TY - JOUR
T1 - The role of atypical MAP kinase 4 in the host interaction with Cryptosporidium parvum
AU - Watanabe, Nina
AU - Bando, Hironori
AU - Murakoshi, Fumi
AU - Sakurai, Riku
AU - Kabir, Mohammad Hazzaz Bin
AU - Fukuda, Yasuhiro
AU - Kato, Kentaro
N1 - Funding Information:
We thank to Dr. M. Matsubayashi (Osaka Prefecture University, Japan) for providing C. parvum HNJ-1 strain used in this study. This study was funded by grants-in-aid for JSPS Research Fellow (21F21101) and Fostering Joint International Research (B:19KK0242) and Scientific Research on Innovative Areas (3805) from the Ministry of Education, Culture, Science, Sports, and Technology (MEXT) of Japan, a Livestock Promotional Subsidy from the Japan Racing Association, the Uehara Memorial Foundation (J200002710), and The Morinaga Foundation for Health & Nutrition (AV602061).
Funding Information:
We thank to Dr. M. Matsubayashi (Osaka Prefecture University, Japan) for providing C. parvum HNJ-1 strain used in this study. This study was funded by grants-in-aid for JSPS Research Fellow (21F21101) and Fostering Joint International Research (B:19KK0242) and Scientific Research on Innovative Areas (3805) from the Ministry of Education, Culture, Science, Sports, and Technology (MEXT) of Japan, a Livestock Promotional Subsidy from the Japan Racing Association, the Uehara Memorial Foundation (J200002710), and The Morinaga Foundation for Health & Nutrition (AV602061).
Publisher Copyright:
© 2023, The Author(s).
PY - 2023/12
Y1 - 2023/12
N2 - Cryptosporidium parvum is an apicomplexan parasite that causes severe zoonotic diarrhea in humans and calves. Since there are no effective treatments or vaccines for infants or immunocompromised patients, it is important to understand the molecular mechanisms of the parasite–host interaction for novel drug discovery. Mitogen-activated protein kinase (MAP kinase) is a key host factor in interactions between host and various pathogens, including parasites. Although the function of conventional MAP kinases against parasite infection has been investigated, that of atypical MAP kinases remains largely unknown. Therefore, we focused on one of the atypical MAP kinases, MAPK4, and its effect on C. parvum infection in human intestinal cells. Here, we report that MAPK4-deficient intestinal cells showed a significant reduction in C. parvum infection. We also show that host MAPK4 has a role in host cell survival from C. parvum infection. In addition, we show that C. parvum requires host MAPK4 for its successful invasion and asexual reproduction. Taken together, our data suggest that MAPK4 is an important host factor contributing to C. parvum infection in human intestinal cells.
AB - Cryptosporidium parvum is an apicomplexan parasite that causes severe zoonotic diarrhea in humans and calves. Since there are no effective treatments or vaccines for infants or immunocompromised patients, it is important to understand the molecular mechanisms of the parasite–host interaction for novel drug discovery. Mitogen-activated protein kinase (MAP kinase) is a key host factor in interactions between host and various pathogens, including parasites. Although the function of conventional MAP kinases against parasite infection has been investigated, that of atypical MAP kinases remains largely unknown. Therefore, we focused on one of the atypical MAP kinases, MAPK4, and its effect on C. parvum infection in human intestinal cells. Here, we report that MAPK4-deficient intestinal cells showed a significant reduction in C. parvum infection. We also show that host MAPK4 has a role in host cell survival from C. parvum infection. In addition, we show that C. parvum requires host MAPK4 for its successful invasion and asexual reproduction. Taken together, our data suggest that MAPK4 is an important host factor contributing to C. parvum infection in human intestinal cells.
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U2 - 10.1038/s41598-023-28269-w
DO - 10.1038/s41598-023-28269-w
M3 - Article
C2 - 36658270
AN - SCOPUS:85146566092
SN - 2045-2322
VL - 13
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 1096
ER -