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"Salivary gland cellular architecture in the Asian malaria vector mosquito Anopheles stephensi"
Anopheles mosquitoes are vectors for malaria, a disease with continued grave outcomes for human health. Transmission of malaria from mosquitoes to humans occurs by parasite passage through the salivary glands (SGs). Previous studies of mosquito SG architecture have been limited in scope and detail....
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Published in: | Parasites & vectors 2015-12, Vol.8 (1), p.617-617, Article 617 |
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description | Anopheles mosquitoes are vectors for malaria, a disease with continued grave outcomes for human health. Transmission of malaria from mosquitoes to humans occurs by parasite passage through the salivary glands (SGs). Previous studies of mosquito SG architecture have been limited in scope and detail.
We developed a simple, optimized protocol for fluorescence staining using dyes and/or antibodies to interrogate cellular architecture in Anopheles stephensi adult SGs. We used common biological dyes, antibodies to well-conserved structural and organellar markers, and antibodies against Anopheles salivary proteins to visualize many individual SGs at high resolution by confocal microscopy.
These analyses confirmed morphological features previously described using electron microscopy and uncovered a high degree of individual variation in SG structure. Our studies provide evidence for two alternative models for the origin of the salivary duct, the structure facilitating parasite transport out of SGs. We compare SG cellular architecture in An. stephensi and Drosophila melanogaster, a fellow Dipteran whose adult SGs are nearly completely unstudied, and find many conserved features despite divergence in overall form and function. Anopheles salivary proteins previously observed at the basement membrane were localized either in SG cells, secretory cavities, or the SG lumen. Our studies also revealed a population of cells with characteristics consistent with regenerative cells, similar to muscle satellite cells or midgut regenerative cells.
This work serves as a foundation for linking Anopheles stephensi SG cellular architecture to function and as a basis for generating and evaluating tools aimed at preventing malaria transmission at the level of mosquito SGs. |
doi_str_mv | 10.1186/s13071-015-1229-z |
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We developed a simple, optimized protocol for fluorescence staining using dyes and/or antibodies to interrogate cellular architecture in Anopheles stephensi adult SGs. We used common biological dyes, antibodies to well-conserved structural and organellar markers, and antibodies against Anopheles salivary proteins to visualize many individual SGs at high resolution by confocal microscopy.
These analyses confirmed morphological features previously described using electron microscopy and uncovered a high degree of individual variation in SG structure. Our studies provide evidence for two alternative models for the origin of the salivary duct, the structure facilitating parasite transport out of SGs. We compare SG cellular architecture in An. stephensi and Drosophila melanogaster, a fellow Dipteran whose adult SGs are nearly completely unstudied, and find many conserved features despite divergence in overall form and function. Anopheles salivary proteins previously observed at the basement membrane were localized either in SG cells, secretory cavities, or the SG lumen. Our studies also revealed a population of cells with characteristics consistent with regenerative cells, similar to muscle satellite cells or midgut regenerative cells.
This work serves as a foundation for linking Anopheles stephensi SG cellular architecture to function and as a basis for generating and evaluating tools aimed at preventing malaria transmission at the level of mosquito SGs.</description><identifier>ISSN: 1756-3305</identifier><identifier>EISSN: 1756-3305</identifier><identifier>DOI: 10.1186/s13071-015-1229-z</identifier><identifier>PMID: 26627194</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Analysis ; Animals ; Anopheles ; Anopheles - cytology ; Antibodies ; Asia ; Cell architecture ; Disease transmission ; Drosophila ; Drosophila melanogaster - cytology ; Fluorescence ; Health aspects ; Insect Vectors ; Malaria ; Microscopy, Confocal ; Microscopy, Fluorescence ; Proteins ; Salivary gland ; Salivary Glands - chemistry ; Salivary Glands - cytology ; Salivary Proteins and Peptides - analysis ; Secretion ; Viral antibodies</subject><ispartof>Parasites & vectors, 2015-12, Vol.8 (1), p.617-617, Article 617</ispartof><rights>COPYRIGHT 2015 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2015</rights><rights>Wells and Andrew. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c594t-660d231417920955ef8a13aa059ce71335c103b9edf2596391e776cad76e0fb13</citedby><cites>FETCH-LOGICAL-c594t-660d231417920955ef8a13aa059ce71335c103b9edf2596391e776cad76e0fb13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667400/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1779737892?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26627194$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wells, Michael B</creatorcontrib><creatorcontrib>Andrew, Deborah J</creatorcontrib><title>"Salivary gland cellular architecture in the Asian malaria vector mosquito Anopheles stephensi"</title><title>Parasites & vectors</title><addtitle>Parasit Vectors</addtitle><description>Anopheles mosquitoes are vectors for malaria, a disease with continued grave outcomes for human health. Transmission of malaria from mosquitoes to humans occurs by parasite passage through the salivary glands (SGs). Previous studies of mosquito SG architecture have been limited in scope and detail.
We developed a simple, optimized protocol for fluorescence staining using dyes and/or antibodies to interrogate cellular architecture in Anopheles stephensi adult SGs. We used common biological dyes, antibodies to well-conserved structural and organellar markers, and antibodies against Anopheles salivary proteins to visualize many individual SGs at high resolution by confocal microscopy.
These analyses confirmed morphological features previously described using electron microscopy and uncovered a high degree of individual variation in SG structure. Our studies provide evidence for two alternative models for the origin of the salivary duct, the structure facilitating parasite transport out of SGs. We compare SG cellular architecture in An. stephensi and Drosophila melanogaster, a fellow Dipteran whose adult SGs are nearly completely unstudied, and find many conserved features despite divergence in overall form and function. Anopheles salivary proteins previously observed at the basement membrane were localized either in SG cells, secretory cavities, or the SG lumen. Our studies also revealed a population of cells with characteristics consistent with regenerative cells, similar to muscle satellite cells or midgut regenerative cells.
This work serves as a foundation for linking Anopheles stephensi SG cellular architecture to function and as a basis for generating and evaluating tools aimed at preventing malaria transmission at the level of mosquito SGs.</description><subject>Analysis</subject><subject>Animals</subject><subject>Anopheles</subject><subject>Anopheles - cytology</subject><subject>Antibodies</subject><subject>Asia</subject><subject>Cell architecture</subject><subject>Disease transmission</subject><subject>Drosophila</subject><subject>Drosophila melanogaster - cytology</subject><subject>Fluorescence</subject><subject>Health aspects</subject><subject>Insect Vectors</subject><subject>Malaria</subject><subject>Microscopy, Confocal</subject><subject>Microscopy, Fluorescence</subject><subject>Proteins</subject><subject>Salivary gland</subject><subject>Salivary Glands - chemistry</subject><subject>Salivary Glands - cytology</subject><subject>Salivary Proteins and Peptides - analysis</subject><subject>Secretion</subject><subject>Viral antibodies</subject><issn>1756-3305</issn><issn>1756-3305</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUk1v1DAQjRCIlsIP4IKscoFDiidO7PiCtKr4WKkSEoWzNXEmu14l8dZOVtBfj5ctpYuQD7Zm3nueeXpZ9hL4BUAt30UQXEHOocqhKHR--yg7BVXJXAhePX7wPsmexbjhXHJdyafZSSFloUCXp5k5v8be7TD8ZKsex5ZZ6vu5x8Aw2LWbyE5zIOZGNq2JLaLDkQ2Y-g7ZLjV9YIOPN7ObPFuMfrumniKLE6XXGN358-xJh32kF3f3Wfb944dvl5_zqy-flpeLq9xWupxyKXlbCChB6SLNWFFXIwhEXmlLCoSoLHDRaGq7otJSaCClpMVWSeJdA-IsWx50W48bsw1uSCsZj878LviwMhgmZ3syuuHALUmyQpfYATY1FjzZJOum4iST1vuD1nZuBmotjVPA_kj0uDO6tVn5nSmlVCXnSeDNnUDwNzPFyQwu7o3FkfwcDShR1wWkpRP09T_QjZ_DmKxKKKWVULUu_qJWmBZwY-fTv3Yvahal1LxSEvZzX_wHlU5Lg7N-pM6l-hHh7REhYSb6Ma1wjtEsr78eY-GAtcHHGKi79wO42afRHNJoUhrNPo3mNnFePTTynvEnfuIX0LbYig</recordid><startdate>20151202</startdate><enddate>20151202</enddate><creator>Wells, Michael B</creator><creator>Andrew, Deborah J</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7SN</scope><scope>7SS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>F1W</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H95</scope><scope>K9.</scope><scope>L.G</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20151202</creationdate><title>"Salivary gland cellular architecture in the Asian malaria vector mosquito Anopheles stephensi"</title><author>Wells, Michael B ; Andrew, Deborah J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c594t-660d231417920955ef8a13aa059ce71335c103b9edf2596391e776cad76e0fb13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Analysis</topic><topic>Animals</topic><topic>Anopheles</topic><topic>Anopheles - cytology</topic><topic>Antibodies</topic><topic>Asia</topic><topic>Cell architecture</topic><topic>Disease transmission</topic><topic>Drosophila</topic><topic>Drosophila melanogaster - cytology</topic><topic>Fluorescence</topic><topic>Health aspects</topic><topic>Insect Vectors</topic><topic>Malaria</topic><topic>Microscopy, Confocal</topic><topic>Microscopy, Fluorescence</topic><topic>Proteins</topic><topic>Salivary gland</topic><topic>Salivary Glands - chemistry</topic><topic>Salivary Glands - cytology</topic><topic>Salivary Proteins and Peptides - analysis</topic><topic>Secretion</topic><topic>Viral antibodies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wells, Michael B</creatorcontrib><creatorcontrib>Andrew, Deborah J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Health & Medical Collection (ProQuest Medical & Health Databases)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Parasites & vectors</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wells, Michael B</au><au>Andrew, Deborah J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>"Salivary gland cellular architecture in the Asian malaria vector mosquito Anopheles stephensi"</atitle><jtitle>Parasites & vectors</jtitle><addtitle>Parasit Vectors</addtitle><date>2015-12-02</date><risdate>2015</risdate><volume>8</volume><issue>1</issue><spage>617</spage><epage>617</epage><pages>617-617</pages><artnum>617</artnum><issn>1756-3305</issn><eissn>1756-3305</eissn><abstract>Anopheles mosquitoes are vectors for malaria, a disease with continued grave outcomes for human health. Transmission of malaria from mosquitoes to humans occurs by parasite passage through the salivary glands (SGs). Previous studies of mosquito SG architecture have been limited in scope and detail.
We developed a simple, optimized protocol for fluorescence staining using dyes and/or antibodies to interrogate cellular architecture in Anopheles stephensi adult SGs. We used common biological dyes, antibodies to well-conserved structural and organellar markers, and antibodies against Anopheles salivary proteins to visualize many individual SGs at high resolution by confocal microscopy.
These analyses confirmed morphological features previously described using electron microscopy and uncovered a high degree of individual variation in SG structure. Our studies provide evidence for two alternative models for the origin of the salivary duct, the structure facilitating parasite transport out of SGs. We compare SG cellular architecture in An. stephensi and Drosophila melanogaster, a fellow Dipteran whose adult SGs are nearly completely unstudied, and find many conserved features despite divergence in overall form and function. Anopheles salivary proteins previously observed at the basement membrane were localized either in SG cells, secretory cavities, or the SG lumen. Our studies also revealed a population of cells with characteristics consistent with regenerative cells, similar to muscle satellite cells or midgut regenerative cells.
This work serves as a foundation for linking Anopheles stephensi SG cellular architecture to function and as a basis for generating and evaluating tools aimed at preventing malaria transmission at the level of mosquito SGs.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>26627194</pmid><doi>10.1186/s13071-015-1229-z</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Animals Anopheles Anopheles - cytology Antibodies Asia Cell architecture Disease transmission Drosophila Drosophila melanogaster - cytology Fluorescence Health aspects Insect Vectors Malaria Microscopy, Confocal Microscopy, Fluorescence Proteins Salivary gland Salivary Glands - chemistry Salivary Glands - cytology Salivary Proteins and Peptides - analysis Secretion Viral antibodies |
title | "Salivary gland cellular architecture in the Asian malaria vector mosquito Anopheles stephensi" |
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