Evidence map›Paper›PMID 39832284›Full record

ArticlePLoS neglected tropical diseases2025

Proteomic characterization and comparison of the infective and adult life stage secretomes from Necator americanus and Ancylostoma ceylanicum.

Yide Wong, Bruce A Rosa, Luke Becker, Mali Camberis, Graham LeGros, Bin Zhan, Maria Elena Bottazzi, Ricardo T Fujiwara, Edita Ritmejeryte, Thewarach Laha and 7 more

Abstract readComparative Study
In one paragraph

Article in PLoS neglected tropical diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Chromosome-ContiguousInternational journal of molecular sciences · 2025
    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

17 authors.

Yide WongAustralian Institute of Tropical Health and Medicine, James Cook University, Cairns, Australia.ORCID https://orcid.org/0000-0001-6049-0177
Bruce A RosaDepartment of Medicine, Washington University School of Medicine in St. Louis, St. Louis, Missouri, United States of America.
Luke BeckerMalaghan Institute of Medical Research, Wellington, New Zealand.
Mali CamberisMalaghan Institute of Medical Research, Wellington, New Zealand.
Graham LeGrosMalaghan Institute of Medical Research, Wellington, New Zealand.
Bin ZhanNational School of Tropical Medicine, Baylor College of Medicine, Houston, Texas, United States of America.
Maria Elena BottazziNational School of Tropical Medicine, Baylor College of Medicine, Houston, Texas, United States of America.
Ricardo T FujiwaraDepartment of Parasitology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Edita RitmejeryteAustralian Institute of Tropical Health and Medicine, James Cook University, Cairns, Australia.
Thewarach LahaDepartment of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Sujittra ChaiyadetDepartment of Tropical Medicine, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Piyanan TaweethavonsawatDepartment of Pathology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand.
Paul J BrindleyDepartment of Microbiology, Immunology & Tropical Medicine, The George Washington University School of Medicine and Health Sciences, Washington, D.C., United States of America.
Bethany K BrackenCharles River Analytics, Cambridge, Massachusetts, United States of America.
Paul R GiacominAustralian Institute of Tropical Health and Medicine, James Cook University, Cairns, Australia.
Makedonka MitrevaDepartment of Medicine, Washington University School of Medicine in St. Louis, St. Louis, Missouri, United States of America.
Alex LoukasAustralian Institute of Tropical Health and Medicine, James Cook University, Cairns, Australia.

Funding

Development of small molecule inhibitors of metabolic enzymes as broad spectrum anthelmintic drugsR01AI159450 · NIAID · WASHINGTON UNIVERSITY · PI JANETKA, JAMES W, MITREVA, MAKEDONKA · 2021 to 2025
$3.9M
NIAID NIH HHS R01 AI159450
6 · The paper itself

Abstract

More than 470 million people globally are infected with the hookworms Ancylostoma ceylanicum and Necator americanus, resulting in an annual loss of 2.1 to 4 million disability-adjusted-life-years. Current infection management approaches are limited by modest drug efficacy, the costs associated with frequent mass drug administration campaigns, and the risk of reinfection and burgeoning drug resistance. Subunit vaccines based on proteins excreted and secreted (ES) by hookworms that reduce worm numbers and associated disease burden are a promising management strategy to overcome these limitations. However, studies on the ES proteomes of hookworms have mainly described proteins from the adult life stage which may preclude the opportunity to target the infective larva. Here, we employed high resolution mass spectrometry to identify 103 and 57 ES proteins from the infective third larvae stage (L3) as well as 106 and 512 ES proteins from the adult N. americanus and A. ceylanicum respectively. Comparisons between these developmental stages identified 91 and 41 proteins uniquely expressed in the L3 ES products of N. americanus and A. ceylanicum, respectively. We characterized these proteins based on functional annotation, KEGG pathway analysis, InterProScan signature and gene ontology. We also performed reciprocal BLAST analysis to identify orthologs across species for both the L3 and adult stages and identified five orthologous proteins in both life stages and 15 proteins that could be detected only in the L3 stage of both species. Last, we performed a three-way reciprocal BLAST on the L3 proteomes from both hookworm species together with a previously reported L3 proteome from the rodent hookworm Nippostrongylus brasiliensis, and identified eight L3 proteins that could be readily deployed for testing using well established rodent models. This novel characterization of L3 proteins and taxonomic conservation across hookworm species provides a raft of potential candidates for vaccine discovery for prevention of hookworm infection and disease.

Indexed as

AncylostomaHelminth ProteinsNecator americanusProteomeSecretomeAnimalsLarvaLife Cycle StagesMass SpectrometryProteomicsHelminth ProteinsProteome

Identifiers

PMID39832284
PMCPMC11745416

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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.