Evidence map›Paper›PMID 24763256›Full record

ArticlePLoS neglected tropical diseases2014

An investigation into the protein composition of the teneral Glossina morsitans morsitans peritrophic matrix.

Clair Rose, Rodrigo Belmonte, Stuart D Armstrong, Gemma Molyneux, Lee R Haines, Michael J Lehane, Jonathan Wastling, Alvaro Acosta-Serrano

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 56 citations in OpenAlex.

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  15. An IntranuclearMicroorganisms · 2020
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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

8 authors at 2 institutions in 1 country.

Clair RoseDepartment of Parasitology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Rodrigo BelmonteDepartment of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Stuart D ArmstrongInstitute for Infection Biology, University of Liverpool, Liverpool, United Kingdom.
Gemma MolyneuxDepartment of Parasitology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Lee R HainesDepartment of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Michael J LehaneDepartment of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Jonathan WastlingInstitute for Infection Biology, University of Liverpool, Liverpool, United Kingdom.
Alvaro Acosta-SerranoDepartment of Parasitology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom; Department of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Liverpool School of Tropical Medicine · GBUniversity of Liverpool · GB

Funding

Wellcome TrustWellcome Trust 093691MA
6 · The paper itself

Abstract

backgroundTsetse flies serve as biological vectors for several species of African trypanosomes. In order to survive, proliferate and establish a midgut infection, trypanosomes must cross the tsetse fly peritrophic matrix (PM), which is an acellular gut lining surrounding the blood meal. Crossing of this multi-layered structure occurs at least twice during parasite migration and development, but the mechanism of how trypanosomes do so is not understood. In order to better comprehend the molecular events surrounding trypanosome penetration of the tsetse PM, a mass spectrometry-based approach was applied to investigate the PM protein composition using Glossina morsitans morsitans as a model organism.

methodsPMs from male teneral (young, unfed) flies were dissected, solubilised in urea/SDS buffer and the proteins precipitated with cold acetone/TCA. The PM proteins were either subjected to an in-solution tryptic digestion or fractionated on 1D SDS-PAGE, and the resulting bands digested using trypsin. The tryptic fragments from both preparations were purified and analysed by LC-MS/MS.

resultsOverall, nearly 300 proteins were identified from both analyses, several of those containing signature Chitin Binding Domains (CBD), including novel peritrophins and peritrophin-like glycoproteins, which are essential in maintaining PM architecture and may act as trypanosome adhesins. Furthermore, 27 proteins from the tsetse secondary endosymbiont, Sodalis glossinidius, were also identified, suggesting this bacterium is probably in close association with the tsetse PM.

conclusionTo our knowledge this is the first report on the protein composition of teneral G. m. morsitans, an important vector of African trypanosomes. Further functional analyses of these proteins will lead to a better understanding of the tsetse physiology and may help identify potential molecular targets to block trypanosome development within the tsetse.

Indexed as

AnimalsChromatography, LiquidGastrointestinal TractMaleMass SpectrometryProteinsProteomeTandem Mass SpectrometryTsetse FliesProteinsProteome

Identifiers

PMID24763256
PMCPMC3998921
OpenAlexW2038782382

What OpenQuestion holds

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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.