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分泌蛋白在小鼠和小牛大脑中的分布

The Distribution of Secretory Proteins in Mouse and Calf Brains.

作者信息

Ushio-Watanabe Nanako, Fujihara Rio, Watanabe Kenichi, Yamada Manabu, Kobayashi Yoshiyasu, Nishikawa Yoshifumi

机构信息

National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Hokkaido 080-8555, Japan.

Kochi Seibu Livestock Hygiene Service Center, Kochi 786-0043, Japan.

出版信息

Microorganisms. 2025 Aug 22;13(9):1970. doi: 10.3390/microorganisms13091970.

DOI:10.3390/microorganisms13091970
PMID:41011303
Abstract

, as well as , secrete proteins that facilitate the invasion of host cells and the regulation of host immune response and metabolism. However, the localization of the secretory proteins in infected animal brains has not been studied in detail. Here, we investigate the brain and intracellular distribution of the secretory proteins in experimentally infected mice and naturally infected calves through histopathology and immunohistochemistry (IHC) to detect surface antigen 1 (NcSAG1), cyclophilin (NcCYP), profilin (NcPF), dense granule protein 6 (NcGRA6), and NcGRA7. These methods revealed that numerous tachyzoites positive for NcSAG1, NcCYP, NcPF, NcGRA6, and NcGRA7 were localized in and around the animals' necrotic lesions, and NcGRA7 was diffusely observed in the necrotic lesions of the infected mice. Moreover, IHC revealed that NcGRA6 and NcGRA7 were distributed in the cytoplasm of infected neurons around the parasites in the infected mice and calves. This suggests that NcGRA6 and NcGRA7 might be directly related to the alteration of neuronal metabolism and activity, and that NcGRA7 might be related to the formation of necrotic lesions.

摘要

以及 ,分泌促进宿主细胞侵袭、宿主免疫反应调节和新陈代谢的蛋白质。然而,分泌蛋白在受感染动物大脑中的定位尚未得到详细研究。在这里,我们通过组织病理学和免疫组织化学(IHC)研究实验感染小鼠和自然感染小牛中分泌蛋白的脑内和细胞内分布,以检测表面抗原1(NcSAG1)、亲环蛋白(NcCYP)、肌动蛋白结合蛋白(NcPF)、致密颗粒蛋白6(NcGRA6)和NcGRA7。这些方法显示,大量NcSAG1、NcCYP、NcPF、NcGRA6和NcGRA7呈阳性的速殖子位于动物坏死病变内及其周围,并且在感染小鼠的坏死病变中广泛观察到NcGRA7。此外,免疫组织化学显示,NcGRA6和NcGRA7分布在感染小鼠和小牛体内寄生虫周围受感染神经元的细胞质中。这表明NcGRA6和NcGRA7可能与神经元代谢和活性的改变直接相关,并且NcGRA7可能与坏死病变的形成有关。

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本文引用的文献

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Estimation of direct economic and productive losses due to abortions caused by in the primary dairy sector of Uruguay.乌拉圭主要乳制品行业因[未提及具体原因]导致的堕胎所造成的直接经济和生产损失估计。
Front Vet Sci. 2025 Mar 26;12:1502742. doi: 10.3389/fvets.2025.1502742. eCollection 2025.
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Modulation of host cell membrane biophysics dynamics by Neospora caninum: A study using LAURDAN fluorescence with hyperspectral imaging and phasor analysis.犬新孢子虫对宿主细胞膜生物物理动力学的调控:一项使用LAURDAN荧光结合高光谱成像和相量分析的研究
J Microsc. 2025 Feb 20. doi: 10.1111/jmi.13395.
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Study of specific immunodominant antigens in different stages of Neospora caninum, Toxoplasma gondii, Sarcocystis spp. and Hammondia spp.
研究刚地弓形虫、弓形虫、肉孢子虫属和哈门氏原虫不同阶段的特异性免疫优势抗原。
Exp Parasitol. 2024 Jul;262:108772. doi: 10.1016/j.exppara.2024.108772. Epub 2024 May 7.
4
Evaluation of Immunodiagnostic Performances of Peroxiredoxin 2 (NcPrx2), Microneme 4 (NcMIC4), and Surface Antigen 1 (NcSAG1) Recombinant Proteins for Bovine Neosporosis.用于牛新孢子虫病的过氧化物还原酶2(NcPrx2)、微线体蛋白4(NcMIC4)和表面抗原1(NcSAG1)重组蛋白的免疫诊断性能评估
Animals (Basel). 2024 Feb 6;14(4):531. doi: 10.3390/ani14040531.
5
Infection Triggers S-phase Arrest and Alters Nuclear Characteristics in Primary Bovine Endothelial Host Cells.感染引发原代牛内皮宿主细胞的S期停滞并改变核特征。
Front Cell Dev Biol. 2022 Aug 5;10:946335. doi: 10.3389/fcell.2022.946335. eCollection 2022.
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Dense granule biogenesis, secretion, and function in Toxoplasma gondii.致密颗粒的生物发生、分泌和功能在刚地弓形虫中。
J Eukaryot Microbiol. 2022 Nov;69(6):e12904. doi: 10.1111/jeu.12904. Epub 2022 Apr 1.
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Microorganisms. 2021 Oct 11;9(10):2133. doi: 10.3390/microorganisms9102133.
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9
From Signaling Pathways to Distinct Immune Responses: Key Factors for Establishing or Combating Infection in Different Susceptible Hosts.从信号通路到不同的免疫反应:在不同易感宿主中建立感染或对抗感染的关键因素
Pathogens. 2020 May 16;9(5):384. doi: 10.3390/pathogens9050384.
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Toxoplasma gondii Parasitophorous Vacuole Membrane-Associated Dense Granule Proteins Regulate Maturation of the Cyst Wall.刚地弓形虫滋养体空泡膜相关致密颗粒蛋白调控囊壁的成熟。
mSphere. 2020 Jan 15;5(1):e00851-19. doi: 10.1128/mSphere.00851-19.