Evidence map›Paper›PMID 27870874›Full record

ArticlePloS one2016

Associations between Season and Gametocyte Dynamics in Chronic Plasmodium falciparum Infections.

Amal A H Gadalla, Petra Schneider, Thomas S Churcher, Elkhansaa Nassir, Abdel-Muhsin A Abdel-Muhsin, Lisa C Ranford-Cartwright, Sarah E Reece, Hamza A Babiker

Abstract read
In one paragraph

Article in PloS one, 2016. 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
–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

18 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Frontiers in cellular and infection microbiology · 2021
    Review
  8. Stressed Out AboutFrontiers in cellular and infection microbiology · 2021
    Review
  9. Article
  10. Article
  11. Prevalence of asymptomaticWellcome open research · 2020
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. 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

8 authors.

Amal A H GadallaDepartment of Biochemistry, Faculty of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
Petra SchneiderInstitutes of Evolution, Immunology and Infection Research, University of Edinburgh, Edinburgh, United Kingdom.
Thomas S ChurcherDepartment of Infectious Disease Epidemiology, Imperial College London, London, United Kingdom.
Elkhansaa NassirMedicinal and Aromatic Plants Research Institute and Traditional Medicine, National Centre for Research, Khartoum, Sudan.
Abdel-Muhsin A Abdel-MuhsinDepartment of Biology, Faculty of Science, University of Hail, Baqaa, Kingdom of Saudi Arabia.
Lisa C Ranford-CartwrightInstitute of Infection, Immunity and Inflammation, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom.
Sarah E ReeceInstitutes of Evolution, Immunology and Infection Research, University of Edinburgh, Edinburgh, United Kingdom.
Hamza A BabikerDepartment of Biochemistry, Faculty of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.

Funding

Medical Research Council MR/K010174/1
6 · The paper itself

Abstract

introductionIn a markedly seasonal malaria setting, the transition from the transmission-free dry season to the transmission season depends on the resurgence of the mosquito population following the start of annual rains. The sudden onset of malaria outbreaks at the start of the transmission season suggests that parasites persist during the dry season and respond to either the reappearance of vectors, or correlated events, by increasing the production of transmission stages. Here, we investigate whether Plasmodium falciparum gametocyte density and the correlation between gametocyte density and parasite density show seasonal variation in chronic (largely asymptomatic) carriers in eastern Sudan. MATERIALS AND

methodsWe recruited and treated 123 malaria patients in the transmission season 2001. We then followed them monthly during four distinct consecutive epidemiological seasons: transmission season 1, transmission-free season, pre-clinical period, and transmission season 2. In samples collected from 25 participants who fulfilled the selection criteria of the current analysis, we used quantitative PCR (qPCR) and RT-qPCR to quantify parasite and gametocyte densities, respectively. RESULTS AND DISCUSSION: We observed a significant increase in gametocyte density and a significantly steeper positive correlation between gametocyte density and total parasite density during the pre-clinical period compared to the preceding transmission-free season. However, there was no corresponding increase in the density or prevalence of total parasites or gametocyte prevalence. The increase in gametocyte production during the pre-clinical period supports the hypothesis that P. falciparum may respond to environmental cues, such as mosquito biting, to modulate its transmission strategy. Thus, seasonal changes may be important to ignite transmission in unstable-malaria settings.

Indexed as

DNA, ProtozoanGerm CellsHumansMalaria, FalciparumMalePlasmodium falciparumSeasonsSudanDNA, Protozoan

Identifiers

PMID27870874
PMCPMC5117706

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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.