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Salivary gland maturation and duct formation in the African malaria mosquito Anopheles gambiae

Mosquito-borne diseases cause one million deaths and hundreds of millions of human infections yearly. With all such diseases, the pathogen must traverse the mosquito salivary gland (SG) for transmission to a new host, making the SGs ideal targets for genetic strategies to block transmission. Prior s...

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Autores principales: Wells, Michael B., Villamor, Jordan, Andrew, Deborah J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428862/
https://www.ncbi.nlm.nih.gov/pubmed/28377572
http://dx.doi.org/10.1038/s41598-017-00672-0
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author Wells, Michael B.
Villamor, Jordan
Andrew, Deborah J.
author_facet Wells, Michael B.
Villamor, Jordan
Andrew, Deborah J.
author_sort Wells, Michael B.
collection PubMed
description Mosquito-borne diseases cause one million deaths and hundreds of millions of human infections yearly. With all such diseases, the pathogen must traverse the mosquito salivary gland (SG) for transmission to a new host, making the SGs ideal targets for genetic strategies to block transmission. Prior studies have elucidated details of SG structure by light and electron microscopy and have deeply explored the salivary transcriptome and proteome. Very little is known, however, about how the unique functional architecture of mosquito SGs is achieved. Using immunohistochemistry and confocal microscopy, we address two questions regarding SGs of the malaria vector Anopheles gambiae. How does the distinct cup-shaped morphology of SG secretory cells arise? And, how does the salivary duct, the structure through which saliva and parasites exit the glands, form? We demonstrate that SG cells begin as cuboidal-shaped cells surrounding a matrix-filled lumen that mature into cup-shaped cells through the formation and fusion of a large pre-apical compartment (PAC) to the apical surface. The secretory duct begins as buds of chitin at the apical surface of individual secretory cells. Further chitin deposition connects these chitin buds to form a contiguous duct that largely separates from the apical surface during PAC fusion.
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spelling pubmed-54288622017-05-15 Salivary gland maturation and duct formation in the African malaria mosquito Anopheles gambiae Wells, Michael B. Villamor, Jordan Andrew, Deborah J. Sci Rep Article Mosquito-borne diseases cause one million deaths and hundreds of millions of human infections yearly. With all such diseases, the pathogen must traverse the mosquito salivary gland (SG) for transmission to a new host, making the SGs ideal targets for genetic strategies to block transmission. Prior studies have elucidated details of SG structure by light and electron microscopy and have deeply explored the salivary transcriptome and proteome. Very little is known, however, about how the unique functional architecture of mosquito SGs is achieved. Using immunohistochemistry and confocal microscopy, we address two questions regarding SGs of the malaria vector Anopheles gambiae. How does the distinct cup-shaped morphology of SG secretory cells arise? And, how does the salivary duct, the structure through which saliva and parasites exit the glands, form? We demonstrate that SG cells begin as cuboidal-shaped cells surrounding a matrix-filled lumen that mature into cup-shaped cells through the formation and fusion of a large pre-apical compartment (PAC) to the apical surface. The secretory duct begins as buds of chitin at the apical surface of individual secretory cells. Further chitin deposition connects these chitin buds to form a contiguous duct that largely separates from the apical surface during PAC fusion. Nature Publishing Group UK 2017-04-04 /pmc/articles/PMC5428862/ /pubmed/28377572 http://dx.doi.org/10.1038/s41598-017-00672-0 Text en © The Author(s) 2017 This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Wells, Michael B.
Villamor, Jordan
Andrew, Deborah J.
Salivary gland maturation and duct formation in the African malaria mosquito Anopheles gambiae
title Salivary gland maturation and duct formation in the African malaria mosquito Anopheles gambiae
title_full Salivary gland maturation and duct formation in the African malaria mosquito Anopheles gambiae
title_fullStr Salivary gland maturation and duct formation in the African malaria mosquito Anopheles gambiae
title_full_unstemmed Salivary gland maturation and duct formation in the African malaria mosquito Anopheles gambiae
title_short Salivary gland maturation and duct formation in the African malaria mosquito Anopheles gambiae
title_sort salivary gland maturation and duct formation in the african malaria mosquito anopheles gambiae
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428862/
https://www.ncbi.nlm.nih.gov/pubmed/28377572
http://dx.doi.org/10.1038/s41598-017-00672-0
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