A monoclonal antibody that tracks endospore formation in the microsporidium Nosema bombycis.

Nosema bombycis, the first identified microsporidium, is a destructive pathogen of the silkworm Bombyx mori and causes severe worldwide economic losses in sericulture. Major microsporidian structural proteins, such as the spore wall protein (SWP), are known to be involved in host invasion. In this s...

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Main Authors: Yanhong Li, Meiling Tao, Fuping Ma, Guoqing Pan, Zeyang Zhou, Zhengli Wu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4374874?pdf=render
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spelling doaj-e0a22d16de1d4f088cec89012afaecd02020-11-24T21:24:26ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01103e012188410.1371/journal.pone.0121884A monoclonal antibody that tracks endospore formation in the microsporidium Nosema bombycis.Yanhong LiMeiling TaoFuping MaGuoqing PanZeyang ZhouZhengli WuNosema bombycis, the first identified microsporidium, is a destructive pathogen of the silkworm Bombyx mori and causes severe worldwide economic losses in sericulture. Major microsporidian structural proteins, such as the spore wall protein (SWP), are known to be involved in host invasion. In this study, the reactivity of the monoclonal antibody 2B10 was tested against an endospore protein of N. bombycis with a molecular weight size at 50-kDa, using Western blotting. The antigen was purified after immunoprecipitation and was further identified as EOB13320 according to MALDI-TOF MS assay. We found that EOB13320 locates to the surface of the different developmental stages of the parasite, mostly the sporoblast stage and the mature spore after immunoelectron microscopy examination. EOB13320 was also widely distributed in the developing endospore, especially at the sporoblast stage. This endospore protein also accumulated in the cytoplasm of both the merogony and sporoblast stages. These results imply that EOB13320 detected by monoclonal antibody 2B10 is expressed throughout the life cycle of the parasite, notably during the stage when the endospore is formed, and that this protein is important for spore-coat formation and parasite maintenance. Our study could be instrumental in the understanding of spore wall formation and will help to gain greater insight into the biology of this parasite.http://europepmc.org/articles/PMC4374874?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Yanhong Li
Meiling Tao
Fuping Ma
Guoqing Pan
Zeyang Zhou
Zhengli Wu
spellingShingle Yanhong Li
Meiling Tao
Fuping Ma
Guoqing Pan
Zeyang Zhou
Zhengli Wu
A monoclonal antibody that tracks endospore formation in the microsporidium Nosema bombycis.
PLoS ONE
author_facet Yanhong Li
Meiling Tao
Fuping Ma
Guoqing Pan
Zeyang Zhou
Zhengli Wu
author_sort Yanhong Li
title A monoclonal antibody that tracks endospore formation in the microsporidium Nosema bombycis.
title_short A monoclonal antibody that tracks endospore formation in the microsporidium Nosema bombycis.
title_full A monoclonal antibody that tracks endospore formation in the microsporidium Nosema bombycis.
title_fullStr A monoclonal antibody that tracks endospore formation in the microsporidium Nosema bombycis.
title_full_unstemmed A monoclonal antibody that tracks endospore formation in the microsporidium Nosema bombycis.
title_sort monoclonal antibody that tracks endospore formation in the microsporidium nosema bombycis.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Nosema bombycis, the first identified microsporidium, is a destructive pathogen of the silkworm Bombyx mori and causes severe worldwide economic losses in sericulture. Major microsporidian structural proteins, such as the spore wall protein (SWP), are known to be involved in host invasion. In this study, the reactivity of the monoclonal antibody 2B10 was tested against an endospore protein of N. bombycis with a molecular weight size at 50-kDa, using Western blotting. The antigen was purified after immunoprecipitation and was further identified as EOB13320 according to MALDI-TOF MS assay. We found that EOB13320 locates to the surface of the different developmental stages of the parasite, mostly the sporoblast stage and the mature spore after immunoelectron microscopy examination. EOB13320 was also widely distributed in the developing endospore, especially at the sporoblast stage. This endospore protein also accumulated in the cytoplasm of both the merogony and sporoblast stages. These results imply that EOB13320 detected by monoclonal antibody 2B10 is expressed throughout the life cycle of the parasite, notably during the stage when the endospore is formed, and that this protein is important for spore-coat formation and parasite maintenance. Our study could be instrumental in the understanding of spore wall formation and will help to gain greater insight into the biology of this parasite.
url http://europepmc.org/articles/PMC4374874?pdf=render
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