Fluorescent in situ hybridization, or 'FISH' is a technique used in molecular microbiology to identify bacteria within formalin fixed tissues. A fluorescent probe that binds to bacterial ribosomes in tissue sections can be visualized using a fluorescent microscope. Our analysis uses a screening 'all bacterial' probe, that binds to most bacterial species. If we identify bacteria, we can use a limited # of additional species specific probes to identify bacterial species (such as E. coli, Staph, Strep, Clostridia, Bartonella ). We do not currently offer probes to detect fungal, mycobacterial, or rickettsial organisms.

FISH analysis of colonic biopsies is a vital adjunct to the diagnosis of Boxer dog colitis, in order to assess colon biopsies for evidence of intramucosal and intracellular bacterial invasion. If bacterial invasion is present, the invading species is usually E. coli, and we use a specific probe to detect E. coli infection. Diagnosis of bacterial invasion helps to formulate a treatment plan, in conjunction with colon culture and antimicrobial susceptibility data. It is important to appreciate that colon culture alone by no means confirms E. coli invasion, and for maximal diagnostic yield, culture data must crucially be interpreted alongside FISH for spatial localization of bacteria.

FISH can also be very helpful in clinical cases where where bacterial involvement is suspected based on clinical or histological evidence, for example in chronic granulomatous diseases, cholangiohepatitis, endocarditis, suppurative pancreatitis, pyelonephritis, lymphadenitis, chronic cystitis.

Yes. We do not require biopsies to be taken into special media for FISH analysis alone. We need a minimum of 5 unstained paraffinised sections, 4-5 microns thick, on charged glass slides.

If, however, you have not already taken biopsies it may be helpful to contact us for advice.

It is extremely unlikely. FISH testing requires specific probes which your regular histology lab is unlikely to have. You may ask your regular histology lab to send slides to us for diagnostic FISH.

The advantages of using FISH as opposed to Gram stain, is that there is much a higher likelihood of visualizing bacteria in tissues using fluorescent beacons. This is particularly true in highly cellular or inflamed tissues, where it can be very difficult to detect and differentiate bacteria from other cell types, inflammatory/necrotic debris and granules. FISH is a highly sensitive technique and can identify a single bacterium.

A negative FISH result does not completely exclude bacterial infection. Reasons for false negatives include the presence of dead/dying bacteria (they must be alive and metabolically active to take up the probe), low bacterial number, a patchy distribution of infection, overfixation, sulfasalazine treatment, and the presence of bacteria with thick cell walls (e.g. Listeria).

The eubacterial probe identifies most bacteria, and FISH MAY enable identification of the bacterial species present if we have the appropriate probe (though we have a limited # of species specific probes). It also does not provide any information on antimicrobial sensitivities.

False positives on FISH are also possible but unlikely, since we use additional probes as positive and negative controls.

No, FISH does not give any information on antimicrobial susceptibility. But it may enable identification of the bacterial species present, and help to ensure an appropriate spectrum and penetration of antimicrobial cover (i.e. Gram + vs Gram -, intracellular vs extracellular).

Currently, we charge a fee of $190 for the first section and $50 for each additional section. This may be subject to change.

Generally, turnaround time is 10-15 days. However, Dr. Simpson is occasionally out of the country or traveling and is therefore unable to read slides promptly. If you are concerned about a long turnaround time, please call before submitting to see what the turnaround time will be.