The Type VI secretion system (T6SS) is a widespread macromolecular structure that delivers protein effectors to both eukaryotic and prokaryotic recipient cells. The current model describes the T6SS as an inverted phage tail composed of a sheath‐like structure wrapped around a tube assembled by stacked Hcp hexamers. Although recent progress has been made to understand T6SS sheath assembly and dynamics, there is no evidence that Hcp forms tubes in vivo. Here we show that Hcp interacts with TssB, a component of the T6SS sheath. Using a cysteine substitution approach, we demonstrate that Hcp hexamers assemble tubes in an ordered manner with a head‐to‐tail stacking that are used as a scaffold for polymerization of the TssB/C sheath‐like structure. Finally, we show that VgrG but not TssB/C controls the proper assembly of the Hcp tubular structure. These results highlight the conservation in the assembly mechanisms between the T6SS and the bacteriophage tail tube/sheath.
This study shows that the Type VI secretion‐associated Hcp protein assembles into tubes in a head‐to‐tail manner. Hcp tube formation requires the VgrG protein and is necessary for proper polymerization of the TssB/C sheath.
The Type VI secretion system (T6SS) protein Hcp assembles tubes in a head‐to‐tail manner which is required for T6SS sheath polymerization.
Hcp1 interacts with the T6SS sheath by directly interacting with the TssB1 subunit.
The assembly of the Hcp tubes is controlled by VgrG.
In Gram‐negative bacteria, the secretion of toxin proteins is achieved by dedicated, specialized machineries called secretion systems. The Type VI secretion system (T6SS) is highly versatile as it delivers protein effectors in either eukaryotic or prokaryotic target cells , . The T6SS is composed of 13 Tss (Type six subunits) core components that assemble a macromolecular complex spanning the cell envelope , . The TssL, TssM and TssJ membrane proteins interact to form the trans‐envelope apparatus , . A number of subunits are evolutionarily, structurally and mechanistically related to proteins that form the tail of contractile bacteriophages. VgrG is a composite protein, structurally related to the trimeric gp27/gp5 hub complex forming the cell‐puncturing device of bacteriophage T4 . The membrane of the target cell is supposed to be disrupted by the tip of the VgrG protein that acts as a syringe. Recently, a PAAR‐like protein has been shown to associate with the tip of VgrG, and by recruiting effector proteins, has been proposed to translocate these proteins into the target cell . The Hcp protein is structurally related to gpV, the major tail tube protein of phage λ. Hcp is an abundant protein of the T6SS that forms a ring‐shaped hexamer , , , . While Hcp tubes have been visualized in vitro , the existence of such tubes in vivo has not been evidenced. In contractile bacteriophages, prior to contraction, the tail tube is surrounded by the sheath in an extended conformation . Upon infection, the phage sheath undergoes an extensive structural transition leading to its contraction and propelling the tail tube towards the target cell interior . Interestingly, the TssB (VipA) and TssC (VipB) proteins assemble large tubular structures extending into the cytoplasm , . The TssB/C sub‐complex exhibits cogwheel‐like cross‐sections resembling the bacteriophage sheath . Time‐lapse fluorescence microscopy further showed that these structures are highly dynamic, oscillating between extended and contracted conformations , , . Based on homology with the bacteriophage it is thought that contraction of the TssB/C tubule propels the Hcp tube towards the exterior and the target cell. In agreement with this model, a recent study has shown that contraction of the T6SS sheath is correlated with prey cell lysis . However, the existence of Hcp tubes has not been demonstrated in vivo. The Hcp crystal structure packing suggested that Hcp hexamers may stack either in a head‐to‐tail , head‐to‐head  or tail‐to‐tail  conformation. However, while the different modes of inter‐rings interactions observed for the different Hcp proteins may reflect differences during assembly, it is formally possible that these packing are crystallographic artifacts and are not physiologically relevant. Similarly, the mode of assembly of the tube protein of contractile tailed phages remains unsolved. Cryo‐electron microscopy images showed that the phage tail tube is a cylinder lacking discernable surface structures , . However, the tail tubes of non‐contractile phages are composed of stacked hexamers positioned offset on each other . We therefore reasoned that an in vivo approach might provide information on Hcp assembly. In this study, we engineered functional cysteine variants of the Hcp1 protein encoded within the enteroaggregative Escherichia coli (EAEC) sci‐1 T6SS gene cluster. We substituted residues at specific positions that discriminate between head‐to‐tail, tail‐to‐tail and head‐to‐head packing. Our results provide strong support for a model in which Hcp1 hexamers form tubular structures in vivo. Importantly, we further demonstrate that the Hcp1 hexamers assemble in an ordered stacked, head‐to‐tail, manner and that this specific assembly is a controlled process requiring other sci‐1 gene products. Finally, we also provide evidence that Hcp1 interacts with the T6SS sheath via direct contacts with the TssB1 subunit and that Hcp1 tube formation is required for sheath polymerization.
Results and Discussion
Hcp is required for T6SS sheath assembly through interaction with TssB
While the TssB and TssC subunits have been postulated to engulf the putative Hcp conduit, experimental data regarding the relationship between Hcp and the sheath‐like proteins are lacking. As TssB1 and TssC1, Hcp1 mainly localizes in the cytoplasm (see further details in the Supplementary Text and Supplementary Fig S1). Using immunoprecipitation we isolated a complex between Hcp1, TssB1 and TssC1 (Fig 1A). This result is in agreement with bioinformatics analyses demonstrating that Hcp, TssB and TssC are functionally linked . To gain further information, we probed pairwise interactions between Hcp1 and TssB1 and TssC1 using bacterial two‐hybrid and co‐immunoprecipitation assays (Fig 1B and C, Supplementary Text, Supplementary Fig S2). Both assays demonstrate that Hcp1 interacts specifically with TssB1, not with TssC1. Specificity experiments between the two T6SS encoded within the EAEC genome showed that Hcp1 does not interact with TssB2. Similarly, although Hcp2 interacts with TssB2, no interaction was detected between Hcp2 and TssB1 (Supplementary Text, Supplementary Fig S2). This set of data supports a model in which Hcp is wrapped by the TssB/C subunits as the bacteriophage tail tube is wrapped by the tail sheath. We next asked whether Hcp1 is required for assembly of the T6SS sheath structure. Several recent reports demonstrated that the TssB protein fused to the superfolder green fluorescent protein (sfGFP) assembles cytosolic tubular structures oscillating between extended and contracted conformations , , . We engineered a plasmid‐borne TssB1‐sfGFP fusion. As previously described , , this fusion protein behaves similarly to the previously described TssB‐sfGFP proteins: (i) it assembles 1‐3 cytoplasmic sheaths per cell, and (ii) the sheath structures oscillate between extended and contracted conformations with dynamics occurring in tens of seconds (Fig 1D, WT). These structures are not visible in a strain deleted of the hcp1 gene, leaving a diffuse fluorescence within the cytoplasm (Fig 1D, Δhcp). This diffuse fluorescence phenotype was complemented by the expression of a WT hcp1 allele from a plasmid (Fig 1D, hcp+). The data suggest that Hcp is required for proper assembly of the T6SS sheath and that the TssB/C proteins build the sheath using the Hcp tube as a scaffold. This is reminiscent of the bacteriophage morphogenesis in which the sheath polymerizes on the tail tube , .
Hcp1 modelling and validation
The EAEC Hcp1 protein was modelled based on the available Hcp three‐dimensional crystal structures from P. aeruginosa, E. tarda and Y. pestis (PDB: 1Y12, 3HE1, 3EAA, 3V4H). The availability of multiple homologous structures offered the opportunity to build a robust multiple sequence alignment, improved and validated based on structural alignments.
To validate the EAEC Hcp1 model, we engineered the N115C variant, in which the asparagine residue at position 115 (Asn‐115) is substituted by a cysteine. The Asn‐115 residue is at the interface of two monomers within the hexamer, and is positioned to face the native cysteine residue (Cys‐38) of the adjacent monomer (Fig 2A). The N115C Hcp1 mutant is functional as shown by its ability to be released in a T6SS‐dependent manner (Supplementary Fig S3). Cells were treated with the oxidative agent copper phenanthroline, washed and free cysteines were blocked using N‐ethylmaleimide (NEM) to avoid artifactual disulfide bond formation upon cell lysis. Analysis of cytoplasmic extracts from cells producing the N115C Hcp1 variant by non‐reducing SDS‐PAGE showed that Hcp1‐N115C migrates as a ladder (Fig 2B), demonstrating formation of disulfide bridges between adjacent monomers. Overall these data validate the EAEC Hcp1 model and the experimental procedure. This model was further validated by the recently released structure of the Hcp1 protein .
Hcp1 hexamers assemble in a head‐to‐tail mode
To further evaluate the ability of Hcp1 to form tubular structures in vivo we reasoned that cysteine residues placed at the interface of two hexamers will form a disulfide bridge if Hcp hexamers polymerize. Our experiment approach draws its inspiration from the in vitro work of Ballister et al . To identify the most probable interfaces between two Hcp hexamers, we modeled dodecamers in a head‐to‐tail, tail‐to‐tail or head‐to‐head orientation (Fig 3A‐C). Interestingly, each of the available Hcp crystal structures describes a different, unique mode of interaction between Hcp hexameric rings: head‐to‐tail (P. aeruginosa Hcp1, ), tail‐to‐tail (P. aeruginosa Hcp3, ), and head‐to‐head (E. tarda EvpC, ). The three templates therefore offer bases for structural predictions regarding all possible stacking modes of EAEC Hcp1 hexamers. In each dodecamer model, the main contact is established by one loop on either side, yielding a limited choice of targets for cysteine substitutions (Fig 3A–C).
Cysteine substitutions were introduced into a cysteine‐less (C38S) variant of the Hcp1 protein. For the head‐to‐tail assembly, cysteine residues were introduced at positions Gly96 (loop 4) and Ser158. Residues Gln24 (loop 1) and Ala95 (loop 4) were targeted for the tail‐to‐tail assembly, while residue Gly48 was mutated for the head‐to‐head assembly. All the Hcp1 variants accumulate at comparable levels and are functional as shown by their release in the extracellular milieu (Supplementary Fig S3).
SDS‐PAGE analyses of cytoplasmic extracts from oxidized cells producing the variants showed that the G96C‐S158C combination leads to the formation of a ladder corresponding to multiple oligomers, while the Q24C‐A95C and G48C combinations remain monomeric (Fig 3D). These data support the hypotheses that (i) Hcp1 assembles into tubular structures in vivo and (ii) that the hexamers are stacked in a head‐to‐tail manner within the tube.
To verify that hexamers are stacked in a head‐to‐tail manner, we engineered tryptophan variants with the rationale that insertion of a bulky tryptophan residue at the hexamer interface will destabilize the assembly of the tubular structure. Indeed, the Hcp1 S158W variant was not functional, as shown by Hcp release assay (Supplementary Fig S4). Identical results were obtained when residues located within the loop facing Ser138 (Asn93 and Gly96) were substituted by tryptophan residues (data not shown). Interestingly, fluorescence microscopy showed that production of the Hcp1 S158W protein prevents formation of dynamic TssB/C sheath structures (Fig 1D, hcpW+), suggesting that Hcp hexamers polymerization into tubes is a prerequisite for T6SS sheath assembly.
Aberrant Hcp1 assembly in the cytoplasm of a sci‐1 T6SS‐deficient strain
We then asked whether the assembly of the Hcp tube requires T6SS components. Formation of Hcp1 hexameric rings remains unaffected in the ∆sci‐1 strain (i.e., which carries a deletion of the sci‐1 T6SS gene cluster; Fig 4A). However, all the cysteine combinations (G96C‐S158C, Q24C‐A95C and G48C) led to the formation of dimers or higher oligomeric forms, demonstrating that, in absence of any T6SS subunit, Hcp1 hexamers can pack in head‐to‐tail, tail‐to‐tail and head‐to‐head assemblies (Fig 4A). From these data we concluded that, while Hcp1 spontaneously forms hexameric rings, proper assembly of Hcp1 tubes in vivo is tightly controlled by Sci‐1 T6SS components. During bacteriophage T4 biogenesis, a complex structure called the baseplate serves as a platform for tail tube/sheath polymerization and triggers sheath contraction as well . The tube initiates its polymerization once the six wedges assemble onto the gp27‐gp5 hub complex . We therefore tested whether Hcp1 assembles tubular structures in absence of VgrG1, the T6SS homologue of the hub complex. As shown in Fig 4B, Hcp1 hexamers do not assemble in head‐to‐tail only in vgrG1 cells, demonstrating that VgrG1 is required for proper assembly of Hcp1 tubes. However, VgrG1, when produced alone in the Δsci‐1 background, is not sufficient to restore the controlled Hcp1 assembly (Fig 4D). Finally, Hcp1 assembly is not impaired in tssB1C1 cells (Fig 4E), a result consistent with phage morphogenesis as bacteriophage T4 sheath‐less tails have been previously observed .
Conclusive remarks and outlook
The current models of Type VI secretion hypothesize that the Hcp proteins assemble into a structure resembling the bacteriophage tail tube . Indeed, in vitro electron microscopy experiments showed that purified Hcp spontaneously assembles into small tubular edifices , . In contractile bacteriophages, the tail tube is surrounded by the sheath and serves as a scaffold during sheath polymerization , . In the T6SS, TssB and TssC form dynamic cytosolic structures resembling the phage sheath, providing further support to the assembly of similar contractile tail structures in both T6SS and bacteriophage T4 , , , , . By analogy with the bacteriophage structure, the cytosolic portion of the T6SS is depicted as a sheath surrounding an Hcp tube. Here, we provide evidence that the EAEC Hcp1 protein interacts with the sheath‐like TssB1/C1 complex through direct contacts with TssB1. Recently, an interaction between Hcp and both TssB and TssC has been reported in Agrobacterium tumefaciens . In our bacterial two‐hybrid and co‐immunoprecipitation assays, we did not detect an interaction between Hcp1 and TssC1. Furthermore, we noted that Hcp1‐TssB1 complex formation was of low affinity since chemical cross‐linking was required to detect this interaction in vivo. This low affinity is compatible with a model in which the Hcp tube slides within the sheath during contraction. In agreement with the results obtained by Kapitein et al using immunofluorescence microscopy , the comparison of T6SS sheath assembly in WT and hcp1 mutant strains using time‐lapse fluorescence microscopy further showed that Hcp1 is required for sheath polymerization: in absence of Hcp1, TssB1‐sfGFP dynamic structures were not observed and the fluorescence was diffuse. Additionally, we found that assembly of the sheath‐like structure is dependent on Hcp1 tube formation as a tryptophan substitution disrupting Hcp1 tubular edifices prevents formation of the T6SS sheath. Although the mechanism by which T6SS sheath polymerization is dependent on Hcp has not been determined here, our data suggest that the TssB/C proteins assemble the sheath using the Hcp tube as a framework, as proposed during bacteriophage T4 tail morphogenesis , .
The cysteine substitution approach revealed that Hcp1 assembles in an ordered manner in vivo in which hexameric rings stack head‐to‐tail onto one another. These results provide the first in vivo demonstration that Hcp subunits form a genuine tubular structure. While these novel data are key to a better understanding of the assembly mechanism of the T6SS, they also bring clues regarding phage structure. Indeed, due to the sheath density in cryo‐electron microscopy images, the assembly mode of the tail tube of contractile phages has not been described yet . However, the tail tube of the non‐contractile bacteriophage λ is composed of 32 stacked hexamers of GpV . Based on the data described here, and on the crystallographic observation that tailed bacteriophages and T6SS tubes are composed of similar building blocks , we propose that these tubes share a common organization. In the case of phages, the tail tube serves as a conduit for DNA and proteins delivery . Interestingly, it was recently shown that protein toxins delivered by the T6SS can be loaded either onto the tip of the VgrG protein  or within the Hcp hexamer . The formation of Hcp tubes therefore suggests that multiple toxins could be stored into the tube and delivered into the target cell by a single shot.
Importantly we show that proper assembly of the Hcp1 tube requires other T6SS subunits. Although the T6SS does not impact formation of the hexameric rings, implying that rings assemble spontaneously, one or several of the T6SS core components are required for proper polymerization of Hcp1 hexamers into tubes. We showed that while the TssB1 and TssC1 proteins are dispensable, VgrG1, the homologue of the gp27‐gp5 hub, is required – but not sufficient – to promote proper Hcp1 assembly. Indeed, during phage tail biogenesis, tube and sheath polymerization is primed by the hub and the tail initiator complex and occurs once the baseplate has been completed. In the T6SS, the components of the baseplate are yet to be identified. The in vivo assay developed in this study may then be used to probe the different subunits of the T6SS and determine which subunit(s) control the ordered Hcp1 assembly. Among other exciting open questions, whether the Hcp tube length is regulated by a tape measure protein such as the bacteriophage T4 gp29 protein and whether dedicated chaperones are required for proper assembly of the Hcp tubes are now under investigation.
In sum, we showed that (i) Hcp form tubes of stacked hexamers, (ii) Hcp tube formation is required for sheath polymerization, (iii) TssB and TssC are not required for Hcp tube formation and (iv) VgrG is required for Hcp assembly. This is reminiscent of phage morphogenesis in which (i) formation of the tail tube initiates onto the central hub of the baseplate and (ii) the sheath is dispensable for tube assembly but use it as a template during polymerization. It is worth to note that subtle differences exist between T6SS tail assembly and bacteriophage tail morphogenesis such as the observations that phage tail tube proteins do not assemble as hexamers by their own or that phage tail tubes are extremely stable. However, the commonalities underlined by this study emphasize that the general mechanism underlying the assembly of these structures is likely conserved.
Materials and Methods
See Supplementary Materials and Methods for details of homology modeling, design of cysteine variants, fractionation, Hcp1 release, bacterial two‐hybrid and co‐immunoprecipitation procedures, and Supplementary Table S1 for list of strains, plasmids and oligonucleotides used in this study.
Bacterial strains, growth conditions and chemicals
Escherichia coli K12 DH5α was used for cloning procedures. The EAEC strain 17‐2 and its Δsci‐1, Δhcp1, ΔvgrG1, ΔtssB1, ΔtssC1 and ΔtssB1‐C1 isogenic derivatives were used for this study. Strains were routinely grown in LB broth at 37°C, with aeration. Plasmids were maintained by the addition of ampicillin (100 μg/ml for K12, 200 μg/ml for EAEC) or chloramphenicol (40 μg/ml). Dichloro (1,10‐phenanthroline) copper(II) (Cu‐oP) and N‐ethylmaleimide (NEM) were purchased from Sigma‐Aldrich.
In vivo disulfide cross‐linking
3 × 1010 exponential growing cells (OD600 ~ 0.6) were incubated with 0.3 mM Cu‐oP for 20 min without agitation. Cells were then harvested by centrifugation and incubated in 10 mM HEPES (pH 7.4), Sucrose 30%, 1 mM EDTA and 2.5 mM NEM for 30 min on ice to block free thiol groups. Cells were pelleted by centrifugation and submitted to a fractionation procedure (see Supplementary Materials and Methods). Cytoplasmic extracts were mixed with loading buffer prior to analysis by SDS‐PAGE and immunoblotting.
Time‐lapse fluorescence microscopy
Overnight cultures of entero‐aggregative E. coli 17‐2 WT or mutant derivative strains carrying plasmid pBAD33‐TssB1–sfGFP were diluted 1:100 into M9 minimal medium supplemented with glycerol (0.2%), vitamin B1 (1 μg/ml), casaminoacids (40 μg/ml), LB (10% v/v) and chloramphenicol 40 μg/ml. Cells were then cultivated for 6 hours to an OD600nm ~ 1.0 in M9 minimal medium to maximize expression of the sci‐1 T6S gene cluster that is up‐regulated in iron‐depleted conditions . Cells were washed in phosphate buffered saline (PBS), resuspended in PBS to an OD600nm ~ 50 and spotted on a thin pad of 1.5% agarose in PBS and covered with a cover slip. Microscopy recordings have been performed as previously described .
Conflict of interest
The authors declare that they have no conflict of interest.
Supplementary Figure 1
Supplementary Figure 2
Supplementary Figure 3
Supplementary Figure 4
Supplementary Table 1
We thank Tâm Mignot for fluorescence microscopy, Laure Journet, Petr Leiman (EPFL, Switzerland) and the members of the Cascales, Lloubès, Cambillau, Bouveret and Sturgis research groups for discussion, Oliver Uderso, Isabelle Bringer and Annick Brun for technical assistance, Patrick Vieira and Lionel Messing for plasmids. Work in the E.C. laboratory is supported by the Centre National de la Recherche Scientifique and a grant from the Agence Nationale de la Recherche (ANR‐10‐JCJC‐1303‐03). Y.R.B. was supported by a doctoral fellowship from the French Ministère de la Recherche.
YRB, JH and EC designed and conceived the experiments; YRB, JH and EC provided tools; YRB, JH and HC performed the experiments; YRB, JH and EC wrote the article.
FundingAgence Nationale de la Recherche ANR‐10‐JCJC‐1303‐03
- © 2014 The Authors