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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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| Publicat a: | J Clin Microbiol |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Microbiology (ASM)
1990
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| Matèries: | |
| Accés en línia: | 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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