Evidence map›Paper›PMID 42205808›Full record

ArticleFrontiers in veterinary science2026

Genotoxicity and gene expression modulation associated with the use of DDVP antiparasitic drugs in aquaculture on

Ad Viralkumar, Lukram Sushil Singh, Gowhar Iqbal, Vivek Shrivastava, Ridhdhisa R Barad, Krinal Mori, Sujit Kumar

Abstract read
In one paragraph

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

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

7 authors.

Ad ViralkumarCollege of Fisheries Science Kamdhenu University Himmatnagar, Gujrat, India.
Lukram Sushil SinghICAR-Central Institute of Fisheries Education, Panch Marg, Yari Road, Mumbai, India.
Gowhar IqbalICAR-Central Institute of Fisheries Education, Panch Marg, Yari Road, Mumbai, India.
Vivek ShrivastavaCollege of Fisheries Science Kamdhenu University Himmatnagar, Gujrat, India.
Ridhdhisa R BaradCollege of Fisheries Science Kamdhenu University Himmatnagar, Gujrat, India.
Krinal MoriCollege of Fisheries Science Kamdhenu University Himmatnagar, Gujrat, India.
Sujit KumarCollege of Fisheries Science Kamdhenu University Himmatnagar, Gujrat, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Parasites are a significant threat to aquaculture, and the application of various antiparasitic chemicals by aquafarmers is a widely practiced strategy to control them. Few antiparasitic drugs are toxic to hosts at higher concentrations and may be genotoxic to them. Genotoxicity tests have been successfully used as indicators of the toxicity of several drugs and environmental pollutants, including heavy metals. The current study was aimed to assess the toxicity of antiparasitic chemicals or drugs at various levels, with special emphasis on genotoxicity in a Zebrafish model. Methods: Adult zebrafish were acclimatized under laboratory conditions and exposed to graded concentrations of dichlorvos to determine acute toxicity (LC25 and LC50) through a 96 h semi-static bioassay. Based on these values, fish were further subjected to sublethal and lethal concentrations for in vivo assessment at 24, 48, 72, and 96 h intervals. Genotoxicity was evaluated using micronucleus and alkaline comet assays on blood and gill tissues. Gene expression analysis of p53, Cyp1a, and Bcl-2 was performed in gill, liver, and kidney tissues using qRT-PCR after RNA isolation and cDNA synthesis. Data were statistically analyzed by one-way ANOVA followed by Tukey's Results: This study investigated the genotoxic potential of dichlorvos in zebrafish using micronucleus and comet assays, along with gene expression analysis of key biomarkers (p53, Cyp1a, and Bcl-2). The 96-hour LC50 and LC25 values of DDVP were determined as 10.6 ppm and 6.78 ppm, respectively. Based on sublethal toxicity, zebrafish ( Conclusion: Overall, dichlorvos exposure induced significant genotoxic effects in zebrafish in a dose- and duration dependent manner. The findings suggest that concentrations below LC25 may be relatively safer for therapeutic use. Further studies are required to check the efficacy of DDVP against different parasites to formulate more specific treatment strategies for sustainable aquaculture practices.

Indexed as

antiparasitic drugaquacultureDanio rerioDDVPgene expressiongenotoxicity

Identifiers

PMID42205808
PMCPMC13201461

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