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dc.contributor.authorBowness, Ruth
dc.contributor.authorBoeree, Martin J
dc.contributor.authorAarnoutse, Rob
dc.contributor.authorDawson, Rodney
dc.contributor.authorDiacon, Andreas
dc.contributor.authorMangu, Chacha
dc.contributor.authorHeinrich, Norbert
dc.contributor.authorNtinginya, Nyanda E
dc.contributor.authorKohlenberg, Anke
dc.contributor.authorMtafya, Bariki
dc.contributor.authorPhillips, Patrick P J
dc.contributor.authorRachow, Andrea
dc.contributor.authorPlemper van Balen, Georgette
dc.contributor.authorGillespie, Stephen H
dc.date.accessioned2015-10-24T23:11:09Z
dc.date.available2015-10-24T23:11:09Z
dc.date.issued2015-02
dc.identifier157165058
dc.identifier604a7382-f89c-43ab-8255-da83fa3fdf50
dc.identifier25344806
dc.identifier84922424155
dc.identifier000350211600013
dc.identifier.citationBowness , R , Boeree , M J , Aarnoutse , R , Dawson , R , Diacon , A , Mangu , C , Heinrich , N , Ntinginya , N E , Kohlenberg , A , Mtafya , B , Phillips , P P J , Rachow , A , Plemper van Balen , G & Gillespie , S H 2015 , ' The relationship between Mycobacterium tuberculosis MGIT time to positivity and cfu in sputum samples demonstrates changing bacterial phenotypes potentially reflecting the impact of chemotherapy on critical sub-populations ' , Journal of Antimicrobial Chemotherapy , vol. 70 , no. 2 , pp. 448-455 . https://doi.org/10.1093/jac/dku415en
dc.identifier.issn0305-7453
dc.identifier.otherORCID: /0000-0001-6537-7712/work/39477821
dc.identifier.otherORCID: /0000-0002-4090-5168/work/59698741
dc.identifier.urihttps://hdl.handle.net/10023/7686
dc.descriptionThis work was supported by EDCTP who fund the PanACEA consortium (IP.2007.32011.011, IP.2007.32011.012, IP.2007.32011.013) and PreDiCT-TB consortium [IMI Joint undertaking grant agreement number 115337, resources of which are composed of financial contribution from the European Union’s Seventh Framework Programme (FP7/2007-2013) and EFPIA companies’ in kind contribution].en
dc.description.abstractObjectives The relationship between cfu and Mycobacterial Growth Indicator Tube (MGIT) time to positivity (TTP) is uncertain. We attempted to understand this relationship and create a mathematical model to relate these two methods of determining mycobacterial load. Methods Sequential bacteriological load data from clinical trials determined by MGIT and cfu were collected and mathematical models derived. All model fittings were conducted in the R statistical software environment (version 3.0.2), using the lm and nls functions. Results TTP showed a negative correlation with log10 cfu on all 14 days of the study. There was an increasing gradient of the regression line and y-intercept as treatment progressed. There was also a trend towards an increasing gradient with higher doses of rifampicin. Conclusions These data suggest that there is a population of mycobacterial cells that are more numerous when detected in liquid than on solid medium. Increasing doses of rifampicin differentially kill this group of organisms. These findings support the idea that increased doses of rifampicin are more effective.
dc.format.extent8
dc.format.extent822327
dc.format.extent492447
dc.language.isoeng
dc.relation.ispartofJournal of Antimicrobial Chemotherapyen
dc.subjectTTPen
dc.subjectM. tuberculosisen
dc.subjectTBen
dc.subjectR Medicine (General)en
dc.subjectNDASen
dc.subjectBDCen
dc.subjectR2Cen
dc.subjectSDG 3 - Good Health and Well-beingen
dc.subject.lccR1en
dc.titleThe relationship between Mycobacterium tuberculosis MGIT time to positivity and cfu in sputum samples demonstrates changing bacterial phenotypes potentially reflecting the impact of chemotherapy on critical sub-populationsen
dc.typeJournal articleen
dc.contributor.sponsorEuropean Commissionen
dc.contributor.institutionUniversity of St Andrews. School of Medicineen
dc.contributor.institutionUniversity of St Andrews. Global Health Implementation Groupen
dc.contributor.institutionUniversity of St Andrews. Gillespie Groupen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.contributor.institutionUniversity of St Andrews. Infection Groupen
dc.identifier.doi10.1093/jac/dku415
dc.description.statusPeer revieweden
dc.date.embargoedUntil2015-10-25
dc.identifier.grantnumberen


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