Mechanisms of the host immune response and helminth-induced pathology during Trichobilharzia regenti (Schistosomatidae) neuroinvasion in mice

PLoS Pathog. 2022 Feb 4;18(2):e1010302. doi: 10.1371/journal.ppat.1010302. eCollection 2022 Feb.

Abstract

Helminth neuroinfections represent serious medical conditions, but the diversity of the host-parasite interplay within the nervous tissue often remains poorly understood, partially due to the lack of laboratory models. Here, we investigated the neuroinvasion of the mouse spinal cord by Trichobilharzia regenti (Schistosomatidae). Active migration of T. regenti schistosomula through the mouse spinal cord induced motor deficits in hindlimbs but did not affect the general locomotion or working memory. Histological examination of the infected spinal cord revealed eosinophilic meningomyelitis with eosinophil-rich infiltrates entrapping the schistosomula. Flow cytometry and transcriptomic analysis of the spinal cord confirmed massive activation of the host immune response. Of note, we recorded striking upregulation of the major histocompatibility complex II pathway and M2-associated markers, such as arginase or chitinase-like 3. Arginase also dominated the proteins found in the microdissected tissue from the close vicinity of the migrating schistosomula, which unselectively fed on the host nervous tissue. Next, we evaluated the pathological sequelae of T. regenti neuroinvasion. While no demyelination or blood-brain barrier alterations were noticed, our transcriptomic data revealed a remarkable disruption of neurophysiological functions not yet recorded in helminth neuroinfections. We also detected DNA fragmentation at the host-schistosomulum interface, but schistosomula antigens did not affect the viability of neurons and glial cells in vitro. Collectively, altered locomotion, significant disruption of neurophysiological functions, and strong M2 polarization were the most prominent features of T. regenti neuroinvasion, making it a promising candidate for further neuroinfection research. Indeed, understanding the diversity of pathogen-related neuroinflammatory processes is a prerequisite for developing better protective measures, treatment strategies, and diagnostic tools.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arginase / metabolism*
  • Biomarkers / metabolism
  • Chemokines / metabolism
  • Disease Models, Animal
  • Eosinophils / metabolism*
  • Female
  • Gene Expression Profiling
  • Host-Parasite Interactions
  • Immunity
  • Major Histocompatibility Complex
  • Mice
  • Mice, Inbred C57BL
  • Neuroglia / parasitology
  • Neurons / parasitology
  • Schistosomatidae / immunology*
  • Spinal Cord / parasitology*
  • Trematode Infections / immunology*
  • Trematode Infections / metabolism*
  • Trematode Infections / pathology

Substances

  • Biomarkers
  • Chemokines
  • Arginase

Grants and funding

TM, RL, BŠ, MM, OV, and PH were supported by the Czech Science Foundation (18-11140S; https://gacr.cz/en), European Regional Development Fund and Ministry of Education, Youth and Sports of the Czech Republic (CZ.02.1.01/0.0/0.0/16_019/0000759; https://ec.europa.eu/regional_policy/en/funding/erdf), and Charles University institutional funding (PROGRES Q43, Cooperatio Biology, UNCE/SCI/012-204072/2018, SVV 260432/2018; https://cuni.cz/UKEN-65.html). OV was supported by Charles University Grant Agency (1374119; https://cuni.cz/UKEN-753.html). Microscopy was performed in the Laboratory of Confocal and Fluorescence Microscopy co-financed by the European Regional Development Fund and the state budget of the Czech Republic (CZ.1.05/4.1.00/16.0347, CZ.2.16/3.1.00/21515; https://ec.europa.eu/regional_policy/en/funding/erdf) and supported by the Czech-BioImaging large RI project LM2018129. Computational resources were supplied by the project "e-Infrastruktura CZ" (e-INFRA LM2018140) provided within the program Projects of Large Research, Development and Innovations Infrastructures, and ELIXIR-CZ projects LM2015047 and LM2018131, part of the international ELIXIR infrastructure supported by Ministry of Education, Youth and Sports of the Czech Republic (https://www.msmt.cz/?lang=2). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.