Response Regulator VxrB Controls Colonization and Regulates the Type VI Secretion System

Summary

Pathogenic bacteria experience varying conditions during infection of human hosts and often use two-component signal transduction systems (TCSs) to monitor their environment. TCS consists of a histidine kinase (HK), which senses environmental signals, and a corresponding response regulator (RR), which mediates a cellular response. The genome of the human pathogen V. cholerae contains a multitude of genes encoding HKs and RRs proteins. In the present study, we systematically analyzed the role of each V. cholerae RR for its role in pathogenesis. We identified a previously uncharacterized RR, VxrB, as a new virulence factor. We demonstrated that VxrB controls expression of the type VI secretion system (T6SS), a virulence nanomachine that directly translocates effectors into bacterial or host cells, thereby facilitating colonization by competing with sister cells and intestinal microbiota. This study represents the first systematic analysis of the role of all RRs in V. cholerae pathogenesis and provides a foundation for understanding the signal transduction pathways controlling V. cholerae pathogenesis.

Introduction

Vibrio cholerae causes the diarrheal disease cholera that affects 3 to 5 million people worldwide every year, resulting in 100,000–120,000 deaths annually [1]. V. cholerae produces a number of virulence factors which facilitate colonization of the intestine and subsequent disease. Major virulence factors are cholera toxin (CT), which is responsible for production of profuse watery diarrhea, and a type IV pilus called the toxin-coregulated pilus (TCP), which is required for intestinal colonization [2]. V. cholerae virulence factors are well known to be under extensive transcriptional control. CT and TCP production are controlled by the transcriptional activator ToxT [3, 4]. Expression of toxT, in turn, is controlled by a virulence regulatory cascade involving the membrane-bound transcriptional activators ToxRS and TcpPH. These two regulators activate toxT transcription directly [5–7]. TcpPH expression is activated by the transcriptional activators AphA and AphB [8, 9]. The quorum sensing (QS) regulatory system is also linked to the virulence gene regulatory cascade through HapR, the master QS regulator, which represses aphA expression [10].

Recently, the type VI secretion system (T6SS) has been identified as a new virulence factor in V. cholerae [11, 12]. T6SSs deliver effector proteins into both eukaryotic and bacterial cells in a contact-dependent manner [12, 13]. V. cholerae has one T6SS system with multiple T6SS effectors: VrgG1 and VrgG3 (valine-glycine repeat protein G), which have actin cross-linking activity and peptidoglycan-degrading activity, respectively [14–17]; TseL, which has lipase activity [15, 18]; and VasX, which perturbs the cytoplasmic membrane of target cells [15, 19]. Activity of these effectors is antagonized by corresponding immunity proteins: TsiV3, TsiV1, and TsiV2, respectively, to prevent killing by strains bearing these proteins [15, 16, 20, 21].

The T6SS can be divided into functional sections consisting of the core structural components, the T6SS effector and immunity proteins, and transcriptional regulators. The base of the T6SS apparatus spans the cell envelope, and is a tube within a tube. The inner tube is composed of polymers of the hemolysin coregulated protein (Hcp). The outer tube, also called the contractile sheath, is formed by polymers of VipA and VipB [14, 22]. The Hcp inner tube is capped with a spike complex of trimeric VgrG proteins. The effectors are delivered by contraction of the VipA/VipB sheath, which in turn results in ejection of the inner tube along with VgrG and the effectors towards the target cell [12].

The genes encoding the T6SS components are organized into one large cluster (VCA0105-VCA0124) and two auxiliary clusters (VCA0017-VCA0022 and VC1415-VC1421) [11, 23]. A key positive transcriptional regulator of the V. cholerae T6SS is VasH (VCA0117), which is related to enhancer binding proteins that activate transcription in a σ54 (RpoN) dependent manner [24, 25]. VasH acts on the T6SS auxiliary clusters and vgrG3 of the large cluster, but does not affect expression of the structural genes encoded in the large T6SS gene cluster [24, 26]. Additionally, Hcp production is positively regulated by the master quorum sensing regulator HapR and the global regulator cyclic AMP (cAMP) receptor protein CRP, and negatively regulated by QS regulator LuxO and by global regulator TsrA, a protein homologous to heat-stable nucleoid-structuring (H-NS) [27, 28]. These studies have thus shown that numerous global regulators control T6SS expression, as well as one specific regulator (VasH).

V. cholerae T6SS studies have mainly focused on the V. cholerae O37 serogroup V52 strain because it assembles a T6SS apparatus constitutively [11]. In this strain, the T6SS is required for cytotoxicity towards Dictyostelium discoideum and J774 macrophages, and induces inflammatory diarrhea in the mouse model [29]. In V. cholerae O1 strain C6706, the T6SS is not constitutively produced and conditions that promote T6SS production are unknown. However, production of T6SS can be achieved in other O1 strains by inactivating mutations in genes encoding the LuxO and TsrA negative regulators. In O1 strains, the T6SS translocates T6SS effectors into macrophages, and increases fecal diarrhea and intestinal inflammation in infant rabbits [27]. It was also shown that the V. cholerae O1 C6706 strain T6SS mediates antagonistic interbacterial interactions during intestinal colonization. A strain unable to produce the TsiV3 immunity protein, which provides immunity against the effector VgrG3, exhibited an intestinal colonization defect only when co-infected with strains harboring an intact T6SS locus and VrgG3 [30]. Although T6SS is regulated and expressed differently between V. cholerae strains, production of this system in multiple strains promotes virulence against both eukaryotic and bacterial cells, suggesting the function is largely conserved but the regulation varies.

Pathogenic bacteria experience varying conditions during infection of human hosts and often use two-component signal transduction systems (TCSs) to monitor their environments [31]. TCSs play important roles in the regulation of virulence factors, metabolic adaptation to host environments, and response to numerous environmental stresses including pH, osmolarity, oxygen availability, bile salts, and antimicrobial peptides [32]. TCS rely on a phosphorelay-based signal transduction system. The prototypical TCS consists of a membrane-bound histidine kinase (HK), which senses environmental signals, and a corresponding response regulator (RR), which mediates a cellular response. Response regulators are typically multi-domain proteins harboring a conserved receiver domain (REC) and C-terminal output domain such as DNA-binding, diguanylate cyclase, or methyltransferase [33–35]. Upon environmental stimulation, the HK catalyzes an ATP-dependent autophosphorylation reaction on a conserved histidine residue. The phosphoryl group is transferred from the HK to a conserved aspartate residue on the RR, eliciting a conformation change and subsequent cellular response [32, 34, 35].

The V. cholerae genome reference genome of O1 EL Tor N16961 strain is predicted to encode 43 HK and 49 RR (http://www.ncbi.nlm.nih.gov/Complete_Genomes/RRcensus.html and http://www.p2cs.org). We also included 3 additional RRs (VpsT, VpsR, QstR) which were not annotated in these databases. Thirteen of these 52 putative RRs have been previously characterized and eight have a role in virulence factor production and host colonization: VarA, LuxO, VieA, PhoB, ArcA, FlrC, CarR, and CheY-3 [36–44]. VarA and LuxO repress production of quorum sensing regulator HapR, which represses expression of aphA and, in turn, TCP and CT production [36, 37], VieA regulates ctxAB expression indirectly by affecting production of ToxT through cyclic diguanylate (c-di-GMP) signaling [38, 39]. The RR for phosphate limitation, PhoB, directly controls expression of a key transcriptional regulator, TcpPH, which activates toxT transcription [40]. The RR ArcA controls adaptation to low oxygen environment of the intestine and positively controls the expression of toxT [41]. CarR regulates glycine and diglycine modification of lipid A, confers polymyxin B resistance, and is required for intestinal colonization, although this phenotype is strain dependent [42]. FlrC controls flagellar biosynthesis and CheY-3 is needed for control of chemotactic motility [43, 44]. Both motility and chemotaxis are known colonization factors for V. cholerae [43]. Together, these results show that RRs shown play a role in intestinal colonization have three basic targets: known virulence regulators and concomitant CT and TCP production; lipid A modification enzymes; or motility and chemotaxis. 39/52, however, were not yet analyzed at the time of this study.

To systematically evaluate the role of V. cholerae TCSs in intestinal colonization, we generated in-frame deletion mutants of each RR gene and analyzed the in vivo colonization phenotypes of the resulting mutants. We found 12 RR were required for wild-type intestinal colonization. One RR in particular had a very strong defect, encoded by genomic locus VCA0566. We determined that VCA0566 (now termed Vibrio type six secretion regulator, vxrB) controls expression of several genes including the T6SS genes. We used multiple methods to substantiate that VxrB is required for expression of the T6SS in vitro and in vivo. Lastly, we report that the T6SS contributes to colonization of the V. cholerae O1 strain used in this study.

Results

Multiple RRs impact intestinal colonization

We have a limited understanding of the V. cholerae TCSs and their role in colonization and adaptation to host environments. To evaluate the importance of the 52 TCS RRs in colonization, we generated in-frame deletion mutants of the 40 RRs. For this analysis, we excluded 12 RR that were either predicted to be involved in chemotaxis (11 CheY, CheV, and CheB proteins) or that we were unable to mutate (VC2368, ArcA) [43, 45]. We then analyzed the ability of 40 RR deletion mutants to colonize the small intestine in an in vivo competition assay where in vivo fitness of a mutant strain is compared to that of wild type strain using the infant mouse infection model (Fig 1A) [46]. While the vast majority of mutants—28—were not different from wild type, we identified 12 RR mutants that had a statistically significant colonization difference as compared to wild type (Fig 1A). We focused on 8 mutants with a statistically significant colonization difference and exhibited at least 1.2-fold difference in CI (Fig 1B). Consistent with previous studies, we identified that ΔVC0719 (phoB), ΔVC1021 (luxO), ΔVC1213 (varA), and ΔVC2135 (flrC) were defective in colonization [36, 37, 40, 44]. The competitive indices (CI) for ΔphoB, ΔluxO, ΔvarA, and ΔflrC were 0.01, 0.02, 0.16, and 0.43, respectively (Fig 1B).

Additionally, we identified a set of genes whose absence slightly but statistically significantly enhanced colonization (at least 1.2 fold higher CI), suggesting that inhibition of their expression and activity may be needed for wild-type colonization. These mutants were ΔVC1050, ΔVC1086, and ΔVC1087, which exhibited subtle and enhanced colonization phenotypes with CIs of 1.43, 1.24, and 1.48, respectively (Fig 1B). VC1050 is classified as an Hnr-type RR, [47] but its function is yet to be determined. VC1086 and VC1087 are part of a predicted eight gene operon encompassing VC1080-VC1087. Both VC1086 and VC1087 have domains that suggest they function in cyclic guanylate (c-di-GMP) regulation. Specifically, VC1086 contains an EAL domain with conserved residues required for enzymatic function, while VC1087 harbors an HD-GYP domain, but this domain lacks the conserved residues required for enzymatic activity.

We also identified one RR that was defective for colonization that had not been previously characterized. This mutant, ΔVCA0566, had a colonization defect with a CI of 0.14 (Fig 1A and 1B). Because this uncharacterized RR was important for colonization, we focused the rest of our studies on this protein.

ΔVCA0566/VxrB impacts colonization

VCA0566 is the second gene of a predicted five gene operon and had been previously annotated as a RR of the OmpR family. The encoded protein, which we named VxrB for reasons described below, is 245 amino acids in length with an N-terminal REC domain and a C-terminal winged helix-turn-helix DNA-binding domain (Fig 2B). Previously characterized members of the OmpR family in V. cholerae include PhoB, CarR, and ArcA [40–42]. Amino acid sequence alignment of the V. cholerae RRs in the OmpR family and the previously characterized E. coli OmpR [48] was used to identify the aspartate residue that is predicted to be phosphorylated in the REC domain (Fig 2A). Since the phosphorylation state of a RR is likely to determine its activity, we mutated the aspartate residue in the REC domain of VxrB to mimic constitutively active (D78E) and inactive (D78A) versions, as used in other work [48], and replaced the wild-type gene in the chromosome with these altered genes. These mutants were competed against wild type in the infant mouse colonization assay to determine if the phosphorylation state of VxrB is important for colonization. In accordance with our initial colonization screen, ΔvxrB displayed a CI of 0.15 (Fig 2B). Somewhat surprisingly, the CI for vxrB::D78A (inactive form) was 0.53, indicating a modest defect in colonization. This result indicates that the “inactive” form of VxrB does not phenocopy the ΔvxrB mutant, suggesting that VxrB harboring D78A substitution is not fully inactive. The CI for vxrB::D78E (active form) is 1.07, suggesting that constitutive activation of VxrB does not significantly impair V. cholerae (Fig 2B). Collectively, these findings suggest that in vivo phosphorylation of VxrB at D78 is likely to be important for its colonization function, but apparently not absolutely required. It is also likely that VxrB may not function by conventional phosphorylation-dependent signal transduction [49].

All members of the vxr operon contribute to in vivo colonization

The first gene of the vxr loci, VCA0565, is annotated as an HK. The other three genes (VCA0567-69) are predicted to encode proteins of unknown function (Fig 3A). We now termed these genes Vibrio type six secretion regulator (vxr) ABCDE and determined that these genes are co-transcribed using RT-PCR and RNAseq analysis (Fig 3A and S1 Fig). Both the genomic context and organization is conserved in the Vibrio species (S2–S4 Figs) and vxr gene products do not share significant sequence similarity with previously characterized proteins.

To gain a better understanding of the role of the vxr operon in colonization, we investigated whether the cognate HK and other genes in the vxr operon also contributed to mouse colonization. In-frame unmarked deletion mutants of vxrA, vxrB, vxrC, vxrD, and vxrE (Fig 3B) were generated and analyzed in an in vivo competition assay. Each mutant was outcompeted, with CIs of 0.35, 0.16, 0.44, 0.66, and 0.70, respectively (Fig 3B). These findings suggest that while vxrA and vxrB genes are critical for colonization in the infant mouse model, contribution of vxrCDE genes appears to be minor.

To further confirm the phenotype of ΔvxrB colonization defect, a wild type copy of vxrB whose expression was driven from its native promoter was inserted into the Tn7 site (located between VC0487 and VC0488) on the chromosome of ΔvxrB. In vivo competition assay of ΔvxrB-Tn7vxrB had a CI of 0.93, similar to wild type levels, where ΔvxrB had a CI of 0.16 (Fig 3B). Thus, the ΔvxrB colonization defect is restored to wild-type levels by introduction of the wild-type copy of vxrB.

VxrB regulates T6SS gene expression

To gain a better understanding of the contribution of VxrB to V. cholerae pathogenesis, we performed high throughput transcriptome sequencing (RNA-seq) analysis to identify the V. cholerae genes controlled by VxrB. We used cells grown under virulence inducing AKI conditions, to mimic the intestinal conditions encountered when we know VxrB is important. 149 genes showed statistically significant differences in gene expression between the wild type and mutant (S2 and S3 Tables). Of these, 80 genes were expressed to greater levels in the ΔvxrB mutant relative to the wild type (S2 Table), while 69 were expressed to lower levels in the ΔvxrB mutant relative to wild type (S3 Table). Of particular interest was the observation that message abundance of most of the T6SS genes in both the large cluster (VCA0105-VCA0124) and the two auxiliary clusters (VCA0017-VCA0022 and VC1415-VC1421) were less in the VxrB mutant relative to wild type (Table 1) (S5 Fig). This finding suggests that VxrB activates expression of the T6SS genes.

VxrB regulates production of T6SS

To further analyze the role of vxrB in T6SS expression and function, we compared the levels of the major T6SS structural component, Hcp, between wild type and ΔvxrB mutant V. cholerae. Quantitative real-time PCR analysis of hcp revealed that the transcript abundance of hcp was decreased by 3.7-fold under AKI conditions and 4.1- fold under LB conditions in the ΔvxrB mutant relative to wild type (Fig 4A). This finding supports that VxrB regulates expression of hcp and is consistent with the RNA-seq analysis. Additionally the levels of the Hcp protein in ΔvxrB were lower than wild type, in both whole cell samples and culture supernatants (Fig 4B). We also determined that complementation of the vxrB mutation (ΔvxrB-Tn7vxrB) restored Hcp to wild-type levels. Because we found lower amounts of Hcp in the supernatant as well as in whole cells, this finding suggests that VxrB is needed to express and secrete Hcp. As negative controls, we included a Δhcp1Δhcp2 mutant because it is unable to produce the Hcp proteins [11, 50]. As expected, no Hcp production was observed in this mutant. Furthermore, complementation of hcp1 in the Δhcp1Δhcp2 mutant partially restored Hcp levels (Fig 4B). Overall these findings suggest that Hcp production is decreased in ΔvxrB mutant.

Next we analyzed whether VxrB was needed for T6SS function, by examining T6SS-mediated interbacterial killing. Killing assays between the V. cholerae and the target E. coli K-12 strain MC4100 showed that wild-type V. cholerae decreased the numbers of E. coli compared to control experiments. This killing was dependent on the T6SS, as shown by greater numbers of E. coli obtained when incubated with V. cholerae Δhcp1Δhcp2 mutant and ΔvasH mutants, consistent with the findings reported by Ishikawa et al. (Fig 4C) [50]. This phenotype was complemented by introduction of either hcp1 or hcp2 into the Tn7 site on the chromosome. Consistent with our transcriptional and protein analysis presented above, we found that ΔvxrB mutants mediated less E. coli killing. These findings suggest that T6SS regulation by VxrB contributes to interbacterial killing.

Since VxrB regulates T6SS expression and is required to for intestinal colonization, we next asked whether the T6SS itself is required for intestinal colonization. We performed in vivo competition assays of a T6SS null mutant (Δhcp1Δhcp2) against wild type in the infant mouse model. We found that the in-vivo CI for Δhcp1Δhcp2 was 0.17 (Fig 5A). In addition, ΔvgrG3 also had an in-vivo CI of 0.26 suggesting that T6SS components are important for intestinal colonization (Fig 5A). This suggests that structural components of the T6SS are needed to colonize the intestine. Furthermore, this finding also suggests that the colonization defect associated with the ΔvxrB mutant could be caused by diminished T6SS production. To evaluate this possibility, we tested the in vivo competition of Δhcp1Δhcp2 against ΔvxrB and found that these strains competed nearly equally with each other (Fig 5C). Furthermore, in-vivo CI of ΔvxrBΔhcp1Δhcp2 triple mutant against ΔvxrB was 0.07 and ΔvxrBΔhcp1Δhcp2 against wt was 0.10. This finding suggests that the colonization defect by ΔvxrB was not solely due to altered expression of T6SS genes and other factors regulated by VxrB also contribute to colonization. It is also likely that T6SS expression is not completely abolished by the vxrB mutation. Indeed, western analysis (Fig 4B) shows that in vxrB mutant Hcp production is reduced but not completely eliminated. Similarly in vitro killing assay shows that vxrB mutant’s interbacterial killing ability is not identical to that of the strain lacking T6SS.

We next asked whether VxrB plays a role in growth in vitro, by performing an in vitro competition assay. ΔvxrB mutants grew equally well as wild type, suggesting that neither had a competitive advantage over the other in vitro (Fig 5B). This outcome suggests that there may be an in vivo signal produced in the infant mouse that triggers T6SS activity and colonization. We also performed single-strain colonization assays in the infant mouse model with ΔvxrB. There was a 12.7-fold decrease in colonization for ΔvxrB compared to wild type (Fig 5D). This finding suggests that the colonization defect by ΔvxrB was not solely dependent on wild type, and possibly could be caused by competition with the normal flora or ability of the mutant to adapt to the infection microenvironment.

Discussion

Systematic mutational phenotypic characterization of TCSs has been performed in only a few bacteria, including Vibrio fischeri, E. coli, Bacillus subtilis, Streptococcus pneumoniae, and Enterococcus faecalis [51–55]. In this study, we systematically analyzed the role of all V. cholerae TCS in colonization of the infant mouse small intestine and identified the RRs that play roles in mouse intestinal colonization. Specifically, ΔVC0719 (phoB), ΔVC1021 (luxO), ΔVC1213 (varA), and ΔVC2135 (flrC), and ΔVCA0566 (vxrB) exhibited intestinal colonization defects while ΔVC1050, ΔVC1086, and ΔVC1087 showed enhanced colonization. Many of the RRs had either no statistically significant defect or minor defects in the infant mouse colonization assay. It remains possible, however, that these RRs have a role in colonization in other infection models.

In vivo transcriptome analysis has been performed on different strains of V. cholerae in the infant mouse and rabbit ileal loop infection models. The analysis of the whole genome expression of V. cholerae O1 El Tor C6706 cells accumulating in the ceca of orally infected infant rabbits and the intestines of orally infected infant mice revealed that expression of the genes encoding RRs is altered during in vivo growth conditions as compared to in vitro growth in nutrient broth and that in vivo expression of TCS also differed between the model systems [56]. In the infant rabbit infection model, expression of seven RR (VC1081, VC1082, VC1155, vieA, VC2702 (cbrR), VCA0210, and VCA1105) was increased and 1 RR (carR) was decreased by more than 2-fold significantly in comparison to V. cholerae cells grown in vitro in nutrient broth. In the infant mouse infection model, expression of 17 RR (vpsR, VC1050, VC1081, VC1082, VC1086, VC1087, VC1155, VC1522, flrC, cbrR, ompR, dct-D2, vxrB, uhpA, vpsT, VCA1086, and VCA1105) and 9 RR (qstR, phoB, VC1348, VC1638, vieB, cpxR, ntrC, VCA0532, pgtA) were either decreased and increased significantly by more than 2-fold, respectively, in comparison to V. cholerae cells grown in vitro in nutrient broth [56]. vxrA and vxrB transcript levels were decreased 2 and 3-fold, respectively, in the experiments reported by Mandlik and colleagues, but did not reach statistical significance [56]. This work all used the V. cholerae O1 El Tor strain C6706, and so it is yet unknown whether vxrB expression is similarly regulated in the O1 El Tor A1552 strain used here.

There have been two other studies that analyzed V. cholerae infection phenotypes on a global scale, although they did not specifically target RR. Together, these studies and ours suggests there is a set of genes required for intestinal colonization across multiple models. Fu et al. used random transposon mutants coupled with insertion site sequencing (Tn-seq) in a rabbit model [30]. They identified insertions in two genes—VC1021 (luxO) and VC1155—that showed 8-15-fold reduction in colonization, while strains harboring insertions into RRs VC1348, vieA, vieB, arcA, VCA0256, uhpA, and pgtA had less than a 5-fold reduction in colonization (p<0.001). Another Tn-seq study using the infant rabbit model identified defects associated with luxO and arcA as above, and additionally phoB and varA [57]. Combining the results of these studies with ours identifies luxO, phoB, and varA, as required for in vivo fitness, and others that are variably identified. Because the Tn-seq work used transposon libraries, it is not known whether all RR were eliminated, so it is possible that their studies missed some critical RR. There are hints in their data, however, that the vxr locus is necessary in these other models as well. While Fu et al. did not identify vxrA or vxrB mutants, they did determine that a strain with an insertion into VCA0567 (vxrC) exhibited a 9-fold reduction in colonization (p<0.0001) [30]. Additionally, Kamp et al. found that a strain with a transposon insertion in VCA0565 (vxrA) had a disadvantage in fitness (mean fitness value of 0.6) when the bacteria from rabbit cecum fluid was placed into pond water for 48 hours at 30°C [57]. Collectively, these studies suggest that the Vxr genes play important roles in V. cholerae colonization and environmental dissemination.

Our study revealed that the RR VxrB plays a significant role in colonization and in vitro inter-bacterial competition through its ability to regulate expression of T6SS genes. Neither vxrB nor any of the vxrABCDE operon members show similarity to previously characterized proteins. The vxr loci are conserved among the Vibrio species Vibrio parahaemolyticus, Vibrio vulnificus, Vibrio harveyi, and V. fischeri. BLAST analysis revealed that VxrA protein exhibits 67–80%, VxrB 79–84%, VxrC 56–68%, VxrD 58–74%, and VxrE 68–81% sequence similarity to the same proteins in other Vibrio species (S2–S4 Figs). We also analyzed the predicted structure and function of the VxrCDE proteins using the protein homology/analogy recognition engine (Phyre) [58]. While VxrC and VxrE could not be modeled with high confidence and sufficient coverage, VxrD exhibited structural similarity to outer membrane protein transport proteins (100% confidence, 90% coverage). These analyses suggest that vxr genomic loci are a part of the ancestral Vibrio genome, and therefore likely have an evolutionarily conserved role in Vibrio biology.

Expression and production of T6SS are tightly regulated at the transcriptional and posttranscriptional levels in a variety of bacterial systems [12, 13, 59]. Environmental signals such as iron limitation, thermoregulation, salinity, envelope stress, indole, and growth on surfaces regulate T6SS expression [59]. In V. cholerae A1552, the strain used here, T6SS genes are expressed when cell are grown in high-osmolarity and low temperature conditions [50]. A recent study revealed that the V. cholerae A1552 T6SS genes are part of the competence regulon and their expression is induced when the bacterium grows on chitinous surfaces in a TfoX-, HapR-, and QstR-dependent manner [60]. Our work presented here identified VxrB as a regulator of the T6SS large gene cluster and the two auxiliary clusters. The predicted cognate HK of VxrB, VxrA, does not exhibit similarity to previously characterized sensory domains. The signals that govern expression and activity of VxrAB and how the VxrAB TCS is integrated into the T6SS regulatory network of V. cholerae are yet to be determined. We determined that while the wild-type strain has a competitive advantage in vivo over ΔvxrB, neither strain had a competitive advantage over the other in vitro. Furthermore, single infection studies showed that ΔvxrB had a significant colonization defect compared to wild type, suggesting that VxrB could be involved in competition with normal flora and that ΔvxrB could have a reduced fitness in infection environment. These observations also suggest that there may be an in vivo signal produced in the infant mouse that triggers T6SS activity and colonization. Our studies thus provided significant new insights into the regulation of T6SS in V. cholerae and provided further support that the T6SS is critical for V. cholerae virulence.

Materials and Methods

Ethics statement

All animal procedures used were in strict accordance with the NIH Guide for the Care and Use of Laboratory Animals [61] and were approved by the UC Santa Cruz Institutional Animal Care and Use Committee (Yildf1206).

Bacterial strains, plasmids, and culture conditions

The bacterial strains and plasmids used in this study are listed in S1 Table. Escherichia coli CC118λpir strains were used for DNA manipulation, and E. coli S17-1λpir strains were used for conjugation with V. cholerae. In-frame deletion mutants of V. cholerae were generated as described earlier [62]. All V. cholerae and E. coli strains were grown aerobically, at 30°C and 37°C, respectively, unless otherwise noted. All cultures were grown in Luria-Bertani (LB) broth (1% Tryptone, 0.5% Yeast Extract, 1% NaCl), pH 7.5, unless otherwise stated. LB agar medium contains 1.5% (wt/vol) granulated agar (BD Difco, Franklin Lakes, NJ). AKI medium contains 0.5% NaCl, 0.3% NaHCO₃, 0.4% Yeast Extract, and 1.5% Peptone, as previously described [63]. Antibiotics were used at the following concentrations: ampicillin 100 μg/ml; rifampicin 100 μg/ml; gentamicin 50 μg/ml; streptomycin 50 μg/ml.

DNA manipulations

An overlapping PCR method was used to generate in-frame deletion constructs of each RR genes using previously published methods [62]. Briefly, a 500–600 bp 5’ flanking sequence of the gene, including several nucleotides of the coding region, was PCR amplified using del-A and del-B primers. del-C and del-D primers were used to amplify the 3’ region of the gene including 500–600 bp of the downstream flanking sequence. The two PCR products were joined using the splicing overlap extension technique [64, 65] and the resulting PCR product, which lacks 80% of amino acids, was digested with two restriction enzymes and ligated to similarly-digested pGP704sacB28 suicide plasmid. Construction of vxrB plasmid harboring point mutations were performed using a similar technique [66] with the following alterations: primers containing the new sequence harboring the point mutations were used in place of the del-B and del-C primers. The deletion constructs were sequenced (UC Berkeley DNA Sequencing Facility, Berkeley, CA) and the clones without any undesired mutations were used. The deletion constructs are listed in S1 Table.

Generation of in-frame deletion mutants and Tn7 complementation strains

The deletion plasmids were maintained in E. coli CC118λpir. Biparental matings were carried out with the wild type V. cholerae and an E. coli S17λpir strain harboring the deletion plasmid. Selection of deletion mutants were done as described [64] and were verified by PCR. The Tn7 complementation V. cholerae strains were generated by triparental matings with donor E. coli S17λpir carrying pGP704-Tn7 with gene of interest, helper E. coli S17λpir harboring pUX-BF13, and V. cholerae strains. Transconjugants were selected on thiosulfate-citrate-bile salts-sucrose (TCBS) (BD Difco, Franklin Lakes, NJ) agar medium containing gentamicin at 30°C. The Tn7 complementation V. cholerae strains were verified by PCR.

Intestinal colonization assay

An in vivo competition assay for intestinal colonization was performed as described previously [46]. Briefly, each of the V. cholerae mutant strains (lacZ⁺) and the fully virulent reference strain (lacZ^-otherwise wild-type)) were grown to stationary phase at 30°C with aeration in LB broth. Mutant strains and wild-type were mixed at 1:1 ratios in 1x Phosphate Buffered Saline (PBS). The inoculum was plated on LB agar plates containing 5-bromo-4-chloro-3-indoyl-β-D-galactopyranoside (X-gal) to differentiate wild-type and mutant colonies and to determine the input ratios. Approximately, 10⁶–10⁷ cfu were intragastrically administered to groups of 5–7 anesthetized 5-day old CD-1 mice (Charles River Laboratories, Hollister, CA). After 20 hours of incubation, the small intestine was removed, weighed, homogenized, and plated on appropriate selective and differential media to enumerate mutant and wild-type cells recovered and to obtain the output ratios. In vivo competitive indices were calculated by dividing the small intestine output ratio by the inoculum input ratio of mutant to wild-type strains. For single strain infections, 10⁷ cfu of each strain, including otherwise wild type (lacZ^-) strain, were intragastrically administrated to 5-day old CD-1 mice. After 20 hours of incubation, the small intestine was harvested and plated on selective media as previously described above. Statistical analyses for competition infections were performed using Wilcoxon Signed Rank Test. Statistical analyses were performed using Prism 5 software (GraphPad Software, Inc., San Diego, CA) using Wilcoxon Signed Rank Test. P values of <0.05 were determined to be statistically significant.

Reverse transcription-PCR

RNA was isolated as described below. The reverse transcription reaction to generate cDNA was carried out using the SuperScript III Reverse Transcriptase (Invitrogen, Carlsbad, CA) according to the manufacturer’s instructions at 25°C for 5 min, 50°C for 1 h, and 70°C for 15 min using 1 μg of RNA in a 20 μl final volume. The product was used in a PCR using suitable primers, and RNA without RT treatment was used as a negative control.

Quantitative real time (qRT) PCR

For qRT-PCR expression analysis, RNA was isolated as described below. cDNA was synthesized using iScript cDNG Synthesis Kit (Bio-Rad, Hercules, CA) from 1 μg of total RNA. Real-time PCR was performed using a Bio-Rad CFX1000 thermal cycler and Bio-RAD CFX96 real-time imager with specific primer pairs (designed within the coding region of the target gene) and SsoAdvanced SYBR green supermix (Bio-Rad, Hercules, CA). Results are from two independent experiments performed in quadruplicate. All samples were normalized to the expression of the housekeeping gene 16S using the Pfaffl method [67]. Relative expression was calculated by normalizing expression at ΔvxrB by that of wt. Statistical analysis was performed using two-tailed student’s t test.

RNA isolation

V. cholerae cells were grown aerobically overnight in LB at 37°C, then diluted 1:100 in fresh 10 ml AKI media in borosilicate glass test tubes (diameter, 15mm; height, 150 mm) and incubated at 37°C without shaking for 4 hours. After 4 hours, 10 ml cultures were transferred to 125 ml flasks (for maximal aerated growth on an orbital shaker (250 rpm) for 2 hours. Aliquots (2 ml) of the cultures were collected and centrifuged for 2 min at room temperature. The cell pellets were immediately resuspended in 1 ml of TRIzol (Invitrogen, Carlsbad, CA) and stored at -80°C. Total RNA was isolated according to the manufacturer’s instructions. To remove contaminating DNA, total RNA was incubated with RNase-free DNase I (Ambion, Grand Island, NY), and an RNeasy mini kit (Qiagen, Valencia, CA) was used to clean up RNA after DNase digestion. Five micrograms of total RNA was treated with a MICROBExpress Kit (Ambion, Grand Island, NY) to remove ribosomal RNA, and the efficiency was confirmed by Bioanalyzer analysis (Agilent Technologies, Santa Clara, CA). Three biological replicates were generated for each condition.

cDNA library construction and Illumina HiSeq sequencing

Libraries for RNA-seq were prepared using NEBNext Ultra Directional RNA Library Prep Kit for Illumina (New England Biolabs, Ipswich, MA). Twelve indexed samples were sequenced per single lane using the HiSeq2500 Illumina sequencing platform for 50 bp single reads (UC Davis Genome Center, UC Davis, CA) and subsequently analyzed and visualized via the CLC Genomics Workbench version 7.5 (Qiagen, Valencia, CA). Samples were mapped to the V. cholerae genome N16961. Differentially regulated genes were identified as those displaying a fold change with an absolute value of 1.5-fold or greater. Statistical significance was determined by Empirical analysis of Digital Gene Expression (edgeR) test where p<0.05 was deemed significant [68].

Analysis of Hcp production and secretion

V. cholerae strains were grown to an OD600 of 2.0, and the culture (25 ml) was centrifuged at 20,000 g for 10 min to obtain whole cell pellets. The culture supernatant containing secreted proteins were filtered through 0.22 μ membranes (Millipore, Billerica, Massachusetts) and secreted proteins in the culture supernatant were precipitated with 13% trichloroacetic acid (TCA) overnight at 4°C, pelleted by centrifugation at 47,000 g for 30 min at 4°C, wash with ice cold acetone and resuspended in 1x PBS containing Complete protease inhibitor (Roche, Basel, Switzerland). Bovine serum albumin (BSA, 100 μg/ml) was added to the culture supernatant prior to TCA precipitation as a control. Protein pellets from whole cell were suspended in 2% sodium dodecyl sulfate (SDS) and protein concentrations were estimated using a Pierce BCA protein assay kit (Thermo Scientific, Rockford, IL). Equal amounts of total protein (20 μg) were loaded onto a SDS 13% polyacrylamide gel electrophoresis (SDS-PAGE). Western blot analyses were performed as described [69] using anti-Hcp polyclonal antiserum provided by the Sun Wai [28], anti-CRP (Neoclone Inc., Madison, WI), and anti-BSA (Santa Cruz Biotech, Santa Cruz, CA). OneMinute Western Blot Stripping Buffer (GM Biosciences, Frederick, MD) was used to remove the Hcp antibodies and the same blot was used again to probe for CRP or BSA. These experiments were conducted with at least three biological replicates.

Bacterial killing assay

Killing assays were performed as described previously [20]. Briefly, bacterial strains were grown overnight on LB plates and resuspended in LB broth containing 340 mM NaCl, as V. cholerae strain A1552 displayed enhanced interbacterial virulence towards E. coli under high osmolarity [50]. V. cholerae and E. coli MC4100 were mixed at a 10:1 ratio and 25 μl was spotted onto LB agar plates containing 340 mM NaCl and incubated at 37°C for 4 hours. Spots were harvested, serially diluted, and plated onto LB plates containing 50 μg/ml of streptomycin to enumerate surviving E. coli prey cells.

In vitro competition assay

The following assay was performed similarly as the intestinal colonization assay except no animal models were used. The V. cholerae mutant strains with wild-type lacZ allele (lacZ⁺) and reference strain (lacZ^-) were grown to stationary phase at 30°C with aeration in LB broth. Mutant strains and wild-type were mixed at 1:1 ratios in 1x PBS. The inoculum was plated on LB agar plates containing X-gal to differentiate colonies formed by the wild-type and mutant strains and to determine the input ratios. The inoculum (50 μl) was spotted on to a LB agar plate and incubated at 37°C. After 20–24 hours of incubation, the 50 μl spots were scraped off the agar plate and resuspended in 1x PBS. The resuspension was serially diluted and plated on appropriate selective and differential media to enumerate mutant and wild type cells recovered and to obtain the output ratios. In vitro competitive indices were calculated by dividing the output ratio by the inoculum input ratio of mutant to wild type strains. Statistical analyses were performed using Wilcoxon Signed Rank Test.

Supporting Information

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