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dc.contributor.authorNg, K.C.S.
dc.contributor.authorNgabonziza, J.C.S.
dc.contributor.authorLempens, P.
dc.contributor.authorde Jong, B.C.
dc.contributor.authorvan Leth, F.
dc.contributor.authorMeehan, Conor J.
dc.date.accessioned2019-11-05T13:35:38Z
dc.date.accessioned2019-11-21T17:00:47Z
dc.date.available2019-11-05T13:35:38Z
dc.date.available2019-11-21T17:00:47Z
dc.date.issued2019-08
dc.identifier.citationNg KCS, Ngabonziza JCS, Lempens P et al (2019) Bridging the TB data gap: in silico extraction of rifampicin-resistant tuberculosis diagnostic test results from whole genome sequence data. PeerJ. 7:e7564.en_US
dc.identifier.urihttp://hdl.handle.net/10454/17491
dc.descriptionYesen_US
dc.description.abstractBackground: Mycobacterium tuberculosis rapid diagnostic tests (RDTs) are widely employed in routine laboratories and national surveys for detection of rifampicinresistant (RR)-TB. However, as next-generation sequencing technologies have become more commonplace in research and surveillance programs, RDTs are being increasingly complemented by whole genome sequencing (WGS). While comparison between RDTs is difficult, all RDT results can be derived from WGS data. This can facilitate continuous analysis of RR-TB burden regardless of the data generation technology employed. By converting WGS to RDT results, we enable comparison of data with different formats and sources particularly for low- and middle-income high TB-burden countries that employ different diagnostic algorithms for drug resistance surveys. This allows national TB control programs (NTPs) and epidemiologists to utilize all available data in the setting for improved RR-TB surveillance. Methods: We developed the Python-based MycTB Genome to Test (MTBGT) tool that transforms WGS-derived data into laboratory-validated results of the primary RDTs—Xpert MTB/RIF, XpertMTB/RIF Ultra, GenoType MDRTBplus v2.0, and GenoscholarNTM+MDRTB II. The tool was validated through RDT results of RR-TB strains with diverse resistance patterns and geographic origins and applied on routine-derived WGS data. Results: The MTBGT tool correctly transformed the single nucleotide polymorphism (SNP) data into the RDT results and generated tabulated frequencies of the RDT probes as well as rifampicin-susceptible cases. The tool supplemented the RDT probe reactions output with the RR-conferring mutation based on identified SNPs. The MTBGT tool facilitated continuous analysis of RR-TB and Xpert probe reactions from different platforms and collection periods in Rwanda. Conclusion: Overall, the MTBGT tool allows low- and middle-income countries to make sense of the increasingly generated WGS in light of the readily available RDT.en_US
dc.description.sponsorshipErasmus Mundus Joint Doctorate Fellowship grant 2016- 1346.en_US
dc.language.isoenen_US
dc.relation.isreferencedbyhttps://doi.org/10.7717/peerj.7564en_US
dc.rights© 2019 Ng et al. Distributed under Creative Commons CC-BY 4.0en_US
dc.subjectMycobacterium tuberculosisen_US
dc.subjectRifampicin-resistant tuberculosisen_US
dc.subjectXpert MTB/RIFen_US
dc.subjectXpertMTB/RIF Ultraen_US
dc.subjectGenoType MDRTBplus v2.0en_US
dc.subjectGenoscholarNTM+MDRTB IIen_US
dc.subjectPythonen_US
dc.subjectNext generation sequencingen_US
dc.subjectWhole genome sequencesen_US
dc.subjectSingle nucleotide polymorphismen_US
dc.titleBridging the TB data gap: in silico extraction of rifampicin-resistant tuberculosis diagnostic test results from whole genome sequence dataen_US
dc.status.refereedYesen_US
dc.date.Accepted2019-07-29
dc.date.application2019-08-26
dc.typeArticleen_US
dc.type.versionPublished versionen_US
dc.date.updated2019-11-05T13:35:42Z
refterms.dateFOA2019-11-21T17:01:25Z


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