TY - JOUR
AU1 - Sitaram, Anand
AU2 - Yin, Yunqiang
AU3 - Zamaitis, Tammy
AU4 - Zhang, Bo
AU5 - Aroian, Raffi V.
AB - Introduction The largest class of bacterial protein virulence factors is pore-forming proteins (PFPs) [1–4]. Produced by many major human pathogens, these are critical virulence factors; many strains that have been deleted for their PFP genes become avirulent or significantly less virulent in lab animals. It is therefore critical to better understand how host cells respond to attack by these toxins. Typically, toxin monomers are secreted or externalized by bacteria, activated by cleavage by host proteases, and oligomerize before being inserted into the plasma membrane and forming pores. PFPs can generally be split into large pore-formers (~30 nm diameter) and small pore-formers (~2 nm diameter). The host range and cellular tropism can be determined by expression of host factors at the membrane that serve as receptors for the toxin. Receptors for different toxins include cholesterol, other lipids, and proteins. Cells that are perforated by toxins are thought to die by osmotic lysis, necrosis, programmed cell death, or dysfunction caused by ion dysregulation. [5]. Cells can mitigate this damage, however, by activating intrinsic cellular defenses or INCED [6–12]. The nematode Caenorhabditis elegans and exposure to PFPs (e.g., Cry5B PFP; [13]) made by the soil bacterium Bacillus thuringiensis have proven to be an invaluable model for discovering and studying INCED pathways by which cells defend against PFPs. These INCEDs include activation and up-regulation of p38 and JNK-like mitogen-activated protein kinase (MAPK) signaling pathways [13,14], the unfolded protein response [9], the hypoxia response [6], endocytosis and membrane shedding [15], and autophagy [7]. Investigation in animal cell culture systems has shown that all of these PFP INCED response processes discovered and/or described in C. elegans are evolutionarily conserved [9,13,14,16]. We previously reported on a C. elegans genome-wide RNAi screen for genes required for INCED against PFPs, in which >16,000 RNAi knock-downs were performed followed by selection and repeat testing at a single dose of Cry5B PFP [13]. This screen yielded 106 hpo genes (hypersensitive to pore-forming toxin). One of the conserved hits included nck-1, the C. elegans homolog of mammalian Nck that is involved in linking tyrosine phosphorylation with localized F-actin polymerization by recruiting several effectors to the plasma membrane, including N-WASP and the Arp2/3 complex [17]. nck-1 is known to be involved in C. elegans axonal guidance, excretory cell and distal tip cell migration, male mating, vulval development, dauer formation, and susceptibility to Orsay virus [18–22]. Here we study the role of nck-1 in PFP INCED, uncovering a key, important, and previously unknown role in vivo between PFP INCED, nck-1 and other F-actin modulating genes, and the filamentous (F-) actin cytoskeleton. Results To follow up on the genome-wide RNAi screen for PFP INCED genes [13], we selected a few hpo genes for dose-dependent Cry5B PFP response assays using RNAi and also looked at the corresponding response of available genetic mutants associated with these hpo genes. From these preliminary follow up studies, the hpo gene nck-1 emerged as a gene of interest. Wild-type N2 C. elegans larvae grown on E. coli expressing RNAi sequences directed against nck-1 were subjected to dose-response mortality assays using purified Cry5B (Fig 1A). nck-1(RNAi) C. elegans hermaphrodites were hypersensitive to Cry5B relative to empty-vector(RNAi) C. elegans hermaphrodites over a wide range of Cry5B PFP concentrations. In these and other experiments below, RNAi of the mitogen-activated protein kinase kinase (MAPKK) sek-1, knockdown of which is known to give a high level of hypersensitivity to Cry5B PFP [14,15], was included as a positive control. These experiments confirm nck-1 is required for normal PFP INCED over a wide range of PFP doses. Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 1. nck-1 loss sensitizes C. elegans to Cry5B. (A) Wild-type N2, (B) glp-4(bn2); rrf-3(pk1426), or (D) VP303 (intestine-specific RNAi) C. elegans were grown from the L1 to L4 stage on E. coli expressing the indicated RNAi, then transferred to liquid culture with purified Cry5B for 6 days, then assayed for survival. (C) Wild-type N2 or nck-1(ok694) null L4s were grown on OP50 E. coli until the L4 stage before being subjected to the same experiment. All data show the mean of three experiments. Error bars here and in other figures represent the standard error of the mean (SEM). Each data point is the average of three independent experiments with three wells/experiment (n = 25–34 worms/well). https://doi.org/10.1371/journal.ppat.1010656.g001 These experiments have a time course of 6 days, and the presence of progeny born during that time can obscure the results, so the thymidine analog 5-fluoro-2’-deoxyuridine (FUdR) was included in the media in Fig 1A to prevent progeny production. To ensure that the presence of FUdR itself did not contribute to the Cry5B hypersensitivity of nck-1-deficient worms, the experiment was repeated using the glp-4(bn2); rrf-3(pk1426) strain, which is hypersensitive to RNAi (due to the rrf-3 mutation) as well as sterile at the assay temperature of 25°C (due to the glp-4 mutation), obviating the need for FUdR. In this background, knockdown of nck-1 also led to hypersensitivity to Cry5B as measured by mortality (Fig 1B). The outcrossed null mutant nck-1(ok694) was viable and fertile, but larvae that were synchronized by standard hypochlorite treatment nevertheless developed at variable speeds. Therefore, L4 larvae were visually identified and handpicked for experiments using the mutant strain. As with wild-type worms knocked down for nck-1 by RNAi, nck-1(ok694) mutants were also hypersensitive to Cry5B compared to wild-type worms, and the effect was more penetrant than in the RNAi experiment (Fig 1C). Because the intestinal epithelium is the tissue directly targeted by the PFP Cry5B [23–25], we also tested whether nck-1 activity is required in the intestinal epithelium itself. Knockdown of nck-1 in the VP303 strain—which preferentially carries out RNAi in the intestine—also led to hypersensitivity to Cry5B (Fig 1D), indicating that nck-1 is required for a cell-autonomous defense process for protection against PFPs. The p38 MAPK pathway, for which sek-1 is the MAPKK, is clearly a central player in cellular defenses against PFPs [5,13,26]. We next tested whether or not nck-1’s role in PFP defenses was part of the p38 MAPK PFP defense pathway. First, we examined the MAPK-dependent activation of the xbp-1-dependent arm of the unfolded protein response (UPR) in response to Cry5B PFP. The hsp-4::gfp worm strain carries a GFP reporter for this response, increasing its fluorescence in response to classic UPR inducers such as tunicamycin or heat shock, but also after worms are fed Cry5B-expressing E. coli for 8 hours [9]. The latter, PFP-induced UPR response is known to be dependent upon MAPK signaling, as it was previously shown to be blocked in animals that carry a secondary mutation in pmk-1, which encodes the C. elegans p38 homolog that is a direct target of SEK-1 kinase activity. Here we similarly found that hsp-4::gfp worms that lacked MAPK signaling due to knockdown of sek-1 showed no increase in GFP signal in response to an 8-hour E. coli-Cry5B feeding exposure (Fig 2A). In contrast, the knockdown of nck-1 did not block Cry5B-induced activation of the UPR. Worms knocked down for sek-1 or nck-1 still showed increased GFP signaling following an 8-hour 30°C heat shock exposure, demonstrating that the hsp-4::gfp response was still intact in those worms (S1 Fig). As a control, worms with a knockdown for xbp-1 showed a loss of even basal levels of reporter activity in response to either stressor (Figs 2A and S1). These results suggested a distinction between a sek-1-mediated and nck-1-mediated PFP response. Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 2. nck-1 works independently of MAPK signaling. (A) hsp-4::gfp C. elegans were grown to the L4 stage on the indicated RNAi bacteria and transferred to E. coli plates expressing empty vector or Cry5B for 8 hours, then subjected to fluorescence microscopy. Scale bar = 0.1mm. (B) sek-1(km4) p38 MAPKK(-) mutant C. elegans were grown on the indicated RNAi bacteria to the L4 stage and then transferred to liquid culture with varying amounts of purified Cry5B and incubated for 6 days before being scored for survival. pmk-1 is p38 MAPK. (C) The reverse experiment to the one in (B), with nck-1(ok694) mutant animals and RNAi of MAPK pathway genes at a single concentration of Cry5B. For (B) and (C), each data point is the average of three independent experiments with three wells/experiment (n = 20–33 worms/well). https://doi.org/10.1371/journal.ppat.1010656.g002 We therefore next directly tested for a genetic interaction between MAPK signaling and nck-1 in toxin defense. sek-1(km4) p38 MAPKK mutant hermaphrodites were subjected to additional knock down of either nck-1 or pmk-1. As expected, pmk-1 knockdown did not increase the PFP sensitivity of hermaphrodites that were already null for the upstream activator sek-1 (Fig 2B). In contrast, nck-1 knockdown did further sensitize sek-1(km4) null hermaphrodites to Cry5B. We also performed this experiment in reverse, knocking down either sek-1 or kgb-1 in nck-1(ok694) null mutants. The kgb-1 gene encodes a JNK-like MAPK that has also been critically implicated in PFP defense in C. elegans [13,14]. Knockdown of either MAPK pathway further sensitized nck-1(ok694) worms to Cry5B (Fig 2C). Taken together, these data demonstrate that nck-1 functions independently of the p38 and JNK-like MAPK signaling pathways for Cry5B PFP defense. We next characterized the specificity of the nck-1-mediated PFP response. Namely, is the hypersensitivity of nck-1 reduction/loss-of-function to Cry5B PFP due to a specific defect in Cry5B PFP responses or to a more generalized inability to protect against even non-PFP stressors that attack the health of the nematode? We therefore next tested the ability of nck-1-deficient animals to withstand other types of stress. Worms that experienced nck-1 RNAi in the intestine alone (the VP303 strain) showed no change in their sensitivity to a prolonged 35°C heat stress (Fig 3A). The intestinal knockdown of nck-1 also did not sensitize worms to the heavy metal copper sulfate (Fig 3B). Global knockdown of nck-1 in N2 did not lead to a change in sensitivity to osmotic stress (Fig 3C) or oxidative stress either (Fig 3D), as assayed by exposure to increasing concentrations of NaCl or H2O2, respectively. Since the tested stresses mentioned to this point are all environmental rather than pathogenic, we also tested the requirement for nck-1 in defense against the pathogenic food source Pseudomonas aeruginosa (PA14), which produces several toxic factors but is not known to produce a PFP. Knockdown of nck-1 did not sensitize the worms to PA14 (Fig 3E). Consistent with previous reports [27], sek-1 knockdown did sensitize worms to PA14 feeding. In all specificity experiments, some empty vector-treated and nck-1(RNAi) worms were tested in parallel to confirm that the RNAi was effective (i.e., that the nck-1(RNAi) worms were hypersensitive to feeding on E. coli expressing Cry5B). Taken together, the results suggest that, whereas some pathways, e.g., p38 MAPK signaling, are known to be utilized as a defense against PFPs as well as other stresses [27–29], the use of nck-1 to protect cells from PFPs appears to be more narrow. Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 3. nck-1 loss does not affect sensitivity to other stressors. (A) VP303 (intestinal-specific RNAi) C. elegans L4 animals grown on RNAi bacteria were incubated at 35°C, with survival determined at each indicated time-point. (B) VP303 L4 animals grown on the indicated RNAi bacteria were transferred to liquid culture with varying amounts of CuSO4 for 6 days at 25°C. (C and D) Wild-type N2 C. elegans grown to the L4 stage on the indicated RNAi were transferred to liquid culture with varying amounts of (C) NaCl for 6 days or (D) H2O2 for 4 hours, before survival was measured. (E) Wild-type C. elegans grown to the L4 stage on the indicated RNAi were transferred to plates spread with Pseudomonas aeruginosa PA14 and survival was followed over the indicated time. For (A), each data point is the average of three independent experiments with one plate/experiment (n = 40–50 worms/plate). For (B), (C), and (D), each data point is the average of three independent experiments with three wells/experiment (n = 27–29 worms/well). The data in (E) are a single representative of three independent trials with comparable results (n = 90 animals/genotype). Logrank analysis shows no significant difference in survival between empty vector and nck-1(RNAi) animals. https://doi.org/10.1371/journal.ppat.1010656.g003 We then investigated whether or not nck-1 protects C. elegans against PFPs other than Cry5B. For this, we tested the requirement for nck-1 in defense against another member of the Bacillus thuringiensis crystal protein family of PFPs, App6A (formerly called Cry6A; [30]). Although Cry5B and App6A are both B. thuringiensis proteins that form pores, the two PFPs are structurally distinct and use different receptors, and C. elegans mutants that are resistant to Cry5B remain sensitive to App6A [13,31–35]. Hence, App6A represents an independent PFP for testing with nck-1 animals. We found that nck-1(ok694) null mutants were visually hypersensitive to feeding on E. coli expressing recombinant App6A, compared to wild-type worms (Fig 4A). Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 4. nck-1 loss sensitizes C. elegans to multiple PFPs. (A) Wild-type N2 or nck-1(ok694) null C. elegans L4s were transferred to plates spread with the indicated percentage of E. coli expressing Cry5B or App6A (formerly Cry6A). Plates were incubated two days at 20°C and then worms were transferred to spot wells and photographed. (B) Wild-type N2 C. elegans grown to the L4 stage on the indicated RNAi bacteria were transferred to plates spread with Vibrio cholerae that do or do not express the PFP cytolysin, and survival was measured after 48 hours. (C) The same experiment as in (B) but using wild-type N2 or mutant C. elegans L4 animals. The data in (A) are representative of three independent trials. For (B) and (C), each data point is the average of three independent experiments with one plate/experiment (n = 50 worms/plate). https://doi.org/10.1371/journal.ppat.1010656.g004 We also tested the sensitivity of C. elegans to Vibrio cholerae cytolysin, a PFP that is active against both mammalian cells and C. elegans [6,36]. C. elegans with an nck-1 deficiency due to either RNAi knockdown (Fig 4B) or genetic mutation (Fig 4C) were much more sensitive to feeding on a cytolysin-positive strain of V. cholerae compared to wild-type worms. C. elegans with a sek-1 deficiency were also much more sensitive to feeding on a cytolysin-positive strain of V. cholerae compared to wild-type worms (Fig 4B). The increased sensitivity of nck-1-deficient animals compared to wild-type animals was not retained when fed V. cholerae lacking cytolysin, although sek-1(km4) null animals (but not sek-1(RNAi) reduction of function animals) were also hypersensitive to the cytolysin-minus strain of V. cholerae, consistent with the fact that sek-1 is more generally involved in stress responses and that V. cholerae may produce other non-PFP virulence factors against C. elegans [37]. Taken together, these data demonstrate that nck-1 shows specificity for defense against multiple PFPs but not the other environmental or pathogenic factors tested. C. elegans intestinal cells that have pores inserted into their apical surface take steps to repair the integrity of the perforated membrane [15]. When worms are given an acute exposure to Cry5B PFP and then immediately fed the fluorescent dye propidium iodide, the ingested dye leaks from the intestinal lumen into the cytoplasm of the intestinal epithelial cells (Fig 5A; top panels). If, however, Cry5B PFP feeding and subsequent propidium iodide dye loading are separated by a ~24-hr recovery period, the ingested dye is confined to the intestinal lumen, as the pores are repaired in the interim (Fig 5A; lower panels) [15]. Loss of RAB-11.1 activity due to partial RNAi knockdown weakens the cell’s ability to repair pores [15]. We asked whether or not NCK-1 was also involved in cellular pore repair. We found that whereas wild-type worms showed almost 100% repair during the ~24-hr recovery period, nck-1(ok694) animals failed to repair dye-permeable pores, similar to rab-11.1 control knockdowns (Fig 5B). Importantly, the nck-1(ok694) mutant did not exhibit an endogenous intestinal permeability to propidium iodide in the absence of PFP exposure (S2 Fig). Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 5. nck-1 loss affects the ability of cells to repair PFP pores. (A) Wild-type C. elegans were grown to the L4 stage on the indicated RNAi bacteria and transferred to Cry5B plates for 1 hour. C. elegans were then either fed propidium iodide within 30 minutes or allowed to recover for 26 hours and then fed propidium iodide. Dye-loaded worms were imaged on slides. Autofluorescent gut granules serve as a surrogate marker indicating the position of the intestinal epithelial cells. Scale bar = 25um. (B) Quantitation of the same type of experiment as in (A) except the strains used were nck-1(ok694) null mutants (grown on standard OP50 E. coli) and N2 (grown on either OP50 or rab-11.1 RNAi E. coli as indicated). “PI leakage” = animals with dye found in intestinal cell cytoplasm. The data represent the mean and SEM of three independent experiments with 50 worms/experiment. https://doi.org/10.1371/journal.ppat.1010656.g005 Following our finding that nck-1 was required for efficient pore repair, we considered how it might function. In mammalian cells, the NCK-1 homolog Nck is an SH2/SH3 adaptor protein that recruits a large number of effector proteins to the plasma membrane following its own recruitment to phosphorylated tyrosine residues. In particular, Nck has been shown to be a potent activator of actin assembly, in part by effectively activating Wiskott-Aldrich Syndrome Protein (WASP)-family proteins so that they in turn activate the Arp2/3 complex, which initiates branched actin filament polymerization. The genome-wide RNAi and toxin hypersensitivity screen that identified nck-1 as a C. elegans PFP defense gene also identified WASP-interacting protein wip-1 as well as three subunits of the C. elegans Arp2/3 complex—arx-3, arx-5, and arx-7—as hpo (PFP defense) genes [13]. Based on these observations, we hypothesized that the nck-1-mediated response to PFPs might also function via the Arp2/3 complex. We confirmed that Arp2/3 subunits are involved in PFP defense. Feeding of undiluted RNAi bacteria against arx-3 or arx-5 led to a significant growth defect in wild-type C. elegans, so the RNAi bacteria were diluted 1:1 with bacteria carrying an empty vector. The level of knockdown afforded by this (50%) dilution was sufficient to qualitatively sensitize worms to Cry5B (Fig 6A). One Arp2/3-encoding gene, arx-5, was chosen for further experimentation. Wild-type worms knocked down for arx-5 also show impaired pore repair (Fig 6B), a phenotype shared with nck-1 mutants. We then looked for genetic interactions between arx-5 and nck-1. Knockdown of arx-5 in the nck-1(ok694) null background did not increase or decrease the sensitivity of the worms to Cry5B, whereas knockdown of sek-1 in the nck-1(ok694) null background displayed increased sensitivity (Fig 6C; just as in the experiment in Fig 2C). Taken together, these results indicate that nck-1 works in the same PFP defense pathway as arx-5—and presumably the rest of the Arp2/3 complex—but separately from the sek-1 MAPK pathway, consistent with the relationship between Nck and Arp2/3 derived from mammalian studies. Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 6. nck-1genetically is in the same pathway with the Arp2/3 complex in PFP defense. (A) N2 worms grown on the indicated RNAi bacteria to the L4 stage and then photographed after two days of feeding on the indicated amount of E. coli-expressed Cry5B. (B) A pore repair assay identical to the one in Fig 5B, but with N2 worms knocked down for sek-1 or arx-5. (C) Survival of nck-1(ok694) worms fed the indicated RNAi bacteria to the L4 stage and then incubated in liquid culture with purified Cry5B for 6 days. The data in Fig 6B represent the mean and SEM of five independent trials (n = 50 worms per trial), while Fig 6C includes data from three independent trials (n = 11 worms/well and three wells/trial). https://doi.org/10.1371/journal.ppat.1010656.g006 In order to identify additional proteins and processes required for defense against PFPs, we undertook a proteomic approach. Other groups have previously reported transcriptomic and/or proteomic changes in C. elegans exposed to Bacillus thuringiensis and have mentioned cytoskeletal proteins among the results list [38,39]. We chose a more targeted approach to finding changes directly attributable to Cry5B PFP exposure. glp-4(bn2) animals were grown at 25°C to block gonad development and thus remove a significant amount of non-intestinal tissue so that a greater percent of the protein analyzed was derived from the intestine (glp-4(bn2) animals have a normal response to Cry5B [14]). L4s were then exposed for 8 hours to E. coli either carrying an empty vector or expressing Cry5B. Worms were then processed for proteomic analysis. The list of hits was narrowed down to ones with a significant p-value (p < 0.05), spectral counts > 2, and at least a 2-fold change up or down in expression in Cry5B-exposed worms relative to worms fed with empty vector bacteria. The resulting 386 proteins with increased abundance and 108 proteins with decreased abundance were then analyzed using the PANTHER classification system [40,41]. Analysis of the proteins increased in abundance in the context of Protein Class gave “hydrolase” as the largest category (47 hits). The second largest category was “cytoskeletal protein” (29 hits), and its largest subcategory was “actin family cytoskeletal protein” (21 hits), including 4 subunits of the Arp2/3 complex (ARX1, ARX2, ARX5, ARX7) (Table 1). Furthermore, the largest Molecular Function category in an overrepresentation test of all upregulated proteins was “actin binding” (p = 4.22E-10), with 13 of 55 reference genes represented. This list was mostly a subset of the “actin family cytoskeletal protein” Protein Class and again included the Arp2/3 subunits ARX5 and ARX7. Other noteworthy proteins increased in abundance included components of MAPK signaling, including MEK2, KGB1, and PMK3. Among the proteins with reduced abundance, only one was associated with the Molecular Function term “actin binding”: TWF2, a homolog of the actin-binding protein twinfilin. NCK1 itself was not identified in the proteomic screen. Note, in our proteomic study (8 hr incubation) and previously published proteomic studies above (12 hr incubation) the extended length of the incubations could have resulted in some animals reaching molting, which could add an additional variable in these experiments. Download: PPT PowerPoint slide PNG larger image TIFF original image Table 1. Actin-related C. elegans glp-4(bn2) proteins altered by Cry5B feeding as detected by proteomics. https://doi.org/10.1371/journal.ppat.1010656.t001 The proteomics results nonetheless lent further strength to the hypothesis that actin regulation plays a role in the cellular response to attack by Cry5B. We tested a few of the genes found in the proteomics screen by RNAi knockdown or with mutant strains to see if they sensitized worms to Cry5B. We found that partial knockdown of erm-1 (Ezrin/Radixin/Moesin-like, involved in linking cortical F-actin to the plasma membrane; [42]) in N2 animals sensitized them to Cry5B feeding (Fig 7A). We obtained the mutant strain dbn-1(ok925) (Drebrin-like, an F-actin-binding protein that changes the helical pitch of actin filaments and decreases rate of F-actin depolymerization; [43]), outcrossed it four times, and subjected it to our standard Cry5B LC50 experiment. Consistent with the fact that DBN1 levels were increased in the Cry5B-treated worms in the proteomics experiment, the null mutant strain was hypersensitive to Cry5B relative to N2 (Fig 7B). We also tested for genetic interaction between erm-1 and either nck-1-mediated or sek-1-mediated PFP responses. sek-1(km4) animals treated with nck-1 RNAi did significantly shift the IC50 (Fig 7C), in accordance with the earlier genetic interaction data (Fig 2B). As with nck-1 RNAi, sek-1(km4) animals treated with 50% erm-1 RNAi also showed a significant hypersensitization to Cry5B based on IC50. These genetic data implicate additional actin-interacting proteins, namely Arp2/3, erm-1 (Ezrin/Radixin/Moesin), and likely dbn-1 (Drebrin), in the mechanism of an nck-1-mediated response to pore-forming proteins that is independent of the p38 MAPK pathway. Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 7. nck-1 genetically functions in the same pathway as other F-actin-interacting proteins in PFP defense. (A) Wild-type N2 C. elegans were grown from the L1 to L4 stage on E. coli expressing the indicated RNAi, then transferred to liquid culture with purified Cry5B for 6 days and assayed for survival. (B) N2 or mutant worms were grown on OP50 E. coli to the L4 stage, then transferred to liquid culture with purified Cry5B for 6 days and assayed for survival. (C) sek-1(km4) mutant C. elegans were grown on the indicated RNAi bacteria to the L4 stage and then transferred to liquid culture with varying amounts of purified Cry5B, incubated for 6 days, and scored for survival. For (A), (B), and (C), each data point is the average of three independent experiments with three wells/experiment (n = 26–40 worms/well). https://doi.org/10.1371/journal.ppat.1010656.g007 To support the conclusion that the actin cytoskeleton plays an important role in PFP defenses, we examined whether changes in F-actin abundance occurred in C. elegans intestinal tissue upon exposure to Cry5B PFP. We therefore exposed N2 and nck-1(ok694) mutant worms to E. coli-expressed Cry5B or empty vector for 2 hours, then transferred the worms to slides, externalized the intestines, and then stained with FITC-phalloidin to visualize F-actin in the exposed internal tissues. The worms were then analyzed on a confocal scope and images were taken of the stained intestines (Fig 8A). There was a qualitative visual decrease in actin staining at the apical surface in wild-type N2 following Cry5B PFP exposure, and in nck-1(ok694) animals relative to wild-type animals in the absence of Cry5B PFP (no toxin) (Fig 8A). Download: PPT PowerPoint slide PNG larger image TIFF original image Fig 8. Cry5B exposure causes a reduction in intestinal F-actin levels. (A) Wild-type N2 or nck-1(ok694) C. elegans L4 animals were fed E. coli-expressed Cry5B or empty vector for 2 hours, permeabilized, and then their internal organs were fixed and stained with FITC-phalloidin. The honeycombed staining is the gonad (labeled G in the upper panels) and the smoother staining is the intestine (I). (B) The integrated density from images (mean pixel intensity x area) of the intestine divided by that of the gonad following the two-hour toxin incubation was graphed. Each dot represents one worm. The data come from three experiments (n = 10 animals per condition and per genotype per trial), and the bars show the mean. Statistical analyses are as described in the Methods. https://doi.org/10.1371/journal.ppat.1010656.g008 To analyze further, we quantitated the intensity of F-actin staining in three independent experiments under these four conditions: wild-type animals not exposed/exposed to Cry5B PFP and nck-1(ok694) animals not exposed/exposed to Cry5B PFP (Fig 8B; see Materials and Methods for details). In order to compare between experiments, we normalized F-actin staining in the intestine to that of the gonad, a tissue that plays no apparent role in Cry5B PFP response [14]. We found that wild-type animals had significantly decreased F-actin upon exposure to Cry5B PFP (Fig 8B). Furthermore, relative to F-actin in the gonad, nck-1(ok694) animals had significantly decreased intestinal F-actin than wild-type animals (Fig 8B; nck-1 itself is expressed in both the intestine and gonad [18]). Conversely, there was not a significant decrease in F-actin in nck-1(ok694) animals upon exposure to Cry5B PFP (Fig 8B), presumably because F-actin levels were already low in nck-1 mutant animals. Taken together, these data indicate that a consequence of intestinal exposure to PFPs in wild-type animals is a reduction in F-actin levels and are consistent with relative stabilization of F-actin in the wild-type intestine by NCK-1. Discussion Here we describe one of the most compelling associations between genes involved in regulating filamentous (F-)actin and in vivo intrinsic cellular defenses (INCED) against pore-forming proteins. We find that nck-1, a gene known to play a central role in regulated F-actin assembly in cells in response to cell signaling, protects C. elegans against small-pore PFPs, genetically functioning in the same pathway as a number of key regulators of F-actin including C. elegans Arp2/3 complex (arx-5), Ezrin/Radixin/Moesin (erm-1), and Drebrin (dbn-1). This role in the nck-1 pathway protecting against small PFP attack is applicable to at least three unrelated PFPs (Cry5B, App6A, VCC) and highly specific in that loss of nck-1 does not result in increased sensitivity to heat stress, heavy metal stress, high salt, oxidative stress, or pathogenic P. aeruginosa bacterial attack. At least part of the role of nck-1/arx-5 in PFP INCED involves enhancing the ability of C. elegans intestinal cell apical membrane to repair the small pores formed by Cry5B. Specific events that could be tied to F-actin-mediated protection against PFP attack include regulation of clathrin-mediated endocytosis or membrane trafficking (e.g., in C. elegans; [15,44]), direct interaction between PFPs and actin [45,46], or generation/maintenance of epithelial junction integrity [47,48]. These results are in contrast to those of the p38 and JNK-like MAPK signaling pathways that are required in C. elegans for defense against pathogenic P. aeruginosa [27], oxidative stress [28], heat stress [29], and heavy metal stress [14]. This positions nck-1 as part of a much more specific response to PFPs than any previously characterized. Consistent with differences in protection against various stressors, nck-1 and p38 and JNK-like MAPK pathways appear to function differently in PFP defense. Microarrays of C. elegans exposed to Cry5B led to the discovery of p38 and JNK-like MAPK signaling as critical mediators of PFP defense, as C. elegans that are deficient in either signaling pathway are quite sensitive to small amounts of toxin [13,14]. Indeed, the majority, but not all, of the genes that were upregulated in response to Cry5B exposure became so in a MAPK-dependent manner [13]. Our results here from hsp-4::gfp staining and double mutant analyses indicate that nck-1/arx-5/erm-1 function separately from the p38 MAPK signaling pathway in PFP INCED. This is the first instance of a major PFP INCED pathway in C. elegans functioning independently of a MAPK pathway. Changes in the actin cytoskeleton by PFPs have been seen in a few instances before, although in general it was not known whether the actin changes are initiated as a means of promoting or resisting pathogenesis [49–51]. An exception was Vega-Cabrera et al. where RNAi of actin led to increased PFP toxicity [46]. Recently, studies on changes in actin remodeling and the role of actin cytoskeleton during plasma membrane damage repair have been reviewed [16]. Interestingly, compounds that stabilize F-actin, like jasplakinolide and phalloidin, were found to hinder the recovery of plasma membrane recovery upon mechanical, laser, or PFP-induced damage. Conversely, F-actin depolymerizing drugs like cytochalasin D and latrunculin increased the speed of repair. There are several important differences between these studies and ours. First, these studies look at repair from membrane damage much larger than that caused by the small-pore PFPs, including by large pore-forming PFPs [5] or by mechanical injury or laser injury. It is possible that defense and repair from smaller pores differs significantly from those caused by much larger plasma membrane disruptions. Second, our study is carried out in vivo in an intact epithelium whereas these studies were carried out in vitro. In the case of bacterial virulence, this is the actual context in which a PFP attack would occur. Third, it is possible that what is most important is actin dynamics and less so the total amount of F- vs G-actin. Our data for the first time indicate that an NCK-1—ARP2/3—ERM F-actin-regulating pathway is important in PFP INCED in C. elegans and, based on the wide range of small-pore PFPs protected against by nck-1, likely in other cells as well. Our results support a model in which small-pore PFPs at the C. elegans apical intestinal membrane destabilize F-actin, which is counteracted by the activity of NCK-1—ARP2/3—ERM, leading to repair of the pores and perhaps other actin-associated INCED processes. Future studies will be directed at determining what other effectors are involved in nck-1-mediated PFP defenses and characterizing more precisely how actin dynamics may be involved in INCED against pore-forming proteins. Materials and methods C. elegans and bacterial strains C. elegans N2 Bristol was maintained using standard techniques [52]. The following strains were used in this study and were purchased from the Caenorhabditis Genetics Center: glp-4(bn2), glp-4(bn2); rrf-3(pk1426), nck-1(ok694) following 4X outcross with lon-2(e678), dbn-1(ok925) following 4X outcross with unc-64(e246), VP303 rde-1(ne219);KbIs7[nhx-2P::rde-1] [53], sek-1(km4), and SJ4005 zcIs4[hsp-4::GFP]. E. coli empty-vector control and Cry5B-expressing strains were JM103-pQE9 and JM103-Cry5B. The App6A gene was subcloned into the BamHI and PstI sites of the vector pQE9 (adding an N-terminal His tag and a seven amino acid extension to the C-terminus) and transformed into JM103 [54]. Feeding RNAi bacterial strains were Escherichia coli HT115 with pL4440 vector derived from the Ahringer RNAi library [55] except for rab-11.1 [15]. RNAi clones were confirmed by plasmid DNA sequencing. In all experiments where arx-5, dbn-1, or erm-1 RNAi bacteria were used, a mixture of equal parts HT115 carrying empty pL4440 and or pL4440 bearing the gene-specific RNAi sequence was prepared. In all experiments where rab-11.1 RNAi bacteria was used, a 17% rab-11.1 mixture was prepared in a similar way. E. coli OP50, Pseudomonas aeruginosa strain PA14 [56], and Vibrio cholerae strains CVD109 Δ(ctxAB zot ace) and CVD110 Δ(ctxAB zot ace) hlyA::(ctxB mer) Hgr were used [57]. Microscopy and image editing Images from qualitative toxicity assays were obtained from assay plates, using an Olympus SZ60 dissecting microscope linked to a Canon Powershot A620 digital camera, and using Canon Remote Capture software or from slides with an Olympus BX60 compound microscope with an UplanFl 10x/0.25NA or 40x/1.35NA objective, mounted to a Spot Insight CCD camera and using Spot software. Actin staining images were taken on a Leica TCS SP8 Spectral Confocal DMi8 Inverted Stage Microscope, with LAS X software. All images within an experiment were taken with identical camera settings. Final images were assembled using Adobe Photoshop and/or GIMP. Quantitative Cry5B assays in liquid media Assays for determining LC50 of C. elegans exposed to purified Cry5B were performed as described [58] with any changes described below. Unless otherwise indicated, all assays were scored after 6 days and included 5-fluoro-2’-deoxyuridine (FUdR; SIGMA) to prevent the appearance of the next generation of larvae that would complicate the experiments [58]. For experiments in which genes were knocked down by feeding RNAi, L1 larvae were synchronized by hypochlorite treatment and plated onto ENG-IA agar plates spread with RNAi bacteria. Animals were grown at 20°C to the L4/young adult stage. OP50 bacteria in the wells were substituted with overnight cultures of RNAi bacteria that were induced with 1 mM IPTG for 1 hr at 37°C before inclusion in wells. Some L1s were plated in parallel on act-5 or unc-22 RNAi to verify RNAi effect. In the assays for Fig 1B, no FUdR was present, and animals were grown to the L4 stage at 25°C. In assays involving nck-1(ok694) mutants, L4 worms were manually transferred into wells. In the assays for Fig 3B and 3C, CuSO4 (SIGMA) or NaCl (SIGMA), respectively, were substituted for Cry5B [15]. In the assays for Fig 3D, L4 animals were put into wells with only S Media and the indicated concentration of H2O2 for four hours at 20°C before scoring. In the assays for Fig 3B, 3C and 3D, a parallel qualitative agar plate assay was performed (described below). Heat stress assay VP303 C. elegans were synchronized by hypochlorite treatment and grown from the L1 stage on ENG-IA agar plates spread with RNAi bacteria. Some L4 animals were used for a qualitative plate assay (described below). One-day adults were transferred to fresh RNAi plates and placed in a 35°C incubator. At the indicated time-points, plates were removed from the incubator, dead worms (unresponsive to touch by an eyelash pick) were removed from the plate, and the plates were replaced in the incubator. C. elegans survival assays PA14 slow-killing assays were performed as described [59], except SK plates seeded with PA14 were incubated overnight at 25C. N2 C. elegans were synchronized by hypochlorite treatment and grown from the L1 stage on ENG-IA agar plates spread with RNAi bacteria. Worms were moved to new SK plates at each timepoint. Some L4 animals were used for a qualitative plate assay (described below). In the Vibrio cholerae assays, CVD109 and CVD110 were inoculated into LB and grown overnight at 30°C. Cultures were then diluted to OD 2.00 and 30 μl were spread on 60mm NG plates and the plates incubated at 25°C overnight. Fifty L4 animals (grown on RNAi bacteria for Fig 4B or OP50 bacteria for Fig 4C) were transferred to each plate and kept at 25°C. Dead worms were removed at 24 hours and remaining live worms moved to a new set of plates. Final survival counts were taken at 48 hours and those results graphed. Some L4 animals were used for a qualitative plate assay (described below). Qualitative agar plate assays Qualitative agar plate assays were performed as described [58]. C. elegans were synchronized and grown to the L4 stage on agar plates spread with either RNAi bacteria or OP50, as required by the experimental design. JM103-pQE9 or JM103-Cry5B bacteria were grown overnight in LB-ampicillin in a 37°C shaker. The next day, the cultures were diluted 10-fold into fresh LB-ampicillin and shaken for 1 hr at 37°C and then 50 μM IPTG was added to induce Cry5B production and the cultures were shaken for 3–4 hours at 30°C. The bacteria were diluted to an OD of 2.00 and spread onto 60mm ENG-IA plates at the indicated concentrations, usually with one set of plates spread with only JM103-pQE9 (0% plates) and another set spread with a 95:5 mixture of JM103-pQE9:JM103-Cry5B (5% plates). Plates were incubated overnight at 25°C and then ten L4 animals were placed on the plates and incubated at 20°C for 2 days. Animals were recovered and placed into glass spot wells with M9 solution with 15 mM sodium azide to paralyze them, and the wells were photographed. In the assays for Fig 4A, an additional set of plates were spread with 5% JM103-App6A, prepared identically to JM103-Cry5B. Unfolded protein response Synchronized hsp-4::gfp animals were grown to the L4 stage at 20°C on ENG-IA agar plates spread with RNAi bacteria. Animals were then transferred to ENG-IA agar plates that had been spread as described above with either JM103-pQE9 (0% plates) or JM103-Cry5B (100% plates) and incubated at 20°C or 30°C for eight hours. Animals were then washed from the plates and mounted in 0.1% NaN3 in M9, on slides made with 5% agar in water with 0.1% NaN3. Pore repair assay The experiment was performed similarly to previously-described ones [15]. Synchronized L1 animals were grown on RNAi or OP50 at 20°C. L4 stage animals were washed off the plates with ddH2O, rinsed once with ddH2O, then transferred to 100% Cry5B plates and incubated for 1 hr at 20°C. After this Cry5B pulse, worms were washed from the plates with M9 and rinsed once. Then some worms were transferred to fresh RNAi plates or OP50 plates and allowed to recover at 20°C for 26 hr, while others were immediately stained as follows. Worms were incubated in M9 with 5 mg/ml serotonin on a rotator for 15 min at room temperature, after which propidium iodide (Sigma) was added. This was incubated 40–60 min on a room-temperature rotator, after which worms were washed twice with M9 media and mounted on slides. Animals were scored positive for cytosolic PI staining if at least one of the enterocytes in the anterior half of the animal was filled with propidium iodide. At least three independent repeats were performed with 50 animals per treatment. Actin staining experiment N2 or nck-1(ok694) L4 animals were transferred to plates that had been spread with JM103 E. coli carrying either the pQE9 empty vector or pQE9/Cry5B and incubated at 20C for 2 hrs. Worms were then transferred to polylysine-treated glass slides in a drop of cutting buffer (5% sucrose, 100 mM NaCl, 0.02 mM levamisole (Acros cat. no. 187870100)) and the heads were sliced off using two syringe needles. The worms were fixed in 1.25% paraformaldehyde for 10 min at room temperature then placed in a Coplin jar to wash for 30 min in PBT (1X PBS, 0.1% Tween-20, 0.1% EDTA, 0.05% NaN3). Worms were then treated with 6.6 μM FITC-labeled phalloidin (SIGMA P5282) for 1 hr at room temperature and washed for 1 hr in PBT. Worms were mounted in Vectashield. Image stacks were acquired on a Leica TCS SP8 Spectral Confocal Microscope with DMi8 Inverted Stage Microscope, using LAS X software. Images were analyzed by selecting a middle slice, drawing a region around the intestine and the gonad in ImageJ, and dividing the Integrated Density of the intestine by that of the gonad. In the data set, there were two outlier animals, one in the N2 untreated group and one in the nck-1(ok694) untreated group, that showed exceptionally high background (>5X the mean integrated density). These animals were removed from analyses. Statistical analyses Statistical analyses were performed and graphs were generated with GraphPad Prism 9.2.0 software (GraphPad, San Diego, CA). In all figures, p-values are written out, in which “n.s.” denotes “not significant.” Sigmoidal graphed data (Figs 1A, 1B, 1D, 2B, 3B, 3C, 3D, 7A, 7B and 7C) were analyzed using Prism’s nonlinear variable slope (four parameters) dose-response model log(test compound concentration; independent variable) vs. response (% alive; dependent variable). An experimental condition was determined to be significantly different from the control if the 95% confidence intervals of the logIC50 value of the two did not overlap. In bar-graph assays comparing two conditions (Figs 1C and 3A), a two-way ANOVA and Sidak’s multiple comparison test were performed. In bar-graph assays comparing three conditions (Figs 2C, 4B, 4C, 5B, 6B and 6C), a two-way ANOVA and Dunnett’s multiple comparison test were performed. For Fig 3E, Kaplan-Meier estimate and the log-rank test were conducted. In Fig 8B, one-way ANOVA and Tukey’s multiple comparison test were conducted. LC50 and 95% confidence intervals are provided in S1 Table. C. elegans and bacterial strains C. elegans N2 Bristol was maintained using standard techniques [52]. The following strains were used in this study and were purchased from the Caenorhabditis Genetics Center: glp-4(bn2), glp-4(bn2); rrf-3(pk1426), nck-1(ok694) following 4X outcross with lon-2(e678), dbn-1(ok925) following 4X outcross with unc-64(e246), VP303 rde-1(ne219);KbIs7[nhx-2P::rde-1] [53], sek-1(km4), and SJ4005 zcIs4[hsp-4::GFP]. E. coli empty-vector control and Cry5B-expressing strains were JM103-pQE9 and JM103-Cry5B. The App6A gene was subcloned into the BamHI and PstI sites of the vector pQE9 (adding an N-terminal His tag and a seven amino acid extension to the C-terminus) and transformed into JM103 [54]. Feeding RNAi bacterial strains were Escherichia coli HT115 with pL4440 vector derived from the Ahringer RNAi library [55] except for rab-11.1 [15]. RNAi clones were confirmed by plasmid DNA sequencing. In all experiments where arx-5, dbn-1, or erm-1 RNAi bacteria were used, a mixture of equal parts HT115 carrying empty pL4440 and or pL4440 bearing the gene-specific RNAi sequence was prepared. In all experiments where rab-11.1 RNAi bacteria was used, a 17% rab-11.1 mixture was prepared in a similar way. E. coli OP50, Pseudomonas aeruginosa strain PA14 [56], and Vibrio cholerae strains CVD109 Δ(ctxAB zot ace) and CVD110 Δ(ctxAB zot ace) hlyA::(ctxB mer) Hgr were used [57]. Microscopy and image editing Images from qualitative toxicity assays were obtained from assay plates, using an Olympus SZ60 dissecting microscope linked to a Canon Powershot A620 digital camera, and using Canon Remote Capture software or from slides with an Olympus BX60 compound microscope with an UplanFl 10x/0.25NA or 40x/1.35NA objective, mounted to a Spot Insight CCD camera and using Spot software. Actin staining images were taken on a Leica TCS SP8 Spectral Confocal DMi8 Inverted Stage Microscope, with LAS X software. All images within an experiment were taken with identical camera settings. Final images were assembled using Adobe Photoshop and/or GIMP. Quantitative Cry5B assays in liquid media Assays for determining LC50 of C. elegans exposed to purified Cry5B were performed as described [58] with any changes described below. Unless otherwise indicated, all assays were scored after 6 days and included 5-fluoro-2’-deoxyuridine (FUdR; SIGMA) to prevent the appearance of the next generation of larvae that would complicate the experiments [58]. For experiments in which genes were knocked down by feeding RNAi, L1 larvae were synchronized by hypochlorite treatment and plated onto ENG-IA agar plates spread with RNAi bacteria. Animals were grown at 20°C to the L4/young adult stage. OP50 bacteria in the wells were substituted with overnight cultures of RNAi bacteria that were induced with 1 mM IPTG for 1 hr at 37°C before inclusion in wells. Some L1s were plated in parallel on act-5 or unc-22 RNAi to verify RNAi effect. In the assays for Fig 1B, no FUdR was present, and animals were grown to the L4 stage at 25°C. In assays involving nck-1(ok694) mutants, L4 worms were manually transferred into wells. In the assays for Fig 3B and 3C, CuSO4 (SIGMA) or NaCl (SIGMA), respectively, were substituted for Cry5B [15]. In the assays for Fig 3D, L4 animals were put into wells with only S Media and the indicated concentration of H2O2 for four hours at 20°C before scoring. In the assays for Fig 3B, 3C and 3D, a parallel qualitative agar plate assay was performed (described below). Heat stress assay VP303 C. elegans were synchronized by hypochlorite treatment and grown from the L1 stage on ENG-IA agar plates spread with RNAi bacteria. Some L4 animals were used for a qualitative plate assay (described below). One-day adults were transferred to fresh RNAi plates and placed in a 35°C incubator. At the indicated time-points, plates were removed from the incubator, dead worms (unresponsive to touch by an eyelash pick) were removed from the plate, and the plates were replaced in the incubator. C. elegans survival assays PA14 slow-killing assays were performed as described [59], except SK plates seeded with PA14 were incubated overnight at 25C. N2 C. elegans were synchronized by hypochlorite treatment and grown from the L1 stage on ENG-IA agar plates spread with RNAi bacteria. Worms were moved to new SK plates at each timepoint. Some L4 animals were used for a qualitative plate assay (described below). In the Vibrio cholerae assays, CVD109 and CVD110 were inoculated into LB and grown overnight at 30°C. Cultures were then diluted to OD 2.00 and 30 μl were spread on 60mm NG plates and the plates incubated at 25°C overnight. Fifty L4 animals (grown on RNAi bacteria for Fig 4B or OP50 bacteria for Fig 4C) were transferred to each plate and kept at 25°C. Dead worms were removed at 24 hours and remaining live worms moved to a new set of plates. Final survival counts were taken at 48 hours and those results graphed. Some L4 animals were used for a qualitative plate assay (described below). Qualitative agar plate assays Qualitative agar plate assays were performed as described [58]. C. elegans were synchronized and grown to the L4 stage on agar plates spread with either RNAi bacteria or OP50, as required by the experimental design. JM103-pQE9 or JM103-Cry5B bacteria were grown overnight in LB-ampicillin in a 37°C shaker. The next day, the cultures were diluted 10-fold into fresh LB-ampicillin and shaken for 1 hr at 37°C and then 50 μM IPTG was added to induce Cry5B production and the cultures were shaken for 3–4 hours at 30°C. The bacteria were diluted to an OD of 2.00 and spread onto 60mm ENG-IA plates at the indicated concentrations, usually with one set of plates spread with only JM103-pQE9 (0% plates) and another set spread with a 95:5 mixture of JM103-pQE9:JM103-Cry5B (5% plates). Plates were incubated overnight at 25°C and then ten L4 animals were placed on the plates and incubated at 20°C for 2 days. Animals were recovered and placed into glass spot wells with M9 solution with 15 mM sodium azide to paralyze them, and the wells were photographed. In the assays for Fig 4A, an additional set of plates were spread with 5% JM103-App6A, prepared identically to JM103-Cry5B. Unfolded protein response Synchronized hsp-4::gfp animals were grown to the L4 stage at 20°C on ENG-IA agar plates spread with RNAi bacteria. Animals were then transferred to ENG-IA agar plates that had been spread as described above with either JM103-pQE9 (0% plates) or JM103-Cry5B (100% plates) and incubated at 20°C or 30°C for eight hours. Animals were then washed from the plates and mounted in 0.1% NaN3 in M9, on slides made with 5% agar in water with 0.1% NaN3. Pore repair assay The experiment was performed similarly to previously-described ones [15]. Synchronized L1 animals were grown on RNAi or OP50 at 20°C. L4 stage animals were washed off the plates with ddH2O, rinsed once with ddH2O, then transferred to 100% Cry5B plates and incubated for 1 hr at 20°C. After this Cry5B pulse, worms were washed from the plates with M9 and rinsed once. Then some worms were transferred to fresh RNAi plates or OP50 plates and allowed to recover at 20°C for 26 hr, while others were immediately stained as follows. Worms were incubated in M9 with 5 mg/ml serotonin on a rotator for 15 min at room temperature, after which propidium iodide (Sigma) was added. This was incubated 40–60 min on a room-temperature rotator, after which worms were washed twice with M9 media and mounted on slides. Animals were scored positive for cytosolic PI staining if at least one of the enterocytes in the anterior half of the animal was filled with propidium iodide. At least three independent repeats were performed with 50 animals per treatment. Actin staining experiment N2 or nck-1(ok694) L4 animals were transferred to plates that had been spread with JM103 E. coli carrying either the pQE9 empty vector or pQE9/Cry5B and incubated at 20C for 2 hrs. Worms were then transferred to polylysine-treated glass slides in a drop of cutting buffer (5% sucrose, 100 mM NaCl, 0.02 mM levamisole (Acros cat. no. 187870100)) and the heads were sliced off using two syringe needles. The worms were fixed in 1.25% paraformaldehyde for 10 min at room temperature then placed in a Coplin jar to wash for 30 min in PBT (1X PBS, 0.1% Tween-20, 0.1% EDTA, 0.05% NaN3). Worms were then treated with 6.6 μM FITC-labeled phalloidin (SIGMA P5282) for 1 hr at room temperature and washed for 1 hr in PBT. Worms were mounted in Vectashield. Image stacks were acquired on a Leica TCS SP8 Spectral Confocal Microscope with DMi8 Inverted Stage Microscope, using LAS X software. Images were analyzed by selecting a middle slice, drawing a region around the intestine and the gonad in ImageJ, and dividing the Integrated Density of the intestine by that of the gonad. In the data set, there were two outlier animals, one in the N2 untreated group and one in the nck-1(ok694) untreated group, that showed exceptionally high background (>5X the mean integrated density). These animals were removed from analyses. Statistical analyses Statistical analyses were performed and graphs were generated with GraphPad Prism 9.2.0 software (GraphPad, San Diego, CA). In all figures, p-values are written out, in which “n.s.” denotes “not significant.” Sigmoidal graphed data (Figs 1A, 1B, 1D, 2B, 3B, 3C, 3D, 7A, 7B and 7C) were analyzed using Prism’s nonlinear variable slope (four parameters) dose-response model log(test compound concentration; independent variable) vs. response (% alive; dependent variable). An experimental condition was determined to be significantly different from the control if the 95% confidence intervals of the logIC50 value of the two did not overlap. In bar-graph assays comparing two conditions (Figs 1C and 3A), a two-way ANOVA and Sidak’s multiple comparison test were performed. In bar-graph assays comparing three conditions (Figs 2C, 4B, 4C, 5B, 6B and 6C), a two-way ANOVA and Dunnett’s multiple comparison test were performed. For Fig 3E, Kaplan-Meier estimate and the log-rank test were conducted. In Fig 8B, one-way ANOVA and Tukey’s multiple comparison test were conducted. LC50 and 95% confidence intervals are provided in S1 Table. Supporting information S1 Table. LC50 values along with 95% confidence intervals associated with experimental results. https://doi.org/10.1371/journal.ppat.1010656.s001 (DOCX) S1 Fig. hsp-4::gfp UPR reporter animals subjected to RNAi are still sensitive to heat shock. hsp-4::gfp worms grown on the indicated RNAi bacteria to the L4 stage, moved to 30°C for heat shock, and then photographed after 8 hours of incubation at that temperature. Scale bar = 0.1mm. https://doi.org/10.1371/journal.ppat.1010656.s002 (TIF) S2 Fig. N2 and nck-1(ok694) animals are not basally permeable to ingested propidium iodide. The indicated C. elegans strains were grown to the L4 stage and subjected to the normal propidium iodide feeding protocol, with no exposure to Cry5B. Scale bar = 25um. https://doi.org/10.1371/journal.ppat.1010656.s003 (TIF) Acknowledgments We thank You-Mie Kim with help on microscopy. Some strains were provided by the CGC, which is funded by NIH Office of Research Infrastructure Programs (P40 OD010440).
TI - A Caenorhabditis elegans nck-1 and filamentous actin-regulating protein pathway mediates a key cellular defense against bacterial pore-forming proteins
JF - PLoS Pathogens
DO - 10.1371/journal.ppat.1010656
DA - 2022-11-14
UR - https://www.deepdyve.com/lp/public-library-of-science-plos-journal/a-caenorhabditis-elegans-nck-1-and-filamentous-actin-regulating-iq4XnKGf06
SP - e1010656
VL - 18
IS - 11
DP - DeepDyve
ER -