Abstract
Borrelia burgdorferi non-sensu lato (s.l.) strains occurred in the Netherlands. A multiplex OspA, FlaB, IGS real time PCR was compared to 16S rRNA/rDNA RT-qPCR with lower average Cycle threshold (Ct) and LOD on strain dilutions. Multiplexing increased sensitivity on CSF samples (n=74), distinguishing B. burgdorferi s.l. from non-s.l. strains.
Keywords:
Borrelia; Lyme; Real time PCR.
Copyright © 2014 Elsevier B.V. All rights reserved.
MeSH terms
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Adult
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Aged
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Antigens, Surface / genetics*
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Bacterial Outer Membrane Proteins / genetics*
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Bacterial Vaccines / genetics*
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Borrelia / classification
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Borrelia / genetics*
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DNA, Ribosomal Spacer*
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Female
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Flagellin / genetics*
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Humans
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Lipoproteins / genetics*
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Lyme Disease / diagnosis*
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Lyme Disease / microbiology*
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Male
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Middle Aged
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Multiplex Polymerase Chain Reaction / methods
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RNA, Ribosomal*
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Real-Time Polymerase Chain Reaction / methods*
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Reproducibility of Results
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Sensitivity and Specificity
Substances
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Antigens, Surface
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Bacterial Outer Membrane Proteins
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Bacterial Vaccines
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DNA, Ribosomal Spacer
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Lipoproteins
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OspA protein
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RNA, Ribosomal
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Flagellin
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flaB flagellin