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Malaria oocysts require circumsporozoite protein to evade mosquito immunity

Malaria parasites are less vulnerable to mosquito immune responses once ookinetes transform into oocysts, facilitating parasite development in the mosquito. However, the underlying mechanisms of oocyst resistance to mosquito defenses remain unclear. Here, we show that circumsporozoite protein (CSP)...

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Autores principales: Zhu, Feng, Zheng, Hong, Chen, Suilin, Zhang, Kun, Qin, Xin, Zhang, Jingru, liu, Taiping, Fan, Yongling, Wang, Liting, Li, Xiaoxu, Zhang, Jian, Xu, Wenyue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184642/
https://www.ncbi.nlm.nih.gov/pubmed/35680915
http://dx.doi.org/10.1038/s41467-022-30988-z
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author Zhu, Feng
Zheng, Hong
Chen, Suilin
Zhang, Kun
Qin, Xin
Zhang, Jingru
liu, Taiping
Fan, Yongling
Wang, Liting
Li, Xiaoxu
Zhang, Jian
Xu, Wenyue
author_facet Zhu, Feng
Zheng, Hong
Chen, Suilin
Zhang, Kun
Qin, Xin
Zhang, Jingru
liu, Taiping
Fan, Yongling
Wang, Liting
Li, Xiaoxu
Zhang, Jian
Xu, Wenyue
author_sort Zhu, Feng
collection PubMed
description Malaria parasites are less vulnerable to mosquito immune responses once ookinetes transform into oocysts, facilitating parasite development in the mosquito. However, the underlying mechanisms of oocyst resistance to mosquito defenses remain unclear. Here, we show that circumsporozoite protein (CSP) is required for rodent malaria oocysts to avoid mosquito defenses. Mosquito infection with CSP(mut) parasites (mutation in the CSP pexel I/II domains) induces nicotinamide adenine dinucleotide phosphate (NADPH) oxidase 5 (NOX5)-mediated hemocyte nitration, thus activating Toll pathway and melanization of mature oocysts, upregulating hemocyte TEP1 expression, and causing defects in the release of sporozoites from oocysts. The pre-infection of mosquitoes with the CSP(mut) parasites reduces the burden of infection when re-challenged with CSP(wt) parasites by inducing hemocyte nitration. Thus, we demonstrate why oocysts are invisible to mosquito immunity and reveal an unknown role of CSP in the immune evasion of oocysts, indicating it as a potential target to block malaria transmission.
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spelling pubmed-91846422022-06-11 Malaria oocysts require circumsporozoite protein to evade mosquito immunity Zhu, Feng Zheng, Hong Chen, Suilin Zhang, Kun Qin, Xin Zhang, Jingru liu, Taiping Fan, Yongling Wang, Liting Li, Xiaoxu Zhang, Jian Xu, Wenyue Nat Commun Article Malaria parasites are less vulnerable to mosquito immune responses once ookinetes transform into oocysts, facilitating parasite development in the mosquito. However, the underlying mechanisms of oocyst resistance to mosquito defenses remain unclear. Here, we show that circumsporozoite protein (CSP) is required for rodent malaria oocysts to avoid mosquito defenses. Mosquito infection with CSP(mut) parasites (mutation in the CSP pexel I/II domains) induces nicotinamide adenine dinucleotide phosphate (NADPH) oxidase 5 (NOX5)-mediated hemocyte nitration, thus activating Toll pathway and melanization of mature oocysts, upregulating hemocyte TEP1 expression, and causing defects in the release of sporozoites from oocysts. The pre-infection of mosquitoes with the CSP(mut) parasites reduces the burden of infection when re-challenged with CSP(wt) parasites by inducing hemocyte nitration. Thus, we demonstrate why oocysts are invisible to mosquito immunity and reveal an unknown role of CSP in the immune evasion of oocysts, indicating it as a potential target to block malaria transmission. Nature Publishing Group UK 2022-06-09 /pmc/articles/PMC9184642/ /pubmed/35680915 http://dx.doi.org/10.1038/s41467-022-30988-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhu, Feng
Zheng, Hong
Chen, Suilin
Zhang, Kun
Qin, Xin
Zhang, Jingru
liu, Taiping
Fan, Yongling
Wang, Liting
Li, Xiaoxu
Zhang, Jian
Xu, Wenyue
Malaria oocysts require circumsporozoite protein to evade mosquito immunity
title Malaria oocysts require circumsporozoite protein to evade mosquito immunity
title_full Malaria oocysts require circumsporozoite protein to evade mosquito immunity
title_fullStr Malaria oocysts require circumsporozoite protein to evade mosquito immunity
title_full_unstemmed Malaria oocysts require circumsporozoite protein to evade mosquito immunity
title_short Malaria oocysts require circumsporozoite protein to evade mosquito immunity
title_sort malaria oocysts require circumsporozoite protein to evade mosquito immunity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184642/
https://www.ncbi.nlm.nih.gov/pubmed/35680915
http://dx.doi.org/10.1038/s41467-022-30988-z
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