Literature DB >> 32893532

Gastrointestinal involvement of COVID-19 and potential faecal transmission of SARS-CoV-2.

Min Song1, Zong-Lin Li2, Ye-Jiang Zhou2, Gang Tian1, Ting Ye1, Zhang-Rui Zeng1, Jian Deng1, Hong Wan1, Qing Li1, Jin-Bo Liu1.   

Abstract

Coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), was found initially in Wuhan, China in early December 2019. The pandemic has spread to 216 countries and regions, infecting more than 23310 000 people and causing over 800 000 deaths globally by Aug. 24, 2020, according to World Health Organization (https://www.who.int/emergencies/diseases/ novel-coronavirus-2019). Fever, cough, and dyspnea are the three common symptoms of the condition, whereas the conventional transmission route for SARS-CoV-2 is through droplets entering the respiratory tract. To date, infection control measures for COVID-19 have been focusing on the involvement of the respiratory system. However, ignoring potential faecal transmission and the gastrointestinal involvement of SARS-CoV-2 may result in mistakes in attempts to control the pandemic.

Entities:  

Keywords:  COVID-19; SARS-CoV-2; Gastrointestinal involvement; Faecal transmission

Mesh:

Substances:

Year:  2020        PMID: 32893532      PMCID: PMC7495406          DOI: 10.1631/jzus.B2000253

Source DB:  PubMed          Journal:  J Zhejiang Univ Sci B        ISSN: 1673-1581            Impact factor:   3.066


Coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), was found initially in Wuhan, China in early December 2019. The pandemic has spread to 216 countries and regions, infecting more than 23310 000 people and causing over 800 000 deaths globally by Aug. 24, 2020, according to World Health Organization (https://www.who.int/emergencies/diseases/ novel-coronavirus-2019). Fever, cough, and dyspnea are the three common symptoms of the condition, whereas the conventional transmission route for SARS-CoV-2 is through droplets entering the respiratory tract. To date, infection control measures for COVID-19 have been focusing on the involvement of the respiratory system. However, ignoring potential faecal transmission and the gastrointestinal involvement of SARS-CoV-2 may result in mistakes in attempts to control the pandemic. The SARS epidemic broke out in 2003, while the Middle East respiratory syndrome (MERS) appeared in 2012, both characterized by fever and respiratory tract infection. Nonetheless, many SARS and MERS patients complained of gastrointestinal symptoms such as diarrhea, vomiting, and abdominal pain (Peiris et al., 2003; Nassar et al., 2018). It was reported that angiotensin-converting enzyme 2 (ACE2) and dipeptidyl peptidase 4 (DPP4) were the functional receptors for the SARS-CoV and the MERS coronavirus (MERS-CoV), respectively, both highly expressed in intestinal epithelial cells (Li et al., 2003; Raj et al., 2013). Not only active viral replication within intestine was confirmed by research, but also SARS-CoV was isolated from intestinal specimens of SARS patients (Leung et al., 2003). Zhou et al. (2017) demonstrated that MERS-CoV could reproduce easily in the small intestine, and that pulmonary infection by MERS-CoV in human DPP4 (hDPP4) mice was secondary to intestinal infection. Clearly, SARS-CoV and MERS-CoV were shown to easily infect intestinal cells, and thus faecal transmission of these viruses seemed very likely. Considering a genome sequence homology of 79% or 50% between SARS-CoV-2 and SARS-CoV or MERS-CoV, respectively, SARS-CoV-2 routinely causes respiratory infection, but it can also target the gastrointestinal system (Lu et al., 2020). A multicenter clinical dataset revealed that COVID-19 patients presenting gastrointestinal symptoms (diarrhea, nausea, or vomiting) accounted for 11.37% (74/651), with diarrhea being the most common symptom accounting for 8.14% (53/651) of all cases. Among the 74 patients with gastrointestinal symptoms, 21 only had gastrointestinal but no respiratory symptoms throughout the course of COVID-19, making up less than a third (28.38%) of patients (21/74). More importantly, the abundance of the more severe illness type was much higher in patients with gastrointestinal symptoms than those without such symptoms (22.97% vs. 8.14%, P<0.001) (Jin et al., 2020). The enzymes ACE2 and transmembrane serine protease 2 (TMPRSS2) have been proven to be cell receptors for SARS-CoV-2, and are abundantly expressed in gastrointestinal cells supporting gastrointestinal infection by SARS-CoV-2 (Lee et al., 2020; Xiao et al., 2020). The RNA of SARS-CoV-2 was detected in the faecal sample in 55.41% (41/74) of all COVID-19 patients. In addition, tests for SARS-CoV-2 RNA in faecal samples remained positive for a mean of 27.9 d, which was much longer than that for respiratory samples with a mean of 11.2 d, while this test was positive for a continuous 33.0 d in one patient after respiratory samples became negative (Wu et al., 2020). It has been established that intestinal epithelium supports SARS-CoV-2 replication, and human small intestinal organoids can serve as an experimental model for SARS-CoV-2 infection (Lamers et al., 2020). Accordingly, live SARS-CoV-2 was detected in faecal samples from two patients, both without gastrointestinal symptoms (Wang et al., 2020). Consequently, the gastrointestinal tract is an optimal target for infection by and the spread of SARS-CoV-2. Regrettably, the COVID-19 outbreak is still ongoing, and the pandemic is becoming increasingly serious with a rapid growth of confirmed disease and death cases. This increasing severity of the pandemic necessitates the enhancement and perfection of current prevention and control measures. Until now, respiratory symptoms and fever are overemphasized, while some non-classical symptoms such as diarrhea have been overlooked, posing an enormous threat to the public. Based on evidence that live SARS-CoV-2 exists in faeces, and viral shedding from the gastrointestinal tract takes longer than that from the respiratory tract, we believe that SARS-CoV-2 can spread easily via faeces. Currently, there are no relevant reports on the faecal occurrence of SARS-CoV-2; however, we speculate that the virus may be derived from the respiratory tract via swallowing or directly from gastrointestinal cells infected by SARS-CoV-2 (Fig. 1). The latest experimental research has revealed that SARS-CoV-2, the stability of which was similar to SARS-CoV under experimental circumstances, could remain viable and infectious for over 3 h in aerosols and 72 h on the surface of plastic or stainless steel (van Doremalen et al., 2020). The aerodynamic nature of SARS-CoV-2 was investigated by measuring viral RNA in aerosols in different areas of two hospitals, with results confirming that the highest concentration of SARS-CoV-2 RNA in aerosols occurred in the patients’ toilet room (19 copies/m3) (Liu et al., 2020). Moreover, SARS-CoV-2 was identified in sewage in Italy (la Rosa et al., 2020). More importantly, the estimated number of COVID-19 cases based on the analysis of untreated wastewater was in reasonable agreement with clinical observations in Australia (Ahmed et al., 2020). All these findings suggest that people exposed to environments contaminated with faeces, such as public toilets or areas with poor sanitation, may be subject to “faecal–aerosol–mucosal transmission” when virus particles touch their noses or eyes. Alternatively, water or food contaminated with faeces may be a source of “fecal– oral transmission” (Fig. 1). Therefore, an effective management and disinfection of areas potentially contaminated with the faeces of COVID-19 patients is considered essential to control the COVID-19 pandemic.
Fig. 1

Potential faecal transmission of SARS-CoV-2

Potential faecal transmission of SARS-CoV-2
  17 in total

1.  Middle East Respiratory Syndrome Coronavirus (MERS-CoV) infection: epidemiology, pathogenesis and clinical characteristics.

Authors:  M S Nassar; M A Bakhrebah; S A Meo; M S Alsuabeyl; W A Zaher
Journal:  Eur Rev Med Pharmacol Sci       Date:  2018-08       Impact factor: 3.507

2.  Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding.

Authors:  Roujian Lu; Xiang Zhao; Juan Li; Peihua Niu; Bo Yang; Honglong Wu; Wenling Wang; Hao Song; Baoying Huang; Na Zhu; Yuhai Bi; Xuejun Ma; Faxian Zhan; Liang Wang; Tao Hu; Hong Zhou; Zhenhong Hu; Weimin Zhou; Li Zhao; Jing Chen; Yao Meng; Ji Wang; Yang Lin; Jianying Yuan; Zhihao Xie; Jinmin Ma; William J Liu; Dayan Wang; Wenbo Xu; Edward C Holmes; George F Gao; Guizhen Wu; Weijun Chen; Weifeng Shi; Wenjie Tan
Journal:  Lancet       Date:  2020-01-30       Impact factor: 79.321

3.  Human intestinal tract serves as an alternative infection route for Middle East respiratory syndrome coronavirus.

Authors:  Jie Zhou; Cun Li; Guangyu Zhao; Hin Chu; Dong Wang; Helen Hoi-Ning Yan; Vincent Kwok-Man Poon; Lei Wen; Bosco Ho-Yin Wong; Xiaoyu Zhao; Man Chun Chiu; Dong Yang; Yixin Wang; Rex K H Au-Yeung; Ivy Hau-Yee Chan; Shihui Sun; Jasper Fuk-Woo Chan; Kelvin Kai-Wang To; Ziad A Memish; Victor M Corman; Christian Drosten; Ivan Fan-Ngai Hung; Yusen Zhou; Suet Yi Leung; Kwok-Yung Yuen
Journal:  Sci Adv       Date:  2017-11-15       Impact factor: 14.136

4.  First detection of SARS-CoV-2 in untreated wastewaters in Italy.

Authors:  Giuseppina La Rosa; Marcello Iaconelli; Pamela Mancini; Giusy Bonanno Ferraro; Carolina Veneri; Lucia Bonadonna; Luca Lucentini; Elisabetta Suffredini
Journal:  Sci Total Environ       Date:  2020-05-23       Impact factor: 7.963

5.  Relative Abundance of SARS-CoV-2 Entry Genes in the Enterocytes of the Lower Gastrointestinal Tract.

Authors:  Jaewon J Lee; Scott Kopetz; Eduardo Vilar; John Paul Shen; Ken Chen; Anirban Maitra
Journal:  Genes (Basel)       Date:  2020-06-11       Impact factor: 4.096

6.  Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMC.

Authors:  V Stalin Raj; Huihui Mou; Saskia L Smits; Dick H W Dekkers; Marcel A Müller; Ronald Dijkman; Doreen Muth; Jeroen A A Demmers; Ali Zaki; Ron A M Fouchier; Volker Thiel; Christian Drosten; Peter J M Rottier; Albert D M E Osterhaus; Berend Jan Bosch; Bart L Haagmans
Journal:  Nature       Date:  2013-03-14       Impact factor: 49.962

7.  Clinical progression and viral load in a community outbreak of coronavirus-associated SARS pneumonia: a prospective study.

Authors:  J S M Peiris; C M Chu; V C C Cheng; K S Chan; I F N Hung; L L M Poon; K I Law; B S F Tang; T Y W Hon; C S Chan; K H Chan; J S C Ng; B J Zheng; W L Ng; R W M Lai; Y Guan; K Y Yuen
Journal:  Lancet       Date:  2003-05-24       Impact factor: 79.321

8.  Evidence for Gastrointestinal Infection of SARS-CoV-2.

Authors:  Fei Xiao; Meiwen Tang; Xiaobin Zheng; Ye Liu; Xiaofeng Li; Hong Shan
Journal:  Gastroenterology       Date:  2020-03-03       Impact factor: 22.682

9.  Enteric involvement of severe acute respiratory syndrome-associated coronavirus infection.

Authors:  Wai K Leung; Ka-Fai To; Paul K S Chan; Henry L Y Chan; Alan K L Wu; Nelson Lee; Kwok Y Yuen; Joseph J Y Sung
Journal:  Gastroenterology       Date:  2003-10       Impact factor: 22.682

10.  Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus.

Authors:  Wenhui Li; Michael J Moore; Natalya Vasilieva; Jianhua Sui; Swee Kee Wong; Michael A Berne; Mohan Somasundaran; John L Sullivan; Katherine Luzuriaga; Thomas C Greenough; Hyeryun Choe; Michael Farzan
Journal:  Nature       Date:  2003-11-27       Impact factor: 49.962

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Journal:  J Zhejiang Univ Sci B       Date:  2021-02-15       Impact factor: 3.066

Review 2.  COVID-19 status quo: Emphasis on gastrointestinal and liver manifestations.

Authors:  Abhishek Bhurwal; Carlos D Minacapelli; Evan Orosz; Kapil Gupta; Christopher Tait; Ishita Dalal; Clark Zhang; Eric Zhao; Vinod K Rustgi
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