Related Experiment Video
Updated: Jul 5, 2026

Methods for Rapid Transfer and Localization of Lyme Disease Pathogens Within the Tick Gut
Published on: February 14, 2011
Direct Capture and Early Detection of Lyme Disease Spirochete in Skin with a Microneedle Patch
Emily Kight1, Rosana Alfaro1, Shiva Kumar Goud Gadila2
1Biomedical Engineering, Vanderbilt University, Nashville, TN 37211, USA.
Abstract:
Borrelia burgdorferi sensu lato family of spirochetes causes Lyme disease (LD) in animals and humans. As geographic territory of ticks expands across the globe, surveillance measures are needed to measure transmission rates and provide early risk testing of suspected bites. The current standard testing of LD uses an indirect two-step serological assay that detects host immune reactivity. Early detection remains a challenge because the host antibody response develops several weeks after infection. A microneedle (MN) device was developed to sample interstitial fluid (ISF) and capture spirochetes directly from skin. After sampling, the MN patch is easily dissolved in water or TE buffer, and the presence of spirochete DNA is detected by PCR. Performance was tested by spiking porcine ear skin with inactivated Borrelia burgdorferi, which had an approximate recovery of 80% of spirochetes. With further development, this simple direct PCR method could be a transformative approach for early detection of the causative agent of Lyme disease and enable rapid treatment to patients when infection is early, and numbers of systemic spirochetes are low.
Insights
A novel microneedle device offers direct detection of Borrelia burgdorferi DNA from skin, potentially enabling earlier Lyme disease diagnosis. This method bypasses the slow antibody response, improving early risk assessment for suspected tick bites.
Area of Science:
- Microbiology
- Infectious Diseases
- Biotechnology
Background:
- Lyme disease (LD) is caused by Borrelia burgdorferi, with expanding tick ranges necessitating improved surveillance.
- Current LD diagnosis relies on indirect serological assays, which are limited by a delayed antibody response, hindering early detection.
Purpose of the Study:
- To develop and evaluate a microneedle (MN) device for direct detection of Borrelia burgdorferi DNA from skin interstitial fluid (ISF).
- To provide a rapid, direct diagnostic method for early Lyme disease detection, overcoming limitations of current serological tests.
Main Methods:
- A microneedle device was designed to collect ISF and capture spirochetes directly from the skin.
- Inactivated Borrelia burgdorferi were used to spike porcine ear skin to assess device performance.
- Spirochete DNA was detected using polymerase chain reaction (PCR) after dissolving the MN patch.
Main Results:
- The microneedle device demonstrated an approximate 80% recovery rate of spiked Borrelia burgdorferi from porcine skin.
- The method allows for direct detection of spirochete DNA, bypassing the need for host immune response.
Conclusions:
- This direct PCR approach using microneedles shows promise for early Lyme disease detection.
- Further development could lead to a transformative tool for rapid diagnosis and timely treatment of Lyme disease.
More Related Videos
Related Concept Videos
Rapid Identification of Pathogens
Rocky Mountain Spotted Fever

