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A mosquito salivary gland protein partially inhibits Plasmodium sporozoite cell traversal and transmission

The key step during the initiation of malaria is for motile Plasmodium parasites to exit the host dermis and infect the liver. During transmission, the parasites in the form of sporozoites, are injected together with mosquito saliva into the skin. However, the contribution of vector saliva to sporoz...

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Autores principales: Schleicher, Tyler R., Yang, Jing, Freudzon, Marianna, Rembisz, Alison, Craft, Samuel, Hamilton, Madeleine, Graham, Morven, Mlambo, Godfree, Tripathi, Abhai K., Li, Yue, Cresswell, Peter, Sinnis, Photini, Dimopoulos, George, Fikrig, Erol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6060088/
https://www.ncbi.nlm.nih.gov/pubmed/30046053
http://dx.doi.org/10.1038/s41467-018-05374-3
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author Schleicher, Tyler R.
Yang, Jing
Freudzon, Marianna
Rembisz, Alison
Craft, Samuel
Hamilton, Madeleine
Graham, Morven
Mlambo, Godfree
Tripathi, Abhai K.
Li, Yue
Cresswell, Peter
Sinnis, Photini
Dimopoulos, George
Fikrig, Erol
author_facet Schleicher, Tyler R.
Yang, Jing
Freudzon, Marianna
Rembisz, Alison
Craft, Samuel
Hamilton, Madeleine
Graham, Morven
Mlambo, Godfree
Tripathi, Abhai K.
Li, Yue
Cresswell, Peter
Sinnis, Photini
Dimopoulos, George
Fikrig, Erol
author_sort Schleicher, Tyler R.
collection PubMed
description The key step during the initiation of malaria is for motile Plasmodium parasites to exit the host dermis and infect the liver. During transmission, the parasites in the form of sporozoites, are injected together with mosquito saliva into the skin. However, the contribution of vector saliva to sporozoite activity during the establishment of the initial infection of the liver is poorly understood. Here we identify a vector protein by mass spectrometry, with similarity to the human gamma interferon inducible thiol reductase (GILT), that is associated with saliva sporozoites of infected Anopheles mosquitoes and has a negative impact on the speed and cell traversal activity of Plasmodium. This protein, referred to as mosquito GILT (mosGILT) represents an example of a protein found in mosquito saliva that may negatively influence sporozoite movement in the host and could lead to new approaches to prevent malaria.
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spelling pubmed-60600882018-07-27 A mosquito salivary gland protein partially inhibits Plasmodium sporozoite cell traversal and transmission Schleicher, Tyler R. Yang, Jing Freudzon, Marianna Rembisz, Alison Craft, Samuel Hamilton, Madeleine Graham, Morven Mlambo, Godfree Tripathi, Abhai K. Li, Yue Cresswell, Peter Sinnis, Photini Dimopoulos, George Fikrig, Erol Nat Commun Article The key step during the initiation of malaria is for motile Plasmodium parasites to exit the host dermis and infect the liver. During transmission, the parasites in the form of sporozoites, are injected together with mosquito saliva into the skin. However, the contribution of vector saliva to sporozoite activity during the establishment of the initial infection of the liver is poorly understood. Here we identify a vector protein by mass spectrometry, with similarity to the human gamma interferon inducible thiol reductase (GILT), that is associated with saliva sporozoites of infected Anopheles mosquitoes and has a negative impact on the speed and cell traversal activity of Plasmodium. This protein, referred to as mosquito GILT (mosGILT) represents an example of a protein found in mosquito saliva that may negatively influence sporozoite movement in the host and could lead to new approaches to prevent malaria. Nature Publishing Group UK 2018-07-25 /pmc/articles/PMC6060088/ /pubmed/30046053 http://dx.doi.org/10.1038/s41467-018-05374-3 Text en © The Author(s) 2018 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
Schleicher, Tyler R.
Yang, Jing
Freudzon, Marianna
Rembisz, Alison
Craft, Samuel
Hamilton, Madeleine
Graham, Morven
Mlambo, Godfree
Tripathi, Abhai K.
Li, Yue
Cresswell, Peter
Sinnis, Photini
Dimopoulos, George
Fikrig, Erol
A mosquito salivary gland protein partially inhibits Plasmodium sporozoite cell traversal and transmission
title A mosquito salivary gland protein partially inhibits Plasmodium sporozoite cell traversal and transmission
title_full A mosquito salivary gland protein partially inhibits Plasmodium sporozoite cell traversal and transmission
title_fullStr A mosquito salivary gland protein partially inhibits Plasmodium sporozoite cell traversal and transmission
title_full_unstemmed A mosquito salivary gland protein partially inhibits Plasmodium sporozoite cell traversal and transmission
title_short A mosquito salivary gland protein partially inhibits Plasmodium sporozoite cell traversal and transmission
title_sort mosquito salivary gland protein partially inhibits plasmodium sporozoite cell traversal and transmission
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6060088/
https://www.ncbi.nlm.nih.gov/pubmed/30046053
http://dx.doi.org/10.1038/s41467-018-05374-3
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