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Plastisphere as a global hotspot for antimicrobial resistance: Systematic review and quantitative synthesis

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Bacteria growing on floating plastic waste swap antibiotic-resistance genes almost 7 times faster than usual, with PVC plastic being the worst offender. This review of 53 studies suggests plastic pollution may be helping create drug-resistant germs in the environment, though it's not yet proof this directly makes people sick, more research is needed.

Study Type Review

Plastic debris provides colonizable surfaces for microbial biofilms, the plastisphere, which is now recognized as a hotspot for antimicrobial resistance (AMR) amplification and dissemination. This PRISMA 2020-compliant synthesis covers 53 studies. Random-effects meta-analysis of 30 conjugation datasets showed enhanced horizontal gene transfer: pooled log response ratio (lnRR) = 1.93 (95% CI: 1.63–2.23), 6.9-fold (95% CI: 5.1–9.3-fold); heterogeneity was high (I 2 = 85.0%; τ 2 = 0.573; Q = 187.6, df = 29) and the 95% prediction interval spanned 1.5–31.3-fold. Polyvinyl chloride (PVC) biofilms showed the largest sub-group effect (lnRR = 2.72; 95% CI: 1.84–3.60; 15.2-fold), and polymer type was significant as a categorical moderator (Q M = 12.3, P = 0.006; R 2 = 29%) but not as a continuous ordinal score ( P = 0.15). Antibiotic resistance gene (ARG) concentrations exceeded paired controls by one to three orders of magnitude (median log 10 enrichment 1.98; 95-fold). Ampicillin resistance in plastisphere-associated Vibrio spp. reached 68.4% (Wilson 95% CI: 57.3–77.8%), with 32.9% multidrug-resistant. A conceptual five-stage genetic reactor lifecycle model is proposed as a heuristic, not a validated framework, identifying dispersal as the least-evidenced stage. A polymer risk hierarchy (PVC > polyethylene (PE) > polystyrene (PS), with polyethylene terephthalate (PET) lowest for ARG enrichment), an exposure–response framework and four Tier-1 knowledge gaps are established. The evidence base is geographically skewed (38% of studies from Chinese systems), and these estimates describe environmental enrichment, not realized clinical risk. They nonetheless justify incorporating polymer-additive regulation and plastisphere resistome surveillance into One Health strategies and the UN Plastics Treaty.

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