tet(X6)

Accession ARO:3005056
Synonym(s)tetX6
CARD Short Nametet(X6)
DefinitionTet(X6) is a tetracycline inactivating enzyme. It is a tet(X) variant.
AMR Gene Familytetracycline inactivation enzyme
Drug Classtetracycline antibiotic
Resistance Mechanismantibiotic inactivation
Resistomes with Perfect MatchesAcinetobacter baumanniig+p+wgs, Acinetobacter indicusp, Acinetobacter johnsoniiwgs, Acinetobacter lwoffiiwgs, Acinetobacter townerip+wgs, Escherichia coliwgs, Proteus columbaeg, Proteus mirabilisp, Providencia alcalifaciensg
Resistomes with Sequence VariantsAcinetobacter baumanniig+p+wgs, Acinetobacter indicusp+wgs, Acinetobacter johnsoniiwgs, Acinetobacter lwoffiiwgs, Acinetobacter townerip+wgs, Escherichia colip+wgs, Proteus columbaeg, Proteus mirabilisp+wgs, Providencia alcalifaciensg, Riemerella anatipestiferg+wgs
Classification8 ontology terms | Show
Parent Term(s)4 ontology terms | Show
+ confers_resistance_to_antibiotic tetracycline [Antibiotic]
+ tetracycline inactivation enzyme [AMR Gene Family]
+ confers_resistance_to_antibiotic minocycline [Antibiotic]
+ confers_resistance_to_antibiotic oxytetracycline [Antibiotic]
Publications

Liu D, et al. 2020. J. Antimicrob. Chemother. 75(6):1428-1431 Identification of the novel tigecycline resistance gene tet(X6) and its variants in Myroides, Acinetobacter and Proteus of food animal origin. (PMID 32068864)

Resistomes

Prevalence of tet(X6) 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 baumannii1.42%0.1%0.01%0%
Acinetobacter indicus0%3.77%5.19%0%
Acinetobacter johnsonii0%0%1.82%0%
Acinetobacter lwoffii0%0%2.63%0%
Acinetobacter towneri0%18.75%3.85%0%
Escherichia coli0%0.01%0.01%0%
Proteus columbae100%0%0%0%
Proteus mirabilis0%1.25%0.17%0%
Providencia alcalifaciens9.09%0%0%0%
Riemerella anatipestifer8.33%0%2.78%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): 750


>gb|QIM09823.1|+|tet(X6) [Proteus genomosp. 6]
MTLLKHKKITIIGAGPVGLTMARLLQQNGVDITVYERDKDQDARIFGGTLDLHRDSGQEAMKRAGLLQTYYDLALPMGVNIVDEKGNILT
TKNVRPENRFDNPEINRNDLRTILLNSLQNDTVIWDRKLVTLEPDKEKWILTFEDKSSETADLVIIANGGMSKVRKFVTDTEVEETGTFN
IQADIHQPEVNCPGFFQLCNGNRLMAAHQGNLLFANPNNNGALHFGISFKTPDEWKSKTRVDFQDRNSVVDFLLKKFSDWDERYKELIRL
TSSFVGLATRIFPLDKSWKSKRPLPITMIGDAAHLMPPFAGQGVNSGLMDALILSDNLTNGKFNSIEEAIENYEQQMFAYGREAQAESII
NETEMFSLDFSFQKLMNL


>gb|MN507533.1|+|36122-37258|tet(X6) [Proteus genomosp. 6]
ATGACTTTACTAAAACATAAAAAAATTACAATAATTGGTGCCGGGCCTGTTGGATTAACAATGGCGAGATTGTTACAGCAAAACGGCGTG
GACATTACAGTTTACGAGAGAGACAAAGACCAAGATGCAAGGATTTTTGGTGGGACACTTGATCTGCACAGGGATTCGGGACAGGAAGCA
ATGAAAAGAGCGGGATTGTTACAAACTTATTATGACTTAGCTTTACCAATGGGTGTAAATATTGTTGATGAAAAGGGCAATATTTTAACC
ACAAAAAATGTAAGACCCGAAAATCGTTTTGACAATCCTGAAATAAACAGAAATGACTTAAGGACTATCCTATTAAATAGTTTACAAAAT
GATACCGTCATTTGGGATAGAAAACTTGTTACCCTTGAACCTGATAAGGAGAAGTGGATACTAACTTTTGAGGATAAATCGAGTGAAACA
GCAGATCTGGTTATTATTGCCAATGGTGGAATGTCTAAAGTAAGAAAATTTGTTACCGACACGGAAGTTGAAGAAACAGGTACTTTCAAT
ATACAAGCCGATATTCATCAACCGGAGGTGAACTGTCCTGGATTTTTTCAGCTTTGCAATGGAAACCGGCTAATGGCTGCTCATCAAGGT
AATTTATTATTTGCGAATCCTAATAATAATGGTGCATTGCATTTTGGAATAAGTTTTAAAACACCTGATGAATGGAAAAGCAAAACGCGG
GTAGATTTTCAAGACAGAAATAGTGTCGTTGATTTTCTCCTGAAAAAATTTTCCGATTGGGACGAACGCTACAAAGAACTGATTCGTTTG
ACATCATCTTTTGTAGGGTTAGCGACACGAATATTTCCCTTAGATAAGTCTTGGAAAAGTAAGCGTCCATTACCCATAACGATGATTGGA
GATGCTGCTCATTTGATGCCTCCTTTTGCAGGACAAGGCGTAAACAGTGGGTTGATGGATGCCTTGATATTGTCGGATAATCTGACCAAT
GGGAAATTTAACAGCATTGAAGAGGCTATTGAAAATTATGAACAGCAAATGTTTGCTTATGGAAGAGAAGCACAGGCAGAATCAATAATA
AACGAAACGGAAATGTTCAGCCTCGACTTTTCTTTCCAAAAACTAATGAATCTATAA