Evidence map›Paper›PMID 39025200›Full record

ArticleInternational journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases2024

A set of diagnostic tests for detection of active Babesia duncani infection.

Meenal Chand, Pratap Vydyam, Anasuya C Pal, Jose Thekkiniath, Dounia Darif, Zeng Li, Jae-Yeon Choi, Ruben Magni, Alessandra Luchini, Laura Tonnetti and 3 more

Abstract read
In one paragraph

Article in International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Human babesiosis: The past, present and future.Expert reviews in molecular medicine · 2025
    Review
  3. Research progress on diagnostic techniques for differentFrontiers in cellular and infection microbiology · 2025
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Meenal ChandDepartment of Internal Medicine, Section of Infectious Diseases, Yale School of Medicine, New Haven, USA.
Pratap VydyamDepartment of Internal Medicine, Section of Infectious Diseases, Yale School of Medicine, New Haven, USA.
Anasuya C PalDepartment of Internal Medicine, Section of Infectious Diseases, Yale School of Medicine, New Haven, USA.
Jose ThekkiniathDepartment of Internal Medicine, Section of Infectious Diseases, Yale School of Medicine, New Haven, USA.
Dounia DarifDepartment of Internal Medicine, Section of Infectious Diseases, Yale School of Medicine, New Haven, USA.
Zeng LiDepartment of Internal Medicine, Section of Infectious Diseases, Yale School of Medicine, New Haven, USA.
Jae-Yeon ChoiDepartment of Internal Medicine, Section of Infectious Diseases, Yale School of Medicine, New Haven, USA.
Ruben MagniSchool of Systems Biology, George Mason University, Fairfax, USA.
Alessandra LuchiniSchool of Systems Biology, George Mason University, Fairfax, USA.
Laura TonnettiScientific Affairs, American Red Cross, Rockville, USA.
Elizabeth J HornLyme Disease Biobank, Portland, USA.
Danielle M TuftsDepartment of Infectious Diseases and Microbiology, University of Pittsburgh School of Public Health, Pittsburgh, USA; Department of Veterinary Tropical Diseases, University of Pretoria, Pretoria, South Africa.
Choukri Ben MamounDepartment of Internal Medicine, Section of Infectious Diseases, Yale School of Medicine, New Haven, USA. Electronic address: choukri.benmamoun@yale.edu.

Funding

Fosinopril analogs for the treatment of human babesiosisR01AI153100 · NIAID · YALE UNIVERSITY · PI BEN MAMOUN, CHOUKRI · 2021 to 2025
$3.6M
Hit-to-Lead Development of the Kalihinol Scaffold for Malaria TreatmentR01AI138139 · NIAID · UNIVERSITY OF CALIFORNIA-IRVINE · PI BEN MAMOUN, CHOUKRI, LE ROCH, KARINE GAELLE · 2018 to 2022
$3.6M
Development of endochin-like quinolones for babesiosis therapyR01AI123321 · NIAID · YALE UNIVERSITY · PI BEN MAMOUN, CHOUKRI · 2017 to 2020
$2.7M
Antigen Discovery and Vaccine Development for Human Babesia ParasitesR01AI152220 · NIAID · YALE UNIVERSITY · PI BEN MAMOUN, CHOUKRI · 2020 to 2024
$2.1M
An antigen-detection assay to diagnose Babesia microti infectionR44AI136118 · NIAID · L2 DIAGNOSTICS, LLC · PI LEDIZET, MICHEL · 2020 to 2022
$2.1M
Parasite-Derived Vesicles in Babesia virulence and Vaccine DevelopmentR56AI177660 · NIAID · YALE UNIVERSITY · PI BEN MAMOUN, CHOUKRI, KASHANCHI, FATAH · 2024 to 2024
$874k
An antigen-detection assay to diagnose Babesia microti infectionR43AI136118 · NIAID · L2 DIAGNOSTICS, LLC · PI LEDIZET, MICHEL · 2018 to 2018
$300k
NIAID NIH HHS R01 AI123321NIAID NIH HHS R01 AI138139NIAID NIH HHS R01 AI152220NIAID NIH HHS R01 AI153100NIAID NIH HHS R43 AI136118NIAID NIH HHS R44 AI136118NIAID NIH HHS R56 AI177660
6 · The paper itself

Abstract

objectivesHuman babesiosis is an emerging and potentially fatal tick-borne disease caused by intraerythrocytic parasites of the Babesia genus. Among these, Babesia duncani is particularly notable for causing severe and life-threatening illness in humans. Accurate diagnosis and effective disease management hinge on the detection of active B. duncani infections. While molecular assays are available to detect the parasite in blood, a reliable method for identifying biomarkers of active infection remains elusive.

methodsWe developed the first B. duncani antigen capture assays, targeting two immunodominant antigens, BdV234 and BdV38. These assays were validated using established in vitro and in vivo B. duncani infection models, and following drug treatment.

resultsThe assays demonstrated no cross-reactivity with other species such as B. microti, B. divergens, Babesia MO1, or Plasmodium falciparum, and can detect as few as 115 infected erythrocytes/µl of blood. Screening of 1731 blood samples from various biorepositories, including samples previously identified as Lyme and/or B. microti-positive, as well as new specimens from wild mice, revealed no evidence of B. duncani infection or cross-reactivity.

conclusionsThese assays hold significant promise for various applications, including point-of-care testing for the early detection of B. duncani in patients, field tests for screening reservoir hosts, and high-throughput screening of blood samples intended for transfusion.

Indexed as

BabesiaBabesiosisAnimalsAntigens, ProtozoanDiagnostic Tests, RoutineErythrocytesFemaleHumansMiceSensitivity and SpecificityAntigens, ProtozoanAntigen Capture AssaysBabesia duncaniELISAHuman babesiosisInfectious diseaseTick-borne diseases

Identifiers

PMID39025200
PMCPMC11914778

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.