Thermus thermophilus uL3 mutations conferring resistance to pleuromutilin antibiotics

Accession ARO:3005081
CARD Short NameTthe_uL3_PLM
DefinitionThermus thermophilus ribosomal protein uL3 containing various mutations conferring resistance to tiamulin. Mutations in the ribosomal protein of uL3 acts by interfering with local rRNA conformation thus conferring resistance.
AMR Gene FamilyRibosomal protein mutation conferring resistance to pleuromutilin antibiotics
Drug Classpleuromutilin antibiotic
Resistance Mechanismantibiotic target alteration
Classification8 ontology terms | Show
Parent Term(s)2 ontology terms | Show
+ confers_resistance_to_antibiotic tiamulin [Antibiotic]
+ Ribosomal protein mutation conferring resistance to pleuromutilin antibiotics [AMR Gene Family]
Publications

Killeavy EE, et al. 2020. Antibiotics (Basel) 9(6): Tiamulin-Resistant Mutants of the Thermophilic Bacterium Thermus thermophilus. (PMID 32526926)

Resistomes

Prevalence of Thermus thermophilus uL3 mutations conferring resistance to pleuromutilin antibiotics among the sequenced genomes, plasmids, and whole-genome shotgun assemblies available at NCBI or IslandViewer for 413 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 GI
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): 400

Legend:

  • discovered in clinical, agricultural, or environmental isolates

  • discovered via laboratory selection experiments

  • ReSeqTB https://platform.reseqtb.org

Published Variants:

PMID: 32526926R144C R144H

>gb|AAS81670.1|-|Thermus thermophilus uL3 mutations conferring resistance to pleuromutilin antibiotics [Thermus thermophilus HB27]
MKGILGVKVGMTRIFRDDRAVPVTVILAGPCPVVQRRTPEKDGYTAVQLGFLPQNPKRVN
RPLKGHFAKAGVEPVRILREIRDFNPEGDTVTVEIFKPGERVDVTGTSKGRGFAGVMKRW
NFAGGPDSHGAHKIHRHPGSIGNRKTPGRVYKGKKMAGHYGAERVTVMNLEVVDVIPEEN
LLLVKGAVPGPNGGLVIVRETKKAAK



>gb|AE017221.1|-|1266023-1266643|Thermus thermophilus uL3 mutations conferring resistance to pleuromutilin antibiotics [Thermus thermophilus HB27]
GTGAAGGGCATCTTGGGCGTCAAGGTGGGCATGACCCGCATCTTCCGCGACGACCGCGCCGTCCCCGTCACGGTCATCCTTGCGGGGCCG
TGCCCCGTGGTGCAGCGCCGCACCCCGGAGAAGGACGGCTACACCGCGGTGCAGCTGGGCTTCCTTCCCCAAAACCCCAAGCGGGTGAAC
CGCCCCCTTAAGGGGCACTTCGCCAAGGCCGGGGTGGAGCCCGTGCGCATCCTGCGGGAGATCCGGGACTTCAACCCCGAAGGCGACACG
GTCACGGTGGAGATCTTCAAGCCCGGGGAGCGCGTGGACGTGACGGGCACCTCCAAGGGCCGGGGCTTCGCCGGCGTGATGAAGCGCTGG
AACTTCGCGGGCGGCCCCGACTCCCACGGCGCCCACAAGATCCACCGCCACCCCGGCTCCATCGGGAACCGCAAGACCCCCGGTCGCGTC
TACAAGGGCAAGAAGATGGCGGGCCACTACGGGGCCGAGCGCGTGACGGTCATGAACCTCGAGGTGGTGGACGTCATCCCCGAGGAGAAC
CTGCTTTTGGTCAAGGGGGCCGTCCCCGGTCCCAACGGCGGCCTGGTCATCGTCCGCGAGACCAAGAAGGCGGCCAAGTGA