Evidence map›Paper›PMID 29570734›Full record

ArticlePloS one2018

Characterization of the adult Aedes aegypti early midgut peritrophic matrix proteome using LC-MS.

Shavonn R Whiten, W Keith Ray, Richard F Helm, Zach N Adelman

Abstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

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

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Intracellular Interactions Between Arboviruses andFrontiers in cellular and infection microbiology · 2021
    Review
  13. Review
  14. Article
  15. Article
  16. 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

4 authors.

Shavonn R WhitenDepartment of Entomology, Texas A&M University, College Station, Texas, United States of America.
W Keith RayDepartment of Biochemistry, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, United States of America.
Richard F HelmDepartment of Biochemistry, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, United States of America.ORCID 0000-0001-5317-0925
Zach N AdelmanDepartment of Entomology, Texas A&M University, College Station, Texas, United States of America.ORCID 0000-0001-5901-7171

Funding

Identification and disruption of mosquito heme transportersR21AI115138 · NIAID · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI ADELMAN, ZACH N. · 2015 to 2016
$417k
NIAID NIH HHS R21 AI115138NIH HHS AI115138
6 · The paper itself

Abstract

The Aedes aegypti mosquito is the principal vector of arboviruses such as dengue, chikungunya, yellow fever, and Zika virus. These arboviruses are transmitted during adult female mosquito bloodfeeding. While these viruses must transverse the midgut to replicate, the blood meal must also reach the midgut to be digested, absorbed, or excreted, as aggregation of blood meal metabolites can be toxic to the female mosquito midgut. The midgut peritrophic matrix (PM), a semipermeable extracellular layer comprised of chitin fibrils, glycoproteins, and proteoglycans, is one such mechanism of protection for the mosquito midgut. However, this structure has not been characterized for adult female Ae. aegypti. We conducted a mass spectrometry based proteomic analysis to identify proteins that comprise or are associated with the adult female Ae. aegypti early midgut PM. Altogether, 474 unique proteins were identified, with 115 predicted as secreted. GO-term enrichment analysis revealed an abundance of serine-type proteases and several known and novel intestinal mucins. In addition, approximately 10% of the peptides identified corresponded to known salivary proteins, indicating Ae. aegypti mosquitoes extensively swallow their own salivary secretions. However, the physiological relevance of this remains unclear, and further studies are needed to determine PM proteins integral for midgut protection from blood meal derived toxicity and pathogen protection. Finally, we describe substantial discordance between previously described transcriptionally changes observed in the midgut in response to a bloodmeal and the presence of the corresponding protein in the PM. Data are available via ProteomeXchange with identifier PXD007627.

Indexed as

Tandem Mass SpectrometryAedesAnimalsChromatography, High Pressure LiquidComputational BiologyFemaleGastrointestinal TractProteomeSalivary GlandsSalivary Proteins and PeptidesProteomeSalivary Proteins and Peptides

Identifiers

PMID29570734
PMCPMC5865745

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.