Neuroinfectiology of an atypical anthrax-causing pathogen in wild chimpanzees

Author:

Gräßle Tobias12,Jäger Carsten34,Kirilina Evgeniya3ORCID,Jaffe Jenny E.25,Carlier Penelope5,Pizarro Andrea6,Jauch Anna3,Reimann Katja4,Lipp Ilona3, ,Wittig Roman M.785,Crockford Catherine785,Weiskopf Nikolaus3910ORCID,Leendertz Fabian H.12,Morawski Markus34

Affiliation:

1. Ecology and Emergence of Zoonotic Diseases, Helmholtz Institute for One Health, Helmholtz Centre for Infection Research

2. Epidemiology of Highly Pathogenic Microorganisms, Robert Koch Institute

3. Department of Neurophysics, Max Planck Institute for Human Cognitive and Brain Sciences

4. Paul Flechsig Institute - Center of Neuropathology and Brain Research, Medical Faculty, University of Leipzig

5. Taï Chimpanzee Project, CSRS, Abidjan, Côte d’Ivoire

6. Tacugama Chimpanzee Sanctuary

7. Ape Social Mind Lab, Institute for Cognitive Sciences Marc Jeannerod, UMR CNRS 5229, University Claude Bernard Lyon 1

8. Evolution of Brain Connectivity Project, Max Planck Institute for Evolutionary Anthropology

9. Felix Bloch Institute for Solid State Physics, Faculty of Physics and Earth Sciences, Leipzig University

10. Wellcome Centre for Human Neuroimaging, UCL Institute of Neurology, University College London

Abstract

Bacillus cereus biovar anthracis ( Bcbva ) is an atypical anthrax-causing bacterium, inflicting wildlife fatalities across African rainforest ecosystems. The pathogen’s virulence in one of our closest living relatives, the chimpanzee, together with human serological evidence, suggests Bcbva is zoonotic. While classical B. anthracis -induced anthrax has been described to affect the central nervous system at a progressive disease-state, the neuroinfectiology of Bcbva is yet unknown. Here we characterised the pathogen’s neuro-invasiveness via gross pathological assessment, ultra-high resolution quantitative Magnetic Resonance Imaging and histological analysis on four brains, which were extracted from naturally deceased wild chimpanzees in Taï National Park, Côte d’Ivoire.Based on macroscopically evident pial vessel congestion and haemorrhages as well as cortical siderosis detected via MRI, we concluded that Bcbva induced meningitis analogous to B. anthracis . Further, histological visualisation of bacteria and leukocytes in the subarachnoid space evidenced the bacterium’s capability to breach the arachnoid barrier. Bcbva was detected in the brain parenchyma of all four cases. This indicates a higher ability to transgress the glia limitans and therefore exhibits a higher neuroinvasiveness compared to B. anthracis that predominantly stays confined to the meninges. Heightened glial fibrillary acidic protein (GFAP) expression but little morphological gliosis suggest a rapid disease progression leading to host-death within hours to a few days after central nervous system invasion.Overall our results reveal Bcbva ’s ability to breach blood-brain barriers which results in a pronounced neuropathogenicity. Bcbva causes extensive damage to the meninges and the brain parenchyma, as well as rapid and massive digestion of brain extracellular matrix in chimpanzees and potentially so in humans in case of zoonotic spillover.

Publisher

eLife Sciences Publications, Ltd

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3