Figures
Abstract
Evidence is growing for a role of Waddlia chondrophila as an agent of adverse pregnancy outcomes in both humans and ruminants. This emerging pathogen, member of the order Chlamydiales, is also implicated in bronchiolitis and lower respiratory tract infections. Until now, the serological diagnosis of W. chondrophila infection has mainly relied on manually intensive tests including micro-immunofluorescence and Western blotting. Thus, there is an urgent need to establish reliable high throughput serological assays. Using a combined genomic and proteomic approach, we detected 57 immunogenic proteins of W. chondrophila, of which 17 were analysed by mass spectrometry. Two novel hypothetical proteins, Wim3 and Wim4, were expressed as recombinant proteins in Escherichia coli, purified and used as antigens in an ELISA test. Both proteins were recognized by sera of rabbits immunized with W. chondrophila as well as by human W. chondrophila positive sera but not by rabbit pre-immune sera nor human W. chondrophila negative sera. These results demonstrated that the approach chosen is suitable to identify immunogenic proteins that can be used to develop a serological test. This latter will be a valuable tool to further clarify the pathogenic potential of W. chondrophila.
Citation: Kebbi-Beghdadi C, Lienard J, Uyttebroeck F, Baud D, Riederer BM, Greub G (2012) Identification of Immunogenic Proteins of Waddlia chondrophila. PLoS ONE 7(1): e28605. https://doi.org/10.1371/journal.pone.0028605
Editor: Georg Häcker, University Freiburg, Germany
Received: June 2, 2011; Accepted: November 11, 2011; Published: January 4, 2012
Copyright: © 2012 Kebbi-Beghdadi et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by the National Swiss Research Fundation, grant 310030-130466. David Baud is supported by the “Société Académique Vaudoise” through the “Paul Blanc” grant and the SICPA (Security Inks Control Partnership Administration) Foundation. Gilbert Greub is supported by the Leenards Foundation through a career award entitled “Bourse Leenards pour la relève académique en médecine clinique à Lausanne”. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The immunogenic proteins and corresponding polypeptides identified in this work have been patented for their use in the detection of antibodies against Waddlia chondrophila and in related diagnostic tests, as well as in vaccines (European patent n°09172401.3, 9th October, 2009). This does not alter the authors' adherence to all the PLoS ONE policies on sharing data and materials.
Introduction
Waddlia chondrophila is an emerging pathogen belonging to the Chlamydiales order, which currently includes six different family-level lineages: the Chlamydiaceae, the Parachlamydiaceae, the Waddliaceae, the Simkaniaceae, the Criblamydiaceae and the Rhabdochlamydiaceae [1], [2]. All members of the Chlamydiales order exhibit a strict intracellular life cycle, with most undergoing a biphasic developmental cycle, beginning with an infectious, but metabolically inactive, elementary body (EB) entering its host cell by endocytosis and converting to a metabolically active reticulate body (RB) replicating by binary fission. At the end of the replication cycle, RBs redifferentiate into EBs, that are released by lysis of the host cell to initiate a new infection cycle [3].
The Chlamydiaceae family comprises well-known human and animal pathogens, of which several are implicated in adverse pregnancy outcomes and in respiratory tract infections in humans and in animals [4], [5], [6]. In recent years, attention has also turned to members of the Parachlamydiaceae, Simkaniaceae and Waddliaceae families, considered to be possible emerging human and animal pathogens. Simkania negevensis and Parachlamydia acanthamoebae are likely implicated in lower respiratory tract infections in humans [7], [8], [9]. Recent reports also indicate an association of P. acanthamoebae with abortion in ruminants [10], [11] and with human fetal loss [4], [12].
W. chondrophila is considered as an abortigenic agent in ruminants. It was isolated from aborted bovine fetuses on two separate occasions, once in USA and once in Germany [13], [14]. Furthermore, a serological study has demonstrated a clear association between anti-Waddlia antibodies and bovine abortion [15] and experimental infection of 2 fetuses with W. chondrophila led to the death of one within 2 weeks [15]. A pathogenic role of W. chondrophila in humans is supported by a serological study conducted on women having experienced sporadic or recurrent miscarriage, which demonstrated a strong association between W. chondrophila seropositivity and adverse pregnancy outcomes [16]. In addition, we recently implemented a real time quantitative PCR for the detection of this pathogen [17] and could report the presence of W. chondrophila DNA in placenta sample of a woman suffering from miscarriage [18]. Waddlia chondrophila was also detected in respiratory tract samples of patients with pneumonia and children with bronchiolitis [17], [19].
Given its obligate intracellular life cycle, W. chondrophila cannot be grown routinely on culture plates used to reveal pathogens and thus would remain undetected by conventional microbiological methods. In humans, the aetiology of miscarriage remains unknown in 50% of cases [16] and there is a clear need for improved methods to detect potential agents such as W. chondrophila. Until now, methods used to detect W. chondrophila infection have relied mainly on molecular techniques [17] or indirectly via seropositivity in micro-immunofluorescence or Western blots [16]. The latter are particularly time consuming and poorly applicable for screening large numbers of samples. Therefore, to further determine the pathogenic role of W. chondrophila in humans and in animals, there is an urgent need to identify immunogenic proteins and to establish a reliable ELISA test.
We recently reported the use of a combined genomic and immuno-proteomic approach, to identify immunogenic proteins of Parachlamydia acanthamoebae [20]. The same approach has also been used to identify immunoreactive proteins of Bartonella quintana and Bartonella henselae [21], [22], [23]. In this study, we combined an immunoproteomic method, i.e. a technique involving 2 dimensional gel electrophoresis followed by immunoblotting, with the complete genomic data of W. chondrophila that became recently available [24], to identify W. chondrophila immunogenic proteins and to establish the basis for a serological diagnostic test.
Results
2D map of W. chondrophila immunoreactive proteins
To identify immunoreactive proteins that could be used in a diagnostic test, elementary bodies of W. chondrophila were lysed and their proteins extracted and separated by 2 dimensional, polyacrylamide gel electrophoresis (2D gels). Bacterial proteins were subsequently either transferred onto nitrocellulose membranes or Coomassie-blue stained. To verify that the purification procedure retrieved only waddlial proteins, we also performed a 2D gel with proteins extracted from a mock control. Coomassie blue staining of this negative control revealed a total absence of proteins (data not shown). To detect immunoreactive proteins, blots were incubated with the serum of a rabbit immunized with W. chondrophila or with the sera of 13 patients previously tested positive for W. chondrophila by immunofluorescence [16], [25]. With the help of the Adobe Photoshop Software, the immunoreactive spots were matched with their corresponding proteins on the Coomassie blue-stained gel, which allowed the detection of 57 immunoreactive proteins (numbered 1 to 57 on Figure 1). The level of recognition of these 57 individual proteins by the 13 human W. chondrophila positive sera tested varied considerably, one being recognized by 92.31% of the sera (12/13) and others being detected by only 1 of the 13 tested sera (7.69%).
Proteins were transferred to nitrocellulose and probed with 13 W. chondrophila positive human sera and with the serum of a rabbit immunized with W. chondrophila. Immunoreactive proteins are numbered (1–57).
To be manually picked from the gel and accurately analyzed by mass spectrometry, a protein must be clearly stained by Coomassie blue and form a well defined spot. We selected 16 protein spots meeting these criteria as well as being recognized by at least 5 human W. chondrophila positive sera (of the 13 tested) and submitted them to mass spectrometry analysis. Spot number 24 was recognized by 4 sera, of which two very strongly, and was included in the analysis (Table 1).
Identification of immunogenic proteins
MALDI TOF MS analysis of 17 individual spots corresponding to immunoreactive proteins resulted in the identification of 13 different proteins, mainly already known chlamydial antigens and proteins described as immunogenic in other bacterial species [22], [26] (Table 2). More interestingly, this immunoproteomic method allowed the detection of two hypothetical proteins, spot #3 (Wim3) and spots #4 and #7 (Wim4). Wim3 has no homology with any known protein and is therefore a very promising candidate for the development of a W. chondrophila specific ELISA test. Wim4 displays no sequence homology with proteins of C. trachomatis and of other members of the Chlamydiaceae family, but partial homologs are found in the genomes of two members of the Parachlamydiaceae family, P. amoebophila (pc1399, 34% identity) and P. acanthamoebae (pah_c029o043, 41% identity) as well as in the draft genomes of two members of the Criblamydiaceae family, Estrella lausannensis (35% identity) and Criblamydia sequanensis (36% identity) (C. Bertelli et al., unpublished results). The sequence homologies are mainly restricted to the C-terminal region (last 100 amino acid residues) of these related proteins. Moreover, the P. acanthamoebae homolog of Wim4 has been previously identified as an immunogenic protein [20]. Interestingly, the W. chondrophila gene wcw_1618, encoding hypothetical protein #4 (Wim4), is located in one of the four type III secretion system (T3SS) genetic clusters present on the bacterial chromosome [24].
Western blot and ELISA with rabbit sera
Most of the 13 identified immunogenic proteins described above have highly conserved homologs in the genomes of other Chlamydiales bacteria (Table 2) and are thus likely to generate cross-reactions if used in an ELISA test. For this reason, only the two hypothetical proteins Wim3 and Wim4 were further considered for the development of a W. chondrophila-specific serological diagnostic tool. In silico analysis of their amino acid sequences revealed the absence of signal peptides and transmembrane domains [27], [28], [29]. Both proteins were expressed in E. coli and purified via a C-terminal His tag. The purified recombinant proteins were detected by Western blot with a rabbit anti-Waddlia serum but not with the corresponding pre-immune serum (data not shown).
Both Wim3 and Wim4 were detected by sera of two rabbits immunized with W. chondrophila in a direct ELISA assay. Serum of rabbit #2 was reactive against the two proteins down to a dilution of 1/256 while serum of rabbit #1 remained reactive at a dilution of 1/4096. Only background reactions were observed with the corresponding pre-immune sera (data not shown). This demonstrated that Wim3 and Wim4 could be detected by the sera from animals immunized with the whole bacterium, supporting their potential use in a serological diagnostic test.
ELISA with human sera
To evaluate the sensitivity and specificity of Wim3 and Wim4 proteins in a W. chondrophila ELISA, we utilized 24 human sera from a previous study [16] and we first determined their positivity or negativity towards W. chondrophila using a micro-immunofluorescence assay (MIF) as gold standard. The sera reactivity was then assessed by direct ELISA using Wim3 and Wim4 as antigens. In order to maximize the signal∶noise ratio of these assays, we performed optimization experiments in which various primary and secondary antibody dilutions as well as different saturation and washing conditions were compared. The optimal assay conditions were determined using ROC analyses (Figure 2). In these optimized conditions, the results obtained with 20 W. chondrophila positive and 4 W. chondrophila negative human sera indicated that both Wim3 and Wim4 assays are able to distinguish the two groups of sera (Figure 3). Considering a threshold value of 0.63, the sensitivity was 100% for the Wim3 assay and, with a threshold value of 0.3, 90% for the Wim4 assay. In addition, sera negative for W. chondrophila and for other members of the Chlamydiales order were not detected neither in the Wim3 nor in the Wim4 assay (specificity of 100% for both assays, see Figure 3).
A. ROC curves obtained using Wim 3 protein as antigen. Combination of buffers used for saturation and dilution of antibodies as well as for washing steps were tested with sera positive and negative for W. chondrophila. See Material and Methods for further description of the assay conditions. B. ROC curves obtained with the Wim3 assay using condition 2 and various dilution of primary and secondary antibodies.
96-well ELISA microplates were coated either with recombinant protein Wim3 or recombinant protein Wim4. Human sera were previously characterized by MIF and are represented as follows: grey circles: W. chondrophila positive (n = 20); black circles: W. chondrophila negative (n = 4). The bar indicates the mean value for each group. Threshold of positivity: 0.63 for Wim3 and 0.30 for Wim4. Results are the mean of three independent experiments. Thresholds were determined by ROC curves analyses (GraphPadPrism).
Discussion
W. chondrophila is now considered as an abortigenic agent in ruminants [13], [14], [15] and as a possible cause of adverse pregnancy outcome in humans [16], [18]. Moreover, bacterial DNA has been detected in respiratory tract samples from patients with pneumonia and from children with bronchiolitis [17], [19]. Recent publications from our group documented the intracellular growth of W. chondrophila in human macrophages, endometrial cells and pneumocytes [30], [31], [32], which further underlines the pathogenic potential of this organism for humans. At present, serological investigation to diagnose W. chondrophila infection relies on a tedious and time-consuming micro-immunofluorescence (MIF) test [16], [25]. Given its pathogenic potential, it is crucial to develop a reliable, sensitive and specific ELISA test for assessing the prevalence of this organism in the human population in large sero-epidemiological studies.
In order to identify immunogenic proteins of W. chondrophila that would be family-specific, we established a combined immunoproteomic and comparative genomics approach utilizing newly available genomic data [24]. This led to the identification of Waddlia proteins, homologs of known chlamydial immunogenic proteins such as chaperonin GroEL (Hsp60), chaperone protein DnaK (Hsp70), elongation factor Tu and leucyl aminopeptidase [33], [34], [35] and of proteins, such as elongation factor G, elongation factor Ts, transcription termination factor rho and 2-oxoglutarate dehydrogenase E3 component which have been described as immunogenic in other bacterial species [22], [26]. This congruence between our results and those reported by other scientists using other approaches supports the relevance of our immunoproteomic method to successfully identify immunogenic proteins. Furthermore, all proteins identified by mass spectrometry were of waddlial origin, a result that reveals the purity of the bacterial preparation, further confirmed by the complete negativity of the 2D gel obtained with the mock control.
Four of the 13 identified proteins (chaperonin GroEL, chaperone protein DnaK, elongation factor Tu and elongation factor Ts) were also described as immunogenic in a similar work conducted on P. acanthamoebae [20]. In addition, W. chondrophila hypothetical protein #4 (Wim4), also identified in this work, is homolog to a P. acanthamoebae hypothetical protein (pah_c029o043), which was previously shown to be immunogenic [20].
Commercially available ELISA tests for the diagnosis of chlamydial infections are usually based on recombinant peptides of the major outer membrane protein (MOMP) or of the 60 kDa cysteine-rich outer membrane protein (OmcB), two major antigens of the organisms belonging to the Chlamydiaceae family [33], [36], [37]. Although, no homolog to MOMP could be identified in the P. acanthamoebae or in the P. amoebophila genomes, a putative cysteine-rich MOMP-family is present in the W. chondrophila genome [20], [24], [38]. However, no protein of this family was identified in the present work, most probably because we had, on purpose, chosen extraction and isolation conditions which should leave the putative waddlial disulphide linked matrix as an insoluble complex. Since our primary aim was to identify unique immunogenic proteins which we could express as fusion-proteins in bacteria for use in a high-throughput ELISA and since disulphide-rich fusion proteins are notoriously difficult to prepare in this manner, we had decided to leave this aspect for a later date. This strategy has the added advantage of easing the preparation of clean 2D gels for proteomic analysis and immunoblotting.
In addition, several other proteins, such as ribosomal proteins S1 and L7/L12, chlamydial protease-like activity factor (CPAF), translocated actin-recruiting protein (TARP) and polymorphic membrane protein D (PmpD), which are well-described antigens of Chlamydiaceae [34], [35], [39], [40] were also not detected in our study on W. chondrophila. Since the corresponding genes are indeed present in the Waddlia genome, these proteins are likely among those that were not chosen for analysis by mass spectrometry, being either weakly immunogenic or poorly expressed in elementary bodies. Alternatively, large proteins such as the waddlial putative Pmp could be under represented due to the 2D gel limitations for large proteins.
Despite these limitations, our strategy proved to be successful, with 2 novel proteins (Wim3 and Wim4) selected (from the 13 identified immunogenic proteins) as promising candidates for the development of a Waddlia-specific ELISA since they display little or no sequence homology with proteins of other members of the Chlamydiales order. Indeed, one recurrent problem of previous serological studies in the chlamydial field was the possible cross reactivity of highly conserved proteins, such as Hsp60, with different bacteria of the same phylogenic order. This limitation was overcome in the present study by the use of a protein not encoded in the genome of any Chlamydiales bacteria sequenced today [20], [41], [42]. In Western blot as well as in ELISA, both recombinant proteins Wim3 and Wim4 reacted with the sera of rabbits immunized with W. chondrophila and not with the corresponding pre-immune sera thus confirming the potential of these two proteins for use in a diagnostic serological test. Wim3 and Wim4 were used in ELISA to assess the reactivity of human sera previously tested by a micro-immunofluorescence (MIF) technique (considered as the gold standard for serological diagnosis) towards W. chondrophila. The sensitivity of the ELISA was 100% for the assay with Wim3 and 90% for the assay with Wim4, using cut off values of 0.63 for the Wim3 assay and of 0.3 for the Wim4 assay, respectively. When considering W. chondrophila negative sera, the specificity of both assays was 100% with the defined cut off values. Thus, the results obtained with Wim3 and Wim4 ELISA were congruent with those obtained by MIF in 100% and 92% of the cases respectively, despite the fact that the antibody response measured is directed against one specific protein in the ELISA and against the whole bacterium in the MIF tests.
In conclusion, by combining genomic and proteomic approaches, this work allowed the identification of an immunogenic protein set for W. chondrophila, of which a number are highly conserved homologs of well-known chlamydial antigens. In addition, we also reported the immunoreactivity of two novel proteins of unknown function, one (Wim3) being specific to W. chondrophila. Preliminary experiments indicated that a direct ELISA test using Wim3 as antigen is able to discriminate between Waddlia positive and Waddlia negative sera as efficiently as micro-immunofluorescence and could be used as an alternative to screen large numbers of samples. Further work is now needed to precisely establish the specificity of this assay, in particular towards other members of the Chlamydiales order.
Methods
Human sera
Human sera were described in previous studies [16], [25]. The clinical studies were approved by the local ethical committees. All sera were tested with an in-house micro- immunmofluorescence method (see below) for reactivity against W. chondrophila. In addition, negative sera were also tested for reactivity against other members of the Chlamydiales order (P. acanthamoebae, E. lausannensis, C. sequanensis, S. negevensis, N. hartmannellae, C. trachomatis, C. pneumoniae and C. psittaci) [16].
Sera from immunized rabbits
Rabbit anti-W. chondrophila sera were obtained by vaccination with W. chondrophila strain ATCC VR-1470 grown in amoebae (see below). Briefly, rabbits were inoculated at days 0, 14, 28 and 56 with 500 µl of PBS containing 5×108 heat-inactivated W. chondrophila. Animals were bled prior to immunization (pre-immune sera) and at day 90.
Culture and purification of Waddlia chondrophila
W. chondrophila strain ATCC VR-1470 was grown at 32°C within Acanthamoeba castellanii strain ATCC 30010 in 25 cm2 or 75 cm2 cell culture flasks (Corning, New York, USA) with 10 or 30 ml of peptone-yeast extract-glucose broth and purified using a sucrose barrier and a gastrografin gradient, as previously described [6], [43]. The same purification procedure was also performed on non-infected A. castellanii (mock control). The purified bacteria were conserved in PBS and 20% glycerol at −80°C.
Crude extract sample preparation and 2D gel electrophoresis
Bacterial cells resuspended in PBS were washed in 10 mM Tris, 5 mM Magnesium acetate, pH 8.0 and then lysed by 5 cycles of short-pulse sonication in lysis buffer (30 mM Tris, 7 M urea, 2 M thiourea, 4% CHAPS, pH 8.5). Proteins were recovered by centrifugation at 6'000 g and their concentration determined using a Bradford assay (Quick Start™ Bradford Protein Assay, Biorad, Hercules, USA).
Two dimensional gel electrophoresis was performed as described by Centeno et al. [44] using approximately 150 µg (mini gels) or 600 µg (midi-gels) of total elementary bodies proteins. Proteins were visualized by Coomassie Blue staining or transferred to nitrocellulose for subsequent immunoblot analyses.
Immunoblot analysis
Nitrocellulose membranes corresponding to 2D gels were blocked by 2 hours incubation with 5% non-fat dry-milk in Tris-buffered saline with 0.05% Tween 20 (TBS), washed 3 times with TBS, 0.5% milk and incubated overnight at 4°C with sera diluted in TBS, 0.5% milk. Membranes were probed either with human sera (dilution 1/8) or with sera of immunized rabbits (dilution 1/25). After 3 subsequent washes with TBS, 0.5% milk, membranes were incubated with horseradish peroxidase-conjugated goat anti-human IgG (Chemicon, Temecula, CA, 1∶500) or horseradish peroxidase-conjugated goat anti-rabbit IgG (Cell Signaling, Allschwill, Switzerland, 1∶1000). Finally, membranes were washed 3 times with TBS and immunoreactive spots were detected either with a chemiluminescence-based kit (LiteAblot™, Euroclone SpA, Pero, Italy) or with 4-chloro-1-naphtol (Sigma-Aldrich, St. Louis, MO, USA).
The same protocol was used for 1D western blots on Wim3 and Wim4 using sera of rabbits immunized with W. chondrophila or preimmune sera at dilution 1/100.
Mass spectrometry
For identification of proteins, Coomassie Blue stained spots were excised from 2D gels and transferred to special 96-well plates (Perkin Elmer Life Sciences). In-gel proteolytic cleavage with sequencing-grade trypsin (Promega, Madison, WI, USA) was performed in the automated workstation Investigator ProGest (Perkin Elmer Life Sciences) according to the protocol of Shevchenko et al. [45]. Digests were evaporated to dryness and resuspended in 3 µl alpha-cyano-hydroxycinnamic acid matrix (5 mg/ml in 60% (v∶v) acetonitrile∶water), of which 0.7 µl were deposed in duplicate on a target plate.
MALDI-MS-MS analysis was performed on a 4700 Proteomics Analyser (Applied Biosystems, Framingham, MA, USA). After MALDI-TOF MS analysis, internal calibration on trypsin autolysis peaks and subtraction of matrix peaks, the 10 most intense ion signals were selected for MS/MS analysis. Non-interpreted peptide tandem mass spectra were used for direct interrogation of W. chondrophila open reading frames using Mascot 2.0 (http://www.matrixscience.com). The mass tolerance for database searches was 50 ppm. With the parameters used, the threshold for statistical significance (p<0.05) corresponded to a MASCOT score of 17, but only scores greater than 30 were considered. Proteins scoring above 80 were automatically considered as valid, while all protein scoring between 30 and 80 were manually validated. Validation included examination of the peptide mass error of individual peptide matches. When proteins could not be identified by MALDI-TOF MS analysis, spots were reanalyzed by LC-MS followed by the same identification procedure as described above.
Cloning, expression and purification of immunogenic proteins
The ORFs corresponding to the immunogenic proteins #3 (Wim3);(ORF wcw_1327) and #4 (Wim4);(ORF wcw_1618) were amplified by PCR and cloned into the pET28 vector (Novagen EMD Chemicals Inc, San Diego, USA). This vector system allows to express the protein of interest fused with a C-terminal 6-His tail. Protein expression was induced during 2.5 hours with 1 mM isopropyl-β-D-thiogalactopyranoside (IPTG, Qbiogen, Basel, Switzerland). The expressed proteins were purified under non denaturating conditions as previously described [20] and concentrated using a MacrosepR 10K (Pall Corporation, Port Washington, USA). Final protein concentrations were determined using the Bradford Quick Start™ assay (Biorad).
Micro-immunofluorescence assay (MIF)
Purified bacteria were inactivated by incubation with 0.3% formalin during 1 hour at room temperature before being spotted on MIF glass slides (12 well diagnostic slides, Menzel, Braunschweig, Germany) previously washed with 70% ethanol. Slides were pre-incubated with PBS 1% BSA during 1.5 hours at room temperature in a humidified chamber, then washed for 5 minutes with PBS 0.03% Tween 20, 5 minutes with PBS and 5 minutes with distilled water. Human sera to be tested were diluted 1/32 in PBS 1% BSA and added to the antigens as a 25 µl drop. After one hour incubation at room temperature in a humidified chamber, slides were washed as before. Slides were then incubated one hour at room temperature with a 1/400 dilution of goat anti human IgH-fluorescein conjugated (Fluoline H, Biomerieux, France) and 150 ng/ml DAPI (dilactate, Molecular Probes, OR, USA) in PBS 1% BSA. After 3 washing steps as before, slides were mounted in Mowiol (Sigma-Aldrich, MO, USA). Positive, negative or doubtful immunofluorescence signals were determined by two independent investigators using an epifluorescent microscope (Axioplan 2, Zeiss, Feldbach, Switzerland) at a magnification of 100×.
ELISA
Optimization of signal∶noise ratio.
To optimize the assay with human sera, different saturation and washing conditions were compared. Buffers used to block and to dilute primary and secondary antibodies were:
condition 1: PBS, 0.1% Tween 20, 1% non-fat dry milk
condition 2: 20 mM Tris-HCl pH 7.5, 0.11 M NaCl, 0.1% Tween-20, 10% FCS, 1% BSA, 1% casein, 1% PEG
condition 3: same as condition 2 but 0.5 M NaCl
condition 4: same as condition 2 but 1 M NaCl
condition 5: same as condition 2 but 1.5 M NaCl
For each condition, a related washing buffer was used:
condition 1: PBS, 0.1% Tween-20
condition 2: 20 mM Tris-HCl pH 7.5, 0.11 M NaCl, 0.1% Tween-20
condition 3: same as condition 2 but 0.5 M NaCl
condition 4: same as condition 2 but 1 M NaCl
condition 5: same as condition 2 but 1.5 M NaCl.
In the optimization phase, human sera were diluted 1/16, 1/32, 1/64 and 1/128. Secondary antibody (horseradish peroxidase-conjugated goat anti-human IgH (Chemicon, Temecula, CA)) was diluted 1/5'000, 1/10'000, 1/25'000 and 1/50'000. The enzymatic reaction with O-phenylenediamine dihydrochloride (OPD) as substrate was stopped with 3M H2SO4 after 5, 15 or 45 minutes and the optical density was read at 492 nm using an ELISA reader (Multiskan Ascent, Thermo Scientific, Waltham, USA). ROC analyses of the ELISA outcome were performed with GraphPad Prism version 5.04 for Windows (GraphPad Software, San Diego, CA, USA).
Wim3 assay.
96-well microplates were coated during 12 hours at 4°C with 100 ng/well of purified protein in carbonate/bicarbonate buffer pH 9.6. Saturation as well as primary and secondary antibody dilutions were performed in 20 mM Tris-HCl pH 7.5, 0.11 M NaCl, 0.1% Tween-20, 10% FCS, 1% BSA, 1% casein, 1% PEG. The saturation step of 1 hour at 37°C was followed by one washing step with 20 mM Tris-HCl pH 7.5, 0.11 M NaCl, 0.1% Tween-20 and a 2 hours incubation at 37°C with primary antibodies diluted 1/64. After 5 washing steps, the plates were incubated during 1 hour at 37°C with a 1/5000 dilution of horseradish peroxidase-conjugated goat anti-human IgH. After 5 washing steps, substrate (1 mg/ml O-phenylenediamine dihydrochloride in citrate buffer) was added and the enzymatic reaction was stopped with 3M H2SO4 after 5 minutes. The optical density was read at 492 nm.
Wim4 assay.
Same protocol as for Wim3 assay except that saturation and primary/secondary antibody dilutions were performed in PBS, 0.1% Tween-20, 1% milk and that washing steps were performed using PBS, 0.1% Tween-20. The enzymatic reaction was stopped after 15 minutes.
When testing rabbit sera, ELISA were performed as described elsewhere [20].
Acknowledgments
We thank Prof. M. Quadroni and the proteomic facility of the University of Lausanne for assisting with mass spectrometry analyses. We also thank I. Riederer (Proteomics Unit, Prilly-Lausanne) for technical help and L. Vaughan (Institute of Veterinary Pathology, Zürich) for careful reading of the manuscript.
Author Contributions
Conceived and designed the experiments: CK BR GG. Performed the experiments: CK FU JL BR. Analyzed the data: CK FU JL BR GG. Contributed reagents/materials/analysis tools: CK DB GG. Wrote the paper: CK GG.
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