key: cord-0796324-rgo5sj5i
authors: Bernard, Sandra C; Simpson, Nandi; Join-Lambert, Olivier; Federici, Christian; Laran-Chich, Marie-Pierre; Maïssa, Nawal; Bouzinba-Ségard, Haniaa; Morand, Philippe C; Chretien, Fabrice; Taouji, Saïd; Chevet, Eric; Janel, Sébastien; Lafont, Frank; Coureuil, Mathieu; Segura, Audrey; Niedergang, Florence; Marullo, Stefano; Couraud, Pierre-Olivier; Nassif, Xavier; Bourdoulous, Sandrine
title: Pathogenic Neisseria meningitidis utilizes CD147 for vascular colonization
date: 2014-06-01
journal: Nat Med
DOI: 10.1038/nm.3563
sha: c1490290ea9d778e4ab19627eaa3ccce3d696368
doc_id: 796324
cord_uid: rgo5sj5i

Neisseria meningitidis is a cause of meningitis epidemics worldwide and of rapidly progressing fatal septic shock. A crucial step in the pathogenesis of invasive meningococcal infections is the adhesion of bloodborne meningococci to both peripheral and brain endothelia, leading to major vascular dysfunction. Initial adhesion of pathogenic strains to endothelial cells relies on meningococcal type IV pili, but the endothelial receptor for bacterial adhesion remains unknown. Here, we report that the immunoglobulin superfamily member CD147 (also called extracellular matrix metalloproteinase inducer (EMMPRIN) or Basigin) is a critical host receptor for the meningococcal pilus components PilE and PilV. Interfering with this interaction potently inhibited the primary attachment of meningococci to human endothelial cells in vitro and prevented colonization of vessels in human brain tissue explants ex vivo and in humanized mice in vivo. These findings establish the molecular events by which meningococci target human endothelia, and they open new perspectives for treatment and prevention of meningococcus-induced vascular dysfunctions. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/nm.3563) contains supplementary material, which is available to authorized users.

N. meningitidis, also referred to as meningococcus, is an obligate human Gram-negative bacterium that normally resides in the nasopharyngeal mucosa without affecting the host, a phenomenon known as carriage 1 . Pathology is initiated when meningococci gain access to the bloodstream, multiply in the blood and disseminate into various tissues, causing meningitis or purpura fulminans, the most severe form of meningococcal invasive disease. Despite antimicrobial therapy, systemic meningococcal infections remain a major cause of mortality and severe neurological sequelae [2] [3] [4] . The endothelium lining blood and lymphatic vessels is a key barrier separating circulating body fluids from host tissues and is a major target for several pathogenic bacteria 5 . A crucial step in the pathophysiology of invasive bloodborne meningococci is their adhesion to and proliferation in both peripheral and brain blood microvessels, a process referred to as vascular colonization 6 . This intimate interaction of meningococci with endothelial cells leads to deregulated inflammatory and coagulation processes, endothelial dysfunction and, ultimately, the breach of endothelial barriers and bacterial dissemination into perivascular tissues 4 . Deciphering the mechanisms that govern this initial pathophysiological step of invasive meningococcal diseases represents an essential development toward the design of new therapeutic approaches to control bacterial infection and subsequent vascular and tissue damage. The capacity of pathogenic capsulated meningococci to interact tightly with human endothelial cells relies on the expression of type IV pili 3, 5 . However, the host cell adhesion receptor that mediates the bacterial attachment to human vessels has remained unknown.

Type IV pili are long filamentous structures that extend from the bacterial cell surface. They mediate adhesion to endothelial cells and signaling events that eventually lead to bacterial translocation through endothelia [7] [8] [9] [10] . These structures are heteromultimeric assemblies of pilin subunits that form helical fibers 11 . The major pilin subunit, PilE, constitutes the essential fiber scaffold and is subject to antigenic variation. Other less abundant ('minor') pilins, such as PilV, PilX and ComP, structurally resemble PilE and participate in various pilus-related functions such as adhesion, bacterial aggregation and DNA uptake, respectively [12] [13] [14] . Both PilE and PilV have been shown to be involved in adhesion to host cells 9, [15] [16] [17] [18] . Furthermore, these two pilins were recently reported to activate the G protein-coupled β 2 -adrenergic receptor (β 2 -AR), which promotes the endothelial signaling events that are subsequent to bacterial adhesion 9, 19 . However, β 2 -AR-depleted endothelial cells, although unable to promote signaling events, still support pilus-mediated bacterial adhesion, thus indicating that the primary meningococcal attachment requires another, yet unidentified, host receptor for type IV pili.

Here, we report that CD147, a member of the immunoglobulin (Ig) superfamily, is a receptor for type IV pilus-mediated adhesion of pathogenic meningococci to human brain or peripheral endothelial cells through interaction with both major and minor pilins-PilE and PilV-and we establish the central role of CD147 for vascular colonization by meningococci in vivo.

CD147 is a candidate endothelial receptor for meningococci To identify candidate receptors for the initial attachment of piliated, capsulated meningococci, we used a gain-of-function strategy in BB19 cells, a dedifferentiated human brain endothelial cell line transformed by papilloma virus that is poorly permissive to meningococcal adhesion under basal conditions. Treatment of BB19 cells with phorbol ester 12-O-tetradecanoylphorbol-13-acetate (TPA), a potent transcriptional regulator, induced enhanced adhesion of the meningococcus strain Nm2C4.3 (Supplementary Fig. 1a) . Treatment with the transcription inhibitor actinomycin D blocked the TPA effect, suggesting the regulated expression of a putative receptor by TPA at the transcriptional level (Supplementary Fig. 1a) . As expected for type IV pilusmediated adhesion, a nonpiliated meningococcal PilE-null mutant (∆pilE) failed to adhere to TPA-treated cells (Supplementary Fig. 1b) . In order to identify upregulated genes in permissive cells, we used a differential, quantitative, large-scale analysis of gene expression (Online Methods) that showed 211 genes upregulated by TPA among 10,478 analyzed genes. Six of them encoded membrane-associated proteins (Supplementary Table 1 ). Among those, four proteins had either limited tissue distribution (sialic acid-binding Ig-type lectin 4 (siglec 4), siglec 11 and delta-and Notch-like epidermal growth factor-related receptor were located mainly in the brain) or limited surface exposure (phosphatidylethanolamine-binding protein). Therefore, we instead focused on the type 1 plasma membrane protein CD147, a member of the Ig superfamily 20 and a well-established marker of brain capillaries 21, 22 , and CD59, a glycosylphosphatidylinositol-anchored glycoprotein known to inhibit membrane attack complex formation in the complement cascade and to induce signaling events 23 . We confirmed that TPA treatment of BB19 cells upregulated expression of CD147 and CD59 ( Supplementary  Fig. 1c) . CD147 expression was enriched at sites of meningococcal adhesion, whereas CD59 was not (Supplementary Fig. 1d) .

We investigated the relevance of CD147 and CD59 as endothelial candidate receptors for meningococcal adhesion using two fully differentiated human endothelial cell lines isolated from either brain (hCMEC/D3) 24 or bone marrow (human bone marrow endothelial cell, HBMEC) 25 capillaries. As observed on TPA-treated BB19 cells, CD59 was not recruited to sites of meningococcal adhesion on HBMECs (Supplementary Fig. 2a) . In noninfected fully polarized hCMEC/D3 or HBMEC monolayers, CD147 was enriched at cell-cell junctions, where it is engaged in homophilic interactions 26, 27 , and was also present at the luminal surface ( Fig. 1a and Supplementary Fig. 2a) . Upon infection with Nm2C4.3, CD147 accumulated at sites of meningococcal adhesion to hCMEC/D3 cells (Fig. 1a) and HBMECs ( Supplementary Fig. 2a) , as already observed for the signaling β 2 -AR receptor 9, 19 . CD147 accumulation occurred rapidly upon contact of diplococci with the cell surface ( Fig. 1b) and was independent of the recruitment of the β 2 -AR, as expected for a receptor mediating initial adhesion (Fig. 1c,d and Supplementary Fig. 3 ). CD147 thus seemed to be a potential endothelial receptor candidate for N. meningitidis.

To establish the role of CD147 in meningococcal adhesion, we transfected endothelial cells with CD147-specific siRNAs. The reduction of CD147 surface expression in hCMEC/D3 cells and HBMECs (75% and 80%, respectively) correlated with decreased meningococcal adhesion to both cerebral or peripheral endothelial cells (65% and 75%, respectively; Fig. 2a,b) . These data were supported by the rescue of meningococcal adhesion in CD147-complemented endothelial cells (Fig. 2b) . Conversely, increased expression of CD147 on HBMECs increased bacterial adherence (Fig. 2c) . This was specific to CD147, as depletion of CD59 did not affect bacterial adhesion to HBMECs ( Supplementary  Fig. 2b) . Furthermore, depletion of CD44 or intercellular adhesion molecule-1 (ICAM-1), two membrane-associated molecules recruited to sites of bacterial adhesion upon type IV pilus-mediated signaling events 7 , did not affect meningococcal adhesion to either hCMEC/D3 cells or HBMECs (Supplementary Fig. 4) .

With the aim of approaching the physiological conditions of shear stress that are encountered in human blood microvasculature, we infected endothelial cells with meningococci in controlled laminar flow chambers that enable the quantification of initial bacterial contacts with the endothelial cell surface 28 . We observed that attenuation of CD147 expression by 65% on hCMEC/D3 cells reduced the number of initial adhesion events by 50% (Fig. 2d) , confirming, under dynamic conditions, the selective effect of CD147 depletion on meningococcal adhesion.

Pathogenic meningococci belong to different capsular groups and show great capacity for antigenic variation in the pilE gene 29 with no alteration in type IV pilus-mediated primary adhesion to host cells 28, 30 . We therefore performed adhesion experiments using meningococcal strains belonging to different capsular serogroups (Z5463, serogroup A; MC58, serogroup B; FAM20, serogroup C; and ROU, serogroup W135) (Fig. 2e) , as well as derivatives of Nm2C4.3 (serogroup C) displaying different variants of the major pilin subunit PilE, designated PilE SA and PilE SB (Fig. 2f) . Reduction of CD147 expression affected the adhesion of these different strains and variants similarly, demonstrating that the capacity of CD147 to support type IV pilus-dependent adhesion was independent of capsular antigen and of antigenic variation of PilE. Competition experiments with CD147-Fc, a soluble recombinant chimeric molecule containing the extracellular domain of CD147 fused to the Fc domain of human IgG1, showed that CD147-Fc caused a 50% reduction in bacterial adhesion to HBMEC cells, whereas soluble ICAM-1-Fc had no effect (Fig. 2g) . To confirm that the extracellular portion of CD147 is a binding site for meningococci, we assayed two antibodies specific for CD147, MEM-M6/1 and MEM-M6/6, which respectively bind to the extracellular N-terminal and the C-terminal Ig domains of CD147, as interaction inhibitors (Supplementary Fig. 5a ). Both antibodies labeled noninfected hCMEC/D3 cells similarly (Supplementary Fig. 5b) , but only MEM-M6/1 efficiently labeled CD147 molecules recruited to bacterial adhesion sites, suggesting that the MEM-M6/6 antibody and meningococci compete for the same binding site in the C-terminal Ig domain of CD147 ( Supplementary  Fig. 5c) . Accordingly, preincubation of hCMEC/D3 cells or HBMECs with the MEM-M6/6 antibody before infection inhibited the initial attachment of Nm2C4.3 under shear stress by 55% and 75%, respectively, whereas the MEM-M6/1 antibody reduced the initial attachment by only 25% and 20% (Fig. 2h) . Overall, our data indicate that CD147 is a critical receptor for the primary attachment of piliated meningococci to both peripheral and brain human endothelial cells.

We next investigated whether the interaction of meningococcus with CD147 was direct by performing meningococcal adhesion experiments using recombinant CD147-Fc immobilized on glass coverslips. Meningococci adhered in a type IV pilus-dependent manner to immobilized CD147-Fc but not to ICAM-1-Fc or noncoated control wells (Fig. 3a) . To identify the bacterial pilus components involved in interaction with CD147, we used Escherichia coli to produce the minor pilins PilV, PilX and ComP, as well as two variants of the major pilin PilE (PilE SA and PilE SB ), as fusion proteins with maltose-binding protein (MBP). Both PilE variants and PilV fusion proteins reduced the adhesion of piliated, capsulated meningococci by 50-60% in competition assays, whereas PilX or ComP had no effect (Fig. 3b) .

We further assessed the direct interaction of CD147 with these pilins using several complementary approaches. First, purified PilE SB or PilV recombinant pilins immobilized on inactivated staphylococci could selectively pull down soluble CD147-Fc (Fig. 3c) . Second, in a protein-protein interaction assay based on oxygen singlet transfer (AlphaScreen), we detected a dose-dependent association with CD147-Fc for both PilE SB and PilV, but not for the other minor pilins (Fig. 3d,e) . This interaction was independent of antigenic variation in the PilE subunit (Supplementary Fig. 6a) and was specific to CD147 (Supplementary Fig. 6b ). As observed above for meningococcal adhesion to human endothelial cells, these interactions were inhibited by the MEM-M6/6 antibody but not by the control anti-ICAM-1 antibody (11C81) (Fig. 3f and Supplementary Fig. 6c) . npg Third, using surface plasmon resonance, we found a specific interaction of PilE SB -or PilV-coated staphylococci with immobilized CD147 (Supplementary Fig. 7) , but we observed no interaction when we used monomeric pilins (data not shown). These results indicate that, despite relatively low affinities of PilE SB and PilV monomers for CD147, their clustering on staphylococci can provide sufficient avidity to CD147, which is consistent with the multimeric organization of pilins within pilus fibers. We then quantified the interaction of PilE variants or PilV with CD147 by atomic force microscopy (AFM) (Fig. 3g) . We observed a load-dependent correlation for the interaction forces of PilE variants or PilV with CD147, further confirming the specificity of this interaction (data not shown). Measured interaction forces with CD147 (62 ± 15 pN, 58 ± 16 pN and 49 ± 12 pN, for PilE SA , PilE SB and PilV, respectively) were only about twofold lower than that between CD147 and its established ligand cyclophilin 31 (128 ± 35 pN) . These data, consistent with a previously described role for PilE and PilV in Neisseria species pilus-mediated adhesion to host cells 9,15-18 , confirm the direct participation of PilE and PilV in the selective interaction of meningococci with CD147.

To establish the role of PilE and PilV in meningococcal adhesion to endothelial cells, we used defective strains of Nm2C4.3. Neither the nonpiliated ∆pilE nor the piliated pilV-null (∆pilV) mutants were able to adhere in vitro to hCMEC/D3 or HBMEC cells (Fig. 4a) . As a control, ∆pilE and ∆pilV complemented strains recovered bacterial adhesion to both endothelial cell lines with an efficiency correlated to the expression level of the complemented proteins (Supplementary Fig. 8a-c) .

To further investigate the specific roles of PilE and PilV in endothelial colonization by meningococci in vivo and because this human specific pathogen does not colonize mouse vessels, we used a humanized mouse model of severe combined immunodeficiency (SCID) mice grafted with human skin, in which functional human blood vessels are maintained within the graft 32, 33 . Although limited to dermal vessels, this model constitutes a unique tool to study meningococcal interaction with human endothelial cells under realistic conditions in a live host. As previously shown 32 , 18 h after bacterial challenge, the Nm2C4.3 wild-type strain massively colonized the human dermal vasculature in a type IV pilus-dependent manner, as we observed no colonization with the nonpiliated ∆pilE derivative (Fig. 4b,c) . Consistent with our in vitro observation, the meningococcal ∆pilV derivative did not associate with vessels in the grafted human skin (Fig. 4b,c) , whereas both ∆pilE and ∆pilV complemented strains colonized human vessels with an efficiency correlating to the expression level of the complemented proteins (Supplementary Fig. 8d-f) . These results establish PilE and PilV as essential bacterial components for in vivo type IV pilus-mediated vascular colonization.

We further analyzed the selective interaction between meningococci and CD147 using an in situ meningococcal infection model of fresh npg human frontal brain tissues obtained from deceased normal subjects, as, in this setting, histological and anatomical characteristics of the brain vessels are conserved. Meningococci incubated with tissue sections established specific tight association with brain vessels, predominantly in Virchow-Robin spaces and in cortical regions ( Fig. 5a and Supplementary Fig. 9) , reminiscent of neuropathological findings in patients with meningococcal meningitis 28, 34 . Adhesion relied on the expression of both PilE and PilV, as ∆pilE or ∆pilV mutants adhered poorly (Fig. 5b-d and Supplementary Fig. 9 ). Upon infection, wild-type meningococci developed microcolonies immediately adjacent to CD147-positive endothelial cells (Fig. 6a) . We also found meningococci in the vicinity of CD147-positive leptomeningeal cells and of cortical brain vessels ( Supplementary  Fig. 10a,b) , but they were not associated with glial or neuronal cells that do not express CD147 (Supplementary Fig. 10c) , indicating a close correlation between meningococcal adhesion to fresh human brain tissue and CD147 expression. Consistent with in vitro cellular models, pretreatment of brain sections with the MEM-M6/6 antibody substantially reduced adhesion of meningococci to human brain vessels, whereas the MEM-M6/1 antibody or the control 11C81 anti-ICAM-1 antibody had no effect (Fig. 6b,c) . Altogether, these data confirm that type IV pilus-mediated adhesion of meningococcus to CD147 is necessary for endothelial cell colonization by this bacterial pathogen.

This study demonstrates that the specific interaction between the meningococcal ligands PilE and PilV and the cellular host receptor CD147 is essential for meningococcal adhesion to human endothelial cells and colonization of human blood vessels, a prerequisite to the major vascular alterations that are the hallmark of invasive meningococcal infections. These results, which help unravel the molecular basis of a key pathophysiological step of meningococcal diseases, are consistent with previous reports suggesting that, in addition to its structural role in the pilus scaffold, the PilE subunit plays a direct role in bacterial adhesion to host cells 15 . PilV has also previously been shown to be required for the adhesion of the closely related Neisseria gonorrhoeae 18 . Interaction with CD147 occurs independently of antigenic variation in the PilE subunit and of possible post-translational modifications. PilE and PilV have relatively low affinities for CD147, whereas multimeric pilins efficiently bind to CD147, indicating a system where avidity is crucial, consistent with the natural organization of pilins in multimeric complexes within pilus fibers. Because endothelial cells, and more particularly brain microvessels, express high levels of CD147, it is likely that CD147 expression level may also contribute to avidity, compensating for the weak affinity of the CD147-meningococcal pilins interaction. How these two pilus components act in concert to create the adhesive phenotype remains to be solved. Identification of the precise PilE and PilV epitopes required for interaction with CD147 will allow the development of targeted antibodies that could prevent type IV pilus-CD147 interaction, opening the path to new vaccine strategies against meningococcal infection.

CD147 is expressed on different cell types, such as erythrocytes and epithelial cells. Pilus-dependent interactions between meningococci and erythrocytes, causing hemagglutination, have been documented in vitro 35, 36 , and meningococci have been described crossing polarized epithelia, indicating that meningococcus might interact with CD147 in a variety of cell types. Notably, several viruses, including HIV-1, severe acute respiratory syndrome coronavirus 37 and measles virus 38 , as well as the bacterial pathogen Listeria monocytogenes 39 , also target CD147 to adhere to and/or invade epithelial cells, indicating that CD147 constitutes an evolutionarily conserved efficient target for pathogens to infect tissues and spread within organisms. CD147 is also known as EMMPRIN, a master regulator of the production of matrix metalloproteinase 40 . It is therefore likely that, in addition to its role in pathogen adhesion and invasion processes, CD147 also contributes to the disruption of the epithelial and endothelial barrier integrity by promoting local production of matrix metalloproteinases.

Whereas CD147 expression is required to support bacterial adhesion to endothelial cells of brain and peripheral origin, β 2 -AR expression is necessary for meningococcus-triggered signaling 8 . β 2 -AR is dispensable for adhesion 9, 19 , but CD147-mediated meningococcal adhesion is a prerequisite for activating the β 2 -AR-β-arrestin signaling pathway, thus suggesting that CD147 and β 2 -AR might cooperate to strengthen meningococcal adhesion and promote subsequent activation of signaling events. Notably, a similar functional association of these two receptors has been reported in the context of erythrocyte infection by the human parasite Plasmodium falciparum, the agent of malaria, although the mechanism of this association is still unknown 41, 42 . The implication of these two receptors in different tissues and in the context of different infectious diseases might reflect a preexisting functional connection between CD147 and β 2 -AR that is hijacked by different pathogens to disseminate and induce multiple organ failure. npg Taken together, our data highlight a key role for CD147 in the cascade of pathophysiological events following meningococcal entry into the bloodstream. Agents or vaccines preventing type IV pilus interaction with CD147 might therefore be highly effective for treatment or prevention of meningococcal infection and associated vascular dysfunction.

Methods and any associated references are available in the online version of the paper. 

Anti-hCD147 mAb (clones MEM-M6/1 and MEM-M6/6) were purchased from AbD Serotec, anti-hCD59 mAb (clone MEM 43/5) from Tebu-Bio, anti-hCD44 mAb (clone J173) from Immunotech, anti-hICAM-1 mAb (clone 18C11) from R&D Systems, anti-human collagen IV (clone PHM12) from Abcam, and anti-GFAP (clone G-A-5) and antivimentin (clone V9) from Sigma-Aldrich. Polyclonal antiserum raised against ezrin was obtained from P. Mangeat. mAb raised against PilE (20D9) and polyclonal antiserum raised against meningococcal 2C4.3 strain were described previously 9 . Secondary antibodies used for immunofluorescence labeling, chromogenic immunohistochemistry and immunoblotting were from Jackson ImmunoResearch Laboratories. Soluble chimeric CD147-Fc-His, ICAM-1-Fc and ALCAM-1-Fc-His molecules were purchased from R&D Systems. DAPI, rhodamine-phalloidin, TPA, actinomycin D, isoproterenol, DAB peroxidase substrate and NBT/BCIP phosphatase alkaline substrate were purchased from Sigma-Aldrich.

Bacterial strains. Nm2C4.3 (formerly clone 12) is a piliated capsulated Opa -Opcvariant of the serogroup C meningococcal clinical isolate 8013 (ref. 43) cultured as described previously 44 . Nm2C4.3 expressing pilin variants PilE SA , PilE SB or GFP were previously described 28, 43 . The pilV mutant was engineered by introduction of an aph3′ resistance cassette into the pilV gene. To complement the pilV mutant, the pilV allele was amplified using primers PilV forward 5′-CCT TAATTAAGGAGTAATTTTATGATGAGTAATAAAATGGAACA-3′ and PilV reverse 5′-CCTTAATTAACTATTTTTTACGATTAGAGAAAGC-3′, containing overhangs with restriction sites for PacI. This PCR fragment was restricted with PacI and cloned into PacI-restricted pGCC4 vector as described before 12 . This placed pilV under the transcriptional control of an IPTG inducible promoter within a DNA fragment corresponding to an intragenic region of the meningococcal chromosome. This pilV construct was then introduced into the chromosome of the ∆pilV mutant by homologous recombination. A similar scheme was used for the construction of a complemented PilE isogenic meningococcus strain. The orf of the pilE gene was inserted, in E. coli, at the PacI restriction site of the PGCC4 plasmid. The primers used to amplify PilE were PilE forward 5′-CTTAATTAAGGAGTAATTTATGAACACCCTTCAAAAAGGTTTTAC-3′ and PilE reverse 5′-CTTAATTAATTAGCTGGCAGATGAATCATCGCG-3′. The inducible pilE construct was inserted ectopically into the chromosome of the Nm2C4.3 strain through transformation, using erythromycin for selection. The wild-type pilE locus was subsequently inactivated through transformation of chromosomal DNA of a previously described aphA3-insertionally inactivated endogenous ∆pilE derivative and selected with kanamycin 17 . Virtually no PilE could be detected in the absence of induction in the resulting ∆pilE/pilE strain, whereas induction yielded up to approximately 5% of the wild-type expression level of PilE, as PilE is one of the most strongly constitutively expressed meningococcal proteins. Phenotypically, despite the low level of PilE complementation induced upon IPTG treatment, the functionality of type IV pili expressed upon PilE complementation was ascertained through restoration of competence (competence frequency <1 × 10 −7 , 1 × 10 −5 and 1 × 10 −4 per µg DNA for ∆pilE, ∆pilE/ pilE and wild-type strains, respectively Cell lines. hCMEC/D3 is a fully differentiated human brain endothelial cell line derived from brain capillaries, produced in the laboratory and which recapitulates the major phenotypic features of the blood-brain barrier 24 . HBMEC is a human endothelial cell line isolated from bone marrow capillaries, provided by B. Weksler, that maintains in vitro most of the characteristics of primary endothelial cells 24 . BB19 is a human brain endothelial cell line transformed by papilloma virus, provided by J.A. Nelson, which has lost most of the phenotypic features of brain endothelial cells 49 .

Cell culture, transfection and infection. To induce bacterial adhesion, BB19 cells were treated with the phorbol ester 12-O-tetradecanoylphorbol-13-acetate (TPA) 10 ng ml −1 , for 10 min, washed and bacterial adhesion measured 48 h after treatment. When indicated, 2 h after TPA treatment, the transcriptional inhibitor actinomycin D was added (1 µg ml −1 , for 4 h), cells were washed and adhesion was measured 42 h later. The hCMEC/D3 and HBMEC cell lines were cultured, transfected and infected as previously described 7, 9 . Plasmid encoding human CD147 was provided by M. Bukrinsky, and plasmid encoding β2 adrenergic receptor fused to YFP (β 2 -AR-YFP) was described previously 50 . To silence the expression of CD147, CD59, CD44, ICAM-1 and β 2 -AR, pools of four siRNA duplexes (ON-TARGET plus SMARTpool siRNA from Dharmacon) were used. The siControl siRNA (Dharmacon) was used as control. 48 h after transfection, efficiency of knockdown was assessed by FACS analysis or by reverse-PCR analysis for β 2 -AR depletion as previously described 9 . When indicated, HBMEC cells were transfected with siRNA targeting the 3′ untranslated region of CD147, 3′-GCUGUCUGGUUGCGCCAUUUU-5′ or control siRNA 3′-AUGUAUUGGCCUGUAUAG-5′ (Eurogentech), and 40 h later, cells were again either mock transfected or transfected with CD147 cDNA coding region. 8 h later, surface expression of CD147 was quantified by FACS analysis and cells were infected concurrently with Nm2C4.3.

Serial analysis of gene expression adapted for downsized extracts. 200 µg of RNA extracted from 2 × 10 7 untreated or TPA-treated BB19 cells 16 h after treatment with TPA were used as a substrate for the serial analysis of gene expression adapted for downsized extracts (SADE) screen carried out as described 51 . Briefly, total RNA was extracted from cells, polyadenylated RNA was selected on oligo-dT columns and tagged cDNA was synthesized from the poly-A RNAs. Concatemers of DNA tags were sequenced, and the number of sequenced tags differentially represented in the two libraries was determined and analyzed using Monte Carlo statistical analysis.

Adhesion assays under static and flow conditions. Meningococcal adhesion on hCMEC/D3, HBMEC and BB19 cells was assayed under both static and shear stress conditions, as previously described 9, 28, 52 . When indicated, meningococci were preincubated with 5 µg ml −1 soluble recombinant human CD147-Fc and ICAM-1-Fc chimera before interaction with HBMEC cells with additional 2 µg ml −1 soluble proteins. Meningococcal adhesion was quantified following a 30-min infection in static conditions. To address the inhibitory effect of antibodies, HBMEC or hCMEC/D3 cells were grown on IBIDI chambers, pretreated for 1 h with 10 µg ml −1 antibodies targeting ICAM-1 (11C81) or CD147 (MEM-M6/1 and MEM-M6/6) and submitted to laminar flow (0.04 dynes/cm 2 ) under an inverted microscope. GFP-expressing bacteria were introduced in the chamber under flow for 10 min, and the number of adherent bacteria was determined, as previously described 28 . For adhesion assays on immobilized proteins, CD147-Fc and ICAM-1-Fc chimera were immobilized on glass slides using a modification of the technique described 53 . Briefly, slides were coated with 0.1% poly-l-lysine, washed with PBS, crosslinked with glutaraldehyde (0.5%), washed, incubated with anti-Fc in assay buffer (PBS with 3% BSA) for 2 h, washed in assay buffer and incubated overnight at 4 °C with 2 µg ml −1 chimeric protein. Slides were washed before infection with meningococcal suspension of OD 600 0.05. After incubation with bacteria, slides were washed three times and fixed. Bacteria were labeled and visualized with a Leica DMI6000 microscope using a 63× oil-immersion objective. The number of adherent bacteria per field was quantified for 30 fields using ImageJ software.

Expression, purification and immobilization of maltose-binding proteinpilin recombinant proteins. Purified pilins were produced as fusion proteins with the maltose-binding protein (MBP), as described before 9 . Fragments of PilE ( SA and SB ), PilV, PilX and ComP lacking the region coding for amino acid residues 1 to 28 of the full-length proteins fused to the MBP were produced in E. coli, purified on amylose resin (New England BioLabs) and immobilized on Staphylococcus aureus (ATCC 25923) expressing specific receptors for the Fc domain of IgG as described before 9 . Coated bacteria were incubated with 1 µg of CD147-Fc chimera for 30 min on ice. After 3 washes, bacteria were lysed with Laemmli buffer, and the quantity of coprecipitated CD147-Fc protein was assessed by immunoblot analysis. Bound CD147-Fc was quantified using ImageJ software. When indicated, hCMEC/D3 cells were pretreated with 10 µg ml −1 of MBP-pilins for 15 min before infection with meningococcal suspension of OD 600 0.05 for 30 min. After incubation with bacteria, cells were npg

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Purification and characterization of eight class 5 outer membrane protein variants from a clone of Neisseria meningitidis serogroup A

Complete genome sequence of Neisseria meningitidis serogroup B strain MC58

Isolation by streptonigrin enrichment and characterization of a transferrin-specific iron uptake mutant of Neisseria meningitidis

Interaction of Neisseria meningitidis with the components of the blood-brain barrier correlates with an increased expression of PilC

Studies of Plasmodium falciparum cytoadherence using immortalized human brain capillary endothelial cells

Detection of β 2-adrenergic receptor dimerization in living cells using bioluminescence resonance energy transfer (BRET)

Serial microanalysis of renal transcriptomes

Invasion of endothelial cells by Neisseria meningitidis requires cortactin recruitment by a PI3-kinase/Rac1 signalling pathway triggered by the lipo-oligosaccharide

MT1-MMP-dependent invasion is regulated by TI-VAMP/VAMP7

Creating biomimetic surfaces through covalent and oriented binding of proteins

Elastic membrane heterogeneity of living cells revealed by stiff nanoscale membrane domains

Elastic properties of the cell surface and trafficking of single AMPA receptors in living hippocampal neurons

Fuzzy logic algorithm to extract specific interaction forces from atomic force microscopy data

The authors declare no competing financial interests.Reprints and permissions information is available online at http://www.nature.com/ reprints/index.html.washed three times and the number of adherent bacteria determined as described above.AlphaScreen. The AlphaScreen technology was used to assess the interaction between MBP-pilin recombinant fusion proteins and CD147-Fc-His or ALCAM-1-Fc-His as a control. The binding reaction was performed using white 384-well Optiplates (PerkinElmer, Whalham, MA, USA) in 20 µl (total reaction volume). The AlphaScreen reagents (anti-MBP-coated Acceptor beads and Nickel chelate-coated Donor beads) were obtained from PerkinElmer. CD147-Fc-His (or ALCAM-1-Fc-His) and MBP-pilins were prepared in 20 mM Tris, pH 7.4, 20 mM NaCl. Donor beads (20 µg/ml) were incubated with CD147-His (0, 100 or 500 nM) for 45 min at room temperature. In parallel, acceptor beads (20 µg ml −1 ) were incubated with MBP-pilins (0, 50 or 500 nM) for 1 h at room temperature in the AlphaScreen reaction buffer (25 mM Tris, pH 7.4 at 20 °C, 20 mM NaCl, 0.1% BSA and 0.05% Tween 20). Next, 10 µl of each of the interacting partners were added to the plate, allowed to incubate for either 2 h or overnight in the dark and at room temperature. In antibody competition assays, 5 µl of MEM-M-6/6 or 11C81 antibodies (at variable concentrations) were added to CD147-Fc-His-Donor beads for 30 min at room temperature before incubation with the MBP-pilin-Acceptor beads. Light signal was detected with the EnVision multilabel plate reader (PerkinElmer).Surface plasmon resonance. Surface plasmon resonance (SPR) experiments were carried out on a Biacore 3000 SPR biosensor (Biacore InternationalAB). CD147-Fc or control ICAM-1-Fc chimera (10 µg ml −1 ) were immobilized onto CM5 chip surfaces at 10 µl min −1 using a standard amine coupling protocol with EDC (1-ethyl-3(3-dimethylaminopropyl) carbodiimide)/NHS (N-hydroxysuccinimide) following the manufacturer's instructions. The density was controlled at an increased response level of 4,600 and 7,200 response units (RU) for ICAM-1-Fc and CD147-Fc, respectively. Soluble monomeric pilins diluted at various concentrations (0.15 to 10 µg ml −1 ) in 10 mM HEPES pH 7.4, 4 mM EDTA, 0.005% (v/v) P20 surfactant or 70 µl of a suspension of pilin-coated staphylococci in PBS pH 7.4 were used as analytes. Analytes were applied at a flow rate of 10 µl min −1 for 5 min followed by a dissociation time of 6 min. Regeneration of the sensorchip surface was performed with 2.5 M NaCl in PBS at 100 µl min −1 for 5 min followed by two washes at 100 µl min −1 with PBS. Output sensorgrams were analyzed using BIAcore BIAnalysis software.Atomic force microscopy. Force spectroscopy was performed between pilins and a CD147-functionalized surface. CD147-Fc-His or control ALCAM-1-Fc-His chimera were deposited on a glass surface using a nitrilotriacetic acid that ensured covalent and oriented binding with the protein 54 . MBP-pilins and control proteins (MBP, cyclophilin) were coated on AFM tips using established protocol known to keep protein functionality intact as previously published 55, 56 . All the experiments were performed at room temperature on a commercial AFM (MultiMode8, Bruker, Santa Barbara, CA) driven under Nanoscope 8.15. MBP-pilins were used at 100 µg ml −1 . Bruker DNP cantilevers with a nominal spring constant of 0.06 N/m and a nominal tip radius of 20 nm were used. True cantilever spring constant was determined using Bruker's thermal tune calibration tool. Experiments were done in force-volume mode operating in 150 mM NaCl, 20 mM HEPES buffer (pH 7.0). Pulling speed was set to 10 µm s −1 on 4 µm 2 areas, 300 nm z ramp, with a relative trigger of 150 pN on the cantilever deflection and a contact time of 200 ms. 6,144 force curves per condition were recorded, using at least 6 different tips. Most nonspecific tip-surface adhesion events were automatically discarded from analysis. Force-distance curves were analyzed as previously described 55 , and binding-unbinding events on the retraction curve were detected according to their shape and size characteristics by a fuzzy logic algorithm fully described in (ref. 57) . Briefly, we considered unbinding events based on the vertical segment size, the V-shape and the angle with the baseline. Statistical analysis was performed using R2.15 where provided data are the peak position mean values ± s.d.Confocal immunofluorescence microscopy. hCMEC/D3, BB19 or HBMEC cells were grown to confluence on Permanox coverslips (Thermo Fisher Scientific) or on Transwell filters (Costar). After the indicated treatments and/or infection, cells were fixed and labeled as previously described 44, 52 . Anti-ezrin antibody (1/1,000), anti-CD44 (1/25) anti-CD147 (MEM-M6/1, 1/100), anti-CD59 (1/100) and rabbit polyclonal serum anti-Nm2C4.3 strain (1/3,000) were used as primary antibodies, and DAPI (0.5 mg ml −1 ) was added to Alexa Fluor-conjugated secondary antibodies (1/300). Image acquisition and analysis were performed with a DMI6000 microscope (Leica, 63×). Series of optical sections were obtained with a confocal spinning disk microscope (Leica, 63×). Three-dimensional (3D) reconstructions were obtained using Imaris software and quantification histograms with ImageJ software (NIH). Quantitative analysis of protein recruitment under bacterial colonies was determined as the proportion of colonies positive for the protein of interest indicated. At least 50 colonies were observed per coverslip. Each experiment was repeated at least 3 times in duplicate or triplicate.Infection of severe combined immunodeficiency mice grafted with human skin. Six-week-old CB17/Icr-Prkdc scid /IcrIcoCrl SCID female mice were purchased from Charles River Laboratories (Saint Germain sur l' Arbresle, France). Human skin tissues were obtained from adult patients undergoing plastic surgery in the Service de Chirurchie Plastique et Reconstructive of the Groupe Hospitalier Saint-Joseph (Paris, France). In accordance with the French legislation, patients were informed and did not refuse to participate in the study. Experimental procedures were performed as previously described 32 , in accordance with the guidelines of the Institut National de la Santé et de la Recherche Médicale. The use of human tissue and the experimental protocol was approved by the Animal Experimentation Ethics Committee of the Université Paris Descartes (consent form CEEA34.O.J.L.039.12). Briefly, mice were prepared for transplantation by shaving the hair of the back and abdominal areas after they received an intraperitoneal injection of ketamine 100 mg kg −1 and xylazine 10 mg kg −1 . A skin flap was created, and a full-thickness human skin graft was placed onto the wound bed. The transplants were held in place with 6-0 nonabsorbable monofilament suture materials, and the flap was then sutured above the transplant. Grafted mice were used for meningococcal infection experiments 1 month after human skin transplantation. Meningococcus strains were grown overnight at 37 °C on GCB agar plates prepared without iron and supplemented with 15 µM deferoxamine (Desferal, Novartis) with appropriate antibiotic. Bacterial colonies were harvested and cultured in RPMI with 1% bovine serum albumin medium and 0.06 µM deferoxamine with gentle agitation to reach the exponential phase of growth. Bacteria were then resuspended in physiological saline containing 20 mg ml −1 of human holotransferrin to promote bacterial growth in vivo (2914HT, R&D systems). Mice were infected intraperitoneally with 0.5 ml of this bacterial suspension to minimize the inoculum required to obtain a reproducible high bacteremia in grafted mice. To assess bacteremia in infected animals, 10 µl of blood was sampled using a heparinized hematocrit glass tube 1 h after injection by puncture in the lateral tail vein, or 18 h after injection by intracardiac puncture on animal killed by intraperitoneal injection of a lethal dose of ketamine and xylazine. Bacterial counts were performed by plating serial dilutions of blood on GCB agar plates. Results were expressed in colony-forming units (CFU) per ml of blood. Biopsy of human skin grafts were carefully collected using a dermatological punch biopsy system and fixed overnight at 4 °C in paraformaldehyde 1%, lysin 75 mM and sodium periodate 100 mM in phosphate buffer. After they were washed in phosphate buffer, the specimens were dehydrated in successive sucrose gradient solutions (10%, 20%, 30% prepared in phosphate buffer 0.1 M) for 2 h at 4 °C each, embedded in OCT and then frozen at −80 °C. 7-µm thick sections of the dermis were immobilized on Superfrost plus microscope slides and analyzed via immunofluorescence. Sections were incubated with the following primary antibodies for 2 h in PBS/BSA 0.1%: monoclonal anti-human collagen IV (1/100) and a rabbit polyclonal serum against the Nm2C4.3 strain (1:3,000). DAPI (0.5 mg ml −1 ) was added to Alexa Fluor-conjugated secondary antibodies (1/300) for 1 h. After additional washing, coverslips were mounted in glycergel (Dako). 3 sections per graft were analyzed using epifluorescence (Zeiss Axiovert, 20×). Quantification analysis of the images (n > 10 per graft) was performed using ImageJ software (NIH). Results are presented as a vascular colonization index corresponding to the area occupied by the fluorescently labeled bacteria in relation to the human vessel area delineated by the anticollagen IV staining ×100, from 6 independent grafts per condition. npg Infection of human brain tissues. Fresh human brain sections were obtained from frontal lobe specimens of macroscopically and histologically normal brain (confirmed by a neuropathologist) of individuals referred to the Department of Forensic Medicine for unexplained out-of-hospital sudden death (consent forms ML1094, PFS 10-008, ClinicalTrials.gov NCT00320099 approved by The Institutional Review Board of the Poincaré Hospital, Versailles-Saint Quentin University and the Agence de la Biomédecine). After freezing of the brain tissue with isopentane cooled in liquid nitrogen, the 7-µm-thick sections containing leptomeninges, cortical ribbon and the underlying white matter were immobilized on Superfrost plus microscope slides and stored at −80 °C. Defrosted sections were rehydrated in PBS for 5 min and incubated for 1 h with medium containing 0.1% BSA before infection with suspensions of bacteria (2 × 10 7 in 150 µl of medium containing 0.1% BSA) for 1 h at 37 °C. Sections were then gently washed horizontally 5 times and fixed in PAF 4% for 10 min at room temperature. When indicated, sections were treated for 1 h with 10 µg ml −1 of antibodies targeting CD147 or ICAM-1 and then washed 3 times before infection by bacteria. Adherent meningococci were detected by chromogenic immunohistochemistry and immunofluorescence analysis. To perform chromogenic immunohistochemistry, after tissue rehydration, sections were incubated overnight with the indicated primary antibodies (monoclonal anti-human CD147 (MEM-M6/1, 1/100) and a rabbit polyclonal serum anti-Nm2C4.3 strain (1/3,000)) and revealed using horseradish peroxidase-coupled secondary donkey anti-mouse antibody and an alkaline phosphatase donkey anti-rabbit (1/500). DAB (brown color) and NBT/BCIP (blue color) were used as chromogens. For immunofluorescence analysis, brain sections were incubated with the following primary antibodies for 2 h in PBS/BSA 0.1%: monoclonal anti-human CD147 (MEM-M6/1, 1/100), anti-GFAP (1/100), anti-human vimentin (1/100) and a rabbit polyclonal serum anti-Nm2C4.3 strain (1/3,000). Alexa Fluor-conjugated phalloidin (1/300) and DAPI (0.5 mg ml −1 ) were added to Alexa Fluorconjugated secondary antibodies (1/300) for 1 h. After additional washing, coverslips were mounted in glycergel (Dako). Entire samples were scanned using Nanozoomer 2.0 (Hamamatsu) and were further analyzed using optical microscopy, epifluorescence (Zeiss Axiovert, 40×) and confocal (spinning disk Leica, 63×) microscopy. Quantification analysis of the fluorescently labeled bacteria that adhered on a 1 mm 2 surface area was performed using ImageJ software. Results are presented as a mean of fluorescence per 100 µm 2 , from two independent experiments. 3D reconstructions were performed on deconvoluted confocal stacks using Imaris software.Statistical analyses. All values are expressed as the mean ± s.e.m. Statistical differences were determined to be significant at P < 0.05. The specific tests used are described in the figure legends. All analyses were performed using GraphPad Prism software. No statistical method was used to predetermine sample size. The investigators were not blinded to allocation during experiments and outcome assessment. The experiments were not randomized.