Detection of the Lyme disease bacterium, Borrelia burgdorferi, by using the polymerase chain reaction and a nonradioisotopic gene probe.
AUTOR(ES)
Wise, D J
RESUMO
A 419-bp region of the flagellin gene sequence of Borrelia burgdorferi was used as a target for the polymerase chain reaction. With a nonradioactively labeled gene-specific probe, sensitivity to as few as 1 to 10 spirochetes was observed. The targeted gene fragment was conserved in the American and European strains of B. burgdorferi tested and among several other pathogenic borreliae.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=270147Documentos Relacionados
- Detection of Borrelia burgdorferi in patients with Lyme disease by the polymerase chain reaction.
- Detection of Borrelia burgdorferi using the polymerase chain reaction.
- Megabase-sized linear DNA in the bacterium Borrelia burgdorferi, the Lyme disease agent.
- Plasmid analysis of Borrelia burgdorferi, the Lyme disease agent.
- DNA microarray analysis of differential gene expression in Borrelia burgdorferi, the Lyme disease spirochete