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. 2001 Jan;39(1):107-10.
doi: 10.1128/JCM.39.1.107-110.2001.

Frequency of rpoB mutations inside and outside the cluster I region in rifampin-resistant clinical Mycobacterium tuberculosis isolates

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Frequency of rpoB mutations inside and outside the cluster I region in rifampin-resistant clinical Mycobacterium tuberculosis isolates

M Heep et al. J Clin Microbiol. 2001 Jan.

Abstract

The prevalence of recently described mutation V176F, located in the beginning of the rpoB gene and associated with rifampin resistance and the wild-type cluster I sequence, was determined by analyzing the distribution of rpoB mutations among 80 rifampin (RIF)-resistant Mycobacterium tuberculosis strains isolated in Germany during 1997. The most frequent rpoB mutations were changes in codon 456 (52 isolates, 65%), followed by changes in codon 441 (13 isolates, 16%) and codon 451 (11 isolates, 14%). The V176F mutation was detected in one isolate of the study population and in 5 of 18 RIF-resistant strains with no cluster I mutation from six previously published studies. In three isolates, a mixture of resistant and susceptible subpopulations (heteroresistance) prohibited the detection of rpoB mutations in the initial analysis; however, in these isolates, cluster I mutations could be verified after a passage on RIF-containing medium. IS6110 DNA fingerprinting of 76 strains revealed eight clusters comprising 27 strains with identical restriction fragment length polymorphism patterns that mainly also show identical rpoB mutations and identical or similar drug resistance patterns. In conclusion, our results indicate that the V176F mutation should be included in molecular tests for prediction of RIF resistance in M. tuberculosis. We further demonstrated that heteroresistance caused by a mixture of mycobacterial subpopulations with different susceptibilities to RIF may influence the sensitivity of molecular tests for detection of resistance.

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Figures

FIG. 1
FIG. 1
Frequencies of rpoB, single and double mutations associated with RIF resistance in a collection of 80 clinical M. tuberculosis isolates from Germany. ∗, Patterns and numbers of double mutations: L436P plus D441G, one; and L436P plus H451Q, one; S437R plus D441V, one; Q438K plus H451D, one; D441Y plus L496V, two; D441V plus L458P, one; S447Q plus S456A, one; S456L plus I486T, one; S456L plus R558C, one; S456W plus E598D, seven.

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