Evidence map›Paper›PMID 18497860›Full record

ArticlePLoS pathogens2008

Intraspecies transmission of BASE induces clinical dullness and amyotrophic changes.

Guerino Lombardi, Cristina Casalone, Antonio D' Angelo, Daniela Gelmetti, Gloria Torcoli, Ilaria Barbieri, Cristiano Corona, Elisa Fasoli, Alessia Farinazzo, Michele Fiorini and 8 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
5.4field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 96 citations in OpenAlex.

  1. Review
  2. Possible alignment of the EU BSE surveillance with the new WOAH provisions.EFSA journal. European Food Safety Authority · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Enhanced neuroinvasion by smaller, soluble prions.Acta neuropathologica communications · 2017
    Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 5 institutions in 1 country.

Guerino LombardiIstituto Zooprofilattico Sperimentale della Lombardia e dell' Emilia Romagna, Brescia, Italy.
Cristina Casalone
Antonio D' Angelo
Daniela Gelmetti
Gloria Torcoli
Ilaria Barbieri
Cristiano Corona
Elisa Fasoli
Alessia Farinazzo
Michele Fiorini
Matteo Gelati
Barbara Iulini
Fabrizio Tagliavini
Sergio Ferrari
Maria Caramelli
Salvatore Monaco
Lorenzo Capucci
Gianluigi Zanusso
University of Verona · ITIstituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia Romagna "Bruno Ubertini" · ITIstituto Zooprofilattico Sperimentale del Piemonte Liguria e Valle d'Aosta · ITFondazione IRCCS Istituto Neurologico Carlo Besta · ITUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The disease phenotype of bovine spongiform encephalopathy (BSE) and the molecular/ biological properties of its prion strain, including the host range and the characteristics of BSE-related disorders, have been extensively studied since its discovery in 1986. In recent years, systematic testing of the brains of cattle coming to slaughter resulted in the identification of at least two atypical forms of BSE. These emerging disorders are characterized by novel conformers of the bovine pathological prion protein (PrP(TSE)), named high-type (BSE-H) and low-type (BSE-L). We recently reported two Italian atypical cases with a PrP(TSE) type identical to BSE-L, pathologically characterized by PrP amyloid plaques and known as bovine amyloidotic spongiform encephalopathy (BASE). Several lines of evidence suggest that BASE is highly virulent and easily transmissible to a wide host range. Experimental transmission to transgenic mice overexpressing bovine PrP (Tgbov XV) suggested that BASE is caused by a prion strain distinct from the BSE isolate. In the present study, we experimentally infected Friesian and Alpine brown cattle with Italian BSE and BASE isolates via the intracerebral route. BASE-infected cattle developed amyotrophic changes accompanied by mental dullness. The molecular and neuropathological profiles, including PrP deposition pattern, closely matched those observed in the original cases. This study provides clear evidence of BASE as a distinct prion isolate and discloses a novel disease phenotype in cattle.

Indexed as

AmyloidAnimalsBiomarkersBrainCattleEncephalopathy, Bovine SpongiformGlial Fibrillary Acidic ProteinImmunohistochemistryMiceMice, TransgenicMuscle, SkeletalPrPC ProteinsAmyloidBiomarkersGlial Fibrillary Acidic ProteinPrPC Proteins

Identifiers

PMID18497860
PMCPMC2374911
OpenAlexW2059742492

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.