Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

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

T. Macháček, B. Šmídová, J. Pankrác, M. Majer, J. Bulantová, P. Horák

. 2020 ; 13 (1) : 426. [pub] 20200820

Jazyk angličtina Země Velká Británie

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc21020251

Grantová podpora
729516 Grantová Agentura, Univerzita Karlova
18-11140S Grantová Agentura České Republiky
CZ.02.1.01/0.0/0.0/16_019/0000759 European Regional Development Fund and Ministry of Education, Youth and Sports of the Czech Republic
PROGRES Q43 Univerzita Karlova v Praze
UNCE/SCI/012 - 204072/2018 Univerzita Karlova v Praze
SVV 260432 Univerzita Karlova v Praze

BACKGROUND: Avian schistosomes, the causative agents of human cercarial dermatitis (or swimmer'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 with Trichobilharzia 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 by T. regenti. The impact of iNOS inhibition by aminoguanidine on parasite burden and growth was then evaluated in vivo. The vulnerability of T. regenti schistosomula to NO and peroxynitrite was assessed in vitro by viability assays and electron microscopy. Additionally, the effect of NO on the activity of T. regenti peptidases 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 of T. regenti cathepsins B1.1 and B2, the peptidases essential for parasite migration and digestion. Peroxynitrite severely damaged the surface tegument of the parasites and decreased their viability in vitro, but rather did not participate in parasite clearance in vivo. CONCLUSIONS: Reactive nitrogen species, specifically NO, do not directly kill T. regenti in 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.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc21020251
003      
CZ-PrNML
005      
20210830101853.0
007      
ta
008      
210728s2020 xxk f 000 0|eng||
009      
AR
024    7_
$a 10.1186/s13071-020-04279-9 $2 doi
035    __
$a (PubMed)32819437
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxk
100    1_
$a Macháček, Tomáš $u Department of Parasitology, Faculty of Science, Charles University, Prague, Czechia. tomas.machacek@natur.cuni.cz
245    10
$a Nitric oxide debilitates the neuropathogenic schistosome Trichobilharzia regenti in mice, partly by inhibiting its vital peptidases / $c T. Macháček, B. Šmídová, J. Pankrác, M. Majer, J. Bulantová, P. Horák
520    9_
$a BACKGROUND: Avian schistosomes, the causative agents of human cercarial dermatitis (or swimmer'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 with Trichobilharzia 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 by T. regenti. The impact of iNOS inhibition by aminoguanidine on parasite burden and growth was then evaluated in vivo. The vulnerability of T. regenti schistosomula to NO and peroxynitrite was assessed in vitro by viability assays and electron microscopy. Additionally, the effect of NO on the activity of T. regenti peptidases 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 of T. regenti cathepsins B1.1 and B2, the peptidases essential for parasite migration and digestion. Peroxynitrite severely damaged the surface tegument of the parasites and decreased their viability in vitro, but rather did not participate in parasite clearance in vivo. CONCLUSIONS: Reactive nitrogen species, specifically NO, do not directly kill T. regenti in 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.
650    _2
$a zvířata $7 D000818
650    _2
$a ptáci $x parazitologie $7 D001717
650    _2
$a centrální nervový systém $x parazitologie $7 D002490
650    _2
$a guanidiny $x farmakologie $7 D006146
650    _2
$a proteiny červů $x účinky léků $x metabolismus $7 D015801
650    _2
$a lidé $7 D006801
650    _2
$a myši $7 D051379
650    _2
$a oxid dusnatý $x farmakologie $7 D009569
650    _2
$a synthasa oxidu dusnatého $x účinky léků $x metabolismus $7 D019001
650    _2
$a proteasy $x účinky léků $x metabolismus $7 D010447
650    _2
$a kyselina peroxydusitá $x farmakologie $7 D030421
650    _2
$a Schistosoma $x účinky léků $x růst a vývoj $x patogenita $7 D012547
650    _2
$a Schistosomatidae $x účinky léků $x růst a vývoj $x patogenita $7 D012551
650    _2
$a schistosomóza $x farmakoterapie $7 D012552
650    _2
$a kůže $x parazitologie $7 D012867
650    _2
$a mícha $x parazitologie $7 D013116
650    _2
$a infekce červy třídy Trematoda $x farmakoterapie $7 D014201
655    _2
$a časopisecké články $7 D016428
700    1_
$a Šmídová, Barbora $u Department of Parasitology, Faculty of Science, Charles University, Prague, Czechia
700    1_
$a Pankrác, Jan $u Department of Parasitology, Faculty of Science, Charles University, Prague, Czechia $u Center for Advanced Preclinical Imaging, First Faculty of Medicine, Charles University, Prague, Czechia
700    1_
$a Majer, Martin $u Department of Parasitology, Faculty of Science, Charles University, Prague, Czechia
700    1_
$a Bulantová, Jana $u Department of Parasitology, Faculty of Science, Charles University, Prague, Czechia
700    1_
$a Horák, Petr $u Department of Parasitology, Faculty of Science, Charles University, Prague, Czechia
773    0_
$w MED00165371 $t Parasites & vectors $x 1756-3305 $g Roč. 13, č. 1 (2020), s. 426
856    41
$u https://pubmed.ncbi.nlm.nih.gov/32819437 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y p $z 0
990    __
$a 20210728 $b ABA008
991    __
$a 20210830101853 $b ABA008
999    __
$a ok $b bmc $g 1690936 $s 1140697
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2020 $b 13 $c 1 $d 426 $e 20200820 $i 1756-3305 $m Parasites & vectors $n Parasit Vectors $x MED00165371
GRA    __
$a 729516 $p Grantová Agentura, Univerzita Karlova
GRA    __
$a 18-11140S $p Grantová Agentura České Republiky
GRA    __
$a CZ.02.1.01/0.0/0.0/16_019/0000759 $p European Regional Development Fund and Ministry of Education, Youth and Sports of the Czech Republic
GRA    __
$a PROGRES Q43 $p Univerzita Karlova v Praze
GRA    __
$a UNCE/SCI/012 - 204072/2018 $p Univerzita Karlova v Praze
GRA    __
$a SVV 260432 $p Univerzita Karlova v Praze
LZP    __
$a Pubmed-20210728

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...