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

Kód výsledku v 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>

Nalezeny alternativní kódy

RIV/00216208:11310/20:10416700

Výsledek na webu

<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>

Jazyk výsledku

angličtina

Název v původním jazyce

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

Popis výsledku v původním jazyce

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.

Název v anglickém jazyce

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

Popis výsledku anglicky

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.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10600 - Biological sciences

Projekt

<a href="/cs/project/GA18-11140S" target="_blank" >GA18-11140S: Mechanismy imunomodulace po napadení hostitele ptačí neuropatogenní schistosomou Trichobilharzia regenti</a><br>

Návaznosti

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

Rok uplatnění

2020

Kód důvěrnosti údajů

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

Název periodika

Parasites &amp; Vectors

ISSN

1756-3305

e-ISSN

—

Svazek periodika

13

Číslo periodika v rámci svazku

1

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

14

Strana od-do

426

Kód UT WoS článku

000567112200001

EID výsledku v databázi Scopus

2-s2.0-85089769357