Blood vessel occlusion by Cryptococcus neoformans is a mechanism for haemorrhagic dissemination of infection

Meningitis caused by infectious pathogens is associated with vessel damage and infarct formation, however the physiological cause is often unknown. Cryptococcus neoformans is a human fungal pathogen and causative agent of cryptococcal meningitis, where vascular events are observed in up to 30% of pa...

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Main Authors: Gibson, Josie F., Bojarczuk, Aleksandra, Evans, Robert J., Kamuyango, Alfred Alinafe, Hotham, Richard, Lagendijk, Anne K., Hogan, Benjamin M., Ingham, Philip William, Renshaw, Stephen A., Johnston, Simon A.
Other Authors: Lee Kong Chian School of Medicine (LKCMedicine)
Format: Article
Language:English
Published: 2022
Subjects:
Online Access:https://hdl.handle.net/10356/161383
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Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-161383
record_format dspace
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Medicine
Blood Vessel Occlusion
Cryptococcus Neoformans
spellingShingle Science::Medicine
Blood Vessel Occlusion
Cryptococcus Neoformans
Gibson, Josie F.
Bojarczuk, Aleksandra
Evans, Robert J.
Kamuyango, Alfred Alinafe
Hotham, Richard
Lagendijk, Anne K.
Hogan, Benjamin M.
Ingham, Philip William
Renshaw, Stephen A.
Johnston, Simon A.
Blood vessel occlusion by Cryptococcus neoformans is a mechanism for haemorrhagic dissemination of infection
description Meningitis caused by infectious pathogens is associated with vessel damage and infarct formation, however the physiological cause is often unknown. Cryptococcus neoformans is a human fungal pathogen and causative agent of cryptococcal meningitis, where vascular events are observed in up to 30% of patients, predominantly in severe infection. Therefore, we aimed to investigate how infection may lead to vessel damage and associated pathogen dissemination using a zebrafish model that permitted noninvasive in vivo imaging. We find that cryptococcal cells become trapped within the vasculature (dependent on their size) and proliferate there resulting in vasodilation. Localised cryptococcal growth, originating from a small number of cryptococcal cells in the vasculature was associated with sites of dissemination and simultaneously with loss of blood vessel integrity. Using a cell-cell junction tension reporter we identified dissemination from intact blood vessels and where vessel rupture occurred. Finally, we manipulated blood vessel tension via cell junctions and found increased tension resulted in increased dissemination. Our data suggest that global vascular vasodilation occurs following infection, resulting in increased vessel tension which subsequently increases dissemination events, representing a positive feedback loop. Thus, we identify a mechanism for blood vessel damage during cryptococcal infection that may represent a cause of vascular damage and cortical infarction during cryptococcal meningitis.
author2 Lee Kong Chian School of Medicine (LKCMedicine)
author_facet Lee Kong Chian School of Medicine (LKCMedicine)
Gibson, Josie F.
Bojarczuk, Aleksandra
Evans, Robert J.
Kamuyango, Alfred Alinafe
Hotham, Richard
Lagendijk, Anne K.
Hogan, Benjamin M.
Ingham, Philip William
Renshaw, Stephen A.
Johnston, Simon A.
format Article
author Gibson, Josie F.
Bojarczuk, Aleksandra
Evans, Robert J.
Kamuyango, Alfred Alinafe
Hotham, Richard
Lagendijk, Anne K.
Hogan, Benjamin M.
Ingham, Philip William
Renshaw, Stephen A.
Johnston, Simon A.
author_sort Gibson, Josie F.
title Blood vessel occlusion by Cryptococcus neoformans is a mechanism for haemorrhagic dissemination of infection
title_short Blood vessel occlusion by Cryptococcus neoformans is a mechanism for haemorrhagic dissemination of infection
title_full Blood vessel occlusion by Cryptococcus neoformans is a mechanism for haemorrhagic dissemination of infection
title_fullStr Blood vessel occlusion by Cryptococcus neoformans is a mechanism for haemorrhagic dissemination of infection
title_full_unstemmed Blood vessel occlusion by Cryptococcus neoformans is a mechanism for haemorrhagic dissemination of infection
title_sort blood vessel occlusion by cryptococcus neoformans is a mechanism for haemorrhagic dissemination of infection
publishDate 2022
url https://hdl.handle.net/10356/161383
_version_ 1759854062055981056
spelling sg-ntu-dr.10356-1613832023-03-05T16:50:58Z Blood vessel occlusion by Cryptococcus neoformans is a mechanism for haemorrhagic dissemination of infection Gibson, Josie F. Bojarczuk, Aleksandra Evans, Robert J. Kamuyango, Alfred Alinafe Hotham, Richard Lagendijk, Anne K. Hogan, Benjamin M. Ingham, Philip William Renshaw, Stephen A. Johnston, Simon A. Lee Kong Chian School of Medicine (LKCMedicine) Institute of Molecular and Cell Biology (A*Star) Singapore Science::Medicine Blood Vessel Occlusion Cryptococcus Neoformans Meningitis caused by infectious pathogens is associated with vessel damage and infarct formation, however the physiological cause is often unknown. Cryptococcus neoformans is a human fungal pathogen and causative agent of cryptococcal meningitis, where vascular events are observed in up to 30% of patients, predominantly in severe infection. Therefore, we aimed to investigate how infection may lead to vessel damage and associated pathogen dissemination using a zebrafish model that permitted noninvasive in vivo imaging. We find that cryptococcal cells become trapped within the vasculature (dependent on their size) and proliferate there resulting in vasodilation. Localised cryptococcal growth, originating from a small number of cryptococcal cells in the vasculature was associated with sites of dissemination and simultaneously with loss of blood vessel integrity. Using a cell-cell junction tension reporter we identified dissemination from intact blood vessels and where vessel rupture occurred. Finally, we manipulated blood vessel tension via cell junctions and found increased tension resulted in increased dissemination. Our data suggest that global vascular vasodilation occurs following infection, resulting in increased vessel tension which subsequently increases dissemination events, representing a positive feedback loop. Thus, we identify a mechanism for blood vessel damage during cryptococcal infection that may represent a cause of vascular damage and cortical infarction during cryptococcal meningitis. Agency for Science, Technology and Research (A*STAR) Nanyang Technological University Published version JFG was supported by an award from the Singapore A*STAR Research Attachment Programme (ARAP) in partnership with the University of Sheffield. Work in the PWI lab was funded by the A*STAR Institute of Molecular and Cell Biology (IMCB) and the Lee Kong Chian School of Medicine. RJE was supported by a British Infection Association postdoctoral fellowship (https://www.britishinfection.org/). AKL was supported by a University of Queensland Postdoctoral Fellowship. BMH by an NHMRC/ National Heart Foundation Career Development Fellowship (1083811). SAJ, AB, RJE, AK and RH, were supported by Medical Research Council and Department for International Development Career Development Award Fellowship MR/J009156/1 (http://www.mrc.ac.uk/). SAJ was additionally supported by a Krebs Institute Fellowship (http:// krebsinstitute.group.shef.ac.uk/), and Medical Research Council Centre grant (G0700091). AK was supported by a Wellcome Trust Strategic Award in Medical Mycology and Fungal Immunology (097377/Z/11/Z). SAR was supported by a Medical Research Council Programme Grant (MR/M004864/1). Light sheet microscopy was carried out in the Wolfson Light Microscopy Facility, supported by a BBSRC ALERT14 award for light-sheet microscopy (BB/M012522/1). 2022-08-30T06:18:27Z 2022-08-30T06:18:27Z 2022 Journal Article Gibson, J. F., Bojarczuk, A., Evans, R. J., Kamuyango, A. A., Hotham, R., Lagendijk, A. K., Hogan, B. M., Ingham, P. W., Renshaw, S. A. & Johnston, S. A. (2022). Blood vessel occlusion by Cryptococcus neoformans is a mechanism for haemorrhagic dissemination of infection. PLoS Pathogens, 18(4), e1010389-. https://dx.doi.org/10.1371/journal.ppat.1010389 1553-7366 https://hdl.handle.net/10356/161383 10.1371/journal.ppat.1010389 35446924 2-s2.0-85128662210 4 18 e1010389 en PLoS Pathogens © 2022 Gibson et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. application/pdf