Evidence map›Paper›PMID 26684756›Full record

ArticlePLoS neglected tropical diseases2015

Generation of a Novel Bacteriophage Library Displaying scFv Antibody Fragments from the Natural Buffalo Host to Identify Antigens from Adult Schistosoma japonicum for Diagnostic Development.

Christopher G Hosking, Hamish E G McWilliam, Patrick Driguez, David Piedrafita, Yuesheng Li, Donald P McManus, Leodevico L Ilag, Els N T Meeusen, Michael J de Veer

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

2 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
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

9 authors at 4 institutions in 1 country.

Christopher G HoskingDepartment of Physiology, Monash University, Clayton, Victoria, Australia.
Hamish E G McWilliamDepartment of Microbiology and Immunology, The University of Melbourne, the Peter Doherty Institute for Infection and Immunity, Parkville, Victoria, Australia.
Patrick DriguezQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
David PiedrafitaSchool of Applied Sciences and Engineering, Federation University, Churchill, Victoria, Australia.
Yuesheng LiQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Donald P McManusQIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Leodevico L IlagBio21 Molecular Sciences and Biotechnology Institute, University of Melbourne, Parkville, Victoria, Australia.
Els N T MeeusenDepartment of Microbiology, Monash University, Clayton, Victoria, Australia.
Michael J de VeerDepartment of Physiology, Monash University, Clayton, Victoria, Australia.
Monash University · AUQIMR Berghofer Medical Research Institute · AUUniversity of Melbourne · AUFederation University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of effective diagnostic tools will be essential in the continuing fight to reduce schistosome infection; however, the diagnostic tests available to date are generally laborious and difficult to implement in current parasite control strategies. We generated a series of single-chain antibody Fv domain (scFv) phage display libraries from the portal lymph node of field exposed water buffaloes, Bubalus bubalis, 11-12 days post challenge with Schistosoma japonicum cercariae. The selected scFv-phages showed clear enrichment towards adult schistosomes and excretory-secretory (ES) proteins by immunofluorescence, ELISA and western blot analysis. The enriched libraries were used to probe a schistosome specific protein microarray resulting in the recognition of a number of proteins, five of which were specific to schistosomes, with RNA expression predominantly in the adult life-stage based on interrogation of schistosome expressed sequence tags (EST). As the libraries were enriched by panning against ES products, these antigens may be excreted or secreted into the host vasculature and hence may make good targets for a diagnostic assay. Further selection of the scFv library against infected mouse sera identified five soluble scFv clones that could selectively recognise soluble whole adult preparations (SWAP) relative to an irrelevant protein control (ovalbumin). Furthermore, two of the identified scFv clones also selectively recognised SWAP proteins when spiked into naïve mouse sera. These host B-cell derived scFvs that specifically bind to schistosome protein preparations will be valuable reagents for further development of a cost effective point-of-care diagnostic test.

Indexed as

Peptide LibraryAnimalsAntibodies, HelminthAntigens, HelminthBlotting, WesternBuffaloesEnzyme-Linked Immunosorbent AssayFluorescent Antibody TechniqueMiceProtein Array AnalysisSchistosoma japonicumSerologic TestsSingle-Chain AntibodiesAntibodies, HelminthAntigens, HelminthPeptide LibrarySingle-Chain Antibodies

Identifiers

PMID26684756
PMCPMC4686158
OpenAlexW2219801302

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LicenceCC BY
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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.