Abstract
This review summarizes research data on SARS-CoV-2 in water environments. A literature survey was conducted using the electronic databases Science Direct, Scopus, and Springer. This complete research included and discussed relevant studies that involve the (1) introduction, (2) definition and features of coronavirus, (2.1) structure and classification, (3) effects on public health, (4) transmission, (5) detection methods, (6) impact of COVID-19 on the water sector (drinking water, cycle water, surface water, wastewater), (6.5) wastewater treatment, and (7) future trends. The results show contamination of clean water sources, and community drinking water is vulnerable. Additionally, there is evidence that sputum, feces, and urine contain SARS-CoV-2, which can maintain its viability in sewage and the urban-rural water cycle to move towards seawater or freshwater; thus, the risk associated with contracting COVID-19 from contact with untreated water or inadequately treated wastewater is high. Moreover, viral loads have been detected in surface water, although the risk is lower for countries that efficiently treat their wastewater. Further investigation is immediately required to determine the persistence and mobility of SARS-CoV-2 in polluted water and sewage as well as the possible potential of disease transmission via drinking water. Conventional wastewater treatment systems have been shown to be effective in removing the virus, which plays an important role in pandemic control. Monitoring of this virus in water is extremely important as it can provide information on the prevalence and distribution of the COVID-19 pandemic in different communities as well as possible infection dynamics to prevent future outbreaks.
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Introduction
The new outbreak of COVID-19 has recently been a serious threat to the health of people around the world. COVID-19 is produced by SARS-CoV-2, which is a single-stranded, positive-sense RNA virus that causes infection and respiratory failure and has led to thousands of deaths (Eslami and Jalili 2020). The current coronavirus pandemic has resulted in huge impacts worldwide. Coronavirus is estimated to infect up to 70% of the world’s population and kill millions of people. The main public health strategy for limiting mortality is to reduce exposure to the virus via physical distancing, which carries tremendous economic costs (Quinete and Hauser-Davis 2021; Stookey et al. 2020).
This abrupt epidemic outbreak of coronavirus disease has currently caused enormous global concerns within the scientific and healthcare community and the general population alike due to the unavailability of human coronavirus vaccines and different virus variants or genetic mutations. Infection with the COVID-19 strain has since spread from Wuhan, China, to approximately 216 countries and territories around the world and has been established as a global pandemic health emergency (Matterne et al. 2020; Kouhsari et al. 2020; Tran et al. 2021). This outbreak is estimated to cause more than 184 324 026confirmed cases of COVID-19, including 3,992,680 deaths (WHO 2021). As of 7th July 2021, a total of 3,032,056,355 vaccine doses were administered.
Faced with this problem, the water is one of the most effective ways to contain the fast-spreading novel coronavirus (COVID-19), however, increased potable water demand and the needs of billions of people living in developing countries that lack access to safe drinking water, facilitate the spread of the virus (Zvobgo and Do 2020). Additionally, the wastewater generated represents a considerable portion of the water consumed, its discharge can contain complex pharmaceuticals, antibiotics, narcotics, radioactive elements, hazardous compounds, and pathogens (Anayah et al. 2021). Wastewater is an ecologically rich environment that contains a plethora of pathogens such as bacteria, fungi, protozoans, toxins, and viruses. Viruses are emerging pathogens and are able to adapt by mutation, recombination, and reassortment and can thus become able to infect new hosts and adjust to new environments. Enteric viruses are among the commonest and most hazardous waterborne pathogens, causing both sporadic and outbreak-related illnesses (Bouseettine et al. 2019). Waterborne enteric viruses, primarily transmitted via fecal-oral route either via person-to-person or interaction or the consumption of contaminated water or food, can pose a serious health hazard to personnel working at wastewater treatment facilities as well as the surrounding community. They find their way into wastewater streams from waste, vomiting, and urine of infected humans as well as animals, hence enter the wastewater stream via infiltration and inflow. Waterborne enteric viruses that are commonly found in wastewater can cause several sporadic cases of diseases and outbreaks because of water or food contamination. Their detection, quantification, and effective removal from wastewater are of great importance because their related diseases result in the death of millions of people across the world, making them a matter of great concern. Adenoviruses (AdVs), coxsackievirus, polioviruses, hepatitis (A and E) viruses, rotaviruses, reoviruses, noroviruses (NoVs), and coronaviruses (including SARS-CoV-2) are examples of some viruses that can be detected in wastewater (Ibrahim et al. 2021; Pandey et al. 2021). The ability of some viruses to travel a much greater distance than bacteria in the soil and eventually to groundwater sources due to their sizes and persistence for a considerable period makes their removal difficult and high risk (Adelodun et al. 2021). Waterborne pathogens, including SARS-CoV-2, can be released into the urban-rural water cycle through domestic sewage, urban runoff, agricultural runoff, and wastewater discharges. For this reason, efficient management of the urban-rural water cycle should be considered, as it is essential to understand the transmission of SARS-CoV-2 through different routes before reaching wastewater effluents or surface water such as oceans, rivers, or lakes.
For this reason, a treatments system for drinking water and wastewater consisting of different physical and chemical treatment units can provide multiple barriers to the alleviation of viruses in water (L. Chen et al. 2021). Abatement of waterborne viruses at different treatment processes is reviewed below (coagulation, sedimentation, filtration, and disinfection) for prevention of sewage discharge into freshwater and saltwater are essential to reduce human exposure to the virus (Naddeo and Liu 2020; Sharifi and Khavarian-Garmsir 2020).
The epidemics and pandemics should be included among the natural disasters to which drinking water and wastewater systems are vulnerable. The services provided by drinking water and wastewater utilities are critical to protecting public health, daily life, and economic well-being (Spearing et al. 2020; States 2020; Anayah et al. 2021).
The present review will focus on (a) analyze the characteristics of SARS-CoV-2 and its effects on public health, (b) identify the analytical method for SARS-CoV-2 detection and quantification in water, (c) evaluate the presence of SARS-CoV-2 in drinking water, natural water, and wastewater; (d) compare its environmental impact through the key findings reported by several authors; (e) it will also provide an overview of the potential transmission risks of this novel coronavirus and how COVID-19 could spread in water resources; (f) water and wastewater treatment polluted with SARS-CoV-2. Monitoring effluents from wastewater treatment plants is important to preventing both environmental contamination and the spread of disease and (g) identify the main trends in this field that help future research.
Definition and features of coronavirus
SARS-CoV-2 structure and classification
SARS-CoV-2 is a member of an enveloped positive-sense single-stranded ribonucleic acid (RNA) virus family named Coronaviridae belonging to the Nidovirales order. It is spherical, has a diameter of approximately 65-125 nm, and has crown-like spikes on the outer surface (Astuti and Ysrafil 2020). Enveloped proteins are involved in several aspects of the virus life cycle, such as assembly, envelope formation, and pathogenesis. Inside the envelope is the helical capsid containing nucleoprotein and the RNA genome (up to 33.5 kilobases (kb) genomes) (La Rosa et al., 2020c; Fehr and Perlman 2015). Coronaviridae is divided into two subfamilies: Coronavirinae and Torovirinae. Coronavirinae is then further classified into alpha, beta, gamma, and delta coronavirus (Ullah et al. 2020). Respiratory infection in humans is usually caused by alpha and beta coronaviruses, which cause mild to severe lower respiratory tract disease. Several human coronaviruses. Middle East respiratory syndrome coronavirus (MERS-CoV), severe acute respiratory syndrome coronavirus (SARS-CoV), and acute respiratory distress syndrome (ARDS)) have been identified, and they can be transmitted by humans via droplets and contact (Chen et al. 2020; Li et al. 2020). Occasionally, new variants of coronaviruses emerge due to their genetic diversity, rapid mutation, high prevalence, and wide distribution (Ullah et al. 2020; Mandal et al. 2020).
Infectious structures of SARS-CoV-2
Coronaviruses usually have a spike (S), envelope (E), membrane (M), and nucleocapsid (N) as structural proteins. Through the S protein, this virus enters the host cell, and it is cut up by the host protease into two functional subunits, S1 and S2, which oversee host cell binding and viral-cellular membrane fusion, respectively. Several CoVs recognize different proteases and entry receptors, where SARS-CoV and SARS-CoV-2 process their S protein by employing the cellular serine called protease TMPRSS2 and subsequent interaction with angiotensin-converting enzyme two (ACE2) cellular receptors (Zhou et al. 2021; Scagnolari et al. 2021). These viral components can be used for drug therapy against COVID-19. The pathophysiology of SARS-CoV-2 is not well understood, but similar to SARS-CoV, viral replication leads to aggressive inflammation and causes acute lung injury (Scagnolari et al. 2021).
This virus infects humans and animals, causing hepatic, gastrointestinal, neurologic, and respiratory illnesses (Ullah et al. 2020).
The effects of SARS-CoV-2 on public health
Global coronavirus disease 2019 (COVID-19) affects the economy, environment, people’s livelihoods, and mainly their health (Rume and Islam 2020). For this reason, several studies have reported its effects on the physical and mental health of children, teenagers, young adults, and elderly adults (Di Santo et al. 2020).
Regarding physical health, COVID-19 is a viral respiratory infection that is easy to spread due to the rapid transmission via the respiratory tract from person to person (Naser et al. 2020). Concerning mental health, people with pre-existing mental illness and substance use disorders will be at increased risk of infection with COVID-19 (Cullen et al. 2020). From 2020 to 2021, the percentage of total studies on the effects of COVID-19 was 44% for mental health and 34% for physical health, while 22% of publications covered both (n = 32 (Banerjee et al. 2020). Table 1 summarizes the effects of COVID-19 on public health linked to age group for comparison.
SARS-CoV-2 transmission
The main route of transmission of SARS-CoV-2 is either by direct contact with an infected subject or indirect contact through a hand-mediated transfer of the virus from contaminated fomites to the mouth, nose, or eyes or via respiratory droplets generated by breathing, sneezing, coughing, etc., (La Rosa et al., 2020a), but knowledge about other potential modes of transmission, e.g., fomite-based, vertical, and fecal-oral transmission, remains sparse (Amirian 2020). The wastewater plumbing system is believed to have acted as a potential route of transmission and caused the superspreading occurrence in Hong Kong due to the transportation of “virus-laden droplets.” The presence of SARS-CoV-2 nucleic acids has been reported in raw wastewater, sewage samples collected from hospitals, and wastewater samples after secondary treatment (Mandal et al. 2020; Sepúlveda-Loyola et al. 2020; Amirian 2020; Lapolla et al. 2020; Ahmed et al. 2020a; Cuevas-Ferrando et al. 2021).
Initial transmission
The bat is the largest natural host of the α- and β-coronaviruses due to its adapted immune system (Kitajima et al. 2020; Street et al. 2020). COVID-19 clinical case-isolated coronavirus has a taxonomic homology > 95% to bat coronavirus (Parthasarathy and Vivekanandan 2021). There is evidence that human coronaviruses have a zoonotic origin (Drexler et al. 2014) and that at some point in their evolution, these viruses became able to infect people. Figure 1 shows the likely mechanism for starting virus transmission.
It was thought that the transmission of SARS-CoV-2 was made possible by the consumption of bats in the food market of the city of Wuhan, and thus transmission to humans was possible (Shereen et al. 2020; Adelodun et al. 2020). Some viruses are easily denatured by the increase in temperature during the food cooking process between 56 and 60 °C (Chida et al. 2021), and SARS-CoV-2 has shown a low affinity for the ACE2 receptor, a protein responsible for initiating the infectious process in human cells, above 40 °C (Shereen et al. 2020; Chida et al. 2021). Thus, consuming this processed food could not be the cause of the initial transmission.
The virus developed the ability to use ACE2 as a receptor in host cells (Street et al. 2020; Wan et al. 2020). This capability may have been the result of the natural evolution of the virus or a modification acquired in another intermediate zoonotic host (Wan et al. 2020). The chances of coming into contact with humans are higher and transmission is more probable (Platto et al. 2020) when you have daily human contact with the animal host for a long time.
Primary transmission mechanism
Primary transmission occurs from contact with droplets that are dispersed by the coughing or sneezing of an infected or asymptomatic individual (Rothan and Byrareddy 2020), and transmission of the virus occurs by person-person contact, which is favored at a distance < 1.5 m (Fig. 1) (Drexler et al. 2014; Manigandan et al. 2020b). Human and social proximity increases the transmission of the virus (Manigandan et al. 2020b).
Primary transmission epithelial cells of the host lung are infected by the virus through recognition of the membrane protein ACE2 by the glycoprotein S of SARS-CoV-2 (Rothan and Byrareddy 2020). The ACE2 protein is expressed primarily in type II alveolar cells, airway epithelial cells, fibroblasts, endothelial cells, and various immune cells (Belete 2020).
Secondary transmission mechanisms
Surfaces contaminated with drops of body fluids from symptomatic or asymptomatic patients, such as door handles, elevator buttons, tables, and glasses, become secondary mechanisms of transmission (Fig. 1) (Shang et al. 2021). Touching surfaces and tools contaminated with the virus increase the risk of contagion (Manigandan et al. 2020b). Transmission is possible through the ocular surface, nose, and mouth (Lu et al. 2020). Medical procedures such as endoscopies or dental treatments can also be a transmission mechanism (Manigandan et al. 2020b). In these transmission mechanisms, there is no direct contact with an infected person; therefore, all different means can be considered secondary mechanisms.
Airborne transmission of SARS-CoV-2 is critical, and this mechanism has been confirmed. hospital room has been isolated (Fig. 1) (Noorimotlagh et al. 2021).
The SARS-CoV-2 virus has been isolated and identified in hospital wastewater (Fig. 1) (Gonçalves et al. 2021). The virus has been identified in fecal excretions, and wastewater from hospitals and households has a high viral concentration of 104 genomic copies/L (GC/L) (Gholipour et al. 2021).
Contact with SARS-CoV-2 wastewater aerosols may be a secondary mechanism of transmission (Fig. 1), and these wastewater aerosols can come into contact with workers in wastewater treatment plants (Gholipour et al. 2021). Hospitalized patients or those isolated at home can spread the virus through wastewater. In countries where wastewater is not treated, the risk of transmission is greater (Adelodun et al. 2020).
Secondary transmission mechanisms represent an important means of contagion, and prevention measures should consider containment strategies to combat SARS-CoV-2 disease by controlling these mechanisms.
Analytical methods for SARS-CoV-2 detection
The recent spread of SARS-CoV-2, exemplifies the critical need for accurate and rapid diagnostic assays. Since the WHO provided the diagnostic protocol on January 13, 2020, clinical and research health laboratories have quickly developed a series of diagnostic kits for COVID-19 (Vogels et al. 2020; Corman et al. 2020).
The most widely used assay is real-time PCR (RT-PCR) (Celis et al. 2021). Which is used for the molecular diagnosis of SARS-CoV-2. Several protocols in laboratories include the RNA extraction and purification process before RT-PCR as a necessary step for the measurement of viral RNA loads, as it isolates genomic RNA from the viral capsid and removes PCR inhibitors from the original material (Deiana et al. 2020).
RT-PCR proceeds with laboratory conversion of viral genomic RNA into DNA by RNA-dependent DNA polymerase (reverse transcriptase), as shown in Fig. 2. This reaction hangs on small DNA sequence primers designed to recognize complementary sequences on the RNA viral genome and the reverse transcriptase to generate a short complementary DNA copy (cDNA) of the viral RNA.
SARS-CoV-2 detection and COVID-19 diagnosis depend on RT-qPCR tests, and results are usually reported as positive or negative. However, the test can also provide a measure of the viral load in the sample, called a cycle threshold value (Tu and O’Leary 2020).
The RT-PCR test provides real-time quantification by reverse transcription of SARS-CoV-2 RNA into DNA, and after performing PCR, the fluorescence signal increases proportionally to the amount of nucleic acid amplified, which allows accurate quantification of RNA in the sample. If the fluorescence reaches a specified threshold within a certain number of PCR cycles (Ct value), the sample is considered positive (Manigandan et al. 2020a). Ct < 40 is considered positive, allowing the detection of very few starting RNA molecules. The cycle threshold (Ct) value from the RT–PCR is inversely proportional (on a logarithmic scale) to viral load; hence, lower Ct values correspond to higher viral loads (Trang et al. 2015).
SARS-CoV-2 detection in environmental water samples
One common method is to quantify the amount of viral RNA in an environmental water sample via RT-qPCR. This method can measure the number of viral RNA copies or genomic copies in water samples such as surface water or wastewater (Rodríguez et al. 2009; Bar-On et al. 2020). However, virus concentration steps will likely be necessary before subsequent detection of SARS-CoV-2 in samples, as shown in Fig. 2 (Nemudryi et al. 2020; Wurtzer et al. 2020a; Medema et al. 2020).
Several methods have been developed for concentrating viruses in water samples, such as electropositive or electronegative membranes. Another membrane-based method used for concentrating viruses in environmental water samples is ultrafiltration, which is based on size exclusion. Other methods, including polyethylene glycol (PEG), ultracentrifugation, and skimmed milk flocculation, have also been used for concentrating viruses from water samples (Lapolla et al. 2020; Haramoto et al. 2020; Sherchan et al. 2020).
Concentration volumes of water are important factors that should be considered in the results of detection of viruses; usually, concentrating < 100 mL of untreated water samples is sufficient to detect enteric viruses (Haramoto et al. 2018; Medema et al. 2020). Detection of SARS-CoV-2 is principally based on RT-qPCR, and their results are usually reported in RNA copies per reaction or genomic copies within a concentration volume, such as liters, milliliters, or cubic meters (Corman et al. 2020; Shirato et al. 2020).
Absolute or relative quantification can be used when calculating the results of the RT-qPCR assay: the first is used to quantify unknown samples by interpolating their quantity from a standard curve, and the second is used to analyze changes in gene expression in a given sample relative to another aqueous reference sample. The calculation methods usually used for relative quantitation are the standard curve method and comparative cycle threshold method, as shown in Fig. 2 (Boulter et al. 2016; Vogels et al. 2020; Arnaout et al. 2020).
Environmental impact associated with SARS-CoV-2 in water
Drinking water
Drinking water is derived from either surface waters, comprising rivers, streams, wetlands, and lakes, or groundwater. However, several contaminants of public health importance naturally occur in these water bodies. For example, metals may originate from natural geochemical lithosphere conditions, and geological processes, in addition to anthropogenic activities, have led to extensive contamination by thousands of chemicals. In general, urbanization and industrialization processes and agriculture and forestry activities are considered the two major contaminant inputs for these freshwater water bodies (Quinete and Hauser-Davis 2021). Currently, clean water sources and community drinking water are vulnerable to stool contamination, and there is evidence that sputum, feces, and urine contain SARS-CoV-2 (Purnama and Susanna 2020; Bilal et al. 2020).
SARS-CoV-2 virus has recently been reported in wastewater. It is possible that patients diagnosed with coronavirus disease are the main route of coronavirus transmission to water and sewage (Tran et al. 2021). Detection of SARS-CoV-2 RNA in wastewater is of interest as it can be used as an early warning method to detect the contact risk associated with untreated water or inadequately treated wastewater (García-Ávila et al. 2020).
Waterborne viruses are different regarding their genome contents and capsid proteins, but such viruses have some common attributes, making them of specific interest concerning the risk of disease endemics related to drinking water infections. According to Hoseinzadeh et al. 2020, water-spread viral pathogens, categorized in terms of moderate to high health importance, consist of adenovirus, astrovirus, hepatitis A and E viruses, rotavirus, norovirus, and other caliciviruses, as well as enteroviruses, including coxsackieviruses and polioviruses. Additionally, urine urinary excretion viruses (e.g., polyomaviruses and cytomegalovirus) have the potential to be disseminated via water. Other viruses (e.g., influenza and coronaviruses) have been considered organisms that are transmittable by drinking water, but the evidence is indecisive. Table 2 shows examples of viruses found in samples of drinking water, and some treatments are reported to remove or reduce these pathogens. SARS-CoV-2 has not yet been found in any drinking water facilities, and per current evidence, it is safe to comment that the risk to drinking water supplies is low if proper precautions are being taken (Bhowmick et al. 2020).
The SARS-CoV-2 virus has been detected in fecal samples and consequently in untreated wastewater. The fecal-oral route of transmission has possible subpathways: contaminated drinking water, contaminated raw and undercooked aquatic, marine, aquacultural, and sewage-irrigated food, and vector-mediated transmission. Contamination of drinking water sources can occur through seepage from sanitation systems (pit latrines and septic tanks), landfills leachates without geomembrane protection towards the shallow groundwater systems. One study reported 99.9% mortality after 10 days in tap water at 23 °C and over 100 days at 4 °C in other types of coronaviruses. This finding also suggests a longer survival time of coronaviruses in tap water than in wastewater (Gwenzi 2021).
Water for human consumption is treated by conventional methods with correct chlorine-based disinfection and ensuring a residual chlorine level of 0.5 mg/L. Chlorine has also been shown to be more effective in inactivating SARS-CoV-2 than chlorine dioxide and other chemical products (García-Ávila et al. 2020). SARS-CoV-2, an enveloped virus, does not survive easily in water and is able to eliminate and inactivate itself efficiently. International and local regulations have launched treatment requirements so that waterborne pathogens, such as viruses, do not attain drinking water systems. The survival of SARS-CoV-2 in wastewater treatment and drinking water supplies is a global concern (García-Ávila et al. 2020).
The World Health Organization (WHO) noted that the accessibility of drinking water is a fundamental condition for the safety of people. It is widely documented how unsafe water has been suspected to be the cause of epidemics since ancient times(Balacco et al. 2020). The absence of evidence on the survival of COVID-19 in drinking water is valuable because it could improve the hygienic conditions of people and prevent the spread of the virus (Balacco et al. 2020; WHO 2021).
Further investigation is urgently required to determine the persistence and infectivity of SARS-CoV-2 in polluted water and sewage as well as the potential of disease transmission via exposure to contaminated water matrices. This might be of critical importance in controlling COVID-19 in vulnerable communities and crisis zones with poor access to water, sanitation, and hygiene (Carraturo et al. 2020; Kassem and Jaafar 2020).
The urban and rural water cycle
Waterborne pathogens, which are divided into three main categories, i.e., viruses, bacteria, and parasites (Bridle 2014), can be released into the urban water cycle through domestic sewage, urban runoff, agricultural runoff, and wastewater discharges (Bar-Or et al. 2020).
Appropriate management of the urban and rural water cycle is essential to contain the spread of SARS-CoV-2 since the disease it causes can spread through fecal-oral routes. Correct disinfection of drinking water and wastewater treatment plants and measures such as prevention of sewage leakage into freshwater resources are essential to reduce human exposure to the virus (Naddeo and Liu 2020; Sharifi and Khavarian-Garmsir 2020).
SARS-CoV-2 can maintain its viability in sewage and the urban-rural water cycle, originating from the fecal discharge of infected patients and moving to different bodies of water through the pathways shown in Fig. 3 (Bhowmick et al. 2020).
Several studies have reported the presence of SARS-CoV-2 in urban and rural sewerage systems. This sewage has the possibility to contaminate freshwater; it can cross untreated effluent discharges to surface water or leaks, as well as affect the supply of traditionally treated graywater, and thus these recycled urban waters also represent possible transmission methods (Mukherjee et al. 2020). Table 3 shows these studies in urban and rural sewage.
According to the table above, multiple authors have detected SARS-CoV-2 in the sewage from urban and rural areas, which confirms its mobility and presence in the water cycle, represented in Fig. 3.
The quantification method used in all studies was real-time polymerase chain reaction (RT-PCR), and virus concentrations were reported as cycle thresholds (Ct) and copy numbers per liter. Ct < 29 values corresponded to raw sewage in India, while countries such as Israel, the USA, and Spain presented Ct > 30 but below cycle 40. It is important to note that a sample is considered positive when the cycle threshold (Ct) took place below cycle 40. In the Northeastern U.S. metropolitan area, a primary sewage sludge exhibited the highest virus RNA copies per liter, and the sewage in Quito contained the lowest copies per liter.
The detected concentrations of SARS-CoV-2 in different countries indicate its high persistence in sewage, and thus the monitoring of the virus in these effluents is extremely important because it can provide information on the prevalence, distribution in communities, and possible infection dynamics to prevent future outbreaks and evaluate virus elimination.
Urban sewer systems are usually more representative samples of communities than wastewater because wastewater is collected from the population through interceptors that are used to divide the study people. If higher viral loads are observed in one interceptor than in the rest, the corresponding service area will be of greater concern for a possible viral outbreak (O’Brien and Xagoraraki 2019). Taking samples in rural areas is more complex than in urban areas due to the nonexistence of wastewater collection systems and the proximity of discharges to surface waters (Polo et al. 2020).
The COVID-19 pandemic influences multiple aspects of urban and rural water areas, such as engineering, sanitary, economic, and social aspects, which will have important effects in the future (Poch et al. 2020). Table 4 summarizes the publications that report the impacts of COVID-19 on the management of the water cycle in urban and rural areas.
As seen in Table 4, there are several impacts of the COVID-19 pandemic on the management of the urban and rural water cycles. In rural communities, impacts such as water supply programs, water scarcity and quality, disruption of activities in agriculture and supply chains, and ensuring water resources to basic needs are mentioned.
On the other hand, urban areas have shown these impacts: the COVID-19 pandemic affects economic-social water aspects, water policies must be improved for equitable distribution and sewage is a critical tool for monitoring the COVID-19 pandemic because SARS-CoV-2 can maintain its viability in sewage. However, a positive effect that some studies report is that the COVID-19 lockdown has reduced water contamination in multiple urban cities.
Surface water
SARS-CoV-2 presence in surface water, including both saltwater and freshwater, was confirmed in some regions with a high prevalence of COVID-19 disease. Moreover, the presence of coronaviruses from anthropogenic activities was confirmed in different water bodies (La Rosa et al. 2020a; Sivakumar 2020).
It is important to understand the mobility of SARS-CoV-2 in the water environment to ensure that public health protection measures are properly established (Naddeo and Liu 2020). However, there are limited data on the presence of viral loads in water bodies due to sewage discharged (Cahill and Morris 2020). It is important to conduct studies that address these issues to develop solutions that help developing countries with poor water and sewage infrastructure (Al Huraimel et al. 2020).
SARS-CoV-2 can be spread to water ecosystems due to leaking sewers or deficient removal after sewage treatment (Wurtzer et al. 2020a). Moreover, rainfall events can increase virus concentrations in natural water systems through combined sewer overflows or failures in wastewater infrastructure (Bogler et al. 2020).
Previous studies reported that viral loads of SARS-CoV-2 are present in the water environment. However, some authors did not detect viral RNA, and others provided a method for the rapid assessment of the SARS-CoV-2 transmission risk, as shown in Table 5.
As seen in Table 5, SARS-CoV-2 was detected in surface water. Rimoldi et al. (2020) reported positive results in three rivers in Milan, Italy; however, the concentration of the virus was not measured.
Guerrero-Latorre et al. (2020) found viral loads in the discharge of raw sewage into urban rivers of Quito, Ecuador, and Weidhaas et al. (2021) detected SARS-CoV-2 RNA in small facilities areas, such as Price River WID.
On the other hand, some authors have studied the presence of SARS-CoV-2 in natural water but have not reported the presence of viral concentrations. Haramoto et al. (2020) reported negative results in samples of river water in Japan, and in the results of Desdouits et al. (2021), none of the seawater samples tested positive for SARS-CoV-2 RNA in different areas of France. Samples tested negative can be affected by dilutions made by an incorrect concentration method, or SARS-CoV-2 did not reach the water environment during sampling at significant levels.
Kumar et al. (2021b) and Shutler et al. (2021) reported viral concentrations in natural water bodies through an assessment of the SARS-CoV-2 transmission risk by modifying pollution analysis methods. Viral load values were very different, < 100 copies/L for small proportions and > 4000 copies/L for large natural water systems, probably due to the large influence of volume.
The detection of SARS-CoV-2 in surface water, such as saltwater and freshwater in rivers, streams, or lakes, has not been sufficiently studied, and the information available is limited, as shown in the table. Moreover, several countries treat their wastewater, so viral loads are considerably lower, although there are also places where wastewater can be discharged into rivers, producing negative impacts due to the presence of human viral pathogens.
The presence and mobility of SARS-CoV-2 in water must be considered because viral RNA copies that are discharged into freshwater and saltwater are a risk of infection for the population in contact with these water bodies (Mahlknecht et al. 2021; Mordecai and Hewson 2020). In addition, studies of water systems could be used to assess the risk of transmission to aquatic and human life and identify countries that are exposed to a high risk of transmission. Additionally, data sources can help to develop viral detection methods to reduce impacts on the environment.
Wastewater
SARS-CoV-2 has been quantified in wastewater through genomic copying (GC), and the air at wastewater treatment plants (WWTPs) has been monitored to determine its presence (Medema et al. 2020). Some stages of wastewater treatment processes can generate aerosols, derived from the collision between water sheets in a mixing, aeration, or grease separation stage. Transmission by exposure to wastewater aerosols is possible in wastewater treatment plants (Cruz-Cruz et al. 2020; Gholipour et al. 2021) (Fig 1).
The presence of viral RNA in wastewater has been determined, even when the prevalence of COVID-19 is low, establishing a correlation between the concentration in wastewater and the reported prevalence of COVID-19 (Medema et al. 2020). Monitoring of SARS-CoV-2 in wastewater represents pandemic status, a wastewater-based epidemiological approach (WBE) (W. Ahmed et al. 2021), and has been developed worldwide as an environmental surveillance approach to inform health authority decision-making (Table 6). This epidemiological basis could help to identify specific areas of increased epidemiological activity; however, its use would be limited to cities with a wastewater collection or sewerage system, without clandestine discharges or open drains.
Although the virus has been determined in wastewater and its concentration is correlated with pandemic behavior, recent studies suggest that the risk of accidental occupational exposure to SARS-CoV-2 in raw sewage, through inhalation in a treatment plant environment, is negligible, with less than 0.3% of the population served by the plant actively infected (Dada and Gyawali 2021). However, other studies indicate that the risk increases as a function of the fraction of the population with an active infection and warn that greater exposure to aerosols may occur if the sewage and wastewater collection system is inadequate. This is a common situation in underdeveloped countries, which may be subject to routes of exposure to the virus by direct ingestion and inhalation of bioaerosol (Zaneti et al. 2021). It is recommended that workers take biosafety measures to reduce risks, such as disinfection of work surfaces with 0.1% hypochlorite, ventilated work areas, keeping areas free of clutter and personal belongings, and use of long-sleeved gowns, biosafety goggles, and disposable gloves (WHO 2020).
The methodology for SARS-CoV-2 RNA quantification may have some limitations; large differences in catchment size, pipe networks, wastewater characteristics, and subsequently hydraulic retention times can modify the viral concentration (W. Ahmed et al. 2021). Therefore, it is important to use the right concentration method. Viral concentration has been observed to improve with precipitation, filtration, ultrafiltration, and ultracentrifugation (Table 6) (Amoah et al. 2020). The detection of viruses in wastewater and drinking water requires methods that are sensitive, resistant to false-positive results, and must be fast and inexpensive (Lahrich et al. 2021). Viral concentration methods are an essential step to accurately detect SARS-CoV-2 RNA in wastewater (Gonçalves et al. 2021).
The quantification of the virus may vary according to the physicochemical characteristics of the wastewater (Table 6). The concentration of SARS-CoV 2 in the wastewater in GC per liter can be variable between 500 GC/L and 2200 GC/mL (Medema et al. 2020; Zhang et al. 2020). According to Medema et al. (2020), this may be related to pandemic status during the analysis. Large particles can protect and contain the virus inside (Wang et al. 2020a), causing unreliable quantification. The sampling method is critical, and 24 h composite samples may be more reliable in showing the daily average (Sherchan et al. 2020). Sampling protocols should consider the inactivation time of the coronavirus and the effect of storage temperature (Cervantes-Avilés et al. 2021).
Due to the risk of hospital wastewater, treatment with sodium hypochlorite has been proposed (Table 6) at concentrations of 800 g/m3; under this condition, the virus concentration was 500 GC/L. To achieve maximum removal, a concentration of 6700 g/m3 was used. Due to the organic matter load of the wastewater matrix and the high concentration of hypochlorite used, the formation of trichloromethane, tribromomethane, bromodichloromethane, and dibromochloromethane compounds was observed, which represents an environmental risk (Wang et al. 2020b).
Wastewater treatment polluted with SARS-CoV-2
Removal of the SARS-CoV-2 virus through chlorine disinfection treatment has been evaluated, and the ecological risks of disinfection byproducts need to be carefully considered. Trichloromethane, tribromomethane, bromodichloromethane, and dibromochloromethane concentrations were 332, 1.9, 5.1, and 0.6 μg/L in the effluents, respectively (Table 7). They show high ecological risks and challenge the surrounding environment receiving disinfected medical wastewater, possessing threats to the ecological system and human health (Wang et al. 2020a).
Conventional wastewater treatment plants (WWTPs) have shown effectiveness in the removal of SARS-CoV-2 (Table 2), which may be related to the removal of solids. These solids can protect the virus, and the treatment must contribute to the removal of solids. Carrillo-Reyes et al. (2021) indicated that the virus may have an affinity for solids. SARS-CoV-2 concentrations are higher in both primary and waste-activated sludge (Kocamemi et al. 2020a). Virus removal in an aseptic tank was low due to the high concentration of solids; this process does not separate and reduces the solid content (Wang et al. 2020a).
The hydrophobic envelope of the virus could explain the affinity of the virus for the solid matrix of the wastewater (Ahmed et al. 2020c), which is explained by the fact that RNA is easier to quantify in the sludge without employing a concentration method, and sludge monitoring has been suggested to serve as an indicator for SARS-CoV-2 surveillance (Carrillo-Reyes et al. 2021). The more efficient the treatment may be in removing solids, the more efficient it will be in removing the virus. The most commonly used methods to improve quantification of the virus in wastewater employ polyethylene glycol to concentrate the viral load (La Rosa, Bonadonna, et al. 2020; Peccia et al. 2020; Zhang et al. 2020).
Virus envelope proteins play a very important role in the process of infection and spread, they can contribute to the strong or weak adhesion of SARS-CoV-2 to its host cell surface, which mainly involves hydrophobic interactions(Jakhmola et al. 2021). These proteins are mostly of a quaternary structure (Duart et al. 2021) and are characterized by hydrophobic interactions (Bhagavan 2002).
The virus concentration can be equal in raw water and primary sludge, and after biological digestion of the sludge, the virus has not been detected (Balboa et al. 2021). Despite the effectiveness of virus removal in raw water and virus denaturation in sludge, chlorination of treated water has been recommended as a final treatment step (Carrillo-Reyes et al. 2021). The combined treatment of thermal hydrolysis and anaerobic digestion prevented the detection of SARS-CoV-2 in sludge effluent of the plant (Balboa et al. 2021).
Although more studies are needed to demonstrate the transmission of the virus via untreated wastewater, the presence of the virus has been demonstrated and poses a risk. Therefore, WWTPs play an important role in controlling the pandemic, as do sewage systems that allow for maximum wastewater collection.
Future trends
The primary mechanism of virus transmission is person-to-person contact (Rothan and Byrareddy 2020); however, we have discussed other possible routes that represent a risk condition. In the future, it will be important to demonstrate the viral load necessary to generate COVID-19. These secondary mechanisms (Fig. 1) represent a risk, but the particular viral load condition for developing the disease is not clear.
Different efforts to control the spread of COVID-19 will increase the water demand and worsen the water quality, leading to additional challenges in water planning and management (Sivakumar 2020). Further studies are needed to determine the survival of SARS-CoV-2 in the environment, clearer mechanisms of transmissibility through sewage, and the potential to infect humans via the fecal-oral route. (Dhama et al. 2021).
The detection and quantification of the virus have confronted difficulties due to the complex composition of the wastewater. The concentration method is an important factor in determining the virus (La Rosa, Iaconelli, et al. 2020a; Carrillo-Reyes et al. 2021; Dhama et al. 2021). Therefore, more sensitive, easy to perform, accessible, and economical techniques are needed to further monitor the pandemic and allow sanitary control to ensure public health. Devices have been suggested for trace detection of SARS-CoV-2 in water. One of the main challenges in the detection/quantification of SARS-CoV-2 in wastewater samples is to generate optimized and standardized protocols (Kitajima et al. 2020), where the risk of transmission is high, as shown in Fig. 4.
WWTPs have shown effectiveness in virus removal (Arora et al. 2020; Jiao Wang et al. 2020a); however, more knowledge is needed about virus sharing through the different stages of the treatments to more clearly determine the most effective removal or denaturation method against the virus.
Disinfection methods used in the drinking water treatment process highly inactivate and efficiently destroy SARS-CoV-2 in water (Tran et al. 2021). However, there is a need to investigate and improve the performance of disinfection technologies to be adopted for the inactivation of SARS-CoV-2 in municipal and hospital wastewater to reduce the related risk. (Mandal et al. 2020; Tran et al. 2021).
The studies compiled in this review are solid antecedents that demonstrate the presence of the SARS-CoV-2 in natural water and wastewater. Some data found, such as the study areas and concentrations of viral loads, would help to quickly relate the presence of the virus in water with the epidemiological and sanitary situation in the future, which could determine the economic and social factors that they intervene in the duration of the disease in different rural or urban communities
Identifying those geographic areas that report the presence of SARS-CoV-2 in water could support future research to predict or control re-outbreaks in surrounding areas. In Italy, viral loads were detected in contiguous rivers and traveled through densely populated areas near the Milan metropolitan area last year and then a re-outbreak occurred in the neighboring city (Lazio).
The need for further research to establish the behavior of the SARS-CoV-2 virus in aquatic systems is a priority to establish efficient methods to concentrate and detect enveloped viruses (and coronavirus in particular) from water matrices and the estimation of the survival of these viruses in natural conditions, at different temperatures and in different types of water. Additionally, the information collected on SARS-CoV-2 in this review aims to facilitate ideas that improve the monitoring of COVID-19 in natural and wastewater in future studies, which would allow investigating the development of the disease in the population. This information would help to determine the stability of the virus in water bodies and to know its possible dynamics in space and time.
The findings discussed in this review would generate options that mitigate the presence of the virus and with it its transmission in drinking water, natural water, and wastewater. Finally, these findings could be used to develop new preventive measures, in addition to healthy distance, temperature measurement, and the use of antibacterial gel, related to the pathways of spread of SARS-CoV-2 in water.
Conclusions
After reviewing 169 references, it was possible to analyze the characteristics of the coronavirus, its transfer routes, detection methods, and its impact on drinking water, surface water, wastewater, and systems that are effective for wastewater treatment.
The presence of SARS-CoV-2 has been demonstrated in the water cycle in both urban and rural areas. One of the routes of transmission of the virus is through the sewage system of domestic origin, i.e., gray water, sewage, soaps and detergents, and toilet paper.
The monitoring of SARS-CoV-2 in wastewater can be a tool that can monitor the behavior of the pandemic. Conventional treatment systems are effective in removing the virus, and a relationship between solid removal and viral load has been observed. WWTPs play an important role in pandemic control.
The transmission of SARS-CoV-2 may be greater in rural areas. Public policies surrounding the urban-rural water cycle have been exposed as deficient and bad in several countries, mainly third world countries.
Some studies have reported the presence of water pathogens including viruses in drinking water. However, SARS-CoV-2 has not yet been found in any drinking water facilities, and it is safe to comment that the risk to drinking water supplies is low.
There is still little information available regarding the existence of SARS-CoV-2 in surface waters; however, more study is needed as its detection in different bodies of water, which are usually in direct contact, is important. These studies should include different natural ecosystems, both terrestrial and aquatic.
The presence of SARS-CoV-2 in surface water should be further studied to determine whether its transmission to different living beings, including humans, is possible and whether it is important to reduce or eradicate possible loads of viruses found in these waters.
Finally, future trends focus on the scope of the present information collected by several authors about the impact of coronavirus SARS-CoV-2 in water to answer the question of how this review could guide future research.
Data availability
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Abbreviations
- ASP:
-
Activated sludge process
- ARDS:
-
Acute respiratory distress syndrome
- ALG:
-
Alum coagulant
- ACE2:
-
Angiotensin-converting enzyme 2
- BDD:
-
Boron-doped diamond
- BBD/Si:
-
Boron-doped diamond/silicon
- CS:
-
Coagulation-sedimentation
- CSOs:
-
Combined sewer overflows
- cDNA:
-
Complementary DNA
- COVID-19:
-
Coronavirus disease 2019
- Ct:
-
Cycle threshold
- DIC:
-
Disseminated intravascular coagulation
- EC-EO:
-
Electrocoagulation-electro-oxidation
- EMV:
-
Electronegative membrane-vortex
- MS2 virus:
-
Escherichia virus MS2
- FF:
-
FeCl3 flocculation
- GI qPCR:
-
Gastrointestinal qPCR
- GC/L:
-
Genomic copies per liter
- HAV:
-
Hepatitis A virus
- HEV:
-
Hepatitis E virus
- HEV-p6:
-
Hepatitis E virus strain Kernow (clone P6)
- AdHu5-GFP:
-
Human adenovirus type 5-green fluorescent protein
- HCOVs:
-
Human coronaviruses
- HepG2/C3A :
-
Human hepatocellular carcinoma cells
- HRT:
-
Hydraulic retention time
- IFA:
-
Immunofluorescence assay
- MF:
-
Microfiltration
- MERS-CoV:
-
Middle East respiratory syndrome coronavirus
- MNV-1:
-
Murine norovirus 1
- PMMoV:
-
Pepper mild mottle virus
- PEG:
-
Polyethylene glycol
- PAX:
-
Prepolymerized aluminum coagulant
- QMRA:
-
Quantitative microbial risk assessment
- qPCR:
-
Quantitative polymerase chain reaction
- RSF:
-
Rapid sand filtration
- RT-PCR:
-
Reverse transcription-polymerase chain reaction
- RNA:
-
Ribonucleic acid
- SARS-COV-2:
-
Severe acute respiratory syndrome coronavirus 2
- SDG:
-
Sustainable development goals
- TMPRSS2:
-
Transmembrane serine protease 2
- UF:
-
Ultrafiltration
- UAE:
-
United Arab Emirates
- UASB:
-
Upflow anaerobic sludge blanket
- ϕX174 virus:
-
Virus that infects the bacterium E. coli
- WAS:
-
Waste-activated sludge
- WWTP:
-
Wastewater treatment plants
- WBE:
-
Wastewater-based epidemiology
- WID:
-
Water improvement district
- WHO:
-
World Health Organization
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The authors would like to acknowledge the support of CONACYT for the scholarship (CVU: 863657) and thank COMECYT for the chair number CAT2021-0016.
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RGN: devised the project, the main conceptual ideas, conducting a research and investigation process. ILH: devised the project, the main conceptual ideas, acquisition of the financial support for the project leading to this publication. LACS: supervised the project, revised it critically for important intellectual content. All authors provided critical feedback and helped shape the research, analysis, and manuscript. All authors read and approved the final manuscript.
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Girón-Navarro, ., Linares-Hernández, I. & Castillo-Suárez, L.A. The impact of coronavirus SARS-CoV-2 (COVID-19) in water: potential risks. Environ Sci Pollut Res 28, 52651–52674 (2021). https://doi.org/10.1007/s11356-021-16024-5
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DOI: https://doi.org/10.1007/s11356-021-16024-5