Real-time PCR for diagnosis and follow-up of toxoplasma reactivation after allogeneic stem cell transplantation using fluorescence resonance energy transfer hybridization probes

被引:134
作者
Costa, JM
Pautas, C
Ernault, P
Foulet, F
Cordonnier, C
Bretagne, S
机构
[1] Hop Amer, Mol Biol Lab, F-92202 Neuilly, France
[2] Hop Henri Mondor, APHP, Serv Hematol Clin, F-94010 Creteil, France
[3] Hop Henri Mondor, APHP, Parasitol Lab, F-94010 Creteil, France
[4] Univ Paris 12, F-94010 Creteil, France
关键词
D O I
10.1128/JCM.38.8.2929-2932.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Toxoplasma reactivation is a life-threatening complication of allogeneic stem cell transplantation. A poor prognosis is probably linked to a difficult diagnosis, based on the detection of evidence of parasites in tissue. We developed a real-time PCR test using fluorescence resonance energy transfer hybridization probes to detect and quantify Toxoplasma gondii DNA in serum. This PCR test gave reproducible quantitative results over a dynamic range of from 0.75 x 10(6) to 0.75 parasites per PCR mixture. Serial samples from four patients with toxoplasma reactivation were evaluated. Three patients had several consecutive PCR-positive samples which corresponded to less than or equal to 0.75 parasites. These three patients became PCR negative during trimethoprim-sulfamethoxazole therapy but never developed clinically apparent toxoplasmosis. In contrast, one patient had an increasing PCR signal, from 1 to 396 parasites in 12 days, and developed cerebral symptoms. The parasite count decreased to 5 parasites in 3 days after pyrimethamine-clindamycin treatment. Real-time quantitative PCR is useful for diagnosis and follow-up of toxoplasma reactivation.
引用
收藏
页码:2929 / 2932
页数:4
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