Evidence map›Paper›PMID 41818208›Full record

ArticlePloS one2026

Development and validation of a synthetic peptide-based field deployable latex slide agglutination test for detection of Tilapia tilapinevirus.

Meshram Supradhnya Namdeo, Megha Kadam Bedekar, Jeena Kezhedath, Kooloth Valappil Rajendran, Anisha Valsalam, Ankita Godavarikar, Pooja Vinde, Sagar Hundare, Khangembam Victoria Chanu, Dimpal Thakuria and 1 more

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Meshram Supradhnya NamdeoICAR-Central Institute of Fisheries Education, Mumbai, India.ORCID https://orcid.org/0000-0002-6046-9703
Megha Kadam BedekarICAR-Central Institute of Fisheries Education, Mumbai, India.ORCID https://orcid.org/0000-0003-3558-7529
Jeena KezhedathICAR-Central Institute of Fisheries Education, Mumbai, India.
Kooloth Valappil RajendranICAR-Central Institute of Fisheries Education, Mumbai, India.
Anisha ValsalamICAR-Central Institute of Fisheries Education, Mumbai, India.
Ankita GodavarikarICAR-Central Institute of Fisheries Education, Mumbai, India.
Pooja VindeSVKM's Mithibai College of Arts, Chauhan Institute of Science and Amrutben Jivanlal College of Commerce and Economic, Mumbai, India.
Sagar HundareICAR-Central Institute of Fisheries Education, Mumbai, India.
Khangembam Victoria ChanuICAR- Central Institute of Coldwater Fisheries Research, Bhimtal, India.
Dimpal ThakuriaICAR- Central Institute of Coldwater Fisheries Research, Bhimtal, India.
Narrotam P SahuICAR-Central Institute of Fisheries Education, Mumbai, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tilapia significantly contributes to global food security and is an affordable protein source for most developing nations. Tilapia tilapinevirus (TiLV) poses a significant economic threat to the global tilapia industry. This study aimed to develop a rapid and accurate detection method for TiLV by synthesizing a monoclonal antibody (MAb) against it. A novel peptide, KLH-CQ, derived from the TiLV sequence, was designed considering physicochemical properties like net cationic charge, amphipathicity, helicity, and hydrophobicity. The KLH-CQ (50 µg) was used to immunize Balb/c mice with Freund's complete adjuvant. The presence of specific antibodies in the mice serum was confirmed by ELISA, which showed a high antibody titre of 2.67:0.12 (mean OD of treated Vs control sera). The mouse with the strongest immune response was used for spleen donor in hybridoma production. Epitope mapping via ELISA screening identified five positive clones (TiLV-MAb 1-5), with the most reactive clone selected for further analysis. Using Classen's method, a cutoff OD value of 1.24 ± 0.45 was determined for virus detection. The selected TiLV-MAb was then used as a probing antibody to develop a latex slide agglutination assay (TiLV-LAT) using passive adsorption method. Validation of the assay with tissue and mucus samples revealed a specificity of 88.37% and a sensitivity of 82.37% for TiLV detection. The overall accuracy of the assay was 83.51%, with positive and negative likelihood ratios of 7.06 and 0.2, respectively. The TiLV-LAT successfully detected TiLV in various tissues, showing variable sensitivity: liver (77.35%), mucus (73.53%), brain (67.92%), and kidney (62.26%). TiLV-LAT developed here has minimized the tedious steps involved in nucleic acid-based detection assays, with the recorded sensitivity and specificity; it can be used as a presumptive diagnosis for testing and point of care/farm site. Moreover, non-lethal sampling and virus testing in mucus samples would be useful for fish health monitoring.

Indexed as

Fish DiseasesPeptidesRNA VirusesTilapiaAnimalsAntibodies, MonoclonalAntibodies, ViralEnzyme-Linked Immunosorbent AssayEpitope MappingFemaleMiceMice, Inbred BALB CAntibodies, MonoclonalAntibodies, ViralPeptides

Identifiers

PMID41818208
PMCPMC12981439

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.