Mycobacterium tuberculosis fgd1 with mutation conferring resistance to delamanid

Accession ARO:3007849
Synonym(s)Rv0407
CARD Short NameMtub_fgd1_DLM
DefinitionMutations in the F420-dependent glucose-6-phosphate dehydrogenase fgd1 which confer resistance to the nitroimidazole antibiotic delamanid.
AMR Gene Familydelamanid-resistant fgd1
Drug Classnitroimidazole antibiotic
Resistance Mechanismantibiotic target alteration
Classification9 ontology terms | Show
Parent Term(s)2 ontology terms | Show
+ confers_resistance_to_antibiotic delamanid [Antibiotic]
+ delamanid-resistant fgd1 [AMR Gene Family]
Publications

Kadura S, et al. 2020. J Antimicrob Chemother 75(8):2031-2043 Systematic review of mutations associated with resistance to the new and repurposed Mycobacterium tuberculosis drugs bedaquiline, clofazimine, linezolid, delamanid and pretomanid. (PMID 32361756)

World Health Organization. 2023. ISBN 978-92-4-008241-0. Catalogue of mutations in Mycobacterium tuberculosis complex and their association with drug resistance. Second Edition. (ISBN 978-92-4-008241-0)

Resistomes

Prevalence of Mycobacterium tuberculosis fgd1 with mutation conferring resistance to delamanid among the sequenced genomes, plasmids, and whole-genome shotgun assemblies available at NCBI or IslandViewer for 414 important pathogens (see methodological details and complete list of analyzed pathogens). Values reflect percentage of genomes, plasmids, genome islands, or whole-genome shotgun assemblies that have at least one hit to the AMR detection model. Default view includes percentages calculated based on Perfect plus Strict RGI hits. Select the checkbox to view percentages based on only Perfect matches to AMR reference sequences curated in CARD (note: this excludes resistance via mutation as references in protein variant models are often wild-type, sensitive sequences).

Prevalence: protein variant model

SpeciesNCBI ChromosomeNCBI PlasmidNCBI WGSNCBI GIGRDI-AMR2
No prevalence data


Detection Models

Model Type: protein variant model

Model Definition: Protein Variant Models (PVM) perform a similar search as Protein Homolog Models (PHM), i.e. detect protein sequences based on their similarity to a curated reference sequence, but secondarily screen query sequences for curated sets of mutations to differentiate them from antibiotic susceptible wild-type alleles. PVMs are designed to detect AMR acquired via mutation of house-keeping genes or antibiotic targets, e.g. a mutated gyrase resistant to aminocoumarin antibiotics. PVMs include a protein reference sequence (often from antibiotic susceptible wild-type alleles), a curated bit-score cut-off, and mapped resistance variants. Mapped resistance variants may include any or all of single point mutations, insertions, or deletions curated from the scientific literature. A Strict RGI match has a BLASTP bit-score above the curated BLASTP cutoff value and contains at least one curated mutation from amongst the mapped resistance variants, while a Loose RGI match has a bit-score less than the curated BLASTP bit-score cut-off but still contains at least one curated mutation from amongst the mapped resistance variants.

Bit-score Cut-off (blastP): 600

PubMed: mutation data hand curated from the scientific literature, evaluated as conferring resistance (R). CRyPTIC: mutation data acquired from the CRyPTIC catalog, evaluated as resistant (R), susceptible (S), or undetermined (U). ReSeqTB: mutation data acquired from the ReSeqTB catalog, evaluated as conferring resistance (Minimal, Moderate, High), not conferring resistance (None), or Indeterminate. WHO: mutation data acquired from the WHO 2023 catalog, evaluated as resistant (R), susceptible (S), or undetermined (U).

MutationMutation typePubMedReSeqTBCRyPTICWHO
V1Varsingle resistance variantno datano datano dataWHO-R

>gb|NP_214921.1|+|Mycobacterium tuberculosis fgd1 with mutation conferring resistance to delamanid [Mycobacterium tuberculosis H37Rv]
MAELKLGYKASAEQFAPRELVELAVAAEAHGMDSATVSDHFQPWRHQGGHAPFSLSWMTA
VGERTNRLLLGTSVLTPTFRYNPAVIAQAFATMGCLYPNRVFLGVGTGEALNEIATGYEG
AWPEFKERFARLRESVGLMRQLWSGDRVDFDGDYYRLKGASIYDVPDGGVPVYIAAGGPA
VAKYAGRAGDGFICTSGKGEELYTEKLMPAVREGAAAADRSVDGIDKMIEIKISYDPDPE
LALNNTRFWAPLSLTAEQKHSIDDPIEMEKAADALPIEQIAKRWIVASDPDEAVEKVGQY
VTWGLNHLVFHAPGHDQRRFLELFQSDLAPRLRRLG



>gb|NC_000962.3|+|490783-491793|Mycobacterium tuberculosis fgd1 with mutation conferring resistance to delamanid [Mycobacterium tuberculosis H37Rv]
GTGGCTGAACTGAAGCTAGGTTACAAAGCATCGGCCGAACAATTCGCACCGCGCGAGCTCGTCGAACTAGCCGTCGCCGCCGAAGCCCAC
GGCATGGACAGCGCGACCGTCAGCGACCATTTTCAGCCTTGGCGCCACCAGGGCGGCCATGCCCCGTTCTCGCTGTCCTGGATGACCGCT
GTCGGCGAACGTACCAACCGGCTGCTGCTGGGCACTTCGGTGCTGACCCCCACCTTCCGCTACAACCCCGCCGTCATCGCTCAGGCTTTC
GCCACCATGGGATGCCTGTACCCGAACCGTGTTTTCCTTGGCGTGGGCACCGGTGAGGCGCTGAACGAAATCGCCACCGGATACGAGGGC
GCCTGGCCGGAGTTCAAGGAGCGGTTCGCCCGGCTGCGTGAATCGGTGGGGCTAATGCGGCAGCTGTGGAGCGGTGACCGCGTCGACTTT
GACGGCGACTATTACCGGCTCAAGGGTGCCTCGATCTACGACGTGCCCGACGGGGGCGTGCCCGTCTACATCGCCGCCGGCGGCCCGGCG
GTGGCCAAGTACGCCGGCCGCGCCGGTGACGGCTTCATCTGTACGTCCGGCAAGGGCGAGGAGCTCTACACCGAGAAGCTGATGCCGGCG
GTACGAGAAGGCGCCGCTGCCGCTGACCGATCCGTCGACGGCATCGACAAGATGATCGAAATCAAGATCTCCTACGACCCCGACCCGGAG
CTGGCATTGAACAACACCCGGTTTTGGGCGCCGCTGTCGTTGACAGCTGAGCAGAAGCACAGCATCGACGACCCGATCGAGATGGAGAAG
GCCGCCGATGCGCTGCCAATCGAACAGATCGCCAAGCGCTGGATCGTGGCGTCGGACCCCGACGAAGCCGTCGAAAAGGTAGGTCAATAC
GTGACATGGGGCCTGAACCACCTGGTATTTCACGCACCAGGACATGACCAGCGCCGGTTTCTGGAGCTCTTCCAGTCGGACCTGGCACCC
AGGTTGCGGCGACTTGGCTGA

Curator Acknowledgements
Curator Description Most Recent Edit