Simultaneous inactivation of antibiotic-resistant bacteria and degradation of antibiotic-resistant genes in alkalised human urine.

The coexistence of pharmaceuticals and microorganisms in source separated urine poses a risk for the development of antimicrobial resistance (AMR), especially when urine-based fertilizers are applied to soils. While prior studies have investigated pathogen inactivation in source-separated wastewater matrices, few have evaluated the simultaneous fate of antibiotic-resistant bacteria (ARBs) and their corresponding resistance genes (ARGs) in real urine matrices, particularly under alkaline conditions. Here, we studied the inactivation of β-lactamase-producing Escherichia coli and vancomycin-resistant Enterococcus faecium and the degradation of their respective ARGs (bla (CTX - M) and van-A) in alkalized, unhydrolyzed urine (pH 10.8 and 12.5) treated with UV (65 W low pressure dichromatic mercury lamp at 185/254 nm), hydrogen peroxide (1.25 g L(-1) H(2)O(2)), and their combination (UV/H(2)O(2)). UV/H(2)O(2) treatment resulted in >7 log(10) inactivation of both ARBs, with inactivation rate constants of -0.058 log(10) cfu min(-1) (E. coli, UV) and -0.093 log(10) cfu min(-1) (E. faecium, UV/H(2)O(2)). In contrast, ARG reduction was limited with UV alone and negligible with H(2)O(2) alone. Gene copy reductions of 3 log10 (bla (CTX - M), k = -0.055 log10 copies min(-1)) and 2 log10 (van-A, k = -0.040 log10 copies min(-1)) were observed under UV/H(2)O(2). Notably, brief storage (>3 h) at pH 12.5 achieved similar ARB inactivation and ARG reduction as 80 min of UV/H(2)O(2) treatment at pH 10.8, offering a low-energy alternative for sanitizing source-separated urine.