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Fu, H.-M.

Publications and source records attributed to Fu, H.-M..

2 recordsLinked to original sources

Microbial community characteristics and stable relationships centered on anammox bacteria revealed by global-scale analysis

Anaerobic ammonium-oxidizing bacteria (AnAOB) play important roles in both artificial wastewater treatment systems and natural ecosystems. To date, AnAOB pure cultures are not available and they tend to coexist with various microbial species. However, anammox community characteristics including the relationships between AnAOB and their companion bacteria at the global perspective and their impacts on anammox metabolism remain unclear. Here, we systematically analyzed the characteristics of anammox communities and the stable relationships concerning AnAOB using a global dataset containing 619 anammox-related amplicons. Different anammox systems showed significant differences in alpha and beta diversity, but shared some core taxa of interest. A total of 89 and 55 core genera and species were identified respectively across anammox communities worldwide, which formed the backbone of artificial anammox systems. Through the analysis of co-abundance networks derived from four distinct artificial anammox systems--biofilm, granular sludge, flocculent sludge, and planktonic cells--we identified 208 stable and 92 limited stable relationships associated with AnAOB. Functional analysis suggested that stable positively-correlated companion bacteria may provide essential cofactors (e.g., molybdenum cofactor, tetrahydrofolate, and coenzyme A) to AnAOB. The companion bacteria which showed limited stable positive correlations with AnAOB in the anammox attachment-growth systems, may mutualize with AnAOB via type pili. This study deepens the understanding of anammox communities, anammox core microbiome, and AnAOB symbiotic relationships. These (limited) stable companion bacteria and corresponding cofactors can potentially guide the development and application of bioaugmentation methods, synthetic anammox communities, and deterioration biomarkers for engineered anammox systems.

microbiology↗

Complete genome-centric analysis reveals functional divergence and adaptive evolution of uncultured bacteria in anammox community

Anaerobic ammonium-oxidation (anammox) bacteria play a crucial role in global nitrogen cycling and wastewater nitrogen removal, but they share symbiotic relationships with various other microorganisms. No pure culture is available for anammox bacteria so far. Although shotgun metagenomics based on short reads has been widely used in anammox research, metagenome-assembled genomes (MAGs) are often discontinuous and highly contaminated, which limits in-depth analyses of anammox communities. Here, for the first time, we performed Pacific Biosciences high-fidelity (HiFi) long-read sequencing on the anammox granule sludge sample from a lab-scale bioreactor, and obtained 30 accurate and complete metagenome-assembled genomes (cMAGs). These cMAGs were obtained by selecting high-quality circular contigs from initial assemblies of long reads generated by HiFi sequencing, eliminating the need for Illumina short reads, binning, and reassembly. One new anammox species and species from three novel families were found in this anammox community. cMAG-centric analysis revealed divergences in general and nitrogen metabolism among members of the anammox community. Furthermore, we identified mobile genetic elements (MGEs) and putative horizontal gene transfer (HGT) events within these cMAGs to explore the adaptive evolution of the community. The results suggest that MGEs and HGT events, particularly transposons containing tnpA in anammox bacteria, might play important roles in the adaptive evolution of this anammox community. The cMAGs generated in the present study could be used to establish of a comprehensive database for anammox bacteria and associated microorganisms. Our findings highlight the advantages of HiFi sequencing for the studies of complex mixed cultures such as anammox communities and advance our understanding of anammox communities.

microbiology↗