4.5 Article

Borrelia multiplex: a bead-based multiplex assay for the simultaneous detection of Borrelia specific IgG/IgM class antibodies

Journal

BMC INFECTIOUS DISEASES
Volume 22, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12879-022-07863-9

Keywords

Borrelia; Lyme Disease; Lyme borreliosis; Multiplex; Immunoassay; Serology

Funding

  1. joint ZIM project Lyme-CytoPlex of the BMWi [FKZ: ZF4585502AJ8]
  2. State Ministry of BadenWurttemberg for Economic Affairs, Labour and Tourism [FKZ: 7-4332.62NMI/55]
  3. German Research Society (Deutsche Forschungsgemeinschaft) [BE1996/1-1]
  4. Helmholtz Association of German Research Centers (HGF) [SO-96]

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A multiplex Borrelia immunoassay was developed in this study, which showed high sensitivity and specificity in detecting antibodies against multiple Borrelia species. This assay provides a cost-effective and time-saving method for the diagnosis and identification of Lyme borreliosis.
Background Lyme borreliosis (LB) is the most common tick-borne infectious disease in the northern hemisphere. The diagnosis of LB is usually made by clinical symptoms and subsequently supported by serology. In Europe, a two-step testing consisting of an enzyme-linked immunosorbent assay (ELISA) and an immunoblot is recommended. However, due to the low sensitivity of the currently available tests, antibody detection is sometimes inaccurate, especially in the early phase of infection, leading to underdiagnoses. Methods To improve upon Borrelia diagnostics, we developed a multiplex Borrelia immunoassay (Borrelia multiplex), which utilizes the new INTELLIFLEX platform, enabling the simultaneous dual detection of IgG and IgM antibodies, saving further time and reducing the biosample material requirement. In order to enable correct classification, the Borrelia multiplex contains eight antigens from the five human pathogenic Borrelia species known in Europe. Six antigens are known to mainly induce an IgG response and two antigens are predominant for an IgM response. Results To validate the assay, we compared the Borrelia multiplex to a commercial bead-based immunoassay resulting in an overall assay sensitivity of 93.7% (95% CI 84.8-97.5%) and a specificity of 96.5% (95%CI 93.5-98.1%). To confirm the calculated sensitivity and specificity, a comparison with a conventional 2-step diagnostics was performed. With this comparison, we obtained a sensitivity of 95.2% (95% CI 84.2-99.2%) and a specificity of 93.0% (95% CI 90.6-94.7%). Conclusion Borrelia multiplex is a highly reproducible cost- and time-effective assay that enables the profiling of antibodies against several individual antigens simultaneously.

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