Enterococcus faecalis gdpD with mutation conferring daptomycin resistance

Accession ARO:3003800
CARD Short NameEfae_gdpD_DAP
DefinitiongdpD is a glycerolphosphodiesterase whose mutations confer resistance to daptomycin.
AMR Gene Familydaptomycin resistant gdpD
Drug Classpeptide antibiotic
Resistance Mechanismantibiotic target alteration
Classification10 ontology terms | Show
Parent Term(s)2 ontology terms | Show
+ daptomycin resistant gdpD [AMR Gene Family]
+ confers_resistance_to_antibiotic daptomycin [Antibiotic]
Publications

Miller C, et al. 2013. Antimicrob Agents Chemother 57(11): 5373-5383. Adaptation of Enterococcus faecalis to daptomycin reveals an ordered progression to resistance. (PMID 23959318)

Resistomes

Prevalence of Enterococcus faecalis gdpD with mutation conferring daptomycin resistance 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): 1000

Legend:

  • discovered in clinical, agricultural, or environmental isolates

  • discovered via laboratory selection experiments

  • ReSeqTB https://platform.reseqtb.org


>gb|AAO81656.1|+|Enterococcus faecalis gdpD with mutation conferring daptomycin resistance [Enterococcus faecalis V583]
MFSYFKNSIVNTLDFLKGTTAYFRDVLLMHGFMLFVLLPLLTSLSKLVLKEGGIDYISYDNLGAIATQHPYVLLTFLLIGLLILLALFFE
FTFLLLSVYFIKKKQPITLTQLLHGTLLQIKKVRGITFLFFLAYFFLILPLSGLTFRSYLLTRVKIPAFILDFIFANRVIIIIGFVLLEL
IILYLAIRLAFALPELILRDVGFRESLKRSWQITKRRFFQILGQFIIIGGTVLGIFTAGYFLIFLGQTAVETFKPEWSLPSAVIAMTLLQ
VMMLLNLVLSSVAIFYIIVDDMEDEGILPDTPEWFTPKSEVRVEWTTFRVVLFCLIAIIFGIGVGTYNTNYLSHTPDRKPVTISHRGVNG
NNGVQNTLDSLIETNKAKPDYVEMDIQETKDHQFIVMHDFNLRALTGVNKRPNQLTLKELTNMNVTENGQTAKMVSFDDYLAKANQLKQR
LLIEIKTTPQDSPDLVQRFVKQYRENIFENGHILHTLTYDTAMALKKEEPRFYVGYVIPFNIVGPPKMPVDFFTMEYSTMNRNFVNAAHH
DGKKVYAWTANDEDVMTRMIFYGVDGIITDQLSLLNETMKTDLENPTYSDKLLNFAIGMG


>gb|AE016830.1|+|1847769-1849571|Enterococcus faecalis gdpD with mutation conferring daptomycin resistance [Enterococcus faecalis V583]
ATGTTTAGTTATTTTAAAAATAGTATTGTGAATACGCTAGATTTTCTTAAAGGGACAACGGCGTATTTTCGCGATGTGCTCTTGATGCAC
GGATTTATGTTATTCGTTCTATTGCCTTTATTGACAAGTTTGTCCAAATTGGTACTCAAAGAAGGTGGGATTGATTATATTTCCTACGAT
AACTTAGGGGCAATTGCTACGCAACATCCCTATGTCCTTTTGACTTTTCTACTAATTGGGCTGTTAATTTTACTGGCGCTCTTTTTTGAA
TTTACCTTTTTATTGCTTAGTGTCTATTTTATTAAGAAAAAGCAACCAATTACTCTAACGCAATTATTGCACGGCACCTTGCTTCAGATC
AAAAAAGTTCGAGGAATTACCTTTCTGTTTTTCCTGGCATATTTCTTTTTGATTTTACCATTAAGTGGGTTAACCTTCCGCTCTTATTTA
TTAACAAGAGTTAAGATTCCAGCCTTTATCTTAGATTTTATTTTTGCAAATCGCGTCATTATTATTATTGGTTTCGTATTGTTAGAACTG
ATTATCTTATATTTAGCGATTCGACTTGCTTTTGCCCTTCCAGAGTTGATTTTACGTGATGTTGGTTTTCGTGAGTCTTTAAAACGTAGT
TGGCAAATTACAAAGCGGCGCTTTTTCCAGATTTTAGGGCAATTTATTATCATTGGAGGAACTGTTTTAGGGATTTTTACGGCTGGCTAT
TTCTTGATATTTTTAGGTCAAACCGCAGTCGAAACGTTTAAACCTGAGTGGTCTTTACCTAGCGCTGTCATCGCTATGACACTCCTTCAG
GTTATGATGCTCTTAAACTTGGTGTTGTCTAGTGTTGCTATTTTTTACATTATTGTTGATGATATGGAAGATGAAGGGATTTTGCCTGAC
ACGCCAGAATGGTTCACCCCGAAATCAGAGGTTCGGGTAGAATGGACCACCTTCAGAGTCGTTCTTTTTTGTTTGATTGCAATCATCTTC
GGAATTGGTGTAGGCACCTATAATACGAATTACCTAAGTCATACACCTGACCGAAAACCGGTTACCATCTCCCATCGTGGTGTTAATGGT
AACAATGGCGTTCAAAACACCTTGGACTCTTTAATCGAGACCAATAAGGCAAAACCTGATTATGTTGAAATGGATATTCAAGAAACCAAA
GACCATCAATTTATTGTCATGCACGATTTTAATTTACGGGCGTTAACGGGCGTTAATAAACGACCGAATCAATTAACACTTAAAGAATTA
ACGAATATGAATGTCACAGAAAATGGTCAAACTGCTAAAATGGTTTCTTTCGATGATTATTTAGCCAAAGCCAATCAATTAAAACAACGT
TTATTAATTGAAATCAAAACCACGCCTCAAGATAGCCCTGATTTAGTACAGCGCTTTGTCAAACAATACCGTGAAAATATTTTTGAAAAC
GGCCATATCCTTCATACCTTAACCTATGATACGGCGATGGCCTTAAAGAAAGAAGAACCACGCTTTTATGTAGGCTACGTTATTCCTTTC
AACATTGTGGGACCGCCTAAAATGCCAGTTGACTTTTTTACTATGGAATACAGTACAATGAATCGTAACTTTGTAAATGCCGCTCATCAT
GATGGGAAAAAGGTTTATGCTTGGACAGCAAATGATGAAGATGTTATGACACGAATGATTTTTTATGGCGTCGATGGCATCATTACCGAT
CAGCTCAGTCTACTGAACGAAACAATGAAAACCGATTTAGAAAACCCAACATACTCCGATAAACTGTTGAATTTCGCTATTGGAATGGGT
TAA