Evidence map›Paper›PMID 27744002›Full record

ArticleArthropod structure & development2016

Immunolocalization of cuticular proteins in Johnston's organ and the corneal lens of Anopheles gambiae.

Laura Vannini, Judith H Willis

Abstract read
In one paragraph

Article in Arthropod structure & development, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

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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

11 citing papers in PubMed.

  1. Article
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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

2 authors.

Laura VanniniDepartment of Cellular Biology, University of Georgia, Athens, GA 30602, USA.
Judith H WillisDepartment of Cellular Biology, University of Georgia, Athens, GA 30602, USA. Electronic address: jhwillis@uga.edu.

Funding

Cuticular proteins of Anopheles gambiaeR01AI055624 · NIAID · UNIVERSITY OF GEORGIA (UGA) · PI WILLIS, JUDITH · 2004 to 2014
$2.8M
NIAID NIH HHS R01 AI055624
6 · The paper itself

Abstract

Previous work with EM immunolocalization examined the intracuticular placement of several antibodies directed against cuticular proteins (CPs) in various structures of Anopheles gambiae. Those structures had long stretches of fairly uniform cuticle. We have now used 19 antibodies directed against members of five CP families on two adult structures with considerable complexity, Johnston's organ and the corneal lens of the compound eye. We also localized chitin with colloidal-gold labeled wheat germ agglutinin. Twelve of these antibodies recognized structures in Johnston's organ. Only 6 were detected in the outer pedicel wall, but the internal structures were more complex with distinct distributions of members of the five CP families in six different structures. The corneal lens had four distinct regions of laminar cuticle. Thirteen of the 15 members of the CPR family were detected, none from the other CP families. Specific antibodies were localized to different regions and in different laminae within a region. The specificity of deployment of cuticular proteins revealed in this study is helping to explain why An. gambiae allocates about 2% of its protein coding genes to structural CPs.

Indexed as

AnimalsAnophelesArthropod ProteinsBlotting, WesternCompound Eye, ArthropodImmunohistochemistryMicroscopy, Electron, TransmissionArthropod ProteinsAntennaeCompound eyeCuticular laminaeEM immunolocalizationMosquito

Identifiers

PMID27744002
PMCPMC5228451

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Registered trials

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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.