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Research Article

Type IV Pilus Proteins Form an Integrated Structure Extending from the Cytoplasm to the Outer Membrane

  • Chengyun Li,

    Affiliations: State Key Laboratory of Microbial Technology, School of Life Science, Shandong University, Jinan, China, Department of Biological Sciences, Virginia Tech, Blacksburg, Virginia, United States of America

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  • Regina A. Wallace,

    Affiliation: Department of Biological Sciences, Virginia Tech, Blacksburg, Virginia, United States of America

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  • Wesley P. Black,

    Affiliation: Department of Biological Sciences, Virginia Tech, Blacksburg, Virginia, United States of America

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  • Yue-zhong Li,

    Affiliation: State Key Laboratory of Microbial Technology, School of Life Science, Shandong University, Jinan, China

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  • Zhaomin Yang mail

    zmyang@vt.edu

    Affiliation: Department of Biological Sciences, Virginia Tech, Blacksburg, Virginia, United States of America

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  • Published: July 26, 2013
  • DOI: 10.1371/journal.pone.0070144
Corrections

2 Sep 2014: The PLOS ONE Staff (2014) Correction: Type IV Pilus Proteins Form an Integrated Structure Extending from the Cytoplasm to the Outer Membrane. PLoS ONE 9(9): e107344. doi: 10.1371/journal.pone.0107344 | View correction

Abstract

The bacterial type IV pilus (T4P) is the strongest biological motor known to date as its retraction can generate forces well over 100 pN. Myxococcus xanthus, a δ-proteobacterium, provides a good model for T4P investigations because its social (S) gliding motility is powered by T4P. In this study, the interactions among M. xanthus T4P proteins were investigated using genetics and the yeast two-hybrid (Y2H) system. Our genetic analysis suggests that there is an integrated T4P structure that crosses the inner membrane (IM), periplasm and the outer membrane (OM). Moreover, this structure exists in the absence of the pilus filament. A systematic Y2H survey provided evidence for direct interactions among IM and OM proteins exposed to the periplasm. For example, the IM lipoprotein PilP interacted with its cognate OM protein PilQ. In addition, interactions among T4P proteins from the thermophile Thermus thermophilus were investigated by Y2H. The results indicated similar protein-protein interactions in the T4P system of this non-proteobacterium despite significant sequence divergence between T4P proteins in T. thermophilus and M. xanthus. The observations here support the model of an integrated T4P structure in the absence of a pilus in diverse bacterial species.

Introduction

Myxococcus xanthus is a gram-negative δ-proteobacterium that utilizes the type IV pilus (T4P) as a motility motor to move over solid surfaces [1]. Bacterial type IV pili (T4P), usually a few micrometers long and 6–7 nm in diameter, are polymeric protein filaments of the monomer pilin [2][4]. The T4P-mediated motility in M. xanthus is known as social (S) motility [2]. This is distinct from the adventurous (A) gliding motility of M. xanthus which is powered by an independent and different motility machinery [5]. T4P in rod-shaped bacteria such as M. xanthus are mostly localized to one of the two cell poles [2], [6], . Their retraction pulls a cell forward in M. xanthus S motility [8], [9] and in the twitching motility of the γ-proteobacterium Pseudomonas aeruginosa, the β-proteobacteria Neisseria meningitidis and Neisseria gonorrhoeae among other bacterial species [7], [10]. It is noteworthy that the T4P is the strongest among known biological motors as a single T4P can produce a stall force well over 100 pN when it retracts [8], [11]. M. xanthus S motility additionally requires extracellular polysaccharides (EPS) to function because M. xanthus EPS mutants are defective in S motility [12], [13]. The current model postulates that a T4P is triggered to retract at its cell proximal end when its distal end binds to EPS that are either associated with the M. xanthus cell surface or deposited on the gliding substratum [5].

About a dozen pil genes are required for T4P to function as a motor (see [1], [10], [14] and references therein). pilA encodes prepilin which is processed to mature pilin by a peptidase. pilM, pilN, pilO, pilP and pilQ usually form an operon in this gene order in M. xanthus and essentially all bacteria with these genes. PilM is a cytoplasmic protein that is likely anchored to the membrane by binding to the cytoplasmic tail of the bitopic transmembrane (TM) protein PilN. Like PilN, PilO is predicted to have a short cytoplasmic N-terminus, a TM helix and a periplasmic domain. PilP is an inner membrane (IM) lipoprotein exposed to the periplasm. PilQ is an outer membrane (OM) secretin which multimerizes to form a channel for the T4P to extend through the OM. PilC is predicted to be a polytopic TM protein with sizeable cytoplasmic domains. PilB and PilT are the two ATPases in the T4P system, the former responsible for T4P extension or assembly and the latter for retraction or disassembly.

In recent years, there have been various reports proposing a T4P IM complex consisting of PilM, PilN, PilO and PilP in P. aeruginosa and Neisseria [15][18]. Such a complex is consistent with the findings in the type II secretion system (T2SS) which is related to the T4P system evolutionarily [14], [19]. For example, the T2SS protein GspL has a single TM helix with a cytoplasmic and a periplasmic domain (GspLcyto and GspLperi). GspLcyto resembles PilM while GspLperi is similar to PilN, providing evidence that PilM and PilN interactions are genuine. The lipoprotein PilP shares structural similarity with the TM protein GspC in the T2SS [20], [21]. Both PilQ and the T2SS protein GspD are members of the secretin family which form channels in the OM [14], [22]. How T4P proteins form a multicomponent machine for its motor function remains an active area of scientific inquiry.

This paper reports our investigation into the interactions among T4P proteins. Besides its motor function in S motility, T4P had been shown to regulate EPS production in M. xanthus [23]. More recently, a suppressor mutation in pilB was discovered that was capable of restoring EPS production to a pilA deletion mutant [24]. The analysis of genetic suppression here suggested an integrated T4P structure consisting of PilB, PilC, PilM, PilN, PilO, PilP and PilQ in vivo. The interactions among these proteins and the formation of this structure are likely independent of a T4P filament because these interactions were observed in a pilA deletion background. Using a yeast two-hybrid (Y2H) system, we demonstrate that the OM protein PilQ can be bridged inward to the IM through interactions in the periplasm with PilP. In addition, Y2H experiments also detected similar interactions among the T4P proteins of the non-proteobacterium Thermus thermophilus. Our findings support an integrated T4P structure capable of extending from the cytoplasm through the IM, periplasm and OM in bacteria on diverse branches of the phylogenetic tree. At least in the proteobacterium M. xanthus, such a structure may form in the absence of the pilus filament.

Materials and Methods

Strains and Growth Conditions

M. xanthus strains used in this study are listed in Table 1. They were grown using CYE medium [25] at 32°C. XL-1 Blue (Stratagene) was the Escherichia coli strain used for plasmid construction, which was grown using Luria-Bertani (LB) medium [26] at 37°C. All plates contained 1.5% agar except CYE soft agar plates which contained 0.4% agar. When necessary, kanamycin, oxytetracycline and ampicillin were supplemented at 100, 15 and 100 µg/ml, respectively, to CYE and/or LB for selection.

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Table 1. Myxococcus xanthus strains used in this study.

doi:10.1371/journal.pone.0070144.t001

Two Saccharomyces cerevisiae strains for the Y2H study, AH109 (MATa, trp1-901, leu2-3, 112, ura3-52, his3-200, gal4Δ, gal80Δ, LYS2::GAL1UAS-GAL1TATA-HIS3, GAL2UAS-GAL2TATA-ADE2, URA3::MEL1UAS-MEL1TATA-lacZ) and Y187 (MATα, ura3-52, his3-200, ade2-101, trp1-901, leu2-3, 112, gal4Δ, met–, gal80Δ, URA3::GAL1UAS-GAL1TATA-lacZ) (Clontech), were grown using YPDA medium [1% Yeast extract, 2% Peptone (Bacto), 2% glucose, 0.003% adenine hemisulfate (pH 6.5)] (Clontech). Synthetic dropout (SD) media with specified nutrients omitted were used for selection and phenotype analysis in Y2H experiments (see later). All yeast cells were grown at 30°C.

Plasmids for M. xanthus Strain Construction

Two sets of plasmids (Table 2) were constructed for use in M. xanthus, one for deleting or replacing M. xanthus wild-type (WT) pil genes and the other for complementing pil deletions. All plasmids were confirmed by restriction digestions, polymerase chain reaction (PCR) and/or DNA sequencing.

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Table 2. Plasmids used in this study.

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The plasmids for pil gene deletions were pWB600 (ΔpilM), pWB601 (ΔpilN), pWB602 (ΔpilO) and, pWB603 (ΔpilP) [27][29]. These plasmids were constructed using pMY7 which is pZErO (Invitrogen) containing the Aeromonas hydrophila galK gene [30]. Deletion alleles, which were obtained using a two-step PCR procedure as described previously [31], were cloned into pMY7 digested with BamHI and EcoRI. The ΔpilM allele deleted codons from 8 to 392, ΔpilN from 6 to 222, ΔpilO from 8 to 189 and ΔpilP from 7 to 197 of their respective genes. In addition, pCL153 (pilBK327A or pilBWA) was used for the replacement of WT pilB (pilB+) with pilBWA (WA stands for Walker A), which was obtained from pWB630 [24] by digestion with HindIII and XbaI and cloned into the same sites in pBJ113.

The plasmids for complementation were pRW143 (pilC), pRW142 (pilM), pRW139 (pilN), pRW141 (pilO), pRW151 (pilP), and pCL179 (pilQ). These plasmids were constructed using the M. xanthus expression plasmid pWB425 as the vector [31]. The target genes were PCR amplified using primers containing KpnI and BamHI at the 5′ and 3′, respectively. These fragments were cloned into the same restriction sites in pWB425. Relative to the coding regions of each gene, pRW143 contains a fragment from 19 base pairs (bp) upstream to 13 bp downstream of pilC, pRW142 from 17 bp upstream to 15 bp downstream of pilM, pRW139 from 14 bp upstream to 17 bp downstream of pilN, pRW141 from 60 bp upstream to 20 bp downstream of pilO, pRW151 from 79 bp upstream to 49 pb downstream of (pilP), and pCL179 from 18 bp upstream to 25 bp downstream of (pilQ).

M. xanthus Strain Construction

All M. xanthus strains (Table 1) are isogenic to the laboratory WT strain DK1622 [2]. The plasmids pWB600 through pWB603 (Table 2) with deletion alleles of pilM through pilP were used for the construction of deletion mutants using DK1622 as the parent as described previously [31]. The resultant single pil deletion mutants are YZ1860 (ΔpilM), YZ1861 (ΔpilN), YZ1862 (ΔpilO), and YZ1863 (ΔpilP). pCL153 were then used to replace pilB+ with pilBWA in these strains to construct YZ1185 through YZ1188. In addition, pCL153 was used to replace pilB+ in DK10417 (ΔpilC), DK11135 (ΔpilG), DK11133 (ΔpilH), DK11122 (ΔpilI) and DK8615 (ΔpilQ) to construct YZ1182, YZ1183, YZ1181, YZ1184 and YZ1189, respectively. To construct YZ1190 and YZ1191, genomic DNA of DK10407 (ΔpilA::tet) was transformed into YZ1189 (ΔpilQ pilBWA) and DK8615 (ΔpilQ) [32][35].

For the complementation of single deletions of pilC, pilM, pilN, pilO, pilP and pilQ, the pRW series of plasmids (Table 2) were transformed into their corresponding deletion strains to construct YZ2214, YZ2225, YZ2215, YZ2226, YZ2234 and YZ1192, respectively.

Assays for S motility and EPS Production

M. xanthus cells in exponential growth were harvested and resuspended in MOPS (morpholinepropanesulfonic acid) buffer (10 mM MOPS (pH 7.6), 2 mM MgSO4) at 5.0×109 cells/ml. For the S-motility assay, 5 µl of the cell suspension was spotted to the center of a soft agar plate which was documented after 5 days of incubation. For EPS analysis, 5 µl of the cell suspension was placed on a CYE plate supplemented with Calcofluor white at 50 µg/ml. Plates were incubated for 6 days and the florescence was documented under ultraviolet (UV) illumination at ~365 nm [23], [29], [31].

Plasmids for Y2H Experiments (Table 2)

The MATCHMAKER System 3 from Clontech was used for the Y2H experiments in this study. The two cloning vectors pGAD (pGADT7) and pGBD (pGBKT7) allow proteins to be fused to the C-terminus of the GAL4 transcription activation domain (GAD) and GAL4 DNA binding domain (GBD), respectively [36]. A fragment with the coding region of interest of a gene from either M. xanthus or T. thermophilus was amplified by PCR and cloned into both pGAD and pGBD restricted by appropriate endonucleases. pGAD-T and pGBD-53, which contain fusions to T-antigen and p53, are provided by Clontech as positive controls.

pCL127, pCL128 and pCL131contain M. xanthus (Mx) PilN, PilP and PilO fused to GAD whereas pCL135, pCL136 and pCL134 contain the same proteins fused to GBD, respectively. Note that the signal peptide of PilP and the TM helices of PilN and PilO are excluded from these constructs. pCL150 and pCL152 contain the same MxPilQ fragment truncated at the C-terminus (PilQ′) in pGBD and pGAD; pCL141 and pCL142 contain the Secretin_N region at the center of MxPilQ (PilQc) in the two Y2H vectors.

Plasmids pCL180 through pCL193 contain fusions of T. thermophilus (Tt) Pil proteins to GAL4 in Y2H vectors (Table 2). pCL180, pCL182 and pCL184 contain TtPilN, TtPilO and TtPilP fused to GAD and pCL182, pCL183 and pCL185 contain the same protein fragments fused to GBD, respectively. The TtPilQ N-terminus is divided into N0, N1 and N2 subdomains. pCL186 through pCL193 contain N0 (PilQ0), N0 and N1 (PilQ01) and all three subdomains (PilQ012) in pGAD and pGBD, respectively.

Y2H Mating Protocol

The plates used for the Y2H mating protocol are SD without (−) tryptophan (Trp), leucine (Leu), histidine (His), adenine (Ade) or their combinations (Clontech). The mating protocol in the manual for the MATCHMAKER system (Clontech) was followed to examine systematic protein-protein interactions in Y2H. Briefly, a pGAD-derived plasmid was transformed into Y187 by selection on SD-Leu and a pGBD-derived plasmid into AH109 by selection on SD-Trp plates. 20 µl of culture of each transformant was placed in the same well of a 96-well plate seeded with 160 µl of YPDA each. After incubation for 18 hours on a rotary shaker, 5 µl of the culture from each well was transferred onto a 150×15 mm2 petri dish with SD-Trp-Leu medium in the same 96-well plate format. After 48–72 hours of incubation, cells were replica plated to SD-Ade and SD-His plates. After 3–5 days of incubation, growth on these plates was scored for the His+ or His and Ade+ or Ade phenotypes. Note that both SD-His and SD-Ade plates were without Trp and Leu. The SD-His plates were additionally supplemented with 2.5 mM 3-Amino-1, 2, 4-triazole (3-AT) which is a competitive inhibitor of the His3 enzyme.

Y2H by Co-transformation

A pair of pGAD- and pGBD-derived plasmids were co-transformed [37] into the yeast strain AH109 by selection on SD-Leu-Trp plates. Transformants were then examined for growth on SD-Ade and SD-His plates and for the expression of β-galactosidase. For the analysis of growth on SD-Ade and SD-His plates, cells in exponential growth were harvested and resuspended in SD medium. 5 µl of cell suspensions at 4×106, 8×105, 1.6×105 and 3.2×104 cells per ml were placed on SD-Ade and SD-His plates in a row from left to right. The growth was documented by photographs after 3 days of incubation. The analysis of β-galactosidase activity was performed as described by the Yeast Protocols Handbook (Clontech) using ONPG (o-nitrophenyl β-D-galactopyranoside) as the substrate. 1 unit of β-galactosidase is defined as the amount that hydrolyzes 1 µmol of ONPG per minute per cell.

Results and Discussion

Deletions of M. xanthus pilM, pilN, pilO, pilP, pilQ and pilC Can Be Complemented

It was observed previously that individual P. aeruginosa pilM, pilN, pilO and pilP mutants could not be complemented by their respective WT genes in trans unless other genes in the same gene cluster or operon were provided as well [15]. These observations were taken as part of the evidence to conclude that PilM, PilN, PilO and PilP formed an inner membrane (IM) complex critical for the stability of the PilQ secretin on the outer membrane (OM) [15]. A similar approach was taken here to examine the complementation of M. xanthus pil mutations as an attempt to study interactions among M. xanthus T4P proteins. Because pilM, pilN, pilO, pilP and pilQ are likely in an operon in M. xanthus as in most other bacteria [1], [10], in-frame deletions of these M. xanthus genes were constructed to minimize polar effects (see Materials and Methods). A pilC deletion was also constructed because PilC may play a key role in organizing an IM complex since it is the only predicted polytopic TM T4P protein [10]. When examined on soft agar plates (Figure 1), all mutants were found to be defective in S motility as anticipated since none was expected to assemble T4P [1], [38].

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Figure 1. pil deletions can be complemented in trans.

S motility was analyzed by colony spreading (or swarming) on soft agar plates as described in Materials and Methods. The pil deletion strains are DK10417 (ΔpilC), YZ1860 (ΔpilM), YZ1861 (ΔpilN), YZ1862 (ΔpilO), YZ1863 (ΔpilP) and DK8615 (ΔpilQ). The complemented stains are YZ2214 (ΔpilC/pilC), YZ2225 (ΔpilM/pilM), YZ2215 (ΔpilN/pilN), YZ2226 (ΔpilO/pilO), YZ2234 (ΔpilP/pilP) and YZ1192 (ΔpilQ/pilQ). The WT strain DK1622 was included on the top center as a control and the scale bar represents 5 mm. See Table 1 for more precise genotypes of the strains.

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Next, plasmids were constructed for complementation of these deletion mutants. Six fragments containing pilC, pilM, pilN, pilO, pilP and pilQ, respectively, were cloned into an expression vector [31] which is able to integrate at the Mx8 phage attachment site (att) on the M. xanthus chromosome. The resulting plasmids were transformed into their respective deletion strains and the transformants were examined on soft agar plates for S motility (Figure 1) which requires fully functional T4P. Unlike the observations in P. aeruginosa [15], these transformants all showed S motility similar to the WT. It is noted that expression of pil genes in trans in these complemented strains are likely lower than in the WT in situ [24], [39]. The previous observation [15] could be explained if T4P assembly is more sensitive to an imbalance of proteins forming a complex in P. aeruginosa than in M. xanthus. Alternatively, the small insertions or scar mutations in P. aeruginosa pil genes [15] could be partially polar on downstream genes.

pilBWA Suppresses the EPS Defect of ΔpilG, ΔpilH & ΔpilI, But Not That of ΔpilC, ΔpilM, ΔpilN, ΔpilO, ΔpilP, or ΔpilQ

Taking advantage of a newly constructed gain-of-function mutation in pilB, an alternative genetic approach was explored to examine if T4P proteins form an integrated structure in M. xanthus. PilB, a cytoplasmic ATPase in the T2SS ATPase superfamily, has been shown to function as the T4P assembly ATPase with ΔpilB mutations leading to a T4P phenotype [6], [40]. Previous results indicated that ΔpilA or any other pil mutants that were T4P were also defective in EPS production, indicating a role for T4P in EPS regulation in M. xanthus [23]. Recently a pilB mutation was found that restored EPS production to a ΔpilA mutant [24]. This mutation, which is referred to as pilBWA or pilBK327A, resulted in the substitution of the strictly conserved lysine (K) 327 with an alanine (A) in the signature Walker A box of such ATPases. To examine if pilBWA could suppress the EPS phenotype resulting from other T4P mutations, the pilB+ allele was replaced by pilBWA in the deletion mutants of pilC, pilM, pilN, pilO, pilP, and pilQ as well as pilG, pilH, and pilI, respectively. The resulting strains were examined on plates containing Calcofluor white, a fluorescent dye that binds to M. xanthus EPS (Figure 2). As indicated by fluorescence, pilBWA suppressed ΔpilG, ΔpilH and ΔpilI in EPS production, but not ΔpilC, ΔpilM, ΔpilN, ΔpilO, ΔpilP, or ΔpilQ.

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Figure 2. pilBWA suppresses some but not all T4P pil deletions in EPS production.

EPS levels were analyzed on plates with the fluorescent dye Calcofluor white (See Materials and Methods). The presence of fluorescence indicates EPS+ and its absence EPS. Each strip shows two strains, the upper is a strain with the indicated mutation(s) in a pilB+ background and the lower in the pilBWA background. Strains used are YZ690 (ΔpilA), YZ1573 (ΔpilA pilBWA), DK10417 (ΔpilC), YZ1182 (ΔpilC pilBWA), YZ1860 (ΔpilM), YZ1185 (ΔpilM pilBWA), DK11135 (ΔpilG), YZ1183 (ΔpilG pilBWA), DK11133 (ΔpilH), YZ1181 (ΔpilH pilBWA), DK11132 (ΔpilI), YZ1184 (ΔpilI pilBWA), YZ1191 (ΔpilA ΔpilQ) and YZ1190 (ΔpilA ΔpilQ pilBWA). pilBWA failed to suppress ΔpilN, ΔpilO, ΔpilP and ΔpilQ as it did ΔpilC and ΔpilM (data not shown).

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The lack of suppression of ΔpilQ by pilBWA was further investigated. PilQ is the secretin that forms a multimeric channel in the OM to allow the passage of the pilus filament through the OM [38]. It was previously reported that a N. meningitidis pilQ mutant assembled T4P in the periplasm likely because a pilQ mutant in an otherwise WT background can still assemble the pilus filament in the periplasm even though it fails to extend through the OM [41], [42]. In addition, mutant PilA or pilins trapped in the IM may negatively influence EPS production [43]. In a pilQ mutant, either periplasmic pili and/or an increase in unassembled pilins in the IM could down regulate EPS levels. To examine if the lack of suppression of ΔpilQ by pilBWA was due to these reasons, we constructed a ΔpilA ΔpilQ pilBWA triple mutant. As shown in Figure 2, pilBWA still failed to restore EPS production to a ΔpilQ ΔpilA mutant. Because pilBWA suppresses ΔpilA (Figure 2) [24], the results here indicate that PilBWA requires PilQ to signal EPS production in M. xanthus in a ΔpilA background or the absence of a pilus.

What are the explanations for this pattern of suppression of pil mutations by pilBWA? The suppression of ΔpilG, ΔpilH and ΔpilI was perhaps not surprising. PilG, PilH and PilI are essential for the translocation of pillin across the IM [33] and their mutants in essence may resemble a ΔpilA mutant due to the lack of pilins and pili. The lack of suppression of ΔpilC and ΔpilM may also have simple explanations. PilM is a cytoplasmic protein [44] and the multi-TM protein PilC is predicted to have sizeable cytoplasmic loops [45]. A frugal explanation would be that PilBWA requires interactions with both PilC and PilM directly or through each other in the cytoplasm in order to signal EPS production. The suppression of ΔpilG, ΔpilH and ΔpilI by pilBWA as well as the lack of suppression of ΔpilC and ΔpilM may therefore be explained parsimoniously with little difficulty.

Without invoking multiple direct and indirect interactions, however, there would be no good explanation for the lack of suppression of ΔpilN, ΔpilO, ΔpilP and ΔpilQ by pilBWA. As has been mentioned in Introduction, PilQ forms an oligomeric passage for the T4P filament on the OM. PilP is a lipoprotein anchored to the IM by a lipid moiety [46]. PilO and PilN are both predicted to have similar membrane topology, each with a cytoplasmic N-terminal tail of a dozen residues, a TM helix followed by the C-terminus in the periplasm [47], [48]. It is known that the N-terminal tail of PilN interacts with PilM in the cytoplasm [44]. Taking into consideration the above structural information and the suppression patterns of various pil mutations by pilBWA in M. xanthus, a reasonable explanation assumes a multi-component complex consisting of all these proteins. To explain the requirement of PilQ for EPS production in a pilBWA background, for example, PilQ in the OM must be connected to the cytoplasmic PilM and/or the IM spanning PilC to affect the activity of PilBWA. This connection through the periplasm and the IM may involve PilP, PilO and/or PilN, but not necessarily the pilus filament. Such a model would explain how PilQ could influence the activity of PilBWA in the cytoplasm and why pilBWA suppresses none of the deletions of pilC, pilM, pilN, pilO and pilP. That is, PilBWA, which likely represents a particular conformation of PilB in vivo [24], must communicate either directly or indirectly with the IM protein PilC and the cytoplasmic protein PilM anchored to the IM by PilN [45]. The other proteins, PilO, PilP and PilQ, must in turn affect the activity of PilBWA indirectly through their interactions with PilC, PilM and/or PilN.

Interactions Among M. xanthus PilN, PilO, PilP and PilQ in Y2H System

The above model envisions an integrated T4P structure with extensive protein-protein interactions that were investigated more directly using the Y2H system. The Y2H mating protocol (See Materials and Methods) was utilized here since it can be used to examine interactions among large numbers of proteins and their domains. In this protocol, a protein or its domain is fused to the C-termini of both the GAL4 activation domain (GAD) and DNA binding domain (GBD) in pGAD and pGBD vectors, respectively (Table 2). The two fusion plasmids are then transformed into two yeast reporter strains of the opposite mating types (Y187: MATα and AH109: MATa), respectively. The two strains are then mated with each other and with others expressing fusions to a different GAL4 domain. After mating, the diploid cells containing a pGAD- and a pGBD-derived plasmids are examined on selective plates without histidine (SD-His) or adenine (SC-Ade) for His+ and Ade+ phenotypes as indicators of the expression of two reporter genes of the Y2H system.

Table 3 represents results for PilN, PilO, PilP and PilQ using this mating protocol. The constructs for PilN and PilO excluded their N-terminal tails and TM domains and those for PilP excluded its predicted lipoprotein signal peptide at the N-terminus [49]. PilQ constructs were designed based on primary sequence conservation (Figure 3A) and secondary structure predictions [50], [51] (data not shown). The PilQ′ construct (Figure 3A and Table 1) excluded the C-terminal secretin region which is predicted to form β-barrels in the OM membrane [51]; the PilQc construct contained the conserved Secretin_N region immediately N-terminal of the more highly conserved secretin domain (Figure 3A). In this experiment, seven pairs of plasmids conferred growth on selective media (Table 3). The results suggested the following four pairwise interactions: PilN-PilO, PilO-PilP, PilP-PilQ and PilQ-PilQ. PilP interacted with both PilQ′ and PilQc (Figure 3A) but not with two other constructs containing the N-termini of PilQ truncated before Secretin_N (data not shown). Therefore, the Secretin_N region may solely contribute to the interaction of PilQ with PilP in M. xanthus. PilP and PilQ′ were the only pair whose interactions were detected in both orientations in reciprocal Y2H vectors while three of the GAL4 fusions (GAD-PilN, GBD-PilO and GBD-PilQc) gave no positive interactions in this Y2H experiment (Table 3). It is noteworthy that the four pairs of interactions detected here (Table 3) are all predicted to be in the periplasm of M. xanthus. Various fragments of PilB, PilM and PilC were also examined, but no interaction between them was detected using this Y2H mating protocol (data not shown).

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Figure 3. Conserved domains of PilQ.

Panel A. Conserved domains of MxPilQ (901 residues) and TtPilQ (757 residues) [58]. The conserved feature are drawn to scale and areindicated by shaded letters below both protein. Each has the PilQ region at their C-terminus consisting of the highly conserved Secretin domain and the region immediately N-terminal of secretin (Secretin_N). Two AMIN domains [59] are found at the N-terminus of MxPilQ but not TtPilQ. The brackets and the labels above indicate the different Y2H constructs and/or subdomains in each protein. Panel B. Structural alignment of the N-termini of TtPilQ and the T2SS secretin GspD from Enterotoxigenic E. coli (ETEC) [50], [55]. The boundaries between N0 and N1 as well as N1 and N2 subdomains in GspD are indicated by arrows (↑). The secondary structure of GspD from crystallography and that of TtPilQ predicted from modeling are indicated below and above the aligned sequences, respectively, with β strands represented by block arrows and α helices by cylinders.

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Table 3. Interactions among M. xanthus Pil proteins detected by Y2H mating protocol.

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The interactions detected by the mating protocol were verified by co-transformation of the yeast strain AH109 and additional analysis of the expression of reporter genes. Briefly, each of the seven pairs of plasmids that gave positive interactions (Table 3) was co-transformed into AH109 and the transformants were examined phenotypically. As a semi-quantitative analysis of the strength of interactions, 5-fold serial dilutions of the transformants were spotted on SD-His and SD-Ade plates as shown in Figures 4A and 4B. The pairs that showed positive interactions in the mating protocol (Table 2) all showed growth on these two selective plates. The expression of β-galactosidase, the third reporter of the Y2H system, confirmed these positive interactions (Figure 5A). When each of the plasmids was co-transformed with an empty Y2H vector, none of them led to the expression of the three reporters (Figures 4A, 4B & 5A), eliminating the possibility of autoactivation by any single GAL4 fusion.

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Figure 4. Pairwise interactions among Pil proteins in Y2H system.

Panels A and B. Interactions among M. xanthus Pil proteins. Panels C, D and E. Interactions among T. thermophilus Pil proteins. The first and second columns on the left of each panel indicate Pil proteins or fragments fused to GAD and GBD in Y2H plasmids by their last letter, respectively. V indicates an empty Y2H vector. N0, N1, N2 and their combinations are represented by their numerals only. Last row in each panel contained the positive control with T-antigen (T) and p53 (53). The left half of each panel shows growth on SD-His and the right on SD-Ade plates, respectively. The spots in each row in a panel were inoculated by serial dilutions of the same yeast cells with the indicated Y2H plasmids. See text and Materials and Methods for details.

doi:10.1371/journal.pone.0070144.g004
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Figure 5. Quantification of β-galactosidase in Y2H experiment.

The upper and lower panels show the β-galactosidase activity for Pil protein interactions in Y2H experiments from M. xanthus and T. thermophilus, respectively. The values for β-galactosidase activity were the average of three independent experiments and samples in each experiment were analyzed in triplicate. See Figure 4 for protein designations under each panel. The bars for the vector controls are shaded for comparison. See text and Materials and Methods for more details.

doi:10.1371/journal.pone.0070144.g005

In summary, the PilQ-PilQ interaction is consistent with its oligomerization in the OM. The PilQ-PilP, PilP-PilO and PilO-PilN pairwise interactions connect PilQ to PilN which interacts with PilM in the cytoplasm [44]. These results are therefore supportive of a model wherein the OM secretin is connected to the cytoplasmic ATPase PilB through a series of physical interactions as proposed based on the suppression of pil mutations by pilBWA in EPS production (Figure 2). The pilus filament is apparently not required for the formation of this integrated T4P complex as pilBWA suppresses ΔpilA yet not a ΔpilA ΔpilQ double mutation (Figure 2).

Similar Interactions Occur Among T. thermophilus T4P Proteins

T4P systems are found in diverse lineages in bacteria [7], [10], but the best experimental systems for T4P studies, which include M. xanthus, P. aeruginosa, and Neisseria sp., are proteobacteria [10]. We used the Y2H system to investigate whether the interactions reported here for M. xanthus are conserved in the non-proteobacterium T. thermophilus (Tt), a thermophile in the deep-rooted Deinococci-Thermus phylum [52]. The motivation for this choice included the prevalent use of thermophilic proteins for structural studies including T. thermophilus T4P proteins [44], [45], [53]. The conservation of protein-protein interactions, if true, would allow the insights from structural studies of T. thermophilus T4P proteins to be applied to experimentally more accessible systems, and vice versa.

Most T4P proteins and their domains are well conserved in different organisms and so is the gene order in the pilM, pilN, pilO, pilP and pilQ gene cluster [10]. There are exceptions when it comes to PilQ and PilP, however [54]. As shown in Figure 3A, except the highly conserved secretin domain and the adjacent Secretin_N region, there is little homology between T. thermophilus PilQ (TtPilQ) and M. xanthus PilQ (MxPilQ) with the latter over 140 residues longer. Moreover, instead of the IM lipoprotein PilP, the gene between pilO and pilQ in T. thermophilus encodes PilW (TtPilW), which is predicted to have a single TM helix with a periplasmic region without homology to any known T4P or T2SS proteins from other bacterial lineages [54]. However, because pilW is in the same chromosomal location as pilP relative to other pil genes, it is possible that PilW may have similar functions as PilP in bridging PilQ to the IM and to other IM T4P proteins in T. thermophilus. The interactions among T. thermophilus PilN, PilO, PilW and PilQ were therefore investigated by Y2H for comparison with M. xanthus T4P proteins.

We first examined the interactions among T. thermophilus PilW, PilO and PilN by cloning their C-termini truncated immediately after their predicted TM helices into the Y2H vectors (Table 2). Pairs of pGAD- and pGBD-derived fusion plasmids were then transformed into the Y2H reporter strain AH109. As shown in Figure 4C, transformants of PilO and PilW constructs as well as those of PilO and PilN grew on SD-His and SD-Ade plates. These observations were further validated by the expression of β-galactosidase (Figure 5B). The results indicate that despite sequence divergence, PilW as well as PilO and PilN interact similarly in T. thermophilus as PilP, PilO and PilN in M. xanthus.

Next, we examined the interactions between TtPilW and TtPilQ. Recall that PilP interacted with the Secretin_N region of MxPilQ in Y2H (PilQc construct in Figures 3A and 4A). Therefore, we tested the interaction of TtPilW with the Secretin_N region of TtPilQ (Figure 3A) using Y2H, but the relevant yeast co-transformants grew on neither SD-His nor SD-Ade (data not shown). Interestingly, while the N-terminus of TtPilQ shares no homology with M. xanthus PilQ (Figure 3A), it does have limited similarity with the periplasmic N-terminus of the T2SS secretin GspD (GspDperi) (Figure 3B). The structure of the N-terminus of TtPilQ can in fact be modeled using the structure of GspDperi as a template [50], [55]. The secondary structure prediction of this modeling is shown in Figure 3B. Using the structures of GspDperi [55] as a guide, the N-terminus of TtPilQperi can be similarly divided into N0, N1 and N2 subdomains (Figure 3B). While these GspDperi subdomains resemble one another in structure to some degree [55], only N0 was shown to interact with GspC which is an ortholog of PilP in T2SS [20]. TtPilW showed interactions with N0 and the combination of N0 and N1 of TtPilQ (TtPilQ0 and TtPilQ01) in Y2H in both orientations as indicated by growth on SD-His and SD-Ade plates (Figure 4D) and by expression of β-galactosidase (Figure 5B). TtPilW was also detected to interact with the three subdomains combined (TtPilQ012) in one orientation (Figure 4C) but not with N1 or N2 individually (data not shown). The strengths of interactions of TtPilW with TtPilQ0 and with TtPilQ01 in both orientations were similar as indicated by growth and β-galactosidase activity (Figures 4D & 5B). These observations suggest that like GspC, TtPilW interacts with the N0 subdomain of its cognate secretin despite the lack of any detectable similarity between TtPilW with GspC or PilP at the level of their primary [54] or predicted higher order structures (data not shown). Such interactions allow the bridging of PilQ to the IM in both T. thermophilus and M. xanthus.

The interaction of TtPilQ with itself was also investigated. Constructs similar to M. xanthus PilQ′ and PilQc gave no indication of interaction using Y2H (data not shown). We additionally examined constructs containing N0, N1 and N2 in various combinations. Only two pairs among them were found to confer interactions in Y2H as shown in Figures 4E and 5B; these are TtPilQ0 with itself and with TtPilQ012. It is interesting to note that in the Y2H system, M. xanthus PilQ-PilQ interactions are mediated by Secretin_N whereas T. thermophilus PilQ-PilQ interactions by N0 (Figures 3, 4 and 5). Nevertheless, these results are consistent with the conservation of structural interactions in the periplasm and the multimerization of PilQ in both the proteobacterium M. xanthus and the non-proteobacterium T. thermophilus.

Concluding Remarks

Our analysis of genetic suppression here suggested an integrated T4P structure in M. xanthus (Figure 6). A systematic Y2H analysis detected the following pairwise interactions among M. xanthus Pil proteins: PilQ-PilQ, PilQ-PilP, PilP-PilO and PilO-PilN. Since PilP is an IM lipoprotein and PilN as well as PilO are integral IM proteins, these interactions allow the OM protein PilQ to communicate with the IM T4P proteins. PilM, while cytoplasmic, is likely anchored to the IM by binding to the cytoplasmic tail of PilN [44], [56]. These results support a model of an integrated T4P structure in M. xanthus because the ability of PilBWA to signal for EPS production requires all of these proteins. This integrated structure would include PilQ in the OM, the TM proteins PilN, PilO and PilC as well as the lipoprotein PilP on the IM. The cytoplasmic proteins PilM and PilB may associate with this structure dynamically as indicated by the genetic suppression patterns by pilBWA. The interactions among these proteins in M. xanthus apparently occur in the absence of the pilus filament as pilBWA suppresses ΔpilA but none of the other pil deletions.

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Figure 6. An integrated T4P structure.

Pil proteins in this model are represented by their single letter designations. OM, outer membrane; IM, inner membrane. This integrated T4P structure, which consists of the indicated Pil protein at the minimum, may exist in the absence of the pilus filament. The interactions of PilB with PilC and PilM are inferred from genetic analysis and they may be either direct or indirect. See main text for details.

doi:10.1371/journal.pone.0070144.g006

Using the same Y2H system, we extended the above interactions to T4P proteins from the non-proteobacterium T. thermophilus. It is especially noteworthy that TtPilW shows interactions with the same T4P proteins as PilP even though they share no detectable structural similarity in silico. Interestingly, the more detailed interactions of TtPilW and TtPilQ resembles those of GspC and GspD in T2SS instead of M. xanthus PilP and PilQ. That is, both PilW and GspC interact with the N0 subdomains of their partner secretin. Similar observations were made recently between PilP and PilQ in P. aeruginosa and N. meningitidis [56], [57]. The findings with T. thermophilus T4P proteins suggest that the interactions among T4P proteins and the formation of an integrated T4P structure are conserved across different bacterial lineages despite extensive sequence and structural divergence. These observations suggest that a discovery in one bacterium may be applicable to related T4P systems in others even when they are evolutionarily distant. While the interactions reported here are mostly consistent with previous reports [[14], [56], [57] and references therein], they are by no means exhaustive as indicated by a recent report on N. meningitidis T4P protein-protein interactions using the bacterial two-hybrid (B2H) system in E. coli [17]. Substantially more interactions were detected in the B2H system, which may require additional verification by alternative approaches because E. coli shares many proteins with N. meningitidis than does yeast with bacteria.

The results here are supportive of other reports in the literature. A very recent publication based on in vitro experiments concluded that P. aeruginosa PilM, PilN, PilO, PilP and PilQ form a transenvelope network that interact with PilA [56]. The results here clearly indicate that a T4P complex can exist independently of PilA or the pilus filament. It was previously observed that certain T4P proteins localize to both cell poles in M. xanthus even though only one of the two poles may actively assemble and disassemble T4P at any given moment [40]. The existence of a T4P complex independent of the pilus filament provides support that the T4P proteins localized to the un-piliated pole may be organized into a complex standing ready for T4P assembly for the directional reversal of T4P mediate bacterial surface motility [38], [40].

Acknowledgments

We thank Dr. Manli Davis for the construction of pMY7.

Author Contributions

Conceived and designed the experiments: ZY YL CL RAW. Performed the experiments: CL RAW WPB. Analyzed the data: CL RAW WPB ZY. Wrote the paper: ZY CL.

References

  1. 1. Wall D, Kaiser D (1999) Type IV pili and cell motility. Mol Microbiol 32: 1–10. doi: 10.1046/j.1365-2958.1999.01339.x
  2. 2. Kaiser D (1979) Social gliding is correlated with the presence of pili in Myxococcus xanthus. Proc Natl Acad Sci USA 76: 5952–5956. doi: 10.1073/pnas.76.11.5952
  3. 3. Wu SS, Kaiser D (1995) Genetic and functional evidence that Type IV pili are required for social gliding motility in Myxococcus xanthus. Mol Microbiol 18: 547–558. doi: 10.1111/j.1365-2958.1995.mmi_18030547.x
  4. 4. Craig L, Pique ME, Tainer JA (2004) Type IV pilus structure and bacterial pathogenicity. Nat Rev Microbiol 2: 363–378. doi: 10.1038/nrmicro885
  5. 5. Mauriello EM, Mignot T, Yang Z, Zusman DR (2010) Gliding motility revisited: how do the myxobacteria move without flagella? Microbiol Mol Biol Rev 74: 229–249. doi: 10.1128/mmbr.00043-09
  6. 6. Jakovljevic V, Leonardy S, Hoppert M, Sogaard-Andersen L (2008) PilB and PilT are ATPases acting antagonistically in type IV pilus function in Myxococcus xanthus. J Bacteriol 190: 2411–2421. doi: 10.1128/jb.01793-07
  7. 7. Mattick JS (2002) Type IV pili and twitching motility. Annu Rev Microbiol 56: 289–314. doi: 10.1146/annurev.micro.56.012302.160938
  8. 8. Clausen M, Jakovljevic V, Sogaard-Andersen L, Maier B (2009) High-force generation is a conserved property of type IV pilus systems. J Bacteriol 191: 4633–4638. doi: 10.1128/jb.00396-09
  9. 9. Shi W, Sun H (2002) Type IV pilus-dependent motility and its possible role in bacterial pathogenesis. Infect Immun 70: 1–4. doi: 10.1128/iai.70.1.1-4.2002
  10. 10. Pelicic V (2008) Type IV pili: e pluribus unum? Mol Microbiol 68: 827–837. doi: 10.1111/j.1365-2958.2008.06197.x
  11. 11. Maier B, Potter L, So M, Long CD, Seifert HS, et al. (2002) Single pilus motor forces exceed 100 pN. Proc Natl Acad Sci U S A 99: 16012–16017. doi: 10.1073/pnas.242523299
  12. 12. Yang Z, Ma X, Tong L, Kaplan HB, Shimkets LJ, et al. (2000) Myxococcus xanthus dif genes are required for biogenesis of cell surface fibrils essential for social gliding motility. J Bacteriol 182: 5793–5798. doi: 10.1128/jb.182.20.5793-5798.2000
  13. 13. Weimer RM, Creighton C, Stassinopoulos A, Youderian P, Hartzell PL (1998) A chaperone in the HSP70 family controls production of extracellular fibrils in Myxococcus xanthus. J Bacteriol 180: 5357–5368.
  14. 14. Giltner CL, Nguyen Y, Burrows LL (2012) Type IV pilin proteins: versatile molecular modules. Microbiol Mol Biol Rev 76: 740–772. doi: 10.1128/mmbr.00035-12
  15. 15. Ayers M, Sampaleanu LM, Tammam S, Koo J, Harvey H, et al. (2009) PilM/N/O/P proteins form an inner membrane complex that affects the stability of the Pseudomonas aeruginosa type IV pilus secretin. J Mol Biol 394: 128–142. doi: 10.1016/j.jmb.2009.09.034
  16. 16. Tammam S, Sampaleanu LM, Koo J, Sundaram P, Ayers M, et al. (2011) Characterization of the PilN, PilO and PilP type IVa pilus subcomplex. Mol Microbiol 82: 1496–1514. doi: 10.1111/j.1365-2958.2011.07903.x
  17. 17. Georgiadou M, Castagnini M, Karimova G, Ladant D, Pelicic V (2012) Large-scale study of the interactions between proteins involved in type IV pilus biology in Neisseria meningitidis: characterization of a subcomplex involved in pilus assembly. Mol Microbiol 84: 857–873. doi: 10.1111/j.1365-2958.2012.08062.x
  18. 18. Tammam S, Sampaleanu LM, Koo J, Manoharan K, Daubaras M, et al. (2013) PilMNOPQ from the Pseudomonas aeruginosa type IV pilus system form a transenvelope protein interaction network that interacts with PilA. J Bacteriol doi: 10.1128/jb.00032-13
  19. 19. McLaughlin LS, Haft RJ, Forest KT (2012) Structural insights into the Type II secretion nanomachine. Curr Opin Struct Biol 22: 208–216. doi: 10.1016/j.sbi.2012.02.005
  20. 20. Korotkov KV, Johnson TL, Jobling MG, Pruneda J, Pardon E, et al. (2011) Structural and functional studies on the interaction of GspC and GspD in the type II secretion system. PLoS Pathog 7: e1002228. doi: 10.1371/journal.ppat.1002228
  21. 21. Golovanov AP, Balasingham S, Tzitzilonis C, Goult BT, Lian LY, et al. (2006) The solution structure of a domain from the Neisseria meningitidis lipoprotein PilP reveals a new beta-sandwich fold. J Mol Biol 364: 186–195. doi: 10.1016/j.jmb.2006.08.078
  22. 22. Korotkov KV, Sandkvist M, Hol WG (2012) The type II secretion system: biogenesis, molecular architecture and mechanism. Nat Rev Microbiol 10: 336–351. doi: 10.1038/nrmicro2762
  23. 23. Black WP, Xu Q, Yang Z (2006) Type IV pili function upstream of the Dif chemotaxis pathway in Myxococcus xanthus EPS regulation. Mol Microbiol 61: 447–456. doi: 10.1111/j.1365-2958.2006.05230.x
  24. 24. Black WP, Jing X, Schubot FD, Yang Z (2013) The PilB ATPase may represent a novel class of signal transducers. submitted.
  25. 25. Campos JM, Zusman DR (1975) Regulation of development in Myxococcus xanthus: effect of 3′:5′-cyclic AMP, ADP, and nutrition. Proc Natl Acad Sci USA 72: 518–522. doi: 10.1073/pnas.72.2.518
  26. 26. Miller JH (1972) Experiments in molecular genetics. Cold Spring Harbor, N.Y.: Cold Spring Harbor Laboratory.
  27. 27. Ueki T, Inouye S, Inouye M (1996) Positive-negative KG cassettes for construction of multi-gene deletions using a single drug marker. Gene 183: 153–157. doi: 10.1016/s0378-1119(96)00546-x
  28. 28. Julien B, Kaiser AD, Garza A (2000) Spatial control of cell differentiation in Myxococcus xanthus. Proc Natl Acad Sci USA 97: 9098–9103. doi: 10.1073/pnas.97.16.9098
  29. 29. Black WP, Yang Z (2004) Myxococcus xanthus chemotaxis homologs DifD and DifG negatively regulate fibril polysaccharide production. J Bacteriol 186: 1001–1008. doi: 10.1128/jb.186.4.1001-1008.2004
  30. 30. Seshadri R, Joseph SW, Chopra AK, Sha J, Shaw J, et al. (2006) Genome sequence of Aeromonas hydrophila ATCC 7966T: jack of all trades. J Bacteriol 188: 8272–8282. doi: 10.1128/jb.00621-06
  31. 31. Black WP, Xu Q, Cadieux CL, Suh SJ, Shi W, et al. (2009) Isolation and characterization of a suppressor mutation that restores Myxococcus xanthus exopolysaccharide production. Microbiology doi: 10.1099/mic.0.031070-0
  32. 32. Wu SS, Kaiser D (1997) Regulation of expression of the pilA gene in Myxococcus xanthus. J Bacteriol 179: 7748–7758.
  33. 33. Wu SS, Wu J, Cheng YL, Kaiser D (1998) The pilH gene encodes an ABC transporter homologue required for type IV pilus biogenesis and social gliding motility in Myxococcus xanthus. Mol Microbiol 29: 1249–1261. doi: 10.1046/j.1365-2958.1998.01013.x
  34. 34. Wall D, Kolenbrander PE, Kaiser D (1999) The Myxococcus xanthus pilQ (sglA) gene encodes a secretin homolog required for type IV pilus biogenesis, social motility, and development. J Bacteriol 181: 24–33.
  35. 35. Wu SS, Kaiser D (1996) Markerless deletions of pil genes in Myxococcus xanthus generated by counterselection with the Bacillus subtilis sacB gene. J Bacteriol 178: 5817–5821.
  36. 36. James P, Halladay J, Craig EA (1996) Genomic libraries and a host strain designed for highly efficient two-hybrid selection in yeast. Genetics 144: 1425–1436.
  37. 37. Gietz RD, Woods RA (2002) Screening for protein-protein interactions in the yeast two-hybrid system. Methods Mol Biol 185: 471–486. doi: 10.1385/1-59259-241-4:471
  38. 38. Nudleman E, Wall D, Kaiser D (2006) Polar assembly of the type IV pilus secretin in Myxococcus xanthus. Mol Microbiol 60: 16–29. doi: 10.1111/j.1365-2958.2006.05095.x
  39. 39. Julien B (2003) Characterization of the integrase gene and attachment site for the Myxococcus xanthus bacteriophage Mx9. J Bacteriol 185: 6325–6330. doi: 10.1128/jb.185.21.6325-6330.2003
  40. 40. Bulyha I, Schmidt C, Lenz P, Jakovljevic V, Hone A, et al. (2009) Regulation of the type IV pili molecular machine by dynamic localization of two motor proteins. Mol Microbiol 74: 691–706. doi: 10.1111/j.1365-2958.2009.06891.x
  41. 41. Carbonnelle E, Helaine S, Nassif X, Pelicic V (2006) A systematic genetic analysis in Neisseria meningitidis defines the Pil proteins required for assembly, functionality, stabilization and export of type IV pili. Mol Microbiol 61: 1510–1522. doi: 10.1111/j.1365-2958.2006.05341.x
  42. 42. Wolfgang M, van Putten JP, Hayes SF, Dorward D, Koomey M (2000) Components and dynamics of fiber formation define a ubiquitous biogenesis pathway for bacterial pili. EMBO J 19: 6408–6418. doi: 10.1093/emboj/19.23.6408
  43. 43. Yang Z, Lux R, Hu W, Hu C, Shi W (2010) PilA localization affects extracellular polysaccharide production and fruiting body formation in Myxococcus xanthus. Mol Microbiol 76: 1500–1513. doi: 10.1111/j.1365-2958.2010.07180.x
  44. 44. Karuppiah V, Derrick JP (2011) Structure of the PilM-PilN inner membrane type IV pilus biogenesis complex from Thermus thermophilus. J Biol Chem 286: 24434–24442. doi: 10.1074/jbc.m111.243535
  45. 45. Karuppiah V, Hassan D, Saleem M, Derrick JP (2010) Structure and oligomerization of the PilC type IV pilus biogenesis protein from Thermus thermophilus. Proteins 78: 2049–2057. doi: 10.1002/prot.22720
  46. 46. Drake SL, Sandstedt SA, Koomey M (1997) PilP, a pilus biogenesis lipoprotein in Neisseria gonorrhoeae, affects expression of PilQ as a high-molecular-mass multimer. Mol Microbiol 23: 657–668. doi: 10.1046/j.1365-2958.1997.2511618.x
  47. 47. Sampaleanu LM, Bonanno JB, Ayers M, Koo J, Tammam S, et al. (2009) Periplasmic domains of Pseudomonas aeruginosa PilN and PilO form a stable heterodimeric complex. J Mol Biol 394: 143–159. doi: 10.1016/j.jmb.2009.09.037
  48. 48. Mattick JS, Whitchurch CB, Alm RA (1996) The molecular genetics of type-4 fimbriae in Pseudomonas aeruginosa—a review. Gene 179: 147–155. doi: 10.1016/s0378-1119(96)00441-6
  49. 49. Goldman BS, Nierman WC, Kaiser D, Slater SC, Durkin AS, et al. (2006) Evolution of sensory complexity recorded in a myxobacterial genome. Proc Natl Acad Sci USA 103: 15200–15205. doi: 10.1073/pnas.0607335103
  50. 50. Kelley LA, Sternberg MJ (2009) Protein structure prediction on the Web: a case study using the Phyre server. Nat Protoc 4: 363–371. doi: 10.1038/nprot.2009.2
  51. 51. Buchan DWA, Ward SM, Lobley AE, Nugent TCO, Bryson K, et al. (2010) Protein annotation and modelling servers at University College London. Nucleic Acids Research 38: W563–W568. doi: 10.1093/nar/gkq427
  52. 52. Battistuzzi FU, Hedges SB (2009) A major clade of prokaryotes with ancient adaptations to life on land. Mol Biol Evol 26: 335–343. doi: 10.1093/molbev/msn247
  53. 53. Burkhardt J, Vonck J, Averhoff B (2011) Structure and function of PilQ, a secretin of the DNA transporter from the thermophilic bacterium Thermus thermophilus HB27. J Biol Chem doi: 10.1074/jbc.m110.212688
  54. 54. Rumszauer J, Schwarzenlander C, Averhoff B (2006) Identification, subcellular localization and functional interactions of PilMNOWQ and PilA4 involved in transformation competency and pilus biogenesis in the thermophilic bacterium Thermus thermophilus HB27. FEBS J 273: 3261–3272. doi: 10.1111/j.1742-4658.2006.05335.x
  55. 55. Korotkov KV, Pardon E, Steyaert J, Hol WG (2009) Crystal structure of the N-terminal domain of the secretin GspD from ETEC determined with the assistance of a nanobody. Structure 17: 255–265. doi: 10.1016/j.str.2008.11.011
  56. 56. Tammam S, Sampaleanu LM, Koo J, Manoharan K, Daubaras M, et al. (2013) PilMNOPQ from the Pseudomonas aeruginosa Type IV Pilus System Form a Transenvelope Protein Interaction Network That Interacts with PilA. J Bacteriol 195: 2126–2135. doi: 10.1128/jb.00032-13
  57. 57. Berry JL, Phelan MM, Collins RF, Adomavicius T, Tonjum T, et al. (2012) Structure and assembly of a trans-periplasmic channel for type IV pili in Neisseria meningitidis. PLoS Pathog 8: e1002923. doi: 10.1371/journal.ppat.1002923
  58. 58. Marchler-Bauer A, Lu S, Anderson JB, Chitsaz F, Derbyshire MK, et al. (2011) CDD: a Conserved Domain Database for the functional annotation of proteins. Nucleic Acids Res 39: D225–229. doi: 10.1093/nar/gkq1189
  59. 59. de Souza RF, Anantharaman V, de Souza SJ, Aravind L, Gueiros-Filho FJ (2008) AMIN domains have a predicted role in localization of diverse periplasmic protein complexes. Bioinformatics 24: 2423–2426. doi: 10.1093/bioinformatics/btn449
  60. 60. Wu SS, Wu J, Kaiser D (1997) The Myxococcus xanthus pilT locus is required for social gliding motility although pili are still produced. Mol Microbiol 23: 109–121. doi: 10.1046/j.1365-2958.1997.1791550.x