Evidence map›Paper›PMID 41291089›Full record

ReviewMicrobial ecology2025

Pelagic Shuttles of Antibiotic Resistance Genes: Zooplankton as Overlooked Vectors Across Space and Food Webs.

Albert Calbet

Abstract readReview
In one paragraph

Review in Microbial ecology, 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. 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

1 author.

Albert CalbetInstitut de Ciències del Mar (ICM-CSIC), Passeig Marítim de la Barceloneta 37-49, 08003 , Barcelona, Spain. acalbet@icm.csic.es.ORCID http://orcid.org/0000-0003-1069-212X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibiotic resistance genes (ARGs) accumulate in aquatic environments, where they create reservoirs and transmission pathways that can undermine antimicrobial treatments and alter the microbial community structure in ways that ultimately affect human and animal health. However, the contribution of zooplankton in these pathways remains critically overlooked. Emerging evidence shows that compared with surrounding water, copepods and cladocerans accumulate ARG loads that are one to two orders of magnitude greater, acting as microbial hotspots that disperse resistant bacteria across seasons and depths. Inside protistan vacuoles, densely packed prey cells undergo conjugation, rapidly accelerating horizontal ARG transfer. Long-term archives reveal persistent ocean-wide dissemination of the class-1 integron integrase (intI1) and sul2 genes since at least the 1970s. Here, I synthesize mechanistic and field evidence, pinpoint knowledge gaps, and recommend priorities: integrate zooplankton into routine ARG surveillance, quantify biofilm-mediated exchanges, and mitigate contamination from coselective pollutants to curb zooplankton-driven ARG propagation. By framing zooplankton-associated ARG dynamics within the broader community ecology of antimicrobial resistance, this mini-review highlights how aquatic food-web processes feed back into the emergence, evolution, and transmission of resistance that concerns for One Health outcomes beyond the clinic.

Indexed as

BacteriaDrug Resistance, BacterialDrug Resistance, MicrobialFood ChainZooplanktonAnimalsAnti-Bacterial AgentsGenes, BacterialGene Transfer, HorizontalAnti-Bacterial AgentsAntibiotic resistance genes (ARGs)Horizontal gene transfer (HGT)Mobile genetic elements (MGEs)One healthPhagotrophic protistsZooplankton

Identifiers

PMID41291089
PMCPMC12774974

What OpenQuestion holds

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LicenceCC BY
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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.