Stability of gametocyte-specific <it>Pfs</it>25-mRNA in dried blood spots on filter paper subjected to different storage conditions

• Main Authors: Pritsch Michael, Wieser Andreas, Soederstroem Victor, Poluda David, Eshetu Teferi, Hoelscher Michael, Schubert Soeren, Shock Jonathan, Loescher Thomas, Berens-Riha Nicole
• Format: Article
• Language: English
• Published: BMC 2012-04-01
• Series: Malaria Journal
• Subjects: Malaria; Gametocytes; <it>Plasmodium falciparum</it>; <it>Pfs</it>25-mRNA; Dried blood spots; Filter paper; Real-time QT-NASBA; Storage conditions; Epidemiology
• Online Access: http://www.malariajournal.com/content/11/1/138

<p>Abstract</p> <p>Background</p> <p>Real-time quantitative nucleic acid sequence-based amplification (QT-NASBA) is a sensitive method for detection of sub-microscopic gametocytaemia by measuring gametocyte-specific mRNA. Performing analysis on fresh whole blood samples is often not feasible in remote and resource-poor areas. Convenient methods for sample storage and transport are urgently needed.</p> <p>Methods</p> <p>Real-time QT-NASBA was performed on whole blood spiked with a dilution series of purified <it>in-vitro</it> cultivated gametocytes. The blood was either freshly processed or spotted on filter papers. Gametocyte detection sensitivity for QT-NASBA was determined and controlled by microscopy. Dried blood spot (DBS) samples were subjected to five different storage conditions and the loss of sensitivity over time was investigated. A formula to approximate the loss of <it>Pfs</it>25-mRNA due to different storage conditions and time was developed.</p> <p>Results</p> <p><it>Pfs</it>25-mRNA was measured in time to positivity (TTP) and correlated well with the microscopic counts and the theoretical concentrations of the dilution series. TTP results constantly indicated higher amounts of RNA in filter paper samples extracted after 24 hours than in immediately extracted fresh blood. Among investigated storage conditions freezing at −20°C performed best with 98.7% of the <it>Pfs</it>25-mRNA still detectable at day 28 compared to fresh blood samples. After 92 days, the RNA detection rate was only slightly decreased to 92.9%. Samples stored at 37°C showed most decay with only 64.5% of <it>Pfs</it>25-mRNA detectable after one month. The calculated theoretical detection limit for 24 h-old DBS filter paper samples was 0.0095 (95% CI: 0.0025 to 0.0380) per μl.</p> <p>Conclusions</p> <p>The results suggest that the application of DBS filter papers for quantification of <it>Plasmodium falciparum</it> gametocytes with real-time QT-NASBA is practical and recommendable. This method proved sensitive enough for detection of sub-microscopic densities even after prolonged storage. Decay rates can be predicted for different storage conditions as well as durations.</p>