Skip directly to site content Skip directly to page options Skip directly to A-Z link Skip directly to A-Z link Skip directly to A-Z link
Volume 20, Number 12—December 2014

Transmission Characteristics of Variably Protease-Sensitive Prionopathy

Article Metrics
citations of this article
EID Journal Metrics on Scopus
Silvio Notari1, Xiangzhu Xiao1, Juan Carlos Espinosa, Yvonne Cohen, Liuting Qing, Patricia Aguilar-Calvo, Diane Kofskey, Ignazio Cali, Laura Cracco, Qingzhong Kong, Juan Maria Torres, and Pierluigi GambettiComments to Author 
Author affiliations: Case Western Reserve University, Cleveland, Ohio, USA (S. Notari, X. Xiao, Y. Cohen, L. Qing, D. Kofskey, I. Cali, L. Cracco, Q. Kong, W. Zou, P. Gambetti); Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria, Madrid, Spain (J.C. Espinosa, P. Aguilar-Calvo, J.M. Torres)

Cite This Article


Variably protease-sensitive prionopathy (VPSPr), a recently identified and seemingly sporadic human prion disease, is distinct from Creutzfeldt-Jakob disease (CJD) but shares features of Gerstmann-Sträussler-Scheinker disease (GSS). However, contrary to exclusively inherited GSS, no prion protein (PrP) gene variations have been detected in VPSPr, suggesting that VPSPr might be the long-sought sporadic form of GSS. The VPSPr atypical features raised the issue of transmissibility, a prototypical property of prion diseases. We inoculated VPSPr brain homogenate into transgenic mice expressing various levels of human PrP (PrPC). On first passage, 54% of challenged mice showed histopathologic lesions, and 34% harbored abnormal PrP similar to that of VPSPr. Surprisingly, no prion disease was detected on second passage. We concluded that VPSPr is transmissible; thus, it is an authentic prion disease. However, we speculate that normal human PrPC is not an efficient conversion substrate (or mouse brain not a favorable environment) and therefore cannot sustain replication beyond the first passage.

Prion diseases include a variety of animal and human conditions that might be sporadic, inherited, or acquired by infection. Despite this diversity, most prion diseases are thought to share the same pathogenetic mechanism whereby the cellular prion protein (PrPC) is templated into an abnormal and pathogenic conformer, commonly identified as scrapie PrP (PrPSc) (1). Therefore, conversion by templating is the basic mechanism that causes disease and sustains disease transmission among humans (2). However, data have shown that propagation, disease manifestation, and transmissibility might occur separately in various ways (3,4).

The phenotype of human prion diseases is highly heterogeneous. This characteristic is largely due to the variable genotype at codon 129, the site of a methionine/valine (MV) polymorphism in the human PrP gene, and the molecular characteristics of the associated PrPSc (5). A further major distinction that has been applied to human prion diseases for years is based on the experimental transmissibility of these diseases to hosts thought to be permissive for exogenous human PrPSc (6). Based on this principle, the sporadic form of Creutzfeldt-Jakob disease (sCJD) belongs to the transmissible disease group, whereas most of the Gerstmann-Sträussler-Scheinker diseases (GSS), a group comprising exclusively inherited forms, were considered difficult to transmit or not transmissible (710). However, an increasing number of findings have challenged this distinction. Replication of infectious PrPSc occurs in the absence of clinical signs in the host, or even in the absence of detectable disease, by histologic and Western blot (WB) examinations. Yet, infectivity can be demonstrated in subsequent passages to more susceptible hosts (9,11,12). Finally, disease transmissibility has recently been demonstrated for a subtype of GSS previously thought to be nontransmissible (8,10,13).

In 2008 and 2010, we introduced a novel human prion disease, presumably sporadic, that we named variably protease-sensitive prionopathy (VPSPr) (1416). VPSPr differs from sCJD in several aspects. The clinical presentation and the frequent slow progression evoke the features of atypical dementias, such as frontotemporal dementia, diffuse Lewy body disease, or normal pressure hydrocephalus (17). The flocculent PrP immunostaining pattern, which includes the frequent presence of PrP peculiar amyloid plaques, differs from those of other sporadic prion diseases. However, the most distinctive VPSPr feature rests on the characteristics of the associated PrPSc, especially the electrophoretic profile and resistance to the commonly used protease, such as proteinase K (PK) (14,15,17). VPSPr-associated, PK-resistant PrPSc (resPrPSc) forms a distinctive 5-band electrophoretic profile, comprising various fragments truncated at the N terminal and at least 1 fragment truncated at both N and C terminals, which consequently lacks the GPI (glycosylphosphatidylinositol) anchor (14). Furthermore, the N-truncated fragments do not include the diglycosylated PrPSc isoforms but only 1 of 2 monoglycosylated and the unglycosylated isoforms (18), and upon cleavage of the glycans, these fragments form 3 PK-resistant WB bands in VPSPr preparations. In contrast, the electrophoretic profile of sCJD resPrPSc is characterized by 3 bands, including diglycosylated, 2 monoglycosylated, and unglycosylated isoform, all of which harbor the GPI anchor and form only 1 band after glycan removal (19). However, VPSPr also occasionally displays small amounts of typical 3 electrophoretic band–forming resPrPSc on WB of basal ganglia and other deep cerebral structures (14). On the whole, the VPSPr 5-band ladder profile is more akin to the electrophoretic profile of PrPSc in most GSS subtypes, although contrary to GSS, no mutation in the PrP gene open reading frame has been observed in VPSPr (1416). Given this similarity, Zou et al. hypothesized that VPSPr is the sporadic form of GSS (15). Like sCJD, VPSPr affects persons harboring each of 3 PrPC 129 genotypes: methionine and valine homozygosity (MM, VV) and MV heterozygosity. The 3 genotypic subtypes of VPSPr differ slightly in clinical presentation, duration, histopathologic features, and PK resistance of the PrPSc (15).

The similarity in the PrPSc electrophoretic profiles with GSS, which was regarded as not transmissible, called into question the transmissibility of VPSPr and prompted use of the term prionopathy rather than prion disease. The present study addresses this issue. Transgenic (Tg) mice expressing various levels of human PrPC harboring methionine (M) or valine (V) at position 129 underwent intracranial inoculation with brain homogenates (BH) from several human case-patients with VPSPr associated with each of the three 129 genotypes (15). Surprisingly, VPSPr was transmitted as an asymptomatic disease characterized by focal accumulation of VPSPr-like PrPSc in the first passage, but no prion disease could be demonstrated in the second passage.

Materials and Methods

VPSPr Case-Patients and Controls

We conducted this study during 2007–2013. Twelve case-patients with VPSPr (6 with VPSPr-129VV, 4 with VPSPr-129MV, and 2 with VPSPr-129MM) provided the inocula used in the first passage. The second passage inocula were obtained from Tg mice challenged at first passage with BH from frontal cortex and putamen of 1 case-patient with VPSPr-129VV and 1 with VPSPr-129MM. Two sets of experiments were conducted to generate negative controls by using Tg mice from the same lines: 1) age-matched Tg mice that were not inoculated and 2) age-matched Tg mice challenged with noninfectious BH from mice of the same genetic background. Positive controls were obtained from the same 129M and 129V Tg mice lines inoculated with BH from 5 subtypes of sCJD, sCJDMM1, sCJDMM2, sCJDVV1, sCJDVV2, and sCJDMV2, maintaining the host/donor homology of codon 129. Finally, six 129V Tg mice were euthanized 35 days postinoculation (dpi) with VPSPr-129VV, and the presence of the inoculum was searched by immunohistochemistry and immunoblotting.

Tg Mice

Four mouse lines with different PrPC expression levels were used. The first line was a Tg362 mouse line expressing human PrPC-129V on a mouse PrPC null background at ≈8-fold normal human brain levels, hereafter identified as Tg(HuPrP129V)×8. This line was generated following previously described methods (20). For the next 2 lines,Tg40 and Tg21 were generated by replacing the mouse PrP open reading frame in the murine half-genomic PrP clone in plasmid pHGPRP (21) with that of human PrP-129M or human PrP-129V as reported (22). The generated Tg mice harbored a wild-type FVB background and bred with FVB/PrP null mice (23) to obtain Tg mice in mouse PrP null FVB background. For the fourth line, the generated Tg40 mouse line expressing human PrPC-129M at ≈1-fold normal mouse brain level, identified as Tg(HuPrP129M)×1, this was then self-bred to obtain the Tg40h mouse line. The generated Tg40h expressing human PrPC-129M at ≈2-fold normal mouse brain levels, was identified as Tg(HuPrP129M)×2. The Tg21 mouse line expressing human PrPC-129V at ≈3-fold normal mouse brain levels was identified as Tg(HuPrP129V) × 3.

Intracerebral Inoculations

Ten percent or 1% BH in 5% glucose or phosphate-buffered saline were generated from the frontal cortex, occipital cortex, or putamen. It was inoculated intracerebrally according to procedures previously described (20,22).

Ethical Considerations

We conducted animal experiments in strict accordance with the recommendations in the guidelines of the Code for Methods and Welfare Considerations in Behavioral Research with Animals (directive 86/609EC). All efforts were made to minimize suffering. Experiments were approved by the Committee on the Ethics of Animal Experiments of the Spanish National Instutute for the Agricultural and Food Research and Technology; permit no. CEEA 2011/046.

Histology and Immunohistochemistry

Standard histologic and immunohistochemical examinations were conducted at 4 brain levels. These were basal ganglia (bregma + ≈0.14 mm), thalamus (bregma – ≈1.46 mm), posterior hippocampus (bregma – ≈2.92 mm), and anterior cerebellum (bregma – ≈6.00 mm), on paraffin sections stained with hematoxylin and eosin or probed with the 3F4 antibody to the prion protein (PrP) (1:1,000–1,400) (24).


Conventional immunoblotting was conducted on frozen brain tissues homogenized in glucose solution to make 10% BH. To detect PK-resistant PrPSc, we mixed the 10% BH with an equal volume of 2× lysis buffer. BH was treated with different amounts of PK (Sigma Chemical Co., St. Louis, MO, USA) ranging from 0 μg/mL to 50 μg/mL. The samples untreated or treated with PK, equivalent to 0.5–2 mg of wet tissues, were loaded onto 15% Tris-HCl Criterion precast gels (Bio-Rad Laboratories, Hercules, CA, USA) for SDS-PAGE (sodium dodecyl sulfate polyacrylamide gel electrophoresis) and immunoblotted with the widely used PrP antibody 3F4 against human PrP106–112 (15) or 1E4 against human PrP97–105 (25) (Cell Sciences, Inc., Canton, MA, USA). When required, PrP was deglycosylated with PNGase F (New England Biolabs, Beverly, MA, USA) before immunoblotting following the manufacturer’s instructions.


First Passage
Histologic and Immunohistochemical Analyses

We found that 54% of the Tg mice belonging to 3 lines expressing 129V or 129M human PrP showed histologic abnormalities after inoculation of BH from 6 persons with symptomatic VPSPr (inoculum from 1 presymptomatic but histopathologically and immunochemically confirmed person with VPSPr did not transmit) (Table 1). All 30 positive Tg mice were asymptomatic until they were culled, after incubation periods of up to 800 days. Although the low number of mice inoculated with VPSPr-129MM made the comparison difficult, no major differences in the rate of transmission were detected between Tg(HuPrP129V) mice challenged with VPSPr-129VV and Tg(HuPrP129M) mice challenged with VPSPr-129MM. Similarly, we detected no significant difference in plaque prevalence between Tg mice expressing PrPC at levels ×8 and ×3 normal (Table 1). Affected Tg mice were observed only when the 129 genotype of the VPSPr inoculum matched that of the host (Table 2); that is, neither positive Tg(HuPrP129M) nor Tg(HuPrP129V) mice were observed after inoculation with VPSPr-129MV and VPSPr-129VV or VPSPr-129MV BH, respectively. However, VPSPr-129MM transmission to Tg(HuPrP129V) was not tested, and Tg(HuPrP129M)×1, but not Tg(HuPrP129M)×2, was used for transmission of VPSPr-129VV.


The histologic lesions included 2 types. The most common lesion consisted of individual or aggregates of prion plaques often in a row preferentially located immediately below the corpus callosum at the border with the alveus of the hippocampus, which might represent the subependymal region of the lateral ventricles. We occasionally saw individual plaques in other periventricular regions but rarely in the parenchyma (Figures 1, 2). The lesion of the second type consisted of focal spongiform degeneration involving the layer lacunosum moleculare of the hippocampus (Figure 1). This lesion was seen almost exclusively in Tg(HuPrP129V)×8 and predominantly after inoculation of VPSPr BH from the basal ganglia. PrP immunostaining intensely enhanced the plaques and demonstrated PrP granular deposits in the focal areas of spongiform degeneration. Although plaques appeared very compact in Tg(HuPrP129V) mice inoculated with VPSPr-129VV, plaques in Tg(HuPrP129M) mice after VPSPr-129MM inoculation were less well formed and were often replaced by loose aggregates of irregular granules (Figure 1). The topographic distribution of the plaque deposits and focal spongiform change are shown in Figure 2.

Neither prion-related lesions nor PrPSc were observed in 23 age-matched Tg(HuPrP129)V×8 mice that had not been inoculated or had undergone inoculations with noninfectious BH (Table 3). As expected, the 3 Tg(HuPrP) mouse lines used for VPSPr transmission easily transmitted sCJD subtypes that were 129 genotypically compatible with the host PrP, indicating that the Tg mice used for VPSPr transmission are competent to propagate classical human prion diseases (Table 3). No PrP immunostaining was detected in the 6 Tg(HuPrP129V)×8 35 dpi with VPSPr-129VV BH.

WB Analysis

Thirteen (34%) of the 38 VPSPr-inoculated Tg(HuPrP129V)×8 mice examined showed a definitively positive WB, despite the mouse BH treatment with a wide range of PK to maximize the recovery of PrPSc, including PrPSc species with low resistance to PK. The 34% prevalence of positive cases harboring detectable PrPSc was nearly half that of PrPSc-positive Tg mice detected at histopathologic examination (Table 1). Tg mouse resPrPSc immunoreacted much more readily with the monoclonal antibody 1E4 than with 3F4, as previously reported for VPSPr PrPSc (14). Probed with 1E4, Tg mouse resPrPSc exhibited a 5-band electrophoretic profile, similar to that of VPSPr (Figure 3). Deglycosylation by PNGase resulted in 3 resPrPSc bands that co-migrated with the analogous VPSPr bands at ≈20 kDa, ≈17 kDa, and ≈7 kDa (Figure 3) (15). No definitely positive WB conducted with standard methods was observed in VPSPr-inoculated Tg(HuPrP129V)×3 and Tg(HuPrP129M)×2 mice (Table 1).

All negative controls, including noninoculated Tg mice and Tg mice inoculated with noninfectious BH, had negative WB. In contrast, WB were positive, with the classical 3-band profile, in all mice from the 3 Tg(HuPrP) lines challenged with BH from different sCJD subtypes used as positive controls (Table 3). WB examination of brains from 3 Tg(HuPrP129V)×8 mice challenged with VPSPr-129VV BH showed no evidence of PrPSc 35 dpi, indicating that the inoculum was too diluted to be detected or no longer present.

Second Passage

The second passage yielded a surprising finding. None of the 13 mice belonging to the Tg(HuPrP129V)×8 and Tg(HuPrP129M)×2 lines showed prion-related histologic lesions or had a definitely positive WB upon secondary transmission, even up to nearly 800 dpi (Table 4).


The experiments reported here, which probed transmissibility of VPSPr to Tg mice expressing human PrPC, yielded puzzling results. On first passage, all hosts remained asymptomatic, but 54% showed focal deposition of PrPSc in the form of prion plaques by immunohistochemical analysis. In 34% of animals, small amounts of resPrPSc were demonstrated by WB (Figures 1, 3). The PrPSc recovered from affected mice recapitulated the electrophoretic profile and immunoreactivity features of the VPSPr-129VV PrPSc, even after removal of the sugar moiety. However, mouse PrPSc was apparently more PK-resistant than the PrPSc from VPSPr-129VV case-patients (Figure 3) (15). In contrast, on second passage, all Tg mice were negative at clinical and histopathologic examinations and harbored no PrPSc that could be definitely identified by WB, even up to 800 dpi.

These findings pose several challenging questions. The first question concerns whether the PrPSc recovered on first passage represents the residual inoculum rather than de novo PrPSc generated by conversion of the host’s PrPC. We believe this possibility is made unlikely by our experiment showing that the PrPSc in the VPSPr inoculum was no longer detectable by immunohistochemical and WB analyses in Tg(HuPrP-129VV) mice 35 dpi. Furthermore, histopathologic changes and PrPSc detection, indicating VPSPr transmission, were observed only when the host and the inoculum were syngenic at PrP codon 129. This genotypic selectivity is not compatible with the notion that the PrPSc detected in the hosts was from the residual inoculum. Finally, several other studies have shown that PrPSc associated with the inoculum is rapidly cleared (12,2630). These observations support the conclusion that histopathologic changes and the PrPSc recovered in the positive VPSPr-challenged mice result from de novo mouse PrPSc generated by templated conversion, although at a very low level. The lack of clinical signs in the affected mice can be easily explained by the characteristics and localization of the plaques and of the spongiform degeneration, both of which affected limited regions depopulated of neuronal cells and processes.

Prion plaques similar in type and topography to those we observed have been reported alone or associated with spongiform degeneration in mice challenged with prions of various origins (9,11,2932). In 3 studies, plaque deposits seem to be especially similar to those observed by us. In the first, the plaques were detected on the second passage of vCJD in Tg mice expressing human PrPC-129V (Tg152) (11,29). The second and third studies used Tg mice expressing mouse PrP harboring the P101L variation (101LL mice), which is the equivalent of the P102L human mutation linked to a GSS subtype (9,30). In the last 2 experiments, Tg101LL mice were challenged with “atypical” P102L GSS (i.e., GSS associated only with 7-kDa PrPSc PK-resistant fragment rather than with the “typical” P102L GSS that is also associated with the classical 3-band resPrPSc) or with BH from TgGSS-22, a Tg mouse model of GSS in which prion disease spontaneously develops (9,30). All affected mice of these 3 studies remained asymptomatic like those of our study, further supporting the notion that focal prion plaque deposition in periventricular regions is not sufficient to produce major clinical signs. Despite the common histopathologic features, these mice were associated with electrophoretically distinct PrPSc species. In the experiment of vCJD transmission, PrPSc harvested from challenged Tg152 mice showed the classical 3 PK-resistant bands as in vCJD, but they displayed a higher molecular mass than in vCJD (11). Minimal quantity of resPrPSc recovered at ≈30 kDa was detected only in 1 of 5 plaque-harboring 101LL mice challenged with atypical P102L GSS (9), whereas 101LL mice inoculated with TgGSS-22 BH showed no detectable PrPSc by WB (30). Although to some extent the variability of the PrPSc electrophoretic profiles between the experiments with Tg101LL and our experiments might be due to variations in WB methods, the PrPSc diversity in these 3 studies and in our study suggests that focal plaque formation at the border between the hippocampus and corpus callosum is not strictly PrPSc strain specific. However, this brief review indicates that peri-hippocampal plaque deposition is preferentially detected in hosts challenged with PrPSc species that form plaques in the natural disease, such as vCJD, GSS, and VPSPr.

The lack of histologic lesions and PrPSc on second passage in both Tg(HuPrP129V) and Tg(HuPrP129M) mice challenged with BH from the most severely affected first-passage mice is unusual. However, comparable findings have been reported in at least 2 previous studies. In the first, 101LL mice challenged with affected TgGSS-22 BH (a Tg mouse in which a GSS-like disease spontaneously develops) harbored fewer plaques on second passage than on first, suggesting decreased replication of the seed on second passage (9,30). In the second study, first passage of BH from cattle affected by bovine spongiform encephalopathy to Tg152 mice (expressing human PrPC-129V) resulted in clinical disease associated with diffuse brain deposition of PrP as demonstrated by immunostaining (11), even though no resPrPSc could be demonstrated by WB. On second passage in the same Tg152 mice, no evidence of prion disease could be demonstrated either by PrP immunostaining or WB, as in our study (11). However, BH from these negative Tg152 produced a full prion disease after inoculation into wild-type FVB mice. This remarkable finding indicates that prion transmissibility (or infectivity) can be sustained in hosts with no demonstrable prion diseases (according to commonly used methods), and that it can be rescued through passage to an appropriate host (11).

Interpreting our findings also in the light of the above data, we propose that normal human PrPC is not a suitable substrate (or mouse brain is not a favorable environment) to sustain conversion to VPSPr PrPSc. Thus, long incubations are required to induce modest and asymptomatic PrPSc deposition. Nevertheless, the PrPSc generated in the host on first passage seems to match the conformation of the PrPSc from the inoculum, based on the finding that PK-resistant PrPSc fragments of similar size are recovered from host and donor preparations. This also indicates that little or no PrPSc adaptation has occurred during the first passage (32). The apparent failure of the second passage to transmit detectable disease might be due to the inadequate amplification of VPSPr PrPSc during primary transmission, which would result in a second passage PrPSc inoculum more diluted than the VPSPr brain extract used in the primary transmission. This line of reasoning raises the possibility that if VPSPr PrPSc were exposed to a favorable PrP substrate (or brain environment), it might replicate efficiently. This conjecture is reinforced by 2 recent findings. First, preliminary findings show that VPSPr can be transmitted to bank voles more easily than to the Tg(HuPrP) used in the present experiments (33). Second, transmissibility of GSS linked to the A117V mutation has been recently demonstrated (10). GSS-A117V is commonly viewed as a “classic” GSS subtype, given the distinct features of its phenotype that is characterized by prominent prion plaques with limited spongiform degeneration and a PrPSc WB profile dominated by a highly PK-resistant fragment of 7–8 kDa (34). Early failures to transmit GSS-A117V and the evidence that the presence of the A117V mutation altered the topology of PrP led to the conclusions that 1) GSS-A117V was not transmissible and 2) its underlying pathogenetic mechanism was not based on a PrPC-to-PrPSc conversion process (8).

After inoculation with BH from GSS-A117V–affected patients, Tg mice expressing human PrP, harboring the A117V mutation, developed a prion disease associated with a histologic phenotype and PrPSc that roughly recapitulated those of the human disease. However, only one fourth of the inoculated mice were symptomatic with incubation periods >600 days, whereas more than half harbored plaques, PrPSc, or both (10). No second passage was reported. This study shows that an allegedly nontransmissible prion disease can be transmitted (at least at first passage) if a suitable host is selected.

In conclusion, we propose that VPSPr is transmissible and, therefore, is an authentic prion disease. However, transmissibility cannot be sustained through serial passages presumably because human PrPC (or the mouse brain environment) cannot efficiently convert and propagate the VPSPr PrPSc species. If this is the case, uncovering the properties of human PrP that are required to replicate more efficiently the prion strains associated with VPSPr may help clarify the PrPSc mode of formation in this intriguing disease.

Dr Notari is an instructor at Case Western Reserve University, Cleveland, Ohio, USA. His research interests include prion diseases with particular focus on the characteristics of PrPSc in different prion strains and their relationships with infectivity.



We thank Miriam Warren and Katie Glisic for their skillful contributions to the histologic study and manuscript editing, respectively.

This study was supported by National Institutes of Health awards AG14359 and NS062787, Centers for Disease Control and Prevention award UR8/CCU515004, Charles S. Britton Fund, and Spanish Ministerio de Ciencia e Innovación AGL2012-37988-C04-04.



  1. Prusiner  SB. Biology and genetics of prions causing neurodegeneration. Annu Rev Genet. 2013;47:6013. DOIPubMed
  2. Surewicz  WK, Apostol  MI. Prion protein and its conformational conversion: a structural perspective. Top Curr Chem. 2011;305:13567. DOIPubMed
  3. Aguzzi  A, Falsig  J. Prion propagation, toxicity and degradation. Nat Neurosci. 2012;15:9369. DOIPubMed
  4. Sandberg  MK, Al-Doujaily  H, Sharps  B, Clarke  AR, Collinge  J. Prion propagation and toxicity in vivo occur in two distinct mechanistic phases. Nature. 2011;470:5402. DOIPubMed
  5. Gambetti  P, Cali  I, Notari  S, Kong  Q, Zou  WQ, Surewicz  WK. Molecular biology and pathology of prion strains in sporadic human prion diseases. Acta Neuropathol. 2011;121:7990. DOIPubMed
  6. Weissmann  C, Flechsig  E. PrP knock-out and PrP transgenic mice in prion research. Br Med Bull. 2003;66:4360. DOIPubMed
  7. Kong  Q, Surewicz  WK, Petersen  RB, Zou  WQ, Chen  SG, Gambetti  P, Inherited Prion Disease. In: Prusiner SB, editor. Prion biology and diseases. 2nd ed. Cold Spring Harbor (NY): Cold Spring Harbor Laboratory Press; 2004. p. 673‒775.
  8. Hegde  RS, Mastrianni  JA, Scott  MR, DeFea  KA, Tremblay  P, Torchia  M, A transmembrane form of the prion protein in neurodegenerative disease. Science. 1998;279:82734. DOIPubMed
  9. Piccardo  P, Manson  JC, King  D, Ghetti  B, Barron  RM. Accumulation of prion protein in the brain that is not associated with transmissible disease. Proc Natl Acad Sci U S A. 2007;104:47127 . DOIPubMed
  10. Asante  EA, Linehan  JM, Smidak  M, Tomlinson  A, Grimshaw  A, Jeelani  A, Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion protein. PLoS Pathog. 2013;9:e1003643. DOIPubMed
  11. Wadsworth  JD, Asante  EA, Desbruslais  M, Linehan  JM, Joiner  S, Gowland  I, Human prion protein with valine 129 prevents expression of variant CJD phenotype. Science. 2004;306:17936. DOIPubMed
  12. Race  R, Meade-White  K, Raines  A, Raymond  GJ, Caughey  B, Chesebro  B. Subclinical scrapie infection in a resistant species: persistence, replication, and adaptation of infectivity during four passages. J Infect Dis. 2002;186(Suppl 2):S16670. DOIPubMed
  13. Hegde  RS, Tremblay  P, Groth  D, DeArmond  SJ, Prusiner  SB, Lingappa  VR. Transmissible and genetic prion diseases share a common pathway of neurodegeneration. Nature. 1999;402:8226. DOIPubMed
  14. Gambetti  P, Dong  Z, Yuan  J, Xiao  X, Zheng  M, Alshekhlee  A, A novel human disease with abnormal prion protein sensitive to protease. Ann Neurol. 2008;63:697708. DOIPubMed
  15. Zou  WQ, Puoti  G, Xiao  X, Yuan  J, Qing  L, Cali  I, Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein. Ann Neurol. 2010;68:16272. DOIPubMed
  16. Head  MW, Yull  HM, Ritchie  DL, Langeveld  JP, Fletcher  NA, Knight  RS, Variably protease-sensitive prionopathy in the UK: a retrospective review 1991–2008. Brain. 2013;136:110215. DOIPubMed
  17. Puoti  G, Bizzi  A, Forloni  G, Safar  JG, Tagliavini  F, Gambetti  P. Sporadic human prion diseases: molecular insights and diagnosis. Lancet Neurol. 2012;11:61828. DOIPubMed
  18. Xiao  X, Yuan  J, Haïk  S, Cali  I, Zhan  Y, Moudjou  M, Glycoform-selective prion formation in sporadic and familial forms of prion disease. PLoS ONE. 2013;8:e58786. DOIPubMed
  19. Gambetti  P, Kong  Q, Zou  W, Parchi  P, Chen  SG. Sporadic and familial CJD: classification and characterization. Br Med Bull. 2003;66:21339. DOIPubMed
  20. Padilla  D, Béringue  V, Espinosa  JC, Andreoletti  O, Jaumain  E, Reine  F, Sheep and goat BSE propagate more efficiently than cattle BSE in human PrP transgenic mice. PLoS Pathog. 2011;7:e1001319 . DOIPubMed
  21. Fischer  M, Rülicke  T, Raeber  A, Sailer  A, Moser  M, Oesch  B, Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie. EMBO J. 1996;15:125564 .PubMed
  22. Kong  Q, Huang  S, Zou  W, Vanegas  D, Wang  M, Wu  D, Chronic wasting disease of elk: transmissibility to humans examined by transgenic mouse models. J Neurosci. 2005;25:79449. DOIPubMed
  23. Sailer  A, Büeler  H, Fischer  M, Aguzzi  A, Weissmann  C. No propagation of prions in mice devoid of PrP. Cell. 1994;77:9678. DOIPubMed
  24. Paxinos  K, Franklin  G, editors. The mouse brain in stereotaxic coordinated. 2nd ed. San Diego (CA): Academic Press; 2001.
  25. Yuan  J, Dong  Z, Guo  JP, McGeehan  J, Xiao  X, Wang  J, Accessibility of a critical prion protein region involved in strain recognition and its implications for the early detection of prions. Cell Mol Life Sci. 2008;65:63143. DOIPubMed
  26. Büeler  H, Aguzzi  A, Sailer  A, Greiner  RA, Autenried  P, Aguet  M, Mice devoid of PrP are resistant to scrapie. Cell. 1993;73:133947. DOIPubMed
  27. Race  R, Raines  A, Raymond  GJ, Caughey  B, Chesebro  B. Long-term subclinical carrier state precedes scrapie replication and adaptation in a resistant species: analogies to bovine spongiform encephalopathy and variant Creutzfeldt-Jakob disease in humans. J Virol. 2001;75:1010612. DOIPubMed
  28. Safar  JG, DeArmond  SJ, Kociuba  K, Deering  C, Didorenko  S, Bouzamondo-Bernstein  E, Prion clearance in bigenic mice. J Gen Virol. 2005;86:291323. DOIPubMed
  29. Wadsworth  JD, Joiner  S, Linehan  JM, Desbruslais  M, Fox  K, Cooper  S, Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice. Proc Natl Acad Sci U S A. 2008;105:388590. DOIPubMed
  30. Piccardo  P, King  D, Telling  G, Manson  JC, Barron  RM. Dissociation of prion protein amyloid seeding from transmission of a spongiform encephalopathy. J Virol. 2013;87:1234956. DOIPubMed
  31. Makarava  N, Kovacs  GG, Savtchenko  R, Alexeeva  I, Budka  H, Rohwer  RG, Genesis of mammalian prions: from non-infectious amyloid fibrils to a transmissible prion disease. PLoS Pathog. 2011;7:e1002419. DOIPubMed
  32. Tamgüney  G, Giles  K, Oehler  A, Johnson  NL, DeArmond  SJ, Prusiner  SB. Chimeric elk/mouse prion proteins in transgenic mice. J Gen Virol. 2013;94:44352. DOIPubMed
  33. Nonno  R, Di Bari  M, Pirisinu  L, D’Agostino  C, Marcon  S, Riccardi  G, Variably protease-sensitive prionopathy is transmissible in bank voles. Prion. 2012;6(S):6‒7.
  34. Pirisinu  L, Nonno  R, Esposito  E, Benestad  SL, Gambetti  P, Agrimi  U, Small ruminant nor98 prions share biochemical features with human Gerstmann-Sträussler-Scheinker disease and variably protease-sensitive prionopathy. PLoS ONE. 2013;8:e66405. DOIPubMed


Cite This Article

DOI: 10.3201/eid2012.140548

1These authors contributed equally to this article.

Table of Contents – Volume 20, Number 12—December 2014


Please use the form below to submit correspondence to the authors or contact them at the following address:

Pierluigi Gambetti or Wenquan Zou, Institute of Pathology, Case Western Reserve University, 2085 Adelbert Rd, Cleveland, OH 44106-4907, USA; or

Send To

character(s) remaining.

Comment submitted successfully, thank you for your feedback.


Page created: November 18, 2014
Page updated: November 18, 2014
Page reviewed: November 18, 2014
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.