The Photorhabdus asymbiotica virulence cassettes deliver protein effectors directly into target eukaryotic cells

Photorhabdus is a highly effective insect pathogen and symbiont of insecticidal nematodes. To exert its potent insecticidal effects, it elaborates a myriad of toxins and small molecule effectors. Among these, the Photorhabdus Virulence Cassettes (PVCs) represent an elegant self-contained delivery mechanism for diverse protein toxins. Importantly, these self-contained nanosyringes overcome host cell membrane barriers, and act independently, at a distance from the bacteria itself. In this study, we demonstrate that Pnf, a PVC needle complex associated toxin, is a Rho-GTPase, which acts via deamidation and transglutamination to disrupt the cytoskeleton. TEM and Western blots have shown a physical association between Pnf and its cognate PVC delivery mechanism. We demonstrate that for Pnf to exert its effect, translocation across the cell membrane is absolutely essential.


Introduction
Bacteria belonging to the Enterobacteriaceae genus Photorhabdus exist in a symbiotic partnership with entomopathogenic Heterorhabditis sp. nematodes. This Entomopathogenic Nematode complex (EPN) comprises a highly efficient symbiosis of pathogens that is commonly used as a biological agent to control crop pests (Forst et al., 1997). The Photorhabdus bacteria are delivered into the hemocoel of the insect, after regurgitation from the worm, where they resist the insect immune response and rapidly kill the host via septicaemic infection. Insect tissues are subsequently bio-converted into a dense soup of Photorhabdus bacteria, which provide a food source to support the replication of the nematode. As food resources are depleted Photorhabdus re-associates with infective juvenile nematodes, and together they emerge from the insect cadaver able to re-infect a new host (Ciche et al., 2008;Somvanshi et al., 2012). Three major species have been formally recognized to date within the genus -P. luminescens, P. asymbiotica, and P. temperata. It should be noted however that with increasing numbers of Photorhabdus genome sequences becoming available, the genus structure is under revision (Machado et al., 2018). In addition to the normal insect life cycle, P. asymbiotica is also the etiological agent of a serious human infection termed Photorhabdosis, which is associated with severe ulcerated skin lesions both at the initial infection foci and later at disseminated distal sites (Gerrard et al., 2004;Gerrard et al., 2006;Gerrard et al., 2003a;Gerrard et al., 2003b).
A fourth class of highly distinct toxin delivery systems first identified in Photorhabdus are the 'Photorhabdus virulence cassettes', or PVCs (Yang et al., 2006). These represent operons of around 16, conserved, structural and synthetic genes (from hereon just described as the structural genes) encoding for a phage 'tailocin' like structure (Ghequire and De Mot, 2015) and one or more tightly linked downstream toxin-effector like genes. Genomic analysis of multiple strains of Photorhabdus revealed they often encode up to five or six copies of the operon, each with unique downstream effector genes (Hapeshi and Waterfield, 2017).
It should be noted that PVC-like elements are not restricted to Photorhabdus as a well-characterized homologous operon can also be found on the pADAP plasmid of the insect pathogenic bacteria Serratia entomophila (Hurst et al., 2004). This system has been named the anti-feeding prophage (AFP), as it is responsible for the cessation of feeding in the New Zealand grass grub host. Recent cryo-electron microscopy studies have revealed that, morphologically, AFP resembles a simplified version of the sheathed tail of bacteriophages such as T4, including a baseplate complex. It also shares features with type-VI secretion systems, with the central tube of the structure having a similar diameter and axial width to the Hcp1 hexamer of P. aeruginosa T6SS (Heymann et al., 2013). One important difference between the PVC and T6SS machinery is that the T6SS relies upon direct contact between host and bacterial cell, and is anchored in to the membrane by a substantial membrane complex whose structure is still being elucidated (Durand et al., 2015), whereas the PVC needle complex is freely released into the surrounding milieu and so can act at a distance.
Furthermore, recent reports have indicated that other more diverse bacteria can also make similar needle complexes for manipulation of eukaryotic hosts. A well-characterized example is the production of analogous devices by the marine bacterium Pseudoalteromonas luteoviolacea ( Figure 1A). These structures are involved in the developmental metamorphosis of the larvae of the tubeworm eLife digest Photorhabdus are the only known group of non-marine bacteria that can produce their own light. These organisms prey on insects, which then glow in the dark once infected. The group also has an unusual weapon system formed of miniscule needle-like structures that can be sent out in the environment. These 'Photorhabdus virulence cassettes' are loaded with toxins that are injected inside host cells; the cassettes alone can kill a caterpillar within minutes. However, it is still unclear how exactly these structures work: are they like poison darts, with the toxin on the outside, or like hypodermic needles, with the toxin within?
Photorhabdus bacteria make lots of deadly substances, so to look at the needles on their own, Vlisidou et al. had them produced by another species of bacteria that does not carry these weapons. The experiments revealed that the cassettes packaged the toxic proteins inside, like a hypodermic needle. Alone in the environment, the toxin cannot penetrate host cells.
Creating the cassettes takes a lot of energy, and a closer look at Photorhabdus showed that, at any given time during an infection, only a small number of bacteria produce them. It is therefore possible that the bacteria share the high cost of making these deadly devices by using a division of labour approach.
With a better understanding of the cassettes, it could one day become possible to harness these molecular machines to control insect pests or parasites.
Hydroides elegans, and they are deployed in outward-facing arrays comprising about 100 contractile structures, with baseplates linked by tail fibres in a hexagonal net (Shikuma et al., 2014). Interrogation of sequence databases with PVC protein sequences suggests many other more diverse tailocin-like systems are yet to be characterized (Sarris et al., 2014 related to the PVCs in Xenorhabdus bovienii CS03, Yersinia ruckeri ATCC29473 and Vibrio campbellii AND4. In addition, evidence of more diverse elements, like that of P. luteoviolacea, can also be seen. To address this, we have recently performed an exhaustive analysis of all available prokaryotic and archaeal genome sequences in the public databases to look at the distribution of pvc-like elements (unpublished data). This suggests that PVC-like nano-syringes and their distant cousins are of enormous ecological and perhaps biomedical significance.
Here we focus on a single Photorhabdus pvc operon (which elaborates the PVCpnf needle complex (Yang et al., 2006) to understand the relationship between the structural genes and the tightly linked effector gene, pnf. We confirm in vivo expression during insect infection and reveal a high level of population heterogeneity of expression in vitro. We demonstrate for the first time the physical association of the Pnf effector toxin protein with the secreted structural needle complex using Western blot and electron microscopy. Furthermore, we prove that the cognate Pnf effector needs to be delivered into the eukaryote cell cytoplasm to exert any measurable effect and confirm its predicted activity targeting small Rho-GTPase target proteins. Taken together this work describes an important new class of protein toxin secretion and injection delivery systems which, unlike the welldescribed Types III, IV and VI systems, can act 'at a distance', requiring no intimate contact between bacteria and host cells.

Results
A bioinformatic analysis of pvc structural operon sequences A comparison of pvc structural operons identified in the genome sequences of Photorhabdus and certain members of other genera, available at the time of publication (Duchaud et al., 2003;Wilkinson et al., 2009;Wilkinson et al., 2010 and our unpublished data), allowed us to define three distinct genetic sub-types. The PVCpnf operon belongs to class I, which has 16 structural genes and three translationally coupled gene blocks, and is of the type typically seen in non-Photorhabdus genera. Class II and III operons differ in the number of structural genes and translationally coupled gene blocks ( Figure 1B). Given the diversity of pvc-operons, and their typically poor annotation in genome sequences, it is necessary here to define a nomenclature protocol to allow reference to any given operon. An example of the method we have adopted is as follows; [Pa ATCC43949 PVCpnf], where Pa ATCC43949 is species and strain, in this case Photorhabdus asymbiotica strain ATCC43949 and PVCpnf is the specific operon within that genome with the suffix referring to one of the tightly linked effectors, in this case the pnf effector gene. We will also include gene identifiers for either end of the operon where appropriate, which in this case would be PAU_03353-PAU_03332, which are the genes for pvc1 and pnf respectively.
With reference to published literature and a detailed bioinformatic analysis of promoter regions upstream of the pvc1 genes, we can identify two distinct, potential cis-operator sequences. Firstly operons belonging to classes I (e.g. PVCpnf) and III (e.g. PVCPaTox) typically encode the highly conserved RfaH operator sequence, GGCGGTAGNNT (Belogurov et al., 2009). RfaH is a conserved anti-termination protein that is known to regulate large operons encoding for extracellular factors in E. coli. It is also believed to be important in ensuring appropriate transcriptional control of horizontally acquired operons (Belogurov et al., 2009). Many of the pvc-operons in Photorhabdus and members of other genera (including Xenorhabdus and Yersinia) encode this operator sequence. An unusual example is the pADAP plasmid encoded Serratia entomophila anti feeding prophage (afp) (Hurst et al., 2004). While the afp promoter also encodes an RfaH operator sequence, it has been demonstrated that it is positively regulated by a tightly linked specific regulator protein, AnfA1 (Hurst et al., 2007;Hurst et al., 2003). This protein is a distant homologue of RfaH suggesting that other class I or III pvc operons are not necessarily under the regulation of the chromosomal RfaH orthologue, but might also be controlled by other diverse regulators that utilise this same operator sequence (Carter et al., 2004). Unfortunately, we were not able to directly test the role of RfaH in pvc-regulation as attempts to knock out the single P. luminescens TT01 rfaH gene were not successful, suggesting an essential role. Secondly, all class II operons (e.g. PVClopT) and certain class I operons (e.g. PVCunits1-4) encode a minimal cryptic conserved sequence motif, CAGGTTGXTGCGG TAGCTAT. In both cases these conserved cis-encoded sequences are located between the pvc1 gene and the transcription start sites, as defined by previous RNA-seq analysis (Mulley et al., 2015 and unpublished data). We speculate that this motif, which we have so far only found in pvc loci, may represent an operator sequence for a cryptic regulator.
Although there is no experimental evidence, several observations suggest that horizontal gene transfer may have been responsible for the dissemination of many observed pvc-operons. These include; the presence of four pvc operons in tandem in P. luminescens TT01 (directly adjacent to a type IV DNA conjugation pilus operon), the presence of multiple pvc operons in any given genome, the suggestion that several operons are regulated by RfaH and the remnants of YhgA-like IS elements and inverted repeats (IR) associated with many of the operons (e.g. the IR sequence 5'-TTATA TTGAA(t/g)GAATATTAAGCAAGAAAC-3' flanking [Pl TT01 PVCu4]). Nevertheless, automatic prediction of horizontal gene transfer regions (HGTs) using Alien Hunter 1.7 (Vernikos and Parkhill, 2006) either did not detect any HGT elements spanning the structural regions of PVCs or in the cases where such an element was detected it was assigned a low confidence score (Figure 1-figure supplement 1).
An analysis of the conservation of individual genes across different pvc operons at both DNA and protein sequence levels suggests that either recombination or diversifying selection is more likely to have occurred in the more 3' regions of the operons (Figure 1-figure supplement 2). This is perhaps no surprise as each pvc operon can be seen to encode different effector genes in the 3' payload region of the operons. An analysis of conservation of protein sequences of the pvc operons showed that within pvc-operons a good deal of variability is possible while presumably retaining the ability to produce a similar macromolecular structure ( Figure 1-figure supplement 3). This is supported by HHPRED structural homology comparisons for equivalent PVC proteins across different operons, despite often-variable primary amino acid sequences (data not shown). We note that the most diverse protein seen in pvc-operons is that of the predicted tail fibre proteins, Pvc13, which we may expect if different pvc-operons are adapted for different host cell targets. Paralogous genes within pvc-operons include pvc1 and pvc5 which encode homologs of Hcp, the inner tube protein of contractile tube mechanisms such as T6SS and phage protein Gp27 and pvc2, À3 and À4 which encode homologues of the outer sheath proteins of phage (Leiman et al., 2010) and T6SS (Russell et al., 2014). A bioinformatic analysis of pvc-operon effector gene sequences A comparison of the 3' effector 'payload regions' of different pvc operons reveals a large diversity of effector genes, with a range of predicted activities, covering a large range of sizes and isoelectric point values (data not shown). Some operons encode only a single putative effector, for example [Pa ATCC43949 PVCPaTox PAU_02249-02230] while others have several, either tandem homologues of one another, for example [Pa ATCC43949 PVCu4 PAU_02790-02808] or entirely unrelated putative effector genes, for example [Pa ATCC43949 PVClopT PAU_02112-02095]. Many effector genes are also tightly linked to transposase gene remnants suggesting they are typically exchanged by horizontal acquisition. This is further supported by the observation that orthologous pvc-operons in the same chromosomal context may have different effector genes in different strains. A good example of this being the unrelated effector genes seen in the orthologous structural 'PVCpnf' operon loci of Pa Kingscliff and Pa ATCC43949 which carry a tyrosine glycosylase and Pnf (this paper) respectively. Analysis with Alien Hunter 1.7, suggests that certain pvc-operon/effector associations are ancestral to any given species. For example, the association of the pvc17 effector with PVCu4, and the multiple linked effectors with the PVClopT operon in both Pa ATCC43949 and Pl TT01 . Conversely other pvc-operons show evidence of recent horizontal acquisition of their 3'linked effectors, for example PVCcif and PVCpnf (not shown).

Expression of PVCpnf in vitro and in vivo
A previous RNA-seq analysis of global transcription in three strains; P. asymbiotica ATCC43949 (Mulley et al., 2015), P. asymbiotica Kingscliff and P. luminescens TT01 (unpublished) showed condition dependent expression of certain pvc-operons but not all. Therefore, due to the diversity of pvc operons and effectors in Photorhabdus, we focused on a single model class I pvc operon, [Pa ATCC43949 PVCpnf], to elucidate the relationship between the conserved structural and effector proteins. This operon was selected as it elaborates a well-defined needle complex structure (as observed by electron microscopy) which has potent insect killing activity when heterologously expressed in E. coli (Yang et al., 2006). This operon has two putative effector genes in the downstream 'payload region', PAU_03337, which shows similarity to adenylate cyclase toxins (e.g. the anthrax Edema Factor and Pseudomonas ExoY toxin) and pnf (PAU_03332). While the predicted activity of PAU_03337 has not been tested directly, when expressed in the NIH-3T3 cell cytoplasm (in transient transfection experiments) it did produce a highly unusual cytoskeleton phenotype (Yang et al., 2006). Pnf (Photorhabdus necrosis factor) is a homologue of the active site domain of the Yersinia CNF2 (Cyto Necrosis Factor 2) toxin, which has small-GTPase deamidase and transglutaminase activities (Knust and Schmidt, 2010).
In order to confirm the expression of this model pvc-operon in Photorhabdus during an insect infection we constructed transcription-translation reporter plasmids in which the promoter regions and the first 150 bp of coding sequence of pvc1, pnf [both from Pa ATCC43949 PVCpnf] and the P. asymbiotica chromosomal rpsM ribosomal 'housekeeping' gene (as a positive control) were genetically fused in frame to a gfpmut2 gene with no start codon (referred to hereon as pvc1::gfp, pnf::gfp and rpsM::gfp reporters). Note, the genomic context and our previous unpublished RT-PCR studies suggested that pnf had its own promoter and could be transcribed independently of the pvc structural genes. As we are unable to transform Pa ATCC43949 itself, these plasmids were transformed into the well-characterised and genetically tractable strain P. luminescens TT01 to provide suitable reporter strains for in vitro and in vivo expression studies. For in vitro studies we cultured the bacteria in LB medium supplemented with Manduca sexta clarified hemolymph and grown to late stationary phase, before microscopic examination ( Figure 2A). For in vivo studies, we injected a low inoculum (c.a. 100 CFU) of the reporter strains into M. sexta, and allowed the infection to establish for 12 hr before macroscopic examination of insect tissues in situ using a (fluorescence) dissecting microscope. We also took hemolymph samples from these insects and visualised the hemocytes and bacteria microscopically using confocal microscopy. This approach provides confidence that the cells showing gfp expression are those in the process of a normal productive infection rather than those carried through in the inoculum. Figure 2A shows expression of GFP reporter from the rpsM positive control and both the pvc1:: gfp and pnf::gfp reporters in LB supplemented with M. sexta hemolymph, although not in all cells of the bacterial population (see below). Furthermore, we also saw expression in bacteria in the ex vivo hemolymph samples taken during infection of live insects ( Figure 2A). It was also possible to confirm expression of pnf::gfp in bacteria attached to the insect trachea in localised putative biofilm masses. In this case, while the expected insect melanisation immune response could be seen to have occurred elsewhere on the trachea, it was notably absent from the pnf expressing bacterial biomass ( Figure 2B).
We subsequently expanded this analysis to include a panel of transcription-translation reporter plasmids for different PVC operons from two different species of Photorhabdus. We cloned around 500 bp of the 5' regions (containing the promoter, translation initiation region and first ATG of pvc1 translationally fused to gfp) of P. luminescens TT01 ; PVCunit1, PVCunit4, PVClopT and PVCcif and from P. asymbiotica PB68.1 ; PVCpnf, PVCunit, PVClopT and PVCcif (see supplementary file 'Reporter construct primers'). Each of the eight reporter constructs were then transformed into the relevant Photorhabdus strain and examined using fluorescent microscopy to assess the expression patterns across growth phases, when grown in LB with aeration and maintaining plasmid marker selection. We initially focused on the P. asymbiotica PB68.1 [PVCpnf] reporter strain as it represents an orthologue of the P. asymbiotica ATCC43949 PVCpnf operon, which is the model operon central to this report. We observed a high level of population heterogeneity in expression, usually with only very few cells expressing GFP at any one time (Figure 2-figure supplement 1). Image analysis provides an objective assessment of heterogeneity, and small percentage of cells expressing Gfp, and thus the pvc-operon (Figure 2-figure supplement 2). Interestingly, a similar pattern of heterogeneity in expression was seen for the other seven operon reporter constructs from both Pa PB68 and Pl TT01 (Figure 2-figure supplements 3 and 4). Note in certain cases we saw no expression at all (e.g. the PVClopT operon of Pa PB68.1 ), which fits with the low or lack of mRNA expression seen in a previous in vitro RNAseq study for the majority of pvc-operons (upublished data). We also assessed  pnf PVC pvc1 pvc5 pvc8 pvc14 pvc15 lysR pnf 1 2 3 4 5 6 7 8 9 1 2 3 4 5 6 7 8 9 1 2 3 4 5 6 7 8 9 1 2 3 4 5 6 7 8 9 1 2 3 4 5 6 7 8 9 1 2 3 4 5 6 7 8 9 1 2 3 4 5 6 7 8 9 pvc15 pnf rpsM C B expression in biofilms grown statically on glass slides and observed the same pattern, though with even fewer cells seen to express GFP (not shown).

Ms
In order to corroborate the observations made using the plasmid-based reporter constructs in P. luminescens TT01 during infection we also performed RT-PCR analysis of transcription of the PVCpnf chromosomal operon in the original Pa ATCC43939 strain. This confirmed transcription across the operon in vitro when the bacteria were grown at either 28˚C or 37˚C, although transcription of certain genes was difficult to detect in vivo during Manduca sexta infections (Figure 3).

The Pnf effector protein is physically associated with the PVC needle complex
We investigated if the Pnf effector protein actually becomes physically associated with the pvcencoded needle complex we had previously visualised by electron microscopy (Yang et al., 2006). While a recent publication has described a cryo-EM structure of this particular PVC needle complex (Jiang et al., 2019), they did not include expression of an effector. In order to investigate if the complex does indeed physically associate with a cognate effector, we raised anti-peptide antibodies against synthetic peptides representing amino acids 206-219 of effector Pnf (TGQKPGNNEWKTGR) and amino acids 130-143 (DGPETELTINGAEE) of the predicted outer sheath protein Pvc2. We then used these antibodies to probe PVCpnf needles expressed from cosmid clones in E. coli. Previously we used 2D-SDS PAGE analysis of PVCpnf needle complex produced by these same cosmid clones to confirm the presence of Pvc2, along with Pvc1, 3, 5, 11, 14 and 16 proteins (Yang et al., 2006 and unpublished data). We confirmed specificity of the Pnf antibody using western blot analysis of extracts of E. coli heterologously expressing Pnf alone.
We first used the anti-Pnf peptide antibody to test for the presence of Pnf protein in supernatants from the native bacterial strain Pa ATCC43949 . We initially tested for the presence of Pnf in clarified supernatants and particulate preparations of stationary phase cultures. Previous studies reporting successful detection of Photorhabdus secreted insecticidal toxins under similar conditions.
We could detect Pnf in preparations enriched for the complexes but not in clarified supernatants. More specifically, the Pnf protein could only be detected in the needle complex fraction of wild-type Pa ATCC43949 which was isolated from 250 ml overnight cultures using DEAE-Sepharose chromatography but not in concentrated supernatant collected from a culture grown from the same starter and under the same conditions. The toxin could only be detected if the needle complexes were first either chemically or physically disrupted before electrophoresis ( Figure 4B). Taken together these findings are consistent with the hypothesis that the Pnf protein is sequestered inside the needle complex or in some other configuration such that the TGQKPGNNEWKTGR epitope is physically hidden from access by the antibody. There is still the potential that the toxin is released in the supernatant but at not detectable amounts in these conditions. Secondly, we enriched needle complexes from insect toxic supernatants of an E. coli cosmid clone that encodes the Pa ATCC43949 PVCpnf operon, as previously described (Yang et al., 2006). The anti-Pnf antibody was used for in situ labelling of Pnf on Transmission Electron Microscopy grids, visualised with negative staining and an anti-rabbit gold-conjugate secondary antibody. It was only possible to detect Pnf protein near the ends of either contracted or damaged needle complexes ( Figure 4A). Note we saw no non-specific labelling when the gold-conjugate secondary antibody was used alone. As the full cryo-EM structure of this model PVCpnf was recently published, it allowed us to examine the location of the epitope we used to raise and anti-peptide antibody to the main outer sheath component Pvc2. While the epitope should indeed be surface exposed based on our analysis, we nevertheless only saw an anti-Pvc2 signal associated with what appeared to be disrupted fragments of needle complexes. We therefore surmise that the secondary structure of Pvc2 in the intact needle abolishes antibody binding to the epitope we selected.
The Pnf protein requires delivery into the eukaryotic cell cytoplasm to exert its effect In a previous publication we reported that injection of an enriched Pa ATCC43949 PVCpnf needle complex preparation; heterologously produced by an E. coli cosmid clone, caused melanisation and death of Galleria mellonella larvae within 30 min. In addition, microscopic analysis of phalloidin stained hemocytes taken from these dying animals revealed the cells were shrunken with highly Pnf Clarified supernatant Needle complex (particle preps) 1 2 3 4 5 6 7 8

No primary (control) Anti-Pvc2
Anti-Pnf A Figure 4. Pnf protein can only be detected in discharged or disrupted needle complexes using antibody based analysis. (A) Representative images of immuno-gold stained transmission electron microscopy grids confirming the Pnf-payload toxin is associated with the needle complex. PVCpnf needle complexes (PVC-NC) were prepared from supernatants of the E. coli 4df10 cosmid clone, which encodes the PVCpnf operon. We used anti-peptide antibodies against Pvc2 (DGPETELTINGAEE) and Pnf (TGQKPGNNEWKTGR) epitopes to localise these protein subunits. The Pvc2 epitope appeared to only become accessible to the antibody when subunits were 'broken off' the ends (white arrows). The Pnf toxin could also only be detected at the ends of broken or contracted suggesting they are contained within the complex (black arrows). (B) Western blot analysis confirms that the Pnf protein can only be detected using the anti-peptide antibody if the needle complex is either chemically or physically disrupted. These preparations were taken from Pa ATCC43949 supernatants. The inability to detect Pnf in clarified supernatants confirms all the protein is associated with the PVC-NC enrichment preparation. Lanes 1 + 5; sonicated samples, 2 + 6; 1M NaCl treatments, 3 + 7; 1% SDS treatments 4 + 8; 1M Urea treatments. Note the PVC-NC appears stable in 1M NaCl. DOI: https://doi.org/10.7554/eLife.46259.015 condensed cytoskeletons, and likely already dead. This effect was abolished by heat denaturing the preparation. In this same publication (Yang et al., 2006) we demonstrated that transient cytoplasmic expression of the Pnf protein caused extensive cytoskeleton re-arrangement and likely cell death in cultured Human HeLa ATCC CCL2 cells, similar to that observed in the ex vivo G. mellonella hemocytes. In an attempt to directly visualise the interaction of the heterologously produced PVCpnf needle complex with insect hemocytes and to determine the initial effects on the cellular morphology, we injected intact or heat denatured PVCpnf needle complex preparations into 5 th instar Manduca sexta larvae before bleeding the animals and preparing their circulating hemocytes for surface examination by cryo-SEM. The surface of hemocytes taken from insects that had been injected with intact complex showed membrane ruffling consistent with the predicted mode of action of the Pnf protein (see below). Furthermore, we could also see linear structures approximately 150 nm in length on the surface of the cells near the sites of membrane ruffles consistent with attached needle complexes. The surface of the control hemocytes taken from insects that had been injected with heat-denatured complex remained relatively smooth and homogeneous and we saw no equivalent linear structures. Figure 5 shows representative images from these experiments. We wished to know if the Pnf effector could exert this toxic effect independently of the needle complex, when applied externally to eukaryotic cells. Therefore, we heterologously expressed (in E. coli) and purified the Pnf protein in addition to a predicted toxoid derivative. The wild-type Pnf protein and toxoid derivative were purified using HisTrap Ni 2+ -affinity columns with the fast phase liquid chromatography (FPLC) AKTA system as described in the methods. SDS-PAGE was used to confirm high levels of purity and that no obvious degradation had occurred. The toxoid was designed based on homology between Pnf and the CNF2 toxin active site, wherein we mutated the cysteine at amino acid position 190 into an alanine (Pnf C190A ). Firstly, neither purified wild type nor toxoid proteins had any obvious toxic effect when injected into cohorts of G. mellonella, even at high doses (data not shown). We subsequently used bioPORTER, a liposome based transfection system, to introduce the purified proteins directly into cultured human cells. We visualised effects on the cytoskeleton and nucleus using TRITC-phalloidin and DAPI staining respectively. The wild type Pnf protein had a very clear effect on the cells, producing phenotypes consistent with those predicted by similarity to the CNF2 toxin. CNF2 is known to modify the cellular Rho GTPases, RhoA, Rac1 and Cdc42. Pnf delivery as a bioPORTER formulation led to the formation of F-actin filaments within 24 B A Figure 5. Visualisation of PVC needle complexes on the cell surface. Cryo-SEM analysis of ex vivo hemocytes from 5 th instar Manduca sexta that had been injected with (A) native or (B) heat inactivated enriched preparations of Pa ATCC43949 PVCpnf needle complexes heterologously produced by the E. coli cosmid clone. Note the abundant linear structures believed to be the PVC needle complex (yellow arrows) and membrane ruffling effect (red arrows) absent from the control treatment. DOI: https://doi.org/10.7554/eLife.46259.016 hr followed by multi-nucleation by 48 hr, phenotypes consistent with the modification of the Rho GTPases. The toxoid derivative, delivered at the same dose using the same approach, produced no changes, giving cellular phenotypes consistent with that of the negative control or of the wild-type Pnf protein topically applied without the bioPORTER transfection agent ( Figure 6). Computational secondary structure predictions of the toxin and toxoid were performed to assess the potential impact of the C190A active site amino acid substitution using the Phyre2 algorithm. We obtained structural predictions (100% confidence score) based on similarity to the known structure of a E. coli CNF1/2 family toxin active site domain (PDB Entry: 1hq0), which revealed only very minor predicted changes ( Figure 6-figure supplement 1).

The pnf protein effector modifies small rho GTPases
Based on homology to CNF2 the effect of Pnf on target cell proteins is predicted to include the modification of several Rho-family GTPases. Therefore, we used western blot assays to examine in  Figure 6. Pnf needs to gain access to the host cell cytoplasm to induce F-actin formation and multi-nucleation in cultured HeLa cells. Wild-type and inactive toxoid mutant Pnf protein was delivered topically using BioPORTER. Cell cytoskeleton is stained with TRITC-Phalloidin and the cell nuclei with DAPI. This gave rise to phenotypes consistent with the molecular targets and that of the Yersinia CNF2 protein homologue. Note we see the F-actin formation by 24 hr (white arrows) preceding extensive multi-nucleation of the host cell by 48 hr (yellow arrows). Note neither application of the Pnf toxoid in a BioPORTER formulation or the purified wild-type Pnf protein without BioPORTER had any observable effect on the cells. DOI: https://doi.org/10.7554/eLife.46259.017 The following figure supplement is available for figure 6: vitro transglutamination and deamidation effects of purified heterologously produced Pnf on purified small GTPases RhoA, Rac1 and Cdc42. The RhoA, Rac1 and Cdc42 were purified from E. coli heterologous expression strains using GSTrap HP affinity columns with the FPLC AKTA system in accordance with previously published protocols, as described in the methods. SDS-PAGE analysis was used to confirm good levels of purity and lack of any significant degradation. Transglutamination is the formation of a covalent bond between a free amine group, as may be found on a lysine residue, and the gamma-carboxamide group of glutamine. As a result protein electrophoretic mobility of the protein is altered. Deamidation is a chemical reaction in which an amide functional group is removed from the protein, which may be detected using deamidated protein specific antibodies. These experiments demonstrated that Pnf induced transglutamination and deamidation of both RhoA and Rac1 (Figure 7), although unlike the reported activity of CNF2, had no effect on Cdc42. As predicted the active site toxoid mutant had no enzymatic activity on any of the three Rho GTPases confirming it was a true toxoid derivative.

Discussion
An analysis of the different subunit proteins of PVCs shows they share several elements in common with other contractile phage-tail derived systems, including the Type VI secretion system (T6SS) (Kapitein and Mogk, 2013) and to a lesser extent R-type pyocins (Taylor et al., 2018  membrane complex for anchoring and synthesis and are freely released from the producing bacterial cell. Therefore, in common with R-type pyocins, they can act at a distance. Secondly, like T6SS but unlike R-type Pyocins, they are evolved to inject bioactive protein effectors into other cells. We hypothesise that the PVCs are evolved to specifically target eukaryotic cells, unlike T6SS, which have been shown to be able to deliver to both eukaryotes and prokaryotic competitors. However, while our previous attempts to show PVCpnf attachment to a range of bacterial species from different genera showed no binding we could detect (data not shown), we cannot rule out the possibility that homologues exist which are able to target prokaryotes. We speculate that these large protein complexes are costly for the cell to produce, consistent with the observation of population heterogeneity of pvc-operon expression. Indeed, uncontrolled heterologous over expression of the Pa ATCC43949 PVClopT and PVCpnf operons in cosmid clones in E. coli, results in deletion of regions of the pvc-operon (confirmed by sequencing) and significant loss of culture viability (not shown). It should be noted that in a natural insect infection the vast majority of the Photorhabdus bacterial population are sacrificial. The majority of the population act as a food source for the replicating nematodes, with very few cells passing into the next generation of infective juvenile nematodes (Ciche et al., 2008). As such the population may restrict PVC production to a limited number of sacrificial cells. We have noted the presence of holin-lysin gene homologues tightly linked to certain pvc-operons, including both 5' and 3' to the Pa ATCC43949 PVCpnf operon which we focus on in this publication. Release by cell lysis would be consistent with the proposed method of release of the related MAC arrays of Pseudoalteromonas (Shikuma et al., 2014). Nevertheless, to date we have not directly observed any cell lysis associated with pvc expression in Photorhabdus itself.
The finding that Pa ATCC43949 PVCpnf, and seven other pvc-operons from Pa PB68 and Pl TT01 (not shown) all show population heterogeneity in expression, at least in vitro, suggests that they are likely deployed in a highly regulated and conservative manner. While it is difficult to fully characterise this heterogeneity in vivo, the PVCpnf GFP reporter strain did show restricted expression to one specific tissue, the insect trachea, and not throughout the body of the animal. In regards to these experiments, it should be noted that we did not see any melanisation response around the bacterial biomass showing GFP. The insect melanisation immune response is typically activated at sites of encapsulation. This is mediated by the recruitment of hemocytes, surrounding and enclosing foreign bodies, and entombing them in melanin. The absence of melanisation around this GFP expressing bacterial mass is consistent with the expression of anti-hemocyte virulence genes, which are likely to include the native Pl TT01 pvc-operons.
Examination of the promoter regions has provided no clue as to the mechanism of population heterogeneity of expression. Nevertheless, the identification of RfaH and a second cryptic conserved potential operator sequence upstream of the pvc1 genes provides a starting point for addressing this in future. Operons containing the second cryptic putative regulatory sequence include [Pl TT01 PVClopT] and [Pl TT01 PVCu4]. Analysis of the supplementary data from a recently published RNA-seq study (Tobias et al., 2017), suggests that these operons may be dependent upon Hfq/ HexA activity (Joyce and Clarke, 2003).
Unlike many of the other genera in which we see pvc-like operons, Photorhabdus genomes encode multiple copies, typically around 5 to 6, suggesting they play important and diverse roles in the life cycle. With this in mind, we examined the conservation of the different subunit genes between operons. We observe a 'break point' in conservation, toward the 3' end of the operons. We postulate this may be due to imprecise recombination events in the 3' payload regions of pvcoperons, where incoming sequences, which have a GC-content that is distinct from the host genome, gradually 'erode' the upstream sequence. Alternatively, it is plausible that the lower GC at the distal end of these long operons (each of~25 kb) may assist in strand separation during transcription, maintaining stoichiometry for these large, multi-subunit structures. Indeed low GC stretches of DNA are common origins of replication because of their reduced strand separation energy (Meijer et al., 1979). However, as yet we do not know whether the pvc1 promoter serves the whole operon, or if there are additional promoters internal to the operon.
Each of the pvc-operons in a Photorhabdus genome encodes multiple paralogous copies of pvc1/ 5 and pvc2/3/4 genes. We were therefore surprised not to see any operons showing signs of genetic degradation. This suggests there is sufficient positive selection for maintaining these multiple operons, with each operon potentially adapted for a specific role. This hypothesis is supported by the high variation in the Pvc13 protein sequences, which we speculate represent the host cell binding fibres. The need to maintain multiple copies of pvc-operons may also have arisen if the structural genes for the needle complexes are specifically adapted for delivery of their cognate cis-linked effector proteins in some way.
Circumstantial evidence from genomic sequences and previous work on the related AFP system of Serratia has suggested the needle complexes serve to deliver the cis-encoded effector proteins. We present here for the first time direct evidence that a linked effector protein does in fact become physically associated with the needle complex. Western blot detection of Pnf from preparations enriched for needle complexes taken from the native Pa ATCC43949 supernatants confirmed it was being expressed in vitro and suggested it was physically associated with the complexes. In addition, physical or chemical disruption was required to release the Pnf protein for detection. When taken alongside the immuno-gold EM observations, showing Pnf could only be seen near contracted or damaged needle complexes, it confirms the protein is either sequestered inside the complex or physically associated in such as way that the TGQKPGNNEWKTGR epitope is not solvent accessible. The anti-Pvc2 antibody is able to specifically detect the protein in Western blots, however it only showed binding to what appeared to be disrupted fragments of needle complexes, again suggesting the relevant epitope is not accessible in the intact native needle complex structure. Indeed, iTasser structural model simulations of a PVC outer sheath Pvc2 protein, using the homologous Pseudomonas 3J9Q PDB structure of an R-type pyocin outer sheath as a model (Ge et al., 2015), supports this idea, suggesting the epitope is partially occluded between adjacent subunits.
While we have not yet directly demonstrated injection of Pnf into host cells by the needle complex, the results of the topical application and bioPORTER transfection experiments confirmed that the Pnf effector absolutely requires a mechanism to facilitate entry into the host cell cytoplasm to exert its effect. We argue the evidence for injection by the needle complex is very strong, and is corroborated by the SEM visualisation of needle-like structures of the correct dimensions on the surface of intoxicated hemocytes. Finally, we have confirmed that Pnf acts in a manner similar to the Yersinia CNF2 toxin, modifying two of the same Rho-GTPases, which correlates with the observed phenotypic effects on the cell.

Insects, bacterial strains and growth conditions
Manduca sexta (Lepidoptera: Sphingidae) were individually reared as described (Reynolds et al., 1985). Briefly, larvae were maintained individually at 25˚C under a photoperiod of 17 hr light: 7 hr dark and fed on an artificial diet based on wheat germ. Larvae 1 day after ecdysis to the 5th instar were used for all experiments. Batches of wax moth larvae (75 g; Livefood UK Ltd, Rooks Bridge, UK) in their final instar stage were stored in the dark at 4˚C and used within a week of receipt. DH5a E. coli (containing various plasmid constructs) were grown on LB agar at 37˚C or in LB liquid, shaking at 200 rpm. Spontaneous rifampicin-resistant mutants of Photorhabdus asymbiotica subsp. asymbiotica Thai (strain PB68.1) (Thanwisai et al., 2012) and Photorhabdus luminescens subsp. laumondii TTO1 (Duchaud et al., 2003) were used in these studies as hosts for reporter plasmids. Photorhabdus were routinely cultured in LB broth or on LB agar supplemented with 0.1% (w/v) pyruvate at 30C or 37˚C (for P. asymbiotica). When required antibiotics were added at the following concentrations: ampicillin (Amp): 100 mg ml À1 , kanamycin (Km): 25 mg ml À1 , chloramphenicol (Cm): 25 mg ml À1 , rifampicin (Rif): 25 mg ml À1 . Human adenocarcinoma HeLa ATCC CCL2 cells (obtained from ATCC culture collection -mycoplasma free) were cultured for 10 passages in Dulbecco's modified Eagle medium (Sigma-Aldrich) containing 4.5 g/L glucose (Sigma-Aldrich), 10% heat-inactivated fetal bovine serum (Sigma-Aldrich), 2 mM glutamine (Sigma-Aldrich), 100 mg /mL penicillin, and 100 mg/ mL streptomycin (Sigma-Aldrich) and incubated at 37˚C and 5% CO 2 .

PVC gene reporter plasmid construction
Translational fusions with the gfpmut2 gene were constructed by PCR in a pACYC184 vector containing the gfpmut2 (pACYC-GFP) (Jacobi et al., 1998) as follows. The pvc1, pnf and rpsM genes (consisting of promoter regions and the first 150 bp of coding sequence) were amplified from P. asymbiotica ATCC43949 genomic DNA and cloned into pACYC-gfp to generate pACYC-afp1-gfp, pACYC-pnf-gfp and pACYC-rpsM-gfp. The constructs were further digested to release the pvc1, pnf or rpsM genes in frame with gfp and the fusion fragments were cloned into pBBR1-MCS (Kanter-Smoler et al., 1994) to generate pBBR1-pvc1-gfp, pBBR1-pnf-gfp and pBBR1-rpsM-gfp. Mating experiments were performed as previously described (Brillard et al., 2002) to transfer plasmid constructs into P. luminescens TTO1 resulting in Pl TTO1 -pvc1-gfp, Pl TTO1 -pnf-gfp and Pl TTO1 -rpsM-gfp. Plasmid stability was confirmed in bacteria harbouring the various constructs isolated after in vivo passages. For the expanded panel of gfp-reporter fusions, the promoter regions for the operons selected, inclusive of the putative RfaH operator sites (if present), and the native RBS and first codon of the pvc1 gene (approximately 500 bp upstream), were cloned in to the pAGAG vector. pAGAG was derivatised from the promoterless pGAG1 gfp bearing plasmid., In brief, pGAG1 was used as a template to amplify gfpmut3* without a start codon using primers pG_GFPfor (5'-aatgtcgaccgtaaaggagaagaacttttc) and pG_GFPrev (5'-aatactagtggatctatttgtatagttcatccatg). The resulting product and the pGAG1 vector were cut by digestion with SalI-HF and SpeI and ligated together, thus replacing the original intact gfpmut3* gene with one that lacks a ribosome binding site and the first ATG codon. This reporter plasmid backbone was used to construct a panel of specific transcription-translation reporter plasmids for different pvc-operon 5' promotor regions. In brief regions 5' to the pvc1 open reading frames from each operon were PCR amplified from P. luminescens strain TT01; PVCu-nit1, PVCunit4, PVClopT and PVCcif and from P. asymbiotica strain PB68.1; PVCPnf, PVCunit, PVClopT and PVCcif. Primers used are shown in Supplementary file 'Reporter construct primers'. All upstream promoter regions were incorporated between the KpnI and BamHI sites of the pAGAG vector. After initial cloning into E. coli, correct constructs, as confirmed by DNA sequencing, were transformed into the relevant Photorhabdus strain (P. luminescens TT01 or P. asymbiotica PB68.1) for fluorescent microscopy studies. (Figure 2-figure supplements 1, 2, 3 and 4).

Image analysis of reporter strain expression heterogeneity
Quantitative image analysis of micrographs of P. asymbiotica PB68.1 harbouring the Pa PB68 PVCpnf pvc1 promoter fusion construct was performed using Fiji. Brightfield images were used to automatically detect the bacteria by converting the image to binary, followed by edge detection and particle analysis with the size of the particles set to 0.5-7 mm 2 . The resulting regions of interest when then used to measure the intensity in the corresponding green channel (for GFP detection). At least four images were used per time point with a minimum total number of cells of 450 for each time point. The control consists of images taken of P. asymbiotica PB68.1 harbouring the negative control plasmid pAGAG and for the purposes of this analysis the mean intensity per cell calculated for each time point were combined to find a threshold value for subtraction of background fluorescence. For the calculation of the percentage number of green cells for each time point, a threshold of 1200 was used above which there were no control cells with this mean intensity value. Raw data can be seen in Figure 2-figure supplement 2-source data 1.

Fluorescent reporter strain assays In vitro experiments
Reporter strains were cultured with shaking aeration in LB liquid medium supplemented with 20% (v/ v) freshly harvested 5 th instar M. sexta clarified hemolymph. To obtain the hemolymph, insects were chilled on ice for 20 min before being bled (by cutting the tip of the tail horn) into a tube on ice, containing 10 ml of saturated Phenol Thio Urea (PTU) solution, which prevents melanisation. Hemolymph was clarified by centrifugation to remove hemocytes and other debris. Bacteria were grown to late stationary phase, before microscopic visualisation using a Leica inverted epi-fluorescent microscope.
In vivo experiments, we injected ca. 100 cells of the reporter strains into cohorts of 5 th instar M. sexta, and allowed the infection to establish before macroscopic examination of insect tissues using a (fluorescence) dissecting microscope. We also took hemolymph samples from these insects and performed microscopic examination of fixed ex vivo hemocytes stained with phalloidin conjugate and confocal microscopy to visualise host cell cytoskeleton and any GFP expression from the recombinant bacteria. Images were acquired with a LSM510 confocal microscope (Leica).
PVC purification from E. coli cosmid clone supernatants and electron microscopy Cosmid libraries of P. asymbiotica ATCC43949 were prepared in E. coli EC100 and arrayed into 96-well microtiter plates by MWG Biotech, Munich, Germany, as described previously (Waterfield et al., 2009b;Daborn et al., 2002). A 250 ml overnight culture of E. coli with the Pa ATCC43949 PVCpnf cosmid (c4DF10) and a wild-type Pa ATCC43949 were grown in LB medium supplemented with 100 mg ml À1 ampicillin (in case of the cosmid strain) at 28˚C with aeration in the dark. The cultures were centrifuged at 6800 x g at 4˚C for 30 min at 4˚C. The supernatants were decanted to remove each cell pellet, and the centrifugation procedure was repeated to remove any remaining cells. Cell-free supernatants were then centrifuged, in small batches, at 150,000 Â g for 90 min at 4˚C to harvest particulate material. The particulate pellets were washed by gentle re-suspension in 1 Â Phosphate Buffered Saline (PBS) before a second centrifugation at 150,000 Â g for 90 min at 4˚C to pellet the particulate material. Each pellet was further separated by DEAE-Sepharose chromatography. 10 ml of particulate material in ice-cold PBS were mixed with an equivalent volume of DEAE-Sepharose CL-6B anion exchanger (in PBS) and the preparation was incubated at room temperature for 15 min. The Sepharose resin was harvested by centrifugation (3,000 Â g), and the supernatant was discarded. The resin was resuspended in 40 ml of ice-cold PBS and again harvested by centrifugation. This washing step was repeated another three times, and the resin was finally resuspended in 10 ml of elution buffer (0.5 M NaCl, 50 mM phosphate buffer [pH 7.4]). The resin was removed by centrifugation, and the supernatant containing the PVCs was again centrifuged at 150,000 Â g for 90 min at 4˚C to pellet the particulate material and concentrate the needle structures in 500 ml of ice-cold PBS. For transmission electron microscopy (TEM) pioloform-covered 300-mesh copper grids that were coated with a fine layer of carbon were used as substrates for the protein fractions. The following four aqueous negative stains were tested with the protein samples: 1% uranyl acetate, 3% ammonium molybdate, 3% methylamine tungstate, and 2% sodium silicotungstate. The preferred stain, 3% methylamine tungstate, produced acceptable contrast and minimum artefacts and was subsequently used for all samples viewed by TEM. The coated grids were exposed to UV light for 16 hr immediately prior to use to ensure adequate wetting of the substrate. A 10 ml drop was applied to the TEM grid, and the protein was allowed to settle for 5 min. Liquid was absorbed with filter paper from the edge of the grid and replaced immediately with 10 ml of filtered negative stain. The drop was partially removed with filter paper, and the grids were allowed to air dry thoroughly before they were viewed with a JEOL 1200EX transmission electron microscope (JEOL, Tokyo, Japan) operating at 80 kV.
Production and isolation of secreted Pnf from wild-type P. asymbiotica ATCC43949 was performed at the same time as the production and isolation of wild-type needle complex in a duplicate culture. Bacterial cultures were grown from the same starter culture and under the same conditions. However, for isolation of secreted proteins, the supernatant was filtered through 0.45 mm and 0.22 mm filters to remove any remaining bacteria and particulate matter. Then it was concentrated using 4% TCA overnight at 4˚C and the next morning washed and resuspended in approximately 10 ml of 50 mM Tris-HCl pH 7.4. The secreted proteins were further concentrated using Amicon filters with NMWL of 10 kDa to 500 ml.

Pnf cloning and heterologous expression for Galleria injection and antibody specificity test
Pnf gene was amplified from P. asymbiotica ATCC43949 genomic DNA (using primers Pnf_NdeI 5'-ATATATCATATGATGTTAAAATATGCTAATCCT-3', Pnf_BamHI 5'-ATATATGGATCCTTATAA-CAACCGTTTTTTAAG-3') and the PCR product was purified and cloned in-frame with a His-tag into the IPTG-inducible expression plasmid pET-15b (Novagen) to create construct pET15b-Pnf. The clone was verified by sequencing and transformed into Arctic Express competent cells (Agilent) for protein expression. A site-directed mutant of Pnf (toxoid) was generated with the QuikChange sitedirected mutagenesis kit (Agilent). To construct the Pnf mutant plasmid pET15b-Pnf C190A , pET15b-Pnf was amplified with FPLC-purified primers designed to generate a Cys to Ala substitution at position 190 (Pnf C190A _for 5'-TCACCGAATATACCATAGTAGCACCGCTCAATGCTCCAGAC-3', Pnf C190A _rev 5'-GTCTGGAGCATTGAGCGGTGCTACTATGGTATATTCGGTGA-3') using the following thermal profile (step 1: 95˚C for 30 s, step 2: 95˚C for 30 s, 55˚C for 60 s, 68˚C for 6 min 45 s for À80˚C glycerol stocks were used to inoculate 5 ml of fresh LB medium supplemented with 0.2% (w/ v) glucose and 100 mgml À1 ampicillin. Bacteria were grown overnight at 30˚C with shaking, and 1 ml of the culture was then harvested, re-suspended in 100 ml of the same medium, and incubated in an orbital incubator at 37˚C until the optical density at 600 nm was 0.7 to 0.9. Cells were then harvested at room temperature by centrifugation at 4,000 rpm for 10 min. The pellet was re-suspended in 100 ml of fresh LB medium supplemented with the 100 mg ml À1 ampicillin and 0.1 mM of the inducer isopropyl-b-d-thiogalactopyranoside (IPTG). Optimized times for inductions were determined experimentally, and cells were then harvested. The bacterial cell pellet was re-suspended in 10 ml of 1x PBS and sonicated (four 20 s sonications at 45 mA using a Branson 450 digital Sonifier fitted with a tapered probe). The freshly sonicated samples were then diluted in 1x PBS for injection into Galleria larvae and for SDS-polyacrylamide gel electrophoresis analysis to confirm expression of the target protein. For toxicity testing cohorts of Galleria larvae (n = 20) were chilled on ice before injection with 10 ml of a dilution series (in sterile PBS) of sonicated cells expressing Pnf or vector control. Insects were then returned to room temperature and observed for 5 days or mortality or morbidity.

Recombinant Pnf and small Rho-GTPase purification
ArcticExpress containing pET-15b-Pnf were initially grown in LB broth supplemented with 100 mg ml À1 ampicillin at 37˚C until OD 0.6 when Pnf expression was induced with a final concentration of 0.1 mM of IPTG at 12˚C for 16 hr to produce soluble Pnf. Pnf was purified over HisTrap Ni 2+ -affinity column with the fast phase liquid chromatography (FPLC) AKTA system as per the manufacturer's protocol (GE Healthcare). Plasmids pGEX-2T-wtRhoA, pGEX-2T-wtRac1 and pGEX-2T-G25K (Cdc42) were gifts from Prof Alan Hall (University College London, London, UK) and were maintained in E. coli DH5a grown on LB agar or in LB broth supplemented with 50 mg ml À1 ampicillin. RhoA, Rac1 and Cdc42 were purified over GSTrap HP affinity columns with the FPLC AKTA system as per the manufacturer's protocol (GE Healthcare).

BioPORTER assay and actin stress fibre analysis
For BioPORTER assays, 80 ml of purified wild type and mutant Pnf proteins (500 mg ml À1 ), or PBS as a negative control, were added to one BioPORTER tube (Genlantis) and resuspended in 920 ml of DMEM. The samples were added to Human HeLa ATCC CCL2 cells (ATCC collection) grown in 6well plates and incubated for 4 hr. BioPORTER/protein or PBS mixes were replaced by fresh complete medium and the cells were incubated for 20-48 hr. To visualise cell morphology and actin cytoskeleton, cells were fixed for 15 min in 4% PBS-formaldehyde, permeabilized with 0.1% Triton X-100 and stained with Tetramethylrhodamine B isothiocyanate (TRITC)-phalloidin (Sigma) and DAPI dihydrochloride (Sigma). Images were acquired with a LSM510 confocal microscope (Leica).

Deamidation and transglutamination of Rho GTPases Deamidation assay
Deamidation assays were done according to previously described procedures (Schmidt et al., 1997) with the following modifications. Briefly, a 20:1 molar ratio of GTPase (RhoA, Rac1 or Cdc42) to toxin was incubated in deamidation buffer (50 mM NaCl, 50 mM Tris-HCl pH 7.4, 5 mM MgCl 2 , 1 mM DTT, 1 mM phenylmethanesulphonyl fluoride) for either 30 min or 2.5 hr at 37˚C. Untreated RhoA served as a negative control. After toxin treatment, samples were concentrated by the addition of 10% trichloroacetic acid and stored overnight at 4˚C. Precipitated proteins were pelleted, washed with acetone, air-dried and resuspended in 20 mM Tris-HCl pH 7.4. Samples were subjected to SDS-PAGE and analysed by Western blotting using either an anti-RhoA (1:1500, Santa Cruz Biotechnology), anti-Rac1 (1:5000, Upstate Biotechnology), or anti-Cdc42 (1:1000, Santa Cruz Biotechnology) monoclonal antibody or rabbit polyclonal antisera (1:2000) that had been raised against a peptide antigen specifically designed to detect modified/deamidated RhoA/Rac1/Cdc42 (Sugai et al., 1999), provided by Prof A. D. O'Brien, Department of Microbiology and Immunology at Uniformed Services University, Maryland, USA). Reactive proteins were detected with either the HRP-conjugated goat anti-mouse IgG (Sigma) or donkey anti-rabbit IgG (1:3000, Sigma) followed by visualization with DAB (Sigma).

Transglutamination assay
Transglutamination assays were done as previously described (Schmidt et al., 1999) with several modifications. Briefly, a 2:1 molar ratio of RhoA to toxin was incubated in transglutamination buffer (50 mM Tris-HCl pH 7.4, 8 mM CaCl 2 , 5 mM MgCl 2 , 1 mM DTT, 1 mM EDTA) in the presence of 50 mM ethylenediamine (which raised the pH of the buffer to 9) for 10 min or 1 hr at 37˚C. As a negative control, RhoA was incubated with ethylenediamine but without toxin. Samples (0.25 mg RhoA/ well) were subjected to SDS-PAGE and then processed for Western blot analyses as described above. Immunoblots were probed with a mouse anti-RhoA monoclonal antibody (1:1500, Santa Cruz Biotechnology) and reactive proteins visualised with DAB after incubation with the HRP-conjugated goat anti-mouse IgG secondary antibody.
A bioinformatic analysis of pvc structural operon sequences DNA sequences for each of the 16 conserved structural loci were clustered syntenically (all pvc1s, all pvc2's etc.). % GC content for each CDS in each syntenic position was calculated (up to 16 observations per locus), and plotted as a boxplot via ggplot2 (Figure 1-figure supplement 2). The average GC content across the full operon, as well as for the whole genome, were plotted as intervals in the plot background to show the PVC loci %GC in contrast. The breakpoint was defined by use of the 'cumSEG' package in R (Muggeo and Adelfio, 2011). Amino acid similarity scores (Figure 1-figure supplement 3) were generated by CLUSTAL Omega (Sievers et al., 2011) multiple sequence alignment, using default parameters. Resulting pairwise alignment scores were plotted as boxplots using ggplot.

RNA purification and RT-PCR
For in vitro transcription analysis, overnight cultures of P. asymbiotica were sub-cultured into liquid LB medium and grown with aeration at 28˚C or 37˚C 200 rpm in the dark. Planktonic cultures were collected at 4, 8 and 24 hr and mixed with a double volume of RNAlater (Ambion) and after 5 min incubation, bacteria were harvested by centrifugation and the pellets stored at À80˚C. For in vivo transcription analysis, overnight cultures of P. asymbiotica were extensively washed in PBS and diluted in Grace's insect media (GIM) to achieve 1000 bacteria per 50 ml of culture. Each M. sexta larvae was injected with 50 ml of P. asymbiotica culture and they were placed in a humid temperaturecontrolled room at 28˚C. After 3 hr or 6 hr of incubation, insects were bled in equal volume of GIM containing 20 mM phenylthiocarbamide (PTC). The sample was initially fractionated into plasma and total hemocytes by centrifugation at 200 x g at 4˚C for 5 min, and plasma was further centrifuged at 6800 x g at 4˚C for 5 min to form a bacterial pellet. For each condition, total RNA was extracted using the RNeasy Mini Kit (Qiagen) and 2 mg total RNA was treated with TURBO DNA-free Kit (Ambion) and subjected to RT-PCR using the Qiagen OneStep RT-PCR kit. Each RT-PCR reaction performed in a volume of 50 ml (containing 100 ng template RNA, 1x QIAGEN OneStep RT-PCR buffer, 400 mM dNTPs, 0.6 mM gene specific primers, 5U RNase inhibitor and 2 ml of QIAGEN One- Step RT-PCR enzyme mix) for 28 cycles.