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DOI 10.1371/journal.pntd.0002954

Медицинская библиотека · PLoS neglected tropical diseases · 2014

Performance of parasitological and molecular techniques for the diagnosis and surveillance of gambiense sleeping sickness.

Mumba Ngoyi Dieudonné, Ali Ekangu Rosine, Mumvemba Kodi Marie France, Pyana Patient Pati, Balharbi Fatima, Decq Mélanie, Kande Betu Victor, Van der Veken Wim, Sese Claude, Menten Joris, Büscher Philippe, Lejon Veerle

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

OBJECTIVES

Recently, improvements have been made to diagnostics for gambiense sleeping sickness control but their performance remains poorly documented and may depend on specimen processing prior to examination. In a prospective study in the Democratic Republic of the Congo, we compared the diagnostic performance of several parasite detection techniques, immune trypanolysis and of m18S PCR on whole blood stored in a stabilisation buffer or dried on filter paper.

METHODS

Individuals with CATT whole blood (WB) titer ≥1∶4 or with clinical signs indicative for sleeping sickness were examined for presence of trypanosomes in lymph node aspirate (LNA) and/or in blood. Blood was examined with Capillary Centrifugation Technique (CTC), mini-Anion Exchange Centrifugation Technique (mAECT) and mAECT on buffy coat (BC). PCR was performed on whole blood (i) stored in guanidine hydrochloride EDTA (GE) stabilisation buffer and (ii) dried on filter paper, and repeatability and reproducibility were assessed. Immune trypanolysis (TL) was performed on plasma.

RESULTS

A total of 237 persons were included. Among 143 parasitologically confirmed cases, 85.3% had a CATT-WB titre of ≥1/8, 39.2% were positive in LNA, 47.5% in CTC, 80.4% in mAECT-WB, 90.9% in mAECT-BC, 95.1% in TL and up to 89.5% in PCR on GE-stabilised blood. PCR on GE-stabilised blood showed highest repeatability (87.8%) and inter-laboratory reproducibility (86.9%). Of the 94 non-confirmed suspects, respectively 39.4% and 23.4% were TL or PCR positive. Suboptimal specificity of PCR and TL was also suggested by latent class analysis.

CONCLUSION

The combination of LNA examination with mAECT-BC offered excellent diagnostic sensitivity. For PCR, storage of blood in stabilisation buffer is to be preferred over filter paper. TL as well as PCR are useful for remote diagnosis but are not more sensitive than mAECT-BC. For TL and PCR, the specificity, and thus usefulness for management of non-confirmed suspects remain to be determined.

Для цитирования: Mumba Ngoyi Dieudonné, Ali Ekangu Rosine, Mumvemba Kodi Marie France, Pyana Patient Pati, Balharbi Fatima, Decq Mélanie, Kande Betu Victor, Van der Veken Wim, Sese Claude, Menten Joris, Büscher Philippe, Lejon Veerle. Performance of parasitological and molecular techniques for the diagnosis and surveillance of gambiense sleeping sickness.. PLoS neglected tropical diseases. 2014. DOI: 10.1371/journal.pntd.0002954.

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