主要虫媒媒介埃及伊蚊间接飞行肌的发育。

Q2 Biochemistry, Genetics and Molecular Biology BMC Developmental Biology Pub Date : 2021-08-26 DOI:10.1186/s12861-021-00242-8
Antonio Celestino-Montes, Salvador Hernández-Martínez, Mario Henry Rodríguez, Febe Elena Cázares-Raga, Carlos Vázquez-Calzada, Anel Lagunes-Guillén, Bibiana Chávez-Munguía, José Ángel Rubio-Miranda, Felipe de Jesús Hernández-Cázares, Leticia Cortés-Martínez, Fidel de la Cruz Hernández-Hernández
{"title":"主要虫媒媒介埃及伊蚊间接飞行肌的发育。","authors":"Antonio Celestino-Montes,&nbsp;Salvador Hernández-Martínez,&nbsp;Mario Henry Rodríguez,&nbsp;Febe Elena Cázares-Raga,&nbsp;Carlos Vázquez-Calzada,&nbsp;Anel Lagunes-Guillén,&nbsp;Bibiana Chávez-Munguía,&nbsp;José Ángel Rubio-Miranda,&nbsp;Felipe de Jesús Hernández-Cázares,&nbsp;Leticia Cortés-Martínez,&nbsp;Fidel de la Cruz Hernández-Hernández","doi":"10.1186/s12861-021-00242-8","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Flying is an essential function for mosquitoes, required for mating and, in the case of females, to get a blood meal and consequently function as a vector. Flight depends on the action of the indirect flight muscles (IFMs), which power the wings beat. No description of the development of IFMs in mosquitoes, including Aedes aegypti, is available.</p><p><strong>Methods: </strong>A. aegypti thoraces of larvae 3 and larvae 4 (L3 and L4) instars were analyzed using histochemistry and bright field microscopy. IFM primordia from L3 and L4 and IFMs from pupal and adult stages were dissected and processed to detect F-actin labelling with phalloidin-rhodamine or TRITC, or to immunodetection of myosin and tubulin using specific antibodies, these samples were analyzed by confocal microscopy. Other samples were studied using transmission electron microscopy.</p><p><strong>Results: </strong>At L3-L4, IFM primordia for dorsal-longitudinal muscles (DLM) and dorsal-ventral muscles (DVM) were identified in the expected locations in the thoracic region: three primordia per hemithorax corresponding to DLM with anterior to posterior orientation were present. Other three primordia per hemithorax, corresponding to DVM, had lateral position and dorsal to ventral orientation. During L3 to L4 myoblast fusion led to syncytial myotubes formation, followed by myotendon junctions (MTJ) creation, myofibrils assembly and sarcomere maturation. The formation of Z-discs and M-line during sarcomere maturation was observed in pupal stage and, the structure reached in teneral insects a classical myosin thick, and actin thin filaments arranged in a hexagonal lattice structure.</p><p><strong>Conclusions: </strong>A general description of A. aegypti IFM development is presented, from the myoblast fusion at L3 to form myotubes, to sarcomere maturation at adult stage. Several differences during IFM development were observed between A. aegypti (Nematoceran) and Drosophila melanogaster (Brachyceran) and, similitudes with Chironomus sp. were observed as this insect is a Nematoceran, which is taxonomically closer to A. aegypti and share the same number of larval stages.</p>","PeriodicalId":9130,"journal":{"name":"BMC Developmental Biology","volume":" ","pages":"11"},"PeriodicalIF":0.0000,"publicationDate":"2021-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8394598/pdf/","citationCount":"1","resultStr":"{\"title\":\"Development of the indirect flight muscles of Aedes aegypti, a main arbovirus vector.\",\"authors\":\"Antonio Celestino-Montes,&nbsp;Salvador Hernández-Martínez,&nbsp;Mario Henry Rodríguez,&nbsp;Febe Elena Cázares-Raga,&nbsp;Carlos Vázquez-Calzada,&nbsp;Anel Lagunes-Guillén,&nbsp;Bibiana Chávez-Munguía,&nbsp;José Ángel Rubio-Miranda,&nbsp;Felipe de Jesús Hernández-Cázares,&nbsp;Leticia Cortés-Martínez,&nbsp;Fidel de la Cruz Hernández-Hernández\",\"doi\":\"10.1186/s12861-021-00242-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Flying is an essential function for mosquitoes, required for mating and, in the case of females, to get a blood meal and consequently function as a vector. Flight depends on the action of the indirect flight muscles (IFMs), which power the wings beat. No description of the development of IFMs in mosquitoes, including Aedes aegypti, is available.</p><p><strong>Methods: </strong>A. aegypti thoraces of larvae 3 and larvae 4 (L3 and L4) instars were analyzed using histochemistry and bright field microscopy. IFM primordia from L3 and L4 and IFMs from pupal and adult stages were dissected and processed to detect F-actin labelling with phalloidin-rhodamine or TRITC, or to immunodetection of myosin and tubulin using specific antibodies, these samples were analyzed by confocal microscopy. Other samples were studied using transmission electron microscopy.</p><p><strong>Results: </strong>At L3-L4, IFM primordia for dorsal-longitudinal muscles (DLM) and dorsal-ventral muscles (DVM) were identified in the expected locations in the thoracic region: three primordia per hemithorax corresponding to DLM with anterior to posterior orientation were present. Other three primordia per hemithorax, corresponding to DVM, had lateral position and dorsal to ventral orientation. During L3 to L4 myoblast fusion led to syncytial myotubes formation, followed by myotendon junctions (MTJ) creation, myofibrils assembly and sarcomere maturation. The formation of Z-discs and M-line during sarcomere maturation was observed in pupal stage and, the structure reached in teneral insects a classical myosin thick, and actin thin filaments arranged in a hexagonal lattice structure.</p><p><strong>Conclusions: </strong>A general description of A. aegypti IFM development is presented, from the myoblast fusion at L3 to form myotubes, to sarcomere maturation at adult stage. Several differences during IFM development were observed between A. aegypti (Nematoceran) and Drosophila melanogaster (Brachyceran) and, similitudes with Chironomus sp. were observed as this insect is a Nematoceran, which is taxonomically closer to A. aegypti and share the same number of larval stages.</p>\",\"PeriodicalId\":9130,\"journal\":{\"name\":\"BMC Developmental Biology\",\"volume\":\" \",\"pages\":\"11\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-08-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8394598/pdf/\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"BMC Developmental Biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1186/s12861-021-00242-8\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Biochemistry, Genetics and Molecular Biology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Developmental Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s12861-021-00242-8","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 1

摘要

背景:飞行是蚊子的一项基本功能,它是交配所必需的,对于雌性蚊子来说,它是吸血所必需的,因此它是一种媒介。飞行依赖于间接飞行肌肉(ifm)的作用,它为翅膀的拍打提供动力。没有关于包括埃及伊蚊在内的蚊子体内ifm发展的描述。方法:采用组织化学和明光显微镜对埃及伊蚊胸部3龄和4龄幼虫(L3龄和L4龄)进行分析。对L3和L4期的IFM原基以及蛹期和成虫期的IFM进行解剖和处理,用phalloidin-rhodamine或TRITC检测F-actin标记,或用特异性抗体免疫检测肌球蛋白和微管蛋白,这些样品通过共聚焦显微镜进行分析。其他样品用透射电子显微镜进行了研究。结果:在L3-L4,背纵肌(DLM)和背腹肌(DVM)的IFM原基在胸部区域的预期位置被识别出来:每个半胸有三个与DLM相对应的原基,前后方向。每半胸对应DVM的其他3个原基为侧位和背侧至腹侧位。在L3至L4阶段,成肌细胞融合导致合胞肌管的形成,随后是肌腱连接(MTJ)的形成,肌原纤维的组装和肌节的成熟。在蛹期观察到肌节成熟过程中z -盘和m -线的形成,在一般昆虫中形成典型的肌凝蛋白粗、肌动蛋白细的六边形晶格结构。结论:本文介绍了埃及伊蚊IFM发育的一般描述,从L3的成肌细胞融合到形成肌管,再到成虫期的肌瘤成熟。在IFM发育过程中,我们观察到埃及伊蚊(线虫目)和黑腹果蝇(短尾目)之间存在一些差异,并观察到与Chironomus的相似性,因为这种昆虫属于线虫目,与埃及伊蚊在分类上更接近,并且具有相同的幼虫期数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Development of the indirect flight muscles of Aedes aegypti, a main arbovirus vector.

Background: Flying is an essential function for mosquitoes, required for mating and, in the case of females, to get a blood meal and consequently function as a vector. Flight depends on the action of the indirect flight muscles (IFMs), which power the wings beat. No description of the development of IFMs in mosquitoes, including Aedes aegypti, is available.

Methods: A. aegypti thoraces of larvae 3 and larvae 4 (L3 and L4) instars were analyzed using histochemistry and bright field microscopy. IFM primordia from L3 and L4 and IFMs from pupal and adult stages were dissected and processed to detect F-actin labelling with phalloidin-rhodamine or TRITC, or to immunodetection of myosin and tubulin using specific antibodies, these samples were analyzed by confocal microscopy. Other samples were studied using transmission electron microscopy.

Results: At L3-L4, IFM primordia for dorsal-longitudinal muscles (DLM) and dorsal-ventral muscles (DVM) were identified in the expected locations in the thoracic region: three primordia per hemithorax corresponding to DLM with anterior to posterior orientation were present. Other three primordia per hemithorax, corresponding to DVM, had lateral position and dorsal to ventral orientation. During L3 to L4 myoblast fusion led to syncytial myotubes formation, followed by myotendon junctions (MTJ) creation, myofibrils assembly and sarcomere maturation. The formation of Z-discs and M-line during sarcomere maturation was observed in pupal stage and, the structure reached in teneral insects a classical myosin thick, and actin thin filaments arranged in a hexagonal lattice structure.

Conclusions: A general description of A. aegypti IFM development is presented, from the myoblast fusion at L3 to form myotubes, to sarcomere maturation at adult stage. Several differences during IFM development were observed between A. aegypti (Nematoceran) and Drosophila melanogaster (Brachyceran) and, similitudes with Chironomus sp. were observed as this insect is a Nematoceran, which is taxonomically closer to A. aegypti and share the same number of larval stages.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
BMC Developmental Biology
BMC Developmental Biology 生物-发育生物学
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: BMC Developmental Biology is an open access, peer-reviewed journal that considers articles on the development, growth, differentiation and regeneration of multicellular organisms, including molecular, cellular, tissue, organ and whole organism research.
期刊最新文献
Dexamethasone priming enhances stemness and immunomodulatory property of tissue-specific human mesenchymal stem cells. Comparative transcriptome analysis uncovers cell wall reorganization and repressed cell division during cotton fiber initiation. Msx1 haploinsufficiency modifies the Pax9-deficient cardiovascular phenotype. Identification of reference genes for gene expression studies among different developmental stages of murine hearts. The miR-200 family in normal mammary gland development.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1