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Journal of Clinical Microbiology, April 1998, p. 1122-1124, Vol. 36, No. 4
Unité de la Tuberculose et des
Mycobactéries, Institut Pasteur, Morne Jolivière, 97165 Pointe-à-Pitre, Guadeloupe, French West Indies
Received 31 October 1997/Returned for modification 22 December
1997/Accepted 14 January 1998
A total of 129 clinical isolates of Mycobacterium
tuberculosis representing 91 patients were typed by a
combination of direct-repeat (DR)-based spoligotyping and
an inter-IS6110-PGRS (polymorphic GC-rich region)-PCR,
also designated double-repetitive-element PCR (DRE-PCR). During the
first phase of this investigation, 72 clinical strains representing 52 patients were initially typed by IS6110-restriction
fragment length polymorphism (RFLP) and DR-RFLP, followed by
spoligotyping and DRE-PCR. In the second phase of this investigation,
the discriminating ability of spoligotyping plus DRE-PCR was studied
for 57 isolates from 39 patients who were suspected to be
epidemiologically linked, and the typing results were later confirmed
by IS6110-RFLP and DR-RFLP analyses. The molecular
clustering of the isolates remained identical irrespective of the
methods used. These results show that the association of two PCR-based
fingerprinting techniques for molecular epidemiology of tuberculosis
has a discriminating ability similar to the
IS6110-RFLP reference method.
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Spoligotyping Followed by Double-Repetitive-Element PCR as
Rapid Alternative to IS6110 Fingerprinting for
Epidemiological Studies of Tuberculosis
*
Corresponding author. Mailing address: Institut
Pasteur, Morne Jolivière, B.P. 484, F-97165 Pointe-à-Pitre
Cedex, Guadeloupe, French West Indies. Phone: 590-893-881. Fax:
590-893-880. E-mail: rastogi{at}ipagua.gp.
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