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Clinical and Vaccine Immunology, July 2007, p. 875-879, Vol. 14, No. 7
1071-412X/07/$08.00+0     doi:10.1128/CVI.00122-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Epitope Length, Genospecies Dependency, and Serum Panel Effect in the IR6 Enzyme-Linked Immunosorbent Assay for Detection of Antibodies to Borrelia burgdorferi

Maria J. C. Gomes-Solecki,^1,3 Luciana Meirelles,¹ John Glass,² and Raymond J. Dattwyler^1,3*

New York Medical College, Valhalla, New York 10595,¹ Brookhaven National Laboratory, Upton, New York 11973,² Biopeptides Corp., Valhalla, New York 10595³

Received 16 March 2007/ Returned for modification 26 April 2007/ Accepted 18 May 2007

Top ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
In the absence of erythema migrans, the basis for diagnosis of Lyme disease is the demonstration of an antibody response against Borrelia burgdorferi in an appropriate clinical setting. The C6 enzyme-linked immunosorbent assay, based on the IR6 region of VlsE, has become widely used in both the United States and Europe. We mapped the antigenic epitopes of IR6 to a shorter sequence that is equivalent in sensitivity and specificity to the full-length IR6 25-residue peptide. In addition, we observed significant differences in sensitivity between serum panels (60 to 100%), indicating that the selection of the serum panels can shape the apparent overall sensitivity of the assay. Contrary to prior reports, the assay sensitivity is greater when the IR6 peptide is derived from the sequence of the same infecting Borrelia genospecies. Using our North American panels and the two panels obtained from European Lyme disease patients, we determined that the IR6 assay that is based on a single genospecies of Borrelia spp. is not optimal for use as a universal diagnostic assay for Lyme disease.

Top ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Lyme disease is the most frequently reported vector-borne disease in the United States and Europe. The only clinical manifestation that is adequate for the diagnosis of Lyme disease is erythema migrans (EM) (18). When present, EM is seen for a limited period of time in early disease. Although in areas of endemicity the presence of bilateral Bell's palsy suggests Lyme disease (2), neither this nor the other clinical manifestations are specific enough, singly or in combination, to determine clinical diagnosis.

In the absence of EM, the basis for diagnosis is the demonstration of an antibody response against Borrelia burgdorferi in an appropriate clinical setting. In North America, a two-tier approach is recommended for serodiagnosis: a sensitive first tier assay followed by a Western blot if the first tier assay is positive or equivocal. Most of the current first tier assays are based on whole B. burgdorferi or recombinant proteins. The sole exception is the C6 peptide assay. This assay, which is based on the IR6 region of the variable surface antigen (VlsE) of B. burgdorferi (C6), is becoming more widely used in both the United States and Europe (3, 6, 8, 14, 17). It is recognized as the most specific of the first tier assays (1), and it has a high degree of sensitivity for disseminated or late Lyme disease (3). Despite its greater performance and previous suggestions that could be used as a single-tier assay (1, 4, 11), lately it has become apparent that the C6 assay is not sufficiently sensitive or specific to develop a single-tier Lyme disease assay (13, 16).

The linear B-cell epitopes within the VlsE IR6 peptide were previously mapped using sera from experimentally infected monkeys, from mice, and from humans clinically diagnosed with Lyme disease using an overlapping peptide technique. That study concluded that the full 25-residue IR6 peptide (IR6-25) was required to maintain antigenicity (5, 7). We observed that the sequence used to design the IR6 peptide was from IP90, a Borrelia garinii strain that has not been found to cause Lyme disease in the United States. In addition, we noted that this relatively conserved region was somewhat long for a single antigenic epitope. Analysis of the chemical properties of this peptide predicted an antigenic region within a much shorter sequence, in the N terminus of this peptide. To test this hypothesis, we remapped the C6 peptide by employing a finely detailed mapping strategy. Considering the chemical properties of this peptide and working from the natural sequence matrix of IR6 from B. burgdorferi sensu stricto, we designed a series of peptides and were able to define the shortest effective IR6 peptide for diagnosis of Lyme disease in the United States. This short version of the IR6 peptide could be the core of a multiantigenic peptide assay that may lead to the development of a single-tier assay for Lyme disease.

Top ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Peptide synthesis. The synthetic peptides were custom synthesized by the Keck Biopolymer Resource at Yale University. The peptides were made by an automated solid-phase methodology using 9-fluorenylmethoxy carbonyl (FMOC) N protection protocols.

ELISA procedure. Immobilization of peptides onto enzyme-linked immunosorbent assay (ELISA) plates was performed as follows. Solutions of crude peptides in 100 mM N,N-methylenebisacrylamide (Bis)-Tris propane buffer (pH 9.7) were used to coat commercial microwell plates (MaxiSorp; Nunc) at 5 µg/ml as follows. One hundred microliters of the solution described above was dispensed in each well. After 1 h of incubation at room temperature, 300 µl of blocking solution (100 mM Bis-Tris propane buffer [pH 9.7], 0.10% Tween 20, 3% skim milk) was added to each well and the mixture was incubated overnight at 4°C. The blocking solution successfully saturates the high antigen binding capacity, leaving low background readings in the control channels. The contents were discarded, and the plate was washed three times using Tris-buffered saline-Tween (TBST) buffer.

A standard procedure for the ELISAs was followed. Human serum was diluted at 1:50 in 100 µl of TBST buffer with 1% skim milk. The samples were added to each well, and the plate was incubated for 1 h at room temperature. Plates were washed three times with TBST buffer. The alkaline phosphatase-conjugated anti-human immunoglobulin G (H+L; Jackson ImmunoResearch, West Grove, PA) antibody was diluted at 1:1,600 in TBST buffer with 1% skim milk; 100 µl of this solution was dispensed onto the plate and incubated for 30 min at room temperature. Plates were washed three times with TBST buffer, and 100 µl of substrate was added (pNPP microwell substrate system; KPL, Gaithersburg, MD) and incubated for 1 h at room temperature. Plates were read at 405 nm on a microplate reader (Spectramax 320; Molecular Devices). A sample was considered positive if it produced an average absorbance superior to the mean of five negative controls plus 3 standard deviations.

Test panels. Our screening panels consist of sera from patients with early Lyme disease and clinically defined as late Lyme disease, patients with syphilis, and patients with rheumatologic disorders as well as from normal healthy donors from an area of endemicity. The clinical characterization of the serum panels is described in Table 1. The Lyme disease serum panels are representative of the population of suburban New York and include samples from children, adults, males, females, whites, and minorities. The panels were randomly selected from our serum bank (from SUNY Stony Brook Lyme Disease Center). They were not preselected in any way.

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TABLE 1. Clinical characterization of the serum panels used in this study

Statistical analysis. The odds ratio (OR) method was used to assess statistical significance. The OR is a measure of effect size particularly important in logistic regression that is a statistical regression model for Bernoulli-distributed dependent variables. The OR is defined as the ratio of the odds of an event occurring in one group to the odds of it occurring in another group.

Top ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Epitope mapping. The sequence used to design the C6 peptide was from a B. garinii strain not found in North America. Because there are amino acid differences between the IR6 sequences from B. garinii (PT7, strain IP90) and B. burgdorferi sensu stricto (strain B31), a prototypic North American strain, we decided to compare the two. We synthesized the 25-mer IR6 segment from both strains with N-terminal cysteinyl residues appended for attachment of biotinyl ligands as described by Liang et al. (5, 8) and compared them against a panel of Lyme disease sera: 55 acute-phase sera characterized by EM, 33 of which were culture confirmed. The results are shown in Table 2. We observed that the peptide that was based on the B. garinii sequence (IP90-25) was less sensitive (41.8%) than the peptide based on the B. burgdorferi B31 sequence (B31-25; 56.4%). An OR of 1.787 indicates the B. burgdorferi sequence is 1.8 times as likely to be more sensitive than the B. garinii sequence.

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TABLE 2. Comparison between B. garinii and B. burgdorferi IR6 test sensitivitiesa

Analysis of the chemical properties of the IR6 peptide by the Kyte-Doolittle hydrophilicity method predicted a large antigenic region within a much shorter sequence in the N terminus of this peptide and a minimal epitope in the C terminus. In order to determine the minimum human active epitope(s) in this region for diagnostic purposes, we employed a finely detailed mapping strategy working from the natural sequence matrix of B. burgdorferi B31 genospecies and used 33 Lyme disease sera defined as EM and culture positive. Liang et al. speculated that the key portion of the human epitope of IR6 was located in the central area of the peptide (7), but they were unable to define it. To test this, we shortened the 25-residue sequence of B31-IR6 from the C terminus until its efficiency at detecting early Lyme disease antibodies dropped. We then returned to the shortened sequence of IR6 and began deleting residues from the N terminus. The results are shown below in Table 3. We found that shortening the C-terminal portion of the peptide by 7 and 8 amino acids showed a trend toward increased sensitivity (B31-17 versus B31-25; OR = 1.552) which indicates that B31-17 is 1.5 times as likely to be more sensitive than B31-25 against the panel tested. In contrast, deletion of the 9th C-terminal residue (B31-16a) and deletion of the first N-terminal residue (B31-16b) caused a decline in B31-17 peptide antibody detection. The OR between IR6-17 and IR6-16a is 2.009, which indicates that IR6-17 is twice as likely to be more sensitive than IR6-16a. Thus, we concluded that the critical immunodiagnostic epitope of the 25-residue IR6 sequence from B. burgdorferi B31 is confined within a 17-residue segment of the IR6 sequence and that the N-terminal sequence is essential for maintenance of antigenicity.

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TABLE 3. B. burgdorferi B31 VlsE-IR6 shortest immunodominant region

Sensitivity and specificity. With these new findings, we wanted to see how this narrowly defined peptide from B. burgdorferi (B31-17) compared to the homologous sequence from B. garinii (IP90-17) as well as to the respective 25-residue peptides, B31-25 and IP90-25. The sensitivities and specificities (Tables 4, 5, and 6) of the four peptides were determined using several panels of clinically defined Lyme disease sera.

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TABLE 4. Comparison between the four IR6 peptides for sensitivity

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TABLE 5. Comparison between the four peptides for specificity

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TABLE 6. Comparison of the sensitivities and specificities of the four IR6 peptides

Differences in sensitivities between the four peptides were significant in detecting B. burgdorferi antibodies in the panel defined as acute, single EM, and early Lyme disease (Table 4 and Table 6). The peptide B31-25 is 1.5 times as likely to be more sensitive than IP90-25 and IP90-17 and 1.3 times as likely to be more sensitive than B31-17 against this panel. In the panel defined as late Lyme, we observed that B31-25 is 1.6 times as likely to be more sensitive than IP90-25 and no differences were observed between B31-25 and the two 17-residue peptides. Overall, we conclude that the peptide based on the B. burgdorferi sensu stricto sequence (B31) is more sensitive than B. garinii IP90, the sequence used to develop the C6 assay. There was no difference in sensitivity between the four peptides in detecting antibodies in sera from patients with specific symptoms of Lyme disease, such as the sera defined in three other panels, acute disseminated (60%), acute neurologic (83.3%), and Lyme disease reinfected (100%).

We tested the specificity of the assay against sera from patients with conditions whose clinical presentation could place Lyme disease in their differential diagnosis (rheumatoid arthritis) or that produce antibodies that can be potentially cross-reactive with anti-B. burgdorferi antibodies (syphilis and systemic lupus erythematosus). Sera from healthy individuals from an area of endemicity were used as a negative control. The most specific peptides were B31-25, IP90-25, and B31-17, which detected the lowest number of cross-reactive samples (Table 5 and Table 6). The IP90-17 peptide was less specific than the other three peptides, detecting the highest percentages of cross-reactive antibodies. This peptide was 2.7 times as likely to detect cross-reactive antibodies as B31-25 and 2.3 times as likely to detect cross-reactive antibodies as B31-17 and IP90-25. The lack of specificity of this peptide against all cross-reactivity panels indicates that it is not appropriate for development of an assay to be used in the United States.

In summary (Table 6), we conclude that the IR6 peptides based on the B. burgdorferi sensu stricto sequence (B31) showed the highest sensitivity and specificity to detect Lyme disease antibodies and that OR determinations for comparisons between the B31-25 and -17 peptides are equivalent (B31-17 versus B31-25, OR = 1.5 against one panel of early Lyme disease; and B31-25 versus B31- 17, OR = 1.3 against a second panel of early Lyme disease).

To finalize this study, we compared the sensitivities of the four peptides to two Lyme disease panels obtained from Europe: a panel from clinically defined Lyme disease Austrian patients and a second panel comprising sera from patients with signs and symptoms suggestive of Lyme disease from Portuguese patients (Table 7). We found that the B31-25 peptide was only 1.3 times as likely to be more sensitive at detecting B. burgdorferi sensu lato antibodies from patients in the Austrian panel than the IP90-25 peptide. In contrast, we found that the IP90-25 peptide was 2.5 times as likely to be more sensitive at detecting anti-B. burgdorferi sensu lato antibodies from patients in the Portuguese panel than B31-25.

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TABLE 7. Comparison between the four IR6 peptides using European serum panels

Top ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
The C6 Lyme ELISA is taking on increasing importance because of its superior characteristics compared to whole-B. burgdorferi-based assays (1, 6, 8). The findings described in this study are noteworthy for three reasons: we have more precisely defined the human IR6 epitope to a shorter sequence that can lead to future improvement of IR6-based assays; the serum panels chosen can shape overall sensitivity of the assay; and, as importantly, we have demonstrated that the IR6 sequences from different genospecies are not fully interchangeable.

Although the IR6-25 peptide was mapped as a single antigenic determinant in humans (7), we observed that this relatively conserved region is somewhat long for a single epitope and we embarked on a series of experiments to remap this region. Rather than using overlapping peptides to determine the minimum human active epitope(s) of this peptide, we employed a finely detailed mapping strategy by serially deleting amino acids from the natural sequence matrix. We used a human serum panel obtained from patients with culture-confirmed early Lyme disease as our source of anti-B. burgdorferi antibodies. We first shortened the 25-residue sequence of IR6 from the C terminus and found that the efficiency to bind antibodies dropped sharply only after the deletion of the 9th C-terminal residue. Then returning to the sequence of IR6 shortened by eight residues at the C terminus, we began deleting residues from the N terminus. Deletion of even the first N-terminal residue caused a decline in antibody detection. Thus, we concluded that the critical immunodiagnostic epitope of the 25-residue IR6 sequence is confined within a 17-residue segment beginning with the N-terminal sequence whose conservation is essential to maintain antigenicity.

This finding, that the epitope encompasses the N terminus of the peptide, does not support what was previously predicted about the IR6 B-cell epitope. Liang et al. hypothesized that the key portion of the human epitope of IR6 was located in the central area of the peptide (7), the core of the epitope, and the key to the tertiary structure of the peptide being a predicted alpha helix comprised of an 11-mer sequence [AA(I or M)(A or V)LRGMAKD]. That hypothesis proposed that the alpha helix anchored the flanking amino acids, that the full 25-residue peptide was required, and that the epitope was most likely discontinuous. We demonstrate that neither the alpha helix nor the full-length peptide is required for the maintenance of the epitope. It also appears that the epitope is more linear than originally hypothesized.

The wide use and acceptance of the C6 assay for detection of anti-B. burgdorferi antibodies (1, 3, 16, 17) and the original finding that the six invariable regions of the VlsE protein are conserved among strains and genospecies of the B. burgdorferi sensu lato complex (5) led to the suggestion that the IR6 regions of any of the genospecies of B. burgdorferi are interchangeable in their ability to bind antibody. We found this not to be the case. Comparing four peptides based on IR6 sequences from B. burgdorferi and B. garinii, we found differences in sensitivities using the acute, single EM Lyme disease and the late-Lyme disease panels. These are the Lyme disease groups that would benefit the most from a sensitive diagnostic assay, especially the early Lyme disease group. In addition, we found that both peptides based on the B. burgdorferi sensu stricto sequence (B31) are more sensitive than B. garinii IP90, the sequence used to develop the C6 assay (8), in these panel groups. This increase in sensitivity is due to the use of the IR6 sequence from B. burgdorferi sensu stricto, the genospecies that infects humans in North America. Furthermore, we observed that there was no difference in sensitivities between the peptides in detecting B. burgdorferi antibodies in the other three panels, defined by clear clinical manifestations of Lyme disease. Most importantly, we observed significant differences in sensitivities between the panels (60 to 100% for the most sensitive peptide), indicating that overall sensitivity of the assay can be affected by the choice of the Lyme disease panel used. These data indicate that in studies of serologic assays, the key factor in determining true test sensitivity is made up of the clinical characteristics of the patients from whom the serum was obtained.

The C6 assay has become the assay of choice both in the United States and Europe, either alone (3, 6, 8, 9, 14, 17) or in combination with other assays (1, 4, 12). Sensitivity of this assay in Europe varies between 91% in a study in The Netherlands against a panel of sera from clinically defined Lyme patients confirmed by immunoblotting (16) and 33% in Italy against a panel of sera from clinically defined Lyme patients with EM confirmed by culture (10). In our study, we found that peptides based in two different Borrelia genospecies detected antibodies to this spirochete with significant differences in sensitivity between two panels of Lyme disease obtained from Europe. The most sensitive peptide for the American panel, based on the B. burgdorferi B31 sequence, showed a trend toward increased sensitivity for the Austrian panel. The fact that the peptide based on the B. garinii sequence was undoubtedly the most sensitive in detecting antibodies in the Portuguese panel of our seroprevalence study shows a degree of genospecificity in the detection of B. burgdorferi sensu lato antibodies, given that in Europe, B. garinii and Borrelia afzelii are the most frequently cultured pathogenic spirochetes from Lyme disease patients. Recently, IR6 peptides from the three pathogenic Borrelia species (B. burgdorferi sensu stricto, B. afzelii, and B. garinii) were analyzed against serum panels from patients with European and American origins, and it was found that B. burgdorferi sensu stricto peptide antibodies correlated well with B. afzelii peptide antibodies and that B. garinii IR6 peptide antibodies were discordant with B. afzelii and with B. burgdorferi peptide antibodies (15). These data correlate with our findings that B. burgdorferi sensu stricto peptide antibodies were detected in the serum panel obtained from Austria (where B. afzelli is most frequent), while B. garinii peptide antibodies were found in the serum panel obtained from Portugal (where the pathogenic Borrelia spp. have not yet been defined). In combination, data from both studies indicate that the IR6 assay that is based on a single genospecies of Borrelia may not be suitable for use as a universal diagnostic assay for Lyme disease. In addition, the data suggest that B. garinii might be one of the predominant species of B. burgdorferii sensu lato that infects humans in Portugal.

 
This study was supported by grants from NIH-NIAID, R44AI058364 (M.G.S.) and R01AI055652 (R.J.D.).

We thank Laura Hannafey and Diana Lombardo for excellent technical support. We would like to thank Margarida Collares-Pereira and the Departments of Neurology and Rheumatology from Instituto de Higiene e Medicina Tropical, in Lisbon, for kindly providing the panel of sera from Portuguese patients. We would like to thank Gerald Seinost and the Department of Medicine of the Medical University of Graz for kindly providing the panel of sera from Austrian patients.

 
* Corresponding author. Mailing address: New York Medical College, BSB Room 308, Valhalla, NY 10595. Fax: (914) 594-4922. E-mail: raymond_dattwyler{at}nymc.edu

Published ahead of print on 30 May 2007.

Top ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 

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Clinical and Vaccine Immunology, July 2007, p. 875-879, Vol. 14, No. 7
1071-412X/07/$08.00+0     doi:10.1128/CVI.00122-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

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