Abstract
Serum samples from persons with Lyme borreliosis, periodontitis, or acute necrotizing ulcerative gingivitis were analyzed by an enzyme-linked immunosorbent assay (ELISA) with and without adsorption and amplification procedures. When biotin and streptavidin reagents were used as an amplification procedure in ELISA without the use of commercially prepared sorbent (Treponema phagedenis biotype Reiter), sensitivity increased. Of the 85 serum samples collected from persons with erythema migrans but no detectable antibodies to Borrelia burgdorferi by standard ELISA, 17 (20%) were reactive after amplification. Adsorption of serum samples with a 1:10 dilution of T. phagedenis biotype Reiter sorbent used in conjunction with amplified ELISA also improved the sensitivity of this method. However, cross-reactivity could not be completely eliminated. An adsorbed-amplified ELISA may be helpful in the diagnosis of Lyme borreliosis in the laboratory, particularly during early weeks of infection, when antibodies to B. burgdorferi can be present at a low concentration.
MeSH Terms
Antibodies, Bacterial/blood
Bacterial Proteins
Biotin
Borrelia burgdorferi Group/immunology
Enzyme-Linked Immunosorbent Assay/methods,statistics & numerical data
False Positive Reactions
Humans
Immunosorbent Techniques
Lyme Disease/diagnosis,immunology
Sensitivity and Specificity
Streptavidin
Chemicals
Antibodies, Bacterial
Bacterial Proteins
Biotin
Streptavidin
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Magnarelli L A
Department of Entomology, Connecticut Agricultural Experiment Station, New Haven 06504.
Anderson J F
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