Table 2.
Agenta | Optimal Standards | Minimal Standardsb | Comments |
---|---|---|---|
Vector‐borne pathogens—testing recommended | |||
Anaplasma phagocytophilum | Seronegative and PCR negative cats | PCR negative cats. Seronegative cats are an acceptable alternative if serologic testing is more economical or yields more rapid turnaround time than PCR. | Seropositive, PCR‐negative cats may be used in endemic regions if no other suitable donor can be identified. |
A. platys | PCR negative cats | No screening | There is no valid serological assay for cats. Infection of cats has only been occasionally documented. |
Bartonella henselae | Seronegative and PCR or culture negative cats | PCR negative cats | Around 70% of seropositive cats are PCR negative. In endemic areas, finding seronegative cats can be difficult and so use of seropositive, PCR negative cats may be needed. |
Other Bartonella spp. | PCR negative cats | No screening | Serologic assays are species‐specific, and assays are not readily available for many species. B. henselae appears to be the most pathogenic species. |
Cytauxzoon felis | PCR negative cats | No screening | Serology is not available. Testing using PCR is strongly recommended for cats with access to the outdoors that reside in endemic regions; cytologic examination of blood smears is not accurate. |
Ehrlichia canis and E. canis‐like | PCR negative cats | No screening | Infection of cats is extremely rare |
Mycoplasma haemofelis | PCR negative cats | PCR negative cats | Serologic assays are not available. Cytologic examination of blood smears is not accurate. The organism is a major primary pathogen and so PCR screening is always optimal. |
“Candidatus Mycoplasma haemominutum” | PCR negative cats | No screening | Serologic assays are not available. Cytologic examination of blood smears is not accurate. The organism is not considered a primary pathogen and is highly prevalent in the cat population, so screening could be considered optional. |
“Candidatus Mycoplasma turicensis” | PCR negative cats | No screening | Serologic assays are not available. “Candidatus M. turicensis” has never been detected using cytologic examination of blood smears, and cytology is not accurate for identification of hemoplasmas. The organism is not considered a primary pathogen and so screening could be considered optional. |
Neorickettsia risticii | PCR negative cats | No screening | Serology is not available. The organism has only rarely been associated with infection in cats |
Non vector‐borne pathogens—testing recommended | |||
Feline leukemia virus | Antigen negative and proviral DNA PCR negative cats | Antigen negative cats | Clinically validated proviral DNA assays are not routinely available in the United States. |
Feline immunodeficiency virus | Antibody negative cats | Antibody negative cats | It is currently not possible to accurately differentiate between an infected cat and an FIV‐vaccinated cat and so all positive cats should be excluded as donors. |
Other pathogens—testing not recommended | |||
Feline coronavirus | No screening | No screening | No documentation of virus transmission by blood transfusion. |
Rickettsia felis | No screening | No screening | While seropositive cats have been detected, the organism has not been found in the blood of cats in the United States. |
Toxoplasmosis | No screening | No screening | No documentation of virus transmission by blood transfusion. |
See the text for further discussion of geographic distribution and risk factors.
See the text for further discussion of specific tests.