primate assay data sheet
Toxoplasma gondii
Test code: X0002
- Qualitative detection of Toxoplasma gondii by
polymerase chain reaction
Infections by Toxoplasma gondii are
prevalent in many species of domestic and wild animals (Dubey,
1993). Although chronic infection of this obligate parasite is
usually asymptomatic, T. gondii has emerged as a major
opportunistic pathogen in the immunocompromised, such as AIDS
patients. Surprisingly, spontaneous cases of fulminating fatal
toxoplasmosis have been reported in adult squirrel monkeys
(Saimiri sciureus) which are immunologically normal (Inoue,
1997). While the disease mechanism of this fatal toxoplasmosis
in squirrel monkeys is not clear, infections of nonhuman
primates with this parasite are common, and it has been shown
that New World monkeys are more susceptible to T. gondii
infection than Old World monkeys (Ruch, 1959). The outbreak of
fatal toxoplasmosis (Cunningham, et al., 1992) is a major
concern in caring for these primate colonies, as a recent
study has indicated the possibility of horizontal transmission
through the respiratory route (Furuta, et al., 2001) in
addition to the fecal-oral route.
The “gold standard” for the detection of
T. gondii in clinical specimens is mouse inoculation and
detection of T. gondii specific antibodies. This method is
sensitive and specific but very time-consuming, taking up to
six weeks to obtain a diagnosis. Cell culture detection of
this parasite is also slow, and lacks sensitivity. PCR
detection of this parasite has been found to be a sensitive,
specific and rapid method for the detection of T. gondii
DNA
in a wide spectrum of samples, such as amniotic fluid (Grover,
et al., 1990), blood (Dupouy-Camet, et al., 1993; Ho-Yen, et
al., 1992), tissue samples (Johnson, et al., 1993) and
cerebrospinal fluid (Cristina, et al., 1993; Farmley, et al.,
1992). Although serology testing can help diagnose recent
infection with this parasite, PCR testing is found to be more
sensitive in identifying acute infection (Hussein, et al.,
2002).
Utilities:
- Confirm the disease causing agent
- Ensure that animal colonies are free of
T. gondii
- Early prevention of spread of this
parasite among a colony
- Minimize personnel exposure to this
parasite
- Safety monitoring of biological products
and vaccines that derive from primates
References:
Dubey, J.P. (1993) Toxoplasma, Neoplasma, Sarcocystis, and
other tissue cyst-forming coccidian of human and animals.
pp1-56. In: Parasitic protozoa (Kreier, P.J. ed), vol. 6, 2nd
ed., Academic Press, Inc., San Diego, California.
Inoue, M. (1997) Acute toxoplasmosis in squirrel monkeys. J.
Vet. Med. Sci. 59:593-595.
Ruch, T.C. (1959). pp.297-299, 313-318, 423-424. In:
Diseases of laboratory primates. W.B. Saunders Co.,
Philadelphia.
Cunningham, A.A., Buxton, D. and Thomson, K.M. (1992) An
epidemic of toxoplasmosis in a captive colony of squirrel
monkeys (Saimiri sciureus). J. Comp. Pathol. 107:207-219.
Furuta, T., Une, Y., Omura, M., Matsutani, N., Nomura, Y.,
Kikuchi, T., Hattori, S. and Yoshikawa, Y. (2001) Horizontal
transmission of Toxoplasma gondii in squirrel monkeys (Saimiri
sciureus). Exp. Anim. 50:299-306.
Grover, M.C., Thulliez, P., Remington, J.S. and Boothroyd,
J.C. (1990) Rapid prenatal diagnosis of congenital Toxoplasma
infection by using polymerase chain reaction and amniotic
fluid. J. Clin. Microbiol. 28:2297-2301.
Dupouy-Camet, J., de Souza, S.L., Maslo, C., Paugam, A.,
Saimot, A.G., Benarous, R., Tourte-Schaefer, C. and Derouin,
F. (1993) Detection of Toxoplasma gondii in venous blood from
AIDS patients by polymerase chain reaction. J. Clin. Microbiol.
31:1866-1869.
Ho-Yen, D.O., Joss, A.W.L., Balflour, A.H., Smyth, E.T.M.,
Baird, D. and Chatterton, J.M.W. (1992) Use of the polymerase
chain reaction to detect Toxoplasma gondii in human blood
samples. J. Clin. Pathol. 45:910-913.
Johnson, J.D., Butcher, P.D., Savva, D. and Holliman, R.E.
(1993) Application of the polymerase chain reaction to the
diagnosis of human toxoplasmosis. J. Infect. 26:147-158.
Cristina, N.H., Pelloux, C., Goulhot, J.P., Brion, P.,
Leclercq, P. and Ambrosis-Thomas, P. (1993) Detection of
Toxoplasma gondii in AIDS patients by the polymerase chain
reaction. Infection 21:150-153.
Farmley, S.F., Goebel, F.D. and Remington, J.S. (1992)
Detection of Toxoplasma gondii in cerebrospinal fluid from
AIDS patients by polymerase chain reaction. J. Clin. Microbiol.
30:3000-3002.
Hussein, A.H., Nagaty, I.M. and Fouad, M.A. (2002)
Evaluation of IgM-ELISA versus PCR in diagnosis of recent
Toxoplasma gondii infection. J Egypt Soc Parasitol. 32:639-46.
Specimen requirement: 1 ml
whole blood in EDTA (purple top) or ACD (yellow top) tube, or
1 ml amniotic fluid, CSF or tissue, shipped overnight at room
temperature; or tissue shipped frozen.
For specimen types other than those listed
here, please call to confirm specimen acceptability and
shipping instructions.
For all specimen types, if there will be a
delay in shipping, or during very warm weather, refrigerate
specimens until shipped and ship with a cold pack unless more
stringent shipping requirements are specified. Frozen
specimens should be shipped so as to remain frozen in transit.
See shipping instructions for
more information.
Turnaround time: 2 business
days
Methodology: Qualitative
PCR
Normal range: Nondetected