Am. J. Respir. Crit. Care Med., Vol 155, No. 3, 03 1997, 1140-1146.
DNA fingerprinting with two probes decreases clustering of Mycobacterium tuberculosis
WJ Burman, RR Reves, AP Hawkes, CA Rietmeijer, Z Yang, H el-Hajj, JH Bates and MD Cave
Department of Public Health, Denver Health and Hospitals, Colorado, USA.
DNA fingerprinting of Mycobacterium tuberculosis is used to study the
epidemiology of tuberculosis, but the specificity of the widely used IS6110
technique has not been validated. Isolates from Denver, Colorado from
December 1988 through June 1994 were fingerprinted with the IS6110
technique. Available records were reviewed for patients whose isolates were
within IS6110-defined clusters, and these isolates were fingerprinted with
an independent technique (pTBN12). Of 189 isolates, 86 (46%) were in
IS6110-defined clusters. Clustering was inversely related to the number of
copies of IS6110, ranging from 12 of 12 (100%) to 37 of 48 (77%) and 37 of
129 (29%) for isolates having one, two to five, and more than five copies
(p < 0.001). Of the 86 isolates clustered with the IS6110 technique, 35
(41%) had unique pTBN12 fingerprints. Discordant results with the two
fingerprinting techniques were more common among isolates having five or
fewer copies of IS6110. Epidemiologic links were identified among four of
35 (11%) patients whose isolates had discordant fingerprinting results, as
compared with 40 of 51 (78%) of those whose isolates matched by both IS6110
and pTBN12. DNA fingerprinting with the IS6110 technique was not a specific
marker of DNA clonality, particularly among isolates having fewer than five
copies of IS6110. The use of a supplemental DNA fingerprinting technique
decreased clustering and improved the correlation between the transmission
links predicted by molecular techniques and epidemiologic investigation.
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Copyright © 1997 American Thoracic Society
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