Skip to main content
Log in

Single-tube nested polymerase chain reaction assay based on flagellin gene sequences for detection ofBorrelia burgdorferi sensu lato

  • Articles
  • Published:
European Journal of Clinical Microbiology and Infectious Diseases Aims and scope Submit manuscript

Abstract

An inherent drawback of nested PCR systems to increase sensitivity of PCR-based assays is that tubes must be opened after the first round of amplification in order to transfer template molecules to the second amplification reaction; this procedure introduces the risk of carry-over contamination of negative specimens. To obviate this disadvantage, a nested PCR assay for detection ofBorrelia burgdorferi in which both amplifications are performed in a single tube that remains closed throughout the entire process was devised. The assay is based on flagellin gene sequences with previously determined species-wide and species-specific properties. The nested PCR system proved to be 1000 times more sensitive than the conventional assay. Using the nested PCR system, ten spirochaetes could be routinely detected by agarose gel electrophoresis alone, whereas the conventional PCR system could detect only 104 spirochaetes under these conditions. After Southern transfer of amplification products and hybridization with32P- or chemiluminescent-labeled probes, the nested PCR system could easily detect a single spirochaete by both means, whereas the sensitivity of the conventional PCR assay varied from 101 (32P) to 103 (chemiluminescence) spirochaetes. This single-tube nested PCR system should be a useful addition to the current range of diagnostic assays for Lyme borreliosis.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Burgdorfer W, Barbour AG, Hayes SF, Benach JL, Grunwaldt E, Davis JP: Lyme disease — a tick-borne spirochetosis? Science 1982, 216: 1317–1319.

    PubMed  Google Scholar 

  2. Johnson RC, Schmid GR, Hyde FW, Steigerwalt AG, Brenner DJ:Borrelia burgdorferi sp. nov.: etiological agent of Lyme disease. International Journal of Systematic Bacteriology 1984, 34: 496–497.

    Google Scholar 

  3. Baranton G, Postic D, Saint Girons I, Boerlin R, Piffaretti JC, Assous M, Grimont PAD: Delineation ofBorrelia burgdorferi sensu stricto,Borrelia garinii sp. nov., and group VS461 associated with Lyme borreliosis. International Journal of Systematic Bacteriology1992, 42: 378–383.

    PubMed  Google Scholar 

  4. Steere AC: Lyme disease. New England Journal of Medicine 1989, 321: 586–596.

    PubMed  Google Scholar 

  5. Berglund J, Eitrem R, Ornstein K, Lindberg A, Ringner Å, Elmrud H, Carlsson M, Runehagen A, Svanborg C, Norby R: An epidemiologic study of Lyme disease in southem Sweden. New England Journal of Medicine 1995, 333: 1319–1324.

    PubMed  Google Scholar 

  6. Nocton JJ, Dressler F, Rutledge BJ, Rys PN, Persing DH, Steere AC: Detection ofBorrelia burgdorferi DNA by polymerase chain reaction in synovial fluid from patients with Lyme arthritis. New England Journal of Medicine 1994, 330: 229–234.

    PubMed  Google Scholar 

  7. Persing DH, Telford SR, Rys PN, Dodge DE, White TJ, Malawista SE, Spielman A: Detection ofBorrelia burgdorferi DNA in museum specimens ofIxodes dammini ticks. Science 1990, 249: 1420–1423.

    PubMed  Google Scholar 

  8. Wallich R, Moter SE, Simon MM, Ebnet K, Heiberger A, Kramer M: TheBorrelia burgdorferi flagellum-associated 41-kilodalton antigen (flagellin): molecular cloning, expression and amplification of the gene. Infection and Immunity 1990, 58: 1711–1719.

    PubMed  Google Scholar 

  9. Jaulhac B, Nicolini R Piemont Y, Monteil H: Detection ofBorrelia burgdorferi in cerebrospinal fluid of patients with Lyme borreliosis. New England Journal of Medicine 1991, 324: 1440.

    Google Scholar 

  10. Lebech A-M, Hindersson R Vuust J, Hansen K: Comparison of in vitro culture and polymerase chain reaction for detection ofBorrelia burgdorferi in tissue from experimentally infected animals. Journal of Clinical Microbiology 1991, 29: 731–737.

    PubMed  Google Scholar 

  11. Krüger WH, Pulz M: Detection ofBorrelia burgdorferi in cerebrospinal fluid by the polymerase chain reaction. Journal of Medical Microbiology 1991, 195: 98–102.

    Google Scholar 

  12. Luft BJ, Steinman CR, Neimark HC, Muralidhar B, Rush T, Finkel MF, Kunkel M, Dattwyler RJ: Invasion of the central nervous system byBorrelia burgdorferi in acute disseminated infection. Journal of the American Medical Association 1992, 267: 1364–1367.

    PubMed  Google Scholar 

  13. Lebech AM, Hansen K: Detection ofBorrelia burgdorferi DNA in urine samples and cerebrospinal fluid samples from patients with early and late Lyme neuroborreliosis by polymerase chain reaction. Journal of Clinical Microbiology 1992, 30: 1646–1653.

    PubMed  Google Scholar 

  14. Schempp C, Bocklage H, Lange R, Kölmel HW, Orfanos CE, Gollnick H: Further evidence forBorrelia burgdorferi infection in morphea and lichen sclerosis et atrophicus confirmed by DNA amplification. Journal of Investigative Dermatology 1993, 100: 717–720.

    PubMed  Google Scholar 

  15. Huppertz H-I, Schmidt H, Karch H: Detection ofBorrelia burgdorferi by nested polymerase chain reaction in cerebrospinal fluid and urine of children with neuroborreliosis. European Journal of Pediatrics 1993, 152: 414–417.

    PubMed  Google Scholar 

  16. Schmidt BL, Aberer E, Stockenhuber C, Klade H, Breier F, Luger A: Detection ofBorrelia burgdorferi DNA by polymerase chain reaction in the urine and breast milk of patients with Lyme borreliosis. Diagnostic Microbiology and Infectious Disease 1995, 21: 121–128.

    PubMed  Google Scholar 

  17. Lebech AM, Clemmensen O, Hansen K: Comparison of in vitro culture, immunohistochemical staining, and PCR for detection ofBorrelia burgdorferi in tissue from experimentally infected animals. Journal of Clinical Microbiology 1995, 33: 2328–2333.

    PubMed  Google Scholar 

  18. Picken RN: Polymerase chain reaction primers and probes derived from fiagellin gene sequences for specific detection of the agents of Lyme disease and North American relapsing fever. Journal of Clinical Microbiology 1992, 30: 99–114.

    PubMed  Google Scholar 

  19. Barbour AG: Isolation and cultivation of Lyme disease spirochetes. Yale Journal of Biological Medicine 1984, 57: 521–525.

    Google Scholar 

  20. Anderson JF, Magnarelli LA, LeFebvre RB, Andreadis TG, McAninch JB, Perng GC, Johnson RC: Antigenically variableBorrelia burgdorferi isolated from cottontail rabbits andIxodes dentatus in rural and urban areas. Journal of Clinical Microbiology 1989, 27: 13–20.

    PubMed  Google Scholar 

  21. Boom R, Sol CJA, Salimans MMM, Jansen CL, Wertheim-van Dillen PME, van der Noordaa J: Rapid and simple method for purification of nucleic acids. Journal of Clinical Microbiology 1990, 28: 495–503.

    PubMed  Google Scholar 

  22. Gaßman GS, Kramer M, Göbel UB, Wallich R: Nucleotide sequence of a gene encoding theBorrelia burgdorferi fiagellin. Nucleic Acids Research 1989, 17: 3590.

    PubMed  Google Scholar 

  23. Jauris-Heipke S, Fuchs R, Motz M, Preac-Mursic V, Schwab E, Soutschek E, Will G, Wilske B: Genetic heterogeneity of the genes coding for the outer surface protein C (OspC) and the fiagellin ofBorrelia burgdorferi. Medical Microbiology and Immunology 1993, 182: 37–50.

    PubMed  Google Scholar 

  24. Wieslander L: A simple method to recover intact high molecular weight RNA and DNA after electrophoretic separation in low gelling temperature agarose gels. Analytical Biochemistry 1979, 98: 305–309.

    PubMed  Google Scholar 

  25. Strle F, Cheng Y, Nelson JA, Picken MM, Bouseman JK, Picken RN: Infection rate ofIxodes ricinus ticks withBorrelia afzelii, Borrelia garinii, andBorrelia burgdorferi sensu stricto. European Journal of Clinical Microbiology & Infectious Diseases 1995, 14: 994–1001.

    Google Scholar 

  26. Picken RN, Cheng Y, Strle F, Cimperman J, Maraspin V, Lotric-Furlan S, Ruzic-Sabljic E, Han D, Nelson JA, Picken MM, Trenholme GM: Molecular characterization ofBorrelia burgdorferi sensu lato from Slovenia revealing significant differences between tick and human isolates. European Journal of Clinical Microbiology & Infectious Diseases 1996, 15: 313–323.

    Google Scholar 

  27. Southern EM: Detection of specific sequences among DNA fragments separated by gel electrophoresis. Journal of Molecular Biology 1975, 98: 503–517.

    PubMed  Google Scholar 

  28. Guy EC, Stanek G: Detection ofBorrelia burgdorferi in patients with Lyme disease by the polymerase chain reaction. Journal of Clinical Pathology 1991, 44: 610–611.

    PubMed  Google Scholar 

  29. Melchers WJG, Meis JF, Rosa PA, Claas ECJ, Nohlmans L, Koopman R, Horrevorts A, Galama J: Amplification ofBorrelia burgdorferi DNA in skin biopsies from patients with Lyme disease. Journal of Clinical Microbiology 1991, 29: 2401–2406.

    PubMed  Google Scholar 

  30. Keller TL, Halperin JJ, Whitman M: PCR detection ofBorrelia burgdorferi DNA in cerebrospinal fluid of Lyme neuroborreliosis patients. Neurology 1992, 42: 32–42.

    Google Scholar 

  31. Williams WV, Callegari P, Freundlich B, Keenan G, Eldridge D, Shin H, Kreitman M, McCallus D, Weiner DB: Molecular diagnosis ofBorrelia burgdorferi infection (Lyme disease). DNA and Cell Biology 1992, 11: 207–213.

    PubMed  Google Scholar 

  32. Pachner AR, Delaney E: The polymerase chain reaction in the diagnosis of Lyme neuroborreliosis. Annals of Neurology 1993, 34: 544–550.

    PubMed  Google Scholar 

  33. Liebling MR, Nishio MJ, Rodriguez A, Sigal LH, Jin T, Louie JS: The polymerase chain reaction for the detection ofBorrelia burgdorferi in human body fluids. Arthritis and Rheumatism 1993, 36: 665–675.

    PubMed  Google Scholar 

  34. Wienecke R, Neubert U, Volkenandt M: Molecular detection ofBorrelia burgdorferi in formalin-fixed, paraffin-embedded lesions of Lyme disease. Journal of Cutaneous Pathology 1993, 20: 385–388.

    PubMed  Google Scholar 

  35. Wienecke R, Zöchling N, Neubert U, Schlüpen E-M, Meurer M, Volkenandt M: Molecular subtyping ofBorrelia burgdorferi in erythema migrans and acrodermatitis chronica atrophicans. Journal of Investigative Dermatology 1994, 103: 19–22.

    PubMed  Google Scholar 

  36. Moter SE, Hofmann H, Wallich R, Simon MM, Kramer MD: Detection ofBorrelia burgdorferi sensu lato in lesional skin of patients with erythema migrans and acrodermatitis chronica atrophicans by ospA-specific PCR. Journal of Clinical Microbiology 1994, 32: 2980–2988.

    PubMed  Google Scholar 

  37. von Stedingk LV, Olsson I, Hanson HS, Åsbrink E, Hovmark A: Polymerase chain reaction for detection ofBorrelia burgdorferi DNA in skin lesions of early and late Lyme borreliosis. European Journal of Clinical Microbiology & Infectious Diseases 1995, 14: 1–5.

    Google Scholar 

  38. Christen HJ, Eiffert H, Ohlenbusch A, Hanefeld F: Evaluation of the polymerase chain reaction for the detection ofBorrelia burgdorferi in cerebrospinal fluid of children with acute peripheral facial palsy. European Journal of Pediatrics 1995, 154: 374–377.

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Picken, M.M., Picken, R.N., Han, D. et al. Single-tube nested polymerase chain reaction assay based on flagellin gene sequences for detection ofBorrelia burgdorferi sensu lato. Eur. J. Clin. Microbiol. Infect. Dis. 15, 489–498 (1996). https://doi.org/10.1007/BF01691317

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01691317

Keywords

Navigation