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Coronavirus disease 2019 (SARS-CoV-2) and colonization of ocular tissues and secretions: a systematic review

Abstract

Coronavirus disease 19 (COVID-19) has been described to potentially be complicated by ocular involvement. However, scant information is available regarding severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) and ocular structures tropism. We conducted a systematic review of articles referenced in PubMed, Cochrane Library, Web of Science and Chinese Clinical Trial Register (ChiCTR) from December 20, 2019 to April 6, 2020, providing information on the presence of SARS-CoV-2 in cornea, conjunctiva, lacrimal sac, and tears. We excluded ongoing clinical  studies as for unobtainable conclusive results. Of 2422 articles, 11 met the inclusion criteria for analysis and were included in the study. None of the studies were multinational. Among the 11 selected papers there were three original articles, one review, four letters, two editorials, and one correspondence letter. Globally, 252 SARS-CoV-2 infected patients were included in our review. The prevalence of ocular conjunctivitis complicating the course of COVID-19 was demonstrated to be as high as 32% in one study only. Globally, three patients had conjunctivitis with a positive tear-PCR, 8 patients had positive tear-PCR in the absence of conjunctivitis, and 14 had conjunctivitis with negative tear-PCR. The majority of the available data regarding SARS-CoV-2 colonization of ocular and periocular tissues and secretions have to be considered controversial. However, it cannot be excluded that SARS-CoV-2 could both infect the eye and the surrounding structures. SARS-CoV-2 may use ocular structure as an additional transmission route, as demonstrated by the COVID-19 patients’ conjunctival secretion and tears positivity to reverse transcriptase-PCR SARS-CoV-2-RNA assay.

摘要

据报道, 冠状病毒疾病-19 (Coronavirus disease 19, COVID-19) 可能因潜在的眼部并发症而变得复杂。然而, 关于重症急性呼吸综合征冠状病毒2型 (Severe Acute Respiratory Syndrome-Coronavirus-2, SARS-CoV-2) 和眼部结构嗜性的信息却很少。我们对2019年12月20日至2020年4月6日在PubMed、Cochrane数据库、科学网和中国临床试验注册中心 (Chinese Clinical Trial Register, ChiCTR)所收录的文章进行了系统回顾, 以提供SARS-CoV-2在角膜、结膜、泪囊和泪液中存在的信息。由于无法获得确定的结果, 我们排除了正在进行的临床试验。在2422篇文章中, 11篇符合纳入标准。这些研究均不是跨国性的。在11篇入选论文中, 有3篇原创文章、1篇综述、4篇快报、2篇社论和1篇通信信函。本文纳入全球范围内252名感染SARS-CoV-2患者。仅一项研究阐述了COVID-19病程中并发眼结膜炎的患病率高达32%。在全部样本中, 有3例结膜炎患者泪液PCR反应呈阳性, 8例无结膜炎患者泪液PCR反应呈阳性, 14例结膜炎患者泪液PCR反应呈阴性。关于SARS-CoV-2在眼部、眼周组织及分泌物中定植的大多数数据目前尚有争议。然而, 不能排除SARS-CoV-2可能感染眼部及其周围结构, 眼部可作为SARS-CoV-2额外的传播途径, 因为COVID-19患者的结膜分泌物和泪液中SARS-CoV-2-RNA逆转录PCR检测呈阳性

Introduction

Coronaviruses (CoVs) are enveloped, non-segmented, positive-sense RNA viruses belonging to the family of Coronaviridae [1]. Although they were not considered as highly pathogenic, mostly causing mild infections in immunocompetent people, in the last 20 years they have been responsible for the outbreak of two epidemic, zoonotic, and respiratory syndromes. In 2002 and 2003 CoVs were responsible of the severe acute respiratory syndrome (SARS) [2,3,4,5,6] and in 2012, of the Middle East Respiratory Syndrome (MERS) [7, 8]. Altogether, they have caused more than 10,000 cumulative cases, with mortality rates of 10% for SARS-CoV, and 37% for MERS-CoV [9].

In more recent times, another CoV hit the headlines for having been described as the cause of a cluster of pneumonia cases in Wuhan, Hubei, China, from December 2019 [9, 10]. On January 31, 2020, the outbreak has been declared by the World Health Organization (WHO) as a Public Health Emergency of International Concern [11]. On February 11, 2020, the WHO officially named the infection due to the virus as coronavirus disease 2019 (COVID‐19) [12]. The Coronavirus Study Group of the International Committee on Taxonomy of Viruses named the etiologic agent of COVID-19 as “severe acute respiratory syndrome related coronavirus 2”, or SARS‐CoV‐2 [13]. On March 11, 2020, the WHO declared COVID-19 a pandemic. As of April 06, 2020, a total of 1,136,862 laboratory-confirmed cases had been documented, with 63,025 confirmed deaths, in 208 countries [14].

SARS-CoV, MERS-CoV, and SARS-CoV-2 etiologic agents belong to the subfamily of betacoronavirus. Interestingly, both SARS-CoV and SARS-CoV-2 uses angiotensin converting enzyme-2 (ACE2) receptor to primarily infect ciliated bronchial epithelial cells and type 2 pneumocytes [15,16,17]. In addition, it has been shown that SARS-CoV and Human Coronavirus NL63 (HCoV-NL63) infections are associated with conjunctivitis, hence suggesting that CoV can shed and even infect ocular tissue [18,19,20].

However, it is still unclear if SARS-CoV-2 can infect or spread through the mucous membranes of the eye. This systematic review will firstly attempt to analyse the current knowledge on SARS-CoV-2 colonization of ocular and periocular tissues and secretions (i.e., cornea, conjunctiva, lacrimal sac, and tears), in order elucidate if conjunctival transmission occurs, and secondarily aims to propose a potential diagnostic tool in the evaluation of suspected, infected patients.

Materials and methods

We performed a systematic review of the Medline (PubMed), Cochrane Library, World of Science (WoS), and Chinese Clinical Trial Register (ChiCTR) [21] from December 2019 to April 05, 2020 to find papers providing information on the presence of SARS-CoV-2 in cornea, conjunctiva, lacrimal sac, and tears (view “Supplementary Material”). PRISMA guidelines were used for this systematic review [22]. Reference lists of identified articles were independently hand-searched by two authors (GGA, CG). Abstracts were examined, and if eligible, full texts and associated reference lists underwent further evaluation for eligibility. The search was then expanded using a snowballing method applied to the references of retrieved papers, which, once identified, were also screened for accordance to our inclusion criteria. Authors were contacted when necessary. All the results were merged using the reference management software Mendeley (V.1.19.4, Mendeley Ltd). All publications were then reassessed by a third reviewer (FA). According to Cohen’s Kappa, interrater agreement was excellent (κ = 1). Notably, though the majority of publications on COVID-19 are from Asia, no language restrictions were imposed, in order to minimize language bias. Due to the scant evidence, both original articles, editorials, letters, and reviews providing evidence (i.e., prevalence, anecdotal report) about SARS-CoV-2 colonization of ocular and periocular tissues and secretions were all included in the study. In addition, both published and unpublished papers were examined in our analysis, but we excluded ongoing clinical studies as for unobtainable conclusive results. To assess risk of bias and quality of primary studies or systematic reviews identified from database searches, we used the Newcastle–Ottawa Scale for cohort studies, the highest score on which is 9 points [23]. After extensive discussion among reviewers, we decided to include also studies with high risk of bias. We did not register the systematic review protocol because we anticipated the paucity of available information on the subject and due to the urgency of the matter.

Results

The initial search identified 2422 articles (2403 from PubMed, 0 from Cochrane Library, 15 from WoS, 0 from ChiCTR, and 4 through other sources). Following the initial screening of titles, abstracts and removal of duplicates, we included 11 articles in our review. None of the studies was multinational. Among the 11 selected papers there were three original articles, one review, four letters, two editorials, and one correspondence letter (Table 1) [24,25,26,27,28,29,30,31,32,33]. Because of the heterogeneity of studies, no meta-analysis was performed.

Table 1 Full list of the selected papers analysed in the systematic review.

Wu et al. investigated ocular manifestations and viral prevalence in the conjunctiva of 38 patients with COVID-19 (mean age: 65.80 ± 16.60 years). Among them, 12 eyes (31.58%) presented with signs suggestive of conjunctivitis and 2 up to 38 conjunctival specimens (5.26%) yielded positive findings for SARS-CoV-2 at RT-PCR. Notably, the two positive conjunctival swabs (2/12, 16.66%) were sampled from patients with ocular symptoms [32].

Fang et al. enrolled 32 COVID-19 patients (age range from 34 to 54). They collected nasal, blood, faecal, urine, saliva, and tears samples to detect SARS-CoV-2 RNA via RT-PCR. Conjunctival swabs resulted as positive in five samples (15.63%). Remarkably, the presence of conjunctivitis or other ocular manifestation was not reported in their letter [33].

Mungmungpuntipantip and Wiwanitkit in their letter to editor did not report any ocular manifestation among the 48 patients met in their practice. However, no conjunctival swab has been sampled and analysed [34].

Xia et al. attempted to elucidate in a prospective study the presence of the novel coronavirus in conjunctival secretions of confirmed SARS–CoV‐2‐infected patients at the First Affiliated Hospital of Zhejiang University from January 26, 2020 to February 9, 2020. Authors tested a total of 60 tear samples and conjunctival secretion samples from 30 patients (mean age = 54.50 ± 14.17 years). Reverse‐transcription polymerase chain reaction (RT-PCR) assay resulted positive for SARS-CoV-2 RNA in two swabs (2/60, 3.33%) from a single patient with conjunctivitis symptoms. The other 58 samples yielded negative RT-PCR results (58/60, 96.66%) and did not show signs of conjunctivitis [29].

Zhou et al. conducted a similar prospective study at Renmin Hospital of Wuhan University from 17 Jan to 28 Jan 2020 on 67 COVID-19 patients (mean age: 35.70 ± 10 years; male/female ratio of 1/1.68). Authors demonstrated conjunctival swab samples positive for SARS–CoV‐2-RNA in one and weakly positive in two patients (3/67, 4.48%). None of the aforementioned patients had conjunctivitis at the time of conjunctival swab collection. In the single patient with conjunctivitis, conjunctival swab was negative for RT-PCR (1/67, 1.50%) [24].

Liang and Wu analysed 37 conjunctival swabs from confirmed SARS-CoV-2-infected patients at Yichang Central People’s Hospital, Hubei. Three out of 37 patients (8.11%) had conjunctivitis. Only one swab (1/37; 2.70%) from a severe patient (as for the Chinese COVID-19 diagnosis protocol [9]) not suffering from conjunctivitis, had positive RT-PCR assay [28].

Peng and Zhou, due to the aforementioned contrasting results, described conjunctivitis as a “coincident event, rather than a causal event of SARS‐CoV‐2 infection of the conjunctiva.”[30].

Qing et al. speculated the possibility that SARS-CoV-2, as a droplet, could mix with tears, and then access the respiratory tract via the nasolacrimal duct, further suggesting that conjunctivitis during the course of COVID-19 may be an incidental event [25].

Li et al. strongly suggests physician to “take particular care when examining patients, because of both the proximity to patients’ nose and mouth, and the potential exposure to tears which may contain the virus” [26, 35]. This hypothesis was used to suggest the need for ophthalmologist to wear goggles during clinical encounter, as expressed by Lu et al. and Li et al. [26, 27].

However, as analysed by Seah and Agrawal, not only is it still unclear whether SARS-CoV-2 may colonize ocular tissue, but we may also speculate upon other ocular manifestations based on the confirmed expression of ACE2 in different other structures of the eye [24, 30, 31].

Discussion

To the best of our knowledge this is the first systematic review summarizing all the data regarding SARS-CoV-2 colonization of ocular and periocular tissues and secretions (i.e., cornea, conjunctiva, lacrimal sac, tears).

This systematic review analysed 252 SARS-CoV-2-infected patients globally who underwent conjunctival swab, and demonstrates the prevalence of ocular conjunctivitis complicating the course of COVID-19 to be as high as 32% (12 patients out 38), differently as what previously stated by the “Report of the WHO‐China Joint Mission on Coronavirus Disease 2019 (COVID‐19)” as low as 0.8% [36]. Altogether, three patients had conjunctivitis with a positive tear-PCR, eight patients had positive tear-PCR in the absence of conjunctivitis, and 14 had conjunctivitis with negative tear-PCR [24, 28, 29, 32, 33]. This inconsistency may be due to a number of factors, including low viral load in conjunctival secretion, inappropriate sample collection or handling leading to sample contamination, and damage to genetic material. Though current RT-PCR is considered an effective technique, it could inevitably lead to false positive and false negative results [37, 38].

The caution for potential ocular transmission of SARS-CoV-2 was first highlighted by one of the experts of the task force who visited Wuhan on early 2020. Despite being fully gowned with protective coat and N95 mask, he was still infected and reported his first symptom being unilateral conjunctivitis, with subsequent fever and catarrhal symptoms 2–3 hours later. The latency period of a few hours from conjunctivitis to respiratory symptoms does not aide in the determination of the route of transmission, since the virus may have entered via the unshielded ocular surface and caused respiratory symptoms around the same time as conjunctivitis, but masking may also have been ineffective, and conjunctivitis was merely a manifestation of SARS-CoV2. It would be useful to further elucidate SARS-CoV-2 binding to the surface of ocular tissues. It has been shown that SARS-CoV-2 cell entry depends on SARS-CoV-2 S protein/ACE2 receptor interaction [39]. Key proteins crucial to the renin–angiotensin–aldosterone system (RAAS) have been widely described in many ocular structures, including the aqueous [40], the pigmented epithelium [41], and the retina [31, 42,43,44,45].

Evidence of the expression of such proteins both in the conjunctiva and in the cornea are limited. The only study trying to address this question with an in vitro model demonstrated ACE2 expression on both corneal and conjunctival cells and also showed effective binding of the S240 proteins of SARS-CoV with ACE2 receptor on both cells and tissues [46].

Furthermore, given the high vascularity of conjunctiva, along with the expression of ACE2 on the surface of endothelial cells [44, 45], it cannot be excluded that the ocular manifestation of SARS-CoV-2 infection may in fact manifest in the form of a local, transient vasculitis [47].

Due to the presence of RAAS proteins expression in different ocular tissues, it can also be speculated that, even in the form of anecdotal event, SARS-CoV-2 may be responsible for other possible ocular manifestations as anterior or posterior uveitis, iridocyclitis, vitritis, or retinal vasculitis [31, 40, 42,43,44,45].

Given the scarce nature of the available evidence regarding SARS-CoV-2 transmission through ocular tissue, no conclusions could be reached either regarding its ability to infect ocular structures or to use the lacrimal duct to reach the respiratory tract, as a novel transmission route [25].

In addition, due to inconsistency in RT-PCR assay results, conjunctival-swab RT-PCR should not be proposed as a standard diagnostic technique for COVID-19.

As it emerged from this analysis, evidence is not only limited, but sorely conflicting too, which determines low strength of the actual available data. In fact, no comparable results emerged in terms of both mean age at recruitment, number of recruited patients, and male/female ratio. In the two original articles and in the editorial reporting clinical data, only RT-PCR was run, while none of the studies reported viral culture [24, 28, 29]. Hence, it cannot be established whether SARS-CoV-2 only colonizes ocular structure or it is able to invade them, inducing conjunctivitis.

It is desirable that, as the current pandemic continues, a better understanding of the viral features with a focus on the viral tropism for ocular structures will emerge.

In the meantime, physicians should stay highly vigilant in recognizing patients with any previous contact at risk and early manifestation of COVID-19, including systemic symptoms and fever. A specific consideration must be dedicated to any ocular inflammatory involvement as a possible presentation. Individual protection kits including goggles are strongly recommended, especially in at risk clinical encounters [35, 48, 49].

References

  1. 1.

    Cui J, Li F, Shi ZL. Origin and evolution of pathogenic coronaviruses. Nat Rev Microbiol. 2019;17:181–92.

    CAS  Article  Google Scholar 

  2. 2.

    Holmes KV. SARS-associated coronavirus. N Engl J Med. 2003;348:1948–51. http://www.ncbi.nlm.nih.gov/pubmed/12748314.

  3. 3.

    Zhong NS, Zheng BJ, Li YM, Poon LLM, Xie ZH, Chan KH, et al. Epidemiology and cause of severe acute respiratory syndrome (SARS) in Guangdong, People’s Republic of China, in February, 2003. Lancet. 2003;362:1353–8.

    CAS  Article  Google Scholar 

  4. 4.

    Drosten C, Günther S, Preiser W, Van der Werf S, Brodt HR, Becker S, et al. Identification of a novel coronavirus in patients with severe acute respiratory syndrome. N Engl J Med. 2003;348:1967–76.

    CAS  Article  Google Scholar 

  5. 5.

    Fouchier RAM, Kuiken T, Schutten M, Van Amerongen G, Van Doornum GJJ, Van Den Hoogen BG, et al. Koch’s postulates fulfilled for SARS virus. Nature. 2003;423:240.

    CAS  Article  Google Scholar 

  6. 6.

    Ksiazek TG, Erdman D, Goldsmith CS, Zaki SR, Peret T, Emery S, et al. A novel coronavirus associated with severe acute respiratory syndrome. N Engl J Med. 2003;348:1953–66.

    CAS  Article  Google Scholar 

  7. 7.

    de Groot RJ, Baker SC, Baric RS, Brown CS, Drosten C, Enjuanes L, et al. Middle East respiratory syndrome coronavirus (MERS-CoV): announcement of the coronavirus study group. J Virol. 2013;87:7790–2.

    Article  Google Scholar 

  8. 8.

    Zaki AM, Van Boheemen S, Bestebroer TM, Osterhaus ADME, Fouchier RAM. Isolation of a novel coronavirus from a man with pneumonia in Saudi Arabia. N Engl J Med. 2012;367:1814–20.

    CAS  Article  Google Scholar 

  9. 9.

    Huang C, Wang Y, Li X, Ren L, Zhao J, Hu Y, et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet. 2020;395:497–506.

    CAS  Article  Google Scholar 

  10. 10.

    Guan W, Ni Z, Hu Y, Liang W, Ou C, He J, et al. Clinical characteristics of coronavirus disease 2019 in China. N Engl J Med. 2020. http://www.nejm.org/doi/10.1056/NEJMoa2002032.

  11. 11.

    Eurosurveillance editorial team. Note from the editors: World Health Organization declares novel coronavirus (2019-nCoV) sixth public health emergency of international concern. Euro Surveill. 2020;25:pii 200131e. https://doi.org/10.2807/1560-7917.ES.2020.25.5.200131e

    Article  Google Scholar 

  12. 12.

    World Health Organization. Novel Coronavirus (2019‐nCoV) Situation Report—22. 2020. https://www.who.int/docs/default-source/coronaviruse/situation-reports/20200211-sitrep-22-ncov.pdf?sfvrsn=fb6d49b1_2.

  13. 13.

    Coronaviridae Study Group of the International Committee on Taxonomy of Viruses. The species Severe acute respiratory syndrome-related coronavirus: classifying 2019-nCoV and naming it SARS-CoV-2. Nature microbiology. 2020;5:536-44.

    Article  Google Scholar 

  14. 14.

    World Health Organisation. Novel coronavirus (COVID-19) situation. 2020. https://experience.arcgis.com/experience/685d0ace521648f8a5beeeee1b9125cd.

  15. 15.

    Li W, Moore MJ, Vasllieva N, Sui J, Wong SK, Berne MA, et al. Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus. Nature. 2003;426:450–4.

    CAS  Article  Google Scholar 

  16. 16.

    Yeo C, Kaushal S, Yeo D. Enteric involvement of coronaviruses: is faecal–oral transmission of SARS-CoV-2 possible? Lancet Gastroenterol Hepatol. 2020;4:335–7.

  17. 17.

    Wang XW, Li J, Guo T, Zhen B, Kong Q, Yi B, et al. Concentration and detection of SARS coronavirus in sewage from Xiao Tang Shan hospital and the 309th Hospital of the Chinese People’s Liberation Army. Water Sci Technol. 2005;52:213–21.

    CAS  Article  Google Scholar 

  18. 18.

    Van Der Hoek L, Pyrc K, Jebbink MF, Vermeulen-Oost W, Berkhout RJM, Wolthers KC, et al. Identification of a new human coronavirus. Nat Med. 2004;10:368–73.

    Article  Google Scholar 

  19. 19.

    Vabret A, Mourez T, Dina J, Van Der Hoek L, Gouarin S, Petitjean J, et al. Human coronavirus NL63, France. Emerg Infect Dis. 2005;11:1225–9.

    Article  Google Scholar 

  20. 20.

    Loon SC, Teoh SCB, Oon LLE, Se-Thoe SY, Ling AE, Leo YS, et al. The severe acute respiratory syndrome coronavirus in tears. Br J Ophthalmol. 2004;88:861–3.

    Article  Google Scholar 

  21. 21.

    Chinese Clinical Trial Register (ChiCTR). The world health organization international clinical trials registered organization registered platform. 2018:3–4. http://www.chictr.org.cn/enindex.aspx.

  22. 22.

    Moher D, Shamseer L, Clarke M, et al. Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015 statement. Syst Rev. 2015;4:1. Published 2015 Jan 1. https://doi.org/10.1186/2046-4053-4-1.

  23. 23.

    Ottawa Hospital Research Institute. The Newcastle-Ottawa Scale (NOS) for assessing the quality of nonrandomised studies in meta-analyses. 2020. http://www.ohri.ca/programs/clinical_epidemiology/oxford.asp.

  24. 24.

    Zhou Y, Zeng Y, Tong Y, Chen C. Ophthalmologic evidence against the interpersonal transmission of 2019 novel coronavirus through conjunctiva. medRxiv. 2020:2020.02.11.20021956.

  25. 25.

    Qing H, Li Z, Yang Z, Shi M, Huang Z, Song J, et al. The possibility of COVID-19 transmission from eye to nose. Acta Ophthalmol. 2020. http://www.ncbi.nlm.nih.gov/pubmed/32189463.

  26. 26.

    Li JPO, Lam DSC, Chen Y, Ting DSW. Novel Coronavirus disease 2019 (COVID-19): the importance of recognising possible early ocular manifestation and using protective eyewear. Br J Ophthalmol. 2020;104:297–8. http://www.ncbi.nlm.nih.gov/pubmed/32086236.

    Article  Google Scholar 

  27. 27.

    Lu C, Liu X, Jia Z. 2019-nCoV transmission through the ocular surface must not be ignored. Lancet. 2020;395:e39. https://linkinghub.elsevier.com/retrieve/pii/S0140673620303135.

    Article  Google Scholar 

  28. 28.

    Liang L, Wu P. There may be virus in conjunctival secretion of patients with COVID-19. Acta Ophthalmol. 2020. http://doi.wiley.com/10.1111/aos.14413.

  29. 29.

    Xia J, Tong J, Liu M, Shen Y, Guo D. Evaluation of coronavirus in tears and conjunctival secretions of patients with SARS‐CoV‐2 infection. J Med Virol. 2020. https://onlinelibrary.wiley.com/doi/abs/10.1002/jmv.25725.

  30. 30.

    Peng Y, Zhou Y-H Is novel coronavirus disease (COVID-19) transmitted through conjunctiva? J Med Virol. 2020. http://www.ncbi.nlm.nih.gov/pubmed/32176356.

  31. 31.

    Seah I, Agrawal R. Can the Coronavirus Disease 2019 (COVID-19) affect the eyes? A review of coronaviruses and ocular implications in humans and animals. Ocul Immunol Inflamm. 2020;1–5. http://www.ncbi.nlm.nih.gov/pubmed/32175797.

  32. 32.

    Wu P, Duan F, Luo C, Liu Q, Qu X, Liang L, et al. Characteristics of ocular findings of patients with coronavirus disease 2019 (COVID-19) in Hubei Province, China. JAMA Ophthalmol. 2020;2019:4–7. http://www.ncbi.nlm.nih.gov/pubmed/32232433.

    Google Scholar 

  33. 33.

    Fang Z, Zhang Y, Hang C, Zhang W, Ai J, Li S. Comparisons of nucleic acid conversion time of SARS-CoV-2 of different samples in ICU and non-ICU patients. J Infect. 2020. https://doi.org/10.1016/j.jinf.2020.03.013.

  34. 34.

    Mungmungpuntipantip R, Wiwanitkit V. Ocular manifestation, eye protection, and COVID-19. Graefes Arch Clin Exp Ophthalmol. 2020;4662. http://www.ncbi.nlm.nih.gov/pubmed/32232568.

  35. 35.

    Lai THT, Tang EWH, Chau SKY, Fung KSC, Li KKW. Stepping up infection control measures in ophthalmology during the novel coronavirus outbreak: an experience from Hong Kong. Graefes Arch Clin Exp Ophthalmol. 2020;1–7. http://www.ncbi.nlm.nih.gov/pubmed/32124000.

  36. 36.

    World Health Organisation. Report of the WHO-China Joint Mission on Coronavirus Disease 2019 (COVID-19). 2020. https://www.who.int/publications-detail/report-of-the-who-china-joint-mission-on-coronavirus-disease-2019-(covid-19).

  37. 37.

    Corman VM, Landt O, Kaiser M, Molenkamp R, Meijer A, Chu DK, et al. Detection of 2019 novel coronavirus (2019-nCoV) by real-time RT-PCR. Eurosurveillance. 2020;25:2000045. https://www.eurosurveillance.org/content/10.2807/1560-7917.ES.2020.25.3.2000045.

    PubMed Central  Google Scholar 

  38. 38.

    Lin C, Ye R, Xia YL. A meta-analysis to evaluate the effectiveness of real-time PCR for diagnosing novel coronavirus infections. Genet Mol Res. 2015;14:15634–41.

    CAS  Article  Google Scholar 

  39. 39.

    Hoffmann M, Kleine-Weber H, Schroeder S, Mü MA, Drosten C, Pö S, et al. SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor article SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor. Cell. 2020;181:1–10. https://doi.org/10.1016/j.cell.2020.02.052.

    Article  Google Scholar 

  40. 40.

    Holappa M, Valjakka J, Vaajanen A. Angiotensin(1-7) and ACE2, “The Hot Spots” of Renin-Angiotensin System, detected in the human aqueous humor. Open Ophthalmol J. 2015;9:28–32.

    CAS  Article  Google Scholar 

  41. 41.

    Tao L, Qiu Y, Fu X, Lin R, Lei C, Wang J, et al. Angiotensin-converting enzyme 2 activator diminazene aceturate prevents lipopolysaccharide-induced inflammation by inhibiting MAPK and NF-kappaB pathways in human retinal pigment epithelium. J Neuroinflammation. 2016;13:35.

    Article  Google Scholar 

  42. 42.

    Reichhart N, Figura A, Skosyrski S, Strauss O. Control of the retinal local RAS by the RPE: An interface to systemic RAS activity. Experimental eye research. 2019;189:107838.

    CAS  Article  Google Scholar 

  43. 43.

    Fletcher EL, Phipps JA, Ward MM, Vessey KA, Wilkinson-Berka JL. The renin-angiotensin system in retinal health and disease: its influence on neurons, glia and the vasculature. Prog Retin Eye Res. 2010;29:284–311.

  44. 44.

    Lovren F, Pan Y, Quan A, Teoh H, Wang G, Shukla PC, et al. Angiotensin converting enzyme-2 confers endothelial protection and attenuates atherosclerosis. Am J Physiol Heart Circ Physiol. 2008;295:H1377-84. http://www.ncbi.nlm.nih.gov/pubmed/18660448.

  45. 45.

    Zhang YH, Zhang Yhuan, Dong XF, Hao QQ, Zhou XM, Yu QT, et al. ACE2 and Ang-(1–7) protect endothelial cell function and prevent early atherosclerosis by inhibiting inflammatory response. Inflamm Res. 2015;64:253–60.

    CAS  Article  Google Scholar 

  46. 46.

    Sun Y, Liu L, Pan X, Jing M. Mechanism of the action between the SARS-CoV S240 protein and the ACE2 receptor in eyes. Int J Ophthalmol. 2006;6:783–6. https://www.researchgate.net/publication/289011231_Mechanism_of_the_action_between_the_SARS-CoV_S240_protein_and_the_ACE2_receptor_in_eyes.

  47. 47.

    Jiang G, Korteweg C. Pathology and pathogenesis of severe acute respiratory syndrome. Am J Pathol. 2007;170:1136–47.

    Article  Google Scholar 

  48. 48.

    Centers for Disease Control and Prevention—CDC. Information for Healthcare Professionals: COVID-19. 2020. https://www.cdc.gov/coronavirus/2019-ncov/hcp/index.html.

  49. 49.

    Chang D, Xu H, Rebaza A, Sharma L, Dela Cruz CS. Protecting health-care workers from subclinical coronavirus infection. Lancet Respir Med. 2020;8:e13.

    CAS  Article  Google Scholar 

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Aiello, F., Gallo Afflitto, G., Mancino, R. et al. Coronavirus disease 2019 (SARS-CoV-2) and colonization of ocular tissues and secretions: a systematic review. Eye 34, 1206–1211 (2020). https://doi.org/10.1038/s41433-020-0926-9

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