Abstract

The efficacy and accepted regimen of antibiotic treatment for Lyme disease has been a point of significant contention among physicians and patients. While experimental studies in animals have offered evidence of post-treatment persistence of Borrelia burgdorferi, variations in methodology, detection methods and limitations of the models have led to some uncertainty with respect to translation of these results to human infection. With all stages of clinical Lyme disease having previously been described in nonhuman primates, this animal model was selected in order to most closely mimic human infection and response to treatment. Rhesus macaques were inoculated with B. burgdorferi by tick bite and a portion were treated with recommended doses of doxycycline for 28 days at four months post-inoculation. Signs of infection, clinical pathology, and antibody responses to a set of five antigens were monitored throughout the ~1.2 year study. Persistence of B. burgdorferi was evaluated using xenodiagnosis, bioassays in mice, multiple methods of molecular detection, immunostaining with polyclonal and monoclonal antibodies and an in vivo culture system. Our results demonstrate host-dependent signs of infection and variation in antibody responses. In addition, we observed evidence of persistent, intact, metabolically-active B. burgdorferi after antibiotic treatment of disseminated infection and showed that persistence may not be reflected by maintenance of specific antibody production by the host.

Highlights

  • A growing public health problem, Lyme disease (LD) is the most commonly reported vectorborne disease in the U.S and Europe [1], inflicting a significant public health burden [2,3,4]

  • Erythematous rashes distal from the tick feeding areas were observed in three monkeys at various time points postinfection

  • What dictates the development of the characteristic rash in humans is not well understood, but could be affected by the genotypic variants of B. burgdorferi present in the tick, prior exposure, and possible co-infections

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Summary

Introduction

A growing public health problem, Lyme disease (LD) is the most commonly reported vectorborne disease in the U.S and Europe [1], inflicting a significant public health burden [2,3,4]. The number of annual cases of LD in the U.S has climbed to over 300,000 [5] and is expected to rise [6, 7]. Diverse responses and post-treatment persistence in the monkey model of Lyme disease study design, data collection and analysis, decision to publish, or preparation of the manuscript

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