Development of a multiplexed bead-based immunoassay for the simultaneous detection of antibodies to 17 pneumococcal proteins
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Presently, several pneumococcal proteins are being evaluated as potential vaccine candidates. Here, we gather novel insights in the immunogenicity of PLY, PsaA, PspA, PspC, NanA, Hyl, PpmA, SlrA, Eno, IgA1-protease, PdBD, BVH-3, SP1003, SP1633, SP1651, SP0189 and SP0376. We developed a multiplex bead-based immunoassay (xMAP® Technology, Luminex Corporation) to simultaneously quantify antibodies against these 17 pneumococcal proteins in serum. The median fluorescence intensity (MFI) values obtained for human pooled serum with the multiplex assay were between 82% and 111% (median 94%) of those obtained with the singleplex assays. For IgG, the coefficient of variation (CV) in serum ranged from 2% to 9%, for IgA, the CV ranged from 3% to 14% and for IgM, the CV ranged from 11% to 15%. Using this immunoassay, we showed that anti-pneumococcal antibody levels exhibited extensive inter-individual variability in young children suffering from invasive pneumococcal disease. All proteins, including the proteins with, as yet, unknown function, were immunogenic. In conclusion, the multiplex Streptococcus pneumoniae immunoassay based on proteins is reproducible. This assay can be used to monitor anti-S. pneumoniae antibody responses in a material- and time-saving manner.
KeywordsInvasive Pneumococcal Disease Pneumococcal Meningitis Multiplex Assay Median Fluorescence Intensity Potential Vaccine Candidate
Streptococcus pneumoniae (S. pneumoniae, pneumococcus) is an important human pathogen that causes life-threatening diseases such as pneumonia and meningitis, as well as less serious but highly prevalent diseases such as otitis media and sinusitis. Between 2002 and 2003, pneumonia accounted for 19% of the 10.6 million deaths per annum among children younger than 5 years of age . Ninety percent of childhood deaths occurred in developing countries , including Bangladesh [3, 4]. The global incidence of pneumococcal meningitis in children is 17 cases per 100,000. The case–fatality rate (CFR) for pneumococcal meningitis is high. In 2000, the global pneumococcal meningitis CFR was 59%, ranging from 29% in the Western Pacific to 73% in Africa .
Fortunately, the availability of the 23-valent capsular polysaccharide and 7-valent pneumococcal conjugate vaccines (PCV23 and PCV7, respectively) has resulted in a dramatic reduction in the morbidity and mortality of pneumococcal diseases. However, the high costs and still limited vaccine-mediated protection, which is restricted to the included serotypes, have prevented its implementation in large-scale immunisation programmes in developing countries. For these reasons, there is considerable interest in designing alternative and more cost-effective strategies. Presently, several pneumococcal proteins are being evaluated as potential vaccine candidates. Optimally, these would provide protection against pneumococcal infection regardless of serotype . To date, the most promising protein vaccine candidates include pneumolysin (PLY), pneumococcal surface adhesin A (PsaA), pneumococcal surface protein A (PspA) and pneumococcal surface protein C (PspC) . These proteins are produced by virtually all clinical isolates of the pneumococcus. PLY is a 53-kDa protein that causes cytolysis, induces complement activation and the production of cytokines and nitric oxide [8, 9, 10, 11, 12]. In addition, PLY has been assigned several functions with respect to modification of the immune response. PLY has recently been shown to interact with Toll-like receptor 4 (TLR-4) . PsaA is a surface-exposed 37-kDa lipoprotein that plays a major role in pneumococcal attachment to the host cell and virulence . PspA is a choline-binding surface protein which inhibits complement-mediated phagocytosis, binds to lactoferrin and, as such, prevents lactoferrin-mediated killing . Antibodies to pneumococcal proteins PspA, PsaA and PLY have been shown to develop early in life [16, 17]. PspC (also known as CbpA or SpsA) acts as an adhesin and binds the complement regulatory protein factor H, to provide resistance to complement [13, 18].
We developed a multiplex bead-based immunoassay using Luminex xMAP® Technology to gather novel insights into the immunogenicity of PLY, PsaA, PspA and PspC and 13 other pneumococcal proteins. With this assay, antibodies to these 17 pneumococcal proteins can be quantified simultaneously. Thus far, for the pneumococcus, this technology was only used for the measurement of antibodies directed to different pneumococcal capsular polysaccharides [19, 20, 21].
Materials and methods
The pneumococcal proteins PLY, PsaA, PspA, PspC, neuraminidase A (NanA), hyaluronidase (Hyl), putative proteinase maturation protein A (PpmA), streptococcal lipoprotein rotamase A (SlrA), α-enolase (Eno), immunoglobulin A1 protease (IgA1-protease), PdBD and BVH-3, SP1003, SP1633, SP1651, SP0189, and SP0376 were used. NanA plays an important role in biofilm formation and promotes pneumococcal brain endothelial cell invasion [22, 23]. Hyl is present on the majority of strains. The enzyme degrades essential components of the host’s extracellular matrix and, as such, it may facilitate bacterial spread in host tissues [13, 24]. PpmA and SlrA, two surface-exposed lipoproteins, have been shown to play a role in virulence and colonisation [25, 26]. Eno has been identified both in the cytoplasm and on the surface of pneumococci and is involved in virulence by the activation of plasmin into plasminogen, a host collagen-degrading enzyme . IgA1-protease plays an important role in pneumococcal colonisation. IgA1-protease modifies IgA1 antibodies so that it promotes rather than inhibits pneumococcal adherence to epithelial cells in a model of colonisation . PdBD is a mutant version of PLY with less cytolytic activity and reduced ability to activate complement . BVH-3 is capable of conferring protection against lethal experimental S. pneumoniae infection. This protein family was also designated Pht (for pneumococcal histidine triad) [30, 31]. SP1003, SP1633, SP1651, SP0189 and SP0376 are pneumococcal proteins with currently unknown functions. Recently, a comprehensive review summarising the surface-exposed virulence factors and their functions was published .
The genes encoding the proteins NanA, PsaA, PspA, PspC, SP1633, SP1651, SP0189, SP0376, Hyl, PLY and PpmA were isolated from S. pneumoniae strain TIGR4 chromosomal DNA and cloned in the vector pOPINF using In-Fusion Technology. Cell extracts were made from the recombinant Escherichia coli (Rosetta) strains and the recombinant proteins purified by immobilised metal affinity chromatography using the poly-His tag added to the N-terminal end of the protein during the cloning procedure. The genes used for the production of the recombinant antigens Eno, SlrA and PpmA were amplified by polymerase chain reaction (PCR) from S. pneumoniae D39. IgA1-protease was amplified from S. pneumoniae TIGR4. The amplified DNA was cloned into a pET11a expression vector (Stratagene) and electrotransformed into E. coli BL21(DE3). The expression of recombinant protein was induced by the addition of isopropyl-β-D-thio-galactoside (IPTG) and the recombinant proteins were purified by Ni+ affinity chromatography, as described previously [16, 25, 32]. The genes encoding BVH-3 and PdBD were cloned into plasmid pPA195 and pPA180, respectively, and transformed into Lactococcus lactis PA1001. The overexpression of BVH-3 and PdBD was induced by nisin, essentially as described previously . The purity of the recombinant proteins was determined by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). The amino acid sequence of the proteins was confirmed with mass spectrometry (Ultraflex MALDI-ToF, Bruker Daltonics).
To quantify antibodies directed against the 17 S. pneumoniae proteins simultaneously, the bead-based flow cytometry technique (xMAP®, Luminex Corporation) was applied. The purified proteins were coupled to fluorescent SeroMAP beads. The coupling procedure was performed as described elsewhere [34, 35]. In each experiment, control beads were included to determine non-specific binding. For control beads, the coupling procedure was followed, except that no S. pneumoniae protein was added. In case of non-specific binding, the median fluorescence intensity (MFI) values were subtracted from the antigen-specific results. As a negative control, PBS-BN was included. Human pooled serum was used as a standard.
Multiplex S. pneumoniae antibody assay
The multiplex assay (serum incubated with the different fluorescence-coloured antigen-coupled beads mixed in one well) was validated by comparing the MFI values for HPS obtained with this multiplex assay with the results for HPS obtained with singleplex assays (serum incubated with individual single-colour antigen-coupled beads in separate wells). After validation, the different antigen-coupled microspheres were mixed to a working concentration of 4,000 beads per colour per well. The procedure used was the same as that described elsewhere [34, 35, 36]. To optimise dilutions, the serum samples of children were diluted 1:25, 1:50 and 1:100 in PBS-BN. The secondary antibodies were diluted 1:50, 1:100 and 1:200 in PBS-BN. Checkerboard titrations were performed. Considering the results of the MFI values and the amounts of serum and secondary antibody needed, optimal serum dilutions were 1:100 for the measurement of IgG and 1:50 for the measurement of antigen-specific IgA and IgM. The optimal secondary antibody dilutions were 1:200 for IgG and 1:100 for IgA and IgM. Measurements were performed on the Luminex 100 instrument (BMD) using Luminex IS software (version 2.2). Tests were performed in duplicate, and the MFI values, reflecting semi-quantitative antibody levels, were averaged.
The multiplexed immunoassay was used to compare differences in anti-pneumococcal antibodies in the serum samples obtained from 54 children under the age of 5 years with clinical suspicion of pneumonia (n = 26) or meningitis (n = 28). Half of these children suffered from pneumonia/meningitis caused by S. pneumoniae and the other half suffered from pneumonia/meningitis caused by a bacterial species other than S. pneumoniae. The serum samples were stored at −80°C until use. The research protocol was approved by the Research Review and Research Ethical Committee of ICDDR,B and written informed consent from the parents was obtained.
The Mann–Whitney U-test was used to compare differences in the anti-pneumococcal antibody levels. Differences were considered to be statistically significant when the two-sided p-values were <0.05.
Results and discussion
Validation of the multiplex assay and reproducibility
The MFI values obtained for HPS with the multiplex assay were between 82% and 111% (median 94%) of those obtained with the singleplex assays. Therefore, it was considered to be legitimate to use the multiplex assay. Serum incubated with control beads resulted in median MFI values for IgG, IgA and IgM of 77 (range, 21–7,210), 92 (range, 15–11,549) and 1,282 (range, 171–7966), respectively. This indicates that there was quite a variable level of non-specific binding that was consistently subtracted from the antigen-specific results. The negative control (PBS-BN) incubated with protein-coupled beads resulted in low MFI values (<10). Inter-assay variation was calculated from the MFI values obtained from serum samples (n = 54) run in two separate assays and averaged per protein and antibody isotype. For IgG, the median coefficient of variation (CV) was 5%, range 2% (PsaA) to 9% (SlrA). For IgA, the median CV was 7%, range 3% (PspC and PsaA) to 14% (SlrA). For IgM, the median CV was 13%, range 11% (SP1633) to 15% (PspC, PpmA and PspA). Earlier studies found equal CVs for inter-assay variation using other types of antigens [20, 34, 37]. Therefore, this new multiplexed anti-pneumococcal immunoassay is considered to be reproducible from experiment to experiment.
In conclusion, using our novel non-polysaccharide-based high-throughput immunological test, we were able to determine the level of antibodies to 17 pneumococcal proteins simultaneously in small-volume serum samples. The requirement for small sample volumes only is a great advantage as compared to enzyme-linked immunosorbent assay (ELISA), especially when limited amounts of samples are available, which is usually the case in young children. Novel antigens can be easily included and combinations of protein and polysaccharide antigens may help in profiling the complete immune response of both patients and healthy individuals to a common opportunistic pathogen, which is especially relevant in children in developing countries.
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