Evidence map›Paper›PMID 38295092›Full record

ArticlePLoS neglected tropical diseases2024

Comparative genomics of Leishmania donovani progeny from genetic crosses in two sand fly species and impact on the diversity of diagnostic and vaccine candidates.

Jovana Sádlová, Matthew Yeo, David S Mateus, Jody Phelan, Le Anh Hai, Tapan Bhattacharyya, Stefan Kurtev, Ondrej Sebesta, Jitka Myskova, Veronika Seblova and 4 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
3.3field-weighted citation impact, top 9% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. 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

14 authors at 4 institutions in 4 countries.

Jovana SádlováDepartment of Parasitology, Faculty of Science, Charles University, Prague, Czech Republic.
Matthew YeoFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London United Kingdom.
David S MateusFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London United Kingdom.
Jody PhelanFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London United Kingdom.
Le Anh HaiFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London United Kingdom.
Tapan BhattacharyyaFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London United Kingdom.ORCID 0000-0003-3385-2536
Stefan KurtevFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London United Kingdom.
Ondrej SebestaLaboratory of Confocal and Fluorescence Microscopy, Faculty of Science, Charles University, Prague, Czech Republic.
Jitka MyskovaDepartment of Parasitology, Faculty of Science, Charles University, Prague, Czech Republic.
Veronika SeblovaDepartment of Parasitology, Faculty of Science, Charles University, Prague, Czech Republic.
Björn AnderssonDepartment of Cell and Molecular Biology, Karolinska Institute, Stockholm, Sweden.
Paola Florez de SessionsGenome Institute of Singapore, Biomedical Sciences Institutes, Agency for Science, Technology and Research, Singapore.
Petr VolfDepartment of Parasitology, Faculty of Science, Charles University, Prague, Czech Republic.
Michael A MilesFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London United Kingdom.
London School of Hygiene & Tropical Medicine · GBCharles University · CZAgency for Science, Technology and Research · SGKarolinska Institutet · SE

Funding

Wellcome Trust
6 · The paper itself

Abstract

Sand fly transmitted Leishmania species are responsible for severe, wide ranging, visceral and cutaneous leishmaniases. Genetic exchange can occur among natural Leishmania populations and hybrids can now be produced experimentally, with limitations. Feeding Phlebotomus orientalis or Phlebotomus argentipes on two strains of Leishmania donovani yielded hybrid progeny, selected using double drug resistance and fluorescence markers. Fluorescence activated cell sorting of cultured clones derived from these hybrids indicated diploid progeny. Multilocus sequence typing of the clones showed hybridisation and nuclear heterozygosity, although with inheritance of single haplotypes in a kinetoplastid target. Comparative genomics showed diversity of clonal progeny between single chromosomes, and extraordinary heterozygosity across all 36 chromosomes. Diversity between progeny was seen for the HASPB antigen, which has been noted previously as having implications for design of a therapeutic vaccine. Genomic diversity seen among Leishmania strains and hybrid progeny is of great importance in understanding the epidemiology and control of leishmaniasis. As an outcome of this study we strongly recommend that wider biological archives of different Leishmania species from endemic regions should be established and made available for comparative genomics. However, in parallel, performance of genetic crosses and genomic comparisons should give fundamental insight into the specificity, diversity and limitations of candidate diagnostics, vaccines and drugs, for targeted control of leishmaniasis.

Indexed as

Leishmania donovaniLeishmaniasis, CutaneousLeishmaniasis, VisceralPhlebotomusPsychodidaeAnimalsCrosses, GeneticGenomics

Identifiers

PMID38295092
PMCPMC10830044
OpenAlexW4391383226

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.