2017
DOI: 10.1093/cid/cix1107
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Surveillance for and Discovery of Borrelia Species in US Patients Suspected of Tickborne Illness

Abstract: These results demonstrate that broad PCR screening followed by MLST is a powerful surveillance tool for uncovering the spectrum of disease-causing Borrelia species, understanding their geographic distribution, and investigating the correlation between B. burgdorferi STs and joint involvement. Detection of Candidatus B. johnsonii in a patient with suspected tickborne disease suggests this species may be a previously undetected cause of illness in humans exposed to bat ticks.

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Cited by 63 publications
(45 citation statements)
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“…This fact is corroborated by largescale studies on post-tick bite febrile illnesses. Indeed, a very small proportion of the tested blood samples were found to be PCR-positive for B. miyamotoi in these previous studies with rates of 0.16% (1/626), 0.84% (97/11,515), 0.33% (7/2150), 0.11% (8/7292) and 0.49% (2/408) [3,4,10,29,30]. In contrast, in Russia, 15.2% (46/302) of the post tick-bite febrile patients [2] were found PCR-positive for B. miyamotoi.…”
Section: Whole Blood Pcrmentioning
confidence: 85%
“…This fact is corroborated by largescale studies on post-tick bite febrile illnesses. Indeed, a very small proportion of the tested blood samples were found to be PCR-positive for B. miyamotoi in these previous studies with rates of 0.16% (1/626), 0.84% (97/11,515), 0.33% (7/2150), 0.11% (8/7292) and 0.49% (2/408) [3,4,10,29,30]. In contrast, in Russia, 15.2% (46/302) of the post tick-bite febrile patients [2] were found PCR-positive for B. miyamotoi.…”
Section: Whole Blood Pcrmentioning
confidence: 85%
“…For Anaplasma and Ehrlichia, a real-time PCR assay that uses hybridization probes and targets the groEL gene, followed by melting temperature analysis of PCR products, was utilized (31). For Borrelia, one to eight housekeeping genes, uvrA, rplB, recG, pyrG, pepX, clpX, nifS, and clpA, were amplified, sequenced, and analyzed (15). For Francisella, a real-time Taqman PCR assay were employed for species identification (32,33).…”
Section: Validation Of Taxonomic Predictionsmentioning
confidence: 99%
“…It is unknown how many of the >13,000 samples represented true tickborne infections, so further work will be necessary to clarify how well this assay performs in that regard. This author group had previously published the results from using a Borrelia genus-targeting broad PCR in 7,292 (presumably overlapping) specimens with similar findings of different Borrelia species and Candidatus B. johnsonii being detected (9). It is reassuring that targeted metagenomics sequencing of the >13,000 samples that they had found as many or more of each species, but still unknown if any of the Borrelia-specific PCR positive samples were not able to be detected by targeted metagenomics.…”
mentioning
confidence: 72%