Suppr超能文献

非典型牛海绵状脑病朊病毒株的人类传播风险评估。

Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strain.

作者信息

Kong Qingzhong, Zheng Mengjie, Casalone Cristina, Qing Liuting, Huang Shenghai, Chakraborty Bikram, Wang Ping, Chen Fusong, Cali Ignazio, Corona Cristiano, Martucci Francesca, Iulini Barbara, Acutis Pierluigi, Wang Lan, Liang Jingjing, Wang Meiling, Li Xinyi, Monaco Salvatore, Zanusso Gianluigi, Zou Wen-Quan, Caramelli Maria, Gambetti Pierluigi

机构信息

Department of Pathology, Case Western Reserve University, Cleveland, OH 44106, USA.

出版信息

J Virol. 2008 Apr;82(7):3697-701. doi: 10.1128/JVI.02561-07. Epub 2008 Jan 30.

Abstract

Bovine spongiform encephalopathy (BSE), the prion disease in cattle, was widely believed to be caused by only one strain, BSE-C. BSE-C causes the fatal prion disease named new variant Creutzfeldt-Jacob disease in humans. Two atypical BSE strains, bovine amyloidotic spongiform encephalopathy (BASE, also named BSE-L) and BSE-H, have been discovered in several countries since 2004; their transmissibility and phenotypes in humans are unknown. We investigated the infectivity and human phenotype of BASE strains by inoculating transgenic (Tg) mice expressing the human prion protein with brain homogenates from two BASE strain-infected cattle. Sixty percent of the inoculated Tg mice became infected after 20 to 22 months of incubation, a transmission rate higher than those reported for BSE-C. A quarter of BASE strain-infected Tg mice, but none of the Tg mice infected with prions causing a sporadic human prion disease, showed the presence of pathogenic prion protein isoforms in the spleen, indicating that the BASE prion is intrinsically lymphotropic. The pathological prion protein isoforms in BASE strain-infected humanized Tg mouse brains are different from those from the original cattle BASE or sporadic human prion disease. Minimal brain spongiosis and long incubation times are observed for the BASE strain-infected Tg mice. These results suggest that in humans, the BASE strain is a more virulent BSE strain and likely lymphotropic.

摘要

牛海绵状脑病(BSE),即牛的朊病毒病,人们普遍认为它仅由一种毒株BSE-C引起。BSE-C可导致人类患上致命的朊病毒病——新型变异型克雅氏病。自2004年以来,在多个国家发现了两种非典型BSE毒株,即牛淀粉样海绵状脑病(BASE,也称为BSE-L)和BSE-H;它们在人类中的传播性和表型尚不清楚。我们通过用来自两头感染了BASE毒株的牛的脑匀浆接种表达人朊病毒蛋白的转基因(Tg)小鼠,研究了BASE毒株的传染性和人类表型。60%的接种Tg小鼠在潜伏期20至22个月后被感染,其传播率高于报道的BSE-C。四分之一感染BASE毒株的Tg小鼠脾脏中出现了致病性朊病毒蛋白异构体,但感染导致散发性人类朊病毒病的朊病毒的Tg小鼠均未出现,这表明BASE朊病毒本质上具有嗜淋巴性。感染BASE毒株的人源化Tg小鼠大脑中的病理性朊病毒蛋白异构体与原始牛BASE或散发性人类朊病毒病的不同。感染BASE毒株的Tg小鼠观察到轻微的脑海绵状变性和较长的潜伏期。这些结果表明,在人类中,BASE毒株是一种毒性更强的BSE毒株,且可能具有嗜淋巴性。

相似文献

1
Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strain.
J Virol. 2008 Apr;82(7):3697-701. doi: 10.1128/JVI.02561-07. Epub 2008 Jan 30.
5
Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans.
Proc Natl Acad Sci U S A. 1999 Dec 21;96(26):15137-42. doi: 10.1073/pnas.96.26.15137.
7
Transgenic models of prion disease.
Arch Virol Suppl. 2000(16):113-24. doi: 10.1007/978-3-7091-6308-5_10.
9
Experimental Infection of Cattle With a Novel Prion Derived From Atypical H-Type Bovine Spongiform Encephalopathy.
Vet Pathol. 2017 Nov;54(6):892-900. doi: 10.1177/0300985817717769. Epub 2017 Jul 21.
10
Transmission barriers for bovine, ovine, and human prions in transgenic mice.
J Virol. 2005 May;79(9):5259-71. doi: 10.1128/JVI.79.9.5259-5271.2005.

引用本文的文献

1
Evaluating the inter-species transmission risk of amyloid beta peptide aggregates via ingestion.
Alzheimers Res Ther. 2024 Jun 7;16(1):123. doi: 10.1186/s13195-024-01487-8.
3
Conventional and State-of-the-Art Detection Methods of Bovine Spongiform Encephalopathy (BSE).
Int J Mol Sci. 2023 Apr 12;24(8):7135. doi: 10.3390/ijms24087135.
4
Glycans are not necessary to maintain the pathobiological features of bovine spongiform encephalopathy.
PLoS Pathog. 2022 Oct 7;18(10):e1010900. doi: 10.1371/journal.ppat.1010900. eCollection 2022 Oct.
5
Non-human primates in prion diseases.
Cell Tissue Res. 2023 Apr;392(1):7-20. doi: 10.1007/s00441-022-03644-7. Epub 2022 Jun 4.
6
Prion Dissemination through the Environment and Medical Practices: Facts and Risks for Human Health.
Clin Microbiol Rev. 2021 Dec 15;34(4):e0005919. doi: 10.1128/CMR.00059-19. Epub 2021 Jul 28.
8
Met -Glu residues in human PrP β2-α2 loop account for evolutionary resistance to prion infection.
Neuropathol Appl Neurobiol. 2021 Jun;47(4):506-518. doi: 10.1111/nan.12676. Epub 2020 Dec 22.

本文引用的文献

2
On the question of sporadic or atypical bovine spongiform encephalopathy and Creutzfeldt-Jakob disease.
Emerg Infect Dis. 2006 Dec;12(12):1816-21. doi: 10.3201/eid1212.060965.
3
Impact of vCJD on blood supply.
Biologicals. 2007 Apr;35(2):79-97. doi: 10.1016/j.biologicals.2007.01.002. Epub 2007 Feb 21.
4
Atypical BSE in Germany--proof of transmissibility and biochemical characterization.
Vet Microbiol. 2006 Oct 31;117(2-4):103-16. doi: 10.1016/j.vetmic.2006.06.016. Epub 2006 Aug 17.
5
Predicting susceptibility and incubation time of human-to-human transmission of vCJD.
Lancet Neurol. 2006 May;5(5):393-8. doi: 10.1016/S1474-4422(06)70413-6.
6
Risk factors for variant Creutzfeldt-Jakob disease: a case-control study.
Ann Neurol. 2006 Jan;59(1):111-20. doi: 10.1002/ana.20708.
7
Chronic wasting disease of elk: transmissibility to humans examined by transgenic mouse models.
J Neurosci. 2005 Aug 31;25(35):7944-9. doi: 10.1523/JNEUROSCI.2467-05.2005.
8
Human prion protein with valine 129 prevents expression of variant CJD phenotype.
Science. 2004 Dec 3;306(5702):1793-6. doi: 10.1126/science.1103932. Epub 2004 Nov 11.
9
Identification of a second bovine amyloidotic spongiform encephalopathy: molecular similarities with sporadic Creutzfeldt-Jakob disease.
Proc Natl Acad Sci U S A. 2004 Mar 2;101(9):3065-70. doi: 10.1073/pnas.0305777101. Epub 2004 Feb 17.
10
Distinct molecular phenotypes in bovine prion diseases.
EMBO Rep. 2004 Jan;5(1):110-5. doi: 10.1038/sj.embor.7400054.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验