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柔嫩艾美耳球虫组织蛋白酶B样半胱氨酸蛋白酶艾美球虫蛋白酶在鸡盲肠无性和有性细胞内发育过程中的定位

Localization of eimeripain, an Eimeria tenella cathepsin B-like cysteine protease, during asexual and sexual intracellular development in chicken ceca.

作者信息

Matsubayashi Makoto, Hatta Takeshi, Miyoshi Takeharu, Sasai Kazumi, Yamaji Kayoko, Shimura Kameo, Isobe Takashi, Kita Kiyoshi, Tsuji Naotoshi

机构信息

National Institute of Animal Health, National Agriculture and Food Research Organization, 3-1-5 Kannondai, Tsukuba, Ibaraki 305-0856, Japan.

出版信息

J Vet Med Sci. 2014 Apr;76(4):531-7. doi: 10.1292/jvms.13-0509. Epub 2013 Dec 20.

DOI:10.1292/jvms.13-0509
PMID:24366155
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4064137/
Abstract

Hemorrhagic diarrhea in poultry is caused by Eimeria tenella, the most pathogenic avian coccidian parasite, and new approaches to treat the disease are continually being sought. Although eimeripain, a cathepsin B-like cysteine protease from E. tenella, has recently been identified as a novel anticoccidial drug target, its localization during the intracellular development of parasites remains unclear. Here, we demonstrate the expression of eimeripain during asexual and sexual development of E. tenella in vivo. Promature eimeripain was detected only in the early immature second generation of schizonts. In contrast, the mature eimeripain was most strongly detected in the middle-sized immature second generation of schizonts. Both promature and mature eimeripain disappeared depending on the maturation level of second generation of schizonts, but were strongly expressed again in the third generation of schizonts. In the sexual stage, both promature and mature eimeripain were detected in the cytoplasm of micro- and macro-gametocytes and zygotes, but expression became weak in zoites forming oocysts. Collectively, our findings suggest that eimeripain might play a key role in the differentiation of intracellular zoites in the ceca and could be an interesting candidate to develop a novel, effective anti-coccidian drug.

摘要

家禽出血性腹泻由最具致病性的禽类球虫寄生虫柔嫩艾美耳球虫引起,人们一直在不断寻求治疗该疾病的新方法。尽管最近已确定来自柔嫩艾美耳球虫的组织蛋白酶B样半胱氨酸蛋白酶艾美蛋白酶是一种新型抗球虫药物靶点,但其在寄生虫细胞内发育过程中的定位仍不清楚。在此,我们证明了艾美蛋白酶在柔嫩艾美耳球虫体内无性和有性发育过程中的表达。仅在早期未成熟的第二代裂殖子中检测到前成熟艾美蛋白酶。相反,在中等大小的未成熟第二代裂殖子中,成熟艾美蛋白酶的检测信号最强。前成熟和成熟的艾美蛋白酶均随着第二代裂殖子的成熟程度而消失,但在第三代裂殖子中再次强烈表达。在有性阶段,在前配子体、大配子体和受精卵的细胞质中均检测到前成熟和成熟的艾美蛋白酶,但在形成卵囊的子孢子中表达减弱。总体而言,我们的研究结果表明,艾美蛋白酶可能在盲肠内细胞内子孢子的分化中起关键作用,并且可能是开发新型有效抗球虫药物的一个有吸引力的候选靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0390/4064137/21ef5e607e2b/jvms-76-531-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0390/4064137/97d73362cb40/jvms-76-531-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0390/4064137/3e33f9bb9d71/jvms-76-531-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0390/4064137/88ee05a13f10/jvms-76-531-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0390/4064137/77b83e4757cb/jvms-76-531-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0390/4064137/a6f391abf464/jvms-76-531-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0390/4064137/21ef5e607e2b/jvms-76-531-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0390/4064137/97d73362cb40/jvms-76-531-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0390/4064137/3e33f9bb9d71/jvms-76-531-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0390/4064137/88ee05a13f10/jvms-76-531-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0390/4064137/77b83e4757cb/jvms-76-531-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0390/4064137/a6f391abf464/jvms-76-531-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0390/4064137/21ef5e607e2b/jvms-76-531-g006.jpg

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Identification of lead compounds targeting the cathepsin B-like enzyme of Eimeria tenella.
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