Evidence map›Paper›PMID 40481536›Full record

ArticleMalaria journal2025

Effects of Plasmodium berghei infection on the expression of salivary gland immune-related genes in the Anopheles stephensi mosquito.

Sakineh Pirahmadi, Zahra Sadat Mousavi Shafi, Zeinab Mohammadi Firouz, Akram Abouie Mehrizi, Jafar J Sani, Hemn Yousefi, Sepideh Siasi, Abbasali Raz, Flora Forouzesh, Leila Darzi

Abstract read
In one paragraph

Article in Malaria journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Salivary gland microbiome ofFrontiers in insect science · 2026
    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

10 authors.

Sakineh PirahmadiMalaria and Vector Research Group (MVRG), Biotechnology Research Center (BRC), Pasteur Institute of Iran, Tehran, Iran. s.pirahmadi2020@googlemail.com.
Zahra Sadat Mousavi ShafiMalaria and Vector Research Group (MVRG), Biotechnology Research Center (BRC), Pasteur Institute of Iran, Tehran, Iran.
Zeinab Mohammadi FirouzMalaria and Vector Research Group (MVRG), Biotechnology Research Center (BRC), Pasteur Institute of Iran, Tehran, Iran.
Akram Abouie MehriziMalaria and Vector Research Group (MVRG), Biotechnology Research Center (BRC), Pasteur Institute of Iran, Tehran, Iran.
Jafar J SaniMalaria and Vector Research Group (MVRG), Biotechnology Research Center (BRC), Pasteur Institute of Iran, Tehran, Iran.
Hemn YousefiMalaria and Vector Research Group (MVRG), Biotechnology Research Center (BRC), Pasteur Institute of Iran, Tehran, Iran.
Sepideh SiasiMalaria and Vector Research Group (MVRG), Biotechnology Research Center (BRC), Pasteur Institute of Iran, Tehran, Iran.
Abbasali RazMalaria and Vector Research Group (MVRG), Biotechnology Research Center (BRC), Pasteur Institute of Iran, Tehran, Iran.
Flora ForouzeshDepartment of Genetics, Faculty of Advanced Science and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.
Leila DarziDepartment of Medical Biotechnology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

Funding

Iran National Science Foundation 4013870Pasteur Institute of Iran 1319
6 · The paper itself

Abstract

backgroundAchieving malaria eradication by 2050 will require the development of novel transmission-blocking strategies alongside existing and emerging control measures. Since the innate immune responses of Anopheles salivary glands determine its vectorial capacity, a detailed assessment of vector-parasite interactions could help identify novel targets that play key roles in the immune response against Plasmodium. In this study, six candidate immune-related genes from Anopheles stephensi salivary gland transcriptomic datasets were selected, and their expression changes were assessed following Plasmodium berghei infection.

methodsUsing RT-qPCR, gene expression profiles at 18 days (early phase) and 21 days (late phase) post-infection were analysed, and the results were compared with those of uninfected mosquitoes.

resultsA significant upregulation of LRIM8A and DEF1 gene expression was observed at both time points, whereas TEP-12 expression was significantly increased only at day 21. However, no significant changes were observed for P37NB, CLIPA4, and CLIPC4. Among the highly expressed genes, LRIM8A exhibited the highest expression during both the early and later phases of salivary gland infection.

conclusionsThe highest expression levels of LRIM8A at both early and late phases of salivary gland infection underscore its potential as a key immune effector. However, further functional assays are required to validate the role of LRIM8A in mosquito innate immunity. A deeper understanding of the immune mechanisms in Anopheles following Plasmodium infection could contribute to the development of novel malaria control strategies.

Indexed as

AnophelesInsect ProteinsMosquito VectorsPlasmodium bergheiSalivary GlandsAnimalsFemaleGene Expression ProfilingImmunity, InnateMalariaTranscriptomeInsect ProteinsAnopheles stephensiGene expressionInnate immunityPlasmodium bergheiSalivary glands

Identifiers

PMID40481536
PMCPMC12144816

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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.