Evidence map›Paper›PMID 23244590›Full record

ArticleMalaria journal2012

A rapid and scalable density gradient purification method for Plasmodium sporozoites.

Mark Kennedy, Matthew E Fishbaugher, Ashley M Vaughan, Rapatbhorn Patrapuvich, Rachasak Boonhok, Narathatai Yimamnuaychok, Nastaran Rezakhani, Peter Metzger, Marisa Ponpuak, Jetsumon Sattabongkot and 3 more

Abstract read
In one paragraph

Article in Malaria journal, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing 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

72 citing papers in PubMed.

  1. Trial
  2. A pleckstrin homology domain protein is involved in crystalloid formation inFrontiers in cellular and infection microbiology · 2026
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  8. Identification of a novel rhoptry protein expressed predominantly inFrontiers in cellular and infection microbiology · 2025
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  10. IdentifyingResearch square · 2024
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  16. Review
  17. Article
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  20. Article

12 more citing papers are in PubMed but not listed here.

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

13 authors.

Mark KennedyCenter for Mosquito Production and Malaria Infection Research, Seattle Biomedical Research Institute, 307 Westlake Avenue North, Suite 500, Seattle, WA 98109, USA.
Matthew E Fishbaugher
Ashley M Vaughan
Rapatbhorn Patrapuvich
Rachasak Boonhok
Narathatai Yimamnuaychok
Nastaran Rezakhani
Peter Metzger
Marisa Ponpuak
Jetsumon Sattabongkot
Stefan H Kappe
Jen C C Hume
Scott E Lindner

Funding

Structural Analysis of DNA Replication Machinery of P. falciparumF32GM083438 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI LINDNER, SCOTT E · 2009 to 2010
$102k
NIGMS NIH HHS F32GM083438
6 · The paper itself

Abstract

backgroundMalaria remains a major human health problem, with no licensed vaccine currently available. Malaria infections initiate when infectious Plasmodium sporozoites are transmitted by Anopheline mosquitoes during their blood meal. Investigations of the malaria sporozoite are, therefore, of clear medical importance. However, sporozoites can only be produced in and isolated from mosquitoes, and their isolation results in large amounts of accompanying mosquito debris and contaminating microbes.

methodsHere is described a discontinuous density gradient purification method for Plasmodium sporozoites that maintains parasite infectivity in vitro and in vivo and greatly reduces mosquito and microbial contaminants.

resultsThis method provides clear advantages over previous approaches: it is rapid, requires no serum components, and can be scaled to purify >107 sporozoites with minimal operator involvement. Moreover, it can be effectively applied to both human (Plasmodium falciparum, Plasmodium vivax) and rodent (Plasmodium yoelii) infective species with excellent recovery rates.

conclusionsThis novel method effectively purifies viable malaria sporozoites by greatly reducing contaminating mosquito debris and microbial burdens associated with parasite isolation. Large-scale preparations of purified sporozoites will allow for enhanced in vitro infections, proteomics, and biochemical characterizations. In conjunction with aseptic mosquito rearing techniques, this purification technique will also support production of live attenuated sporozoites for vaccination.

Indexed as

AnimalsAnophelesCentrifugation, Density GradientDisease Models, AnimalFemaleHumansLiverMalariaMiceParasitologyPlasmodiumPlasmodium falciparumPlasmodium vivaxPlasmodium yoeliiSporozoitesVirulence

Identifiers

PMID23244590
PMCPMC3543293

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LicenceCC BY
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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.