Evidence map›Paper›PMID 33272316›Full record

ArticleParasites & vectors2020

Endochin-like quinolone-300 and ELQ-316 inhibit Babesia bovis, B. bigemina, B. caballi and Theileria equi.

Marta G Silva, Reginaldo G Bastos, J Stone Doggett, Michael K Riscoe, Sovitj Pou, Rolf Winter, Rozalia A Dodean, Aaron Nilsen, Carlos E Suarez

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Synthesis of Deuterated Endochin-Like Quinolones.Journal of labelled compounds & radiopharmaceuticals · 2024
    Article
  5. Article
  6. Article
  7. Parasite powerhouse: A review of the Toxoplasma gondii mitochondrion.The Journal of eukaryotic microbiology · 2022
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  8. Structure-activity relationships ofExpert opinion on drug discovery · 2022
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  9. HarnessingVaccines · 2022
    Review
  10. Article
  11. Dual inhibition of theFrontiers in veterinary science · 2022
    Article
  12. Lactate Dehydrogenase as a Potential Therapeutic Drug Target to ControlFrontiers in cellular and infection microbiology · 2022
    Article
  13. 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

9 authors at 4 institutions in 1 country.

Marta G Silva *Department of Veterinary Microbiology and Pathology, College of Veterinary Medicine, Washington State University, Pullman, WA, USA. marta_silva@wsu.edu.
Reginaldo G Bastos *Department of Veterinary Microbiology and Pathology, College of Veterinary Medicine, Washington State University, Pullman, WA, USA.
J Stone DoggettOregon Health and Science University, 3181 SW Sam Jackson Blvd., Portland, Oregon, 97239, USA.
Michael K RiscoeOregon Health and Science University, 3181 SW Sam Jackson Blvd., Portland, Oregon, 97239, USA.
Sovitj PouVA Portland Health Care System, 3710 SW US Veterans Hospital Road, Portland, OR, 97239, USA.
Rolf WinterVA Portland Health Care System, 3710 SW US Veterans Hospital Road, Portland, OR, 97239, USA.
Rozalia A DodeanVA Portland Health Care System, 3710 SW US Veterans Hospital Road, Portland, OR, 97239, USA.
Aaron NilsenOregon Health and Science University, 3181 SW Sam Jackson Blvd., Portland, Oregon, 97239, USA.
Carlos E SuarezDepartment of Veterinary Microbiology and Pathology, College of Veterinary Medicine, Washington State University, Pullman, WA, USA. carlos.suarez@usda.gov.
Oregon Health & Science University · USVA Portland Health Care System · USWashington State University · USAgricultural Research Service · US

Funding

Optimizing ELQs for Treatment and Prevention of MalariaR01AI100569 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI Michael Kevin RISCOE · 2014 to 2026
$8.0M
Development of a Sustained Release Injectable Formulation for Long-Term Delivery of ELQsR01AI141412 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI RISCOE, MICHAEL KEVIN · 2019 to 2022
$3.2M
Optimizing ELQs for Treatment and Prevention of MalariaR56AI100569 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI RISCOE, MICHAEL KEVIN · 2012 to 2012
$574k
Pharmachin Optimization and TestingI01BX003312 · VA · PORTLAND VA MEDICAL CENTER · PI RISCOE, MICHAEL KEVIN · 2016 to 2025
–
Agricultural Research Service 2090-32000-039-00DBLRD VA I01 BX001421BLRD VA i01 BX003312BLRD VA I01 BX003312BLRD VA I01 BX004522BLRD VA IK2 BX002440BLRD VA IK6 BX004857International Development Research Centre 108525-001National Institute of Allergy and Infectious Diseases R01AI141412NIAID NIH HHS R01 AI100569NIAID NIH HHS R01 AI141412NIAID NIH HHS R56 AI100569NIH HHS AI100569U.S. Department of Defense PR181134U.S. Department of Veterans Affairs Biomedical Laboratory Research and Development BX002440U.S. Department of Veterans Affairs (US) BX004522VA Research 14S-RCS001
6 · The paper itself

Abstract

backgroundThe most common apicomplexan parasites causing bovine babesiosis are Babesia bovis and B. bigemina, while B. caballi and Theileria equi are responsible for equine piroplasmosis. Treatment and control of these diseases are usually achieved using potentially toxic chemotherapeutics, such as imidocarb diproprionate, but drug-resistant parasites are emerging, and alternative effective and safer drugs are needed. The endochin-like quinolones (ELQ)-300 and ELQ-316 have been proven to be safe and efficacious against related apicomplexans, such as Plasmodium spp., with ELQ-316 also being effective against Babesia microti, without showing toxicity in mammals.

methodsThe inhibitory effects of ELQ-300 and ELQ-316 were assessed on the growth of cultured B. bovis, B. bigemina, B. caballi and T. equi. The percentage of parasitized erythrocytes was measured by flow cytometry, and the effect of the ELQ compounds on the viability of horse and bovine peripheral blood mononuclear cells (PBMC) was assessed by monitoring cell metabolic activity using a colorimetric assay.

resultsWe calculated the half maximal inhibitory concentration (IC

conclusionsThe compounds ELQ-300 and ELQ-316 showed significant inhibitory activity on the main parasites responsible for bovine babesiosis and equine piroplasmosis at doses that are tolerable to host cells. These ELQ drugs may be viable candidates for developing alternative protocols for the treatment of bovine babesiosis and equine piroplasmosis.

Indexed as

AnimalsAntiprotozoal AgentsBabesiaBabesiosisErythrocytesHorse DiseasesHorsesLeukocytes, MononuclearQuinolonesTheileriaTheileriasisAntiprotozoal AgentsQuinolonesBabesia bigeminaBabesia bovisBabesia caballiBovine babesiosisELQ-300Endochin-like quinolonesEquine piroplamsosisnnELQ-316Theileria equi

Identifiers

PMID33272316
PMCPMC7712603
OpenAlexW3099300450

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.