Evidence map›Paper›PMID 28578678›Full record

ArticleParasites & vectors2017

Changes in the neuropeptide content of Biomphalaria ganglia nervous system following Schistosoma infection.

Tianfang Wang, Min Zhao, Di Liang, Utpal Bose, Satwant Kaur, Donald P McManus, Scott F Cummins

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

17 citing papers in PubMed, 55 citations in OpenAlex.

  1. Peptidomic Identification of Behaviour-Modulating Putative Neuropeptides inInternational journal of molecular sciences · 2026
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  7. FMRF-NHThe Journal of comparative neurology · 2021
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  12. Temporal transcriptome change ofCell & bioscience · 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

7 authors at 3 institutions in 2 countries.

Tianfang WangGenecology Research Centre, Faculty of Science, Health and Education, University of the Sunshine Coast, Maroochydore DC, Queensland, 4558, Australia. twang@usc.edu.au.ORCID http://orcid.org/0000-0002-4876-7767
Min ZhaoGenecology Research Centre, Faculty of Science, Health and Education, University of the Sunshine Coast, Maroochydore DC, Queensland, 4558, Australia.
Di LiangGenecology Research Centre, Faculty of Science, Health and Education, University of the Sunshine Coast, Maroochydore DC, Queensland, 4558, Australia.
Utpal BoseGenecology Research Centre, Faculty of Science, Health and Education, University of the Sunshine Coast, Maroochydore DC, Queensland, 4558, Australia.
Satwant KaurInstitute of Environment, Health and Societies, Brunel University London, Kingston Lane, London, UB8 3PH, UK.
Donald P McManusMolecular Parasitology Laboratory, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, 4006, Australia.
Scott F CumminsGenecology Research Centre, Faculty of Science, Health and Education, University of the Sunshine Coast, Maroochydore DC, Queensland, 4558, Australia. scummins@usc.edu.au.
University of the Sunshine Coast · AUBrunel University of London · GBQIMR Berghofer Medical Research Institute · AU

Funding

NIAID NIH HHS HHSN272201000005CNIAID NIH HHS HHSN272201000005I
6 · The paper itself

Abstract

backgroundMolluscs, including snails, are prone to parasite infection, which can lead to massive physiological and behavioural changes, yet many of the molecular components involved remain unresolved. Central to this point is the neural system that in snails consists of several ganglia that regulate the animals' physiology and behaviour patterns. The availability of a genomic resource for the freshwater snail Biomphalaria glabrata provides a mean towards the high throughput analysis of changes in the central nervous system (CNS) following infection with Schistosoma miracidia.

resultsIn this study, we performed a proteomic analysis of the B. glabrata CNS at pre-patent infection, providing a list of proteins that were further used within a protein-protein interaction (PPI) framework against S. mansoni proteins. A hub with most connections for both non-infected and infected Biomphalaria includes leucine aminopeptidase 2 (LAP2), which interacts with numerous miracidia proteins that together belong to the immunoglobulin family of cell adhesion related molecules. We additionally reveal the presence of at least 165 neuropeptides derived from the precursors of buccalin, enterin, FMRF, FVRI, pedal peptide 1, 2, 3 and 4, RYamide, RFamide, pleurin and others. Many of these were present at significantly reduced levels in the snail's CNS post-infection, such as the egg laying hormone, a neuropeptide required to initiate egg laying in gastropod molluscs.

conclusionsOur analysis demonstrates that LAP2 may be a key component that regulates parasite infection physiology, as well as establishing that parasite-induced reproductive castration may be facilitated by significant reductions in reproduction-associated neuropeptides. This work helps in our understanding of molluscan neuropeptides and further stimulates advances in parasite-host interactions.

Indexed as

AminopeptidasesAnimalsBiomphalariaCentral Nervous SystemGangliaHigh-Throughput Screening AssaysHost-Parasite InteractionsMiceNeuropeptidesProtein Interaction MapsProteomicsSchistosomaSchistosoma mansoniSchistosomiasisSequence AlignmentAminopeptidasesbuccalinNeuropeptidespedal peptideBiomphalariaCentral nervous systemHost-parasite interactionNeuropeptidePre-patent infectionProtein-protein interactionProteomicsSchistosoma

Identifiers

PMID28578678
PMCPMC5455113
OpenAlexW2620903866

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.