2011
DOI: 10.1016/j.meegid.2010.09.011
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IS6110-based global phylogeny of Mycobacterium tuberculosis

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Cited by 21 publications
(22 citation statements)
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“…Forty three samples (24.4%) grouped under "unassigned" group. Common fragments seen were exactly the same as the earlier published report by Thorne et al, (2011) except for an additional fragment, 78.4 G, for the CAS lineage. A dendrogram was generated using only the IS6110 FAFLP data ( Figure 2) confirming again the above mentioned lineages in relation to the PGGs.…”
Section: Analysis Of Data Using Bionumerics Software V61supporting
confidence: 78%
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“…Forty three samples (24.4%) grouped under "unassigned" group. Common fragments seen were exactly the same as the earlier published report by Thorne et al, (2011) except for an additional fragment, 78.4 G, for the CAS lineage. A dendrogram was generated using only the IS6110 FAFLP data ( Figure 2) confirming again the above mentioned lineages in relation to the PGGs.…”
Section: Analysis Of Data Using Bionumerics Software V61supporting
confidence: 78%
“…It has been demonstrated previously that IS6110 FAFLP PCR can be used to delineate the phylogeny of MTBC as shared common fragments can determine the different lineages in a geographical location by comparison with a reference database collection [7]. As limited lineage information is available from strains in Nepal, we have applied the IS6110 method published recently on mapping the IS6110 sites in H37Rv [9] and also carried out rpoB sequencing to further characterize strains from this important region.…”
Section: Discussionmentioning
confidence: 99%
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“…In parallel, the discovery of the Direct Repeat (DR) locus polymorphism, based on the presence/absence of short spacer sequences connecting the DR sequences, and the development of the spacer oligonucleotide typing (spoligotyping) methodology [12], introduced a further tool for genetic analysis of the M. tuberculosis complex that soon became the most practiced typing system used in studies of genetic diversity [13]. In general, the polymorphisms probed by RD deletion analysis and spoligotyping turn out to be largely congruent, as they reflect the clonal population structure of the M. tuberculosis complex [5], [14][16], so that the spoligotype families are generally regarded as sublineages within the LSP-defined main lineages [17]; in certain cases, however, spoligotype homoplasy, i.e. identical molecular pattern of the DR locus in strains belonging to different evolutionary lineages, likely resulting from convergent evolution, has been reported [17][23].…”
Section: Introductionmentioning
confidence: 99%
“…The insertion sequence “IS6110" is a transposable element which is present in the members of MTB complex in multiple copies (up to 25 copies), except M. bovis BCG which harbours a single copy and absent in other mycobacteria 13,14. For those reasons the insertion sequence “IS6110” has been reported as the most common target used for the MTB diagnosis in the clinical samples and demonstrated that the detection rate of MTB complex targeting “IS6110” was higher than that of microscopy or MTB culturing with a considerable time 7,12,15,16.…”
Section: Introductionmentioning
confidence: 99%