Phages are increasingly recognized for their importance
in microbial
aggregates, including their influence on microbial ecosystem services
and biotechnology applications. However, the adaptive strategies and
ecological functions of phages in different aggregates remain largely
unexplored. Herein, we used membrane bioreactors to investigate bacterium–phage
interactions and related microbial functions within suspended and
attached microbial aggregates (SMA vs AMA). SMA and AMA represent
distinct microbial habitats where bacterial communities display distinct
patterns in terms of dominant species, keystone species, and bacterial
networks. However, bacteria and phages in both aggregates exhibited
high lysogenicity, with 60% lysogenic phages in the virome and 70%
lysogenic metagenome-assembled genomes of bacteria. Moreover, substantial
phages exhibited broad host ranges (34% in SMA and 42% in AMA) and
closely interacted with habitat generalist species (43% in SMA and
49% in AMA) as adaptive strategies in stressful operation environments.
Following a mutualistic pattern, phage-carried auxiliary metabolic
genes (pAMGs; 238 types in total) presumably contributed to the bacterial
survival and aggregate stability. The SMA-pAMGs were mainly associated
with energy metabolism, while the AMA-pAMGs were mainly associated
with antioxidant biosynthesis and the synthesis of extracellular polymeric
substances, representing habitat-dependent patterns. Overall, this
study advanced our understanding of phage adaptive strategies in microbial
aggregate habitats and emphasized the importance of bacterium–phage
symbiosis in the stability of microbial aggregates.