Evidence map›Paper›PMID 25784701›Full record

ArticlemBio2015

Cyclic GMP balance is critical for malaria parasite transmission from the mosquito to the mammalian host.

Viswanathan Lakshmanan, Matthew E Fishbaugher, Bob Morrison, Michael Baldwin, Michael Macarulay, Ashley M Vaughan, Sebastian A Mikolajczak, Stefan H I Kappe

Open access · goldAbstract read
In one paragraph

Article in mBio, 2015. 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
2.3field-weighted citation impact, top 11% 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, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Plasticity and therapeutic potential of cAMP and cGMP-specific phosphodiesterases inComputational and structural biotechnology journal · 2022
    Article
  4. Review
  5. mBio · 2021
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. The protozoan parasiteComputational and structural biotechnology journal · 2020
    Article
  12. Article
  13. Review
  14. Article
  15. The MicronemalFrontiers in cellular and infection microbiology · 2018
    Article
  16. Review
  17. Article
  18. Cold Spring Harbor perspectives in medicine · 2017
    Review
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 at 2 institutions in 1 country.

Viswanathan LakshmananSeattle Biomedical Research Institute (Seattle BioMed), Seattle, Washington, USA.
Matthew E FishbaugherSeattle Biomedical Research Institute (Seattle BioMed), Seattle, Washington, USA.
Bob MorrisonSeattle Biomedical Research Institute (Seattle BioMed), Seattle, Washington, USA.
Michael BaldwinSeattle Biomedical Research Institute (Seattle BioMed), Seattle, Washington, USA.
Michael MacarulaySeattle Biomedical Research Institute (Seattle BioMed), Seattle, Washington, USA.
Ashley M VaughanSeattle Biomedical Research Institute (Seattle BioMed), Seattle, Washington, USA.
Sebastian A MikolajczakSeattle Biomedical Research Institute (Seattle BioMed), Seattle, Washington, USA.
Stefan H I Kappestefan.kappe@seattlebiomed.org.
Center for Infectious Disease Research · USUniversity of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledTransmission of malaria occurs during Anopheles mosquito vector blood meals, when Plasmodium sporozoites that have invaded the mosquito salivary glands are delivered to the mammalian host. Sporozoites display a unique form of motility that is essential for their movement across cellular host barriers and invasion of hepatocytes. While the molecular machinery powering motility and invasion is increasingly well defined, the signaling events that control these essential parasite activities have not been clearly delineated. Here, we identify a phosphodiesterase (PDEγ) in Plasmodium, a regulator of signaling through cyclic nucleotide second messengers. Reverse transcriptase PCR (RT-PCR) analysis and epitope tagging of endogenous PDEγ detected its expression in blood stages and sporozoites of Plasmodium yoelii. Deletion of PDEγ (pdeγ(-)) rendered sporozoites nonmotile, and they failed to invade the mosquito salivary glands. Consequently, PDEγ deletion completely blocked parasite transmission by mosquito bite. Strikingly, pdeγ(-) sporozoites showed dramatically elevated levels of cyclic GMP (cGMP), indicating that a perturbation in cyclic nucleotide balance is involved in the observed phenotypic defects. Transcriptome sequencing (RNA-Seq) analysis of pdeγ(-) sporozoites revealed reduced transcript abundance of genes that encode key components of the motility and invasion apparatus. Our data reveal a crucial role for PDEγ in maintaining the cyclic nucleotide balance in the malaria parasite sporozoite stage, which in turn is essential for parasite transmission from mosquito to mammal. IMPORTANCE: Malaria is a formidable threat to human health worldwide, and there is an urgent need to identify novel drug targets for this parasitic disease. The parasite is transmitted by mosquito bite, inoculating the host with infectious sporozoite stages. We show that cellular signaling by cyclic nucleotides is critical for transmission of the parasite from the mosquito vector to the mammalian host. Parasite phosphodiesterase γ is essential for maintaining cyclic nucleotide balance, and its deletion blocks transmission of sporozoites. A deeper understanding of the signaling mechanisms involved in transmission might inform the discovery of novel drugs that interrupt this essential step in the parasite life cycle.

Indexed as

LocomotionAnimalsAnophelesCyclic GMPGene DeletionGene Expression ProfilingHumansPhosphoric Diester HydrolasesPlasmodium yoeliiReverse Transcriptase Polymerase Chain ReactionSalivary GlandsCyclic GMPPhosphoric Diester Hydrolases

Identifiers

PMID25784701
PMCPMC4453516
OpenAlexW2100808589

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.