| アイテムタイプ |
学術雑誌論文 / Journal Article(1) |
| 公開日 |
2026-03-13 |
| タイトル |
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タイトル |
Trafficking and organization of cyst wall components into a robust biphasic structure in Entamoeba |
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言語 |
en |
| 言語 |
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言語 |
eng |
| 資源タイプ |
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資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
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資源タイプ |
journal article |
| 著者 |
Vo, Tam Kha
Yoshida, Hiroki
Mi-ichi, Fumika
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| 抄録 |
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内容記述タイプ |
Abstract |
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内容記述 |
Entamoeba histolytica, a protozoan parasite, causes amebiasis. Amebiasis is mainly transmitted by oral ingestion of cysts. Cysts are produced in the large intestine of humans from proliferative trophozoites by a cell differentiation process called encystation. The Entamoeba cyst wall consists of chitins and proteins that include chitinase and Jacob and Jessie lectins. During encystation, these components are synthesized and layered around encysting Entamoeba cells. The structures of these components are well studied; however, the detailed timings of their synthesis (the transcription of the encoding genes and the translation of the resulting mRNAs) and of changes in their localization during encystation are poorly understood. Here, we performed quantitative RT-PCR and an approach combining western blotting and immunofluorescence, confocal, and immunoelectron microscopy to analyze Entamoeba invadens cells that were sampled with short-time intervals during encystation. A chitinase inhibitor, D-B-09, which disrupts the compression of chitin fibers was used to analyze component interaction with chitin fibers. All genes encoding cyst wall proteins were stage-specifically transcribed and translated, and post-translationally modified forms of Jacob1/3 were trafficked to the cyst wall before Jessie3a and Chitinase1/4 were simultaneously localized in the cyst wall. The trafficking of Jacob lectins to the cyst wall and their co-localization with chitin fibers in encysting cells were not affected by D-B-09, while the localization of Jessie protein was impaired, indicating that localizations of Jacob and Jessie lectins are spatially different positions via different modes in cyst wall. These results indicate that cyst wall components are functionally linked and that they play different roles during Entamoeba cyst wall formation. Immunoelectron microscopy confirmed the immunofluorescence and confocal microscopy results. Importantly, immunoelectron microscopy also indicated that the Entamoeba cyst wall consists of a biphasic structure of electron-light (inner) and electron-dense (outer) areas. |
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言語 |
en |
| 書誌情報 |
en : PLOS Pathogens
巻 22,
号 2,
p. art. no. e1013940,
発行日 2026-02-26
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| 出版者 |
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出版者 |
Public Library of Science |
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言語 |
en |
| ISSN |
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収録物識別子タイプ |
EISSN |
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収録物識別子 |
1553-7374 |
| DOI |
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関連タイプ |
isIdenticalTo |
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識別子タイプ |
DOI |
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関連識別子 |
https://doi.org/10.1371/journal.ppat.1013940 |
| 権利 |
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権利情報 |
© 2026 Vo et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
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言語 |
en |
| 著者版フラグ |
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出版タイプ |
VoR |
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出版タイプResource |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
| 引用 |
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内容記述タイプ |
Other |
|
内容記述 |
PLOS Pathogens, 22, art. no. e1013940; 2026 |
|
言語 |
en |
PLOSP22_e1013940.pdf (3.3 MB)
