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Unraveling dual feeding associated molecular complexity of salivary glands in the mosquito Anopheles culicifacies
Mosquito salivary glands are well known to facilitate meal acquisition, however the fundamental question on how adult female salivary gland manages molecular responses during sugar versus blood meal uptake remains unanswered. To investigate these responses, we analyzed a total of 58.5 million raw re...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4542284/ https://www.ncbi.nlm.nih.gov/pubmed/26163527 http://dx.doi.org/10.1242/bio.012294 |
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author | Sharma, Punita Sharma, Swati Mishra, Ashwani Kumar Thomas, Tina Das De, Tanwee Rohilla, Suman Lata Singh, Namita Pandey, Kailash C. Valecha, Neena Dixit, Rajnikant |
author_facet | Sharma, Punita Sharma, Swati Mishra, Ashwani Kumar Thomas, Tina Das De, Tanwee Rohilla, Suman Lata Singh, Namita Pandey, Kailash C. Valecha, Neena Dixit, Rajnikant |
author_sort | Sharma, Punita |
collection | PubMed |
description | Mosquito salivary glands are well known to facilitate meal acquisition, however the fundamental question on how adult female salivary gland manages molecular responses during sugar versus blood meal uptake remains unanswered. To investigate these responses, we analyzed a total of 58.5 million raw reads generated from two independent RNAseq libraries of the salivary glands collected from 3–4 day-old sugar and blood fed Anopheles culicifacies mosquitoes. Comprehensive functional annotation analysis of 10,931 contigs unraveled that salivary glands may encode diverse nature of proteins in response to distinct physiological feeding status. Digital gene expression analysis and PCR validation indicated that first blood meal significantly alters the molecular architecture of the salivary glands. Comparative microscopic analysis also revealed that first blood meal uptake not only causes an alteration of at least 12–22% of morphological features of the salivary glands but also results in cellular changes e.g. apoptosis, confirming together that adult female salivary glands are specialized organs to manage meal specific responses. Unraveling the underlying mechanism of mosquito salivary gene expression, controlling dual feeding associated responses may provide a new opportunity to control vector borne diseases. |
format | Online Article Text |
id | pubmed-4542284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Company of Biologists |
record_format | MEDLINE/PubMed |
spelling | pubmed-45422842015-09-16 Unraveling dual feeding associated molecular complexity of salivary glands in the mosquito Anopheles culicifacies Sharma, Punita Sharma, Swati Mishra, Ashwani Kumar Thomas, Tina Das De, Tanwee Rohilla, Suman Lata Singh, Namita Pandey, Kailash C. Valecha, Neena Dixit, Rajnikant Biol Open Research Article Mosquito salivary glands are well known to facilitate meal acquisition, however the fundamental question on how adult female salivary gland manages molecular responses during sugar versus blood meal uptake remains unanswered. To investigate these responses, we analyzed a total of 58.5 million raw reads generated from two independent RNAseq libraries of the salivary glands collected from 3–4 day-old sugar and blood fed Anopheles culicifacies mosquitoes. Comprehensive functional annotation analysis of 10,931 contigs unraveled that salivary glands may encode diverse nature of proteins in response to distinct physiological feeding status. Digital gene expression analysis and PCR validation indicated that first blood meal significantly alters the molecular architecture of the salivary glands. Comparative microscopic analysis also revealed that first blood meal uptake not only causes an alteration of at least 12–22% of morphological features of the salivary glands but also results in cellular changes e.g. apoptosis, confirming together that adult female salivary glands are specialized organs to manage meal specific responses. Unraveling the underlying mechanism of mosquito salivary gene expression, controlling dual feeding associated responses may provide a new opportunity to control vector borne diseases. The Company of Biologists 2015-07-10 /pmc/articles/PMC4542284/ /pubmed/26163527 http://dx.doi.org/10.1242/bio.012294 Text en © 2015. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Sharma, Punita Sharma, Swati Mishra, Ashwani Kumar Thomas, Tina Das De, Tanwee Rohilla, Suman Lata Singh, Namita Pandey, Kailash C. Valecha, Neena Dixit, Rajnikant Unraveling dual feeding associated molecular complexity of salivary glands in the mosquito Anopheles culicifacies |
title | Unraveling dual feeding associated molecular complexity of salivary glands in the mosquito Anopheles culicifacies |
title_full | Unraveling dual feeding associated molecular complexity of salivary glands in the mosquito Anopheles culicifacies |
title_fullStr | Unraveling dual feeding associated molecular complexity of salivary glands in the mosquito Anopheles culicifacies |
title_full_unstemmed | Unraveling dual feeding associated molecular complexity of salivary glands in the mosquito Anopheles culicifacies |
title_short | Unraveling dual feeding associated molecular complexity of salivary glands in the mosquito Anopheles culicifacies |
title_sort | unraveling dual feeding associated molecular complexity of salivary glands in the mosquito anopheles culicifacies |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4542284/ https://www.ncbi.nlm.nih.gov/pubmed/26163527 http://dx.doi.org/10.1242/bio.012294 |
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