Evidence map›Paper›PMID 27723436›Full record

ArticleThe Journal of parasitology2017

Transient Expression of Plasmodium berghei MSP8 and HAP2 in the Marine Protozoan Parasite Perkinsus marinus.

Emma R Cold, Gerardo R Vasta, José A Fernández Robledo

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of parasitology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Perkinsus marinus in bioreactor: growth and a cost-reduced growth medium.Journal of industrial microbiology & biotechnology · 2023
    Article
  2. Article
  3. From the raw bar to the bench: Bivalves as models for human health.Developmental and comparative immunology · 2019
    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

3 authors at 1 institution in 1 country.

Emma R ColdBigelow Laboratory for Ocean Sciences, East Boothbay, Maine 04544.
Gerardo R VastaBigelow Laboratory for Ocean Sciences, East Boothbay, Maine 04544.
José A Fernández RobledoBigelow Laboratory for Ocean Sciences, East Boothbay, Maine 04544.
Bigelow Laboratory for Ocean Sciences · US

Funding

A Heterologous Expression System for Apicomplexa GenesR21AI076797 · NIAID · UNIVERSITY OF MD BIOTECHNOLOGY INSTITUTE · PI FERNANDEZ-ROBLEDO, JOSE A · 2009 to 2010
$356k
NIAID NIH HHS R21 AI076797
6 · The paper itself

Abstract

Perkinsus marinus is a protozoan parasite of molluscs that can be propagated in vitro in a defined culture medium, in the absence of host cells. We previously reported that P. marinus trophozoites can be transfected with high efficiency by electroporation using a plasmid based on MOE, a highly expressed gene, and proposed its potential use as a "pseudoparasite." This is a novel gene expression platform for parasites of medical relevance for which the choice of the surrogate organism is based on phylogenetic affinity to the parasite of interest, while taking advantage of the whole engineered surrogate organism as a vaccination adjuvant. Here we improved the original transfection plasmid by incorporating a multicloning site, an enterokinase recognition sequence upstream of GFP, and a His-tag and demonstrate its potential suitability for the heterologous expression of Plasmodium sp. genes relevant to the development of anti-malarial vaccines. Plasmodium berghei HAP2 and MSP8, currently considered candidate genes for a malaria vaccine, were cloned into p[MOE]:GFP, and the constructs were used to transfect P. marinus trophozoites. Within 48 hr of transfection we observed fluorescent cells indicating that the P. berghei genes fused to GFP were expressed. The expression appeared to be transient for both P. berghei genes, as florescence of the transfectants diminished gradually over time. Although this heterologous expression system will require optimization for integration and constitutive expression of Plasmodium genes, our results represent attainment of proof for the "pseudoparasite" concept we previously proposed, as we show that the engineered P. marinus system has the potential to become a surrogate system suitable for expression of Plasmodium spp. genes of interest, which could eventually be used as a malaria vaccine delivery platform. The aim of the present study was to test the ability of marine protozoan parasite P. marinus to express genes of P. berghei .

Indexed as

Malaria VaccinesAlveolataAnimalsAntigens, ProtozoanFemaleGene Expression RegulationGenetic VectorsMalariaMalePlasmidsPlasmodium bergheiProtozoan ProteinsTransfectionAntigens, ProtozoanMalaria Vaccinesmerozoite surface protein 8, PlasmodiumProtozoan Proteins

Identifiers

PMID27723436
PMCPMC7759765
OpenAlexW2530100358

What OpenQuestion holds

Textmetadata
LicenceTDM
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.