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Detection of Borrelia burgdorferi infection in Ixodes dammini ticks with the polymerase chain reaction.

The polymerase chain reaction (PCR) was used to amplify DNA sequences of the etiologic agent of Lyme disease, Borrelia burgdorferi, and was applied to the detection of the spirochete in its tick vector. The target for PCR amplification was the OSP-A gene of strain B31; analysis of isolates from diff...

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Publicado en:J Clin Microbiol
Autores principales: Persing, D H, Telford, S R, Spielman, A, Barthold, S W
Formato: Artigo
Lenguaje:Inglês
Publicado: American Society for Microbiology (ASM) 1990
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Acceso en línea:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC269663/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1969867/
https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jcm.28.3.566-572.1990
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