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Article

DNA Sequencing Diagnosis of Off-Season Spirochetemia with Low Bacterial Density in Borrelia burgdorferi and Borrelia miyamotoi Infections

1
Department of Pathology, Milford Hospital, 300 Seaside Ave., Milford, CT 06460, USA
2
Origins of Health, LLC, 279 New Britain Road Berlin, CT 06037, USA
3
My Path Medical, 20 Park Plaza, 804, Boston, MA 02116, USA
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2014, 15(7), 11364-11386; https://doi.org/10.3390/ijms150711364
Received: 12 May 2014 / Revised: 17 June 2014 / Accepted: 19 June 2014 / Published: 25 June 2014
(This article belongs to the Section Molecular Pathology, Diagnostics, and Therapeutics)
A highly conserved 357-bp segment of the 16S ribosomal RNA gene (16S rDNA) of Borrelia burgdorferi sensu lato and the correspondent 358-bp segment of the Borrelia miyamotoi gene were amplified by a single pair of nested polymerase chain reaction (PCR) primers for detection, and the amplicons were used as the templates for direct Sanger DNA sequencing. Reliable molecular diagnosis of these borreliae was confirmed by sequence alignment analysis of the hypervariable regions of the PCR amplicon, using the Basic Local Alignment Search Tool (BLAST) provided by the GenBank. This methodology can detect and confirm B. burgdorferi and B. miyamotoi in blood samples of patients with off-season spirochetemia of low bacterial density. We found four B. miyamotoi infections among 14 patients with spirochetemia, including one patient co-infected by both B. miyamotoi and B. burgdorferi in a winter month when human exposure to tick bites is very limited in the Northeast of the U.S.A. We conclude that sensitive and reliable tests for these two Borrelia species should be implemented in the microbiology laboratory of hospitals located in the disease-endemic areas, for timely diagnosis and appropriate treatment of the patients at an early stage of the infection to prevent potential tissue damages. View Full-Text
Keywords: DNA sequencing; same-nested PCR; Borrelia burgdorferi; Borrelia miyamotoi; 16S rDNA; off-season spirochetemia; Lyme disease DNA sequencing; same-nested PCR; Borrelia burgdorferi; Borrelia miyamotoi; 16S rDNA; off-season spirochetemia; Lyme disease
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MDPI and ACS Style

Lee, S.H.; Vigliotti, J.S.; Vigliotti, V.S.; Jones, W.; Moorcroft, T.A.; Lantsman, K. DNA Sequencing Diagnosis of Off-Season Spirochetemia with Low Bacterial Density in Borrelia burgdorferi and Borrelia miyamotoi Infections. Int. J. Mol. Sci. 2014, 15, 11364-11386. https://doi.org/10.3390/ijms150711364

AMA Style

Lee SH, Vigliotti JS, Vigliotti VS, Jones W, Moorcroft TA, Lantsman K. DNA Sequencing Diagnosis of Off-Season Spirochetemia with Low Bacterial Density in Borrelia burgdorferi and Borrelia miyamotoi Infections. International Journal of Molecular Sciences. 2014; 15(7):11364-11386. https://doi.org/10.3390/ijms150711364

Chicago/Turabian Style

Lee, Sin H., Jessica S. Vigliotti, Veronica S. Vigliotti, William Jones, Thomas A. Moorcroft, and Katherine Lantsman. 2014. "DNA Sequencing Diagnosis of Off-Season Spirochetemia with Low Bacterial Density in Borrelia burgdorferi and Borrelia miyamotoi Infections" International Journal of Molecular Sciences 15, no. 7: 11364-11386. https://doi.org/10.3390/ijms150711364

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