key: cord-0940169-8je1spxs
authors: Osman, Ikram Omar; Melenotte, Cléa; Brouqui, Philippe; Million, Matthieu; Lagier, Jean-Christophe; Parola, Philippe; Stein, Andréas; La Scola, Bernard; Meddeb, Line; Mege, Jean-Louis; Raoult, Didier; Devaux, Christian A.
title: Expression of ACE2, Soluble ACE2, Angiotensin I, Angiotensin II and Angiotensin-(1-7) Is Modulated in COVID-19 Patients
date: 2021-06-14
journal: Front Immunol
DOI: 10.3389/fimmu.2021.625732
sha: 76f55a0723c64ffd20481b9e0a6c7c5ecb141581
doc_id: 940169
cord_uid: 8je1spxs

The etiological agent of COVID-19 SARS-CoV-2, is primarily a pulmonary-tropic coronavirus. Infection of alveolar pneumocytes by SARS-CoV-2 requires virus binding to the angiotensin I converting enzyme 2 (ACE2) monocarboxypeptidase. ACE2, present on the surface of many cell types, is known to be a regulator of blood pressure homeostasis through its ability to catalyze the proteolysis of Angiotensin II (Ang II) into Angiotensin-(1-7) [Ang-(1-7)]. We therefore hypothesized that SARS-CoV-2 could trigger variations of ACE2 expression and Ang II plasma concentration in SARS-CoV-2-infected patients. We report here, that circulating blood cells from COVID-19 patients express less ACE2 mRNA than cells from healthy volunteers. At the level of circulating cells, this ACE2 gene dysregulation mainly affects the monocytes, which also show a lower expression of membrane ACE2 protein. Moreover, soluble ACE2 (sACE2) plasma concentrations are lower in prolonged viral shedders than in healthy controls, while the concentration of sACE2 returns to normal levels in short viral shedders. In the plasma of prolonged viral shedders, we also found higher concentrations of Ang II and angiotensin I (Ang I). On the other hand, the plasma levels of Ang-(1-7) remains almost stable in prolonged viral shedders but seems insufficient to prevent the adverse effects of Ang II accumulation. Altogether, these data evidence that the SARS-CoV-2 may affect the expression of blood pressure regulators with possible harmful consequences on COVID-19 outcome.

Similarly to the severe acute respiratory syndrome coronavirus (SARS-CoV) that emerged in Asia in 2003, SARS-CoV-2 is a Betacoronavirus lineage 2b/Sarbecovirus which found its origin in a coronavirus circulating in wildlife and to which humans are susceptible (1, 2) . The SARS-CoV and SARS-CoV-2 are genetically close and shared 79.5% nucleotide identity (3) (4) (5) (6) . SARS-CoV-2, is the etiological agent of coronavirus disease 2019 . First described in Chinese patients hospitalized in December 2019, COVID-19 cases were then reported in many countries and the original virus as well as its variants have actually spread worldwide (6) (7) (8) . Although not very symptomatic for the majority of those infected, the SARS-CoV-2 can be responsible for severe forms of COVID-19 characterized by multiple organ dysfunction syndrome (MODS) (9, 10) as well as acute respiratory distress syndrome (ARDS), with high fatality risk (11) . In 16 months, the COVID-19 pandemic caused more than 3.4 million deaths and 164 million confirmed cases -(the COVID-19 Dashboard at Johns Hopkins University May 18, 2021: https://coronavirus.jhu.edu/ map.html).

Venous thromboembolism is a relatively common side effect of SARS-CoV-2 infection (up to one-third of critical COVID-19 cases), characterized by acute pulmonary embolism or intravascular coagulopathy that predisposes the patients to thrombotic events (12) (13) (14) . Elevated D-dimers upon admission of patients is a biomarker of pulmonary embolism and is associated with increased mortality (15) . Cytokines (such as IL-6) production is increased in severe COVID-19 and contributes in the "cytokine storm" leading to obstructive thrombo-inflammatory syndrome (16) (17) (18) . Anticoagulants are considered a possible therapy to reduce the harmful circle of inflammation-coagulation-fibrosis observed in severe forms of COVID-19 (19, 20) . To further explore the physiopathology of COVID-19, it is necessary to focus research on the viral receptor, the ACE2 molecule, and its function. The ACE2 expressed at the surface of human alveolar pneumocytes is the receptor for the spike proteins (S1) of SARS-CoV-2 (21) (22) (23) . Cell surface expression of ACE2 is however not limited to pneumocytes as the ACE2 gene is differentially expressed in human tissues, offering a broad spectrum of cellular targets to the virus including enterocytes and the arterial and venous endothelial cells (24) (25) (26) (27) .

The interaction between S1 and ACE2 does not solely allow viruses attachment to target cells, it could possibly disturb the function of ACE2. Indeed, ACE2, a 805 amino acids type I cellsurface zinc-dependent monocarboxypeptidase, catalyzes the hydrolysis of the active vasoconstrictor octapeptide Ang II [Asp-Arg-Val-Tyr-Ile-His-Pro-Phe] to the heptapeptide Ang-(1-7) and free L-Phe, thus controlling blood pressure (28) (29) (30) (31) . Therefore, ACE2 antagonizes the vasoconstrictor and profibrotic effects of Ang II both by reducing the synthesis of Ang II and by catalyzing the transformation of Ang II into Ang-(1-7) (32) . ACE2 can also exert its functions through cleavage of Ang I (the precursor of Ang II) into Ang- (1) (2) (3) (4) (5) (6) (7) (8) (9) , which can get further metabolized into Ang-(1-7) (33) . Characterizing possible dysregulation of the renin angiotensin aldosterone system (RAAS) in SARS-CoV-2 infected patients, could help explain why one of the main comorbidities related to COVID-19 is hypertension (HT) (34, 35) . It may also encourage the use of new classes of molecules such as soluble human recombinant ACE2 (shrACE2) (36) , in the treatment of COVID-19. Indeed, it has recently been reported that the administration of shrACE2 to severe COVID-19 patients quickly improved their condition (37) .

It has previously been reported that SARS-CoV, which uses ACE2 for binding to cells as does SARS-CoV-2, modulates the expression of ACE2 (38) (39) (40) . We have recently hypothesized (41) that a SARS-CoV-2-induced decrease in ACE2 expression and/ or inhibition of ACE2 peptidase function could result in a feedback control leading to increased production of Ang II expected to aggravate the severity of COVID-19. To investigate this hypothesis we studied the expression of ACE2 mRNA, ACE2 cell-surface protein, as well as the plasma concentrations of soluble ACE2 (sACE2), Ang I, Ang II, and Ang-(1-7), in 44 patients (30 prolonged viral shedders -and 14 short viral shedders) compared to 15 healthy volunteers. We found here that the concentrations of these biomarkers are significantly affected during COVID-19 and we suggest that these changes are likely conducive to worsening the patient's condition.

This prospective pilot study included 44 patients with a confirmed diagnosis of SARS-CoV-2 infection diagnosed at the IHU Mediterraneé Infection in Marseille. These patients have all been tested positive for SARS-CoV-2 in their nasopharyngeal samples as evidenced by a quantitative reverse transcriptasepolymerase chain reaction (qRT-PCR) which uses specific primers for the E gene of this virus. The qRT-PCR were considered positive when the cycle threshold (Ct) was below 30, as previously reported (42) . The severity of the disease was determined according to the WHO classification (43) . Before inclusion, the patients were all subjected to a clinical examination including a pulmonary examination by low dose scanner and their blood pressure was recorded. The inclusion period began on 3 June 2020 and continued until the authorized number of patients was reached. Patients were distributed in two groups: i) prolonged viral shedders (nasopharyngeal SARS-CoV-2 PCR ≥10 days from the first consultation) and, ii) short viral shedders (nasopharyngeal SARS-CoV-2 PCR<10 days from the first consultation). A control group was composed with healthy volunteers. All patients included in this study received 600 mg of hydroxychloroquine (HCQ) daily during 10 days (plus or minus 1 day) and azithromycin was added to their treatment during the first 5 days. This therapy, routinely used at the IHU Mediterraneé Infection, as previously described (44, 45) , was initiated with the informed consent of the patient and after verification of the absence of contraindications. A follow up of the patients' viral load was performed to monitor the effectiveness of treatment and the course of the disease at days 0, 3, 6 and 10. Deidentified clinical information was collected from the standard clinical care units of the IHU Mediterraneé Infection, in accordance with regulations in force in France. Most of the patient samples used in this study were collected between 1 and 3 days after the treatment had been stopped (with exception of two samples collected 5 days after the end of treatment, and samples from 2 other patients collected 7 days and 10 days respectively after the end of treatment). Samples (10 mL Paxgene tube and 5mL EDTA tube), were collected and divided into the predefined two patients groups and control group, respectively. All healthy volunteers (students and non-nursing staff with no symptoms) were tested negative for SARS-CoV-2 by qRT-PCR (Ct>34).

This research protocol registered as ANSM N°2020-a00864-35, was submitted to ethical review by the French Participants Protection Committee (CPP East III; CPP president: Dr. P. Peton) -and received ethical approval prior to participant's enrolment (CPP 20.04.09/N°:20.04.01.83219/N°7626; Principal investigator, C. Devaux, Research Director at CNRS; Assay promotor: IHU Mediterraneé Infection: Prof Didier Raoult, Director). All patients were informed of the nature of the study and provided written consent. The volume of peripheral blood sampled agreed with the volume authorized in type 2 human biological research (RIPH type 2) and was approved by the ethics committee for this study. All clinical data were deidentified before being made available to the principal investigator and collaborators in respect with the European General Data Protection Regulation (GDPR).

5 mL of blood samples was collected from patients and healthy donors into an Ethylenediaminetetraacetate (EDTA) tube (Sigma Aldrich, Saint-Quentin Fallavier, France), and allowed to clot at room temperature. The plasma was collected, then centrifuged at 1500g for 10 min and stored at -20°C until use.

Peripheral blood mononuclear cells (PBMCs) were recovered from blood samples using Ficoll (Eurobio, Les Ulis, France) density gradient centrifugation followed by harvesting of PBMCs. Monocytes were isolated by adherence to culture dishes for 2 hours at 37°C and directly lysed for qRT-PCR without being harvested.

Ribonucleic Acid (RNA) Extraction and Quantitative-Reverse Transcription Polymerase Chain Reaction (qRT-PCR) RNAs were extracted from whole blood using PAXgene blood RNA kit (QIAGEN SA) with a DNase I step to eliminate DNA contaminants, according to the manufacturer instructions. The quantity and quality of the RNA was evaluated using a Nanodrop 1000 spectrophotometer (Thermo Science). The first-strand cDNA was obtained using oligo(dT) primers and Moloney murine leukemia virus-reverse transcriptase (MMLV-RT kit; Life Technologies), using 200 ng of purified RNA. The amplification cycles were performed using a real time PCR Mastercycler gradient (Eppendorf, Montesson, France). The qPCR experiments were performed using s peci fi c oligonucleotide primers (Specific primers were designed using the Primer3 software) and hot-start polymerase (SYBR Green Fast Master Mix; Roche Diagnostics). The specific primers used were Angiotensin Convertase Enzyme (ACE2) primers (forward primer: CAGGGAACAGGTAGAGGACATT and reverse primer: CAGAGGGTGAACATACAGTTGG) and the housekeeping b-Actin primers (forward: AGGAAGGAAGGCT GGAAGAG and reverse: GGAAATCGTGCGTGACATTA). The amplification cycles were performed using a C1000 Touch Thermal cycler (Biorad, Marnes-La-Coquette, France). The results of qRT-PCR were normalized using the housekeeping gene b-Actin (ACTB) and expressed as Relative Quantity (RQ= 2 -DCT ), where DCt = (Ct Target − Ct Actin ). The threshold cycle (Ct) was defined as the number of cycles required to detect the fluorescent signal.

Quantification of Plasma solubleACE2, Angiotensin I, Angiotensin II, and Angiotensin-(1-7)

The quantity of soluble ACE2, Angiotensin I, Angiotensin II, and Angiotensin-(1-7) in the plasma of healthy volunteers and COVID-19 patients was determined using Elisa kits (FineTest, Wuhan, China) that require small sample volume and obviate the need for prior sample extraction or enrichment. Plasma samples were rapidly processed and kept at -20°C until used, as suggested by Chappell et al. (46, 47) . All studied samples were tested on the same day. The experiments were performed according to the manufacturer's instructions, using 100 µL of plasma per assay. The minimal detectable concentration of human soluble ACE2, Angiotensin I, Angiotensin II, Angiotensin-(1-7) were 391 pg/mL, 125 pg/mL pg/mL, 31.2 pg/mL, and 15.6 pg/mL, respectively. The concentrations in each molecule were calculated by comparison to standard curves.

Flow cytometry was used to study the membrane expression of ACE2 as well as specific biomarkers on PBMCs. Cells were analyzed according to fluorescence intensity using an anti-ACE2-monoclonal antibody (mAb) labeled with Alexa Fluor 488 (R&D Systems, Minneapolis, USA) and mAb anti-CD3-PC5, anti-CD20-PC7, anti-CD16-PE, and anti-CD14-APC purchased from Beckman (Beckman coulter, Villepinte, France). Fluorescence intensity was measured using a Canto II cytofluorometer (Becton Dickinson, Biosciences, Le Pont de Claix, France) and the results were analyzed using a BD FACSDiva software v.6. 1.3 (Becton Dickinson, New Jersey, USA).

Data were analyzed using a non-parametric Mann-Whitney U test to compare healthy donors, patients with COVID-19 and healed COVID-19 individuals. The results are presented as the median with confidence interval. A p value <0.05 was considered statistically significant. The data were submitted to multivariate principal component analysis (PCA) biplot (score plot + loading plot) (RStudio) and hierarchical clustering heatmap analysis (ClustVis). The R studio program (RStudio, USA) was used to generate the correlation matrix for the biomarkers of interest after a Pearson's test that measuring the linear correlation for two variables or Spearman's test for the not normally distributed correlation.

All COVID-19 patients included had mild to moderate disease and recovered from COVID-19 infection. Patients were divided into two groups. The first group, hereafter named prolonged viral shedders (patients with viral persistence 10 days after diagnosis of infection), was composed of 30 patients having difficulties to clear the virus, among whom 5 men and 25 women (mean age: 46 ± 13 years). The second group, hereafter named short viral shedders (patients with rapid viral clearance at day 6 after diagnosis of infection), included 14 patients -, among whom 7 men and 7 women (mean age: 41 ± 12 years) ( Table 1) . Most samples (40/44) were collected between 11 and 13 days after SARS-CoV-2 diagnosis (i.e. less than 5 days after the test turned negative on the nasopharyngeal sample for the prolonged viral shedders and more than 5 days after qRT-PCR turned negative on nasopharyngeal sample for the short viral shedders group), whereas 4 samples were collected between 15 and 20 days post-diagnosis due to the unavailability of patients. A group of 15 healthy volunteers was included in this study as control among which 7 males -and 8 females (mean age: 34.8 ± 14 years).

In order to assess the effect of SARS-CoV-2 on the ACE2 gene expression in patients with COVID-19, we used qRT-PCR to compare the ACE2 mRNA expression in circulating cells from 30 prolonged viral shedders and 14 short viral shedders with 15 healthy volunteers ( Figure 1A ). When the median values of ACE2 mRNA expression were compared among groups, a lower expression of ACE2 mRNA was observed in the prolonged viral shedders compared to the healthy volunteers (median values 0.722 x 10 -3 versus 1.433 x 10 -3 ). Yet, this result appeared not statistically significant according to Mann-Whitney test (p=0.0577). This lower ACE2 gene expression was also observed in the short viral shedders compared to the healthy volunteers (median values 0.540 x 10 -3 versus 1.433 x 10 -3 ), and 

100% ( even more accentuated then in the prolonged viral shedders group. The lower expression of ACE2 mRNA in short viral shedders was statistically significant -(p=0.0307). In addition, there were no significant differences between the two groups of patients (p=0.2771). We confirmed these results by investigating the expression of ACE2 mRNA in PBMCs, instead of the whole blood circulating cells (the difference resides in the lack polynuclear cells in PBMCs) ( Figure 1B) examined by flow cytometry. Between 8 and 40% of PBMCs expressed detectable ACE2 at their surface. ACE2 expression at the surface of PBMCs from the prolonged viral shedders (n=16) and the short viral shedders (n=12), was quantified and compared to that of PBMCs from the healthy volunteers (n=12) ( Figure 1C) . Surprisingly, the percentage of PBMCs expressing membrane-bound ACE2 was almost stable or even slightly higher in the two groups of patients compared to the healthy volunteers.

Although ACE2 mRNA expression was lower in PBMCs from COVID-19 patients than in PBMCs from healthy volunteers, this does not result in a lower expression of the ACE2 protein on the total population of PBMCs. To try to understand this apparent paradox, the expression of ACE2 on the surface of separated cell populations was studied. The modulation of ACE2 cell-surface expression differed from one cell population to another as illustrated by the significantly higher number of CD3 + T cells expressing ACE2 in the COVID-19 patients groups, while there was an absence of modulation in the CD20 + B cells and CD16 + / HLA-DR + monocytic/dendritic cells expressing ACE2 compared to cell populations from healthy volunteers ( Figure S1 ; Supplementary Data). However, we observed ( Figure 2A ) a slight but significantly lower number of CD14 + /HLA-DR + monocytes that expressed membrane-bound ACE2 in the prolonged viral shedders (n=16). This lower expression of ACE2 in monocytes was confirmed using qRT-PCR ( Figure 2B) . A significantly lower ACE2 mRNA expressionwas found in monocytic cells from the prolonged viral shedders (n=6; p=0.0043) and the short viral shedders (n=6; p=0.0087), compared to the same cell type in healthy volunteers (n=6).

The release of soluble ACE2 (sACE2) in plasma was investigated using an ELISA assay ( Figure 3A ). Plasma samples from two patients were not available; thus, only 29/30 patients from the prolonged viral shedders group and 13/14 patients from the short viral shedders group were tested. The expression of sACE2 was found heterogeneous among the healthy control group. In the healthy controls group, 3 individuals were found with higher concentrations of sACE2 than the other group members, among which a 32 years old man characterized by a high expression of ACE2 mRNA. In the prolonged viral shedders, there was also a strong heterogeneity with 5 patients -for whom the expression was much higher than for the 25 other members of the group. All 5 patients were women, including two with high blood pressure, but none of them had elevated expression of ACE2 mRNA.

Regarding the short viral shedders, the results were more homogeneous. Despite these individual variations, what is remarkable according to a Mann-Whitney test, is that the plasma concentration of sACE2 was found to be significantly lower in the prolonged viral shedders, compared to the healthy volunteers' group (19396 pg/mL versus 22600 pg/mL; p=0.0156). It should also be noted that the short viral shedders had a plasma concentration of sACE2 of 22141 pg/mL, which was not significantly different from the healthy control group (p=0.153).

Since ACE2 is a key peptidase that regulates the -RAAS, it was of major importance to investigate the plasma concentration of the main peptides of this system. The quantification of Ang I, a peptide resulting from the cleavage of the angiotensinogen by renin was performed as it serves as upstream precursor for Ang II production following hydrolysis by the ACE peptidase. In addition, since ACE2 mRNA expression was found to be lower in patients with COVID-19, it was of interest to study whether this modification affected the plasma concentrations of Angiotensin metabolites. For this purpose, we used Ang I and Ang II ELISA kits. The comparison of Ang I concentrations found in healthy volunteers (median=1496 pg/mL), with that from COVID-19 patients showed a significantly higher Ang I in both prolonged viral shedders (median= 2979 pg/mL; p=0.0029) and short viral shedders (median= 3603 pg/mL; p=0.0001) ( Figure 3B ). Next, Ang II was quantified in the patient's plasma and that of the healthy volunteers. This study showed that the -Ang II concentration was higher in the prolonged viral shedders (median= 921 pg/mL; p=0.0338) and short viral shedders (median= 1038 pg/mL; p=0.0158), than in the healthy volunteers (median=746 pg/mL) ( Figure 3C ). The differences between the two groups of patients and the healthy volunteers were found to be significant according to a Mann-Whitney test -It is noteworthy that the plasma concentration of Ang II was extremely high in two patients from the prolonged viral shedders group, two women (49 years old and 54 years old, respectively)without documented history of high blood pressure and anti-HT treatment. Their kalemia values were also in the normal range (4.06 mmol/L and 4.1 mmol/L, respectively).

The finding that Ang II accumulated in the plasma of COVID-19 patients prompted us to study the plasma concentrations of Ang-(1-7), the downstream molecule of the RAAS pathway. We studied the Ang-(1-7) plasma concentrations in the 3 studied groups ( Figure 3D ). Indeed we found a slightly higher plasma concentrations of Ang-(1-7) in the prolonged viral shedders (median: 554 pg/mL) than in the short viral shedders (median: 436 pg/mL). We noted in particular a strong expression of Ang-(1-7) in three prolonged viral shedders, one being the patient with the highest plasma concentration of Ang II in this group, the second patient was a 81 years old woman with HT (candesartan medication; kalemia: 3.68 mmol/L), while the third patient was a 52 years old man with no known history of HT (kalemia: 3.82 mmol/L). However, compared to the Ang-(1-7) plasma concentrations found with samples from healthy volunteers (median: 510 pg/mL), the higher Ang-(1-7) concentrations measured in samples from prolonged viral shedders was not statistically significant.

Regarding the differences of angiotensin metabolites concentrations between the two groups of patients and the healthy volunteers they were found to be significant according to a Mann-Whitney test and were also confirmed by the principal component analysis and hierarchical clustering heatmap ( Figure 4 and Figure S2 ; Supplementary Data) which show that the two groups of COVID-19 patients behave differently from the control group for all parameters studied. In fact, it appears that higher concentrations in Ang I correlate with higher concentrations in Ang-(1-7) (r=0.49, p <0.006 in prolonged viral shedders and r=0.74, p=0.0036 in short viral shedders). Regarding Ang II, we found that higher concentrations in Ang II also correlate with higher concentrations in Ang-(1-7) and this effect was statistically significant (r=0.60, p <0.001 in prolonged viral shedders and r=0.89, <0.001 in short viral shedders). Yet, as shown in Figure 3D , we also found a statistically significant decrease in Ang-(1-7) between prolonged viral shedders (median: 554 pg/mL) and short viral shedders (median: 436 pg/mL; p=0.00402).

During the past year, in vitro and in silico studies allowed to analyze interactions between SARS-CoV-2 and ACE2 (48) (49) (50) . This has led many clinical research teams to hypothesize that soon after infection of people, SARS-CoV-2 is likely to trigger a dysfunction of ACE2 and subsequently variations in the balance between Ang II and Ang-(1-7), contributing to worsening hypertension and releasing of proinflammatory cytokines, especially IL-6, thereby accelerating -atherogenesis (35, 51) . ACE2 is thought to act in an opposing manner to its homologue, angiotensin-converting enzyme (ACE), by inactivating the vasoconstrictor peptide Ang II and generating the vasodilator fragment, Ang-(1-7) (52). As illustrated by Figure 5 , we report here -evidence that ACE2 mRNA and ACE2 protein expression, as well as sACE2, Ang I, Ang II and Ang-(1-7) plasma concentrations are modulated during COVID-19. Because the size of the studied cohort is small to meet the recommendations of the ethical committee, this impacted our statistical analyses. This work should later be reproduced with a larger cohort of patients, including patients with severe forms of COVID-19. Moreover, in order to conduct this study, we only had access to blood samples, because it is a simple medical act, not particularly invasive, and it can be performed with the informed consent of the patient in agreement with the ethics committee' instructions. Although the ACE2 gene is usually considered poorly expressed in immune cells, the expression of ACE2 mRNAs was previously reported in a subset of CD14 + CD16human monocytes (53) , opening to us the possibility of conducting a study using circulating blood cells. However, -it should be kept in mind that it is mainly at the level of the pulmonary, vascular, renal, and cardiac epithelial tissues that the impact of the SARS-CoV-2 should be the greatest -(54-56). There is not such limitation for the quantification of plasma compounds (sACE2, Ang I, Ang II and Ang-(1-7). Regarding the cohort of 44 patients we studied, there is a possible bias due to sex ratio, genetic polymorphism, age, and treatment. In our studied, men represented only 16.6% of the COVID-19 patients group while, in general, about two-thirds of symptomatic COVID-19 are men. Moreover, we did not get information on the sequences of the ACE and ACE2 genes of the patients while ACE and ACE2 ethnic polymorphisms were reported (57) (58) (59) (60) (61) (62) . Regarding the plasma concentration of sACE2, literature reports that males express little higher ACE2 than females (54, 63, 64) . In the two groups of COVID-19 patients, among 44 individuals, seven were known to have a history of hypertension and two more were found with high blood pressure at the time of clinical examination. In the prolonged viral shedders group, 4 patients showed hypokalemia while 2 patients showed hyperkalemia, and in the short viral shedders group, 2 patients showed hyperkalemia. Finally, it cannot be excluded that the treatment taken by the patients might modify the ability of the virus to bind to the ACE2 since hydroxychloroquine -was suggested to mediate a deficit in the glycosylation of ACE2 (65, 66) . Despite the high heterogeneity of ACE2 mRNA expression from individual to individual within each group, we observed alower ACE2 mRNA expression in both COVID-19 patient groups compared to the healthy volunteers. It is worth noting that the level of ACE2 mRNA expression in the healthy volunteers group was highly heterogeneous, particularly regarding three volunteers, a 63-years-old male, a 26-years-old female, and a 32-years-old male, who had high basal ACE2 mRNA expression. The difference in ACE2 mRNA expression in peripheral blood cells was significant between the healthy control group and the short viral shedders (p=0.0307), as if the expression of ACE2 retained the imprint of the infection for some time after nasopharyngeal SARS-CoV-2 qRT-PCR has turned negative. In the COVID-19 patient groups, one patientwith an ACE2 expression significantly higher than the mean value for this group was a 47-years-old obese woman on analgesic therapy. Her COVID-19 history was marked by an extended viral carriage during 21 days. In the group of short viral shedders, the three patients with the slightly higher ACE2 mRNA expression were male patients, a 57-years-old patient with hypertension (196/85) and hyperkalemia (4.65 mmol/L) a 66-years-old patient also with above-normal blood pressure (159/95) and a normal kalemia of 3.97 mmol/L, both patients were on anti-HT treatment, -and a 35-year-old male patient (kalemia: 3.91 mmol/ L), treated for allergy and inflammatory bronchial obstruction. 7) and also Ang I to Ang-(1-9) next converted in Ang-(1-7) by ACE peptidase, leading to protective signal through MAS-receptor. This is the physiological state. The upper-right panel illustrates the possible dysfunction of signals when SARS-CoV-2 is attached to its ACE2 receptor. Under this condition Ang-(1-7) synthesis through ACE2 is likely decreased, Ang II accumulates and, increased Ang II binding to AT1R -leads to proinflammatory signals that ultimately will trigger both tissues damage (in particular lungs and heart) and hypertension. The lower -panel illustrates that during COVID-19, the ACE2 mRNA expression is reduced leading to low surface expression of ACE2 (and plasma sACE2), Ang II is in excess in plasma, yet Ang-(1-7) remains synthesized through the NEP/TOP alternative pathway where neprilysin (NEP) and thimet oligopeptidase (TOP) convert Ang I to Ang-(1-7). However, the median value of ACE2 mRNA expression in those patients groups remained lower than the median value of ACE2 mRNA expression in the healthy control group, which is consistent with earlier data obtained in vitro -with Sarbecovirus (39) . In the absence of Sarbecovirus infection, reduced levels of ACE2 expression were previously reported in cardiac tissues linked to HT, dyslipidemia and/or heart failure (67, 68) . The lower ACE2 mRNA expression observed in COVID-19 patients could also be the result of a feedback regulation loop orchestrated by Ang II. It was previously reported that the over-expression of Ang II decreased ACE2 mRNA production in rat cardiac myocytes and fibroblasts (69). This ACE2 mRNA down-regulation was blocked by losartan, an Ang II receptor blocker (ARB), and by inhibitors of MAP kinases, suggesting that Ang II triggers AT1 receptor signaling that leads to Erk1/Erk2 activation and modulation of ACE2 gene expression (69) .

During the quantitative analysis of membrane ACE2 by flow cytometry, no decrease in expression of this molecule was observed on PBMCs and populations of T-cells, B-cells and CD16 + monocytic/dendritic cells from COVID-19 patients. This was surprising given that there is a decrease in the expression of the ACE2 transcript in PBMCs of COVID-19 patients. It may be due to a lower sensitivity of flow cytometry compared to qRT-PCR. In addition, the mean expression of ACE2 on the surface of PBMCs does not exceed 35%, which is perhaps too low to measure detectable variations at the protein level. Yet we found a significantly lower membrane-bound ACE2 in a population of CD14 + /HLA-DR + monocytes from prolonged viral shedders, that corroborates with the down regulation of ACE2 transcription in monocytic cells. It is consistent with a previous report indicating that in symptomatic COVID-19 patients the percentage of CD14 + /HLA-DR + monocytes increase in the PBMCs while the CD14 low CD16 + inflammatory monocytes decrease as they leave the bloodstream and homing tissues (70) . Moreover, we found lower plasma concentrations of sACE2 in the prolonged viral shedders consistent with the reduction of ACE2 mRNA expression. Indeed, similarly to other Sarbecoviruses (71, 72) it can be hypothesized that the binding of the SARS-CoV-2 spike to cell-membrane anchored ACE2 modulates ACE2 expression. In a murine animal model, it was observed that Ang II-mediated decrease of ACE2 at the surface of cardiomyocyte was accompanied by the concomitant increase in cell-surface expression of the ADAM17 sheddase (73, 74) , suggesting a possible cleavage of membrane-bound ACE2 and shedding of sACE2. It was also previously reported that a recombinant SARS-CoV expressing the HCoV-NL63 spike, another human coronavirus using ACE2 for cell entry, trigger shedding of sACE2 (75) . The sACE2 molecule could be considered a possible candidate for monitoring the evolution of COVID-19.

Here we found that the plasma concentrations of Ang I and Ang II are significantly higher in the COVID-19 patients -than in healthy volunteers. It might have seemed reasonable to hypothesize that if, in COVID-19 patients, ACE2 expression was decreased and the Ang II plasma concentration became high, the risk of hypertension could be high. In the prolonged viral shedders group, 7 out of 30 patients had a history of HT and 4 showed evidence of HT during the clinical examination. Two cases (2/23, 8 .7%) of HT were discovered at the time of their clinical examination (a patient with blood pressure of 180/30 and hypokalemia at 3.45 mmol/L, and another with blood pressure of 137/65 and a kalemia of 4.1 mmol/L). In the short viral shedders group,-2 -patients had HT but they were already known for HT prior to the discovery of their COVID-19. It is worth noting that both Ang I and Ang II remained very high in plasma samples of short viral shedders even after the specific SARS-CoV-2 qRT-PCR on nasopharyngeal samples has turned negative. The medical management of hypertension involves the use of RAAS inhibitors, such as angiotensin converting enzyme inhibitors (ACEis) and Ang II Receptor Blockers (ARBs), considered to up-regulate the cell surface expression of ACE2, with the possible adverse effects of increasing the susceptibility to SARS-CoV-2 of patients who receive these treatments (76, 77) . Recently we found that ARBs (azilsartan, eprosartan, irbesartan, olmesartan, losartan, telmisartan, and valsartan) trigger a downregulation of the AT1R mRNA and an over-expression of ACE2 mRNA synthesis in Vero E6 cells that correlates with increased SARS-CoV-2 production (78). However, using a model of mice treated with captopril (ACEi) or telmisartan (ARB), Wysocki and colleagues reported a profound decrease in kidney ACE2 protein and increase in cytosolic ACE2 protein, but this effect was not found in lung (79) . Nonetheless, another study reported that ACEis reduced ACE2 expression in lungs (80) . In previous opinion papers, we and others (32, 76, (81) (82) (83) strongly encouraged to rapidly evaluate whether the -RAAS inhibitors are more beneficial than harmful in severe COVID-19 patients. This question was -the source of intense debate among cardiologists - (41, 74, 84) , with supporters of the temporary discontinuation of the treatment during COVID-19 to avoid viral over-replication and rapid cell-to-cell propagation of the virus, while others considered that discontinuing treatment could also worsen the general health status of patients and that maintaining treatment could have a favorable effect by acting as a vasodilator, antioxidant and anti-inflammatory through the action of Ang-(1-7) on MAS-receptors. Although we had not enough patients with HT medication to draw definitive conclusion, our preliminary observation suggests that being on HT medication could promote a faster return to normal ACE2 gene expression. It corroborates recent data indicating that maintaining therapy against HT improve the clinical outcome of COVID-19 patients (85) (86) (87) .

The lower expression of ACE2 was consistent with the observed accumulation of Ang II in COVID-19 patients. Therefore, it may be surprising to find no major difference between the three groups studied with respect to the quantification of the Ang-(1-7) in plasma samples. In particular, we noted a higher Ang-(1-7) expression in three prolonged viral shedders, a 49-years-old woman with HT and the highest plasma concentrations of Ang II, a 81-yearsold woman with HT and a high plasma concentration of sACE2, and a 52-years-old man with no known history of HT. A transcription of the ACE2 gene should result in a reduced capacity of this peptidase to cleave Ang II -. However, Ang-(1-7) production did not collapsed in COVID-19 patients and was slightly higher than in healthy volunteers. It cannot be excluded that ACE2 mRNA expression in PBMCs is valuable for this tissues only and that ACE2 may remain expressed on other cell types leading to cleavage of Ang II that is produced in excess in COVID-19 patients, allowing synthesis of Ang-(1-7) (88). However, it is much more likely that an alternative pathway independent of ACE2, contributes to the biosynthesis of Ang-(1-7). The comparison of intrarenal Ang I, Ang II and Ang-(1-7) in wild type mice and tisACE -/mice lacking the ACE, revealed that the Ang I and Ang II levels were decreased by 80% in tisACE -/mice, whereas the Ang-(1-7) levels were sustained (89) . It was also reported that Ang-(1-7) can be formed directly from Ang I through peptidases including the endopeptidases neprilysin (NEP), a 95 kDa membrane-anchored metalloendopeptidase located on the vascular surface of blood vessels and the thimet oligopeptidase (TOP), a 80KDa soluble metalloendopeptidase, which both hydrolyzes Ang I to form Ang-(1-7) (90) (91) (92) . This suggests that in COVID-19 patients the ACE2-independent pathway of peptide generation is efficient to trigger Ang-(1-7) biosynthesis from Ang I when the Ang-(1-7) production through Ang II cleavage by ACE2 is impaired. This should be further studied, as Ang-(1-7) generation was previously reported capable to achieve protection against Ang II-mediated lung injury and cardiovascular risks (84, 93, 94) . However, the plasma concentration of Ang II in COVID-19 patients is probably too high so that its harmful effects are not offset by the protective action of Ang-(1-7). As previously reported (95) , it is also likely that the high plasma concentration of Ang II triggers overproduction of aldosterone through AT1 receptor stimulation, which may be at least in part responsible of the hypokaliemia observed in some COVID-19 patients.

In conclusion, we report evidence that during the COVID-19, a decrease in the expression of ACE2 mRNA and cell-surface ACE2 is observed and that prolonged viral shedders forms of COVID-19 are associated with low plasma concentrations of sACE2. As a result, Ang II is no longer metabolized by ACE2 and its plasma concentrations increase. However, this has no direct impact on the plasma concentrations of Ang-(1-7) which remain stable in COVID-19 patients. This suggests that when the ACE2 pathway is less efficient or totally ineffective, Ang-(1-7) is produced by metabolism of Ang I likely by the neprilysin and/ or thimet oligopeptidase. The high plasma concentration of Ang I in COVID-19 patients should favor this pathway. Although the plasma concentration of Ang-(1-7) remains stable in COVID-19 patients, it appears to be insufficient to prevent the harmful effects of Ang II.

The original contributions presented in the study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding author.

The studies involving human participants were reviewed by French Participants Protection Committee (CPP East III; CPP president: Dr. P. Peton) prior to commencement of the study and received ethical approval CPP 20 

We are grateful to all the clinical, technical and paramedical staffs of the hospitalization units and laboratories for their expert assistance. We thank the students and our colleagues from the Mediterranean Infection IHU who volunteered to join the healthy control group. We thank Aissatou Bailo-Diallo, Orlane Soldani, Andriamiharimamy Rajaonison and Youssouf Seŕeḿef or helpful technical discussions. We thank the Cookie Trad company for English editing.

The Comparison of percent cells expressing ACE2 and ACE2 MFI on cell samples from prolonged viral shedders (n=12), patients short viral shedders (n=12) and healthy volunteers (n=12). The gating was performed using different cluster differentiationspecific mAb allowing to select subpopulation of lymphocytes CD3 + T-cells, CD20 + B-cells and HLA-DR + /CD16 + monocytic/dendritic cells. The left panels indicate the percent of cells expressing ACE2 with respect to the cells subpopulation analyzed while the right panels are the histograms of ACE2 cell surface expression (MFI).

Supplementary Figure 2 | Correlation matrix (R studio used to generate the matrix) between sACE2 and angiotensin metabolites in different groups of COVID-19 patients and healthy volunteers. The upper panels show the correlation matrix of the different biomarkers of interest for the group of healthy volunteers (left) and prolonged viral shedders (right), while the correlation matrix for the short viral shedders is shown in the lower left panel. For the not normally distributed correlation (Healthy control and prolonged viral shedders) we used Spearman's correlation and for the short viral shedders we used the Pearson's correlation. The table at the lower right part of the figure summarizes the correlation analyses (Pearson test) between sACE2 and the different metabolites Ang I, Ang II, Ang-(1-7) in each group.

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