Evidence map›Paper›PMID 36351999›Full record

ArticleScientific reports2022

Identification of a TNF-TNFR-like system in malaria vectors (Anopheles stephensi) likely to influence Plasmodium resistance.

Subhashini Srinivasan, Chaitali Ghosh, Shrestha Das, Aditi Thakare, Siddharth Singh, Apoorva Ganesh, Harsh Mahawar, Aadhya Jaisimha, Mohanapriya Krishna, Aritra Chattopadhyay and 7 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 13 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

17 authors at 5 institutions in 2 countries.

Subhashini SrinivasanInstitute of Bioinformatics and Applied Biotechnology, Biotech Park, Electronic City Phase I, Bengaluru, 560100, India. ssubha@ibab.ac.in.
Chaitali Ghosh *Tata Institute for Genetics and Society (TIGS), Center at inStem, Bellary Road, GKVK Campus, Bengaluru, 560065, India.
Shrestha Das *Institute of Bioinformatics and Applied Biotechnology, Biotech Park, Electronic City Phase I, Bengaluru, 560100, India.
Aditi Thakare *Institute of Bioinformatics and Applied Biotechnology, Biotech Park, Electronic City Phase I, Bengaluru, 560100, India.
Siddharth SinghInstitute of Bioinformatics and Applied Biotechnology, Biotech Park, Electronic City Phase I, Bengaluru, 560100, India.
Apoorva GaneshInstitute of Bioinformatics and Applied Biotechnology, Biotech Park, Electronic City Phase I, Bengaluru, 560100, India.
Harsh MahawarInstitute of Bioinformatics and Applied Biotechnology, Biotech Park, Electronic City Phase I, Bengaluru, 560100, India.
Aadhya JaisimhaInstitute of Bioinformatics and Applied Biotechnology, Biotech Park, Electronic City Phase I, Bengaluru, 560100, India.
Mohanapriya KrishnaInstitute of Bioinformatics and Applied Biotechnology, Biotech Park, Electronic City Phase I, Bengaluru, 560100, India.
Aritra ChattopadhyayInstitute of Bioinformatics and Applied Biotechnology, Biotech Park, Electronic City Phase I, Bengaluru, 560100, India.
Rishima BorahInstitute of Bioinformatics and Applied Biotechnology, Biotech Park, Electronic City Phase I, Bengaluru, 560100, India.
Vikrant SinghInstitute of Bioinformatics and Applied Biotechnology, Biotech Park, Electronic City Phase I, Bengaluru, 560100, India.
Soumya MTata Institute for Genetics and Society (TIGS), Center at inStem, Bellary Road, GKVK Campus, Bengaluru, 560065, India.
Naveen KumarTata Institute for Genetics and Society (TIGS), Center at inStem, Bellary Road, GKVK Campus, Bengaluru, 560065, India.
Sampath KumarTata Institute for Genetics and Society (TIGS), Center at inStem, Bellary Road, GKVK Campus, Bengaluru, 560065, India.
Sunita SwainTata Institute for Genetics and Society (TIGS), Center at inStem, Bellary Road, GKVK Campus, Bengaluru, 560065, India. sunita.swain@tigs.res.in.
Suresh SubramaniTIGS, University of California San Diego, La Jolla, CA, 92093, USA.
Institute of Bioinformatics and Applied Biotechnology · INBiotech Park · INTata Institute for Genetics and Society · INInstitute for Stem Cell Biology and Regenerative Medicine · INUniversity of California, San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Identification of Plasmodium-resistance genes in malaria vectors remains an elusive goal despite the recent availability of high-quality genomes of several mosquito vectors. Anopheles stephensi, with its three distinctly-identifiable forms at the egg stage, correlating with varying vector competence, offers an ideal species to discover functional mosquito genes implicated in Plasmodium resistance. Recently, the genomes of several strains of An. stephensi of the type-form, known to display high vectorial capacity, were reported. Here, we report a chromosomal-level assembly of an intermediate-form of An. stephensi strain (IndInt), shown to have reduced vectorial capacity relative to a strain of type-form (IndCh). The contig level assembly with a L50 of 4 was scaffolded into chromosomes by using the genome of IndCh as the reference. The final assembly shows a heterozygous paracentric inversion, 3Li, involving 8 Mbp, which is syntenic to the extensively-studied 2La inversion implicated in Plasmodium resistance in An. gambiae involving 21 Mbp. Deep annotation of genes within the 3Li region in the IndInt assembly using the state-of-the-art protein-fold prediction and other annotation tools reveals the presence of a tumor necrosis factor-alpha (TNF-alpha) like gene, which is the homolog of the Eiger gene in Drosophila. Subsequent chromosome-wide searches revealed homologs of Wengen (Wgn) and Grindelwald (Grnd) genes, which are known to be the receptors for Eiger in Drosophila. We have identified all the genes in IndInt required for Eiger-mediated signaling by analogy to the TNF-alpha system, suggesting the presence of a functionally-active Eiger signaling pathway in IndInt. Comparative genomics of the three type-forms with that of IndInt, reveals structurally disruptive mutations in Eiger gene in all three strains of the type-form, suggesting compromised innate immunity in the type-form as the likely cause of high vectorial capacity in these strains. This is the first report of the presence of a homolog of Eiger in malaria vectors, known to be involved in cell death in Drosophila, within an inversion region in IndInt syntenic to an inversion associated with Plasmodium resistance in An. gambiae.

Indexed as

AnophelesMalariaPlasmodiumAnimalsChromosome InversionDrosophilaMosquito VectorsTumor Necrosis Factor-alphaTumor Necrosis Factor-alpha

Identifiers

PMID36351999
PMCPMC9646898
OpenAlexW4308735528

What OpenQuestion holds

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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.