Literature DB >> 12084158

Brain and buffy coat transmission of bovine spongiform encephalopathy to the primate Microcebus murinus.

Nöelle Bons1, Sylvain Lehmann, Nadine Mestre-Francès, Dominique Dormont, Paul Brown.   

Abstract

BACKGROUND: More than 100 cases of variant CJD resulting from infections with bovine spongiform encephalopathy (BSE) have accumulated in the United Kingdom since 1995. Concern about the possibility of secondary transmissions via blood and blood components donated by infected individuals has prompted a variety of international donor deferral policies that will continue until laboratory and epidemiologic evidence provides a consensus about potential risk. STUDY DESIGN AND METHODS: BSE was passaged through macaque monkeys and then adapted to the prosimian microcebe (Microcebus murinus). Brain homogenate and buffy coat from an affected microcebe were separately inoculated intracerebrally into three healthy microcebes (two animals received brain and one received buffy coat).
RESULTS: All three inoculated microcebes became ill after incubation periods of 16 to 18 months. Clinical, histopathologic, and immunocytologic features were similar in each of the recipients.
CONCLUSION: Buffy coat from a symptomatic microcebe infected 17 months earlier with BSE contained the infectious agent. This observation represents the first documented transmission of BSE from the blood of an experimentally infected primate, which in view of rodent buffy coat infectivity precedents and the known host range of BSE is neither unexpected nor cause for alarm.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12084158     DOI: 10.1046/j.1537-2995.2002.00098.x

Source DB:  PubMed          Journal:  Transfusion        ISSN: 0041-1132            Impact factor:   3.157


  11 in total

Review 1.  Leucoreduction of blood components: an effective way to increase blood safety?

Authors:  Maria Bianchi; Stefania Vaglio; Simonetta Pupella; Giuseppe Marano; Giuseppina Facco; Giancarlo M Liumbruno; Giuliano Grazzini
Journal:  Blood Transfus       Date:  2015-12-16       Impact factor: 3.443

Review 2.  Molecular neurology of prion disease.

Authors:  J Collinge
Journal:  J Neurol Neurosurg Psychiatry       Date:  2005-07       Impact factor: 10.154

3.  B cells and platelets harbor prion infectivity in the blood of deer infected with chronic wasting disease.

Authors:  Candace K Mathiason; Jeanette Hayes-Klug; Sheila A Hays; Jenny Powers; David A Osborn; Sallie J Dahmes; Karl V Miller; Robert J Warren; Gary L Mason; Glenn C Telling; Alan J Young; Edward A Hoover
Journal:  J Virol       Date:  2010-03-10       Impact factor: 5.103

4.  All clinically-relevant blood components transmit prion disease following a single blood transfusion: a sheep model of vCJD.

Authors:  Sandra McCutcheon; Anthony Richard Alejo Blanco; E Fiona Houston; Christopher de Wolf; Boon Chin Tan; Antony Smith; Martin H Groschup; Nora Hunter; Valerie S Hornsey; Ian R MacGregor; Christopher V Prowse; Marc Turner; Jean C Manson
Journal:  PLoS One       Date:  2011-08-17       Impact factor: 3.240

5.  Plasmacytoid dendritic cells sequester high prion titres at early stages of prion infection.

Authors:  Rocio Castro-Seoane; Holger Hummerich; Trevor Sweeting; M Howard Tattum; Jacqueline M Linehan; Mar Fernandez de Marco; Sebastian Brandner; John Collinge; Peter-Christian Klöhn
Journal:  PLoS Pathog       Date:  2012-02-16       Impact factor: 6.823

6.  White blood cell-based detection of asymptomatic scrapie infection by ex vivo assays.

Authors:  Sophie Halliez; Emilie Jaumain; Alvina Huor; Jean-Yves Douet; Séverine Lugan; Hervé Cassard; Caroline Lacroux; Vincent Béringue; Olivier Andréoletti; Didier Vilette
Journal:  PLoS One       Date:  2014-08-14       Impact factor: 3.240

Review 7.  Variant CJD. 18 years of research and surveillance.

Authors:  Abigail B Diack; Mark W Head; Sandra McCutcheon; Aileen Boyle; Richard Knight; James W Ironside; Jean C Manson; Robert G Will
Journal:  Prion       Date:  2014-11-01       Impact factor: 3.931

8.  Paracrine diffusion of PrP(C) and propagation of prion infectivity by plasma membrane-derived microvesicles.

Authors:  Vincenzo Mattei; Maria Grazia Barenco; Vincenzo Tasciotti; Tina Garofalo; Agostina Longo; Klaus Boller; Johannes Löwer; Roberta Misasi; Fabio Montrasio; Maurizio Sorice
Journal:  PLoS One       Date:  2009-04-01       Impact factor: 3.240

9.  Plasminogen-based capture combined with amplification technology for the detection of PrP(TSE) in the pre-clinical phase of infection.

Authors:  Christiane Segarra; Daisy Bougard; Mohammed Moudjou; Hubert Laude; Vincent Béringue; Joliette Coste
Journal:  PLoS One       Date:  2013-07-24       Impact factor: 3.240

Review 10.  Detection of Pathognomonic Biomarker PrPSc and the Contribution of Cell Free-Amplification Techniques to the Diagnosis of Prion Diseases.

Authors:  Hasier Eraña; Jorge M Charco; Ezequiel González-Miranda; Sandra García-Martínez; Rafael López-Moreno; Miguel A Pérez-Castro; Carlos M Díaz-Domínguez; Adrián García-Salvador; Joaquín Castilla
Journal:  Biomolecules       Date:  2020-03-19
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.