tet(X3)

Accession ARO:3004719
Synonym(s)tetX3
CARD Short Nametet(X3)
DefinitionA tetracyline resistance gene located on an approximately 300-kb plasmid, designated p47AB. It inactivates all tetracyclines, including tigecycline, eravacycline, and omadacycline.Adjacent to insertion sequence ISVsa3 on the conjugative plasmid.
AMR Gene Familytetracycline inactivation enzyme
Drug Classtetracycline antibiotic, glycylcycline
Resistance Mechanismantibiotic inactivation
Resistomes with Perfect MatchesAcinetobacter baumanniip+wgs, Acinetobacter indicusg+p+wgs, Acinetobacter johnsoniip+wgs, Acinetobacter juniip+wgs, Acinetobacter lwoffiiwgs, Acinetobacter nosocomialisp+wgs, Acinetobacter pittiip+wgs, Acinetobacter townerip+wgs
Resistomes with Sequence VariantsAcinetobacter baumanniip+wgs, Acinetobacter indicusg+p+wgs, Acinetobacter johnsoniip+wgs, Acinetobacter juniip+wgs, Acinetobacter lwoffiiwgs, Acinetobacter nosocomialisp+wgs, Acinetobacter pittiip+wgs, Acinetobacter townerip+wgs
Classification9 ontology terms | Show
Parent Term(s)3 ontology terms | Show
+ tetracycline inactivation enzyme [AMR Gene Family]
+ confers_resistance_to_antibiotic tigecycline [Antibiotic]
+ confers_resistance_to_antibiotic tetracycline [Antibiotic]
Publications

He T, et al. 2019. Nat Microbiol : Emergence of plasmid-mediated high-level tigecycline resistance genes in animals and humans. (PMID 31133751)

Resistomes

Prevalence of tet(X3) 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 homolog model (view sequences)

SpeciesNCBI ChromosomeNCBI PlasmidNCBI WGSNCBI GI
Acinetobacter baumannii0%0.36%0.07%0%
Acinetobacter indicus4.76%20.75%2.6%0%
Acinetobacter johnsonii0%1.39%9.09%0%
Acinetobacter junii0%16.67%1.49%0%
Acinetobacter lwoffii0%0%2.63%0%
Acinetobacter nosocomialis0%1.64%1.15%0%
Acinetobacter pittii0%0.99%0.85%0%
Acinetobacter towneri0%18.75%11.54%0%
Escherichia coli0%0%0%0%
Show Perfect Only


Detection Models

Model Type: protein homolog model

Model Definition: Protein Homolog Models (PHM) detect protein sequences based on their similarity to a curated reference sequence, using curated BLASTP bitscore cut-offs. Protein Homolog Models apply to all genes that confer resistance through their presence in an organism, such as the presence of a beta-lactamase gene on a plasmid. PHMs include a reference sequence and a bitscore cut-off for detection using BLASTP. A Perfect RGI match is 100% identical to the reference protein sequence along its entire length, a Strict RGI match is not identical but the bit-score of the matched sequence is greater than the curated BLASTP bit-score cutoff, Loose RGI matches have a bit-score less than the curated BLASTP bit-score cut-off.

Bit-score Cut-off (blastP): 760


>gb|QBQ85438.1|+|tet(X3) [Acinetobacter baumannii]
MTMRIDTDKQMNLLSDKNVAIIGGGPVGLTMAKLLQQNGIDVSVYERDNDREARIFGGTLDLHKGSGQEAMKKAGLLQTYYDLALPMGVN
IADEKGNILSTKNVKPENRFDNPEINRNDLRAILLNSLENDTVIWDRKLVMLEPGKKKWTLTFENKPSETADLVILANGGMSKIRSFVTD
TQVEETGTFNIQADILQPEINCPGFFQLCNGNRLMAGHQGILLFANPNNNGALYLGISFKTPDEWKNKIPLDFQDRNSVADFLLKRFSKW
SEVYKQLIRSVSTFQCLPTRKFPLNNDWKSNRPLPITMIGDAAHLMSPFAGQGVNTGLLDALILSENLTNGEFTSIENAIENYEQQMFVY
AKDTQDESTENETEMFSPNFSFQKLLNL


>gb|MK134375.1|+|6174-7340|tet(X3) [Acinetobacter baumannii]
ATGACAATGCGAATAGATACAGACAAACAAATGAATTTACTTAGTGATAAGAACGTTGCAATAATTGGTGGTGGACCCGTTGGACTGACT
ATGGCAAAATTATTACAGCAAAACGGCATAGACGTTTCAGTTTACGAAAGAGACAACGACCGAGAGGCAAGAATTTTTGGTGGAACCCTT
GACCTACACAAAGGTTCAGGTCAGGAAGCAATGAAAAAAGCGGGATTGTTACAAACTTATTATGACTTAGCCTTACCAATGGGTGTAAAT
ATTGCTGATGAAAAAGGCAATATTTTATCCACAAAAAATGTAAAGCCCGAAAATCGATTTGACAATCCTGAAATAAACAGAAATGACTTA
AGGGCTATCTTGTTGAATAGTTTAGAAAACGACACGGTTATTTGGGATAGAAAACTTGTTATGCTTGAACCTGGTAAGAAGAAGTGGACA
CTAACTTTTGAGAATAAACCGAGTGAAACAGCAGATTTGGTTATTCTTGCCAATGGTGGAATGTCGAAAATAAGGAGCTTTGTTACCGAC
ACGCAAGTTGAAGAAACCGGTACTTTCAACATCCAAGCTGATATTCTTCAACCGGAAATAAACTGTCCCGGATTTTTTCAGCTATGCAAC
GGCAACCGATTAATGGCGGGACATCAGGGCATTTTATTGTTTGCCAATCCCAATAATAATGGTGCATTGTATTTAGGAATTAGTTTTAAA
ACGCCCGATGAATGGAAAAATAAAATTCCCTTAGATTTTCAGGACAGAAACAGCGTTGCCGATTTTTTATTGAAAAGATTTTCCAAATGG
AGTGAAGTTTACAAACAATTAATACGTTCGGTATCAACATTTCAATGCTTGCCCACAAGGAAATTTCCTTTGAACAATGATTGGAAAAGT
AACCGTCCATTACCCATAACAATGATTGGCGATGCTGCTCATTTGATGTCGCCTTTTGCAGGACAGGGTGTAAATACGGGATTATTGGAT
GCTTTGATATTGTCTGAAAACCTTACAAACGGAGAATTTACAAGTATTGAAAATGCCATCGAAAACTACGAACAACAAATGTTTGTTTAT
GCAAAAGATACGCAGGACGAATCGACAGAAAACGAAACCGAAATGTTTAGTCCCAATTTTTCGTTTCAAAAATTATTGAATCTATAA