Table.
Mutations in mgrB, phoP and phoQ genes among the colistin-resistant Klebsiella pneumoniae
| Isolate ID | Source | Colistin MIC (µg/ml) | MLST | Carbapenemase | mgrB | phoP | phoQ | Accession number |
|---|---|---|---|---|---|---|---|---|
| Kp1 | Blood | 16 | ST86 | Nil | Nil | Alanine 114 arginine (0.22) | Leucine 209 cysteine (0.00*) | bPAW96459.1 cNRQZ01000030.1 |
| Kp2 | Blood | 32 | ST11 | Nil | Elongated mgrB of 55 amino acids | Nil | Nil | aPBD34554.1 |
| Kp3 | Blood | 16 | ST14 | OXA48-like | Nil | Nil | Tryptophan 161 leucine (0.30) | cMH211110 |
| Kp4 | Blood | 32 | ST14 | OXA48, NDM | No amplification | Nil | Tryptophan 161 leucine (0.30) | cMH211111 |
| Kp5 | Blood | 32 | ST14 | OXA48-like | Truncated by IS1R of IS1 family | Nil | Nil | aMH590725 |
| Kp6 | Blood | 8 | ST231 | OXA48-like | Premature stop codon at 21st amino acid and change in the sequence of protein after 10th amino acid | Nil | Nil | aMH807824 |
| Kp7 | Blood | 8 | ST15 | KPC | Truncated by IS903B group of IS5 family | Nil | Nil | aMH590724 |
| Kp8 | Blood | 16 | ST231 | OXA48-like | Truncated by ISKpn14 of IS1 family | Nil | Nil | aMH590726 |
| Kp9 | CSF | 16 | ST14 | OXA48-like | Truncated by ISKpn26 of IS5 family | Nil | Changes from 218 to 239 and 436 to 448 amino acids | aMH590727 cMH807825 |
| Kp10 | Exudate | 8 | ST23 | NDM | Nil | Nil | Glycine 117 aspartic acid (1.00) | cMH211112 |
| Kp11 | Exudate | 4 | ST2096 | OXA48-like | Nil | Nil | Valine 370 glutamic acid (0.03*) | cMH211113 |
| Kp12 | Exudate | 32 | ST14 | OXA48, NDM | Cysteine to glycine at 28th amino acid (0.00*) | Threonine 151 Alanine (0.00*) | Nil | aMH337365 bMH211116 |
| Kp13 | Exudate | 16 | ST147 | OXA48, NDM | Nil | Glutamic acid 22 lysine (0.49) | Nil | bMH211117 |
| Kp14 | Exudate | 32 | ST231 | OXA48-like | Premature stop codon at 21st amino acid and change in the sequence of protein after 10th amino acid | Nil | Nil | aMH807823 |
| Kp15 | Respiratory | 32 | ST14 | NDM | Cysteine to glycine at 28th amino acid (0.00*) | Nil | Leucine 172 glutamine (0.01*); Tryptophan 182 serine (0.04*) | aMH337366 cMH211114 |
| Kp16 | Respiratory | 8 | ST231 | OXA48-like | Nil | Nil | Valine444^, phenylalanine 445 glycine (0.00*) | cMH211115 |
| Kp17 | Respiratory | 8 | ST147 | OXA48-like | Methionine to arginine first amino acid (0.00*) | Nil | Nil | aMH590728 |
| Kp18 | Respiratory | 16 | ST231 | OXA48-like | Premature stop codon at 21st amino acid and change in the sequence of protein after 10th amino acid | Nil | Nil | aMH337364 |
| Kp19 | Respiratory | 8 | ST2957 | KPC-9 | No mutation; associated with IS102 of IS5 family | Nil | Proline 424 leucine (0.37) V446W (0.00*), change from 448th amino acid | aPAT25546.1 cCJ307_16160 |
amgrB accession number; bphoP accession number; cphoQ accession number. Numbers in parenthesis indicate the SIFT score; values with *<0.05 show that the mutation affects the protein function. #Position of insertion in mgrB gene. ^Indicates Valine deletion at 444th position in phoQ. MLST, multilocus sequence typing; SIFT, sorting intolerant from tolerant; MIC, minimum inhibitory concentration; IS, insertion sequence