Lyme borreliosis, ticks and Borrelia species
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This issue of the Wiener klinische Wochenschrift contains review papers on clinical and diagnostic aspects of Lyme borreliosis, on hard ticks as vectors of human pathogens and on recent discussion on the taxonomy of borreliae. We will learn about approaches for the management of infectious diseases transmitted by hard ticks established during the past 30 years at the Lyme Disease Diagnostic Center, New York Medical College, Valhalla, NY, USA . We also include an article on Viennese long-term experience with Borrelia burgdorferi sensu lato infections that has enabled the diagnosis and successful treatment of rare manifestations of Lyme neuroborreliosis presenting as dementia-like syndromes . An article on ticks as vectors explains what makes ixodid ticks such efficient transmitters of pathogens . In addition, a paper on the proposal for a new genus name for the Borrelia burgdorferi sensu lato complex, which has triggered fierce debate, illuminates the background from the viewpoint of a molecular microbiologist .
The terms Lyme borreliosis or Lyme disease have also become terms for medically unexplained symptoms such as fatigue, joint pain, muscle pain and difficulties with memory and concentration . It is useful, therefore, to outline here what Lyme borreliosis includes.
The infection cycle is linked to the blood meals of the respective development stages of the ticks: larvae, nymphs and adults. About 30% of nymphal ticks in central Europe are infected with Lyme borreliae. The risk of infection for humans is highest from May to September. Lyme borreliae were discovered in 1982 and identified in 1984 as a new Borrelia species, named Borrelia burgdorferi in honour of its discoverer Willy Burgdorfer. More than 20 genospecies are now included under the umbrella term B. burgdorferi sensu lato. In Europe, the species pathogenic for humans are B. afzelii, B. garinii, B. bavariensis, B. burgdorferi sensu stricto, and occasionally B. spielmanii and B. lusitaniae; in North America, B. burgdorferi sensu stricto and in certain areas B. mayonii. The transmission of Lyme borreliae occurs on average 24 h (6–48 h) after a blood meal. There is no transmission from person to person and there is no evidence of diaplacental transmission.
Clinical manifestations include the following:
Painless, bluish red nodule or spot, usually on the earlobe, ear helix, nipple or scrotum; more common in children (especially at the ear) than in adults.
Acrodermatitis chronica atrophicans
Neurologic manifestations are summarized under the term Lyme neuroborreliosis. In adults mainly meningopolyradiculitis (Bannwarth’s syndrome), meningitis, rare encephalitis, myelitis, and very rarely cerebral vasculitis. Children present mainly with facial palsy and/or mild meningitis.
Recurrent attacks or persistent, objective joint swelling in one or a few large joints. Exclusion of other causes necessary.
Rare: acute atrioventricular (I–III) conduction disorder, arrhythmia; also possible myocarditis, pancarditis. Exclusion of other causes necessary.
Very rare: conjunctivitis, uveitis, papillitis, episcleritis, keratitis.
Suitable specimens are full blood, EDTA blood and citrate blood; cerebrospinal fluid, synovia, synovialis, and biopsies, primarily skin biopsy.
Direct detection of the pathogens
Direct detection of borreliae by cultivation and/or nucleic amplification techniques (PCR). In controlled clinical trials, these techniques for detection of borreliae in body fluids, tissue samples, biopsies, and ticks should be limited to specialized laboratories.
Indirect detection of borrelial infection
Detection of specific antibodies should be requested only when there is sound clinical suspicion and according to diagnostic/management guidelines . Results of untargeted searches have very poor predictive diagnostic value. Principle of serology: a two-tier procedure. The first tier using immunofluorescence assay, enzyme-linked immunosorbent assay, chemiluminescence, etc. detects antibodies of classes IgG and IgM against B. burgdorferi sensu lato; the second tier uses immunoblotting, line-blotting or other technique with a relevant number of immunodominant Borrelia antigens to verify specificity. Seropositivity requires that both the first and the second tier are positive. Serological methods have become established as a diagnostic aid in suspected Lyme borreliosis and numerous products from different manufacturers are on the market. The principle of the two-tier procedure still pertains. The band pattern of an immunoblot together with the relative concentration of antibodies in the first tier screening test allows greater certainty in the diagnosis in clinical manifestations with a broad spectrum of differential diagnoses, such as arthritis. Nonetheless, a positive blot pattern does not indicate a definite clinical manifestation of Lyme borreliosis or an active event. Without clinical signs and symptoms there is no disease.
A persisting delusion is that the mere serological result “Borrelia IgM positive” requires antibiotic treatment. It should be remembered that the prevalence of serum antibodies to B. burgdorferi sensu lato in healthy adults is, e. g. in Austria, approximately 23% (20–30%) for IgG and about 18% (14–23%) for IgM.
In the following serological constellations, and in the absence of signs and symptoms of Lyme borreliosis, antibiotic treatment should be carefully considered: a) IgM and/or IgG positive without signs of disease → no treatment. Laboratories should refrain from interpreting as “active Lyme borreliosis, antibiotic treatment required”; b) IgM and IgG negative in a patient with erythema migrans → treatment is necessary (comment: erythema migrans is a clinical diagnosis, no reason for serology); c) IgM negative, IgG positive without signs of disease: in most cases this indicates an earlier Borrelia spp. infection (borrelial IgG antibodies can persist for long periods of time) and antibiotic treatment is certainly not indicated.
Treatment with antibiotics is usually for 2–4 weeks and most patients recover uneventfully. Detailed information on the manifestations, diagnosis and treatment of Lyme borreliosis may be obtained from the references listed below [7, 8].
The publications in this issue of the Wiener klinische Wochenschrift should be considered a stimulus to obtain further information on Lyme borreliosis, by review and original work, and on other tick-borne diseases.
Conflict of interest
G. Stanek is an unpaid member of the steering committee of ESGBOR, the European Society of Clinical Microbiology and Infectious Diseases (ESCMID) Study Group on Lyme Borreliosis.
- 6.Stanek G, Fingerle V, Hunfeld KP, Jaulhac B, Kaiser R, Krause A, Kristoferitsch W, O’Connell S, Ornstein K, Strle F, Gray J. Lyme borreliosis: clinical case definitions for diagnosis and management in Europe. Clin Microbiol Infect. 2011;17:69–79. https://doi.org/10.1111/j.1469-0691.2010.03175.x.CrossRefPubMedGoogle Scholar