Nested PCR Assay for Detection of Granulocytic Ehrlichiae

Robert F. Massung(Centers for Disease Control and Prevention), Kim Slater(Centers for Disease Control and Prevention), Jessica H. Owens(Centers for Disease Control and Prevention), William L. Nicholson(Centers for Disease Control and Prevention), Thomas N. Mather(University of Rhode Island), Victoria B. Solberg(Walter Reed Army Institute of Research), James G. Olson(Centers for Disease Control and Prevention)
Journal of Clinical Microbiology
April 1, 1998
Cited by 468Open Access
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Abstract

A sensitive and specific nested PCR assay was developed for the detection of granulocytic ehrlichiae. The assay amplifies the 16S rRNA gene and was used to examine acute-phase EDTA-blood and serum samples obtained from seven humans with clinical presentations compatible with human granulocytic ehrlichiosis. Five of the seven suspected cases were positive by the PCR assay using DNA extracted from whole blood as the template, compared with a serologic assay that identified only one positive sample. The PCR assay using DNA extracted from the corresponding serum samples as the template identified three positive samples. The sensitivity of the assay on human samples was examined, and the limit of detection was shown to be fewer than 2 copies of the 16S rRNA gene. The application of the assay to nonhuman samples demonstrated products amplified from template DNA extracted from Ixodes scapularis ticks collected in Rhode Island and from EDTA-blood specimens obtained from white-tailed deer in Maryland. All PCR products were sequenced and identified as specific to granulocytic ehrlichiae. A putative variant granulocytic ehrlichia 16S rRNA gene sequence was detected among products amplified from both the ticks and the deer blood specimens.


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