Gut microbiota is of critical importance to host health. Aryl hydrocarbon receptor (AhR) is found to be closely involved in the regulation of gut microbial dynamics. However, it is still not clear how AhR signaling shapes the gut microbiota. In the present study, adult zebrafish were acutely exposed to an AhR antagonist (CH223191), an AhR agonist (polychlorinated biphenyl 126; PCB126) or their combination for 7 d. Overall intestinal health and gut microbial community were temporally monitored (1 d, 3 d and 7 d) and inter-compared among different groups. The results showed that single exposure to PCB126 significantly disrupted the overall health of intestines (i.e., neural signaling, inflammation, epithelial barrier integrity, oxidative stress). However, CH223191 failed to inhibit but enhanced the physiological toxicities of PCB126, implying the involvement of extra mechanisms rather than AhR in the regulation of intestinal physiological activities. Dysbiosis of gut microbiota was also caused by PCB126 over time as a function of sex. It is intriguing that CH223191 successfully abolished the holistic effects of dioxin on gut microbiota, which inferred that growth of gut microbes was directly controlled by AhR activation without the involvement of host feedback modulation. When coming to detailed alterations at certain taxon, both antagonistic and synergistic interactions existed between CH223191 and dioxin, depending on fish sex, exposure duration and bacterial species. Correlation analysis found that gut inflammation was positively associated with pathogenic Legionella bacteria, but was negatively associated with epithelial barrier integrity, suggesting that integral intestinal epithelial barrier can prevent the influx of pathogenic bacteria to induce inflammatory response. Overall, this study has deciphered, for the first time, the direct regulative effects of AhR activity on gut microbiota. Future research is warranted to elucidate the specific mechanisms of AhR action on certain bacterial population.

Cooling tower emissions have become an increasingly common hazard to the environment (air polluting, ice formation and salts deposition) and to the health (Legionella disease) in the last decades. Several environmental policies have emerged in recent years limiting cooling tower emissions but they have not prevented an increasing intensity of outbreaks.Since the level of emissions depends mainly on cooling tower component design and the operating conditions, this paper deals with an experimental investigation of the amount of emissions, drift and PM10, emitted by a cooling tower with different configurations (drift eliminators and distribution systems) and working under several operating conditions. This objective is met by the measurement of cooling tower source emission parameters by means of the sensitive paper technique. Secondary objectives were to contextualize the observed emission rates according to international regulations.Our measurements showed that the drift rates included in the relevant international standards are significantly higher than the obtained results (an average of 100 times higher) and hence, the environmental problems may occur. Therefore, a revision of the standards is recommended with the aim of reducing the environmental and human health impact. By changing the operating conditions and the distribution system, emissions can be reduced by 52.03% and 82% on average. In the case of drift eliminators, the difference ranges from 18.18% to 98.43% on average. As the emissions level is clearly influenced by operating conditions and components, regulation tests should be referred to default conditions. Finally, guidelines to perform emission tests and a selection criterion of components and conditions for the tested cooling tower are proposed.

In developing countries, many urban rivers are suffering from heavy contamination by untreated sewage, which implies great microbial risks. However, information regarding the bacterial pathogen diversity and distribution in urban rivers is highly limited. In this study, 41 water samples of fifteen rivers and eight samples from two sewage treatment plants in Changzhou City of Yangtze River Delta were sampled. Next-generation sequencing and a self-built reference pathogen database were used to investigate the diversity of enteric and environmental pathogens. The results indicated that the studied urban rivers were harboring diverse potential pathogen species, which primarily included enteric pathogens in Arcobacter and Bacteroides, and environmental pathogens in Acinetobacter, Aeromonas and Pseudomonas. Quantification of twelve pathogens/indicators of interest by qPCR showed that Escherichia coli, Enterococcus faecalis, Campylobacter jejuni, Arcobacter cryaerophilus, Acinetobacter johnsonii, Acinetobacter lwoffii and Aeromonas spp. were abundant, with median values ranging from 3.30 to 5.85 log10 copies/100 mL, while Salmonella, Legionella pheumophila, Mycobacterium avium, Pseudomonas aeruginosa and Staphylococcus aureus were infrequently quantified. The pollution of nutrients and human intestinal microorganisms indicated by specific markers were found to be prevalent but with different levels in the rivers. The correlation analyses revealed that the diversity (p < 0.01) and concentrations (p < 0.05) of the enteric pathogens highly correlated to the human fecal marker abundances, which indicated that the enteric pathogens in the urban rivers were likely to have originated from domestic sewage. The environmental pathogens, which are different from the enteric ones, showed various distribution patterns, and some of them were more abundant in the rivers of rich nutrient. Our findings provide a comprehensive understanding of the bacterial pathogen distribution and influencing factors in urban rivers that are impacted by domestic sewage, thereby establishing the foundation for urban water management.

The bacterial diversity in ballast water from five general cargo ships calling at the Port of Houston was determined with ion semiconductor DNA sequencing (Ion Torrent PGM) of PCR amplified 16S rRNA genes. Phylogenetic analysis revealed that the composition of bacteria in ballast water did not resemble that of typical marine habitats or even open ocean waters where BWEs occur. The predominant group of bacteria in ships conducting BWEs was the Roseobacter clade within the Alphaproteobacteria. In contrast, Gammaproteobacteria were predominant in the ship that did not conduct a BWE. All the ships contained human, fish, and terrestrial plant pathogens as well as bacteria indicative of fecal or activated sludge contamination. Most of the 60 pathogens had not been detected in ballast water previously. Among these were the human pathogens Corynebacterium diptheriae and several Legionella species and the fish pathogens Francisella piscicida and Piscirickettsia salmonis.

Ethidium monoazide bromide (EMA) and propidium monoazide (PMA), in combination with amplicon-based sequencing (ABS) and quantitative polymerase chain reaction (qPCR) assays, were compared for the detection of viable bacterial species in rainwater. The ABS α- and β-diversity indices indicated that, in comparison to the untreated samples, both EMA and PMA reduced the detection of non-viable bacteria in the rainwater samples. However, while comparable results were obtained for the detection of the most abundant bacterial families and genera in the rainwater samples for both the EMA and PMA pre-treatments; the EMA pre-treatment produced highly significant differences in the relative abundance of the dominant bacterial families and genera, and significantly decreased the detection of “unclassified” bacteria in comparison to the untreated samples (i.e. unclassified genera: untreated 46.7% versus EMA-treated 39.7%). Additionally, the inclusion of EMA and PMA allowed for the increased detection of less abundant pathogenic bacteria in the rainwater samples, such as Clostridium, Listeria and Streptococcus spp. The qPCR assays also indicated that the EMA and PMA pre-treatments were comparable for the detection of intact and potentially viable Acinetobacter, Legionella and Pseudomonas spp. The combination of viability pre-treatments with ABS thus offers a comprehensive monitoring approach to detect less abundant bacterial genera and/or pathogens, which may pose a health risk to the end-users (prioritise target organisms) of unpiped environmental water sources. Moreover, the subsequent combination of the viability pre-treatments with qPCR allows for the specific detection and quantification of these pathogenic genera, which increases analysis sensitivity and allows for the application of risk assessment and water safety strategies.

Regular monitoring and measurement of Legionella in tower water and preventive measures against contamination are particularly important in hospitals. This study aimed at risk assessment and disease burden because of legionella presence in cooling towers of Iran’s central hospitals. Then its correlation with temperature, pH, turbidity, residual chlorine, and EC was investigated by the Pearson test. The health risk and burden of diseases caused by Legionella exposure were determined using QMRA and DALY models. Statistical analysis and modeling were performed in MATLAB₂₀₁₈. Of the total samples, 30–43% was infected with Legionella. The mean concentrations in hospital A and B were 5–102.5 ± 10 and 5–89.7 ± 0.7 CFU/L, respectively. Among environmental factors, turbidity and pH were the most effective factors in increasing and decreasing Legionella concentration, respectively. According to the QMRA model, the risks of Legionella infections and annual mortality in both hospitals were 0.2–0.3, 0–0.19, 2–2.9 × 10⁻⁵, and 0–0.7 × 10⁻⁵, respectively, which was higher than the acceptable risk range for Legionella (10-4–10-7). However, the trend of its change was negatively correlated with time (RB = − 0.77). According to the results, the concentration of Legionella and the exposure risk in both hospitals were higher than the permissible range, which is necessary to decrease to 0.1 current concentrations.

The aim of this study was to evaluate the efficiency of a passive point-of-use treatment system, namely, a polyvinyl (alcohol) (PVA) nanofiber membrane/activated carbon column, for the treatment of harvested rainwater. The efficiency of SMI-Q10 [quaternized poly (styrene-co-maleimide)] nanofiber membrane disks placed in a filtration assembly for the treatment of surface water (Plankenburg River, Western Cape, South Africa) and harvested rainwater was also assessed. Two rainwater harvesting tanks were installed at the Welgevallen Experimental farm, Stellenbosch, South Africa, with the filtration system intermittently attached to the tanks for collection of rainwater samples throughout the study period. Parameters used to monitor the filtration systems included heterotrophic bacteria, Escherichia coli, and total coliform enumeration and the presence/absence of adenovirus. When compared to drinking water guidelines, the results indicated that 3 L of potable water could be produced by the synthesized PVA nanofiber membrane/activated carbon column. However, PCR assays indicated that adenovirus and numerous bacteria such as Klebsiella spp., Legionella spp., Pseudomonas spp., and Yersinia spp. were not effectively removed by the filtration system utilized. Additionally, the SMI-Q10 nanofiber membrane disks did not remove viruses from the river or tank water samples as bovine adenovirus 3 strain, simian adenovirus, and human adenovirus A strain were detected in all water samples analyzed. Thus, while the microfiltration system was efficient in reducing the level of indicator organisms to within drinking water standards, further optimization of the electrospun filtration membranes is required as molecular analysis revealed that numerous opportunistic bacterial pathogens and viruses persisted after filtration.

The incidence of Legionella and Acanthamoeba spp. was correlated to microbial indicator analysis and physico-chemical characteristics of rainwater harvested from catchment areas constructed from galvanized zinc, Chromadek®, and asbestos, respectively. Quantitative PCR (qPCR) analysis indicated that no significant difference (p > 0.05) in copy numbers of Legionella spp. and Acanthamoeba spp. was recorded in tank water samples collected from the respective roofing materials. However, significant positive Spearman (ρ) correlations were recorded between the occurrences of Legionella spp. gene copies vs. nitrites and nitrates (p = 0.05) in all tank water samples. Significant positive correlations were also established between Acanthamoeba spp. vs. barium (p = 0.03), magnesium (p = 0.02), sodium (p = 0.02), silicon (p = 0.05), arsenic (p = 0.03), and phosphate (p = 0.01), respectively. Additionally, while no significant correlations were observed between Legionella spp. vs. the indicator bacteria (p > 0.05), positive correlations were observed between Acanthamoeba spp. vs. total coliforms (p = 0.01) and Acanthamoeba spp. vs. Escherichia coli (p = 0.02), respectively. Results obtained in the current study thus indicate that the incidence of Acanthamoeba and Legionella spp. in harvested rainwater was not influenced by the roofing material utilized. Moreover, it is essential that the microbial quality of rainwater be assessed before this water source is implemented for potable and domestic uses as untreated harvested rainwater may lead to legionellosis and amoebae infections.

The use of lagooning as a complementary natural method of treating secondary effluents of wastewater treatment plants has been employed as an affordable and easy means of producing reclaimed water. However, using reclaimed water for some purposes, for example, for food irrigation, presents some risks if the effluents contain microbial pathogens. Classical bacterial indicators that are used to assess faecal contamination in water do not always properly indicate the presence of bacterial or viral pathogens. In the current study, the presence of faecal indicator bacteria (FIB), heterotrophic bacterial counts (HBC), pathogens and opportunistic pathogens, such as Legionella spp., Aeromonas spp., Arcobacter spp., free-living amoeba (FLA), several viral indicators (human adenovirus and polyomavirus JC) and viral pathogens (noroviruses and hepatitis E virus) were analysed for 1 year in inlet and outlet water to assess the removal efficiency of a lagooning system. We observed 2.58 (1.17–4.59) and 1.65 (0.15–3.14) log reductions in Escherichia coli (EC) and intestinal enterococci (IE), respectively, between the inlet and outlet samples. Genomic copies of the viruses were log reduced by 1.18 (0.24–2.93), 0.64 (0.12–1.97), 0.45 (0.04–2.54) and 0.72 (0.22–2.50) for human adenovirus (HAdV), JC polyomavirus (JCPyV) and human noroviruses (NoV GI and GII), respectively. No regrowth of opportunistic pathogens was observed within the system. FLA, detected in all samples, did not show a clear trend. The reduction of faecal pathogens was irregular with 6 out of 12 samples and 4 out of 12 samples exceeding the EC and IE values, specified in the Spanish legislation for reclaimed water (RD 1620/2007). This data evidences that there is a need for more studies to evaluate the removal mechanisms of lagooning systems in order to optimize pathogen reduction. Moreover, surveillance of water used to irrigate raw edible vegetables should be conducted to ensure the fulfilment of the microbial requirements for the production of safe reclaimed water.

In recent years, the occurrence of Legionella in wastewater treatment plants (WWTP) has often been reported. However, until now there is limited knowledge about the factors that promote Legionella’s growth in such systems. The aim of this study was to investigate the chemical wastewater parameters that might be correlated to the concentration of Legionella spp. in WWTP receiving industrial effluents. For this purpose, samples were collected at different processes in three WWTP. In 100 % of the samples taken from the activated sludge tanks Legionella spp. were detected at varying concentrations (4.8 to 5.6 log GU/mL) by the quantitative real-time polymerase chain reaction method, but not by the culture method. Statistical analysis with various parameters yielded positive correlations of Legionella spp. concentration with particulate chemical oxygen demand, Kjeldahl nitrogen and protein concentration. Amino acids were quantified in wastewater and activated sludge samples at concentrations that may not support the growth of Legionella, suggesting that in activated sludge tanks this bacterium multiplied in protozoan hosts.