The following are general guidelines for submitting samples for testing at the BADDL. For specific testing requirements, select a lab section below or contact the laboratory directly at (321) 697-1400.
Select a lab section to learn more.
Anatomic sites likely to contain anaerobic bacteria contributing to the disease process are closed cavities such as peritoneal cavity, joint space, and para-nasal sinus. The following specimens are generally unacceptable for culture of non-spore-forming anaerobic bacteria:
When submitting fecal or cloacal specimens, understand the laboratory's identification schemes to allow the ruling out of pathogens:
Culture and sensitivity are separate tests to be requested. Most bacteria recovered from submitted specimens are environmental or commensal and do not warrant antimicrobial sensitivity testing.
Be sure to submit a sufficient amount of serum for testing. Almost every test in our laboratory requires 0.5 to 1 ml of serum.
All tubes, containers, bags, slides and swabs submitted must be adequately labeled. Specimen type, name of the patient, and information pertinent to the practitioner should be included on the label.
Blood film must be prepared as soon as possible to minimize artifactual cellular changes. Smears should be rapidly dried with a blow dryer to eliminate artifacts of air-drying red blood cells. Make sure the distribution of cells is even and thin.
To prevent serum hemolysis, it is ideal to submit only chilled serum instead of whole blood for testing. Specimens must be submitted and processed as soon as possible.
For cytologies, smears of aspirates or imprints of tumors and skin lesions should be prepared immediately following collection, air-dried, and then fixed in methanol or sprayed with a commercial fixative such as Spray-cyte prior to shipment. Plastic stacking-type slide containers tend to better prevent slide breakage during transit as compared to flat cardboard or plastic slide holders. If cytology is required on a fluid, slides should be immediately prepared after the specimen is collected and/or the fluid placed in a fixative solution (an EDTA blood tube is usually ideal) and shipped chilled overnight. A red top tube of the fluid can also be submitted chilled (and shipped overnight) for culture or other testing if desired.
When submitting cytological specimens, make a thin preparation. Material should be located at one edge of the slide and homogeneously smeared. It is recommended to submit two smears, one with no fixative, and the second cytospray-fixed right after the specimen is smeared.
Fluids must be submitted in a plastic or glass tube. For safety purposes, no syringes and/or needles should be submitted.
It is important to submit and process the fluids as soon as possible for cytopathological evaluation. If the fluid is not to be processed within the next 24 hours, it is recommended to add 1/4 parts of alcohol to the total fluid volume. Or 1/4 parts of alcohol in 3/4 parts of specimen. Bloody fluid can be submitted in a purple-top (EDTA) tube for good preservation.
Please indicate on the submission form if alcohol was added to the specimen.
After obtaining the sample, the cotton tip must be gently rolled on a glass slide. The already-prepared smear must immediately be cytosprayed or air-dried. Do not leave the smear in the open as it can get contaminated.
The swab should not be submitted for cytopathological testing. The swab is only useful for bacteriological, mycotic evaluation. The cells dry out and die when left in the swab.
For best results, specimens intended for histopathological or immunohistochemical examination should be submitted in 10% formalin. Formalin must penetrate the tissue completely to preserve detail critical to accurate microscopic evaluation. For this reason, tissue must be completely immersed in a generous quantity of formalin (a tissue-to-formalin ratio of 1:10 is ideal). Large specimens (greater than 2 centimeters in diameter) should be partially incised (every 1 centimeter or so) so that fixative can penetrate the tissue.
It is preferred that the cadaver be submitted chilled instead of frozen. However, the carcass should be frozen prior to shipment if the interval between the animal's death and receipt at the laboratory will be more than three days.
The cadaver submitted must be fresh, since the gross and microscopic evaluation of the cadaver is hindered by advanced postmortem autolysis. The normal microflora invades all tissues and organs; therefore, a reliable bacterial analysis cannot be made. Autolysis also hinders other testing, including but not limited to microscopic examination of tissues, fluid evaluation and virus isolation.
The cadaver must be put inside a sealed bag to prevent leaking, with enough ice packs and absorbent material. Body and ice packs should be placed inside a Styrofoam box and an external cardboard box.
Packaging must meet the following conditions:
NOTE: According to the U.S. Department of Transportation, any person who knowingly violates a requirement of the Federal Hazardous Material Transportation law is liable for a civil penalty of not more than $27,500 and not less than $250 for each violation.
Complete, bilateral samples of brain stem, hippocampus and cerebellum are required for rabies testing. A diagnostic test for rabies requires the examination of a complete cross-section of the brain stem and the cerebellum (including the vermis, right and left lobes). If the cerebellum is not available, a diagnosis can be made by examination of brainstem and hippocampi (right and left). If possible, submit the head of large animals and the entire body of small animals.
When submitting only the brain, submit the entire brain. Submit fresh, chilled tissues only; do not fix the brain in chemical preservatives. Refrigerate, do not freeze specimens for rabies testing prior to shipping. However, if specimens have been inadvertently frozen, they may yield satisfactory results; do not thaw them prior to shipping.
Collect whole blood in a covered test tube.
Allow blood to clot by leaving the sample undisturbed at room temperature for 15-30 minutes.
Remove clot by centrifuging sample at 1000-2000 x g for 10 minutes. The resulting supernatant is the serum.
If collected in a serum separator tube, the sample is ready to package and ship. If a serum separator tube was not used, transfer the liquid component (serum) into a clean tube using a transfer pipette.
Refrigerate samples at 2-8 degrees C until ready to ship or transport.
Ship or transport on ice to maintain sample integrity.
EIA AGID testing will only be offered for serum samples indicated for export purposes, or if the sample handling/storage does not match the quality standards for EIA ELISA testing. For all other EIA testing requests, the EIA ELISA test will be run by default regardless of whether AGID has been requested on the EIA submission form.
EIA samples must be submitted by a Category II federally accredited veterinarian authorized to perform accredited duties in the state where the sample originated, or a state for federal animal health official.
A complete and legible USDA VS 10-11: Equine Infectious Anemia Laboratory Test form, Veterinary Services Process Streamlining (VSPS) EIA Test Form, or Global Vet Link (GLV) Laboratory Submittal Form must accompany each sample to be tested.
Sample tubes must be uniquely identifiable. Tubes should be labeled at minimum with the animal’s name. If two or more animals in the same shipment have the same name, additional information should be included in order to identify each sample (e.g., owner’s last name, GVL/VSPS ID, etc.). Samples that are not uniquely identifiable will not be tested.
Per USDA guidelines, EIA samples older than 30 days will be rejected as they do not reflect the current exposure status of the horse.
Follow serum collection guidelines as listed above. Separated serum should be transported on ice to maintain sample integrity.
Samples exhibiting hemolysis are not suitable for EIA ELISA testing. Samples with slight to moderate hemolysis will be tested by AGID.
Grossly hemolyzed or contaminated samples will not be tested.
Testing schedule is as follows:
Equine viral arteritis (EVA) testing requires separated serum and should be sent on ice. Ice packs should be contained in sealed plastic bags to prevent leakage.
All samples should be clearly labeled and accompanied by a completed Equine Viral Arteritis Submission Form [ Adobe PDF Document ]. Please note if multiple samples are to be combined or placed on separate reports.
EVA testing is scheduled on Tuesdays and Fridays. All results will be reported on Mondays and Fridays.
If the animal has been vaccinated for EVA or has a prior history of a positive EVA test, please make a note on the submission form. The lab will then complete a titer on the sample at the initial testing, which will give the veterinarian quicker results.
For additional assistance, call (321) 697-1400.