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2009
DOI: 10.3201/eid1510.090463
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Discriminatory Ability of Hypervariable Variable Number Tandem Repeat Loci in Population-based Analysis ofMycobacterium tuberculosisStrains, London, UK

Abstract: Hypervariable loci should be included in standardized panels because they can provide consistent comparable results in multiple settings.

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Cited by 24 publications
(24 citation statements)
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“…Loci QUB3232 and QUB11a have been previously found to have a higher mutation rate regarding allelic diversity in M. tuberculosis and were therefore considered hypervariable (27); nevertheless, their use remains controversial as they may contribute to improved discrimination in determined settings (15). Conflicting findings may be due to variations between different lineages (31) or between species; e.g., allelic diversities may differ in M. bovis (18,19). For the additional 16 isolates of different spoligotypes, QUB3232 was also the most discriminatory locus, followed by ETR-A and QUB11a.…”
mentioning
confidence: 41%
“…Loci QUB3232 and QUB11a have been previously found to have a higher mutation rate regarding allelic diversity in M. tuberculosis and were therefore considered hypervariable (27); nevertheless, their use remains controversial as they may contribute to improved discrimination in determined settings (15). Conflicting findings may be due to variations between different lineages (31) or between species; e.g., allelic diversities may differ in M. bovis (18,19). For the additional 16 isolates of different spoligotypes, QUB3232 was also the most discriminatory locus, followed by ETR-A and QUB11a.…”
mentioning
confidence: 41%
“…1 and 2. Equally, the number of clusters may be reduced by increasing the number of MIRU-VNTR markers used for analysis or by using further analytical techniques, as has been demonstrated for discriminative analysis of M. tuberculosis (27,28). Pulmonary disease was more common among clustered cases than among unique cases.…”
Section: Discussionmentioning
confidence: 99%
“…Crude DNA extracts were isolated from cultures by heating (95°C, 30 min), followed by sonication (20 min). Isolates were genotyped using spoligotyping and variable-number tandem-repeat (VNTR) typing with a standardized panel of 24 loci as described previously (21,32,44,45). The VNTR loci 3232, 3336, 2163A, and 1982 were used, in addition to the standard panel (44).…”
Section: Methodsmentioning
confidence: 99%