Evidence map›Paper›PMID 34445959›Full record

ArticleBMC developmental biology2021

Development of the indirect flight muscles of Aedes aegypti, a main arbovirus vector.

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 and 1 more

Open access · hybridAbstract read
In one paragraph

Article in BMC developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 34% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Antonio Celestino-MontesDepartamento de Infectómica y Patogénesis Molecular, Centro de Investigación y de Estudios Avanzados del IPN, Av. Instituto Politécnico Nacional # 2508, San Pedro Zacatenco, G. A. Madero, 07360, México City, México.
Salvador Hernández-MartínezCentro de Investigación Sobre Enfermedades Infecciosas, Instituto Nacional de Salud Pública, Av. Universidad # 655, Santa María Ahuacatitlán, 62100, Cuernavaca, Morelos, México.
Mario Henry RodríguezCentro de Investigación Sobre Enfermedades Infecciosas, Instituto Nacional de Salud Pública, Av. Universidad # 655, Santa María Ahuacatitlán, 62100, Cuernavaca, Morelos, México.
Febe Elena Cázares-RagaDepartamento de Infectómica y Patogénesis Molecular, Centro de Investigación y de Estudios Avanzados del IPN, Av. Instituto Politécnico Nacional # 2508, San Pedro Zacatenco, G. A. Madero, 07360, México City, México.
Carlos Vázquez-CalzadaDepartamento de Infectómica y Patogénesis Molecular, Centro de Investigación y de Estudios Avanzados del IPN, Av. Instituto Politécnico Nacional # 2508, San Pedro Zacatenco, G. A. Madero, 07360, México City, México.
Anel Lagunes-GuillénDepartamento de Infectómica y Patogénesis Molecular, Centro de Investigación y de Estudios Avanzados del IPN, Av. Instituto Politécnico Nacional # 2508, San Pedro Zacatenco, G. A. Madero, 07360, México City, México.
Bibiana Chávez-MunguíaDepartamento de Infectómica y Patogénesis Molecular, Centro de Investigación y de Estudios Avanzados del IPN, Av. Instituto Politécnico Nacional # 2508, San Pedro Zacatenco, G. A. Madero, 07360, México City, México.
José Ángel Rubio-MirandaDepartamento de Infectómica y Patogénesis Molecular, Centro de Investigación y de Estudios Avanzados del IPN, Av. Instituto Politécnico Nacional # 2508, San Pedro Zacatenco, G. A. Madero, 07360, México City, México.
Felipe de Jesús Hernández-CázaresDepartamento de Biología Celular, Centro de Investigación y de Estudios Avanzados del IPN, Av. Instituto Politécnico Nacional # 2508, San Pedro Zacatenco, G. A. Madero, 07360, México City, México.
Leticia Cortés-MartínezDepartamento de Infectómica y Patogénesis Molecular, Centro de Investigación y de Estudios Avanzados del IPN, Av. Instituto Politécnico Nacional # 2508, San Pedro Zacatenco, G. A. Madero, 07360, México City, México.
Fidel de la Cruz Hernández-HernándezDepartamento de Infectómica y Patogénesis Molecular, Centro de Investigación y de Estudios Avanzados del IPN, Av. Instituto Politécnico Nacional # 2508, San Pedro Zacatenco, G. A. Madero, 07360, México City, México. cruzcruz@cinvestav.mx.ORCID 0000-0002-7276-7513
Instituto Politécnico Nacional · MXInstituto Nacional de Salud Pública · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFlying 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.

methodsA. 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.

resultsAt 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.

conclusionsA 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.

Indexed as

AedesArbovirusesAnimalsDrosophila melanogasterMosquito VectorsSarcomeresAedes aegyptiDorsal—longitudinal musclesDorsal–ventral musclesIndirect flight musclesMuscle developmentMyoblastMyofibrilMyotubeSarcomere

Identifiers

PMID34445959
PMCPMC8394598
OpenAlexW3196093062

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.