Ecological risks of sulfonamides and quinolones degradation intermediates: Toxicity, microbial community, and antibiotic resistance genes

Abstract

The ecological risks posed by incompletely degraded antibiotic intermediates in aquatic environments warrant significant attention. This study investigated the degradation mechanisms of sulfonamides (sulfadiazine, sulfamethoxazole) and quinolones (ciprofloxacin, norfloxacin) during thermally activated persulfate (TAP) treatment. The main degradation mechanisms for sulfonamides involved S-N bond cleavage and –NH₂ oxidation mediated by sulfate and hydroxyl radicals, whereas quinolone degradation occurred primarily through piperazine ring cleavage facilitated by a single linear oxygen. Toxic degradation intermediates were found to be enriched with bacteria in real water samples, including Aeromonas (SDZ-50, 9.61%), Acinetobacter (SMZ-50, 21.91%), unclassified Archaea (CIP-50, 19.32%), and Herbaspirillum (NOR-50, 17.36%). Meanwhile, the abundance of sulfonamide-associated antibiotic resistance genes (ARGs) (sul1 and sul2) and quinolone-associated ARGs (mfpA, emrA, and lfrA) significantly increased, with SMZ-50 and NOR-50 reaching 659.34 and 2009.98 RPKM, respectively. Correlation analysis revealed differences in host diversity and composition driven by the same classes of antibiotics and their intermediates.