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Multiplex polymerase chain reaction detection of enteropathogens in sewage in Norway
Acta Veterinaria Scandinavicavolume 61, Article number: 11 (2019)
The primary objective of this small-scale study was to investigate the occurrence of enteropathogens in sewage (municipal wastewater) in Norway using the commercially available FilmArray® multiplex polymerase chain reaction (PCR) system with the gastrointestinal (GI) panel. Our findings indicate that DNA/RNA of several enteropathogens are present simultaneously in Norwegian wastewater systems. The spectre was broad even in smaller communities. With some exceptions, occurrence corresponded more or less to the reported cases of infectious human gastrointestinal disease in the same geographical regions. The effects of different sewage purification techniques were assessed on a limited number of samples indicating that neither chemical nor biological treatment was sufficiently effective to reduce gene material from the pathogens to undetectable levels. Further studies are required to assess the performance and suitability FilmArray® multiplex PCR when used on collective sewage samples in outbreak situations. Additionally, screening sewage samples using multiplex-PCR could be valuable in order to detect new and emerging pathogens and for preliminary analysis of samples before proceeding to more work demanding confirmatory techniques.
Detection and identification of enteropathogens in environmental samples have traditionally relied on a combination of different diagnostic tools, including microscopy, enrichment, culture, antigen–antibody-interaction based tests and polymerase chain reaction (PCR) based molecular techniques. Multiplex PCR assays permit rapid detection of nucleic acids from multiple infectious agents, including bacteria, viruses and parasites and analysis of sewage (municipal wastewater) to provide early warning of foodborne outbreaks was previously suggested . This study applied the commercially available FilmArray® multiplex PCR system (BioFire-bioMérieux, France) to explore the occurrence of enteropathogens in municipal wastewater, in the south eastern part of Norway. The FilmArray® Gastrointestinal (GI) panel is US Food and Drug Administration (FDA)-approved for diagnostic purposes on clinical faecal samples. However, limited data are available regarding its performance on environmental samples .
In this study, occurrence of pathogen specific molecular markers (DNA/RNA) was compared to the reported prevalence of the corresponding diseases in humans in the corresponding region, the sewage purification techniques and the size of the populations.
Sampling was conducted during winter/spring/early summer 2018 at various municipal wastewater treatment facilities (n = 11), located along the course of the river Glomma. One litre of untreated and treated wastewater was collected in sterile bottles from each treatment plant. Samples were prepared by filtrating 900 mL of sampled water through Sleicher & Schull 597 filter paper under vacuum assistance. Filters from each sample were subsequently homogenized in the remaining 100 mL of sample using a stomacher 400 Seward. FilmArray® reagent pouches were loaded with 500 µL of homogenated sample, 1.5 mL hydrating solution FilmArray® Injection Vial-GI before analysis by FilmArray® system using the gastrointestinal (GI) panel targeting 22 different pathogens.
Analysis identified molecular markers of different Escherichia coli pathotypes, Yersinia enterocolitica and Campylobacter spp. indicating that these are the most prevalent bacterial pathogens in untreated sewage (Table 1). Enteroaggregative E. coli (EAEC) and Y. enterocolitica were detected at all sampling sites, while Campylobacter spp. was detected at 8 out of 11 sampling sites. These findings are partially compatible with reported human cases of gastrointestinal infections in the same geographical area and period . According to the Norwegian Surveillance System for Communicable Diseases (MSIS), the most frequently diagnosed enteropathogens in the same municipalities are in descending order: Campylobacter spp., Salmonella enterica sp. enterica biovars, and various E. coli pathotypes . Our frequent detection of Y. enterocolitica does not match the single reported case of clinical disease in the region, which could be due to a number of reasons such as underreporting, subclinical carriers, low target specificity (pathogenic vs. non-pathogenic strains), environmental/animal sources and the ability of this agent to grow and survive in wastewater systems. Earlier studies utilizing traditional culture-based methods have demonstrated Yersinia spp. occurrence in 54% to 90% of sewage samples, where a majority of isolates have been non-pathogenic to humans [4, 5]. Clostridium difficile was detected at one site, while according to surveillance data constituting one of the most frequently diagnosed agents of gastrointestinal disease. Infection by C. difficile is typically acquired by hospitalized patients undergoing antibacterial therapy; this may account for the relatively high number of reported cases . Salmonella spp. were detected at a moderate number of sites, confirming the low prevalent Salmonella status in Norway compared to other European countries, where Salmonella spp. have been shown to occur more frequently in sewage .
Molecular markers of all five viral agents included in the FilmArray ® GI-panel were detected by the screening of untreated sewage. Adenovirus was detected at every sampled site, which coincides with its frequent isolation at regional medical diagnostic laboratories, and earlier publications describing Adenovirus as the enteric virus most commonly isolated from wastewater [8, 9]. Rotavirus was detected at 7 out of 11 sampled sites, despite constituting only a small share of diagnosed cases of viral diarrheal disease in the region. Rotavirus infection in adults typically proceeds asymptomatically or with mild clinical signs, influencing the degree to which cases are reported . Norovirus and Sapovirus were both detected at 6 sites. Sapoviruses are generally considered less pathogenic than Norovirus, which may explain its frequent isolation in sewage compared to its reduced clinical relevance (Table 1).
Sample analysis demonstrated Giardia lamblia as the most frequent protozoan agent found in untreated sewage. The parasite was detected in 9 out of 11 sites. Cryptosporidium spp. and Entamoeba spp. were both isolated once each, while traces of genetic material from Cyclospora cayetanensis was not found. Detection of Giardia spp. in the absence of Cryptosporidium spp. at a majority of test sites was an unexpected finding, and is neither consistent with MSIS clinical data nor earlier surveys of sewage parasite occurrence . According to disease surveillance, Entamoeba histolytica is a sporadic finding, and Cyclospora cayetanensis has not yet been isolated in Norway , both of which is in accordance with our findings.
The samples were collected from sewage treatment plants of which different purification techniques were used (Table 2). We collected samples pre and post purification to evaluate any differences in detection frequency as a result of the treatment process. Mechanical treatment, comprising filtration or sieving, had no reducing effect on the number of pathogen species detected. The increase of pathogens after mechanical treatment could be explained by the addition of septic waste after the filtration. Chemical treatment with flocculation and sedimentation resulted in a 50% reduction in the number of identified pathogens, this is in accordance with the reduction in coliform bacteria reported by Curtis . Further reduction was observed subsequent to a final biological purification step. However, pathogens were still detected in several of the samples after the chemical and biological treatment steps. Whether this represent viable cells or nucleic material from dead cells only remains to be elucidated. Nevertheless, our results indicate that sewage might be a source of environmental spread of genetic material from enteropathogens in Norway.
Grouping sampled treatment facilities according to population size, while removing atypical plants or plants serving atypical populations (1 plant removed due to recent direct septical sludge disposal into the system, 1 plant removed due to a large proportion of temporary inhabitants), permit the comparison of the pathogen profile of untreated sewage from different sized populations (Table 3). Molecular markers of a wide range of pathogens were present even in smaller wastewater systems without any reported ongoing local outbreaks. These findings highlight the importance of carriers and asymptomatic shedders in disease transmission, persistence of genetic material and possibly the ability for some enteropathogens to survive and grow in wastewater systems [13, 14]. It is also important to emphasize that most of the pathogens included in the panel are zoonotic. The rodent populations in the sewage systems, animal droppings from the surface run-off in the combined sewer and food industry (animal products) may have contributed to the findings.
The prevalence of molecular markers of enteropathogens, as determined by the FilmArray® GI system, is partially compatible with reported cases of gastrointestinal infections in the corresponding geographical areas. This indicates the applicability of multiplex PCR on sewage samples for the rapid culture-independent pathogen detection as an early warning in outbreak situations, particularly in confined areas such as military camps or hospitals when baseline levels are known. However, several factors might limit and challenge the use of this tool in outbreak investigations such as lack of proper baseline measures, inability to differentiate between dead and live cells, persistence of agents/nucleic acids in the sewage system, asymptomatic shedders and the risk of false positives/negatives in complex sewage samples. As such, these issues should be addressed in follow-on studies to guide the interpretation of this tool when used in outbreak investigations. Nevertheless, the FilmArray® GI system seems to be a promising tool for the preliminary rapid screening of sewage samples before proceeding to more work demanding confirmatory analysis techniques.
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ØØ and EHM planned the study. KA and ØØ collected the samples. KA and ØØ performed the laboratory analyses. ØØ and EHM obtained the funding and coordinated the study. ØØ, KA and EHM drafted the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Availability of data and materials
The datasets analysed during the current study available from the corresponding author on reasonable request.
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The authors would like to thank the Norwegian Armed Forces Joint Medical Services and the Norwegian Defence Research Establishment for funding.
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