Evidence map›Paper›PMID 23349974›Full record

ArticlePloS one2013

Application of a qPCR assay in the investigation of susceptibility to malaria infection of the M and S molecular forms of An. gambiae s.s. in Cameroon.

Anne Boissière, Geoffrey Gimonneau, Majoline T Tchioffo, Luc Abate, Albert Bayibeki, Parfait H Awono-Ambéné, Sandrine E Nsango, Isabelle Morlais

Erratum issuedAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing 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

42 citing papers in PubMed.

  1. Article
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  5. Limited association betweenEvolutionary applications · 2023
    Article
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  7. GigaByte (Hong Kong, China) · 2023
    Article
  8. Using qPCR to compare the detection ofFrontiers in parasitology · 2023
    Article
  9. Article
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  13. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Anne BoissièreUnité mixte de recherche MIVEGEC (IRD 224- CNRS 5290-UM1-UM2), Institut de Recherche pour le Développement, Montpellier, France.
Geoffrey Gimonneau
Majoline T Tchioffo
Luc Abate
Albert Bayibeki
Parfait H Awono-Ambéné
Sandrine E Nsango
Isabelle Morlais

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plasmodium falciparum is the causative agent of malaria, a disease that kills almost one million persons each year, mainly in sub-Saharan Africa. P. falciparum is transmitted to the human host by the bite of an Anopheles female mosquito, and Anopheles gambiae sensus stricto is the most tremendous malaria vector in Africa, widespread throughout the afro-tropical belt. An. gambiae s.s. is subdivided into two distinct molecular forms, namely M and S forms. The two molecular forms are morphologically identical but they are distinct genetically, and differ by their distribution and their ecological preferences. The epidemiological importance of the two molecular forms in malaria transmission has been poorly investigated so far and gave distinct results in different areas. We have developed a real-time quantitative PCR (qPCR) assay, and used it to detect P. falciparum at the oocyst stage in wild An. gambiae s.s. mosquitoes experimentally infected with natural isolates of parasites. Mosquitoes were collected at immature stages in sympatric and allopatric breeding sites and further infected at the adult stage. We next measured the infection prevalence and intensity in female mosquitoes using the qPCR assay and correlated the infection success with the mosquito molecular forms. Our results revealed different prevalence of infection between the M and S molecular forms of An. gambiae s.s. in Cameroon, for both sympatric and allopatric populations of mosquitoes. However, no difference in the infection intensity was observed. Thus, the distribution of the molecular forms of An. gambiae s.s. may impact on the malaria epidemiology, and it will be important to monitor the efficiency of malaria control interventions on the two M and S forms.

Indexed as

AdultAnimalsAnophelesCameroonFemaleGenetic Predisposition to DiseaseGenotypeHumansInsect VectorsMalaria, FalciparumOocystsPlasmodium falciparumPolymerase Chain Reaction

Identifiers

PMID23349974
PMCPMC3551906

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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.