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Diversity in new flagellum tip attachment in bloodstream form African trypanosomes
The closely related parasites Trypanosoma brucei, T. congolense, and T. vivax cause neglected tropical diseases collectively known as African Trypanosomiasis. A characteristic feature of bloodstream form T. brucei is the flagellum that is laterally attached to the side of the cell body. During the c...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826329/ https://www.ncbi.nlm.nih.gov/pubmed/36056717 http://dx.doi.org/10.1111/mmi.14979 |
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author | Smithson, Laura Ihuoma Akazue, Pearl Findlater, Lucy Gwira, Theresa Manful Vaughan, Sue Sunter, Jack D. |
author_facet | Smithson, Laura Ihuoma Akazue, Pearl Findlater, Lucy Gwira, Theresa Manful Vaughan, Sue Sunter, Jack D. |
author_sort | Smithson, Laura |
collection | PubMed |
description | The closely related parasites Trypanosoma brucei, T. congolense, and T. vivax cause neglected tropical diseases collectively known as African Trypanosomiasis. A characteristic feature of bloodstream form T. brucei is the flagellum that is laterally attached to the side of the cell body. During the cell cycle, the new flagellum is formed alongside the old flagellum, with the new flagellum tip embedded within a mobile transmembrane junction called the groove. The molecular composition of the groove is currently unknown, which limits the analysis of this junction and assessment of its conservation in related trypanosomatids. Here, we identified 13 proteins that localize to the flagellar groove through a small‐scale tagging screen. Functional analysis of a subset of these proteins by RNAi and gene deletion revealed three proteins, FCP4/TbKin15, FCP7, and FAZ45, that are involved in new flagellum tip attachment to the groove. Despite possessing orthologues of all 13 groove proteins, T. congolense and T. vivax did not assemble a canonical groove around the new flagellum tip according to 3D electron microscopy. This diversity in new flagellum tip attachment points to the rapid evolution of membrane‐cytoskeleton structures that can occur without large changes in gene complement and likely reflects the niche specialization of each species. |
format | Online Article Text |
id | pubmed-9826329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98263292023-01-09 Diversity in new flagellum tip attachment in bloodstream form African trypanosomes Smithson, Laura Ihuoma Akazue, Pearl Findlater, Lucy Gwira, Theresa Manful Vaughan, Sue Sunter, Jack D. Mol Microbiol Research Articles The closely related parasites Trypanosoma brucei, T. congolense, and T. vivax cause neglected tropical diseases collectively known as African Trypanosomiasis. A characteristic feature of bloodstream form T. brucei is the flagellum that is laterally attached to the side of the cell body. During the cell cycle, the new flagellum is formed alongside the old flagellum, with the new flagellum tip embedded within a mobile transmembrane junction called the groove. The molecular composition of the groove is currently unknown, which limits the analysis of this junction and assessment of its conservation in related trypanosomatids. Here, we identified 13 proteins that localize to the flagellar groove through a small‐scale tagging screen. Functional analysis of a subset of these proteins by RNAi and gene deletion revealed three proteins, FCP4/TbKin15, FCP7, and FAZ45, that are involved in new flagellum tip attachment to the groove. Despite possessing orthologues of all 13 groove proteins, T. congolense and T. vivax did not assemble a canonical groove around the new flagellum tip according to 3D electron microscopy. This diversity in new flagellum tip attachment points to the rapid evolution of membrane‐cytoskeleton structures that can occur without large changes in gene complement and likely reflects the niche specialization of each species. John Wiley and Sons Inc. 2022-09-14 2022-11 /pmc/articles/PMC9826329/ /pubmed/36056717 http://dx.doi.org/10.1111/mmi.14979 Text en © 2022 The Authors. Molecular Microbiology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Smithson, Laura Ihuoma Akazue, Pearl Findlater, Lucy Gwira, Theresa Manful Vaughan, Sue Sunter, Jack D. Diversity in new flagellum tip attachment in bloodstream form African trypanosomes |
title | Diversity in new flagellum tip attachment in bloodstream form African trypanosomes |
title_full | Diversity in new flagellum tip attachment in bloodstream form African trypanosomes |
title_fullStr | Diversity in new flagellum tip attachment in bloodstream form African trypanosomes |
title_full_unstemmed | Diversity in new flagellum tip attachment in bloodstream form African trypanosomes |
title_short | Diversity in new flagellum tip attachment in bloodstream form African trypanosomes |
title_sort | diversity in new flagellum tip attachment in bloodstream form african trypanosomes |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826329/ https://www.ncbi.nlm.nih.gov/pubmed/36056717 http://dx.doi.org/10.1111/mmi.14979 |
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