Table 6-1.
Categorization of Antigen Detection Methods
| TECHNIQUE | TARGET | ADVANTAGES | DISADVANTAGES | EXAMPLE | NEW ADVANCES | COMMENTS |
|---|---|---|---|---|---|---|
| Cytology/biopsy | Whole organism | Fast, inexpensive, highly specific | Organism may not be in sample collected; training required to evaluate sample; labor-intensive | Histoplasma capsulatum in lung aspirate | Immunostaining, flow cytometry | Negative test does not rule out infection. |
| Microbiology | Whole organism | 24–48hr; can provide antimicrobial susceptibility; possible to perform indirect measurement of growth (gas production) | Limited by the growth traits of the organism (i.e., intracellular, fastidious, slow growth) | Salmonella, Mycobacterium spp. | Automation | Testing is limited to readily culturable organisms; cannot be used for viruses. |
| ELISA | Surface antigen, peptide | Easy to perform; rapid results; inexpensive; highly sensitive; patient-side testing available | FeLV, Dirofilaria, Giardia spp. | Molecular techniques for development of highly specific monoclonal antibodies | Substrate (blood, feces) differs depending on the organism. | |
| Latex agglutination | Surface antigen | Easy to perform; rapid results; inexpensive | Cryptococcus neoformans | Negative test does not rule out infection. | ||
| PCR | Nucleic acid sequence | Sensitive and specific; can detect minute amounts of DNA and RNA | Can detect residual organisms that are dead after successful treatment | Ehrlichia canis, FIV | Assay formats and equipment that minimize contamination and provide substantiating information (amplicon melting temperatures) | False negatives because of inhibitors; false positives because of contamination can occur; no established quality control protocols. |