Evidence map›Paper›PMID 35167626›Full record

ArticlePLoS pathogens2022

Chromosome-level genome of Schistosoma haematobium underpins genome-wide explorations of molecular variation.

Andreas J Stroehlein, Pasi K Korhonen, V Vern Lee, Stuart A Ralph, Margaret Mentink-Kane, Hong You, Donald P McManus, Louis-Albert Tchuem Tchuenté, J Russell Stothard, Parwinder Kaur and 11 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
6.1field-weighted citation impact, top 2% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  13. Trematode Genomics and Proteomics.Advances in experimental medicine and biology · 2024
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  19. Article
  20. 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

21 authors at 10 institutions in 5 countries.

Andreas J StroehleinFaculty of Veterinary and Agricultural Sciences, The University of Melbourne, Parkville, Victoria, Australia.
Pasi K KorhonenFaculty of Veterinary and Agricultural Sciences, The University of Melbourne, Parkville, Victoria, Australia.
V Vern LeeDepartment of Biochemistry and Pharmacology, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Parkville, Australia.
Stuart A RalphDepartment of Biochemistry and Pharmacology, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Parkville, Australia.
Margaret Mentink-KaneNIH-NIAID Schistosomiasis Resource Center, Biomedical Research Institute, Rockville, Maryland, United States of America.
Hong YouImmunology Department, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Donald P McManusImmunology Department, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Louis-Albert Tchuem TchuentéFaculty of Sciences, University of Yaoundé I, Yaoundé, Cameroon.
J Russell StothardDepartment of Parasitology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Parwinder KaurUWA School of Agriculture and Environment, The University of Western Australia, Perth, Western Australia, Australia.
Olga DudchenkoThe Center for Genome Architecture, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.
Erez Lieberman AidenUWA School of Agriculture and Environment, The University of Western Australia, Perth, Western Australia, Australia.
Bicheng YangBGI Australia, Oceania, BGI Group, CBCRB Building, Herston, Queensland, Australia.
Huanming YangBGI-Shenzhen, Shenzhen, China.
Aidan M EmeryParasites and Vectors Division, The Natural History Museum, London, United Kingdom.
Bonnie L WebsterParasites and Vectors Division, The Natural History Museum, London, United Kingdom.
Paul J BrindleySchool of Medicine & Health Sciences, Department of Microbiology, Immunology & Tropical Medicine, George Washington University, Washington DC, United States of America.
David RollinsonParasites and Vectors Division, The Natural History Museum, London, United Kingdom.
Bill C H ChangFaculty of Veterinary and Agricultural Sciences, The University of Melbourne, Parkville, Victoria, Australia.
Robin B GasserFaculty of Veterinary and Agricultural Sciences, The University of Melbourne, Parkville, Victoria, Australia.
Neil D YoungFaculty of Veterinary and Agricultural Sciences, The University of Melbourne, Parkville, Victoria, Australia.ORCID 0000-0001-8756-229X
The University of Melbourne · AUNatural History Museum · GBQIMR Berghofer Medical Research Institute · AUThe University of Western Australia · AUBaylor College of Medicine · USBGI Group (China) · CNBiomedical Research Institute · USGeorge Washington University · USLiverpool School of Tropical Medicine · GBUniversité de Yaoundé I · CM

Funding

Center for Genome ImagingRM1HG011016 · NHGRI · HARVARD MEDICAL SCHOOL · PI WU, CHAO-TING · 2021 to 2025
$12.2M
GENOME WIDE MAPPING OF LOOPS USING IN SITU HI-CUM1HG009375 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI LIEBERMAN-AIDEN, EREZ · 2017 to 2021
$4.7M
NHGRI NIH HHS RM1 HG011016NHGRI NIH HHS UM1 HG009375
6 · The paper itself

Abstract

Urogenital schistosomiasis is caused by the blood fluke Schistosoma haematobium and is one of the most neglected tropical diseases worldwide, afflicting > 100 million people. It is characterised by granulomata, fibrosis and calcification in urogenital tissues, and can lead to increased susceptibility to HIV/AIDS and squamous cell carcinoma of the bladder. To complement available treatment programs and break the transmission of disease, sound knowledge and understanding of the biology and ecology of S. haematobium is required. Hybridisation/introgression events and molecular variation among members of the S. haematobium-group might effect important biological and/or disease traits as well as the morbidity of disease and the effectiveness of control programs including mass drug administration. Here we report the first chromosome-contiguous genome for a well-defined laboratory line of this blood fluke. An exploration of this genome using transcriptomic data for all key developmental stages allowed us to refine gene models (including non-coding elements) and annotations, discover 'new' genes and transcription profiles for these stages, likely linked to development and/or pathogenesis. Molecular variation within S. haematobium among some geographical locations in Africa revealed unique genomic 'signatures' that matched species other than S. haematobium, indicating the occurrence of introgression events. The present reference genome (designated Shae.V3) and the findings from this study solidly underpin future functional genomic and molecular investigations of S. haematobium and accelerate systematic, large-scale population genomics investigations, with a focus on improved and sustained control of urogenital schistosomiasis.

Indexed as

Genetic VariationGenome, ProtozoanTranscriptomeAnimalsChromosomesGenes, ProtozoanGenomeGenome-Wide Association StudySchistosoma haematobiumSchistosomiasis haematobiaSequence Analysis, DNA

Identifiers

PMID35167626
PMCPMC8846543
OpenAlexW4213033048

What OpenQuestion holds

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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.