TABLE 6.
ESBL detection techniques
| Technique type | Test | Advantages | Disadvantages | Reference(s) |
|---|---|---|---|---|
| Clinical microbiology | Standard NCCLS interpretive criteria | Easy to use, performed in every lab | ESBLs not always “resistant” | 78, 111 |
| NCCLS ESBL confirmatory test | Easy to use and interpret | Sensitivity depends on choice of oxyimino-cephalosporin | 111 | |
| Double-disk approximation test | Easy to use, easy to interpret | Distance of disk placement for optimal sensitivity not standardized | 76, 169, 71 | |
| Three-dimensional test | Sensitive, easy to interpret | Not specific for ESBLS, labor intensive | 169 | |
| Etest ESBL strips | Easy to use | Not always easy to interpret, not as sensitive as double-disk test | 183 | |
| Vitek ESBL test | Easy to use, easy to interpret | Reduced sensitivity | 149, 164 | |
| Molecular detection | DNA probes | Specific for gene family (e.g., TEM or SHV) | Labor intensive, cannot distinguish between ESBLs and non-ESBLs, cannot distinguish between variants of TEM or SHV | 7, 55, 70 |
| PCR | Easy to perform, specific for gene family (e.g., TEM or SHV) | Cannot distinguish between ESBLs and non-ESBLs, cannot distinguish between variants of TEM or SHV | 42, 90, 116 | |
| Oligotyping | Detects specific TEM variants | Requires specific oligonucleotide probes, labor intensive, cannot detect new variants | 117 | |
| PCR-RFLP | Easy to perform, can detect specific nucleotide changes | Nucleotide changes must result in altered restriction site for detection | 116 | |
| PCR-SSCP | Can distinguish between a number of SHV variants | Requires special electrophoresis conditions | 106, 107 | |
| LCR | Can distinguish between a number of SHV variants | Requires a large number of oligonucleotide primers | 80 | |
| Nucleotide sequencing | The gold standard, can detect all variants | Labor intensive, can be technically challenging, can be difficult to interpret manual methods | 25 |