Evidence map›Paper›PMID 31113385›Full record

ArticleBMC infectious diseases2019

Molecular evidence supports the expansion of visceral leishmaniasis towards non-program districts of Nepal.

Mitesh Shrestha, Medha Khatri-Chhetri, Ram Chandra Poudel, Jyoti Maharjan, Shyam Prakash Dumre, Krishna Das Manandhar, Basu Dev Pandey, Sher Bahadur Pun, Kishor Pandey

Abstract read
In one paragraph

Article in BMC infectious diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
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  4. Review
  5. Article
  6. The role of CD4Frontiers in cellular and infection microbiology · 2024
    Review
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  10. Review
  11. Article
  12. Article
  13. Article
  14. Emergence of cutaneous leishmaniasis in Nepal.Tropical medicine and health · 2021
    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.

Mitesh ShresthaMolecular Biotechnology Unit, Nepal Academy of Science and Technology (NAST), Khumaltar, GPO box: 3323, Lalitpur, Nepal.
Medha Khatri-ChhetriMolecular Biotechnology Unit, Nepal Academy of Science and Technology (NAST), Khumaltar, GPO box: 3323, Lalitpur, Nepal.
Ram Chandra PoudelMolecular Biotechnology Unit, Nepal Academy of Science and Technology (NAST), Khumaltar, GPO box: 3323, Lalitpur, Nepal.
Jyoti MaharjanMolecular Biotechnology Unit, Nepal Academy of Science and Technology (NAST), Khumaltar, GPO box: 3323, Lalitpur, Nepal.
Shyam Prakash DumreDepartment of Immunogenetics, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Krishna Das ManandharCentral Department of Biotechnology, Tribhuvan University, Kathmandu, Nepal.
Basu Dev PandeySukraraj Tropical and Infectious Disease Hospital, Kathmandu, Nepal.
Sher Bahadur PunSukraraj Tropical and Infectious Disease Hospital, Kathmandu, Nepal.
Kishor PandeyMolecular Biotechnology Unit, Nepal Academy of Science and Technology (NAST), Khumaltar, GPO box: 3323, Lalitpur, Nepal. pandey_kishor@hotmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVisceral Leishmaniasis (VL) is caused by a protozoan parasite Leishmania donovani that is transmitted to humans by an infected female sandfly, Phlebotomus argentipes. VL is common in the Indian sub-continent including Nepal and efforts for its elimination are ongoing. However, expansion of disease towards the higher altitude areas, previously considered as VL free in Nepal, may impact the ability to achieve the elimination target by 2020.

methodsThis was an exploratory study, where VL suspected patients living exclusively in the non-program districts of Nepal and presenting with fever > 2 weeks and splenomegaly was included. The patients' blood samples were collected, and DNA was extracted. DNA was subjected to PCR amplification and subsequent sequencing. Additionally, past 10 years data of VL cases from the national databases were analysed to see the trends of the disease in program and non program districts.

resultsAnalysis of the past 10 years data revealed that trend of VL cases significantly decreased in the program districts (p = 0.001) while it increased in the non-program districts (p = 0.002). The national trend for overall incidence of VL also significantly decreased over this time period. Limited number of patients' samples (n = 14) were subjected to molecular investigation, and four patients were found to be positive for Leishmania species by PCR. Interestingly, these cases in non-program districts were indeed also L. donovoni complex. All four patients were male with age ranges from 10 to 68 years. GenBank BLAST of the obtained DNA sequences confirmed identified specimens as L. donovani complex. We identified additional VL cases from non-program districts (including the high lands) of Nepal, indicating that the infection could be an emerging threat for the non-program areas of Nepal.

conclusionThe demonstration of VL cases in areas initially considered non-endemic has raised concern about on-going transmission in those regions and may trigger subsequent government plan and action to include those areas in the elimination program. Thus, the government should consider revising the disease control programs to accommodate non-program districts for achieving the VL elimination goal set for 2020.

Indexed as

AdolescentAdultAgedAnimalsChildHumansIncidenceLeishmania donovaniLeishmaniasis, VisceralMaleMiddle AgedNepalPhlebotomusPolymerase Chain ReactionYoung AdultHigh altitudeNepalNon-program districtsVisceral leishmaniasis

Identifiers

PMID31113385
PMCPMC6528229

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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.