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Cryptococcus neoformans ex vivo capsule size is associated with intracranial pressure and host immune response in HIV-associated cryptococcal meningitis.

Robertson, EJ; Najjuka, G; Rolfes, MA; Akampurira, A; Jain, N; Anantharanjit, J; von Hohenberg, M; Tassieri, M; Carlsson, A; Meya, DB; et al. Robertson, EJ; Najjuka, G; Rolfes, MA; Akampurira, A; Jain, N; Anantharanjit, J; von Hohenberg, M; Tassieri, M; Carlsson, A; Meya, DB; Harrison, TS; Fries, BC; Boulware, DR; Bicanic, T (2014) Cryptococcus neoformans ex vivo capsule size is associated with intracranial pressure and host immune response in HIV-associated cryptococcal meningitis. J Infect Dis, 209 (1). pp. 74-82. ISSN 1537-6613 https://doi.org/10.1093/infdis/jit435
SGUL Authors: Harrison, Thomas Stephen Bicanic, Tihana

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Abstract

BACKGROUND: The Cryptococcus neoformans polysaccharide capsule is a well-characterized virulence factor with immunomodulatory properties. The organism and/or shed capsule is postulated to raise intracranial pressure (ICP) in cryptococcal meningitis (CM) by mechanical obstruction of cerebrospinal fluid (CSF) outflow. Little is known regarding capsule phenotype in human cryptococcosis. We investigated the relationship of ex vivo CSF capsular phenotype with ICP and CSF immune response, as well as in vitro phenotype. METHODS: In total, 134 human immunodeficiency virus (HIV)-infected Ugandan adults with CM had serial lumbar punctures with measurement of CSF opening pressures, quantitative cultures, ex vivo capsule size and shedding, viscosity, and CSF cytokines; 108 had complete data. Induced capsular size and shedding were measured in vitro for 48 C. neoformans isolates. RESULTS: Cryptococcal strains producing larger ex vivo capsules in the baseline (pretreatment) CSF correlated with higher ICP (P = .02), slower rate of fungal clearance (P = .02), and paucity of CSF inflammation, including decreased CSF white blood cell (WBC) count (P < .001), interleukin (IL)-4 (P = .02), IL-6 (P = .01), IL-7 (P = .04), IL-8 (P = .03), and interferon γ (P = .03). CSF capsule shedding did not correlate with ICP. On multivariable analysis, capsule size remained independently associated with ICP. Ex vivo capsular size and shedding did not correlate with that of the same isolates grown in vitro. CONCLUSIONS: Cryptococcal capsule size ex vivo is an important contributor to virulence in human cryptococcal meningitis.

Item Type: Article
Additional Information: © The Author 2013. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
Keywords: CSF, Cryptococcus neoformans, HIV, cryptococcal meningitis, human, immune response, intracranial pressure, polysaccharide capsule, AIDS-Related Opportunistic Infections, Adult, Analysis of Variance, Antifungal Agents, Cerebrospinal Fluid, Cryptococcus neoformans, Cytokines, Female, Fungal Capsules, Humans, Intracranial Pressure, Male, Meningitis, Cryptococcal, Phenotype, Polysaccharides, Uganda, Viscosity, Cerebrospinal Fluid, Humans, Cryptococcus neoformans, AIDS-Related Opportunistic Infections, Meningitis, Cryptococcal, Polysaccharides, Cytokines, Antifungal Agents, Analysis of Variance, Intracranial Pressure, Phenotype, Viscosity, Adult, Uganda, Female, Male, Fungal Capsules, Cryptococcus neoformans, cryptococcal meningitis, HIV, polysaccharide capsule, intracranial pressure, immune response, CSF, human, Science & Technology, Life Sciences & Biomedicine, Immunology, Infectious Diseases, Microbiology, IMMUNOLOGY, INFECTIOUS DISEASES, MICROBIOLOGY, Cryptococcus neoformans, cryptococcal meningitis, HIV, polysaccharide capsule, intracranial pressure, immune response, CSF, human, CEREBROSPINAL-FLUID PRESSURE, VIRULENCE FACTORS, INFECTION, MENINGOENCEPHALITIS, POLYSACCHARIDE, AIDS, CLEARANCE, DIAGNOSIS, ANTIGEN, BURDEN, Microbiology, 11 Medical And Health Sciences, 06 Biological Sciences
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: J Infect Dis
ISSN: 1537-6613
Language: eng
Dates:
DateEvent
1 January 2014Published
14 August 2013Published Online
30 July 2013Accepted
Publisher License: Creative Commons: Attribution 3.0
Projects:
Project IDFunderFunder ID
U01 AI089244NIAID NIH HHSUNSPECIFIED
K23AI073192NIAID NIH HHSUNSPECIFIED
R21NS065713NINDS NIH HHSUNSPECIFIED
P30 AI051519NIAID NIH HHSUNSPECIFIED
R21 A1087564PHS HHSUNSPECIFIED
100714Wellcome Trusthttp://dx.doi.org/10.13039/100004440
WT 089966Wellcome Trusthttp://dx.doi.org/10.13039/100004440
R21 NS065713NINDS NIH HHSUNSPECIFIED
U01AI089244NIAID NIH HHSUNSPECIFIED
R01 AI059681NIAID NIH HHSUNSPECIFIED
K23 AI073192NIAID NIH HHSUNSPECIFIED
PubMed ID: 23945372
Web of Science ID: WOS:000329157000012
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URI: https://openaccess.sgul.ac.uk/id/eprint/103763
Publisher's version: https://doi.org/10.1093/infdis/jit435

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