ABSTRACT
Here, we present the draft genome sequence of an anaerobic ammonium-oxidizing bacterium (AnAOB), “Candidatus Brocadia,” which was enriched in an anammox reactor. A 3.2-Mb genome sequence comprising 168 contigs was assembled, in which 2,765 protein-coding genes, 47 tRNAs, and one each of 5S, 16S, and 23S rRNAs were annotated. No evidence for the presence of a nitric oxide-forming nitrite reductase was found.
GENOME ANNOUNCEMENT
Anaerobic ammonium oxidation (anammox) is a microbial bioprocess in which ammonium (NH4+) and nitrite (NO2−) are converted to dinitrogen (N2) gas via the generation of hydrazine (N2H4) (1), and it is considered a more energy efficient and effective N removal bioprocess than conventional wastewater treatment systems (1). All known anaerobic ammonia-oxidizing bacteria (AnAOB) belong to the phylum Planctomycetes, with five “Candidatus” genera defined (1, 2). We established an enrichment protocol to target anammox organisms in a sequencing batch reactor seeded with return activated sludge from a water reclamation plant (Public Utilities Board, Singapore). The reactor was fed synthetic wastewater containing ammonium and nitrite and operated at 35°C. Within 6 weeks, simultaneous ammonium and nitrite depletion was observed, along with the appearance of a reddish-brown biofilm on the walls of the reactor, which is highly characteristic of anammox biofilms (1). Fluorescent in situ hybridization (FISH) analysis conducted on day 120 postinoculation, using the Amx820 probe (3), indicated the presence of anammox bacteria. The wall biofilm was then sampled, and shotgun metagenomics was performed on an Illumina MiSeq run using 300-bp paired end sequencing (Illumina). Following read filtering, we analyzed these data using RiboTagger (4) and observed ∼70% relative abundance for genus “Candidatus Brocadia” (V4 ribotag annotated against SILVA release 119) (5).
We constructed a metagenome assembly using Newbler v 2.9 (454 Life Sciences) and employed the CONCOCT program to cluster these contigs into 27 putative genome bins (6). The most abundant bin contained 168 contigs (length, 1,527 to 114,900 bp; mean, 19,210 bp) and had a total sequence length of 3.27 Mb, with an average GC content of 42.3%. Analysis with CheckM (7) showed this genome to have a high completeness (98.8%) and low contamination rate (1.7%), and it was annotated to the marker set lineage UID2565, which is selective for “Candidatus Brocadiaceae.” We annotated predicted genes with Prokka (v1.10) (8), finding that this draft genome sequence encodes 2,765 genes, 47 tRNAs, and 3 rRNA genes. Using the CheckM SSUfinder module (7), one 16S gene of length 1,572 bp was identified from this bin, which, when analyzed using the SILVA Incremental Aligner (SINA) (9), was annotated to “Candidatus Brocadia,” with 94% sequence identity. Collectively, these data suggest that we have recovered a new member of genus “Candidatus Brocadia.”
This draft genome sequence encodes gene clusters relating to core anammox metabolism, including 9 multiheme hdh/hao-like proteins, the three subunits of hzs (hydrazine synthase), and a single three-subunit nitrate reductase/oxidoreductase (nxr) (10). The presence in anammox bacteria of nitrite reductases, either nitric oxide (NO)-forming and/or ammonia-forming, remains subject to considerable uncertainty (10). Using a sequence similarity network approach that incorporates all protein sequences from (i) the present metagenome assembly, (ii) all extant draft genomes, and (iii) all known nitrate reductases, we identified a gene in the current draft genome that has an 88% average amino acid identity (AAI) and a 100% alignment overlap with ammonia-forming nitrite reductase in the genome of “Candidatus Brocadia sinica JPN1” (E = 1 × 10−257) and, at a lower level of support, with an ammonia-forming nitrite reductase in genus Rhodopirellula (53% AAI; 94% alignment overlap; E = 1 × 10−146). We did not find any clear evidence for the presence of an NO-forming nir gene, consistent with results of previous investigations of the genus “Candidatus Brocadia” (10–13).
Accession number(s).
The draft genome described in this paper has been deposited at DDBJ/ENA/GenBank under the accession number PJZV00000000. The raw sequence data from the reactor community are available via NCBI BioProject accession number PRJNA383754.
ACKNOWLEDGMENTS
This research was supported in part by the Singapore National Research Foundation and the Ministry of Education under the Research Centre of Excellence Programme and in part by the Singapore National Research Foundation grants 1102-IRIS-10-03 and 1301-IRIS-59.
We thank Nguyen Thi Quynh Ngoc for performing DNA extraction, Larry Liew for assistance with sampling, Sara Swathi and Eganathan Kaliyamoorthy for laboratory measurements, and Yeshi Cao, Azhar Kasmani, Roslan Dawi, Hui Yui, Bee Hong Kwok, Winson Lay, and Yangshuo Gu of the Public Utilities Board for their assistance and collaboration.
Footnotes
Citation Liu X, Arumugam K, Natarajan G, Seviour TW, Drautz-Moses DI, Wuertz S, Law Y, Williams RBH. 2018. Draft genome sequence of a “Candidatus Brocadia” bacterium enriched from activated sludge collected in a tropical climate. Genome Announc 6:e00406-18. https://doi.org/10.1128/genomeA.00406-18.
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