Evidence map›Paper›PMID 31547813›Full record

ArticleMalaria journal2019

Differential expression of var subgroups and PfSir2a genes in afebrile Plasmodium falciparum malaria: a matched case-control study.

Himanshu Gupta, Beatriz Galatas, Gloria Matambisso, Lidia Nhamussua, Pau Cisteró, Quique Bassat, Aina Casellas, Eusébio Macete, John J Aponte, Charfudin Sacoor and 5 more

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2019. 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
2.0field-weighted citation impact, top 14% 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, 11 citations in OpenAlex.

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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

15 authors at 3 institutions in 2 countries.

Himanshu GuptaISGlobal, Hospital Clínic - Universitat de Barcelona, Barcelona, Spain. himanshu.gupta@isglobal.org.ORCID http://orcid.org/0000-0003-1391-8358
Beatriz GalatasISGlobal, Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
Gloria MatambissoCentro de Investigação em Saúde de Manhiça, Manhiça, Mozambique.
Lidia NhamussuaCentro de Investigação em Saúde de Manhiça, Manhiça, Mozambique.
Pau CisteróISGlobal, Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
Quique BassatISGlobal, Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
Aina CasellasISGlobal, Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
Eusébio MaceteCentro de Investigação em Saúde de Manhiça, Manhiça, Mozambique.
John J AponteISGlobal, Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
Charfudin SacoorCentro de Investigação em Saúde de Manhiça, Manhiça, Mozambique.
Pedro AlonsoISGlobal, Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
Francisco SaúteISGlobal, Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
Caterina GuinovartISGlobal, Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
Pedro AideCentro de Investigação em Saúde de Manhiça, Manhiça, Mozambique.
Alfredo MayorISGlobal, Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
Manhiça Health Research Centre · MZBarcelona Institute for Global Health · ESInstitució Catalana de Recerca i Estudis Avançats · ES

Funding

Bill & Melinda Gates Foundation OPP1115265Overseas Postdoctoral Fellowship by Department of Science & Technology, Government of India SB/OS/PDF-043/2015-16
6 · The paper itself

Abstract

backgroundPoor knowledge on the afebrile Plasmodium falciparum biology limits elimination approaches to target asymptomatic malaria. Therefore, the association of parasite factors involved in cytoadhesion, parasite multiplication and gametocyte maturation with afebrile malaria was assessed.

methodsPlasmodium falciparum isolates were collected from febrile (axillary temperature ≥ 37.5 °C or a reported fever in the previous 24 h) and afebrile (fever neither at the visit nor in the previous 24 h) individuals residing in Southern Mozambique. var, PfSir2a and Pfs25 transcript levels were determined by reverse transcriptase quantitative PCRs (RT-qPCRs) and compared among 61 pairs of isolates matched by parasite density, age and year of sample collection.

resultsThe level of varC and PfSir2a transcripts was higher in P. falciparum isolates from afebrile individuals (P ≤ 0.006), while varB and DC8 genes (P ≤ 0.002) were higher in isolates from individuals with febrile infections. After adjusting the analysis by area of residence, doubling the relative transcript unit (RTU) of varC and PfSir2a was associated with a 29.7 (95% CI 4.6-192.3) and 8.5 (95% CI 1.9-32.2) fold increases, respectively, of the odds of being afebrile. In contrast, doubling the RTU of varB and DC8 was associated with a 0.8 (95% CI 0.05-0.6) and 0.2 (95% CI 0.04-0.6) fold changes, respectively, of the odds of being afebrile. No significant differences were found for Pfs25 transcript levels in P. falciparum isolates from afebrile and febrile individuals.

conclusionsvar and gametocyte-specific transcript patterns in febrile and afebrile infections from southern Mozambique matched by age, parasite density and recruitment period suggest similar transmissibility but differential expression of variant antigens involved in cytoadhesion and immune-evasion.

Indexed as

Gene ExpressionAdolescentAdultCase-Control StudiesChildChild, PreschoolCross-Sectional StudiesFemaleHumansInfantInfant, NewbornMalaria, FalciparumMaleMozambiquePlasmodium falciparumProtozoan Proteinserythrocyte membrane protein 1, Plasmodium falciparumProtozoan ProteinsAfebrile malariaGametocytesMozambiquePfSir2avar genes

Identifiers

PMID31547813
PMCPMC6755688
OpenAlexW2975723932

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LicenceCC BY
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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.