Drinking water quality in regional Hunter New England, New South Wales, Australia, 2001-2015

The objective of this study was to evaluate the effectiveness of drinking water quality verification monitoring as a means of improving preventive measures on drinking water quality management in regional New South Wales (NSW), Australia. Water sampling and E. coli detection data were obtained from the NSW Drinking Water Database. Statistical analysis was performed using Incidence Rate Ratios to compare the relationship between the proportion of samples collected to the tests allocated based on population served (sampling adequacy), E. coli detection and the relationship between sampling adequacy and E. coli detections over time. Sampling adequacy and E. coli detections significantly improved during the study period. Sampling adequacy was significantly lower in smaller populations (IRR = 0.83, p = 0.036). E. coli detections were significantly increased in smaller communities (IRR = 4.3, p = 0.01) and in summer (IRR = 2.7, p = < 0.001). There was a strong inverse correlation between improved sampling adequacy and decreased E. coli detections (Spearman’s rho = −0.821; p < 0.0001). This research has highlighted the value of continued assistance to water utilities in the implementation of drinking water management systems to improve drinking water safety. © 2020, © 2020 Engineers Australia

Sma-miR-277 family predicted targets downregulated in developing female parasites.

<p>Fold change expression (Log₂) of high confidence targets of sma-miR-277 family during the development of male and female worms in two conditions: paired (solid line red) and unpaired (dashed green). Black lines represent the mean expression of genes in paired (solid black line) and unpaired (dashed black line) worms.</p

Sma-miR-277 and sma-miR-4989 belong to a gene cluster.

<p>(A) The genomic locus in Chromosome 4 of sma-miR-277 and sma-miR-4989 suggests they belong to a gene cluster. The average distance between genes (represented by coloured boxes) is 109 bases. Here the mature miRNAs (sma-miR2-277 and sma-miR-4989) and passenger miRNAs are represented with coverage plot and aligned reads from one of the small RNA libraries. (B) Predicted stem-loop structures for sma-miR-277 and sma-miR-4989 –individual cases. Mature miRNAs are located in the 3’-end of the hairpin. (C) Due to the cluster organisation of sma-miR-277/sma-miR-4989, it is likely that they are transcribed as one precursor RNA molecule. This figure represents the predicted stem-loop structure for sma-miR-277/sma-miR-4989 when arising from a larger transcript.</p

Sma-miR-4989 is expressed in the cells surrounding the oesophagus and cells of the tegument in adult worms.

<p>Whole mount <i>in situ</i> hybridisation for (A) <i>cathepsin B</i>, (B) sma-miR-124a-3p (<i>124a</i>), and (C) sma-miR-4989. (D) Fluorescence <i>in situ</i> hybridisation showing the colocalization of sma-miR-4989 with four co-expressed tegument-specific mRNAs (<i>calpain</i>, <i>npp-5</i>, <i>annexin</i> and <i>gtp-4</i>). Nuclei are stained with DAPI and shown in blue. Anterior of worms is to the left in A-C. Scale Bars: A-C 100 μm; D 10 μm.</p

Sma-miR-4989 is significantly up-regulated during male and female maturation.

<p>Fold change expression of sma-miR-4989 during development of juvenile to adult worms in male (blue bars) and females (red bars) as measured by RT-qPCR. Samples were collected at the time points (days post infection) indicated in the x-axis from murine hosts infected with pooled (mixed sex) cercariae. Each barplot represents the mean of three biological replicates. T-tests were performed between 49 d.p.i. and 28 d.p.i. and were both significant with p-value ≤ 0.01. Error bars show the standard error of the mean, based on three biological replicates.</p

High confidence targets of the sma-miR-277 family identified with a combined approach (Sylamer, miRanda and TargetScan with conservation).

<p>F = female; M = male.</p

MiRNA target prediction based on both miRNA-unaware and miRNA-guided approaches.

<p>(A) Sylamer enrichment landscape plots for 7mers in male (top) and female (bottom) expression data. The x-axis represents a list of transcripts, ranked from more expressed in juveniles to more expressed in adults. The y-axis represents the significance values acquired for each 7mer at each position in the ranked list of transcripts. Coloured boxes represent the fraction of transcripts significantly (adjusted p-value < 0.01) differentially expressed between juvenile and adult worm as found using DESeq2. These transcripts were subsequently filtered based on the presence of the 7mers TGCATTT or GCATTTA as found by Sylamer. The resulting sets are referred to as Male and Female Sylamer genes. (B) Venn Diagram showing the intersection of Male and Female Sylamer genes with schistosome-conserved miRNA targets as found using TargetScan with conservation + miRanda. The overlap represents transcripts with highly conserved sma-miR-277 target sites across the three <i>Schistosome</i> spp (S. <i>mansoni</i>, <i>S</i>. <i>haematobium</i> and S. <i>japonicum</i>) that are also significantly down regulated during worm development.</p