High-Resolution Temporal and Spatial Patterns of Virome in Wastewater Treatment Systems

Wastewater treatment plants (WWTPs) are considered reservoirs of viruses, but the diversity and dynamic changes of viruses are not well understood. In this study, we recovered 8478 metagenomic viral contigs (mVCs; >5 kb) from two WWTPs (Shatin, 2806; Shek Wu Hui, 5672) in Hong Kong. Approximately 60% of the mVCs were poorly covered (<35% of genes in identified mVCs) by the current NCBI and IMG/VR viral databases. The temporal profile of the newly identified mVCs among 98 Shatin AS samples collected monthly (for approximately 9 years) revealed the presence of periodic dynamics at an interval of approximately one year (341 days). The spatial distribution pattern of the virome in the wastewater treatment systems showed that shared viral clusters (viral populations categorized based on shared gene content and network analysis) can be globally found among similar samples of wastewater treatment systems, indicating the presence of core viral communities among geographically isolated wastewater treatment systems. These results not only supplemented the current virome database of engineered systems but also, to some extent, expanded the understanding of long-term cyclical development and spatial distributions of viral communities in wastewater treatment systems

Characteristics of assembled scaffolds and the retrieved CAP IIC HKU-2 draft genome.

<p>Characteristics of assembled scaffolds and the retrieved CAP IIC HKU-2 draft genome.</p

Exploring the Shift in Structure and Function of Microbial Communities Performing Biological Phosphorus Removal

<div><p>A sequencing batch reactor fed mainly by acetate was operated to perform enhanced biological phosphorus removal (EBPR). A short-term pH shock from 7.0 to 6.0 led to a complete loss of phosphate-removing capability and a drastic change of microbial communities. 16S rRNA gene pyrosequencing showed that large proportions of glycogen accumulating organisms (GAOs) (accounted for 16% of bacteria) bloomed, including <i>Candidatus</i> Competibacter phosphatis and <i>Defluviicoccus</i>-related tetrad-forming organism, causing deteriorated EBPR performance. The EBPR performance recovered with time and the dominant <i>Candidatus</i> Accumulibacter (Accumulibacter) clades shifted from Clade IIC to IIA while GAOs populations shrank significantly. The Accumulibacter population variation provided a good opportunity for genome binning using a bi-dimensional coverage method, and a genome of Accumulibacter Clade IIC was well retrieved with over 90% completeness. Comparative genomic analysis demonstrated that Accumulibacter clades had different abilities in nitrogen metabolism and carbon fixation, which shed light on enriching different Accumulibacter populations selectively.</p></div

Venn diagram of conserved and unique genes for four Accumulibacter genomes of Clade IIC.

<p>Venn diagram of conserved and unique genes for four Accumulibacter genomes of Clade IIC.</p

Phosphorus removal and sludge sampling for 16S rRNA gene pyrosequencing from the SBR performing EBPR.

<p>The pH of solution in the SBR was maintained at 7.2 ± 0.1 except at 60 d when accidentally overdosed acidic solution to decrease pH to 6.0 for around 20 h.</p

Maximum likelihood phylogenetic tree of Accumulibacter <i>ppk1</i> gene sequences.

<p>The <i>ppk1</i> genes of the reconstructed Accumulibacter genomes are indicated in green, while those from clone library of sludges A and C are colored in orange. Seven and nine partial <i>ppk1</i> gene sequences with 99% identity were obtained from sludge A and C respectively. Reference sequences attached with their accession numbers are extracted from NCBI database. Node labels refer to bootstrap support values and <i>Rhodocyclus tenuis ppk1</i> gene is employed as the outgroup sequence.</p

The ANI and orthologous genes shared by each pair of Accumulibacter genomes.

<p>The ANI and orthologous genes shared by each pair of Accumulibacter genomes.</p

Relative abundances of <i>ppk1</i> genes of different clades in the microbial communities.

<p>The abundance of Accumulibacter was calculated according to the copy numbers of Accumulibacter and bacterial 16S rRNA genes by qPCR analysis. Meanwhile the 2 copies of <i>rrn</i> operon in CAP IIA UW-1 and 4 copies of <i>rrn</i> operon in the available bacterial finished genomes have been taken into account. The proportions of different <i>ppk1</i> genes in one sample was estimated by the copy numbers obtained from the qPCR assay using primer sets targeting <i>ppk1</i> genes of specific clades.</p

Table_S1 – Supplemental material for Split chimeric antigen receptor-modified T cells targeting glypican-3 suppress hepatocellular carcinoma growth with reduced cytokine release

Supplemental material, Table_S1 for Split chimeric antigen receptor-modified T cells targeting glypican-3 suppress hepatocellular carcinoma growth with reduced cytokine release by Xuan Liu, Jianyun Wen, Honglei Yi, Xiaorui Hou, Yue Yin, Guofu Ye, Xuedong Wu and Xiaotao Jiang in Therapeutic Advances in Medical Oncology</p