TY - JOUR
T1 - Characterization of the gene expression patterns in the murine liver following intramuscular administration of baculovirus
AU - Iyori, Mitsuhiro
AU - Ogawa, Ryohei
AU - Emran, Talha Bin
AU - Tanbo, Shuta
AU - Yoshida, Shigeto
N1 - Publisher Copyright:
Copyright © 2021 Cognizant, LLC.
PY - 2021
Y1 - 2021
N2 - Intramuscular administration of wild-type baculovirus is able to both protect against Plasmodium sporozoite challenge and eliminate liver-stage parasites via a Toll-like receptor 9-independent pathway. To investigate its effector mechanism(s), the gene expression profile in the liver of baculovirus-administered mice was characterized by cDNA microarray analysis. The ingenuity pathway analysis gene ontology module revealed that the major gene subsets induced by baculovirus were immune-related signaling, such as interferon signaling. A total of 40 genes commonly upregulated in a Toll-like receptor 9-independent manner were included as possible candidates for parasite elimination. This gene subset consisted of NT5C3, LOC105246895, BTC, APOL9a/b, G3BP3, SLC6A6, USP25, TRIM14, and PSMB8 as the top 10 candidates according to the special unit. These findings provide new insight into effector molecules responsible for liver-stage parasite killing and, possibly, the development of a new baculovirus-mediated prophylactic and therapeutic biopharmaceutical for malaria.
AB - Intramuscular administration of wild-type baculovirus is able to both protect against Plasmodium sporozoite challenge and eliminate liver-stage parasites via a Toll-like receptor 9-independent pathway. To investigate its effector mechanism(s), the gene expression profile in the liver of baculovirus-administered mice was characterized by cDNA microarray analysis. The ingenuity pathway analysis gene ontology module revealed that the major gene subsets induced by baculovirus were immune-related signaling, such as interferon signaling. A total of 40 genes commonly upregulated in a Toll-like receptor 9-independent manner were included as possible candidates for parasite elimination. This gene subset consisted of NT5C3, LOC105246895, BTC, APOL9a/b, G3BP3, SLC6A6, USP25, TRIM14, and PSMB8 as the top 10 candidates according to the special unit. These findings provide new insight into effector molecules responsible for liver-stage parasite killing and, possibly, the development of a new baculovirus-mediated prophylactic and therapeutic biopharmaceutical for malaria.
KW - Baculovirus
KW - CDNA microarray
KW - Interferon signaling
KW - Liver
KW - Plasmodium
UR - http://www.scopus.com/inward/record.url?scp=85108124126&partnerID=8YFLogxK
U2 - 10.3727/105221620X16039045978676
DO - 10.3727/105221620X16039045978676
M3 - 学術論文
C2 - 33115550
AN - SCOPUS:85108124126
SN - 1052-2166
VL - 20
SP - 147
EP - 155
JO - Gene Expression The Journal of Liver Research
JF - Gene Expression The Journal of Liver Research
IS - 3
ER -