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J. Bacteriol., 01 1996, 78-84, Vol 178, No. 1
D van Soolingen, PE de Haas, RM Blumenthal, K Kremer, M Sluijter, JE Pijnenburg, LM Schouls, JE Thole, MW Dessens-Kroon, JD van Embden and PW Hermans
Restriction endonuclease PvuII plays a central role in restriction fragment
length polymorphism analysis of Mycobacterium tuberculosis complex isolates
with IS6110 as a genetic marker. We have investigated the basis for an
apparent dichotomy in PvuII restriction fragment pattersn observed among
strains of the M. tuberculosis complex. The chromosomal regions of two
modified PvuII restriction sites, located upstream of the katG gene and
downstream of an IS1081 insertion sequence, were studied in more detail. An
identical 10-bp DNA sequence (CAGCTGGAGC) containing a PvuII site was found
in both regions, and site-directed mutagenesis analysis revealed that this
sequence was a target for modification. Strain-specific modification of
PvuII sites was identified in DNA from over 80% of the nearly 800 isolates
examined. Furthermore, the proportion of modifying and nonmodifying strains
differs significantly from country to country.
Copyright © 1996, American Society for Microbiology
Host-mediated modification of PvuII restriction in Mycobacterium tuberculosis
Laboratory for Bacteriology and Antimicrobial Agents, National Institute of Public Health and Environmental Protection, Bilthoven, The Netherlands.
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