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Journal of Clinical Microbiology, June 1999, p. 2087-2089, Vol. 37, No. 6
National Institute of Neurological Diseases
and Stroke, National Institutes of Health, Bethesda, Maryland
20892,1 and Department of Neurology,
Georgetown University School of Medicine, Washington, D.C.
200072
Received 10 November 1998/Returned for modification 14 January
1999/Accepted 18 March 1999
We are investigating the neuropathogenesis of Lyme disease caused
by Borrelia burgdorferi in a nonhuman primate model. In the
past, two separate pieces of tissue had to be used when both analyzing
for the presence of the spirochete and examining the host response to
infection. We have modified a procedure to purify DNA from the same
sample after the extraction of RNA. The remaining material containing
the DNA was precipitated, and residual organic reagent was removed
prior to deproteinization and extraction of the DNA. This procedure now
allows us to both assay for the presence of the Lyme microorganism and
analyze the host response in the same tissue preparation.
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Isolation of DNA after Extraction of RNA To Detect the Presence
of Borrelia burgdorferi and Expression of Host
Cellular Genes from the Same Tissue Sample
*
Corresponding author. Present address: Department of
Neurosciences, Bldg. MSB H506, University of Medicine and Dentistry of New Jersey, 185 S. Orange Ave., Newark, NJ 07103. Phone: (973) 972-7407. Fax: (973) 972-5059. E-mail: pachner{at}UMDNJ.edu.
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