2017
DOI: 10.1128/jcm.00510-17
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T2 Magnetic Resonance Assay-Based Direct Detection of Three Lyme Disease-Related Borrelia Species in Whole-Blood Samples

Abstract: In early Lyme disease (LD), serologic testing is insensitive and seroreactivity may reflect active or past infection. In this study, we evaluated a novel assay for the direct detection of three species of Borrelia spirochetes in whole blood. The T2 magnetic resonance (T2MR) assay platform was used to amplify Borrelia DNA released from intact spirochetes and to detect amplicon. Analytical sensitivity was determined from blood spiked with known concentrations of spirochetes, and the assay's limit of detection wa… Show more

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Cited by 11 publications
(5 citation statements)
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“…Recently, T2 magnetic resonance assay was evaluated to detect Candida spp. and some bacteria in whole blood (Mylonakis et al, 2015 ; Snyder et al, 2017 ; Peker et al, 2018 ). In the present study, we evaluated the Magicplex TM Sepsis test (MP), comparing it with conventional BC.…”
Section: Discussionmentioning
confidence: 99%
“…Recently, T2 magnetic resonance assay was evaluated to detect Candida spp. and some bacteria in whole blood (Mylonakis et al, 2015 ; Snyder et al, 2017 ; Peker et al, 2018 ). In the present study, we evaluated the Magicplex TM Sepsis test (MP), comparing it with conventional BC.…”
Section: Discussionmentioning
confidence: 99%
“…While standard PCR methods have limited sensitivity for LD, due to low numbers of B. burgdorferi in tissue and body fluids, various strategies can improve sensitivity without compromising specificity 32,33,37,38 . These include starting with larger specimen volumes, using target enrichment methods, and employing unconventional signal detection methods, including targeting multicopy Borrelia phage genes [39][40][41] .…”
Section: Advancements In Lyme Disease Diagnostics: Overcoming Limitat...mentioning
confidence: 99%
“…While standard PCR methods have limited sensitivity for LD, due to low numbers of B. burgdorferi in tissue and body fluids, various strategies can improve sensitivity without compromising specificity [33,34,38,39]. These include starting with larger specimen volumes, using target enrichment methods, and employing unconventional signal detection methods, including targeting multicopy Borrelia phage genes [40][41][42]. This direct detection is particularly essential for recognizing various Borrelia strains that might not be captured through standard serology testing.…”
Section: Advancements In Lyme Disease Diagnostics: Overcoming Limitat...mentioning
confidence: 99%