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  Research articleUltra-sensitive detection of prion protein fibrils by flow cytometry in blood from cattle affected with bovine spongiform encephalopathyLothar Trieschmann1 1ACGT ProGenomics AG, Weinbergweg 22, D-06120 Halle (Saale), Germany 2Institute of Virology, Technical University of Munich, Biedersteinerstrasse 29, D-80802 Munich, Germany
BMC Biotechnology 2005, 5:26doi:10.1186/1472-6750-5-26 The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1472-6750/5/26
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2005 Trieschmann et al; licensee BioMed Central Ltd. AbstractBackgroundThe definite diagnosis of prion diseases such as Creutzfeldt-Jakob disease (CJD) in humans or bovine spongiform encephalopathy (BSE) in cattle currently relies on the post mortem detection of the pathological form of the prion protein (PrPSc) in brain tissue. Infectivity studies indicate that PrPSc may also be present in body fluids, even at presymptomatic stages of the disease, albeit at concentrations well below the detection limits of currently available analytical methods. ResultsWe developed a highly sensitive method for detecting prion protein aggregates that takes advantage of kinetic differences between seeded and unseeded polymerization of prion protein monomers. Detection of the aggregates was carried out by flow cytometry. In the presence of prion seeds, the association of labelled recombinant PrP monomers in plasma and serum proceeds much more efficiently than in the absence of seeds. In a diagnostic model system, synthetic PrP aggregates were detected down to a concentration of approximately 10-8 nM [0.24 fg/ml]. A specific signal was detected in six out of six available serum samples from BSE-positive cattle. ConclusionWe have developed a method based on seed-dependent PrP fibril formation that shows promising results in differentiating a small number of BSE-positive serum samples from healthy controls. This method may provide the basis for an ante mortem diagnostic test for prion diseases. BackgroundA group of fatal transmissible neurodegenerative diseases, including Creutzfeld-Jakob disease (CJD), bovine spongiform encephalopathy (BSE), chronic wasting disease (CWD) and scrapie, is caused by an unusual infectious agent that has been termed prion [1]. Prions consist of an aberrant isoform (PrPSc) of the normal cellular prion protein (PrPC). PrPC is a cell surface glycoprotein expressed in neurons [2] and other cell types [3,4]. The precise physiological function of the cellular prion protein is not known yet. PrPSc differs from PrPC in its higher content of β-sheet structure [5,6], its partial resistance to protease digestion [7], and its tendency to form large aggregates [8]. PrPSc propagates by converting the cellular prion protein to the PrPSc conformation [9]. PrPSc aggregates accumulate predominantly in the central nervous system (CNS), and definitive diagnosis of prion diseases currently relies on the post mortem detection of PrPSc in CNS tissue by immunohistochemistry, Western blotting, or ELISA [10]. Transmission studies indicate that prions may also be present in blood, potentially allowing for ante mortem diagnosis, but the sensitivity of the currently available analytical methods is insufficient for the detection of the extremely low prion titers that can be expected in body fluids [11]. Here, we report the development of a method based on kinetic differences between seeded and unseeded aggregation of prion protein that allows the detection of PrP aggregates in blood down to attomolar concentrations by flow cytometry. Results and discussionDetection of synthetic prion protein aggregates in serum or plasmaKinetic differences between seeded and spontaneous polymerization of peptide monomers can be used for the detection of amyloid β-protein aggregates in the cerebrospinal fluid of Alzheimer's disease patients [15]. Here, we extend the principle of seeded polymerization to the detection of prion protein aggregates. While trying to establish conditions for the labeling of synthetic prion protein aggregates with a fluorescently labeled prion protein probe, we observed that the formation of prion protein aggregates proceeds much less efficiently in serum or plasma (not shown) than in PBS (Fig. 1). This inhibition is probably caused by interactions of the prion protein probe with serum proteins.
Next, we found that the addition of preformed prion protein aggregates to plasma can partially overcome this inhibition (Fig. 2). The preformed aggregates presumably function as seeds that facilitate the formation of new aggregates in the inhibitory environment of plasma. The seeds stimulated the formation of prion protein aggregates at all concentrations tested, from 5 nM [120 ng/ml] to 10-8 nM [0.24 fg/ml] (Fig 2C). The average ratio of event counts in seeded samples to those in samples without seeds was 6.4. The number of events, however, was not proportional to the seed concentration, but remained relatively constant over the whole concentration range. Thus, the seed-dependent formation of prion protein aggregates can be used to detect extremely low amounts (down to the attomolar range) of spiked prion protein aggregates in blood.
Analysis of serum from clinical-stage, BSE-positive cattleStudies demonstrating the transmission of prion diseases by blood transfusion suggest that prions are present in the blood of afflicted animals and people, even at pre-symptomatic stages of the disease [16-18]. We used the method of seed-dependent fibril formation to analyze serum from six confirmed cases of clinical-stage, BSE-positive cattle and four controls. Based on the spiking experiments described above, our hypothesis was that any PrPSc aggregates present in serum may act as seeds for the formation of easily detectable amounts of labeled PrP aggregates, whereas in the absence of seeds the formation of PrP aggregates would be inhibited. The serum samples from BSE-positive cattle and controls from healthy cattle were incubated with 10 nM of a FITC-labeled bovine PrP probe at 37°C for 20 h with continuous shaking, followed by analysis in a flow cytometer. All six BSE-samples could be clearly distinguished by a population of events that was absent in the controls (Fig. 3A–J, green dots in region R3; quantification in fig. 3K).
ConclusionWe have developed a method based on seed-dependent PrP fibril formation that shows promising results in differentiating a small number of BSE-positive serum samples from healthy controls. More samples need to be tested in order to validate its potential as an ante mortem diagnostic test for BSE and other prion diseases. MethodsBiological fluidsSerum samples from six confirmed cases of BSE in cattle and four control animals were obtained from BFAV, Insel Riems, Germany. Control plasma was obtained from a blood bank. Labeling of prion proteinRecombinant full-length bovine PrP was produced as described previously [12,13]. The purified protein was labeled with a FITC-labeling kit (Roche) according to the manufacturer's instructions. Preparation of fibrils from recombinant prion protein25 μM of unlabeled bovine prion protein in PBS containing 0.2 % SDS was incubated for 10 min at room temperature, followed by a twentyfold dilution with PBS. For fibril formation, the diluted reaction mixture was incubated for 48 h at room temperature [14]. PrP fibril formation in serum or plasmaRecombinant FITC-labeled bovine prion protein was incubated in 150 μl serum or plasma at a concentration of 5 or 10 nM for 5–10 min. at 20°C, shaking at 550 rpm in an Eppendorf thermomixer, followed by an increase of the temperature to 37°C h at constant shaking speed. The incubation was continued for 20 h. Samples were then analyzed by flow cytometry. Flow cytometryAnalysis of the samples was carried out on a FACSVantage flow cytometer (BD Biosciences) at room temperature, measurement time was 30 sec per sample. Authors' contributionsLT participated in the design of the study, carried out the measurements and drafted the manuscript. ANS participated in the analysis of the data. EM prepared the recombinant protein. KK and ST were also involved in protein expression and purification. HS participated in the design and coordination of the study. GB conceived of the study and helped to draft the manuscript. All authors read and approved the final manuscript. AcknowledgementsThis work was kindly supported by grant No. 0312711A from the BMBF (Bundesministerium für Bildung und Forschung) in the context of the German National TSE Research Platform. The authors gratefully acknowledge the help of the TSE Research Platform, Munich, and the BFAV Riems, Germany, with respect to the kind gift of biological material in the context of this study. References
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