Printer Friendly

Distribution and quantitative estimates of variant Creutzfeldt-Jakob disease prions in tissues of clinical and asymptomatic patients.

Prion diseases, or transmissible spongiform encephalopathies (TSEs), are fatal neurodegenerative disorders that occur naturally in sheep (scrapie), cattle (bovine spongiform encephalopathy [BSE]), and humans (Creutzfeldt-Jakob disease [CJD]). A key event in the pathogenesis of TSEs is the conversion of the normal cellular prion protein ([PrP.sup.C], encoded by the PRNP gene) into an abnormal disease-associated isoform ([PrP.sup.Sc]) in tissues of infected animals. [PrP.sup.C] is completely degraded after controlled digestion with proteinase K in the presence of nondenaturing detergents. In contrast, [PrP.sup.Sc] is N terminally truncated under the same conditions, resulting in a proteinase K-resistant prion ([PrP.sup.res]) (1).

In 1996, a new form of CJD, termed variant CJD (vCJD) was identified in the United Kingdom. vCJD is believed to result from zoonotic transmission of the BSE agent, probably as a consequence of dietary exposure to BSE-contaminated meat products (2,3). The total number of clinical cases of vCJD thus far identified is limited (227 patients worldwide at the time of writing this article). However, the estimated prevalence of asymptomatic vCJD in populations exposed to the BSE agent is uncertain (4).

In the United Kingdom, 32,441 appendix samples collected during surgery from patients born during 1941-1985 have been tested for abnormal prion protein accumulation by using immunohistochemical analysis. This study reported a vCJD prevalence estimate of 1/2,000 in persons in these age cohorts (95% CI 1/3,500-1/1,250) (5). No comparable data are available concerning the prevalence of asymptomatic vCJD in other countries, although BSE exposure is known to have occurred in several countries in continental Europe, as judged by cases of vCJD that are not attributable to exposure in the United Kingdom (http://www.cjd.ed.ac.uk/documents/ worldfigs.pdf).

Over the past 2 decades, several studies have reported on the distribution of the vCJD agent in tissues of infected patients (6-8). Most of these studies did not detect the vCJD agent outside the nervous system (central, peripheral, and autonomic) and lymphoid tissues. However, the sensitivity of detection techniques for [PrP.sup.res] used in these investigations was limited.

Protein misfolding cyclic amplification (PMCA) is believed to mimic prion replication in vitro, but in an accelerated form, which enables amplification of minute amounts of [PrP.sup.Sc] and prion infectivity (9). In PMCA, a [PrP.sup.C]-containing substrate is combined with a seed that might contain otherwise undetectable amounts of [PrP.sup.Sc]. After repeated cycles of incubation and sonication, the amount of [PrP.sup.Sc] increases to levels at which they can be detected by using conventional biochemical techniques. Recently, our group and others have shown that PMCA can detect endogenous vCJD agent in patient biologic fluids such as urine and blood (10,11).

In this study, we evaluated the relative sensitivity of PMCA versus that of bioassay in mice for detection of the vCJD agent. We estimated by using PMCA the level of vCJD prions in 21 tissues collected from 4 patients who died of symptomatic vCJD and from a patient with asymptomatic vCJD. We also determined whether vCJD prion levels, as estimated by using PMCA, were consistent with infectious titers, as estimated by bioassay with transgenic mice.

Methods

Ethics Statements

All animal experiments were performed in compliance with institutional and French national guidelines and in accordance with the European Community Council Directive 86/609/EEC. Animal experiments that were part of this study (national registration no. 01734.01) were approved by the local ethic committee of the Ecole Nationale Veterinaire de Toulouse (Toulouse, France). Mouse inoculations were performed under anesthesia with isofulorane. Mice that displayed clinical signs of disease were anesthetized with isofluorane before being humanely killed by inhalation of C[O.sub.2].

Human samples were obtained from the United Kingdom National CJD Research and Surveillance Unit Brain and Tissue Bank, which is part of the Medical Research Council Edinburgh Brain Bank (Edinburgh, Scotland, UK). Tissue samples were pseudo-anonymized by using a Brain Bank reference number. All case-patients in the United Kingdom provided informed consent. Use of samples in this study was approved by the East of Scotland Research Ethics Service for the Edinburgh Brain Bank (16/ES/0084).

vCJD and Control Patients

We investigated tissues from 4 clinical vCJD case-patients (vCJD-1-vCJD-4) and 1 asymptomatic person with vCJD who had received a transfusion of packed erythrocytes from a donor who subsequently died from vCJD (12). Tissues from 2 non-vCJD-affected patients were used as controls. For case-patients who provided appropriate consent, the entire PRNP gene coding sequence was established to exclude pathogenic mutations in this gene (13,14).

Mouse Bioassays

Bioassays were performed by using mice expressing bovine PrP (tgBov-tg110) as described (15,16). These mice were observed daily and their neurologic status was assessed weekly. When clinically progressive TSE symptoms were evident, or at the end of their lifespan, the animals were euthanized. Survival time was expressed as the mean [+ or -] SD days postinoculation of mice positive for [PrP.sup.res]. For mice that showed no clinical signs, they were humanely killed at the end of their natural lifespan (600-800 days). In these instances, incubation periods are reported as >600 days postinoculation, which corresponded to survival time observed for [greater than or equal to] 3 of 6 mice.

Estimation of Infectious Prion Titers

We estimated infectious titer in a reference 10% (wt/vol) frontal cortex homogenate from a clinical vCJD patient by using endpoint titration (intracerebral route) in tgBov mice. Infectious titer (50% lethal dose/g intracerebral in tgBov mice) was estimated by using the Spearman method.

The titer of prion infectivity in vCJD-affected patient bone marrow samples was estimated by using the method of Arnold et al. (17). This method uses the probability of survival (attack rate at each dilution) and the individual mouse incubation periods at each dilution to estimate infectious load and is thus able to provide more accurate estimation of titer than using either attack rate or incubation period data alone.

PMCA Reactions

A transgenic mouse line that expresses ovine [A.sub.136][R.sub.154][Q.sub.171] PrP variant [PrP.sup.C] (tgShXI) was used to prepare the PMCA substrate as described (18,19). PMCA amplification was performed as described (11). Each PMCA experiment included a reference vCJD sample (10% brain homogenate) as a control for the amplification efficiency. Unseeded controls (1 unseeded control for 8 seeded reactions) were also included in each experiment. For each tested dilution of each sample, [greater than or equal to] 4 replicates were tested in 2 independent experiments. For each sample, the highest dilution showing [greater than or equal to] 50% of positive replicates (presence of detectable [PrP.sup.res] in the reaction as assessed by using Western blotting) was determined.

Detection of Abnormal PrP by Western Blotting and Paraffin-Embedded Tissue Blotting

Extraction of proteinase K-resistant abnormal PrP and Western blotting were performed as described (11). Immunodetection was performed by using 2 PrP-specific monoclonal antibodies, Sha31 (1 [micro]g/mL) (20), and 12B2 (4 [micro]g/mL) (21), which recognize amino acid sequences YEDRYYRE (145-152), and WGQGG (89-93), respectively. Paraffin-embedded tissue blotting was performed as described (22,23).

Results

Sensitivity of vCJD Agent Detection by PMCA and Bioassay

To determine the relative sensitivity of PMCA, we retitrated a reference sample (10% cerebral cortex homogenate from a vCJD-affected patient) that had previously undergone endpoint titration (IC inoculation route; Table 1) in bovine PrP-expressing mice (tgBov). Amplification of a 10-fold serial dilution of this sample (6 individual replicates/dilution point) demonstrated that 4 PMCA rounds (24 hours/round, i.e., 96 h) were sufficient to reach the maximum sensitivity level of the assay. Additional PMCA rounds did not improve the analytical sensitivity of the assay or the number of positive replicates (Table 2; Figure 1). On the basis of these results, we estimated by using the Spearman method that the seeding activity of the isolate was [10.sup.11] 50% seeding activity/per g. Bioassay endpoint titration data for the same sample in tgBov mice showed an infectious titer of [10.sup.7.7] [LD.sub.50]/g. When we took into account the 4-fold lower amount of material used to seed the PMCA reaction compared with material used in mouse inoculations, we found that the PMCA protocol used was 465 times more sensitive than the bioassay of tgBov mice for detection of vCJD prions.

PMCA for Control and vCJD Patients

We complied basic demographic data for vCJD and control patients (Table 3). A 10-fold dilution series of 10% homogenates from the vCJD-affected and non-vCJD-afected control patients was prepared, and this series was subjected to 4 rounds of PMCA. Amplification products from each round were tested for [PrP.sup.res] using by Western blotting (Table 4; Figure 2).

We found that none of the reactions seeded with tissue homogenates from non-CJD controls were positive for [PrP.sup.res] (Table 4). In contrast, PMCA reactions seeded with tissues from the 4 symptomatic vCJD patients were positive for [PrP.sup.res] (Table 4; Figure 2). As expected, among tested tissues, brain homogenates (temporal cortex) showed the highest seeding activity (highest [PrP.sup.res]-positive dilution [10.sup.-8]). All lymphoid organs tested also showed seeding activity, but the highest PMCA-positive dilution varied according to the organs tested from [10.sup.-2] (thymus) to [10.sup.-6] (distal ileum and tonsil). Moreover, for a given lymphoid organ, [less than or equal to] [10.sup.2]-fold differences was observed in seeding activity, depending on the patient and sample tested. These data indicate that for symptomatic vCJD patients, lymphoid organs contain [10.sup.2]-[10.sup.6]-fold less prion seeding activity than the same amount of brain tissue (Table 4).

Salivary gland, adrenal gland, liver, and bone marrow from the 4 symptomatic vCJD patients showed positive reactions by PMCA (Figures 2, 3). Using the highest dilution to show a positive reaction as a measure of seeding activity, we found that the vCJD agent in these tissues was [10.sup.3]-[10.sup.6]-fold lower than that for the brain. [PrP.sup.res] was also detected by PMCA reactions seeded with heart, liver, kidney, skeletal muscle, several endocrine/exocrine glands (pancreas, thyroid), and gonads, from some, but not all, of the 4 clinical vCJD patients. Positive tissues contained a level of vCJD seeding activity that was equivalent to those observed in distal ileum (i.e., [10.sup.3]-[10.sup.6]-fold lower than for the brain). Irrespective of the tissue used to seed the PMCA reactions, the [PrP.sup.res] Western blot profile for positive reactions was indistinguishable from that observed in reactions seeded with the vCJD brain control (Figure 3).

Analysis of Tissues from an Asymptomatic vCJD-Infected Person

Prion seeding activity was not detected in the brain (temporal cortex) of the asymptomatic vCJD-affected patient, who was infected with a PRNP gene codon 129 heterozygote (Met/[Val.sub.129]) prion (12) (Table 4; Figure 2). PMCA reactions seeded with dorsal root ganglia or trigeminal ganglia homogenates from this patient showed negative results. However, seeding activity was detected in the pituitary gland (highest [PrP.sup.res]-positive dilution [10.sup.-2]). In addition, as for the symptomatic vCJD patient, PMCA amplification readily detected vCJD prions in all lymphoid organs tested from this asymptomatic person. On the basis of PMCA results, the vCJD agent load in lymphoid organs in this asymptomatic patient infected with the PRNP gene codon 129 Met/[Val.sub.129] prion was similar to those for patients infected with Met/[Met.sub.129] prions during the clinical stage of disease.

In addition to findings for lymphoid organs, prion seeding activity was detectable in certain peripheral tissues (salivary gland, lung, and liver) from this patient (Tables 4; Figures 2, 3). Certain tissues, such as bone marrow or adrenal gland, that contained a substantial prion seeding activity in the clinically affected patients showed negative results. Again, the [PrP.sup.res] Western blot profile for positive reactions was indistinguishable from that observed for reactions seeded with the vCJD brain control.

vCJD Infectivity in Bone Marrow

To test whether PMCA seeding activity in peripheral tissues from vCJD patients correlated with infectivity, we inoculated bone marrow samples from the symptomatic patient into tgBov mice. Clinical TSE was observed in mice that were inoculated with each of the 4 bone marrow samples. The [PrP.sup.res] Western blot profile and the [PrP.sup.res] distribution pattern, as assessed by paraffin-embedded tissue blotting for brain of the bone marrow-inoculated mice, were identical to those observed in tgBov mice inoculated with the vCJD brain control sample (Figure 4).

Data obtained for mice inoculated with bone marrow samples were also used to estimate prion infectivity levels in these samples. For this purpose, we applied the method of Arnold et al. (77). This method combines the probability of survival (attack rate) and the individual mouse incubation period to provide an estimation of infectious titers. We used data corresponding to endpoint titration in tgBov mice for reference vCJD sample (frontal cortex from a clinical vCJD patient) (Table 1) to derive the relationship between prion titer of inoculum and the probability of infection and length of the incubation period (Figure 5). We found that bone marrow samples had an infectious titer that ranged from [10.sup.2.3][LD.sub.50]/g through [10.sup.4.7] [LD.sub.50]/g in tgBov mice (Table 5).

These values are consistent with a [10.sup.3]-[10.sup.5] lower infectivity load in bone marrow samples than in the reference vCJD brain sample. Consistent with the PMCA results (Table 4), we found that prion load in bone marrow samples (highest [PrP.sup.res]-positive dilution [[10.sup.-3]-[10.sup.-5]]) was also [10.sup.3]-[10.sup.5]-fold lower than for the reference vCJD isolate (highest [PrP.sup.res]-positive dilution [[10.sup.-8]]). These results strongly support the idea that PMCA seeding activity provides a reliable estimate of the prion load in tissues from vCJD-infected patients.

Discussion

Most previous studies with tissue from vCJD patients have failed to identify consistent accumulation of the vCJD agent outside the nervous and lymphoreticular systems. However, data obtained in this study clearly demonstrate the presence of vCJD prions in a wide and unexpected variety of peripheral tissues.

Natural scrapie and experimental BSE in sheep are 2 models of orally transmitted prion diseases (24,25). In both diseases, the agent accumulates in the lymphoreticular system and the enteric nervous system during the early preclinical phase of the incubation period. Moreover, an early and persistent prionemia is observed in asymptomatic infected animals (26,27). These features were also observed in vCJD in humans and in view of the likely origin of vCJD (oral exposure to BSE agent), these similarities have led to a consensus that BSE and scrapie in sheep and vCJD in human have a common pathogenesis (28).

Although vCJD prions in a variety tissues, such as bone marrow, kidney, salivary gland, skeletal muscle, pancreas, liver, or heart, might be surprising, each of these tissue has already been demonstrated to accumulate prion infectivity or abnormal prion protein in TSE-infected sheep (29-33). Because low levels of infectivity have been reported in blood fractions from a vCJD-affected patient, such widespread tissue positivity might be derived from residual blood, rather than from the solid tissue in these samples (16). However, this proposal seems unlikely because in whole blood PMCA amplification inhibitors preclude detection of endogenous vCJD agent by this method (11,34-36).

The patient in our study who was infected with a prion containing PRNP gene codon 129 Met/Val is 1 of only 2 identified vCJD agent-infected persons known to have died of other causes before onset clinical symptoms of vCJD, and the only person who provided consent to sample autopsy tissues for research. For this patient, all previous investigations did not detect abnormal prion protein or infectivity in the brain (12,37). The negative PMCA results e obtained for cerebral cortex, dorsal root ganglia, and trigeminal ganglia tissue from this patient are consistent with a lack of central nervous system involvement at the time of death. However, PMCA seeding activity in the pituitary gland was surprising in this instance.

The presence of abnormal prion protein accumulation in the pituitary gland and other circumventricular organs before deposition of [PrP.sup.res] in surrounding brain has been reported in TSE-infected sheep (38). However, this phenomenon in animals does not represent the main route for neuroinvasion and is a probable consequence of hematogenous dissemination of the TSE agent through the fenestrated capillary system of the circumventricular organs, which is substantially more permeable than the other capillaries in the brain (blood-brain barrier). Therefore, this finding might be a consequence of the hematogenous route of secondary vCJD in this person (by transfusion of packed erythrocytes from a vCJD-infected donor), in contrast to the oral route of infection in primary clinical vCJD cases (12).

vCJD prions were detected in certain peripheral tissues from the patients infected with a prion containing the PRNP gene codon 129 Met/Val. Although distribution of vCJD seeding activity in lymphoreticular tissues was similar to that observed for symptomatic vCJD patients, several tissues that were positive in clinically affected patients were negative in this heterozygous asymptomatic person. These findings suggest that involvement of some peripheral tissues might occur at a later stage in the incubation period than others, or that they could involve recirculation of the agent from the central nervous system (i.e., centrifugal spread in a late state). However, we cannot discount the possibility that that these differences in tissue distribution are caused by the hematogenous route of infection in this person (as opposed to the probable oral route in patients with clinical vCJD) or the difference between the PRNP gene codon 129 genotype of the asymptomatic vCJD-affected person (PRNP gene codon 129 Met/Val) and persons with clinical vCJD (PRNP gene codon 129 Met/Met).

Irrespective of the actual explanation for these differences, the presence of vCJD agent in peripheral tissues of patients during preclinical and clinical stage of the disease indicates the potential for iatrogenic transmission of this fatal neurologic condition by surgical procedures. Furthermore, this finding shows that, for certain peripheral tissues, a level of infectivity equivalent to an end stage titer (and attendant risk) is reached at a preclinical stage.

Several hundred cases of iatrogenic CJD have been reported worldwide. These cases appear to result from transmission of sporadic CJD, and most cases have occurred in recipients of human dura mater grafts or after administration of human growth hormone extracted from cadaveric pituitaries (39). Although in sporadic CJD the distribution of the agent is largely restricted to the nervous system (central and peripheral), the wide distribution of the vCJD agent in the asymptomatic infected patient we report might serve to increase the range of medical procedures, including dentistry, organ transplant, and surgery involving nondisposable equipment, that might result in iatrogenic transmission of vCJD (40-43).

Nevertheless, >20 years after identification of the first vCJD patients, only 5 cases that are a probable consequence of iatrogenic vCJD transmission are known, all in the United Kingdom and associated with blood and blood products. These cases were caused by transfusion of non-leukocyte-depleted erythrocyte concentrates or by treatment involving large amounts of pooled plasma from the United Kingdom that were known to include donations from persons who later showed development of vCJD (12,44-46).

None of the 220 other vCJD cases identified worldwide have been linked to any other medical or dental procedure. Whereas this fact is reassuring, it would be unwise to disregard the threat that vCJD still poses for public health. Despite the relatively low number (n = 178) of vCJD clinical cases observed in the United Kingdom, the most recent epidemiologic studies indicate that [approximately equal to]1 of 2,000 persons in the United Kingdom could be infected with the vCJD agent (as indicated by the presence of abnormal prion protein detected by immunohistochemical analysis of lymphoid follicles in the appendix). Each asymptomatic vCJD-infected person represents a potential source of secondary infection. The data in our report offer an opportunity for refining measures that were implemented in many countries to limit the risk for vCJD iatrogenic transmission. The apparent concordance between PMCA biochemical and infectivity bioassay data, and the higher analytical sensitivity of PMCA, suggest that future research need not rely exclusively on time-consuming and costly animal bioassay.

Our results indicate the need for vCJD screening assays. After more than a decade of effort, several vCJD blood detection tests have reached a stage in their development that could enable their evaluation as screening or confirmatory assays (11,47,48). In particular, there is now a strong case for use of PMCA in a highly sensitive and specific blood test for vCJD, as indicated by our previous studies (11,16) and studies by Bougard et al. (35) and Concha-Marambio et al. (36). The relationship shown here between [PrP.sup.res] amplification by PMCA and detection of infectivity by bioassay indicates that PMCA seeding activity is a good surrogate marker of infectivity and could provide a sound basis for a vCJD blood test for use with blood or tissue donors.

This study was supported in part by the Department of Health Policy Research Programme and the Scottish Government. The National CJD Research and Surveillance Unit is supported by the Policy Research Program of the Department of Health and the Scottish Government (DH121/5061). The Edinburgh Brain Bank is supported by the Medical Research Council (MRC grant G0900580). The Unite Mixte de Recherche 1225, Ecole Nationale Veterinaire de Toulouse was supported by the European Union FEDER/INTERREG (EFA282/13 TRANSPRION), the Institut National de la Recherche Agronomique Institut Carnot en Sante Animale, and an Agence Nationale Recherche grant (Unmasking Blood Prions; ANR-15-CE18-0028).

Dr. Douet is a research scientist and assistant lecturer in ophthalmology at the National Veterinary School of Toulouse, Toulouse, France. His primary research interests are the pathogenesis of the prion disease with special emphasis on the iatrogenic risk of transmission.

References

(1.) McKinley MP, Bolton DC, Prusiner SB. A protease-resistant protein is a structural component of the scrapie prion. Cell. 1983; 35:57-62. http://dx.doi.org/10.1016/0092-8674(83)90207-6

(2.) Bruce ME, Will RG, Ironside JW, McConnell I, Drummond D, Suttie A, et al. Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent. Nature. 1997; 389:498-501. http://dx.doi.org/10.1038/39057

(3.) Collinge J, Sidle KC, Meads J, Ironside J, Hill AF. Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD. Nature. 1996; 383:685-90. http://dx.doi.org/ 10.1038/383685a0

(4.) Garske T, Ghani AC. Uncertainty in the tail of the variant Creutzfeldt-Jakob disease epidemic in the UK. PLoS One. 2010; 5:e15626. http://dx.doi.org/10.1371/journal.pone.0015626

(5.) Gill ON, Spencer Y, Richard-Loendt A, Kelly C, Dabaghian R, Boyes L, et al. Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey. BMJ. 2013; 347:f5675. http://dx.doi.org/10.1136/ bmj.f5675

(6.) Wadsworth JD, Joiner S, Hill AF, Campbell TA, Desbruslais M, Luthert PJ, et al. Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay. Lancet. 2001; 358:171-80. http://dx.doi.org/10.1016/S0140-6736(01)05403-4

(7.) Haik S, Faucheux BA, Sazdovitch V, Privat N, Kemeny JL, Perret-Liaudet A, et al. The sympathetic nervous system is involved in variant Creutzfeldt-Jakob disease. Nat Med. 2003; 9:1121-3. http://dx.doi.org/10.1038/nm922

(8.) Head MW, Ritchie D, Smith N, McLoughlin V, Nailon W, Samad S, et al. Peripheral tissue involvement in sporadic, iatrogenic, and variant Creutzfeldt-Jakob disease: an immunohistochemical, quantitative, and biochemical study. Am J Pathol. 2004; 164:143-53. http://dx.doi.org/10.1016/ S0002-9440(10)63105-7

(9.) Saborio GP, Permanne B, Soto C. Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding. Nature. 2001; 411:810-3. http://dx.doi.org/10.1038/35081095

(10.) Moda F, Gambetti P, Notari S, Concha-Marambio L, Catania M, Park KW, et al. Prions in the urine of patients with variant Creutzfeldt-Jakob disease. N Engl J Med. 2014; 371:530-9. http://dx.doi.org/10.1056/NEJMoa1404401

(11.) Lacroux C, Comoy E, Moudjou M, Perret-Liaudet A, Lugan S, Litaise C, et al. Preclinical detection of variant CJD and BSE prions in blood. PLoS Pathog. 2014; 10:e1004202. http://dx.doi.org/ 10.1371/journal.ppat.1004202

(12.) Peden AH, Head MW, Ritchie DL, Bell JE, Ironside JW. Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient. Lancet. 2004; 364:527-9. http://dx.doi.org/ 10.1016/S0140-6736(04)16811-6

(13.) Uro-Coste E, Cassard H, Simon S, Lugan S, Bilheude JM, Perret-Liaudet A, et al. Beyond [PrP.sup.res] type 1/type 2 dichotomy in Creutzfeldt-Jakob disease. PLoS Pathog. 2008; 4:e1000029. http://dx.doi.org/10.1371/journal.ppat.1000029

(14.) Moreno CR, Moazami-Goudarzi K, Laurent P, Cazeau G, Andreoletti O, Chadi S, et al. Which PrP haplotypes in a French sheep population are the most susceptible to atypical scrapie? Arch Virol. 2007; 152:1229-32. http://dx.doi.org/10.1007/s00705-007-0956-7

(15.) Castilla J, Gutierrez Adan A, Brun A, Pintado B, Ramirez MA, Parra B, et al. Early detection of [PrP.sup.res] in BSE-infected bovine PrP transgenic mice. Arch Virol. 2003; 148:677-91. http://dx.doi.org/10.1007/s00705-002-0958-4

(16.) Douet JY, Zafar S, Perret-Liaudet A, Lacroux C, Lugan S, Aron N, et al. Detection of infectivity in blood of persons with variant and sporadic Creutzfeldt-Jakob disease. Emerg Infect Dis. 2014; 20:114-7. http://dx.doi.org/10.3201/eid2001.130353

(17.) Arnold ME, Hawkins SA, Green R, Dexter I, Wells GA. Pathogenesis of experimental bovine spongiform encephalopathy (BSE): estimation of tissue infectivity according to incubation period. Vet Res. 2009; 40:8. http://dx.doi.org/10.1051/vetres:2008046

(18.) Groschup MH, Buschmann A. Rodent models for prion diseases. Vet Res. 2008; 39:32. http://dx.doi.org/10.1051/vetres:2008008

(19.) Douet JY, Lacroux C, Corbiere F, Litaise C, Simmons H, Lugan S, et al. PrP expression level and sensitivity to prion infection. J Virol. 2014; 88:5870-2. http://dx.doi.org/10.1128/JVI.00369-14

(20.) Feraudet C, Morel N, Simon S, Volland H, Frobert Y, Creminon C, et al. Screening of 145 anti-PrP monoclonal antibodies for their capacity to inhibit [PrP.sup.Sc] replication in infected cells. J Biol Chem. 2005; 280:11247-58. http://dx.doi.org/10.1074/jbc.M407006200

(21.) Langeveld JP, Jacobs JG, Erkens JH, Bossers A, van Zijderveld FG, van Keulen LJ. Rapid and discriminatory diagnosis of scrapie and BSE in retro-pharyngeal lymph nodes of sheep. BMC Vet Res. 2006; 2:19. http://dx.doi.org/10.1186/1746-6148-2-19

(22.) Cassard H, Torres JM, Lacroux C, Douet JY, Benestad SL, Lantier F, et al. Evidence for zoonotic potential of ovine scrapie prions. Nat Commun. 2014; 5:5821. http://dx.doi.org/10.1038/ ncomms6821

(23.) Lacroux C, Corbiere F, Tabouret G, Lugan S, Costes P, Mathey J, et al. Dynamics and genetics of [PrP.sup.Sc] placental accumulation in sheep. J Gen Virol. 2007; 88:1056-61. http://dx.doi.org/10.1099/ vir.0.82218-0

(24.) Andreoletti O, Berthon P, Marc D, Sarradin P, Grosclaude J, van Keulen L, et al. Early accumulation of PrP(Sc) in gut-associated lymphoid and nervous tissues of susceptible sheep from a Romanov flock with natural scrapie. J Gen Virol. 2000; 81:3115-26. http://dx.doi.org/10.1099/0022-1317-81-12-3115

(25.) Foster JD, Parnham DW, Hunter N, Bruce M. Distribution of the prion protein in sheep terminally affected with BSE following experimental oral transmission. J Gen Virol. 2001; 82:2319-26. http://dx.doi.org/10.1099/0022-1317-82-10-2319

(26.) Lacroux C, Vilette D, Fernandez-Borges N, Litaise C, Lugan S, Morel N, et al. Prionemia and leukocyte-platelet-associated infectivity in sheep transmissible spongiform encephalopathy models. J Virol. 2012; 86:2056-66. http://dx.doi.org/10.1128/ JVI.06532-11

(27.) Houston F, Foster JD, Chong A, Hunter N, Bostock CJ. Transmission of BSE by blood transfusion in sheep. Lancet. 2000; 356:999-1000. http://dx.doi.org/10.1016/S0140-6736(00)02719-7

(28.) Hilton DA. Pathogenesis and prevalence of variant CreutzfeldtJakob disease. J Pathol. 2006; 208:134-41. http://dx.doi.org/ 10.1002/path.1880

(29.) Tamguney G, Richt JA, Hamir AN, Greenlee JJ, Miller MW, Wolfe LL, et al. Salivary prions in sheep and deer. Prion. 2012; 6:52-61. http://dx.doi.org/10.4161/pri.6.1.16984

(30.) Andreoletti O, Simon S, Lacroux C, Morel N, Tabouret G, Chabert A, et al. [PrP.sup.Sc] accumulation in myocytes from sheep incubating natural scrapie. Nat Med. 2004; 10:591-3. http://dx.doi.org/10.1038/nm1055

(31.) Chianini F, Cosseddu GM, Steele P, Hamilton S, Hawthorn J, Siso S, et al. Correlation between infectivity and disease associated prion protein in the nervous system and selected edible tissues of naturally affected scrapie sheep. PLoS One. 2015; 10:e0122785. http://dx.doi.org/10.1371/journal.pone.0122785

(32.) Hadlow WJ, Kennedy RC, Race RE. Natural infection of Suffolk sheep with scrapie virus. J Infect Dis. 1982; 146:657-64. http://dx.doi.org/10.1093/infdis/146.5.657

(33.) Garza MC, Monzon M, Marin B, Badiola JJ, Monleon E. Distribution of peripheral PrP(Sc) in sheep with naturally acquired scrapie. PLoS One. 2014; 9:e97768. http://dx.doi.org/10.1371/ journal.pone.0097768

(34.) Castilla J, Saa P, Soto C. Detection of prions in blood. Nat Med. 2005; 11:982-5.

(35.) Bougard D, Brandel JP, Belondrade M, Beringue V, Segarra C, Fleury H, et al. Detection of prions in the plasma of presymptomatic and symptomatic patients with variant Creutzfeldt-Jakob disease. Sci Transl Med. 2016; 8:370ra182. http://dx.doi.org/10.1126/scitranslmed.aag1257

(36.) Concha-Marambio L, Pritzkow S, Moda F, Tagliavini F, Ironside JW, Schulz PE, et al. Detection of prions in blood from patients with variant Creutzfeldt-Jakob disease. Sci Transl Med. 2016; 8:370ra183. http://dx.doi.org/10.1126/scitranslmed.aaf6188

(37.) Bishop MT, Diack AB, Ritchie DL, Ironside JW, Will RG, Manson JC. Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt-Jakob disease. Brain. 2013; 136:1139-45. http://dx.doi.org/10.1093/brain/ awt032

(38.) Siso S, Gonzalez L, Jeffrey M. Neuroinvasion in prion diseases: the roles of ascending neural infection and blood dissemination. Interdiscip Perspect Infect Dis. 2010; 2010:747892. http://dx.doi.org/10.1155/2010/747892

(39.) Brown P, Brandel JP, Sato T, Nakamura Y, MacKenzie J, Will RG, et al. Iatrogenic Creutzfeldt-Jakob disease, final assessment. Emerg Infect Dis. 2012; 18:901-7. http://dx.doi.org/ 10.3201/eid1806.120116

(40.) Flechsig E, Hegyi I, Enari M, Schwarz P, Collinge J, Weissmann C. Transmission of scrapie by steel-surface-bound prions. Mol Med. 2001; 7:679-84.

(41.) Taylor D. Inactivation of the BSE agent. C R Biol. 2002; 325:75-6. http://dx.doi.org/10.1016/S1631-0691(02)01386-0

(42.) Molesworth A, Yates P, Hewitt PE, Mackenzie J, Ironside JW, Galea G, et al. Investigation of variant Creutzfeldt-Jakob disease implicated organ or tissue transplantation in the United Kingdom. Transplantation. 2014; 98:585-9. http://dx.doi. org/10.1097/TP.0000000000000105

(43.) Jayanthi P, Thomas P, Bindhu P, Krishnapillai R. Prion diseases in humans: oral and dental implications. N Am J Med Sci. 2013; 5:399-403. http://dx.doi.org/10.4103/1947-2714.115766

(44.) Peden A, McCardle L, Head MW, Love S, Ward HJ, Cousens SN, et al. Variant CJD infection in the spleen of a neurologically asymptomatic UK adult patient with haemophilia. Haemophilia. 2010; 16:296-304. http://dx.doi.org/10.1111/j.1365-2516. 2009.02181.x

(45.) Llewelyn CA, Hewitt PE, Knight RS, Amar K, Cousens S, Mackenzie J, et al. Possible transmission of variant CreutzfeldtJakob disease by blood transfusion. Lancet. 2004; 363:417-21. http://dx.doi.org/10.1016/S0140-6736(04)15486-X

(46.) Lefrere JJ, Hewitt P. From mad cows to sensible blood transfusion: the risk of prion transmission by labile blood components in the United Kingdom and in France. Transfusion. 2009; 49:797-812. http://dx.doi.org/10.1111/j.1537-2995.2008.02044.x

(47.) Edgeworth JA, Farmer M, Sicilia A, Tavares P, Beck J, Campbell T, et al. Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assay. Lancet. 2011; 377:487-93. http://dx.doi.org/10.1016/S0140-6736(10)62308-2

(48.) Jackson GS, Burk-Rafel J, Edgeworth JA, Sicilia A, Abdilahi S, Korteweg J, et al. A highly specific blood test for vCJD. Blood. 2014; 123:452-3. http://dx.doi.org/10.1182/blood-2013-11-539239

Jean Y. Douet, Caroline Lacroux, Naima Aron, Mark W. Head, Severine Lugan, Cecile Tillier, Alvina Huor, Herve Cassard, Mark Arnold, Vincent Beringue, James W. Ironside, Olivier Andreoletti

Author affiliations: Institut National de la Recherche Agronomique, Toulouse, France (J.Y. Douet, C. Lacroux, N. Aron, S. Lugan, C. Tillier, A. Huor, H. Cassard, O. Andreoletti); University of Edinburgh, Edinburgh, Scotland, UK (M.W. Head, J.W. Ironside); Animal and Plant Health Agency, Loughborough, UK (M. Arnold); Institut National de la Recherche Agronomique, Jouy-en-Josas, France (V. Beringue)

DOI: http://dx.doi.org/10.3201/eid2306.161734

Address for correspondence: Olivier Andreoletti, Unite Mixte de Recherche 1225, Ecole Nationale Veterinaire de Toulouse, 23 Chemin des Cappelles, Toulouse 31076, France; email: o.andreoletti@envt.fr

Caption: Figure 1. Western blots of variant Creutzfeldt-Jakob disease (vJCD) proteinase K-resistant prions ([PrP.sup.res]) analyzed by protein misfolding cyclic amplification (PMCA) in tissues of clinical and asymptomatic patients. PMCAs were seeded with a 10-fold serial dilutions of a reference vCJD brain homogenate (10% wt/ vol, [10.sup.-2] - [10.sup.-10] dilutions). This homogenate had been endpoint titrated by bioassay in bovine prion (PrP)-expressing mice (tgBov, intracerebral route, [10.sup.7.7] 50% lethal dose/g). PMCA substrate was prepared by using brains from transgenic mice overexpressing the ARQ variant of sheep prion protein. An unseeded (lane U) reaction was included as a specificity control. PMCAs were subjected to 6 rounds of amplification, each composed of 96 cycles (sonication for 10 s and incubation for 14.5 min at 39.5[degrees]C) in a Qsonica700 Sonicator (Qsonica LLC, Newtown, CT, USA). After each round, reaction products (1 volume) were mixed with fresh substrate (9 volumes) to seed the following round. Part of the same product was analyzed by Western blotting for abnormal [PrP.sup.res] (Sha31 antibody epitope YEDRYYRE). A sheep scrapie sample (WB cont) was included as a control on each gel. WB, Western blot.

Caption: Figure 2. Protein misfolding cyclic amplification (PMCA) of peripheral tissues from patients with variant Creutzfeldt-Jakob disease (vCJD). PMCA reactions were seeded with a 10-fold dilution series of vCJD tissue homogenates (10-2-10-9) obtained postmortem from CJD-infected patients. At least 4 replicates of each sample dilution were tested in 2 independent PMCA experiments. Patients vCJD-1 (A), vCJD-2 (B), vCJD-3 (C), and vCJD-4 (D) died of clinical vCJD. These 4 patients were infected with prions containing methionine at codon 129 of the PRNP gene (homozygote). Patient vCJD-A (E) died during an asymptomatic or preclinical stage of the disease. This patient was infected with a prion containing methionine/valine at codon 129 of the PRNP gene (heterozygote). PMCA substrate was prepared by using brains from transgenic mice overexpressing the ARQ variant of sheep prion protein. Unseeded reactions and a reaction seeded with tissues from 2 non-vCJD-infected control patients (NC-1 and NC-2; Table 3) were included as specificity controls. PMCAs were subjected to 4 rounds of amplification, each composed of 96 cycles (sonication for 10 s and incubation for 14.5 min at 39.5[degrees]C) in a Qsonica700 Sonicator (Qsonica LLC, Newtown, CT, USA). After each round, reaction products (1 vol) were mixed with fresh substrate (9 vol) to seed the following round. Part of the same product was analyzed by Western blotting for abnormal proteinase K-resistant prions ([PrP.sup.res]) (Sha31 antibody epitope YEDRYYRE). For each round, the highest dilution showing a positive Western blot result in at least half of the replicates tested is indicated. Circles, round 1; V round 2; A, round 3; squares, round 4. Neg, negative.

Caption: Figure 3. Western blots of proteinase K-resistant prions ([PrP.sup.res]) in PMCA reactions seeded with peripheral tissues. PMCA reactions were seeded with a 10-fold dilution series ([10.sup.-2]-[10.sup.-9]) of variant Creutzfeldt-Jakob disease (vCJD) tissue homogenates that had been collected postmortem from vCJD patients during the clinical stage (symptomatic vCJD patient 1-vCJD patient 4 [P1-P4]) or at an asymptomatic or preclinical stage of the disease (vCJD asymp) (Table 2). Reactions seeded with tissues from 2 non-vCJD patients (Table 2) were used as controls, and an unseeded (lane U) reaction was included as a specificity control. Reactions were then subjected to 4 amplification rounds, each composed of 96 cycles (sonication for 10 s and incubation for 14.5 min at 39.5[degrees]C) in a Qsonica 700 Sonicator (Qsonica LLC, Newtown, CT, USA). PMCA reactions were analyzed by using Western blotting for abnormal [PrP.sup.res] (Sha31 antibody epitope YEDRYYRE). A sheep scrapie sample and a vCJD reference isolate were used as controls. For the 7 tissues tested, the dilution of tissue homogenates used to seed the PMCA reactions is indicated below the immunoblots. Cont, control; WB, Western blot.

Caption: Figure 4. Detection of proteinase K-resistant prions ([PrP.sup.res]) by using Western blotting and paraffin-embedded tissue (PET) blotting of brains of transgenic mice expressing bovine PrP (tgBov). A) [PrP.sup.res] WB of a vCJD sample (frontal cortex), tgBov mice (brain) inoculated with the same vCJD reference isolate, bone marrow samples from vCJDaffected patients (vCJD 1-vCJD-4 [P1-P4]; Table 2), and a nonvCJD control (NC-1; Table 2). A scrapie isolate (WB cont) and a noninoculated tgBov brain (vCJD brain) homogenate were included as controls. [PrP.sup.res] immunodetection was performed by using Sha31 monoclonal antibody ([epitope.sub.145] [YEDRYYRE.sub.152]) and 12B2 epitope ([epitope.sub.89][WGQGG.sub.93]). B) PET blotting of [PrP.sup.res] distribution in coronal section (thalamus level) of tgBov mice inoculated with a reference vCJD isolate (10% brain homogenate) or bone marrow (10% tissue homogenate) from 2 vCJD patients (vCJD-1 and vCJD3; Table 2) at the clinical stage of disease. Immunodetection of [PrP.sup.res] was performed by using Sha31 monoclonal antibody ([epitope.sub.145] [YEDRYYRE.sub.152]). Cont, control; NI, not inoculated; WB, Western blot. Scale bar indicates 120 [micro]m.

Caption: Figure 5. Dose-response relationship for A) incubation period am B) probability of infection of bovine PrP-expressing mice. Data were derived from an endpoint titration of 10% (wt/vol) frontal cortex homogenate from a patient with variant Creutzfeldt-Jakob disease. This homogenate was inoculated into tgBov mice (20 [micro]L by intracerebral [ic] route; Table 1). This procedure was used to establish a model that estimates infectious titer in a homogenate on the basis of incubation period and the probability of infection in inoculated mice. Model plots are indicated by solid lines. +, observed value. [LD.sub.50], 50% lethal dose.
Table 1. Endpoint titration of reference sample from a patient
with vCJD in tgBov mice expressing bovine prion protein *

                  Transmission in tgBov mice

               No. positive      Mean [+ or -] SD,
Dilution      mice/no. tested      incubation, d

Undiluted           6/6           249 [+ or -] 2
[10.sup.-1]         6/6           283 [+ or -] 15
[10.sup.-2]         6/6           316 [+ or -] 21
[10.sup.-3]         6/6           342 [+ or -] 10
[10.sup.-4]         6/6           453 [+ or -] 66
[10.sup.-5]         2/6         479, 495 ([dagger])
[10.sup.-6]         1/6           502 ([dagger])
[10.sup.-7]         0/6                >700

* A 10% (wt/vol) homogenate was prepared by using frontal cortex
from a clinically affected patient with vCJD. Groups of 6 tgBov mice
were inoculated intracerebrally with 20 [micro]L of serial 10-fold
dilutions of this homogenate. Mice were considered positive when
abnormal prion protein deposition was detected in the brain. vCJD,
variant Creutzfeldt-Jakob disease.

([dagger]) Dilutions at which <50% of mice were positive.

Table 2. Endpoint titration of PMCA seeding activity in a reference
brain sample from a patient with vCJD *

                Reference vCJD 10% brain homogenate dilution series,
                no. of positive PMCA reactions/no. reactions conducted

Amplification   [10.sup.-2]   [10.sup.-3]   [10.sup.-4]   [10.sup.-5]
round

1                   6/6           6/6           0/6           0/6
2                   6/6           6/6           5/6           3/6
3                   6/6           6/6           6/6           6/6
4                   6/6           6/6           6/6           6/6
5                   6/6           6/6           6/6           6/6
6                   6/6           6/6           6/6           6/6

                Reference vCJD 10% brain homogenate dilution series,
                no. of positive PMCA reactions/no. reactions conducted

Amplification   [10.sup.-6]   [10.sup.-7]   [10.sup.-8]   [10.sup.-9]
round

1                   0/6           0/6           0/6           0/6
2                   0/6           0/6           0/6           0/6
3                   3/6           0/6           0/6           0/6
4                   6/6           5/6           2/6           0/6
5                   6/6           5/6           2/6           0/6
6                   6/6           5/6           2/6           0/6

                Reference vCJD 10% brain homogenate dilution series,
                no. of positive PMCA reactions/no. reactions conducted

Amplification   [10.sup.-10]
round

1                   0/6
2                   0/6
3                   0/6
4                   0/6
5                   0/6
6                   0/6

* A 10% (wt/vol) homogenate was prepared by using frontal cortex
from a symptomatic patient with vCJD (same homogenate as in Table
1). Samples were serially diluted 10-fold ([10.sup.-2]-[10.sup.-10])
before being used to seed PMCA reactions. Six individual replicates
of each sample dilution were tested. PMCA substrate was prepared by
using brains from transgenic mice overexpressing the ARQ variant of
sheep prion protein. PMCAs were subjected to 6 rounds of
amplification, each composed of 96 cycles (sonication for 10 s and
incubation for 14.5 min at 39.5[degrees]C) in a Qsonica700 Sonicator
(Qsonica LLC, Newtown, CT, USA). After each round, reaction products
(1 volume) were mixed with fresh substrate (9 volumes) to seed the
following round. Part of the same product was analyzed by Western
blotting for abnormal [PrP.sup.res] by using Sha31 antibody epitope
YEDRYYRE. Values are number of [PrP.sup.res] Western Blot-positive
replicates corresponding to each round and each dilution. PMCA,
protein misfolding cyclic amplification; [PrP.sup.res], proteinase
K-resistant prion; vCJD, variant Creutzfeldt-Jakob disease.

Table 3. Characteristics of 5 patients with vCJD and 2 controls in
study of distribution and quantitative estimates of variant prions
in tissues *

Patient                    Diagnosis             Sex   Year of
identification                                          death
no.

vCJD-1                       vCJD                 M     1999
vCJD-2                       vCJD                 F     2000
vCJD-4                       vCJD                 M     2000
vCJD-3                       vCJD                 M     2001
vCJD-A                 Asymptomatic vCJD          F     2004
NC-1              No CJD (tumor, infarction,      F     2005
                           ischemia)
NC-2             No CJD (Alzheimer's disease,     F     2010
                     infarction, ischemia)

Patient          Age, y, at     Disease      PRNP gene
identification     death      duration, mo   codon 129
no.

vCJD-1               33            18           MM
vCJD-2               17            18           MM
vCJD-4               26            10           MM
vCJD-3               26            10           MM
vCJD-A               82            NA           MV
NC-1                 85            NA           MM

NC-2                 80            NA           MM

Patient            PRNP gene
identification     mutations
no.

vCJD-1           None detected
vCJD-2           None detected
vCJD-4           None detected
vCJD-3           None detected
vCJD-A           None detected
NC-1             No consent for
                   sequencing
NC-2             None detected

* NA, not applicable; vCJD, variant Creutzfeldt-Jakob disease.

Table 4. Protein misfolding cyclic amplification reactions seeded
with tissue homogenate from vCJD and control patients *

Tissue                            Clinical vCJD patients,
                               [Met.sub.129]/[Met.sub.129]

                   vCJD-1        vCJD-2        vCJD-3        vCJD-4

Frontal cortex   [10.sup.-8]   [10.sup.-8]   [10.sup.-8]   [10.sup.-8]
Pituitary            NA            NA            NA            NA
  gland
Trigeminal           NA            NA            NA            NA
  ganglia
Dorsal root          NA            NA            NA            NA
  ganglia
Cervical lymph   [10.sup.-5]   [10.sup.-4]   [10.sup.-4]   [10.sup.-3]
  node
Tonsil           [10.sup.-3]   [10.sup.-4]   [10.sup.-6]   [10.sup.-3]
Appendix         [10.sup.-4]   [10.sup.-4]   [10.sup.-4]   [10.sup.-3]
Distal Ileum     [10.sup.-3]   [10.sup.-5]   [10.sup.-5]   [10.sup.-2]
Spleen           [10.sup.-4]   [10.sup.-4]   [10.sup.-5]   [10.sup.-4]
Thymus               NA        [10.sup.-3]   [10.sup.-2]   [10.sup.-2]
Lung             [10.sup.-2]   [10.sup.-2]       --            --
Heart            [10.sup.-2]   [10.sup.-2]       --            --
Liver            [10.sup.-4]   [10.sup.-2]   [10.sup.-2]   [10.sup.-4]
Kidney           [10.sup.-2]   [10.sup.-3]       --        [10.sup.-3]
Salivary gland   [10.sup.-4]   [10.sup.-3]   [10.sup.-2]   [10.sup.-3]
Pancreas         [10.sup.-2]       --        [10.sup.-2]   [10.sup.-4]
Thyroid          [10.sup.-2]       --        [10.sup.-2]   [10.sup.-2]
Adrenal gland    [10.sup.-3]   [10.sup.-3]   [10.sup.-3]   [10.sup.-4]
Bone marrow      [10.sup.-4]   [10.sup.-5]   [10.sup.-3]   [10.sup.-4]
Skeletal         [10.sup.-4]   [10.sup.-2]       --            NA
  muscle
Testis               --            NA            --        [10.sup.-3]
Ovary                NA        [10.sup.-4]       NA            NA

Tissue           Preclinical vCJD   Non-vCJD controls,
                     patient,       [Met.sub.129]/
                  [Met.sub.129]/    [Met.sub.129]
                  [Val.sub.129]

                      vCJD-A        NC-1   NC-2

Frontal cortex          -            --     --
Pituitary          [10.sup.-2]       --     --
  gland
Trigeminal              -            --     --
  ganglia
Dorsal root             -            --     --
  ganglia
Cervical lymph     [10.sup.-4]       NA     NA
  node
Tonsil             [10.sup.-3]       NA     --
Appendix           [10.sup.-2]       --     --
Distal Ileum       [10.sup.-3]       --     --
Spleen             [10.sup.-3]       --     --
Thymus             [10.sup.-2]       NA     NA
Lung               [10.sup.-3]       --     --
Heart                   --           --     --
Liver              [10.sup.-2]       --     --
Kidney                  --           --     --
Salivary gland     [10.sup.-2]       --     --
Pancreas                --           --     --
Thyroid                 --           --     --
Adrenal gland           --           --     --
Bone marrow             --           --     --
Skeletal                --           --     --
  muscle
Testis                  NA           NA     NA
Ovary                   NA           NA     NA

* PMCA reactions were seeded with 10-fold serial dilutions of 10%
tissues homogenates ([10.sup.-2]-[10.sup.-9]) that had been
collected postmortem from 4 symptomatic vCJD patients
(vCJD-1-vCJD-4) or an asymptomatic vCJD-infected person (vCJD-A). At
least 4 replicates of each sample dilution were tested in 2
independent PMCA experiments. Prions from patients vCJD-1-vCJD-4
were homozygous for methionine at codon 129 of the PRNP gene. Prion
from patient vCJD-A was heterozygous (methionine/valine) at codon
129 of the PRNP gene. PMCA substrate was prepared by using brains
from transgenic mice overexpressing the ARQ variant of sheep prion
protein. Reactions seeded with tissues from 2 non-vCJD-infected
control patients (NC-1 and NC-2) were included as negative controls.
PMCAs were subjected to 4 rounds of amplification, each composed of
96 cycles (sonication for 10 s and incubation for 14.5 min at
39.5[degres]C) in a Qsonica700 Sonicator (Qsonica LLC, Newtown, CT,
USA). PMCA reactions were analyzed by Western blotting for
proteinase K-resistant PrP by using Sha31 antibody epitope YEDRYYRE.
Values are the highest dilution that resulted in a positive Western
blot result in [greater than or equal to] 50% of the tested
replicates after 4 PMCA amplification rounds. NA, not applicable;
PMCA, protein misfolding cyclic amplification; PrP, prion protein;
vCJD, variant Creutzfeldt-Jakob disease; --, negative.

Table 5. Bone marrow sample bioassay in bovine PrP-expressing mice
(tgBov) for 4 patients with vCJD *

                   Transmission in tgBov mice

Sample        No. positive/no.   Mean [+ or -] SD
              inoculated mice     incubation, d

vCJD-1              5/5          458 [+ or -] 37
vCJD-2              6/6          373 [+ or -] 35
vCJD-3              4/6          504 [+ or -] 10
vCJD-4              6/6          447 [+ or -] 91
PBS control         0/6                >600

                      Mean infectious titer,
                      [LD.sub.50]/g (95% CI)
Sample

vCJD-1        [10.sup.3.1] ([10.sup.2.6]-[10.sup.3.5])
vCJD-2        [10.sup.4.7] ([10.sup.4.3]-[0.sup.5.2])
vCJD-3        [10.sup.2.3] ([10.sup.1.8]-[10.sup.2.7])
vCJD-4        [10.sup.4.0] ([10.sup.3.4]-[0.sup.4.5])
PBS control                     NA

*A 10% wt/vol bone marrow homogenate prepared from 4 symptomatic
vCJD patients (Table 3) was inoculated intracerebrally into 6 tgBov
mice (20 [micro]L/mouse). One mouse (inoculated with homogenate from
patient vCJD-1) died within the first few days after intercerebral
inoculation. Mice were euthanized when they showed clinical signs of
prion infection or after 600-d postinoculation. Mice were considered
prion infected when abnormal PrP deposition was detected in brain.
Infectious prion titers were estimated by using the method of Arnold
et al. (17). The method uses the probability of survival (attack
rate at each dilution) and the individual mouse incubation periods
at each dilution to estimate infectious load. Infectious titers are
given as estimated values. LD50, 50% lethal dose; NA, not
applicable; PBS, phosphate-buffered saline; PrP; prion protein;
vCJD, variant Creutzfeldt-Jakob disease.
COPYRIGHT 2017 U.S. National Center for Infectious Diseases
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2017 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:RESEARCH
Author:Douet, Jean Y.; Lacroux, Caroline; Aron, Naima; Head, Mark W.; Lugan, Severine; Tillier, Cecile; Huo
Publication:Emerging Infectious Diseases
Article Type:Report
Date:Jun 1, 2017
Words:8058
Previous Article:Relative risk for ehrlichiosis and lyme disease in an area where vectors for both are sympatric, New Jersey, USA.
Next Article:Creutzfeldt-Jakob [croyts'felt-yak"ob] disease.
Topics:

Terms of use | Privacy policy | Copyright © 2019 Farlex, Inc. | Feedback | For webmasters