Evidence map›Paper›PMID 19634714›Full record

ArticleIndian journal of experimental biology2009

High-throughput screening of amastigotes of Leishmania donovani clinical isolates against drugs using a colorimetric beta-lactamase assay.

Swati Mandal, Mahendra Maharjan, Sudipto Ganguly, Mitali Chatterjee, Sarman Singh, Frederick S Buckner, Rentala Madhubala

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in Indian journal of experimental biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Reporter gene systems: A powerful tool forCurrent research in microbial sciences · 2022
    Article
  4. Article
  5. Article
  6. Challenges and Tools for In VitroPathogens (Basel, Switzerland) · 2021
    Review
  7. Review
  8. Evaluation of synergy between host and pathogen-directed therapies against intracellular Leishmania donovani.International journal for parasitology. Drugs and drug resistance · 2019
    Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Visceral leishmaniasis treatment: What do we have, what do we need and how to deliver it?International journal for parasitology. Drugs and drug resistance · 2012
    Review
  16. Article
  17. Visceral leishmaniasis: experimental models for drug discovery.The Indian journal of medical research · 2011
    Review
  18. Novel arylimidamides for treatment of visceral leishmaniasis.Antimicrobial agents and chemotherapy · 2010
    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

7 authors at 1 institution in 1 country.

Swati MandalSchool of Life Sciences, Jawaharlal Nehru University, New Delhi 110 067, India.
Mahendra Maharjan
Sudipto Ganguly
Mitali Chatterjee
Sarman Singh
Frederick S Buckner
Rentala Madhubala
Jawaharlal Nehru University · IN

Funding

Research Training on Intracellular Pathogens including Plasmodium, Leishmania andD43TW000924 · FIC · UNIVERSITY OF WASHINGTON · PI STUART, KENNETH D · 1997 to 2010
$1.2M
FIC NIH HHS D43 TW000924FIC NIH HHS D43TW000924
6 · The paper itself

Abstract

A simple colorimetric beta-lactamase assay for quantifying Leishmania amastigotes in macrophages grown in microtiter plates has been reported. The beta-lactamase gene was integrated into the rRNA region of the genome, thereby allowing for high-level stable expression of the enzyme. Both visceral leishmaniasis (VL) and post-kala azar dermal leishmaniasis (PKDL) isolates were transfected with beta-Lactamase gene. These beta-lactamase-expressing promastigotes were used for infecting intracellular J774A.1 macrophages in vitro. Quantification was done by a colorimetric readout with CENTA beta-lactamase as substrate and with an optical density plate reader. The assay was carried out in 96-well plates. Results obtained demonstrate that this methodology could be a valuable high-throughput screening assay for checking efficacy of anti-leishmanial drugs in the clinical isolates.

Indexed as

AnimalsAntiprotozoal Agentsbeta-LactamasesBiological AssayGenes, ReporterHumansLeishmania donovaniLeishmaniasis, CutaneousLeishmaniasis, VisceralAntiprotozoal Agentsbeta-Lactamases

Identifiers

PMID19634714
PMCPMC3127289
OpenAlexW1546173330

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.