Original Research ARTICLE
Identification of Genes Involved in Biogenesis of Outer Membrane Vesicles (OMVs) in Salmonella enterica Serovar Typhi
- 1Laboratorio de Genética y Patogénesis Bacteriana, Facultad de Ciencias de la Vida, Universidad Andres Bello, Santiago, Chile
- 2Escuela de Química y Farmacia, Facultad de Medicina, Universidad Andres Bello, Santiago, Chile
- 3Center of Applied Nanosciences, Universidad Andres Bello, Santiago, Chile
- 4Unidad de Microbiología, Hospital Clínico Universidad de Chile, Santiago, Chile
- 5Microbiota-Host Interactions and Clostridia Research Group, Facultad de Ciencias de la Vida, Universidad Andres Bello, Santiago, Chile
Outer membrane vesicles (OMVs) are nano-sized proteoliposomes discharged from the cell envelope of Gram-negative bacteria. OMVs normally contain toxins, enzymes and other factors, and are used as vehicles in a process that has been considered a generalized, evolutionarily conserved delivery system among bacteria. Furthermore, OMVs can be used in biotechnological applications that require delivery of biomolecules, such as vaccines, remarking the importance of their study. Although it is known that Salmonella enterica serovar Typhi (S. Typhi), the etiological agent of typhoid fever in humans, delivers toxins (e.g., HlyE) via OMVs, there are no reports identifying genetic determinants of the OMV biogenesis in this serovar. In the present work, and with the aim to identify genes participating in OMV biogenesis in S. Typhi, we screened 15,000 random insertion mutants for increased HlyE secretion. We found 9 S. Typhi genes (generically called zzz genes) determining an increased HlyE secretion that were also involved in OMV biogenesis. The genes corresponded to ompA, nlpI, and tolR (envelope stability), rfaE and waaC (LPS synthesis), yipP (envC), mrcB (synthesis and remodeling of peptidoglycan), degS (stress sensor serine endopeptidase) and hns (global transcriptional regulator). We found that S. Typhi Δzzz mutants were prone to secrete periplasmic, functional proteins with a relatively good envelope integrity. In addition, we showed that zzz genes participate in OMV biogenesis, modulating different properties such as OMV size distribution, OMV yield and OMV protein cargo.
Outer membrane vesicles (OMVs) are nano-sized proteoliposomes (20–200 nm) discharged from the cell envelope of Gram-negative bacteria in a process that does not involve cell lysis or death (Schwechheimer and Kuehn, 2015). OMVs normally contain toxins, enzymes and other factors, and are used as vehicles in a process that has been considered a generalized, evolutionarily conserved delivery system among bacteria (Schwechheimer and Kuehn, 2015). In pathogenic bacteria, OMVs can be directly delivered into host cells during infection. Many virulence factors are secreted via this pathway, such as the vacuolating toxin VacA of Helicobacter pylori and the HlyE hemolysin in Salmonella enterica serovar Typhi (S. Typhi) (Wai et al., 2003; Ricci et al., 2005). On the other hand, and due to their immunogenicity and ability to display antigens, OMVs can be incorporated into vaccine preparations. Since OMVs are metabolically inert, they represent fewer risks compared with live-cell vaccines (van der Pol et al., 2015). Nevertheless, increasing protective responses generated by OMVs, engineering the inclusion of protective antigens, and reducing OMV-mediated toxicity remain challenges in this field (van der Pol et al., 2015).
Evidence indicates that OMV biogenesis relies on three main mechanisms: (1) dissociation of the outer membrane in specific zones lacking proper attachments to underlying structures (e.g., peptidoglycan) (Yeh et al., 2010; Park et al., 2012); (2) the presence of misfolded proteins, which accumulates in nanoterritories where crosslinks between peptidoglycan and other components of bacterial envelope are either locally depleted or displaced (Schwechheimer and Kuehn, 2015); and (3) some changes in LPS composition also modulate OMV biogenesis, presumably by generating a differential curvature, fluidity, and/or charge in the outer membrane (Elhenawy et al., 2016). In this sense, identification of genes involved in such processes has been progressively gaining attention.
Global incidence of typhoid fever, a severe disease produced by S. Typhi (Enterobacteriaceae), is estimated to cause over 21 million cases worldwide, with approximately 220,000 deaths each year (Crump et al., 2008). The full progression of this disease was commonly observed in the pre-antibiotic era, resulting in 30% mortality. Antibiotics greatly reduced mortality, but emergence of multi-resistant strains represents a serious issue. Thus, a deeper knowledge of S. Typhi pathogenesis and the molecular determinants of the progression toward a systemic infection are needed to develop new approaches to treat or prevent typhoid fever in the future. At present, OMVs biogenesis is poorly understood in Salmonella enterica, and unknown in S. Typhi. Studies performed in S. enterica serovar Typhimurium (S. Typhimurium) reveal that some changes in LPS composition, observed in ΔpagL mutants (lipid A deacylase), negatively affects OMV biogenesis (Elhenawy et al., 2016). Nevertheless, it is necessary to be cautious before directly extrapolating data from S. Typhimurium to S. Typhi, a common practice. There are differences in biogenesis, composition and activity of OMVs between species, presumably due to the particular ecological niche of each pathogen (McBroom and Kuehn, 2007). S. Typhi and S. Typhimurium, albeit closely related, exhibit considerable differences regarding host range and disease progression. While S. Typhi infects only humans, producing a systemic infection, S. Typhimurium infects a broad range of hosts, producing only a self-limited gastroenteritis in humans (Parkhill et al., 2001). Remarkably, pagL is a pseudogene (i.e., a non-functional gene) in S. Typhi (Parkhill et al., 2001). For that reason, data obtained from S. Typhimurium (and much less from Escherichia coli) cannot be directly extrapolated to S. Typhi without an experimental approach (Urrutia et al., 2014).
As stated, identifying genes involved in OMV biogenesis is the first approach to understand mechanisms potentially involved in modulating OMV properties, such as size distribution and protein cargo selection. Nevertheless, such identification is challenging. In S. Typhi, OMVs proved to be the delivery mechanism for at least two virulence factors: the typhoid toxin and the HlyE cytolysin (Wai et al., 2003; Guidi et al., 2013). Remarkably, these toxins are not produced by S. Typhimurium (McClelland et al., 2000; Fuentes et al., 2008), reinforcing the fact that an experimental strategy must be performed to better understand the role of OMVs in S. Typhi. In S. Typhi, HlyE (ClyA) is a periplasmic hemolysin that contributes to invasion of epithelial cells (Fuentes et al., 2008). Although hlyE is expressed under standard growth conditions, S. Typhi WT is not hemolytic on blood agar (Fuentes et al., 2008). Previously, we reported that S. Typhi ΔompA exhibits hemolysis on blood agar due to an increased secretion of HlyE (Fuentes et al., 2008). Since OmpA participates in OMVs biogenesis in other Enterobacteriaceae (Deatherage et al., 2009), we hypothesized that S. Typhi ΔompA presents an increased HlyE secretion due to changes in OMV production. In this sense, we reasoned that S. Typhi derivatives exhibiting increased HlyE secretion, evidenced by hemolysis on blood agar under standard growth conditions, will present changes in OMV biogenesis. In the present work, and with the aim to identify genes participating in OMV biogenesis in S. Typhi, we screened 15,000 random insertion mutants for increased HlyE secretion. We found 9 S. Typhi genes (generically called zzz genes) involved in OMV biogenesis, corresponding to ompA, nlpI, and tolR (envelope stability), rfaE and waaC (LPS synthesis), yipP (also known as envC), mrcB (synthesis and remodeling of peptidoglycan), degS (stress sensor serine endopeptidase) and hns (global transcriptional regulator). All these genes encode functions related to envelope stability, accumulation of misfolded proteins, or to LPS composition. In general, S. Typhi Δzzz mutants were found to present an increased production of OMVs, which exhibited a distinct size distribution and protein cargo compared with the OMVs derived from the WT, supporting the role of zzz gene in OMV biogenesis in S. Typhi.
Materials and Methods
Bacterial Strains, Media and Culture Conditions
Salmonella enterica serovar Typhi strain STH2370 (S. Typhi WT) (Valenzuela et al., 2014) was obtained from the Infectious Diseases Hospital Lucio Córdova, Chile. S. enterica serovar Typhimurium ATCC14028s (S. Typhimurium WT) was obtained from the Instituto de Salud Pública, Chile. Strains were routinely grown in liquid culture using Luria Bertani medium (Bacto peptone, 10 g/L; Bacto yeast extract, 5 g/L; NaCl, 5 g/L; prepared in phosphate buffer pH 7.0) at 37°C, with aeration. When required, medium was supplemented with kanamycin (50 mg/ml), chloramphenicol (20 mg/ml), ampicillin (50 mg/ml), Xgal (5-bromo-4-chloro-3-indolyl-β-D-galactopyranoside) (40 μg/ml), or agar (15 g/L).
Random Insertional Mutagenesis
Mutagenesis was performed using the EZ-Tn5 < R6Kγori/KAN-2 > transposome (Epicenter®) as previously described (see detailed description in Supplementary Figure 1) (Goryshin et al., 2000). We screened 15,000 mutants to cover all the genome, and hemolytic colonies were selected for further analyses. As the next step, a “clean mutagenesis” (backcross) of the corresponding gene interrupted by the transposon (i.e., the zzz gene) was performed in a S. Typhi WT background using Red-Swap recombination (Datsenko and Wanner, 2000) yielding S. Typhi Δzzz::FRT mutants. For the experiments presented in this work, at least two different S. Typhi Δzzz clones, independently generated, were tested in each case. All mutants were corroborated by PCR amplification, as described (Datsenko and Wanner, 2000). S. Typhi Δzzz::FRT ΔhlyE::kan double mutants were constructed using the Red/Swap method (Datsenko and Wanner, 2000) iteratively.
S. Typhi hlyE-3 × FLAG was constructed as previously described (Fuentes et al., 2009). S. Typhi Δzzz::FRT hlyE-3 × FLAG was constructed by moving the hlyE-3 × FLAG (kanR) allele over the corresponding S. Typhi Δzzz::FRT mutant as described (Toro et al., 1998). A full list with the primers used in this study is presented in the Supplementary Table 1.
To complement the S. Typhi Δzzz mutants, we amplified the corresponding zzz genes (using primers listed in Supplementary Table 1) prior to cloning them into the pCR TOPO TA® plasmid according to the manufacturer’s instructions.
Quantitative RT-PCR Assay
Quantitative RT-PCR was performed as described (Jofre et al., 2014). Briefly, total mRNA from the strains grown in LB broth (approximately OD600 = 1.4), was extracted using TRIzol reagent (Invitrogen) as described by the manufacturer. RNA was precipitated with isopropanol for 10 min at room temperature, washed with ice-cold 70% v/v ethanol and resuspended in DEPC-treated water, prior to the treatment with DNase I to remove any trace of DNA. Purity of extracted RNA was determined by spectrometry. Reverse transcription and relative quantification of each mRNA was performed as previously described (Jofre et al., 2014). Experiments were performed in three biological and technical triplicates. Statistical significance of differences in the relative expression data was determined using Kruskal–Wallis with Dunn’s test as post hoc analysis to compare with the WT. A full list with the primers used in this study is presented in the Supplementary Table 1.
Immunodetection Analysis and SDS–PAGE
Strains carrying the epitope-tagged hlyE gene were grown in LB at 37°C with shaking to stationary phase (approximately OD600 = 1.1). For the whole lysate, bacterial pellets were resuspended in 1 mL of Tris–HCl pH 8.0 and sonicated on ice during 100 s. For the supernatant fraction, proteins were previously precipitated using 1/4 volume of trichloroacetic acid, incubated at 4°C for 10 min, and centrifuged at 15,000 ×g for 10 min. The pellet was washed twice with cold acetone and finally resuspended in Tris–HCl 100 mM pH 8.0. Bradford method (Bradford, 1976) was used to calculate the volume of the whole lysate containing 60 μg of proteins for each strain to be tested (load control). An equivalent volume was used for the corresponding supernatant fraction. Proteins were resolved by 12% SDS–PAGE, transferred to poly(vinylidene difluoride) membranes and stained with Ponceau S to confirm the protein load as previously described (Stochaj et al., 2006). Western blot was performed as described, using Hsp60 as load control (Jofre et al., 2014; Ortega et al., 2016).
The same procedure described for the SDS–PAGE was used to qualitatively assess the exported proteins of S. Typhi WT and S. Typhi Δzzz mutants.
In the case of OMV proteins, OMVs obtained from either S. Typhi WT or S. Typhi Δzzz mutants (corresponding to 12 μg of proteins) were resolved by SDS–PAGE and visualized with silver stain.
Bioassay for Determining β-Lactamase Release
First, strains expressing β-lactamase (bla gene) from a single chromosomal copy were constructed by the chromosomal insertion of pNFB9. pNFB9 is a plasmid that contains the bla gene, the attachment site for the phage Gifsy-1 (attPG1) and the respective integrase int (Lemire et al., 2008), allowing its integration into the attBG1 chromosomal site of S. Typhi (naturally empty) (Valenzuela et al., 2014), yielding the strain S. Typhi attBG1::pNFB9 (Lac- AmpR). The same procedure was performed for all the mutants (i.e., S. Typhi Δzzz) to generate the corresponding AmpR derivatives. Spots of S. Typhi attBG1::pNFB9 (WT background), and S. Typhi Δzzz attBG1::pNFB9 derivatives (Δzzz backgrounds) were plated over a lawn of S. Typhimurium ATCC14028s ΔompD::MudJ (106 cfu, Lac+ AmpS, reporter strain) previously spread on a LB agar plate supplemented with ampicillin and Xgal. For semi-quantitative assay to assess export of β-lactamase, supernatants from the strains described above was obtained (OD600 = 1.1), filtered (0.45 μm), precipitated with trichloroacetic acid (as described above), serially diluted and used for the bioassay. In all cases, export of functional β-lactamase was inferred by the growth of blue satellite colonies.
Assay of Resistance to Deoxycholic Acid and Vancomycin
Bacteria were grown in LB with shaking at 37°C to OD600 = 0.5 or 1.1, prior to being treated during 2 h with sodium deoxycholate 0.5% or PBS (control) at 37°C. Percentage of survival was calculated as following: (cfu treated with sodium deoxycholate/cfu with PBS) × 100, relative to S. Typhi WT. To determine sensitivity to vancomycin, a Kirby-Bauer assay was performed as reported (Villagra et al., 2012), using vancomycin disks loaded with 30 μg of antibiotic.
Preparation of Bacterial Samples for Atomic Force Microscopy (AFM)
Preparation of bacterial samples was performed as described (Azari et al., 2013) with modifications. Briefly, bacterial suspensions (OD600 = 1.1) were centrifuged and washed three times with PBS. Aliquots were applied onto the surface of circular coverslips and allowed to dry. Bacterial cell surfaces were imaged in contact mode or optical fiber cantilevers [n-type silicon cantilevers (f 1/4 37.2 kHz; k 1/4 0.01–0.60 N/m; tip radius of 10 nm)], using a Nanonics MultiView MV1000. Analysis was performed with the Gwyddion 2.42 software.
Determination of β-Galactosidase Release
S. Typhi WT and S. Typhi Δzzz derivatives were transformed with a religated pCR TOPO TA® multicopy plasmid (Lac+), producing strains constitutively expressing β-galactosidase (since S. Typhi lacks the lacI gene) (Valenzuela et al., 2014). All the strains were tested in LB plates supplemented with ampicillin and Xgal before the assays. For the assay, bacteria were cultured in LB to approximately OD600 1.1, prior to obtaining the pellet and the supernatant fraction by centrifugation. β-galactosidase activity was determined as described (Fuentes et al., 2009). The percentage of β-galactosidase release was calculated as (β-galactosidase activity of supernatant)/[(β-galactosidase activity of supernatant + β-galactosidase activity of pellet)] × 100.
OMV Isolation, Quantification and Size Measurement
To isolate OMVs, we followed a previously reported protocol, with modifications (Liu et al., 2016b). Bacteria were grown in LB at 37°C with shaking (approximately to OD600 = 1.1), prior being centrifuged 10 min at 5400 ×g at 4°C. The pellet was discarded, and the supernatant fraction was filtered (0.45 μm), ultrafiltered with Ultracel® 100 kDa ultrafiltration disks (Amicon Bioseparations), and ultracentrifuged 3 h at 150000 ×g at 4°C (Thermo Scientific™ Sorvall™ WX, Rotor AH-629). The supernatant was discarded, and the pellet resuspended in 1 ml DPBS. OMVs were stored at -20°C until their use. We quantified OMV yield as by determining the both protein content (BCA assay) and lipid content (FM4-64 molecular probe), and normalizing by CFU/ml (McBroom et al., 2006; Deatherage et al., 2009). We determined OMV size as described (Deatherage et al., 2009). Briefly, OMV size (diameter) was measured from at least 3 TEMs of 3 independent OMV extracts per strain in Adobe Photoshop using the ruler tool. Results were presented in diameter ranges of 3 nm, where 3 represents 1 to 3 nm. All OMVs larger than 60 nm were grouped in the last category (60+ nm).
Transmission Electronic Microscopy
Outer membrane vesicle extracts were bound to formvar-coated slot grids, stained with 1% aqueous uranyl acetate for 1 min, and viewed with a Philips Tecnai 12 (Biotwin) transmission electron microscope.
Mass spectrometry based on Matrix Assisted Laser Desorption Ionization Time-of-Flight (MALDI-TOF) was performed in a VITEK® MS device (bioMérieux) (wavelength: 337.1 nm, beam divergence: 3.5 × 3 mrad; rate repetition and pulse duration: 3 ns/60 Hz; Maximum output: 150 μJ/pulse). Data were processed by Acquisition Software. Experiments were performed in biological duplicate, using two independent OMV extracts.
Generation of S. Typhi Hemolytic Mutants by Random Insertional Mutagenesis
Although the cytolysin/hemolysin hlyE is efficiently expressed in rich media at 37°C, S. Typhi WT exhibits no hemolysis when cultured on blood agar plates (Jofre et al., 2014). Taking advantage of this feature, we performed a random insertional mutagenesis based on the EZ-Tn5 < R6Kγori/KAN-2 > transposome (Supplementary Figure 1) to find S. Typhi mutants with an increased HlyE secretion. To this purpose, we screened 15,000 random mutants (approximately 3 times the total number of S. Typhi genes, to cover the whole genome) (Porwollik et al., 2004; Valenzuela et al., 2014) on blood agar plates. Twenty-three clearly hemolytic colonies were identified and used for further analyses, including the identification of the corresponding interrupted genes (Figure 1A and Table 1). To corroborate that the observed hemolytic phenotype was effectively due to the loss of function of the identified genes, we performed a “clean” deletion by Red-Swap recombination (Datsenko and Wanner, 2000) for each identified gene in a S. Typhi WT background prior to testing the hemolytic phenotype of the resulting mutants. Some “clean” deletion mutants showed no hemolysis (Table 1), strongly suggesting that the hemolytic phenotype could be due to a secondary, spontaneous mutation or to polar effects attributed to the presence of the transposon. In these cases, genes were discarded. By contrast, 9 clean mutants (collectively called S. Typhi Δzzz::FRT) conserved the hemolytic phenotype and were used for further analysis (Figure 1B and Supplementary Figure 2).
Figure 1. (A) Screening showing a hemolytic derivative (yellow arrow) found after random mutagenesis with Tn5. (B) Hemolysis on blood agar plates of Salmonella enterica serovar Typhi (S. Typhi) Δzzz::FRT mutants generated by Red-Swap recombination (Datsenko and Wanner, 2000). The WT and the mutants (stationary phase, 5 μl) were placed over blood agar plates and incubated during 12 h to reveal hemolysis. (C) The hemolysis depends on the presence of hlyE. All the S. Typhi Δzzz::FRT ΔhlyE::kan double mutants lost the hemolytic phenotype, demonstrating that HlyE is the responsible of such phenotype. In the figure we show an example with S. Typhi WT, S. Typhi ΔompA::FRT, and S. Typhi ΔompA::FRT ΔhlyE::kan. The WT and the mutants were placed (stationary phase, 5 μl) over blood agar plates and incubated during 12 h to reveal hemolysis. (D) qRT-PCR to determine the hlyE expression in each mutant. In all the cases, the experiments were performed with 2 different clones for each mutant, in both technical and biological triplicate. Dark gray bar shows positive (∗∗p < 0.01) statistically significant differences compared with S. Typhi WT (n = 3 for each case, Kruskal–Wallis with Dunn’s test as post hoc analysis). (E) Secretion of HlyE to the supernatant fraction. S. Typhi hlyE-3 × FLAG (WT background) and S. Typhi Δzzz::FRT hlyE-3 × FLAG mutants (Δzzz background, indicated with the corresponding name of the deleted gene in the figure) were used to perform WB to detect HlyE-3 × FLAG in the supernatant (SN) or in the whole lysate (W). Detection of Hsp60 was performed as load control. In all cases, bacteria were grown in LB to stationary phase. This is a representative experiment of n = 5.
To determine that the observed hemolysis depends on the presence of hlyE, we generated S. Typhi Δzzz::FRT ΔhlyE::kan double mutants. We were unable to detect hemolysis in the double mutants, showing that hlyE was effectively the genetic determinant of this phenotype (Figure 1C and Supplementary Figure 2).
To assess whether the Δzzz deletions affected hlyE transcription, we performed qRT-PCR. As shown in Figure 1D, Δzzz deletions did not affect hlyE transcription, indicating that the hemolytic phenotype exhibited by the S. Typhi Δzzz mutants is more likely due to an increased HlyE secretion than to an increased hlyE expression. The only exception was observed with S. Typhi Δhns, where the hlyE transcript was highly abundant compared with the WT, showing that H-NS contributes to the repression of hlyE expression (Figure 1D).
To corroborate that Δzzz deletions contribute to an increased HlyE secretion, we epitope-tagged HlyE (Jofre et al., 2014), prior to analyzing the supernatant and the whole bacterial lysate by Western Blot. As shown in Figure 1E, almost all the mutants exhibited similar amounts of HlyE in the whole lysate. The increased production of HlyE, detected in the Δhns genetic background, can be attributed to the increased amount of hlyE mRNA in this same background (Figure 1D). On the other hand, the presence of HlyE in the supernatant fraction, as an indicator of HlyE secretion, was clearly increased in all the tested mutants in comparison with the WT (Figure 1E).
Altogether, these results indicated that deletions of zzz genes produced an increased HlyE liberation.
Δzzz Deletions Are Involved in Releasing Distinct, Functional Proteins
Since periplasmic proteins are prone to be secreted via OMVs (Haurat et al., 2011), increased secretion of periplasmic, functional proteins, such as β-lactamase, has been considered a typical feature of hypervesiculating mutants (Schwechheimer and Kuehn, 2015). To determine whether Δzzz deletions promote the release of periplasmic proteins, different from HlyE, we constructed a S. Typhi parental strain harboring one copy of the bla (β-lactamase) gene stably inserted into the chromosome (i.e., S. Typhi ΔattBG1::pNFB9). We used this strain to construct the S. Typhi ΔattBG1::pNFB9 Δzzz double mutants. To determine whether Δzzz deletions improve β-lactamase secretion, we performed a satellite-based bioassay. As shown in Figure 2A, all the S. Typhi ΔattBG1::pNFB9 Δzzz mutants allowed the growth of blue, satellite colonies around a spot of bacteria plated over a lawn of a Lac+ AmpS reporter strain. By contrast, no satellites were observed with the S. Typhi ΔattBG1::pNFB9 strain (WT background) (Figure 2A). As a semi-quantitative approximation, dilutions of precipitated proteins obtained from the corresponding supernatants were tested as described above. As shown in Figure 2B, some Δzzz mutants seem to secrete higher amounts of β-lactamase, since it was possible to observe blue satellites even in the most diluted samples (e.g., ΔrfaE, ΔtolR, and ΔdegS), whereas other S. Typhi Δzzz mutants only allowed the growth of satellites with the most concentrated samples (e.g., ΔompA, ΔwaaC, ΔnlpI, and Δhns). On the other hand, S. Typhi ΔattBG1::pNFB9 (WT background) supernatant was unable to allow the growth of satellites, even in the most concentrated sample. These results strongly suggest that Δzzz mutants release distinct amounts of proteins. To test this hypothesis, we compared the amount of total released proteins from S. Typhi WT and S. Typhi Δzzz mutants. We found that S. Typhi ΔdegS secreted 30% more proteins into supernatant fraction compared with the WT (Figure 2C). This result might explain the increased secretion of both HlyE and β-lactamase in this mutant. Nevertheless, we observed that S. Typhi ΔompA, ΔmrcB, ΔwaaC, ΔrfaE, ΔnlpI, ΔyibP, and ΔtolR were undistinguishable from the WT regarding the amount of total secreted proteins (Figure 2C). On the other hand, S. Typhi Δhns released approximately 25% fewer proteins (Figure 2C). These data suggest that the increased secretion of HlyE and β-lactamase cannot be merely explained by a generalized protein hypersecretion, at least in these last cases, suggesting that periplasmic proteins are prone to be secreted due to another phenomenon. These results prompted us to qualitatively assess the exported proteins by SDS–PAGE. As control, we loaded proteins obtained from the respective whole lysate. As shown in Figure 2D, S. Typhi Δzzz mutants seem to secrete a distinct pattern of proteins (including distinct abundance and diversity).
Figure 2. Δzzz mutants release a distinct pattern of proteins. (A) S. Typhi ΔattBG1::pNFB9 (Lac-, and AmpR due to the presence of bla gene stably inserted in the chromosome in one copy, WT background) and S. Typhi ΔattBG1::pNFB9 Δzzz::FRT double mutants (Lac- AmpR; Δzzz background, indicated with the corresponding name of the deleted gene in the figure) were plated (stationary phase, 5 μl) over a lawn of a reporter strain (Lac+ AmpS) previously spread on a plate with Xgal and ampicillin. Release of functional β-lactamase was evidenced as the presence of blue, satellite colonies after 8 h of incubation. This is a representative experiment of n = 3. (B) Semi-quantitative assay to assess the export of periplasmic proteins (i.e., β-lactamase). Supernatant obtained from the same strains described in (A) was obtained and filtered (0.45 μm). Proteins were precipitated with trichloroacetic acid, serially diluted, and plated (5 μl) over a lawn of a reporter strain, as indicated in (A). This is a representative experiment of n = 3. (C) SDS–PAGE showing proteins exported into the supernatant from S. Typhi WT and S. Typhi Δzzz mutants. Bacteria were cultured in LB to stationary phase, prior to obtaining proteins from the supernatant fraction as described in the Section “Materials and Methods.” Proteins from the whole lysate were used as load control. We performed this same assay with two different clones for each mutant, obtaining similar results. This is a representative experiment of n = 5. (D) Protein release of WT and S. Typhi Δzzz mutants. S. Typhi WT or S. Typhi Δzzz mutants were cultured in LB with shaking at 37°C for 16, 24, or 38 h (approximately OD600 in each case = 1.1, stationary phase). Then, bacteria were centrifuged (15,000 × g for 5 min) to obtain the pellet and the supernatant fractions. Supernatant was filtered (0.45 μm) and proteins were precipitated with trichloroacetic acid as described in Materials and Methods. Protein content was determined for both fractions to calculate the % of protein release as (proteins in the supernatant fraction)/[(proteins in the supernatant fraction)+(proteins in the pellet fraction)]. In all cases, values were corrected by OD600. In the figure, we showed relative values to the WT at 16 h as reference. In each case, 2 independent clones were tested, with both technical and biological triplicate. Two-way ANOVA with Tukey as post hoc test was performed (∗∗∗p < 0.001 and ∗∗∗∗p < 0.0001). No statistically significant differences were found among 16, 24, and 38 h for each mutant.
All these results show that S. Typhi Δzzz mutants can secrete a distinct pattern of proteins, including functional periplasmic proteins such as HlyE and β-lactamase.
Characterization of S. Typhi Δzzz Regarding the Envelope Integrity
It has been reported that S. Typhimurium mutants lacking OmpA, LppAB, Pal, TolA, or TolB exhibit an increased production of OMVs (Deatherage et al., 2009). Nevertheless, those mutants also present severe problems regarding membrane integrity, leading to high susceptibility to bile acids (e.g., sodium deoxycholate). This phenomenon was also observed in other Gram-negative bacteria (McBroom et al., 2006). In this sense, it has been proposed that mutants producing more subtle changes in envelope crosslinking can reveal more physiological conditions involved in OMVs biogenesis (i.e., “subtle mutants”). To check the envelope integrity and to determine whether the S. Typhi Δzzz mutants are more susceptible to sodium deoxycholate, bacteria grown to approximately OD600 = 0.5 were challenged with 0.5% deoxycholate or PBS (control) for 2 h. As shown in Figure 3A, only S. Typhi ΔompA and S. Typhi ΔyibP exhibited a statistically significant increased susceptibility to sodium deoxycholate. The same experiment performed with bacteria grown to approximately OD600 = 1.1, and including complementation of the mutations, gave similar results (Supplementary Figure 3). To further estimate the envelope integrity, we determined the relative susceptibility to vancomycin by a Kirby–Bauer assay. Gram-negative bacteria are intrinsically resistant to vancomycin because of the limit of diffusible molecules through the bacterial envelope (Pimenta et al., 1999). Thus, an increased susceptibility to vancomycin could be interpreted as an increased permeability. We found that almost all the S. Typhi mutants exhibited complete resistance to vancomycin, except for S. Typhi ΔompA and S. Typhi ΔyibP (Figure 3B). These same mutants showed increased sensitivity to sodium deoxycholate, strongly suggesting that the envelope may be compromised in these cases. The remaining mutants were undistinguishable from the WT strains (i.e., “subtle mutants”). Remarkably, when S. Typhimurium and the corresponding S. Typhimurium Δzzz mutants were evaluated, a different pattern of sensitivity was observed (Supplementary Figure 4), reinforcing the fact that data obtained from S. Typhimurium cannot be freely extrapolated to S. Typhi without an experimental approach.
Figure 3. Resistance to deoxycholic acid and vancomycin, and β-galactosidase release of S. Typhi WT and Δzzz mutants. (A) Resistance to sodium deoxycholate 0.5%. Bacteria were grown in LB with shaking at 37°C to OD600 = 0.5, prior to being treated during 2 h with sodium deoxycholate 0.5% or PBS (control) at 37°C. Percentage of survival was calculated as (cfu treated with sodium deoxycholate/cfu with PBS) × 100, and the relative values with respect to the WT were shown. (B) Kirby–Bauer assay to determine the sensitivity to vancomycin (30 μg in the paper disk) of S. Typhi WT and S. Typhi Δzzz mutants. The Y-axis shows the growth inhibition halo (diameter) measured in mm. 6 mm corresponds to the technique detection limit determined by the paper disk diameter. (C) Determination of β-galactosidase release. S. Typhi WT and S. Typhi Δzzz mutants expressing β-galactosidase (from a religated version of pCR TOPO TA [Lac+] plasmid) were grown in LB to stationary phase prior to obtaining the pellet and the supernatant fraction by centrifugation. β-galactosidase of each fraction was determined and used to calculate the enzyme release as stated in Materials and Methods. In all cases, dark gray and white bars show positive and negative (∗p < 0.05, ∗∗p < 0.01) statistically significant differences, compared with S. Typhi WT (n = 4 for each case, Kruskal–Wallis with Dunn’s test as post hoc analysis).
To better characterize the S. Typhi Δzzz mutants regarding their envelope integrity, we assessed the release of cytoplasmic proteins. β-galactosidase release has been used as an indicator of cell disruption in many cell types, including S. enterica (Kong et al., 2008). Thus, we transformed the pCR TOPO TA® religated, multicopy plasmid (lacZ+) into S. Typhi WT and S. Typhi Δzzz mutants, to generate the corresponding Lac+ version of these strains. Since S. Typhi lacks lacI (Parkhill et al., 2001; Valenzuela et al., 2014), the Lac+ phenotype is constitutive and presented no statistically differences among S. Typhi Δzzz mutants (Supplementary Figure 5). As shown in Figure 3C, the ratio of β-galactosidase activity in the supernatant versus total β-galactosidase activity indicated leakage of cytoplasmic enzymes. Although most S. Typhi Δzzz mutants seem to release more β-galactosidase than the WT, only S. Typhi ΔyibP and ΔdegS exhibited statistically significant differences. Since it has been considered that a ratio superior to 0.5 could correspond to cell lysis (Kong et al., 2008), we speculate that S. Typhi ΔyibP and ΔdegS present some leakage of cytoplasmic enzymes, where bacterial lysis is not the most important factor, and such leakage is less pronounced in the other S. Typhi Δzzz mutants. Altogether, these results show that most S. Typhi Δzzz can be considered as “subtle mutants” since they exhibit a good envelope integrity and a relatively low leakage of cytoplasmic proteins, even though the reporter gene (lacZ) is in a high gene dosage in this case.
Characterization of Outer Membrane Vesicles Produced by S. Typhi Δzzz Mutants
At this point, we have evidence arguing for the role of zzz genes in OMV biogenesis: (1) all the S. Typhi Δzzz mutants export increased amounts of periplasmic proteins (i.e., HlyE and β-lactamase) (Figures 1, 2), where S. Typhi HlyE is known to be secreted via OMVs (Wai et al., 2003); (2) S. Typhi Δzzz mutants have a distinct protein secretion into the supernatant fraction (Figure 3); (3) all S. Typhi Δzzz mutants, except for S. Typhi ΔompA and S. Typhi ΔyibP, exhibited a good envelope integrity, compared with the WT (Figure 3); and (4) all zzz genes, except hns, encode functions clearly related to the bacterial envelope (Table 1). In this context, we examined bacterial surface by AFM to determine whether Δzzz deletions produce envelope changes that could be associated to OMV biogenesis. AFM allows obtaining high-resolution images of bacterial samples, measuring structures in scales from molecules to cells (Liu and Wang, 2010). As shown in Figure 4, S. Typhi WT exhibited a smooth surface. By contrast, we found that, in all the cases, S. Typhi Δzzz mutants presented some changes in bacterial surface, such as waves, protrusions, creases or structural modifications that could correspond to envelope evaginations, consistent with a potential hypervesiculator phenotype (see Supplementary Figure 6 to complement the analysis). In the case of S. Typhi ΔyibP, we found two cell configurations: filament-like (Supplementary Figure 7) and isolated (Figure 4). On the other hand, several structures, consistent with released OMVs, can be observed in S. Typhi Δzzz mutants. Similar images obtained by AFM have been previously interpreted as OMV release (Wai et al., 2003; Chatterjee and Chaudhuri, 2011; Thoma et al., 2018). In this sense, ompA has been previously reported as involved OMV biogenesis in S. Typhimurium (Deatherage et al., 2009), and zzz genes are encoding different functions related to the bacterial envelope. For these reasons, we hypothesized that S. Typhi Δzzz are producing distinct OMVs, exhibiting different structural features, such as the size distribution, and potentially distinct OMV cargo. Thus, we isolated OMVs from S. Typhi WT and Δzzz mutants, prior to observing them with transmission electronic microscopy. As shown in Figure 5A, S. Typhi Δzzz mutants produced morphologically distinct OMVs, showing different mean sizes and more variability compared with OMVs produced by the S. Typhi WT. Δzzz deletions affected OMV size and/or OMV size distribution, where S. Typhi ΔompA, ΔtolR, ΔdegS, and Δhns tended to produce bigger OMVs compared with the WT, S. Typhi ΔmrcB produced smaller OMVs, and S. Typhi ΔwaaC was prone to produce both smaller and bigger OMVs. Nevertheless, all mutants seemed to produce more variable OMVs regarding their size, when compared with WT OMVs (Figure 5B and Supplementary Figure 8, see Supplementary Table 2 for statistical analysis). In addition, we observed that the increased β-lactamase release found in S. Typhi ΔattBG1::pNFB9 Δzzz double mutants (Figure 2) depends, at least in part, on the secretion of OMVs (Supplementary Figure 9). On the other hand, we were able to observe the direct release of OMVs from S. Typhi ΔtolR and ΔdegS, where differences in OMV size were also evident (Supplementary Figure 10).
Figure 4. Atomic force microscopy (AFM) of S. Typhi WT and S. Typhi Δzzz mutants. AFM images of bacterial surface. Bacteria were cultured in LB at 37°C with shaking to stationary phase. The black bar corresponds to 1 μm. In each case, a representative experiment is shown (n = at least 3).
Figure 5. Deletion of zzz genes impacts on the distribution of Outer Membrane Vesicle (OMV) size. (A) OMV extracts were observed by transmission electronic microscopy (TEM). The black bar corresponds to 200 nm. In all cases the horizontal field width and the magnification corresponded to 1.5 μm and 60000×, respectively. The black, gray, or white arrowhead show OMVs with different sizes. In each case, a representative experiment is shown (n = at least 3). (B) Size distribution of OMVs produced either by S. Typhi WT or S. Typhi Δzzz mutants. OMV size was obtained from TEMs (see Materials and Methods, Supplementary Table 2 and Supplementary Figure 7 for details). Dark bar contains the median for each case.
To determine the OMV yield of S. Typhi Δzzz mutants, we performed two independent strategies. To this end, we cultured both the S. Typhi WT and the S. Typhi Δzzz in LB to stationary phase (OD600 = 1.1), and OMVs were extracted. Then, we determined the protein content of OMVs as an indicator of abundance, as previously described, normalizing with CFU/ml (Deatherage et al., 2009). As shown in Figure 6A and Supplementary Figure 11, S. Typhi ΔtolR and S. Typhi ΔdegS clearly presented more proteins in the OMV fraction, whereas S. Typhi ΔompA, ΔmrcB, ΔrfaE, ΔyibP, and Δhns exhibited a slight but consistent increase in the OMV protein content. On the other hand, S. Typhi ΔnlpI exhibited similar results compared with S. Typhi WT and, strikingly, S. Typhi ΔwaaC seems to present less proteins in the OMV fraction. Considering that the heterogeneity in OMV size and the leakage of cytoplasmic proteins, such as in the ΔdegS mutant, could affect the protein content in the OMV fraction, we also performed a direct quantification of lipids in OMV preparation for vesicle quantification, as previously described. As well as for protein content, we also normalized our results with CFU/ml in each case (McBroom et al., 2006). As shown in Figure 6A and Supplementary Figure 11, the lipid content determination corroborated the results obtained with the protein content determination. An increase in both protein and lipid content in the OMV fraction have been previously interpreted as an increased OMV yield, and vice versa (McBroom et al., 2006; Deatherage et al., 2009; Schwechheimer et al., 2015). Interestingly, S. Typhi ΔwaaC released more HlyE and β-lactamase to the supernatant, compared with the WT, when 5 μl of a stationary culture were plated on agar plates (Figures 1, 2), but produced less OMVs per CFU. This result could be explained by the fact that S. Typhi ΔwaaC exhibited 10-fold more CFU/ml in a stationary culture, compared with the WT (Supplementary Figure 12).
Figure 6. (A) OMV production of S. Typhi WT and S. Typhi Δzzz mutants. Bacteria were grown in LB to stationary phase, and OMVs were extracted. Relative fold of OMV production was obtained by quantitating both the protein and lipid content (McBroom et al., 2006; Deatherage et al., 2009; Schwechheimer et al., 2015), normalizing to CFU/ml, and dividing by (CFU/ml)-normalized OMV production obtained with the S. Typhi WT. (B) MALDI-TOF mass spectrometry of OMV extracts. Arrows indicate differences with S. Typhi WT (n = 2, representative experiment). (C) SDS–PAGE of OMV extracts obtained from S. Typhi WT and S. Typhi Δzzz mutants. Proteins were visualized by silver staining.
Altogether, these results indicate that zzz genes participate in the OMV biogenesis, affecting OMV production. This assertion is supported by the AFM (Figure 4), where Δzzz mutants seem to show structures potentially corresponding to a hypervesiculating phenotype.
As stated above, protein cargo selection is a process that should occur during OMV biogenesis (Schwechheimer and Kuehn, 2015). Since zzz genes participate in the OMV biogenesis, we expect that cargo in OMVs derived from S. Typhi Δzzz mutants should be affected. To test this hypothesis, we performed MALDI-TOF mass spectrometry of OMVs extracts. We found that most mutants produced OMVs presenting MALDI-TOF profiles that were very similar to that obtained with the WT OMVs, except for S. Typhi ΔnlpI-derived OMVs, which exhibited slight differences (Supplementary Figure 13), and OMVs obtained from S. Typhi ΔtolR and ΔdegS (Figure 6B), which showed more evident differences. These results indicate that, at least for tolR and degS, zzz genes participate in processes that modulate OMV cargo. To observe potential differences in protein cargo in an independent way, we visualized OMV proteins with SDS–PAGE. As shown in Figure 6C, OMVs derived from S. Typhi WT exhibited few observable proteins, with a high abundance of a protein of approximately 55 kDa (plausibly corresponding to flagellin). This pattern is similar to OMV extracts derived from other WT S. enterica serovars (Liu et al., 2016a, 2017). We observed that protein cargo of OMVs derived from S. Typhi Δzzz mutants was different to that observed for the WT OMVs, corroborating the role of these genes in OMV cargo selection. Interestingly, when OMVs obtained from S. Typhi ΔmrcB were analyzed, we also observed differences in comparison with the WT OMVs. Although OMVs derived from S. Typhi WT and S. Typhi ΔmrcB presented a similar MALDI-TOF pattern (Supplementary Figure 13), it is possible that more subtle differences cannot be detected by the methods performed in this work. Accordingly, albeit many bands are shared between WT OMVs and ΔmrcB OMVs (Figure 6C), their abundance differs. The same could be extrapolated to the other Δzzz mutants. In this sense, a more profound study must be performed to determine how exactly zzz are affecting OMV cargo.
According to these results, we conclude that zzz genes participate in OMV biogenesis in S. Typhi, affecting OMV size distribution, OMV production, and, at least for tolR and degS, we conclude that zzz are involved in OMV cargo selection.
In this work, we aimed to identify genes involved in OMV biogenesis in S. Typhi. To this purpose, we performed a transposon-based screening that allowed identifying 9 genes that participate in OMV biogenesis. The fact that many of the identified genes were found more than once in the screening (Table 1), and considering that the screening allowed us identifying ompA and hns, two genes already reported as involved in HlyE secretion and in repression of hlyE expression, respectively (Oscarsson et al., 2002; Fuentes et al., 2008), indicates that the screening depth was suitable, and the whole genome was explored. Although transposon mutagenesis was previously described as a useful tool to identify genes potentially involved in HlyE export in an HlyE-overproducing E. coli strain (Wyborn et al., 2004a), to our knowledge, this is the first time that the hemolytic phenotype is used to identify genes involved in OMV biogenesis.
Our analysis showed that ompA, tolR and nlpI (envelope stability), rfaE and waaC (LPS synthesis), yipP, mrcB (synthesis and remodeling of peptidoglycan), degS (stress sensor serine endopeptidase) and hns (global transcriptional regulator) were involved in HlyE-dependent hemolysis in S. Typhi. We showed that this phenotype is mainly due to an increased export of HlyE rather than to an increased hlyE expression, except for the S. Typhi Δhns mutant. The role of HNS in hlyE repression was already reported for S. Typhi (Oscarsson et al., 2002) and E. coli (Wyborn et al., 2004b).
Outer membrane vesicle biogenesis is poorly understood (Deatherage et al., 2009) and unknown in S. Typhi. Nevertheless, there is evidence showing that this process mainly relies on the dissociation of the outer membrane in specific zones lacking proper attachments to underlying structures (e.g., peptidoglycan). Studies performed in E. coli revealed that envelope stability comes from three main crosslinks: OmpA, an outer membrane protein linked to peptidoglycan (Park et al., 2012), LppAB, highly abundant outer membrane lipoproteins covalently crosslinked to peptidoglycan (Mizushima, 1984) and the Tol-Pal complex, a cell division component that contributes to envelope stability also by interacting with peptidoglycan (Cascales et al., 2002; Gerding et al., 2007; Yeh et al., 2010). When these crosslinks decrease, production of OMVs increases, and vice versa. Accordingly, S. Typhimurium mutants lacking OmpA, LppAB, Pal, TolA, or TolB exhibit an increased production of OMVs (Deatherage et al., 2009). Nevertheless, these mutants also present severe problems regarding membrane integrity, leading to high susceptibility to bile acids and cellular leakage (Sonntag et al., 1978; McBroom et al., 2006; Deatherage et al., 2009). In this work, we found that ompA is involved in OMV biogenesis in S. Typhi, reinforcing the fact that the screening was suitable to identify OMV-related genes in this serovar. Interestingly, S. Typhimurium ΔompA (Deatherage et al., 2009) apparently produces smaller OMVs than S. Typhi ΔompA (Figure 5), remarking potential differences regarding OMV biogenesis between these two serovars. On the other hand, we were unable to find mutants in the Braun (murein) lipoprotein gene lpp. The genome of S. Typhimurium presents two copies of lpp (i.e., lppA or lpp1, and lppB or lpp2) (Sha et al., 2004). Similarly, S. Typhi genome also harbors two copies of lpp (Parkhill et al., 2001; Valenzuela et al., 2014). This fact might remark a limitation of the screening, indicating that genes encoding redundant functions related to OMV biogenesis cannot be identified with the proposed strategy. However, this same finding remarks an advantage of the screening, showing that the identified genes encode specific functions that are not redundant regarding OMV biogenesis. In other words, each zzz gene contributes to OMV biogenesis in S. Typhi by a specific, unique mechanism, underlying the contribution of this work. This point is supported by the fact that S. Typhi Δzzz mutants produce distinct OMVs regarding size distribution, abundance and protein cargo.
TolR, part of the Tol-Pal system (TolA, TolB, TolQ, and TolR), is an inner membrane protein related to the peptidoglycan-binding stator from the flagellum in E. coli. The Tol-Pal systems contribute to maintaining integrity of the outer membrane (Deatherage et al., 2009). Although TolR is conserved among Gram-negative bacteria, some important structural differences among related bacteria have been reported (Wojdyla et al., 2015). TolA, TolB, and Pal have been shown to affect OMV biogenesis in S. Typhimurium (Deatherage et al., 2009), albeit we were unable to find the corresponding encoding genes as implicated in S. Typhi OMVs. As stated, it is possible that differences in the Tol-Pal system between these two serovars could explain this result. For instance, TolA determines an increase resistance to bile in S. Typhi, compared with S. Typhimurium (Lahiri et al., 2011), and tolR encodes functions involved in motility only in S. Typhimurium, and E. coli (Santos et al., 2014), but not in S. Typhi (Supplementary Figure 14). Interestingly, in this work we showed that S. Typhi ΔtolR produce high amount of OMVs, without an important compromise of the cell envelope, presenting the same resistance to deoxycholate than the WT (i.e., a “subtle mutant). By contrast, S. Typhimurium Δpal, ΔtolA, and ΔtolB mutants exhibit a highly compromised envelope stability (Deatherage et al., 2009), suggesting that deletions in different components of the Tol-Pal systems are not fully equivalent. In support of this point, we found that S. Typhimurium ΔtolR produces only 2-fold more OMVs compared with S. Typhimurium WT, remarking another difference between S. Typhi and S. Typhimurium (Supplementary Figure 15).
NlpI, a lipoprotein that participates in the balance of peptidoglycan breakdown and synthesis, partially determines (around 40%) the formation of Lpp-peptidoglycan crosslinks (Schwechheimer et al., 2015). In this sense, E. coli ΔnlpI exhibits an increased OMVs production compared to the otherwise isogenic parental strain, without evident leakage of cytoplasmic proteins (i.e., E. coli ΔnlpI is a subtle mutant) (McBroom et al., 2006; Schwechheimer et al., 2015). According to our results, S. Typhi ΔnlpI (as well as ΔmrcB, ΔwaaC, ΔrfaE, ΔyibP, ΔtolR, ΔdegS, and Δhns) can be also considered subtle mutants since OMV production is independent of envelope instability in this serovar (Figure 3). In the best scenario, it might be possible to modify OMV production without compromising bacterial global envelope integrity, providing a potential improved genetic background to perform further OMV proteomic analyses (with few contamination of cytoplasmic proteins) or for biotechnological purposes (Bonnington and Kuehn, 2014; Schwechheimer and Kuehn, 2015). On the other hand, although nlpI has been associated to hypervesiculation in other Gram-negative bacteria (e.g., Actinobacillus pleuropneumoniae) (Antenucci et al., 2017), its role in S. enterica is less known, where it has been linked to biofilm formation and acclimatization in S. Typhimurium (Rouf et al., 2011a,b).
It has been stated that LPS remodeling triggers formation of OMVs in S. enterica (Bonnington and Kuehn, 2016; Elhenawy et al., 2016). Nevertheless, although several genes are involved in LPS synthesis, we only found, waaC and rfaE in the screening. The waaC gene encodes a heptosyltransferase, an enzyme that catalyzes the transfer of the first heptose to the lipid A in the core region of the LPS, as described for E. coli (Durka et al., 2012). On the other hand, rfaE encodes an enzyme harboring two domains that catalyze the synthesis of the LPS core precursor ADP-L-glycero-D-manno-heptose, as reported for E. coli (Valvano et al., 2000). Although these two enzymes (WaaC and RfaE) work together in the same LPS synthetic pathway, they are not redundant. In fact, although both waaC and rfaE affect OMV biogenesis in S. Typhi, S. Typhi ΔwaaC produced less OMVs than the WT, whereas S. Typhi ΔrfaE can be considered as a hypervesiculating strain. In support of this, a deletion in waaC in S. Typhimurium inhibits vesiculation (Liu et al., 2016b). Nevertheless, waaC and rfaE seem to be only partially equivalent between S. Typhimurium and S. Typhi, since their respective deletions apparently affect in different ways the motility of these two serovars (Supplementary Figure 14). As stated, changes in LPS composition can affect OMV production, presumably by generating local nanoterritories in the outer membrane. These nanoterritories could exhibit differential curvature, fluidity, and/or charge, making the membrane more or less prone to be discharged, depending on the modification (Haurat et al., 2011). Furthermore, only a subset of genes involved in LPS have shown to participate in OMV biogenesis (Haurat et al., 2011; Elhenawy et al., 2016), assertion that is supported by the results of our screening.
The mrcB gene encodes the PBP-1b (penicillin binding protein). In E. coli, PBP-1b corresponds to a bifunctional enzyme (transglycosidase and transpeptidase activity) that participates in synthesis of peptidoglycan (Sauvage et al., 2008; Kumar et al., 2012). Since changes in peptidoglycan dynamics (i.e., decrease in covalent cross-links between outer membrane and bacterial wall) can induce OMV production, we speculate that mrcB encodes functions that could also contribute to this process in S. Typhi. In support of this, it has been reported that PBP-1b provides an important physical link between the inner and outer membranes at the division site in E. coli (Markovski et al., 2016). Thus, the lack of mrcB could impact on envelope stability, affecting vesiculation. On the other hand, yibP (also known as envC) encodes an enzyme showing a murein hydrolytic activity related to peptidoglycan hydrolysis associated with cell division. YibP interacts with FtsX and FtsZ in bacterial septa (Yang et al., 2011), as well as with amidases that cleave the septal murein and promotes daughter cell separation (Bernhardt and de Boer, 2004). The lack of yibP results in defects of septation, producing filament-like cells in E. coli (Hara et al., 2002), a phenotype that we also found in S. Typhi ΔyibP (Supplementary Figure 7). Interestingly, it has been stated that the interactions of the outer membrane, the peptidoglycan and the inner membrane at division septa contribute to the envelope integrity and modulate localized release of OMVs, affecting both the size distribution and the protein content of the OMVs in S. Typhimurium (Deatherage et al., 2009). In this sense, our results with the S. Typhi ΔyibP could be indicating that specific or particular functions related to septa formation are also involved in OMV biogenesis. To our knowledge, neither mrcB nor yibP were previously described to be associated to OMV biogenesis.
In S. Typhimurium and in E. coli, degS encodes an inner-membrane-anchored periplasmic endopeptidase belonging to the HtrA family (Rhodius et al., 2006; Clausen et al., 2011). In presence of unfolded proteins (e.g., outer membrane proteins), DegS cleaves the cytoplasmic moiety of RseA (also known as anti-σE), releasing σE and activating the transcription of genes involved in repair and/or elimination of misfolded periplasmic proteins (Missiakas et al., 1997). DegS could participate in OMV biogenesis by both a direct and an indirect mechanism: First, in absence of DegS, misfolded proteins could accumulate in the periplasmic space. This accumulation in distinct nanoterritories may cause displacement or depletion of local crosslinks, destabilizing the bacterial envelope and inducing vesiculation (Bonnington and Kuehn, 2014; Schwechheimer and Kuehn, 2015). And second, the lack of DegS impairs the activation (release) of σE. In this sense, the impairment of the σE pathway positively affects vesiculation, as shown for E. coli (Button et al., 2007; McBroom and Kuehn, 2007).
The hns gene encodes the global regulator H-NS reported to silence genes acquired by horizontal transfer by counteracting transcription of AT-rich promoter-like regions (Singh et al., 2014). Accordingly, H-NS acts as a repressor of hlyE, belonging to the SPI-18, a genomic locus presumably acquired by horizontal transfer in S. Typhi (Oscarsson et al., 2002; Fuentes et al., 2008). Interestingly, we found that hns is also involved in OMV biogenesis in this serovar. Previously, it has been reported that E. coli Δhns exhibits an increased OMV yield, supporting the role of hns in OMV biogenesis in Enterobacteriaceae (Horstman and Kuehn, 2002; Sanchez-Torres et al., 2010). Although the mechanism by which H-NS participates in OMV biogenesis is unknown, it is possible that this regulator is involved in the expression of other genetic determinants of vesiculation, as previously proposed (Horstman and Kuehn, 2002).
Regarding the regulation of vesiculation, it has been shown that HlyE secretion, which occurs via OMVs in S. Typhi (Wai et al., 2003), is indirectly promoted by the downregulation of OmpA in presence of epinephrine or norepinephrine, hormones that are abundant in the gut or in macrophages exposed to LPS (Furness, 2000; Flierl et al., 2007, 2009; Karavolos et al., 2011). Thus, the identification of new genetic determinants of OMV biogenesis in S. Typhi could contribute to a better understanding of how vesiculation is regulated during the normal infective cycle. In other words, the study of zzz regulation, in the OMV context, could provide clues about the exact role of HlyE in the normal infective cycle. Furthermore, even though there are no good animal models for S. Typhi, these mutants could be also used in future tissue culture and macrophage studies.
Since proteins are the most significant determinants of OMV functions (Lee et al., 2016), identification of OMV-associated proteins is crucial. In this work, we showed that that some Δzzz deletions affected protein content of S. Typhi-derived OMVs. It has been stated that genes involved in OMVs biogenesis are also involved in inclusion/exclusion of proteins in OMVs, supporting the assertion that OMV cargo selection is determined during OMV biogenesis (Schwechheimer and Kuehn, 2015). For instance, Pseudomonas aeruginosa lacking OprF, a homologous of OmpA, exhibits an increased production of OMVs. Furthermore, OprF impacts on OMV cargo, modulating both abundance and diversity of OMV-associated proteins (Wessel et al., 2013). On the other hand, DegP, a chaperone participating in protein-folding quality control of OM proteins (Clausen et al., 2011), contributes to both OMV protein cargo selection and to OMVs functions in Vibrio cholerae (Altindis et al., 2014). OMVs from V. cholerae ΔdegP lack proteins involved in biofilm formation; thereby, these mutants are impaired in biofilm biogenesis (Wessel et al., 2013). Remarkably, DegP is important in OMV biogenesis in E. coli (McBroom et al., 2006). Furthermore, deletion of genes contributing to LPS composition affects OMV production in S. Typhimurium (Elhenawy et al., 2016), as well as OMV production, cargo selection, and even OMV size in P. aeruginosa (Murphy et al., 2014). All this evidence argues that genes implicated in different stages of OMV biogenesis are also involved in OMV cargo selection, potentially determining OMV functions and other properties such as OMV size (Yoon, 2016).
Since OMVs are vehicles for bacterial proteins, their study will allow getting a better insight of the communication occurring between bacteria–host cells, potentially allowing the identification of new proteins involved in virulence. On the other hand, since OMVs can also be used to deliver heterologous antigens in vaccine design (van der Pol et al., 2015), a better understanding of OMV biogenesis in S. enterica, a species used to develop recombinant attenuated vaccines (Curtiss et al., 2010), will allow engineering improved OMVs. Thus, the study of OMVs produced by S. Typhi Δzzz mutants could potentially contribute to better comprehend their role in the infection cycle, but also for the development of improved biotechnological tools.
This manuscript is dedicated to Prof. Guido C. Mora, for a whole life devoted to science and for his contribution to the microbiology in Chile and the world.
JN performed the experiments of the Figures 1–3 and Supplementary Figures 1–7, 14. AS peformed the experiments of the Figures 4–6A,C and Supplementary Figures 8–12, 15. CO critically read the manuscript and co-directed the project. DO contributed with the data for Figure 4 and Supplementary Figure 6. BB contributed with the data for Figure 6B and Supplementary Figure 13. FG and IC critically read the manuscript and discussed the results. JF designed and discussed all the experiments, designed all the figures, wrote the manuscript, and directed the project.
This work was funded by FONDECYT 1181638.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
We are grateful to Dr. Ramiro Arratia-Pérez for instrumental facilities. We thank Lionello Bossi and Nara Figueroa-Bossi for the kind donation of the pNFB9 plasmid.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmicb.2019.00104/full#supplementary-material
Antenucci, F., Fougeroux, C., Bosse, J. T., Magnowska, Z., Roesch, C., Langford, P., et al. (2017). Identification and characterization of serovar-independent immunogens in Actinobacillus pleuropneumoniae. Vet. Res. 48:74. doi: 10.1186/s13567-017-0479-5
Azari, F., Nyland, L., Yu, C., Radermacher, M., Mintz, K. P., and Ruiz, T. (2013). Ultrastructural analysis of the rugose cell envelope of a member of the Pasteurellaceae family. J. Bacteriol. 195, 1680–1688. doi: 10.1128/JB.02149-12
Bernhardt, T. G., and de Boer, P. A. (2004). Screening for synthetic lethal mutants in Escherichia coli and identification of EnvC (YibP) as a periplasmic septal ring factor with murein hydrolase activity. Mol. Microbiol. 52, 1255–1269. doi: 10.1111/j.1365-2958.2004.04063.x
Bonnington, K. E., and Kuehn, M. J. (2016). Outer membrane vesicle production facilitates LPS remodeling and outer membrane maintenance in Salmonella during environmental transitions. mBio 7:e01532-16. doi: 10.1128/mBio.01532-16
Bradford, M. M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72, 248–254. doi: 10.1016/0003-2697(76)90527-3
Button, J. E., Silhavy, T. J., and Ruiz, N. (2007). A suppressor of cell death caused by the loss of sigmaE downregulates extracytoplasmic stress responses and outer membrane vesicle production in Escherichia coli. J. Bacteriol. 189, 1523–1530. doi: 10.1128/JB.01534-06
Cascales, E., Bernadac, A., Gavioli, M., Lazzaroni, J. C., and Lloubes, R. (2002). Pal lipoprotein of Escherichia coli plays a major role in outer membrane integrity. J. Bacteriol. 184, 754–759. doi: 10.1128/JB.184.3.754-759.2002
Chatterjee, D., and Chaudhuri, K. (2011). Association of cholera toxin with Vibrio cholerae outer membrane vesicles which are internalized by human intestinal epithelial cells. FEBS Lett. 585, 1357–1362. doi: 10.1016/j.febslet.2011.04.017
Crump, J. A., Ram, P. K., Gupta, S. K., Miller, M. A., and Mintz, E. D. (2008). Part I. Analysis of data gaps pertaining to Salmonella enterica serotype Typhi infections in low and medium human development index countries, 1984-2005. Epidemiol. Infect. 136, 436–448. doi: 10.1017/S0950268807009338
Curtiss, R. III, Xin, W., Li, Y., Kong, W., Wanda, S. Y., Gunn, B., et al. (2010). New technologies in using recombinant attenuated Salmonella vaccine vectors. Crit. Rev Immunol. 30, 255–270. doi: 10.1615/CritRevImmunol.v30.i3.30
Datsenko, K. A., and Wanner, B. L. (2000). One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products. Proc. Natl. Acad. Sci. U.S.A. 97, 6640–6645. doi: 10.1073/pnas.120163297
Deatherage, B. L., Lara, J. C., Bergsbaken, T., Rassoulian Barrett, S. L., Lara, S., and Cookson, B. T. (2009). Biogenesis of bacterial membrane vesicles. Mol. Microbiol. 72, 1395–1407. doi: 10.1111/j.1365-2958.2009.06731.x
Durka, M., Buffet, K., Iehl, J., Holler, M., Nierengarten, J. F., and Vincent, S. P. (2012). The inhibition of liposaccharide heptosyltransferase WaaC with multivalent glycosylated fullerenes: a new mode of glycosyltransferase inhibition. Chemistry 18, 641–651. doi: 10.1002/chem.201102052
Elhenawy, W., Bording-Jorgensen, M., Valguarnera, E., Haurat, M. F., Wine, E., and Feldman, M. F. (2016). LPS remodeling triggers formation of outer membrane vesicles in Salmonella. mBio 7:e00940-16. doi: 10.1128/mBio.00940-16
Flierl, M. A., Rittirsch, D., Nadeau, B. A., Chen, A. J., Sarma, J. V., Zetoune, F. S., et al. (2007). Phagocyte-derived catecholamines enhance acute inflammatory injury. Nature 449, 721–725. doi: 10.1038/nature06185
Flierl, M. A., Rittirsch, D., Nadeau, B. A., Sarma, J. V., Day, D. E., Lentsch, A. B., et al. (2009). Upregulation of phagocyte-derived catecholamines augments the acute inflammatory response. PLoS One 4:e4414. doi: 10.1371/journal.pone.0004414
Fuentes, J. A., Jofre, M. R., Villagra, N. A., and Mora, G. C. (2009). RpoS- and Crp-dependent transcriptional control of Salmonella Typhi taiA and hlyE genes: role of environmental conditions. Res. Microbiol. 160, 800–808. doi: 10.1016/j.resmic.2009.09.016
Fuentes, J. A., Villagra, N., Castillo-Ruiz, M., and Mora, G. C. (2008). The Salmonella Typhi hlyE gene plays a role in invasion of cultured epithelial cells and its functional transfer to S. Typhimurium promotes deep organ infection in mice. Res. Microbiol. 159, 279–287. doi: 10.1016/j.resmic.2008.02.006
Gerding, M. A., Ogata, Y., Pecora, N. D., Niki, H., and De Boer, P. A. (2007). The trans-envelope Tol-Pal complex is part of the cell division machinery and required for proper outer-membrane invagination during cell constriction in E. coli. Mol. Microbiol. 63, 1008–1025. doi: 10.1111/j.1365-2958.2006.05571.x
Goryshin, I. Y., Jendrisak, J., Hoffman, L. M., Meis, R., and Reznikoff, W. S. (2000). Insertional transposon mutagenesis by electroporation of released Tn5 transposition complexes. Nat. Biotechnol. 18, 97–100. doi: 10.1038/72017
Guidi, R., Levi, L., Rouf, S. F., Puiac, S., Rhen, M., and Frisan, T. (2013). Salmonella enterica delivers its genotoxin through outer membrane vesicles secreted from infected cells. Cell. Microbiol. 15, 2034–2050. doi: 10.1111/cmi.12172
Hara, H., Narita, S., Karibian, D., Park, J. T., Yamamoto, Y., and Nishimura, Y. (2002). Identification and characterization of the Escherichia coli envC gene encoding a periplasmic coiled-coil protein with putative peptidase activity. FEMS Microbiol. Lett. 212, 229–236. doi: 10.1111/j.1574-6968.2002.tb11271.x
Haurat, M. F., Aduse-Opoku, J., Rangarajan, M., Dorobantu, L., Gray, M. R., Curtis, M. A., et al. (2011). Selective sorting of cargo proteins into bacterial membrane vesicles. J. Biol. Chem. 286, 1269–1276. doi: 10.1074/jbc.M110.185744
Horstman, A. L., and Kuehn, M. J. (2002). Bacterial surface association of heat-labile enterotoxin through lipopolysaccharide after secretion via the general secretory pathway. J. Biol. Chem. 277, 32538–32545. doi: 10.1074/jbc.M203740200
Jofre, M. R., Rodriguez, L. M., Villagra, N. A., Hidalgo, A. A., Mora, G. C., and Fuentes, J. A. (2014). RpoS integrates CRP, Fis, and PhoP signaling pathways to control Salmonella Typhi hlyE expression. BMC Microbiol. 14:139. doi: 10.1186/1471-2180-14-139
Karavolos, M. H., Bulmer, D. M., Spencer, H., Rampioni, G., Schmalen, I., Baker, S., et al. (2011). Salmonella Typhi sense host neuroendocrine stress hormones and release the toxin haemolysin E. EMBO Rep. 12, 252–258. doi: 10.1038/embor.2011.4
Kong, W., Wanda, S. Y., Zhang, X., Bollen, W., Tinge, S. A., and Roland, K. L. (2008). Regulated programmed lysis of recombinant Salmonella in host tissues to release protective antigens and confer biological containment. Proc. Natl. Acad. Sci. U.SA. 105, 9361–9366. doi: 10.1073/pnas.0803801105
Kumar, A., Sarkar, S. K., Ghosh, D., and Ghosh, A. S. (2012). Deletion of penicillin-binding protein 1b impairs biofilm formation and motility in Escherichia coli. Res. Microbiol. 163, 254–257. doi: 10.1016/j.resmic.2012.01.006
Lahiri, A., Ananthalakshmi, T. K., Nagarajan, A. G., Ray, S., and Chakravortty, D. (2011). TolA mediates the differential detergent resistance pattern between the Salmonella enterica subsp. enterica serovars Typhi and Typhimurium. Microbiology 157, 1402–1415. doi: 10.1099/mic.0.046565-0
Lee, J., Kim, O. Y., and Gho, Y. S. (2016). Proteomic profiling of Gram-negative bacterial outer membrane vesicles: current perspectives. Proteomics Clin. Appl. 10, 897–909. doi: 10.1002/prca.201600032
Lemire, S., Figueroa-Bossi, N., and Bossi, L. (2008). A singular case of prophage complementation in mutational activation of recET orthologs in Salmonella enterica serovar Typhimurium. J. Bacteriol. 190, 6857–6866. doi: 10.1128/JB.00769-08
Liu, Q., Yi, J., Liang, K., Hu, B., Zhang, X., Curtiss, R. III, et al. (2016a). Outer membrane vesicles from flagellin-deficient Salmonella enterica serovar Typhimurium induce cross-reactive immunity and provide cross-protection against heterologous Salmonella challenge. Sci. Rep. 6:34776. doi: 10.1038/srep34776
Liu, Q., Yi, J., Liang, K., Liu, T., Roland, K. L., Jiang, Y., et al. (2016b). Outer membrane vesicles derived from Salmonella Typhimurium mutants with truncated LPS induce cross-protective immune responses against infection of Salmonella enterica serovars in the mouse model. Int. J. Med. Microbiol. 306, 697–706. doi: 10.1016/j.ijmm.2016.08.004
Liu, Q., Yi, J., Liang, K., Zhang, X., and Liu, Q. (2017). Outer membrane vesicles derived from Salmonella enteritidis protect against the virulent wild-type strain infection in a mouse model. J. Microbiol. Biotechnol. 27, 1519–1528. doi: 10.4014/jmb.1705.05028
Markovski, M., Bohrhunter, J. L., Lupoli, T. J., Uehara, T., Walker, S., Kahne, D. E., et al. (2016). Cofactor bypass variants reveal a conformational control mechanism governing cell wall polymerase activity. Proc. Natl. Acad. Sci. U.S.A. 113, 4788–4793. doi: 10.1073/pnas.1524538113
McBroom, A. J., Johnson, A. P., Vemulapalli, S., and Kuehn, M. J. (2006). Outer membrane vesicle production by Escherichia coli is independent of membrane instability. J. Bacteriol. 188, 5385–5392. doi: 10.1128/JB.00498-06
McBroom, A. J., and Kuehn, M. J. (2007). Release of outer membrane vesicles by Gram-negative bacteria is a novel envelope stress response. Mol. Microbiol. 63, 545–558. doi: 10.1111/j.1365-2958.2006.05522.x
McClelland, M., Florea, L., Sanderson, K., Clifton, S. W., Parkhill, J., Churcher, C., et al. (2000). Comparison of the Escherichia coli K-12 genome with sampled genomes of a Klebsiella pneumoniae and three Salmonella enterica serovars, Typhimurium, Typhi and Paratyphi. Nucleic Acids Res. 28, 4974–4986. doi: 10.1093/nar/28.24.4974
Missiakas, D., Mayer, M. P., Lemaire, M., Georgopoulos, C., and Raina, S. (1997). Modulation of the Escherichia coli sigmaE (RpoE) heat-shock transcription-factor activity by the RseA, RseB and RseC proteins. . Mol. Microbiol. 24, 355–371. doi: 10.1046/j.1365-2958.1997.3601713.x
Murphy, K., Park, A. J., Hao, Y., Brewer, D., Lam, J. S., and Khursigara, C. M. (2014). Influence of O polysaccharides on biofilm development and outer membrane vesicle biogenesis in Pseudomonas aeruginosa PAO1. J. Bacteriol. 196, 1306–1317. doi: 10.1128/JB.01463-13
Ortega, A. P., Villagra, N. A., Urrutia, I. M., Valenzuela, L. M., Talamilla-Espinoza, A., Hidalgo, A. A., et al. (2016). Lose to win: marT pseudogenization in Salmonella enterica serovar Typhi contributed to the surV-dependent survival to H2O2, and inside human macrophage-like cells. Infect. Genet. Evol. 45, 111–121. doi: 10.1016/j.meegid.2016.08.029
Oscarsson, J., Westermark, M., Lofdahl, S., Olsen, B., Palmgren, H., Mizunoe, Y., et al. (2002). Characterization of a pore-forming cytotoxin expressed by Salmonella enterica serovars Typhi and Paratyphi A. Infect. Immun. 70, 5759–5769. doi: 10.1128/IAI.70.10.5759-5769.2002
Park, J. S., Lee, W. C., Yeo, K. J., Ryu, K. S., Kumarasiri, M., Hesek, D., et al. (2012). Mechanism of anchoring of OmpA protein to the cell wall peptidoglycan of the gram-negative bacterial outer membrane. FASEB J. 26, 219–228. doi: 10.1096/fj.11-188425
Parkhill, J., Dougan, G., James, K. D., Thomson, N. R., Pickard, D., Wain, J., et al. (2001). Complete genome sequence of a multiple drug resistant Salmonella enterica serovar Typhi CT18. Nature 413, 848–852. doi: 10.1038/35101607
Pimenta, A. L., Young, J., Holland, I. B., and Blight, M. A. (1999). Antibody analysis of the localisation, expression and stability of HlyD, the MFP component of the E. coli haemolysin translocator. Mol. Gen. Genet. 261, 122–132. doi: 10.1007/s004380050949
Porwollik, S., Boyd, E. F., Choy, C., Cheng, P., Florea, L., Proctor, E., et al. (2004). Characterization of Salmonella enterica subspecies I genovars by use of microarrays. J. Bacteriol. 186, 5883–5898. doi: 10.1128/JB.186.17.5883-5898.2004
Rhodius, V. A., Suh, W. C., Nonaka, G., West, J., and Gross, C. A. (2006). Conserved and variable functions of the sigmaE stress response in related genomes. PLoS Biol. 4:e2. doi: 10.1371/journal.pbio.0040002
Ricci, V., Chiozzi, V., Necchi, V., Oldani, A., Romano, M., Solcia, E., et al. (2005). Free-soluble and outer membrane vesicle-associated VacA from Helicobacter pylori: two forms of release, a different activity. Biochem. Biophys. Res. Commun. 337, 173–178. doi: 10.1016/j.bbrc.2005.09.035
Rouf, S. F., Ahmad, I., Anwar, N., Vodnala, S. K., Kader, A., Romling, U., et al. (2011a). Opposing contributions of polynucleotide phosphorylase and the membrane protein NlpI to biofilm formation by Salmonella enterica serovar Typhimurium. J. Bacteriol. 193, 580–582. doi: 10.1128/JB.00905-10
Rouf, S. F., Anwar, N., Clements, M. O., and Rhen, M. (2011b). Genetic analysis of the pnp-deaD genetic region reveals membrane lipoprotein NlpI as an independent participant in cold acclimatization of Salmonella enterica serovar Typhimurium. FEMS Microbiol. Lett. 325, 56–63. doi: 10.1111/j.1574-6968.2011.02416.x
Sanchez-Torres, V., Maeda, T., and Wood, T. K. (2010). Global regulator H-NS and lipoprotein NlpI influence production of extracellular DNA in Escherichia coli. Biochem. Biophys. Res. Commun. 401, 197–202. doi: 10.1016/j.bbrc.2010.09.026
Santos, T. M., Lin, T. Y., Rajendran, M., Anderson, S. M., and Weibel, D. B. (2014). Polar localization of Escherichia coli chemoreceptors requires an intact Tol-Pal complex. Mol. Microbiol. 92, 985–1004. doi: 10.1111/mmi.12609
Sauvage, E., Kerff, F., Terrak, M., Ayala, J. A., and Charlier, P. (2008). The penicillin-binding proteins: structure and role in peptidoglycan biosynthesis. FEMS Microbiol. Rev. 32, 234–258. doi: 10.1111/j.1574-6976.2008.00105.x
Schwechheimer, C., Rodriguez, D. L., and Kuehn, M. J. (2015). NlpI-mediated modulation of outer membrane vesicle production through peptidoglycan dynamics in Escherichia coli. Microbiologyopen. 4, 375–389. doi: 10.1002/mbo3.244
Sha, J., Fadl, A. A., Klimpel, G. R., Niesel, D. W., Popov, V. L., and Chopra, A. K. (2004). The two murein lipoproteins of Salmonella enterica serovar Typhimurium contribute to the virulence of the organism. Infect. Immun. 72, 3987–4003. doi: 10.1128/IAI.72.7.3987-4003.2004
Singh, S. S., Singh, N., Bonocora, R. P., Fitzgerald, D. M., Wade, J. T., and Grainger, D. C. (2014). Widespread suppression of intragenic transcription initiation by H-NS. Genes Dev. 28, 214–219. doi: 10.1101/gad.234336.113
Sonntag, I., Schwarz, H., Hirota, Y., and Henning, U. (1978). Cell envelope and shape of Escherichia coli: multiple mutants missing the outer membrane lipoprotein and other major outer membrane proteins. J. Bacteriol. 136, 280–285.
Thoma, J., Manioglu, S., Kalbermatter, D., Bosshart, P. D., Fotiadis, D., and Müller, D. J. (2018). Protein-enriched outer membrane vesicles as a native platform for outer membrane protein studies. Commun. Biol. 1:23. doi: 10.1038/s42003-018-0027-5
Toro, C. S., Mora, G. C., and Figueroa-Bossi, N. (1998). Gene transfer between related bacteria by electrotransformation: mapping Salmonella typhi genes in Salmonella typhimurium. J. Bacteriol. 180, 4750–4752.
Urrutia, I. M., Fuentes, J. A., Valenzuela, L. M., Ortega, A. P., Hidalgo, A. A., and Mora, G. C. (2014). Salmonella Typhi shdA: pseudogene or allelic variant? Infect. Genet. Evol. 26, 146–152. doi: 10.1016/j.meegid.2014.05.013
Valenzuela, C., Ugalde, J. A., Mora, G. C., Alvarez, S., Contreras, I., and Santiviago, C. A. (2014). Draft Genome Sequence of Salmonella enterica Serovar Typhi Strain STH2370. Genome Announc. 2:e00104-14. doi: 10.1128/genomeA.00104-14
Valvano, M. A., Marolda, C. L., Bittner, M., Glaskin-Clay, M., Simon, T. L., and Klena, J. D. (2000). The rfaE gene from Escherichia coli encodes a bifunctional protein involved in biosynthesis of the lipopolysaccharide core precursor ADP-L-glycero-D-manno-heptose. J. Bacteriol. 182, 488–497. doi: 10.1128/JB.182.2.488-497.2000
Villagra, N. A., Fuentes, J. A., Jofre, M. R., Hidalgo, A. A., Garcia, P., and Mora, G. C. (2012). The carbon source influences the efflux pump-mediated antimicrobial resistance in clinically important Gram-negative bacteria. J. Antimicrob. Chemother. 67, 921–927. doi: 10.1093/jac/dkr573
Wai, S. N., Lindmark, B., Soderblom, T., Takade, A., Westermark, M., Oscarsson, J., et al. (2003). Vesicle-mediated export and assembly of pore-forming oligomers of the enterobacterial ClyA cytotoxin. Cell 115, 25–35. doi: 10.1016/S0092-8674(03)00754-2
Wessel, A. K., Liew, J., Kwon, T., Marcotte, E. M., and Whiteley, M. (2013). Role of Pseudomonas aeruginosa peptidoglycan-associated outer membrane proteins in vesicle formation. J. Bacteriol. 195, 213–219. doi: 10.1128/JB.01253-12
Wojdyla, J. A., Cutts, E., Kaminska, R., Papadakos, G., Hopper, J. T., Stansfeld, P. J., et al. (2015). Structure and function of the Escherichia coli Tol-Pal stator protein TolR. J. Biol. Chem. 290, 26675–26687. doi: 10.1074/jbc.M115.671586
Wyborn, N. R., Clark, A., Roberts, R. E., Jamieson, S. J., Tzokov, S., Bullough, P. A., et al. (2004a). Properties of haemolysin E (HlyE) from a pathogenic Escherichia coli avian isolate and studies of HlyE export. Microbiology 150, 1495–1505.
Wyborn, N. R., Stapleton, M. R., Norte, V. A., Roberts, R. E., Grafton, J., and Green, J. (2004b). Regulation of Escherichia coli hemolysin E expression by H-NS and Salmonella SlyA. J. Bacteriol. 186, 1620–1628.
Yang, D. C., Peters, N. T., Parzych, K. R., Uehara, T., Markovski, M., and Bernhardt, T. G. (2011). An ATP-binding cassette transporter-like complex governs cell-wall hydrolysis at the bacterial cytokinetic ring. Proc. Natl. Acad. Sci. U.S.A. 108, E1052–E1060. doi: 10.1073/pnas.1107780108
Yeh, Y. C., Comolli, L. R., Downing, K. H., Shapiro, L., and Mcadams, H. H. (2010). The Caulobacter Tol-Pal complex is essential for outer membrane integrity and the positioning of a polar localization factor. J. Bacteriol. 192, 4847–4858. doi: 10.1128/JB.00607-10
Keywords: Outer membrane vesicles, Salmonella Typhi, ompA, mrcB, rfaE, yibP, tolR, degS
Citation: Nevermann J, Silva A, Otero C, Oyarzún DP, Barrera B, Gil F, Calderón IL and Fuentes JA (2019) Identification of Genes Involved in Biogenesis of Outer Membrane Vesicles (OMVs) in Salmonella enterica Serovar Typhi. Front. Microbiol. 10:104. doi: 10.3389/fmicb.2019.00104
Received: 11 September 2018; Accepted: 17 January 2019;
Published: 04 February 2019.
Edited by:Marie-Joelle Virolle, Centre National de la Recherche Scientifique (CNRS), France
Reviewed by:Haijian Zhou, National Institute for Communicable Disease Control and Prevention (China CDC), China
Ben Davies Tall, U.S. Food and Drug Administration, United States
G. Marcela Rodriguez, Rutgers, The State University of New Jersey, United States
Copyright © 2019 Nevermann, Silva, Otero, Oyarzún, Barrera, Gil, Calderón and Fuentes. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Juan A. Fuentes, firstname.lastname@example.org