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Shedding of SARS-CoV-2 in Feces and Urine and Its Potential Role in Person-to-person Transmission and the Environment-based Spread of COVID-19

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Date 2020 Aug 25
PMID 32836117
Citations 194
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Abstract

The recent detection of SARS-CoV-2 RNA in feces has led to speculation that it can be transmitted via the fecal-oral/ocular route. This review aims to critically evaluate the incidence of gastrointestinal (GI) symptoms, the quantity and infectivity of SARS-CoV-2 in feces and urine, and whether these pose an infection risk in sanitary settings, sewage networks, wastewater treatment plants, and the wider environment (e.g. rivers, lakes and marine waters). A review of 48 independent studies revealed that severe GI dysfunction is only evident in a small number of COVID-19 cases, with 11 ± 2% exhibiting diarrhea and 12 ± 3% exhibiting vomiting and nausea. In addition to these cases, SARS-CoV-2 RNA can be detected in feces from some asymptomatic, mildly- and pre-symptomatic individuals. Fecal shedding of the virus peaks in the symptomatic period and can persist for several weeks, but with declining abundances in the post-symptomatic phase. SARS-CoV-2 RNA is occasionally detected in urine, but reports in fecal samples are more frequent. The abundance of the virus genetic material in both urine (ca. 10-10 gc/ml) and feces (ca. 10-10 gc/ml) is much lower than in nasopharyngeal fluids (ca. 10-10 gc/ml). There is strong evidence of multiplication of SARS-CoV-2 in the gut and infectious virus has occasionally been recovered from both urine and stool samples. The level and infectious capability of SARS-CoV-2 in vomit remain unknown. In comparison to enteric viruses transmitted via the fecal-oral route (e.g. norovirus, adenovirus), the likelihood of SARS-CoV-2 being transmitted via feces or urine appears much lower due to the lower relative amounts of virus present in feces/urine. The biggest risk of transmission will occur in clinical and care home settings where secondary handling of people and urine/fecal matter occurs. In addition, while SARS-CoV-2 RNA genetic material can be detected by in wastewater, this signal is greatly reduced by conventional treatment. Our analysis also suggests the likelihood of infection due to contact with sewage-contaminated water (e.g. swimming, surfing, angling) or food (e.g. salads, shellfish) is extremely low or negligible based on very low predicted abundances and limited environmental survival of SARS-CoV-2. These conclusions are corroborated by the fact that tens of million cases of COVID-19 have occurred globally, but exposure to feces or wastewater has never been implicated as a transmission vector.

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References
1.
Wu Z, McGoogan J . Characteristics of and Important Lessons From the Coronavirus Disease 2019 (COVID-19) Outbreak in China: Summary of a Report of 72 314 Cases From the Chinese Center for Disease Control and Prevention. JAMA. 2020; 323(13):1239-1242. DOI: 10.1001/jama.2020.2648. View

2.
Sassi H, Reynolds K, Pepper I, Gerba C . Evaluation of hospital-grade disinfectants on viral deposition on surfaces after toilet flushing. Am J Infect Control. 2018; 46(5):507-511. DOI: 10.1016/j.ajic.2017.11.005. View

3.
Robilotti E, Deresinski S, Pinsky B . Norovirus. Clin Microbiol Rev. 2015; 28(1):134-64. PMC: 4284304. DOI: 10.1128/CMR.00075-14. View

4.
Coetzee B, Kagee A . Structural barriers to adhering to health behaviours in the context of the COVID-19 crisis: Considerations for low- and middle-income countries. Glob Public Health. 2020; 15(8):1093-1102. DOI: 10.1080/17441692.2020.1779331. View

5.
Drosten C, Seilmaier M, Corman V, Hartmann W, Scheible G, Sack S . Clinical features and virological analysis of a case of Middle East respiratory syndrome coronavirus infection. Lancet Infect Dis. 2013; 13(9):745-51. PMC: 7164791. DOI: 10.1016/S1473-3099(13)70154-3. View