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Morphogenesis of Plasmodium zoites is uncoupled from tensile strength

A shared feature of the motile stages (zoites) of malaria parasites is a cortical cytoskeletal structure termed subpellicular network (SPN), thought to define and maintain cell shape. Plasmodium alveolins comprise structural components of the SPN, and alveolin gene knockout causes morphological abno...

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Autores principales: Tremp, Annie Z, Carter, Victoria, Saeed, Sadia, Dessens, Johannes T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3912903/
https://www.ncbi.nlm.nih.gov/pubmed/23773015
http://dx.doi.org/10.1111/mmi.12297
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author Tremp, Annie Z
Carter, Victoria
Saeed, Sadia
Dessens, Johannes T
author_facet Tremp, Annie Z
Carter, Victoria
Saeed, Sadia
Dessens, Johannes T
author_sort Tremp, Annie Z
collection PubMed
description A shared feature of the motile stages (zoites) of malaria parasites is a cortical cytoskeletal structure termed subpellicular network (SPN), thought to define and maintain cell shape. Plasmodium alveolins comprise structural components of the SPN, and alveolin gene knockout causes morphological abnormalities that coincide with markedly reduced tensile strength of the affected zoites, indicating the alveolins are prime cell shape determinants. Here, we characterize a novel SPN protein of Plasmodium berghei ookinetes and sporozoites named G2 (glycine at position 2), which is structurally unrelated to alveolins. G2 knockout abolishes parasite transmission and causes zoite malformations and motility defects similar to those observed in alveolin null mutants. Unlike alveolins, however, G2 contributes little to tensile strength, arguing against a cause-effect relationship between tensile strength and cell shape. We also show that G2 null mutant sporozoites display an abnormal arrangement of their subpellicular microtubules. These results provide important new understanding of the factors that determine zoite morphogenesis, as well as the potential roles of the cortical cytoskeleton in gliding motility.
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spelling pubmed-39129032014-02-06 Morphogenesis of Plasmodium zoites is uncoupled from tensile strength Tremp, Annie Z Carter, Victoria Saeed, Sadia Dessens, Johannes T Mol Microbiol Research Articles A shared feature of the motile stages (zoites) of malaria parasites is a cortical cytoskeletal structure termed subpellicular network (SPN), thought to define and maintain cell shape. Plasmodium alveolins comprise structural components of the SPN, and alveolin gene knockout causes morphological abnormalities that coincide with markedly reduced tensile strength of the affected zoites, indicating the alveolins are prime cell shape determinants. Here, we characterize a novel SPN protein of Plasmodium berghei ookinetes and sporozoites named G2 (glycine at position 2), which is structurally unrelated to alveolins. G2 knockout abolishes parasite transmission and causes zoite malformations and motility defects similar to those observed in alveolin null mutants. Unlike alveolins, however, G2 contributes little to tensile strength, arguing against a cause-effect relationship between tensile strength and cell shape. We also show that G2 null mutant sporozoites display an abnormal arrangement of their subpellicular microtubules. These results provide important new understanding of the factors that determine zoite morphogenesis, as well as the potential roles of the cortical cytoskeleton in gliding motility. John Wiley & Sons Ltd 2013-08 2013-07-05 /pmc/articles/PMC3912903/ /pubmed/23773015 http://dx.doi.org/10.1111/mmi.12297 Text en 2013 The Authors. Molecular Microbiology published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Tremp, Annie Z
Carter, Victoria
Saeed, Sadia
Dessens, Johannes T
Morphogenesis of Plasmodium zoites is uncoupled from tensile strength
title Morphogenesis of Plasmodium zoites is uncoupled from tensile strength
title_full Morphogenesis of Plasmodium zoites is uncoupled from tensile strength
title_fullStr Morphogenesis of Plasmodium zoites is uncoupled from tensile strength
title_full_unstemmed Morphogenesis of Plasmodium zoites is uncoupled from tensile strength
title_short Morphogenesis of Plasmodium zoites is uncoupled from tensile strength
title_sort morphogenesis of plasmodium zoites is uncoupled from tensile strength
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3912903/
https://www.ncbi.nlm.nih.gov/pubmed/23773015
http://dx.doi.org/10.1111/mmi.12297
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