Nitric oxide debilitates the neuropathogenic schistosome Trichobilharzia regenti in mice, partly by inhibiting its vital peptidases

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F20%3A10416700" target="_blank" >RIV/00216208:11110/20:10416700 - isvavai.cz</a>

Alternative codes found

RIV/00216208:11310/20:10416700

Result on the web

<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=QoL9ZkQa-L" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=QoL9ZkQa-L</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1186/s13071-020-04279-9" target="_blank" >10.1186/s13071-020-04279-9</a>

Result language

angličtina

Original language name

Nitric oxide debilitates the neuropathogenic schistosome Trichobilharzia regenti in mice, partly by inhibiting its vital peptidases

Original language description

Background: Avian schistosomes, the causative agents of human cercarial dermatitis (or swimmer&apos;s itch), die in mammals but the mechanisms responsible for parasite elimination are unknown. Here we examined the role of reactive nitrogen species, nitric oxide (NO) and peroxynitrite, in the immune response of mice experimentally infected withTrichobilharzia regenti, a model species of avian schistosomes remarkable for its neuropathogenicity. Methods: Inducible NO synthase (iNOS) was localized by immunohistochemistry in the skin and the spinal cord of mice infected byT. regenti. The impact of iNOS inhibition by aminoguanidine on parasite burden and growth was then evaluatedin vivo. The vulnerability ofT. regentischistosomula to NO and peroxynitrite was assessedin vitroby viability assays and electron microscopy. Additionally, the effect of NO on the activity ofT. regentipeptidases was tested using a fluorogenic substrate. Results: iNOS was detected around the parasites in the epidermis 8 h post-infection and also in the spinal cord 3 days post-infection (dpi). Inhibition of iNOS resulted in slower parasite growth 3 dpi, but the opposite effect was observed 7 dpi. At the latter time point, moderately increased parasite burden was also noticed in the spinal cord.In vitro, NO did not impair the parasites, but inhibited the activity ofT. regenticathepsins B1.1 and B2, the peptidases essential for parasite migration and digestion. Peroxynitrite severely damaged the surface tegument of the parasites and decreased their viabilityin vitro, but rather did not participate in parasite clearancein vivo. Conclusions: Reactive nitrogen species, specifically NO, do not directly killT. regentiin mice. NO promotes the parasite growth soon after penetration (3 dpi), but prevents it later (7 dpi) when also suspends the parasite migration in the CNS. NO-related disruption of the parasite proteolytic machinery is partly responsible for this effect.

Czech name

—

Czech description

—

Type

J_imp - Article in a specialist periodical, which is included in the Web of Science database

CEP classification

—

OECD FORD branch

10600 - Biological sciences

Project

<a href="/en/project/GA18-11140S" target="_blank" >GA18-11140S: Mechanisms of host immunomodulation by Trichobilharzia regenti, an avian neuropathogenic schistosome</a><br>

Continuities

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year

2020

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Parasites &amp; Vectors

ISSN

1756-3305

e-ISSN

—

Volume of the periodical

13

Issue of the periodical within the volume

1

Country of publishing house

GB - UNITED KINGDOM

Number of pages

14

Pages from-to

426

UT code for WoS article

000567112200001

EID of the result in the Scopus database

2-s2.0-85089769357