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      Observations about sexual and other routes of SARS‐CoV‐2 (COVID‐19) transmission and its prevention

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          Abstract

          Sexual contact has been proposed as a route of transmission for the SARS‐CoV‐2 virus, which raises the question of alternate routes of transmission. 1 Angiotensin‐converting enzyme (ACE)2 receptors (ACE2‐R) may be present in epidermal basal cells, including those at the base of hair follicles, sebaceous and eccrine glands, smooth muscle cells, vascular endothelial cells, renal epithelial cells, and potentially even the testis. 2 Recent research shows that although the testicles do carry ACE2‐R and that some patients might present with symptoms of viral orchitis, viral DNA is not found within seminal fluid after infection. Furthermore, it is postulated that the viral load is likely to be too low to cross the blood–testis barrier, and that ACE2‐R concentration in the testis may be insufficient to permit viral entry. 3 However, other types of sexual contact, such as oral–anal contact, may also be implicated in transmission, given that rectal swab testing is positive even with negative nasopharyngeal swabs. 1 , 4 It therefore seems relevant to ask whether all tissues that express ACE2‐R are receptive to viral entry, and if they can also be a source of viral shedding. Although some authors have suggested that there is no evidence of sexual transmission for SARS‐CoV‐2, it is still an interesting hypothesis to bear in mind, as it could place some sexual minorities at disproportionately higher risk. At this time, we think nasopharyngeal swabs probably remain the standard of diagnosis. The faecal–oral route, whether through sexual contact or not, is quickly becoming a recognized route of viral transmission. 4 The wildlife markets at the epicentre of the outbreak are notoriously overcrowded and unhygienic. In such places, faecal contamination of food could be an overlooked source of human–human transmission, similar to that seen in diseases such as cholera and dysentery. If this is true, then the potential for SARS‐CoV‐2 to spread in refugee camps or the slums of cities in poorer nations is very real. This certainly needs to be addressed urgently as part of various strategies so that public health authorities, who are already enforcing social isolation, do not lock people down in situations where they can spread the virus easily because of lack of access to clean water. Keeping all this in mind, we recommend that hygiene rules be very strictly adhered to: nails cut as short as possible, hair tied back (it too can be contaminated with the virus) and avoidance of eyelash extensions. It would also be good to shave beards, taking into account the sebum secretion in beard hair; however, this could be a problem for those who need to maintain beards for religious purposes. Absolutely any tool used for personal hygiene (tweezers, scissors, comb, etc.) should be disinfected as often as appropriate, and of course, under no circumstances be lent to other people. We propose that further study should be directed towards the theoretically possible skin–skin transmission, either directly or through vectors such as pets, flies, mosquitoes (by portage) or Demodex folliculorum, which can be proliferated either as spinulosis that roughens the skin of the cheeks and thorax, or in patients with rosacea. 5

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          Characteristics of pediatric SARS-CoV-2 infection and potential evidence for persistent fecal viral shedding

          We report epidemiological and clinical investigations on ten pediatric SARS-CoV-2 infection cases confirmed by real-time reverse transcription PCR assay of SARS-CoV-2 RNA. Symptoms in these cases were nonspecific and no children required respiratory support or intensive care. Chest X-rays lacked definite signs of pneumonia, a defining feature of the infection in adult cases. Notably, eight children persistently tested positive on rectal swabs even after nasopharyngeal testing was negative, raising the possibility of fecal–oral transmission.
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            No evidence of SARS-CoV-2 in semen of males recovering from COVID-19

            Objective To describe detection of SARS-CoV-2 in seminal fluid of patients recovering from COVID-19 and describe the expression profile of ACE2 and TMPRSS2 within the testicle. Design observational, cross-sectional study Setting Tertiary referral center Patients Thirty-four adult Chinese males diagnosed with COVID-19 through confirmatory quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR) from pharyngeal swab samples Intervention None Main Outcome Measures Identification of SARS-CoV-2 on qRT-PCR of single ejaculated semen samples. Semen quality was not assessed. Expression patterns of ACE2 and TMPRSS2 in the human testis are explored through previously published single-cell transcriptome datasets. Results Six patients (19%) demonstrated scrotal discomfort concerning for viral orchitis around the time of COVID-19 confirmation. SARS-CoV-2 was not detected in semen after a median of 31 days (IQR: 29-36 days) from COVID-19 diagnosis. Single-cell transcriptome analysis demonstrates sparse expression of ACE2 and TMPRSS2, with almost no overlapping gene expression. Conclusions SARS-CoV-2 was not detected in the semen of patients recovering from COVID-19 one month after COVID-19 diagnosis. ACE2-mediated viral entry of SARS-CoV-2 into target host cells is unlikely to occur within the human testicle based on ACE2 and TMPRSS2 expression. The long-term effects of SARS-CoV-2 on male reproductive function remain unknown.
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              Sexual transmission of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2): A new possible route of infection?

              To the Editor: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the virus responsible for the coronavirus disease (COVID-19), first identified in Wuhan, China, in December 2019, and that has now actually spread worldwide. The human-to-human transmission routes hitherto recognized include direct transmission, through cough, sneeze, droplet inhalation, and contact transmission, comprising contact with oral, nasal, and eye mucous membranes. To date, COVID-19 has not been reported to be sexually transmitted. However, a series of data raises the possibility that sexual intercourse could be an additional direct way of infection. This hypothesis mainly derives from the recent evidence of a likely fecal-oral transmission. 1 The exact mechanisms by which SARS-CoV-2 interacts with the gastrointestinal tract is unknown. However, angiotensin-converting enzyme II (ACE2) seems to be used by the virus as a receptor to enter cells. ACE2 messenger RNA is highly expressed in the gastrointestinal system, and immunofluorescent data show that the ACE2 protein is abundantly present in the glandular cells of rectal epithelia. 2 , 3 In addition, SARS-CoV-2 RNA identification and intracellular staining of viral nucleocapsid protein in rectal epithelia demonstrated that the virus infects such epithelial cells.2, 3, 4 The recognition of viral RNA from feces indicates that virions are secreted from the virus-infected cells.2, 3, 4 Moreover, SARS-CoV-2 can also be transmitted through the saliva, and ACE2 has been detected on the mucosa of oral cavity, which is rich in epithelial cells. 4 Therefore, if saliva and feces are both capable of carrying the virus and ACE2 is expressed both in the glandular cells of rectal epithelia and oral mucosa, how can we be sure that sexual intercourse does not represent another way of contagion? We thus hypothesize that practice of certain sexual behaviors could constitute an additional way for the contagion, both directly (eg through oral-anal contacts), or indirectly (eg with exposure of the rectal mucosa to the saliva for lubrication during anal sex). This issue could be particularly noteworthy if considering that a patient with COVID-19 is actually considered cured after at least 2 upper respiratory tract samples negative for SARS-CoV-2 are collected at ≥24-hour intervals. Nevertheless, it has been demonstrated that patients can persistently test positive on rectal swabs even after negative results for nasopharyngeal testing. 5 This means that the gastrointestinal tract may continue shedding the virus and that fecal-oral, or eventually sexual, transmission may be possible despite the apparent recovery. Indeed, some authors recommend that real-time reverse transcription polymerase chain reaction be routinely performed to test for SARS-CoV-2 from feces. 3 Patients' sexual habits are often not investigated. These observations highlight the need for physicians, and dermatologists in particular, to strongly discourage sexual practices if infected during the pandemic COVID-19. Indeed, beyond the hypothesized possibility of a direct sexual transmission, sexual intercourse involves close contact that inevitably expose individuals to the risk of contagion. Refining the questions in epidemiologic surveys and conducting extensive studies of the mucosal sites (genitals included) of SARS-CoV-2 shedding may perhaps confirm our hypothesis, allowing for a greater understanding about SARS-CoV-2 transmission routes and effective strategies to control infection spread.
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                Author and article information

                Contributors
                thomas.nadasdy@gmail.com
                Journal
                Clin Exp Dermatol
                Clin. Exp. Dermatol
                10.1111/(ISSN)1365-2230
                CED
                Clinical and Experimental Dermatology
                John Wiley and Sons Inc. (Hoboken )
                0307-6938
                1365-2230
                30 May 2020
                : 10.1111/ced.14274
                Affiliations
                [ 1 ] Department of Dermatology St Parascheva Clinical Hospital of Infectious Diseases Galati Romania
                [ 2 ] Department of Dermatology Faculty of Medicine and Pharmacy/Clinical Department, Medical and Pharmaceutical Research Unit/Competitive Interdisciplinary Research Integrated Platform ReForm‐UDJG Dunărea de Jos University Galati Romania
                [ 3 ] N. Paulescu National Institute of Diabetes Bucharest Romania
                Author information
                https://orcid.org/0000-0003-4290-7068
                https://orcid.org/0000-0002-1196-8100
                https://orcid.org/0000-0003-0774-7396
                Article
                CED14274
                10.1111/ced.14274
                7267151
                32369619
                f5432814-005b-4782-9fcd-c8f6b2841dd3
                © 2020 British Association of Dermatologists

                This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.

                History
                : 30 April 2020
                : 01 May 2020
                Page count
                Figures: 0, Tables: 0, Pages: 2, Words: 1527
                Categories
                Viewpoints in dermatology ● Correspondence
                Viewpoints in Dermatology
                Correspondence
                Custom metadata
                2.0
                corrected-proof
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.8.3 mode:remove_FC converted:03.06.2020

                Dermatology
                Dermatology

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