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PfMAP-2 is essential for male gametogenesis in the malaria parasite Plasmodium falciparum
In malaria parasites, male gametogenesis is a proliferative stage essential for parasite transmission to the mosquito vector. It is a rapid process involving three rounds of genome replication alternating with closed endomitoses, and assembly of axonemes to produce eight flagellated motile microgame...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368081/ https://www.ncbi.nlm.nih.gov/pubmed/32681115 http://dx.doi.org/10.1038/s41598-020-68717-5 |
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author | Hitz, Eva Balestra, Aurélia C. Brochet, Mathieu Voss, Till S. |
author_facet | Hitz, Eva Balestra, Aurélia C. Brochet, Mathieu Voss, Till S. |
author_sort | Hitz, Eva |
collection | PubMed |
description | In malaria parasites, male gametogenesis is a proliferative stage essential for parasite transmission to the mosquito vector. It is a rapid process involving three rounds of genome replication alternating with closed endomitoses, and assembly of axonemes to produce eight flagellated motile microgametes. Studies in Plasmodium berghei have highlighted tight regulation of gametogenesis by a network of kinases. The P. berghei MAPK homologue PbMAP-2 is dispensable for asexual development but important at the induction of axoneme motility. However, in P. falciparum, causing the most severe form of human malaria, PfMAP-2 was suggested to be essential for asexual proliferation indicating distinct functions for MAP-2 in these two Plasmodium species. We here show that PfMAP-2 is dispensable for asexual growth but important for male gametogenesis in vitro. Similar to PbMAP-2, PfMAP-2 is required for initiating axonemal beating but not for prior DNA replication or axoneme formation. In addition, single and double null mutants of PfMAP-2 and the second P. falciparum MAPK homologue PfMAP-1 show no defect in asexual proliferation, sexual commitment or gametocytogenesis. Our results suggest that MAPK activity plays no major role in the biology of both asexual and sexual blood stage parasites up until the point of male gametogenesis. |
format | Online Article Text |
id | pubmed-7368081 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73680812020-07-22 PfMAP-2 is essential for male gametogenesis in the malaria parasite Plasmodium falciparum Hitz, Eva Balestra, Aurélia C. Brochet, Mathieu Voss, Till S. Sci Rep Article In malaria parasites, male gametogenesis is a proliferative stage essential for parasite transmission to the mosquito vector. It is a rapid process involving three rounds of genome replication alternating with closed endomitoses, and assembly of axonemes to produce eight flagellated motile microgametes. Studies in Plasmodium berghei have highlighted tight regulation of gametogenesis by a network of kinases. The P. berghei MAPK homologue PbMAP-2 is dispensable for asexual development but important at the induction of axoneme motility. However, in P. falciparum, causing the most severe form of human malaria, PfMAP-2 was suggested to be essential for asexual proliferation indicating distinct functions for MAP-2 in these two Plasmodium species. We here show that PfMAP-2 is dispensable for asexual growth but important for male gametogenesis in vitro. Similar to PbMAP-2, PfMAP-2 is required for initiating axonemal beating but not for prior DNA replication or axoneme formation. In addition, single and double null mutants of PfMAP-2 and the second P. falciparum MAPK homologue PfMAP-1 show no defect in asexual proliferation, sexual commitment or gametocytogenesis. Our results suggest that MAPK activity plays no major role in the biology of both asexual and sexual blood stage parasites up until the point of male gametogenesis. Nature Publishing Group UK 2020-07-17 /pmc/articles/PMC7368081/ /pubmed/32681115 http://dx.doi.org/10.1038/s41598-020-68717-5 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Hitz, Eva Balestra, Aurélia C. Brochet, Mathieu Voss, Till S. PfMAP-2 is essential for male gametogenesis in the malaria parasite Plasmodium falciparum |
title | PfMAP-2 is essential for male gametogenesis in the malaria parasite Plasmodium falciparum |
title_full | PfMAP-2 is essential for male gametogenesis in the malaria parasite Plasmodium falciparum |
title_fullStr | PfMAP-2 is essential for male gametogenesis in the malaria parasite Plasmodium falciparum |
title_full_unstemmed | PfMAP-2 is essential for male gametogenesis in the malaria parasite Plasmodium falciparum |
title_short | PfMAP-2 is essential for male gametogenesis in the malaria parasite Plasmodium falciparum |
title_sort | pfmap-2 is essential for male gametogenesis in the malaria parasite plasmodium falciparum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368081/ https://www.ncbi.nlm.nih.gov/pubmed/32681115 http://dx.doi.org/10.1038/s41598-020-68717-5 |
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