Understanding the biofilm microbiome and antibiotic resistome
evolution
in drinking water distribution systems (DWDSs) is crucial to ensure
the safety of drinking water. We explored the 10 month evolution of
the microbial community, antibiotic resistance genes (ARGs), mobile
gene elements (MGEs) co-existing with ARGs and pathogenic ARG hosts,
and the ARG driving factors in DWDS biofilms using metagenomics assembly.
Sampling season was critical in determining the microbial community
and antibiotic resistome shift. Pseudomonas was the primary biofilm colonizer, and biofilms diversified more
as the formation time increased. Most genera tended to cooperate to
adapt to an oligotrophic environment with disinfectant stress. Biofilm
microbial community and antibiotic resistome assembly were mainly
determined by stochastic processes and changed with season. Metagenome
assembly provided the occurrence and fates of MGEs co-existing with
ARGs and ARG hosts in DWDS biofilms. The abundance of ARG- and MGE-carrying
pathogen Stenotrophomonas maltophilia was high in summer. It primarily harbored the aph(3)-IIb, multidrug transporter, smeD,
and metallo-beta-lactamase ARGs, which were transferred
via recombination. The microbial community was the most crucial factor
driving the antibiotic resistance shift. We provide novel insights
about the evolution of pathogens and ARGs and their correlations in
DWDS biofilms to ensure the safety of drinking water.