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Journal of Clinical Microbiology, June 2000, p. 2248-2253, Vol. 38, No. 6
Department of Medical Microbiology,
University of Zürich, 8028 Zürich, Switzerland
Received 28 December 1999/Returned for modification 23 February
2000/Accepted 24 March 2000
Using broad-spectrum primers, we have amplified, cloned, and
sequenced a 620-bp fragment of the "Tropheryma
whippelii" heat shock protein 65 gene (hsp65) from
the heart valve of a patient with Whipple's endocarditis. The deduced
amino acid sequence shows high similarity to those from actinobacteria,
confirming that "T. whippelii" is indeed a member of
this phylum. Based on the nucleotide sequence, we have developed a
"T. whippelii"-specific seminested PCR. Seventeen
patients shown to be positive by 16S ribosomal DNA (rDNA) PCR and/or
internal transcribed spacer (ITS) PCR were also positive by
hsp65 PCR. All 33 control specimens from patients without
Whipple's disease and negative for "T. whippelii" by
both seminested 16S rDNA and ITS PCR remained negative. All amplicons
digested with XhoI revealed an identical restriction pattern. Eight of the 17 hsp65 amplicons representing all
three previously described ITS types were sequenced. Three of the
amplicons showed slight differences, but none of the mutations detected affected the amino acid sequence of the corresponding protein. We
conclude that the hsp65 gene is a suitable target for the
specific detection of "T. whippelii." Its product
represents a putative antigen for a future serodiagnostic assay.
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Cloning and Sequencing of a Part of the Heat Shock
Protein 65 Gene (hsp65) of "Tropheryma
whippelii" and Its Use for Detection of "T.
whippelii" in Clinical Specimens by PCR
*
Corresponding author. Mailing address: Department of
Medical Microbiology, University of Zürich, Gloriastrasse 30, CH-8028 Zürich, Switzerland. Phone: 41 (1) 634 27 00. Fax: 41 (1)
634 49 06. E-mail: altwegg{at}immv.unizh.ch.
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