 0.5 % Triton X-100 (5 min, RT), incubated again with the blocking buffer and then with Alexa Fluor® conjugated phalloidin to stain F-actin (2 μM, 45 min, RT) or sequentially with antibodies against proteins of interest (see list above) followed by relevant Alexa Fluor® conjugated secondary antibodies (1 h, RT). In some assays, cell permeabilization was performed straight after fixation prior to immunostaining. In the assays performed with both ΔMyoA tachyzoites and the fluorescent Alexa 594 dextran (500 μg/mL, 10 kDa), ARPE-19 and HFF cells were fixed after 10 or 20 min of interaction and permeabilized with Triton X-100 (0.01 % in PBS, 5 min, RT). Mouse serum against ROP2 and anti-mouse Alexa Fluor® conjugated secondary antibodies were used to stain the PV membrane [37]. Cells were mounted in Mowiol® 4-88 (Sigma-Aldrich, St Louis, MO, USA) and analyzed within 24 h by confocal microscopy using the Eclipse Ti inverted microscope.

Invasion assays
About 2 × 10 4 U2OS and ARPE-19 cells were plated in a 96-well plate to obtain 80 % confluency 24 h later. Cells were starved in 0.01 % FCS for 12-16 h prior to the assay and were pre-treated as follows: (1) with JLY as described in [26] with 20 μM Y27632 for 10 min prior to addition of 8 μM jasplakinolide and 5 μM latrunculin B for an additional 10 min before extensive washing in medium and immediate contact with ΔMyoA tachyzoites, (2) with jasplakinolide alone (1 μM) for 15 min and treated as indicated for JLY inhibitors, (3) with blebbistatin (25 μM), Y27632 (20 μM) separately or in combination for 15 min with the drugs kept during the invasion assays due to the high reversibility of both compounds, and (4) with wortmannin (10 μM) for 30 min that was washed out prior to the invasion assay. ΔMyoA tachyzoites were settled on top of the cells by gentle centrifugation (2 min, 250 g) and incubated at 37°C and 5 % CO 2 for 15 min before PFA fixation. Following sequential labeling of extra-and intracellular tachyzoites with anti-TgP30 and anti-TgGRA1 antibodies and differential fluorophore-coupled secondary antibodies, respectively, prior and post TX-100 permeabilization, Hoechst 33242 was added to label all nuclei (mammalian cells and parasites), and the samples were automatically scanned at a magnification of × 20 under an Olympus Scan^R automated inverted microscope (3 wells per condition, 16 fields of acquisition per well). Image processing with the Cell^R software successively included signal-to-noise ratio optimization to allow cell nuclei segmentation, channel-associated image detection, and image subtraction (extracellular zoites subtracted from extra-plus intracellular tachyzoites), and intracellular tachyzoite segmentation using an edge detection algorithm. The whole assay including imaging procedure was applied to samples of untreated pre-starved ARPE-19 and HFF cells that were incubated in complete medium supplemented with 20 % FCS but no phenol red with ΔMyoA tachyzoites to which Alexa 594 dextran (500 ug/mL) was added for 10 min after the parasite centrifugation step. Samples were fixed in PFA, permeabilized, and stained with anti-T. gondii ROP2 antibodies to observe macropinosomes and nascent PVs. Control of the efficiency of macropinocytosis inhibitors was performed under the conditions used for invasion assays and assessed by quantifying the number of macropinosomes positive for fluorescent Alexa 594 dextran (500 μg/ mL, 10 kDa) as described [56]. Statistics were performed with GraphPad Prism software. To check whether JLY treatment was cytotoxic for the U2OS cells, we assessed viability by pre-loading them with cell-permeant calcein-AM (0.5 μM final dilution) and Hoechst 33258 (1.5 μM final dilution) reagents (15 min, RT) before JLY exposure. Drugs were removed and the amount of green (i.e., live) and blue (i.e., total) fluorescent cells was measured over a 2-h period using semi-automatic imaging (×20) with an Olympus Scan^R automated inverted microscope under conditions similar to those used for the invasion assays in P96-well plates (N = 1 experiment). Reversibility of the JLY effect on cell invasion was measured under the same conditions (N = 3 experiments).

Additional files
Additional file 1: Movie 1. ΔMyoA tachyzoite entering HeLa cell expressing the CAAX-mC PM reporter by progressive wrapping through host cell PM ruffles. Scale bar: 5 μm. (AVI 1484 kb)