Evidence map›Paper›PMID 34570778›Full record

ArticlePLoS neglected tropical diseases2021

Characterization of the β-tubulin gene family in Ascaris lumbricoides and Ascaris suum and its implication for the molecular detection of benzimidazole resistance.

Sara Roose, Russell W Avramenko, Stephen M J Pollo, James D Wasmuth, Shaali Ame, Mio Ayana, Martha Betson, Piet Cools, Daniel Dana, Ben P Jones and 8 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.7field-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

8 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
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  4. Review
  5. The turkey ascarid, Ascaridia dissimilis, as a model genetic system.International journal for parasitology · 2023
    Article
  6. Article
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  8. 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

18 authors at 5 institutions in 5 countries.

Sara RooseDepartment of Virology, Parasitology and Immunology, Ghent University, Merelbeke, Belgium.ORCID 0000-0002-0072-9649
Russell W AvramenkoDepartment of Comparative Biology and Experimental Medicine, Faculty of Veterinary Medicine, Host-Parasite Interactions (HPI) Research Training Network, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0002-0638-1700
Stephen M J PolloDepartment of Ecosystem and Public Health, Faculty of Veterinary Medicine, Host-Parasite Interactions (HPI) Research Training Network, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0001-9252-4976
James D WasmuthDepartment of Ecosystem and Public Health, Faculty of Veterinary Medicine, Host-Parasite Interactions (HPI) Research Training Network, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0002-9516-212X
Shaali AmePublic Health Laboratory-Ivo de Carneri, Chake Chake, United Republic of Tanzania.
Mio AyanaDepartment of Virology, Parasitology and Immunology, Ghent University, Merelbeke, Belgium.
Martha BetsonDepartment of Veterinary Epidemiology and Public Health, University of Surrey, Guildford, Surrey, United Kingdom.
Piet CoolsDepartment of Virology, Parasitology and Immunology, Ghent University, Merelbeke, Belgium.ORCID 0000-0003-2980-5307
Daniel DanaDepartment of Virology, Parasitology and Immunology, Ghent University, Merelbeke, Belgium.
Ben P JonesDepartment of Veterinary Epidemiology and Public Health, University of Surrey, Guildford, Surrey, United Kingdom.ORCID 0000-0003-3843-9417
Zeleke MekonnenInstitute of Health, Faculty of Health Science, School of Medical Laboratory Science, Jimma University, Jimma, Ethiopia.
Arianna MorosettiDepartment of Comparative Biology and Experimental Medicine, Faculty of Veterinary Medicine, Host-Parasite Interactions (HPI) Research Training Network, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0002-1579-9084
Abhinaya VenkatesanDepartment of Comparative Biology and Experimental Medicine, Faculty of Veterinary Medicine, Host-Parasite Interactions (HPI) Research Training Network, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0002-9036-1357
Johnny VlaminckDepartment of Virology, Parasitology and Immunology, Ghent University, Merelbeke, Belgium.ORCID 0000-0002-3601-9825
Matthew L WorkentineDepartment of Ecosystem and Public Health, Faculty of Veterinary Medicine, Host-Parasite Interactions (HPI) Research Training Network, University of Calgary, Calgary, Alberta, Canada.
Bruno LeveckeDepartment of Virology, Parasitology and Immunology, Ghent University, Merelbeke, Belgium.
John S GilleardDepartment of Comparative Biology and Experimental Medicine, Faculty of Veterinary Medicine, Host-Parasite Interactions (HPI) Research Training Network, University of Calgary, Calgary, Alberta, Canada.
Peter GeldhofDepartment of Virology, Parasitology and Immunology, Ghent University, Merelbeke, Belgium.
University of Calgary · CAGhent University · BEJimma University · ETUniversity of Surrey · GBPublic Health Laboratory Ivo de Carneri · TZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe treatment coverage of control programs providing benzimidazole (BZ) drugs to eliminate the morbidity caused by soil-transmitted helminths (STHs) is unprecedently high. This high drug pressure may result in the development of BZ resistance in STHs and so there is an urgent need for surveillance systems detecting molecular markers associated with BZ resistance. A critical prerequisite to develop such systems is an understanding of the gene family encoding β-tubulin proteins, the principal targets of BZ drugs. METHODOLOGY AND PRINCIPAL

findingsFirst, the β-tubulin gene families of Ascaris lumbricoides and Ascaris suum were characterized through the analysis of published genomes. Second, RNA-seq and RT-PCR analyses on cDNA were applied to determine the transcription profiles of the different gene family members. The results revealed that Ascaris species have at least seven different β-tubulin genes of which two are highly expressed during the entire lifecycle. Third, deep amplicon sequencing was performed on these two genes in more than 200 adult A. lumbricoides (Ethiopia and Tanzania) and A. suum (Belgium) worms, to investigate the intra- and inter-species genetic diversity and the presence of single nucleotide polymorphisms (SNPs) that are associated with BZ resistance in other helminth species; F167Y (TTC>TAC or TTT>TAT), E198A (GAA>GCA or GAG>GCG), E198L (GAA>TTA) and F200Y (TTC>TAC or TTT>TAT). These particular SNPs were absent in the two investigated genes in all three Ascaris populations. SIGNIFICANCE: This study demonstrated the presence of at least seven β-tubulin genes in Ascaris worms. A new nomenclature was proposed and prioritization of genes for future BZ resistance research was discussed. This is the first comprehensive description of the β-tubulin gene family in Ascaris and provides a framework to investigate the prevalence and potential role of β-tubulin sequence polymorphisms in BZ resistance in a more systematic manner than previously possible.

Indexed as

AnimalsAnthelminticsAscariasisAscaris lumbricoidesAscaris suumBenzimidazolesDrug ResistanceHumansTubulinAnthelminticsbenzimidazoleBenzimidazolesTubulin

Identifiers

PMID34570778
PMCPMC8496844
OpenAlexW3203136030

What OpenQuestion holds

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LicenceCC BY
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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.