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Characterization of essential eggshell proteins from Aedes aegypti mosquitoes
BACKGROUND: Up to 40% of the world population live in areas where mosquitoes capable of transmitting the dengue virus, including Aedes aegypti, coexist with humans. Understanding how mosquito egg development and oviposition are regulated at the molecular level may provide new insights into novel mos...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10576393/ https://www.ncbi.nlm.nih.gov/pubmed/37833714 http://dx.doi.org/10.1186/s12915-023-01721-z |
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author | Isoe, Jun Simington, Carter J. Oscherwitz, Max E. Peterson, Alyssa J. Rascón, Alberto A. Massani, Brooke B. Miesfeld, Roger L. Riehle, Michael A. |
author_facet | Isoe, Jun Simington, Carter J. Oscherwitz, Max E. Peterson, Alyssa J. Rascón, Alberto A. Massani, Brooke B. Miesfeld, Roger L. Riehle, Michael A. |
author_sort | Isoe, Jun |
collection | PubMed |
description | BACKGROUND: Up to 40% of the world population live in areas where mosquitoes capable of transmitting the dengue virus, including Aedes aegypti, coexist with humans. Understanding how mosquito egg development and oviposition are regulated at the molecular level may provide new insights into novel mosquito control strategies. Previously, we identified a protein named eggshell organizing factor 1 (EOF1) that when knocked down with RNA interference (RNAi) resulted in non-melanized and fragile eggs that did not contain viable embryos. RESULTS: In this current study, we performed a comprehensive RNAi screen of putative A. aegypti eggshell proteins to identify additional proteins that interact with intracellular EOF1. We identified several proteins essential for eggshell formation in A. aegypti and characterized their phenotypes through a combination of molecular and biochemical approaches. We found that Nasrat, Closca, and Polehole structural proteins, together with the Nudel serine protease, are indispensable for eggshell melanization and egg viability. While all four proteins are predominantly expressed in ovaries of adult females, Nudel messenger RNA (mRNA) expression is highly upregulated in response to blood feeding. Furthermore, we identified four additional secreted eggshell enzymes that regulated mosquito eggshell formation and melanization. These enzymes included three dopachrome-converting enzymes (DCEs) and one cysteine protease. All eight of these eggshell proteins were essential for proper eggshell formation. Interestingly, their eggshell surface topologies in response to RNAi did not phenocopy the effect of RNAi-EOF1, suggesting that additional mechanisms may influence how EOF1 regulates eggshell formation and melanization. CONCLUSIONS: While our studies did not identify a definitive regulator of EOF1, we did identify eight additional proteins involved in mosquito eggshell formation that may be leveraged for future control strategies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-023-01721-z. |
format | Online Article Text |
id | pubmed-10576393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105763932023-10-15 Characterization of essential eggshell proteins from Aedes aegypti mosquitoes Isoe, Jun Simington, Carter J. Oscherwitz, Max E. Peterson, Alyssa J. Rascón, Alberto A. Massani, Brooke B. Miesfeld, Roger L. Riehle, Michael A. BMC Biol Research Article BACKGROUND: Up to 40% of the world population live in areas where mosquitoes capable of transmitting the dengue virus, including Aedes aegypti, coexist with humans. Understanding how mosquito egg development and oviposition are regulated at the molecular level may provide new insights into novel mosquito control strategies. Previously, we identified a protein named eggshell organizing factor 1 (EOF1) that when knocked down with RNA interference (RNAi) resulted in non-melanized and fragile eggs that did not contain viable embryos. RESULTS: In this current study, we performed a comprehensive RNAi screen of putative A. aegypti eggshell proteins to identify additional proteins that interact with intracellular EOF1. We identified several proteins essential for eggshell formation in A. aegypti and characterized their phenotypes through a combination of molecular and biochemical approaches. We found that Nasrat, Closca, and Polehole structural proteins, together with the Nudel serine protease, are indispensable for eggshell melanization and egg viability. While all four proteins are predominantly expressed in ovaries of adult females, Nudel messenger RNA (mRNA) expression is highly upregulated in response to blood feeding. Furthermore, we identified four additional secreted eggshell enzymes that regulated mosquito eggshell formation and melanization. These enzymes included three dopachrome-converting enzymes (DCEs) and one cysteine protease. All eight of these eggshell proteins were essential for proper eggshell formation. Interestingly, their eggshell surface topologies in response to RNAi did not phenocopy the effect of RNAi-EOF1, suggesting that additional mechanisms may influence how EOF1 regulates eggshell formation and melanization. CONCLUSIONS: While our studies did not identify a definitive regulator of EOF1, we did identify eight additional proteins involved in mosquito eggshell formation that may be leveraged for future control strategies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-023-01721-z. BioMed Central 2023-10-13 /pmc/articles/PMC10576393/ /pubmed/37833714 http://dx.doi.org/10.1186/s12915-023-01721-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Isoe, Jun Simington, Carter J. Oscherwitz, Max E. Peterson, Alyssa J. Rascón, Alberto A. Massani, Brooke B. Miesfeld, Roger L. Riehle, Michael A. Characterization of essential eggshell proteins from Aedes aegypti mosquitoes |
title | Characterization of essential eggshell proteins from Aedes aegypti mosquitoes |
title_full | Characterization of essential eggshell proteins from Aedes aegypti mosquitoes |
title_fullStr | Characterization of essential eggshell proteins from Aedes aegypti mosquitoes |
title_full_unstemmed | Characterization of essential eggshell proteins from Aedes aegypti mosquitoes |
title_short | Characterization of essential eggshell proteins from Aedes aegypti mosquitoes |
title_sort | characterization of essential eggshell proteins from aedes aegypti mosquitoes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10576393/ https://www.ncbi.nlm.nih.gov/pubmed/37833714 http://dx.doi.org/10.1186/s12915-023-01721-z |
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