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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)...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-9184642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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