MCR-2.2

Accession ARO:3004502
CARD Short NameMCR-2.2
DefinitionAn MCR-2 phosphoethanolamine transferase and polymyxin resistance gene variant identified in Moraxella isolated from pigs in Great Britain.
AMR Gene FamilyMCR phosphoethanolamine transferase
Drug Classpeptide antibiotic
Resistance Mechanismantibiotic target alteration
Classification14 ontology terms | Show
Parent Term(s)4 ontology terms | Show
+ confers_resistance_to_antibiotic colistin A [Antibiotic]
+ confers_resistance_to_antibiotic colistin B [Antibiotic]
+ evolutionary_variant_of MCR-2.1
+ MCR phosphoethanolamine transferase [AMR Gene Family]
Publications

AbuOun M, et al. 2017. J. Antimicrob. Chemother. 72(10):2745-2749 mcr-1 and mcr-2 variant genes identified in Moraxella species isolated from pigs in Great Britain from 2014 to 2015. (PMID 29091227)

Poirel L, et al. 2017. J. Antimicrob. Chemother. 72(10):2947-2949 MCR-2-mediated plasmid-borne polymyxin resistance most likely originates from Moraxella pluranimalium. (PMID 29091193)

Resistomes

Prevalence of MCR-2.2 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 homolog model

SpeciesNCBI ChromosomeNCBI PlasmidNCBI WGSNCBI GIGRDI-AMR2
No prevalence data


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): 1000


>gb|ASK49941.1|+|MCR-2.2 [Moraxella pluranimalium]
MTSQHSWYRYSINPFVLMGLVALFLAATANLTFFEKAMAVYPVSDNLGFIISMAVALMGAMLLIVVLLSYRYVLKPVLILLLIMGAVTSY
FTDTYGTVYDTTMLQNAMQTDQAESKDLMNLAFFVRIIGLGVLPSVLVAFAKVNYPTWGKGLIQRAMTWGVSLVLLLVPIGLFSSQYASF
FRVHKPVRFYINPITPIYSVGKLASIEYKKATAPTDTIYHAKDAVQTTKPSERKPRLVVFVVGETARADHVQFNGYGRETFPQLAKVDGL
ANFSQVTSCGTSTAYSVPCMFSYLGQDDYDVDTAKYQENVLDTLDRLGVDILWRDNNSDSKGVMDKLPTTQYFDYKSATNNTICNTNPFN
ECRDVGMLVGLDDYVSANNGKDMLIMLHQMGNHGPAYFKRYDEQFAKFTPVCEGNELAKCEHQSLINAYDNALLATDDFIAKSIDWLKTH
EANYDVAMLYVSDHGESLGENGVYLHGMPNAFAPKEQRAVPAFFWSNNTTFKPTASDTVLTHDAITPTLLKLFDVTADKVKDRTAFIQ


>gb|MF176239.1|+|1-1617|MCR-2.2 [Moraxella pluranimalium]
ATGACATCACAGCACTCTTGGTATCGCTACTCCATCAATCCTTTTGTACTGATGGGTTTGGTGGCGTTATTTTTGGCGGCAACAGCGAAC
CTGACATTTTTTGAAAAAGCGATGGCGGTCTATCCTGTATCGGATAACTTAGGCTTTATCATCTCAATGGCGGTTGCACTGATGGGTGCT
ATGCTATTGATTGTCGTGCTATTATCCTATCGCTATGTGCTAAAGCCTGTGCTGATTTTATTACTTATCATGGGTGCGGTGACGAGCTAT
TTTACCGATACTTATGGCACGGTCTATGATACCACCATGCTCCAAAATGCCATGCAAACCGACCAAGCTGAATCTAAAGACTTGATGAAT
TTGGCGTTTTTTGTGCGGATTATCGGGCTTGGCGTGTTGCCAAGTGTGTTGGTCGCATTTGCCAAAGTCAATTATCCAACATGGGGCAAA
GGCCTGATTCAGCGTGCGATGACGTGGGGTGTCAGCCTTGTGCTGTTGCTTGTGCCGATTGGGCTATTTAGCAGTCAGTATGCGAGTTTC
TTTCGGGTGCATAAGCCAGTGCGTTTTTATATCAATCCGATTACGCCGATTTATTCGGTGGGCAAGCTTGCCAGTATCGAGTACAAAAAA
GCCACTGCACCAACAGACACCATCTATCATGCCAAAGATGCCGTGCAGACCACCAAGCCTAGCGAGCGTAAGCCACGCCTAGTAGTGTTC
GTCGTCGGTGAGACGGCGCGTGCTGACCATGTGCAGTTCAATGGCTATGGCCGTGAGACTTTCCCACAGCTTGCCAAAGTTGATGGCTTG
GCGAATTTTAGCCAAGTGACATCGTGTGGCACATCGACAGCGTATTCTGTGCCGTGTATGTTTAGCTATTTGGGTCAAGATGACTATGAT
GTCGATACCGCCAAATACCAAGAAAATGTGCTAGATACGCTTGACCGCTTGGGCGTGGATATCTTGTGGCGTGATAATAATTCAGACTCA
AAAGGCGTGATGGATAAGCTACCTACCACGCAGTATTTTGATTATAAATCAGCGACCAACAACACCATCTGTAACACCAATCCCTTTAAT
GAATGCCGTGATGTCGGTATGCTTGTTGGGCTAGATGACTATGTCAGTGCCAATAATGGCAAAGATATGCTCATCATGCTACACCAAATG
GGCAATCATGGGCCGGCGTACTTTAAGCGTTATGATGAGCAATTTGCCAAATTCACCCCTGTGTGCGAAGGCAATGAGCTTGCCAAATGC
GAACACCAATCACTCATCAATGCCTATGATAATGCACTACTTGCCACCGATGATTTTATCGCCAAAAGTATCGATTGGCTAAAAACACAT
GAAGCAAACTACGATGTCGCTATGCTCTATGTCAGCGACCACGGCGAGAGCTTGGGCGAGAATGGTGTCTATCTGCATGGTATGCCAAAT
GCCTTTGCACCAAAAGAACAGCGAGCCGTGCCTGCGTTTTTTTGGTCAAATAATACGACATTCAAGCCAACTGCCAGCGACACTGTGCTG
ACGCATGATGCGATTACCCCGACATTGCTTAAGCTGTTTGATGTCACAGCCGACAAGGTCAAAGACCGCACGGCATTTATCCAGTAA

Curator Acknowledgements
Curator Description Most Recent Edit