Table I.
Bioluminescence | Fluorescent Proteins | Targeted Fluorescent Probes | |
---|---|---|---|
Advantages | • Inherently low background. • Amenable to longitudinal studies • Close mimics of natural bacterial strains • Ability to detect infection recovery |
• Amenable to longitudinal studies • Near-IR versions under development • No substrate needed • Ability to detect infection recovery |
• Bright near-IR probes are best for deep tissue • Activatable by enzymes • Possible translation to clinic • Multimodal probes under development |
Disadvantages | • Limited tissue penetration of visible luminescence • Bacteria must be encoded with genetic reporter • Signal can vary • Substrate is often needed |
• Limited tissue penetration of visible emission • Autofluorescence • Bacteria must be encoded with genetic reporter |
• Probe preparation • Probe may affect bacteria function • Probes may be toxic or decompose • Not ideal for longitudinal studies. |
Best Use of Method | • Study of bacterial pathogenesis • Antibiotic screening |
• Study of bacterial pathogenesis • Antibiotic screening |
• Detection of bacteria which do not express genetic reporters. • Clinical potential |
How to Get Access to the Method | • Academic literature • Instrumentation vendors |
• Academic literature • Instrumentation vendors |
• Academic literature • Instrumentation vendors |
References | [3] | [7] | [15] |
Relevent Patents | [40] | [41] | [N/A] |