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Mating mediates morphophysiological changes in the spermathecae of Coptotermes gestroi queens
Insect spermathecae play a crucial role in sperm storage and maintenance prior to egg fertilization. Within eusocial insects, this structure is well studied in the Hymenoptera, whose queens copulate during a short period early in life and store sperm for up to decades. Within Isoptera, sperm storage...
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Published in: | Entomologia experimentalis et applicata 2023-05, Vol.171 (5), p.361-373 |
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description | Insect spermathecae play a crucial role in sperm storage and maintenance prior to egg fertilization. Within eusocial insects, this structure is well studied in the Hymenoptera, whose queens copulate during a short period early in life and store sperm for up to decades. Within Isoptera, sperm storage and maintenance inside the spermatheca are poorly understood, especially due to the presence of a sperm‐providing king. Here, we compared the morphometric and morphophysiological features of the spermathecae of virgin and mated queens of the invasive termite Coptotermes gestroi (Wasmann) (Isoptera: Rhinotermitidae). The spermatheca comprises a finger‐shaped reservoir divided into two regions and a duct limited by a narrow transition. The superficial spermatheca area, as well as the luminal area, increase significantly after insemination, even among queens whose reproductive activity was reduced, suggesting that sperm storage continues during such conditions. The secretion of proteins and polysaccharides into the spermathecal lumen was a remarkable feature for both virgin and 4‐year‐old queens, although the concentration of the secreted content increased in the latter group. It suggests that spermatheca activation occurs before pairing, but its secretory activity intensifies to nourish and provide energy for the stored spermatozoa. Ultrastructure of the spermathecal epithelium showed a bicellular unit, composed of a secretory cell and associated canal cells. Secretory vesicles of various electron densities were observed next to the receiving canal of the secretory cells in both virgin and 2‐year‐old queens. Nevertheless, strongly electron‐dense vesicles were only recorded for mated queens, which were associated with the increasing synthesis of proteins. The occurrence of rough endoplasmic reticulum and richness of mitochondria reinforces the protein synthesis and transport of contents towards the spermathecal lumen. In conclusion, the spermatheca of C. gestroi undergoes morphometric and physiological changes after mating, and further analysis may provide insights into the chemical nature of the spermathecal secretion prior to and after this event.
The spermathecae of Coptotermes gestroi (Isoptera: Rhinotermitidae) females secrete proteins and polysaccharides prior to copulation. After mating, the secretion of compounds increases, to nourish and maintain the stored sperm. Morphometric changes also occur in the spermatheca after mating, a likely consequence of the |
doi_str_mv | 10.1111/eea.13253 |
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The spermathecae of Coptotermes gestroi (Isoptera: Rhinotermitidae) females secrete proteins and polysaccharides prior to copulation. After mating, the secretion of compounds increases, to nourish and maintain the stored sperm. Morphometric changes also occur in the spermatheca after mating, a likely consequence of the sperm storage and secretory activity of the spermathecal epithelium (composed of class III secretory cells). Ultrastructural features such as rough endoplasmic reticulum, mitochondria richness, and electron‐dense vesicles suggest synthesis and secretion of proteins.</description><identifier>ISSN: 0013-8703</identifier><identifier>EISSN: 1570-7458</identifier><identifier>DOI: 10.1111/eea.13253</identifier><language>eng</language><publisher>Amsterdam: Wiley Subscription Services, Inc</publisher><subject>Blattaria ; Canals (anatomy) ; Coptotermes gestroi ; Endoplasmic reticulum ; Epithelium ; eusocial insect ; Eusociality ; Fertilization ; histochemistry ; Insects ; Isoptera ; Maintenance ; Mating ; Mitochondria ; pest species ; Polysaccharides ; Protein biosynthesis ; Protein synthesis ; Protein transport ; Proteins ; Queens ; reproductive system ; Rhinotermitidae ; Saccharides ; Secretion ; Secretory vesicles ; Sperm ; sperm storage ; Spermatheca ; Spermatozoa ; termite ; Ultrastructure ; Vesicles</subject><ispartof>Entomologia experimentalis et applicata, 2023-05, Vol.171 (5), p.361-373</ispartof><rights>2022 Netherlands Entomological Society.</rights><rights>2023 The Netherlands Entomological Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2973-81b560b723a76f0eb9909c4f9b7a91e143a5d4e94c95c00b7db873376b9ec23d3</citedby><cites>FETCH-LOGICAL-c2973-81b560b723a76f0eb9909c4f9b7a91e143a5d4e94c95c00b7db873376b9ec23d3</cites><orcidid>0000-0002-4584-9839 ; 0000-0002-8874-5538</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Silva, Iago Bueno</creatorcontrib><creatorcontrib>Costa‐Leonardo, Ana Maria</creatorcontrib><title>Mating mediates morphophysiological changes in the spermathecae of Coptotermes gestroi queens</title><title>Entomologia experimentalis et applicata</title><description>Insect spermathecae play a crucial role in sperm storage and maintenance prior to egg fertilization. Within eusocial insects, this structure is well studied in the Hymenoptera, whose queens copulate during a short period early in life and store sperm for up to decades. Within Isoptera, sperm storage and maintenance inside the spermatheca are poorly understood, especially due to the presence of a sperm‐providing king. Here, we compared the morphometric and morphophysiological features of the spermathecae of virgin and mated queens of the invasive termite Coptotermes gestroi (Wasmann) (Isoptera: Rhinotermitidae). The spermatheca comprises a finger‐shaped reservoir divided into two regions and a duct limited by a narrow transition. The superficial spermatheca area, as well as the luminal area, increase significantly after insemination, even among queens whose reproductive activity was reduced, suggesting that sperm storage continues during such conditions. The secretion of proteins and polysaccharides into the spermathecal lumen was a remarkable feature for both virgin and 4‐year‐old queens, although the concentration of the secreted content increased in the latter group. It suggests that spermatheca activation occurs before pairing, but its secretory activity intensifies to nourish and provide energy for the stored spermatozoa. Ultrastructure of the spermathecal epithelium showed a bicellular unit, composed of a secretory cell and associated canal cells. Secretory vesicles of various electron densities were observed next to the receiving canal of the secretory cells in both virgin and 2‐year‐old queens. Nevertheless, strongly electron‐dense vesicles were only recorded for mated queens, which were associated with the increasing synthesis of proteins. The occurrence of rough endoplasmic reticulum and richness of mitochondria reinforces the protein synthesis and transport of contents towards the spermathecal lumen. In conclusion, the spermatheca of C. gestroi undergoes morphometric and physiological changes after mating, and further analysis may provide insights into the chemical nature of the spermathecal secretion prior to and after this event.
The spermathecae of Coptotermes gestroi (Isoptera: Rhinotermitidae) females secrete proteins and polysaccharides prior to copulation. After mating, the secretion of compounds increases, to nourish and maintain the stored sperm. Morphometric changes also occur in the spermatheca after mating, a likely consequence of the sperm storage and secretory activity of the spermathecal epithelium (composed of class III secretory cells). Ultrastructural features such as rough endoplasmic reticulum, mitochondria richness, and electron‐dense vesicles suggest synthesis and secretion of proteins.</description><subject>Blattaria</subject><subject>Canals (anatomy)</subject><subject>Coptotermes gestroi</subject><subject>Endoplasmic reticulum</subject><subject>Epithelium</subject><subject>eusocial insect</subject><subject>Eusociality</subject><subject>Fertilization</subject><subject>histochemistry</subject><subject>Insects</subject><subject>Isoptera</subject><subject>Maintenance</subject><subject>Mating</subject><subject>Mitochondria</subject><subject>pest species</subject><subject>Polysaccharides</subject><subject>Protein biosynthesis</subject><subject>Protein synthesis</subject><subject>Protein transport</subject><subject>Proteins</subject><subject>Queens</subject><subject>reproductive system</subject><subject>Rhinotermitidae</subject><subject>Saccharides</subject><subject>Secretion</subject><subject>Secretory vesicles</subject><subject>Sperm</subject><subject>sperm storage</subject><subject>Spermatheca</subject><subject>Spermatozoa</subject><subject>termite</subject><subject>Ultrastructure</subject><subject>Vesicles</subject><issn>0013-8703</issn><issn>1570-7458</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp1kE1PwzAMhiMEEmNw4B9E4sShW9I0y3KcpvIhDXGBI4rS1F0ztU1JMqH9ewLlii-27Md-rRehW0oWNMUSQC8oyzk7QzPKBclEwdfnaEYIZdlaEHaJrkI4EEKEkHSGPl50tMMe91BbHSHg3vmxdWN7CtZ1bm-N7rBp9bBPMzvg2AIOI_hep8powK7BWzdGF1MvIQmL3ln8eQQYwjW6aHQX4OYvz9H7Q_m2fcp2r4_P280uM7kU6S9a8RWpRM60WDUEKimJNEUjK6ElBVowzesCZGEkNySBdbUWjIlVJcHkrGZzdDfdHb1LyiGqgzv6IUmqXEgmeSESP0f3E2W8C8FDo0Zve-1PihL1455K7qlf9xK7nNgv28Hpf1CV5Wba-AbXfXHB</recordid><startdate>202305</startdate><enddate>202305</enddate><creator>Silva, Iago Bueno</creator><creator>Costa‐Leonardo, Ana Maria</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><orcidid>https://orcid.org/0000-0002-4584-9839</orcidid><orcidid>https://orcid.org/0000-0002-8874-5538</orcidid></search><sort><creationdate>202305</creationdate><title>Mating mediates morphophysiological changes in the spermathecae of Coptotermes gestroi queens</title><author>Silva, Iago Bueno ; Costa‐Leonardo, Ana Maria</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2973-81b560b723a76f0eb9909c4f9b7a91e143a5d4e94c95c00b7db873376b9ec23d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Blattaria</topic><topic>Canals (anatomy)</topic><topic>Coptotermes gestroi</topic><topic>Endoplasmic reticulum</topic><topic>Epithelium</topic><topic>eusocial insect</topic><topic>Eusociality</topic><topic>Fertilization</topic><topic>histochemistry</topic><topic>Insects</topic><topic>Isoptera</topic><topic>Maintenance</topic><topic>Mating</topic><topic>Mitochondria</topic><topic>pest species</topic><topic>Polysaccharides</topic><topic>Protein biosynthesis</topic><topic>Protein synthesis</topic><topic>Protein transport</topic><topic>Proteins</topic><topic>Queens</topic><topic>reproductive system</topic><topic>Rhinotermitidae</topic><topic>Saccharides</topic><topic>Secretion</topic><topic>Secretory vesicles</topic><topic>Sperm</topic><topic>sperm storage</topic><topic>Spermatheca</topic><topic>Spermatozoa</topic><topic>termite</topic><topic>Ultrastructure</topic><topic>Vesicles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Silva, Iago Bueno</creatorcontrib><creatorcontrib>Costa‐Leonardo, Ana Maria</creatorcontrib><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Entomologia experimentalis et applicata</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Silva, Iago Bueno</au><au>Costa‐Leonardo, Ana Maria</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mating mediates morphophysiological changes in the spermathecae of Coptotermes gestroi queens</atitle><jtitle>Entomologia experimentalis et applicata</jtitle><date>2023-05</date><risdate>2023</risdate><volume>171</volume><issue>5</issue><spage>361</spage><epage>373</epage><pages>361-373</pages><issn>0013-8703</issn><eissn>1570-7458</eissn><abstract>Insect spermathecae play a crucial role in sperm storage and maintenance prior to egg fertilization. Within eusocial insects, this structure is well studied in the Hymenoptera, whose queens copulate during a short period early in life and store sperm for up to decades. Within Isoptera, sperm storage and maintenance inside the spermatheca are poorly understood, especially due to the presence of a sperm‐providing king. Here, we compared the morphometric and morphophysiological features of the spermathecae of virgin and mated queens of the invasive termite Coptotermes gestroi (Wasmann) (Isoptera: Rhinotermitidae). The spermatheca comprises a finger‐shaped reservoir divided into two regions and a duct limited by a narrow transition. The superficial spermatheca area, as well as the luminal area, increase significantly after insemination, even among queens whose reproductive activity was reduced, suggesting that sperm storage continues during such conditions. The secretion of proteins and polysaccharides into the spermathecal lumen was a remarkable feature for both virgin and 4‐year‐old queens, although the concentration of the secreted content increased in the latter group. It suggests that spermatheca activation occurs before pairing, but its secretory activity intensifies to nourish and provide energy for the stored spermatozoa. Ultrastructure of the spermathecal epithelium showed a bicellular unit, composed of a secretory cell and associated canal cells. Secretory vesicles of various electron densities were observed next to the receiving canal of the secretory cells in both virgin and 2‐year‐old queens. Nevertheless, strongly electron‐dense vesicles were only recorded for mated queens, which were associated with the increasing synthesis of proteins. The occurrence of rough endoplasmic reticulum and richness of mitochondria reinforces the protein synthesis and transport of contents towards the spermathecal lumen. In conclusion, the spermatheca of C. gestroi undergoes morphometric and physiological changes after mating, and further analysis may provide insights into the chemical nature of the spermathecal secretion prior to and after this event.
The spermathecae of Coptotermes gestroi (Isoptera: Rhinotermitidae) females secrete proteins and polysaccharides prior to copulation. After mating, the secretion of compounds increases, to nourish and maintain the stored sperm. Morphometric changes also occur in the spermatheca after mating, a likely consequence of the sperm storage and secretory activity of the spermathecal epithelium (composed of class III secretory cells). Ultrastructural features such as rough endoplasmic reticulum, mitochondria richness, and electron‐dense vesicles suggest synthesis and secretion of proteins.</abstract><cop>Amsterdam</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1111/eea.13253</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-4584-9839</orcidid><orcidid>https://orcid.org/0000-0002-8874-5538</orcidid></addata></record> |
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subjects | Blattaria Canals (anatomy) Coptotermes gestroi Endoplasmic reticulum Epithelium eusocial insect Eusociality Fertilization histochemistry Insects Isoptera Maintenance Mating Mitochondria pest species Polysaccharides Protein biosynthesis Protein synthesis Protein transport Proteins Queens reproductive system Rhinotermitidae Saccharides Secretion Secretory vesicles Sperm sperm storage Spermatheca Spermatozoa termite Ultrastructure Vesicles |
title | Mating mediates morphophysiological changes in the spermathecae of Coptotermes gestroi queens |
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