| Accession | ARO:3000999 |
| CARD Short Name | TEM-135 |
| Definition | TEM-135 is a broad-spectrum beta-lactamase found in Salmonella enterica. |
| AMR Gene Family | TEM beta-lactamase |
| Drug Class | penam, penem, cephalosporin, monobactam |
| Resistance Mechanism | antibiotic inactivation |
| Resistomes with Perfect Matches | Cronobacter sakazakiip, Escherichia albertiiwgs, Escherichia colig+p+wgs, Escherichia fergusoniiwgs, Klebsiella pneumoniaewgs, Neisseria gonorrhoeaep+wgs, Salmonella entericap+wgs, Shigella sonneiwgs |
| Resistomes with Sequence Variants | Cronobacter sakazakiip, Escherichia albertiiwgs, Escherichia colig+p+wgs, Escherichia fergusoniiwgs, Klebsiella pneumoniaewgs, Neisseria gonorrhoeaep+wgs, Salmonella entericap+wgs, Shigella sonneiwgs |
| Classification | 17 ontology terms | Show + process or component of antibiotic biology or chemistry + mechanism of antibiotic resistance + determinant of antibiotic resistance + antibiotic molecule + antibiotic inactivation [Resistance Mechanism] + antibiotic inactivation enzyme + hydrolysis of antibiotic conferring resistance + beta-lactam antibiotic + cephem + hydrolysis of beta-lactam antibiotic by serine beta-lactamase + penam [Drug Class] + beta-lactamase + penem [Drug Class] + ampicillin [Antibiotic] + class A beta-lactamase + cephalosporin [Drug Class] + monobactam [Drug Class] |
| Parent Term(s) | 2 ontology terms | Show |
| Publications | Pasquali F, et al. 2005. J Antimicrob Chemother 55(4): 562-565. Physical linkage of Tn3 and part of Tn1721 in a tetracycline and ampicillin resistance plasmid from Salmonella Typhimurium. (PMID 15731203) Yan J, et al. 2019. Int. J. Antimicrob. Agents 54(3):361-366 High prevalence of TEM-135 expression from the Asian plasmid in penicillinase-producing Neisseria gonorrhoeae from Hangzhou, China. (PMID 31202926) |
Prevalence of TEM-135 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).
| Species | NCBI Chromosome | NCBI Plasmid | NCBI WGS | NCBI GI |
|---|---|---|---|---|
| Cronobacter sakazakii | 0% | 2.56% | 0% | 0% |
| Escherichia albertii | 0% | 0% | 0.65% | 0% |
| Escherichia coli | 0.02% | 0.23% | 0.25% | 0% |
| Escherichia fergusonii | 0% | 0% | 2.17% | 0% |
| Klebsiella pneumoniae | 0% | 0% | 0.09% | 0% |
| Neisseria gonorrhoeae | 0% | 5.1% | 1.44% | 0% |
| Salmonella enterica | 0% | 0.05% | 0.09% | 0% |
| Shigella sonnei | 0% | 0% | 0.29% | 0% |
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): 500