2014
Life cycle of Cryptosporidium muris in two rodents with different responses to parasitization
MELICHEROVÁ, Janka, Jana ILGOVÁ, Martin KVÁČ, Bohumil SAK, Břetislav KOUDELA et. al.Základní údaje
Originální název
Life cycle of Cryptosporidium muris in two rodents with different responses to parasitization
Autoři
MELICHEROVÁ, Janka (703 Slovensko, garant, domácí), Jana ILGOVÁ (703 Slovensko, domácí), Martin KVÁČ (203 Česká republika), Bohumil SAK (203 Česká republika), Břetislav KOUDELA (203 Česká republika) a Andrea VALIGUROVÁ (703 Slovensko, domácí)
Vydání
Parasitology, Cambridge University Press, 2014, 0031-1820
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10600 1.6 Biological sciences
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 2.560
Kód RIV
RIV/00216224:14310/14:00073486
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000331903700013
Klíčová slova česky
cryptosporidia development gastric oocyst pathology Type II merogony
Klíčová slova anglicky
cryptosporidia development gastric oocyst pathology Type II merogony
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 8. 5. 2019 10:59, doc. RNDr. Andrea Bardůnek Valigurová, Ph.D.
Anotace
V originále
This study focuses on mapping the life cycle of Cryptosporidium muris in two laboratory rodents; BALB/c mice and the southern multimammate rat Mastomys coucha, differing in their prepatent and patent periods. Both rodents were simultaneously experimentally inoculated with viable oocysts of C. muris (strain TS03). Animals were dissected and screened for the presence of the parasite using a combined morphological approach and nested PCR (SSU rRNA) at different times after inoculation. The occurrence of first developmental stages of C. muris in stomach was detected at 2.5 DPI. The presence of Type II merogony, appearing 36 hours later than Type I merogony, was confirmed in both rodents. Oocysts exhibiting different size and thickness of their wall were observed from 5 DPI onwards in stomach of both host models. The early phase of parasitisation in BALB/c mice progressed rapidly, with a prepatent period of 7.5–10 days; whereas in M. coucha, the developmental stages of C. muris were first observed 12 hours later in comparison with BALB/c mice and prepatent period was longer (18–21 days). Similarly, the patent periods of BALB/c mice and M. coucha differed considerably, i.e. 10–15 days versus chronic infection throughout the life of the host, respectively.
Návaznosti
GAP505/11/1163, projekt VaV |
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GPP506/10/P372, projekt VaV |
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