|
|
 |
|
REVIEW ARTICLE |
|
Year : 2020 | Volume
: 9
| Issue : 6 | Page : 244-247 |
|
Diabetes and coronavirus infections (SARS-CoV, MERS-CoV, and SARS-CoV-2)
Azadeh Haghi Navand1, Saber Soltani2, Mona Moghadami3, Parastoo Hosseini2, Sepideh Nasimzadeh1, Milad Zandi2
1 Virology Department, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran 2 Department of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran 3 Department of Medical Biotechnology, School of Medicine, Babol University of Medical Science, Babol, Iran
Date of Submission | 17-Apr-2020 |
Date of Decision | 17-Sep-2020 |
Date of Acceptance | 15-Oct-2020 |
Date of Web Publication | 02-Nov-2020 |
Correspondence Address: Milad Zandi Department of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran Iran
 Source of Support: None, Conflict of Interest: None
DOI: 10.4103/2221-6189.299178

Diabetes, as the major cause of hyperglycemia, is a chronic metabolic disease. Immune system disorders caused by diabetes can increase the risk of respiratory diseases. Thus, diabetes is considered to be a major risk factor for viral respiratory infections such as coronavirus infections. Coronaviruses are members of the Coronaviridae, which has caused three outbreaks from 2003 to 2020. Patients with coronavirus infection in the lower and upper respiratory tract could show mild to severe symptoms. In this review, we focus on the relationship between diabetes and three coronaviruses: SARS-CoV, MERS-CoV, and SARS-CoV-2. Keywords: Diabetes; Coronavirus; SARS-CoV; MERS-CoV; SARS-CoV-2
How to cite this article: Navand AH, Soltani S, Moghadami M, Hosseini P, Nasimzadeh S, Zandi M. Diabetes and coronavirus infections (SARS-CoV, MERS-CoV, and SARS-CoV-2). J Acute Dis 2020;9:244-7 |
How to cite this URL: Navand AH, Soltani S, Moghadami M, Hosseini P, Nasimzadeh S, Zandi M. Diabetes and coronavirus infections (SARS-CoV, MERS-CoV, and SARS-CoV-2). J Acute Dis [serial online] 2020 [cited 2021 Apr 19];9:244-7. Available from: http://www.jadweb.org/text.asp?2020/9/6/244/299178 |
1. Introduction | |  |
Diabetes is one of the most common metabolic diseases (a metabolic disorder) with a wide presence around the world[1]. According to new findings, a total of 463 million people worldwide are living with diabetes[2]. Diabetes, an aging-associate disease with a higher prevalence among people aged over 60 years, is considered to be the major cause of microvascular diseases such as retinopathy, nephropathy, and neuropathy[3],[4]. Besides, it has been suggested that the immune system functions, including chemotaxis, phagocytosis, intracellular apoptosis, and respiratory burst can be negatively impacted by hyperglycemia that is the most prominent feature of diabetes[5]. Therefore, diabetic patients are more prone to infectious diseases[6]. As a result, these patients are more likely to develope respiratory infections, especially with more severe disease symptoms[5],[6]. It is worthy to note that the incidence of influenza infection among diabetic patients is 6 times higher than the non-diabetic population. Similarly, the mortality rate of pneumonia or influenza is higher in diabetic patients[7]. In addition, diabetes is associated with an increased risk of viral respiratory diseases such as coronaviruses[8]. Hence, early detection would be an effective strategy in preventing severe complications in diabetic patients.
Coronaviruses are the members of the Coronaviridae. This family is composed of two subfamilies, including Coronavirinae and Torovirinae. The subfamily Coronavirine consists of four genera, known as alpha-coronavirus, beta-coronavirus, gamma-coronavirus, and delta-coronavirus[9]. SARS-CoV, MERS-CoV, and SARS-CoV-2 belong to the beta-coronavirus genus. Coronaviruses can cause illnesses ranging from the common cold to severer respiratory diseases such as severe acute respiratory syndrome (SARS) and Middle East respiratory syndrome (MERS), which are both zoonotic[10],[11],[12]. Researchers have found that MERS-CoV and SARS-CoV are transmitted from camels[13] and civet cats to humans, respectively[14].
SARS-CoV-2 is a member of Coronaviridae, which has caused coronavirus disease 2019 (COVID-19)[15]. COVID-19 was declared a worldwide pandemic by World Health Organization (WHO) on 11 March 2020[16]. Same with SARS-CoV and MERS-CoV, SARS-CoV-2 is a zoonotic virus, and it is transmitted from animals to humans[17]. According to the obtained evidence, the lower respiratory tract is the main target of SARS-CoV-2 infection[18], and it can also affect other organs[19]. Due to the the considerable worldwide concerns about the emergence of novel coronaviruses like SARS-CoV-2, and susceptibility of diabetic patients to viral infections, this review aims to explore the relationship between diabetes and three emerging coronaviruses including SARS-CoV, MERS-CoV, and SARS-CoV-2 .
2. SARS-CoV | |  |
SARS-CoV can cause a viral respiratory disease referred to as SARS[20]. SARS-CoV enters host cells through the binding of it’s spike glycoprotein to angiotensin-converting enzyme 2 (ACE2)[21], ACE2, as a cellular receptor of SARS-CoV, is highly expressed in a variety of cells including alveolar epithelial cells, small superficial enterocytes, and endothelial cells in the heart and kidneys[22]. Studies have indicated that the entry of SARS-CoV into pancreatic islets is mediated by ACE2 that can damage pancreatic beta cells and cause acute diabetes[23]. On the other hand, chronic hyperglycemia in diabetic patients can induce acidosis, which can restrain the phagocytic activity of immune cells. Thus diabetes can be a major cause of death in patients with SARS infection[24]. Furthermore, SARS-CoV infection has a crucial role in the onset of secondary hyperglycemia[25].
3. MERS-CoV | |  |
MERS-CoV was first identified in Saudi Arabia in June 2012[11]. According to surveys, the mortality rate of MERS was approximately 35%[26]. In the early stages, the common symptoms are shortness of breath and other respiratory problems, as well as severe respiratory difficulties, fever, coughing[27], gastrointestinal complications such as diarrhea occur[28]. Human dipeptidyl peptidase 4 (DDP4), which is also known as CD26, is the cell receptor of MERS-CoV. As a type 2 transmembrane protein, DDP4 enzyme is expressed on the surface of a variety of cells, including the immune cells. By affecting the function of the immune cells, DPP4 can modulate the immune system[29]. The expression of this multifunctional enzyme is dysregulated in numerous diseases such diabetes, and it can lead to inflammation in type 2 diabetes via various mechanisms. Therefore, DDP4 has key roles in coronavirus-infection in patients with type 2 diabetes[26],[30]. Some studies showed that DPP4 inhibitors may increase the risk of pneumonia via the suppression of immune system, so the treatment of type 2 diabetes patients with DPP4 is controversial[27],[28],[31],[32]. As mentioned above, MERS-CoV binds to DPP4, the cellular receptor, to enter the host cells through its surface spike (S) protein. The viral entry is subsequently followed by the membrane fusion of the virus and the host cell[33]. A study conducted on diabetic rats infected with MERS-CoV showed delayed and prolonged inflammatory response in their lungs[34]. It also indicated a decrease in inflammatory cytokines, macrophages, and T cells in diabetic mice[35]. Thus, it can be proposed that diabetes can cause the dysfunction of the immune system so that the immune system fails to respond to infections. This may explain why diabetic patients are susceptible to severe MERS-CoV infections and are more prone to severe influenza, pneumonia, and other respiratory infections. The increase in the severity of the disease in diabetic mice infected by MERS virus can be attributed to an unregulated immune response which leads to a more severe and prolonged lung pathology[34]. Overall, MERS-CoV has close association with diabetes.
4. SARS-CoV-2 | |  |
SARS-CoV-2 induced COVID-19 is an ongoing pandemic, which has raised worldwide concern. SARS-CoV-2 is a new member of the Coronaviridae family and belongs to the genus beta-coronavirus[36],[37]. Malaise, fever, dry cough, and shortness of breath are the main signs of COVID-19, but a runny nose, headache, diarrhea, and sore throat are less prevalent. Other complications of the COVID-19 include acute respiratory distress syndrome, acute heart damage, secondary infections, abnormal clotting, sepsis, damages to the liver, and kidneys[38].
SARS-CoV-2, like SARS-CoV, employs the same receptor to enter the target cell where the virus replicates and spreads into other cells in the respiratory tract[36]. SARS-CoV-2 and SARS-CoV share a sequence similarity of 76% in their S proteins. SARS-CoV-2 binds to ACE2 through S glycoprotein[39]. The spike glycoprotein of SARS-CoV-2 is a structural protein which consists of two subdomains:, including S1 and S2. The sequence of the S1 domain is variable and plays a role in binding to ACE2, and the S2 domain with a conserved sequence integrates the viral membrane into the cell membrane[39]. It has been shown that amino acid 493 in the receptor-binding domain of S glycoprotein plays an important role in ACE2 binding[40],[41].
According to the available data from the WHO, the mortality rate of COVID-19 is estimated between 3%-4% and almost 80% of death cases aged over 60 years, and 75% of them had underlying health conditions such as diabetes[42]. In fact, diabetes down-regulates the immune system functions, and it is considered to be a risk factor for exacerbation of COVID-19 disease.
5. Association between diabetes, SARS, MERS, and COVID-19 | |  |
It has been suggested that the cellular receptors are crucial factors in the association between diabetes mellitus (DM) and coronavirus infections including SARS, MERS, and COVID-19[43],[44]. In addition, age is another risk factor for coronavirus diseases since age affects the expression and distribution of ACE2[44]. The regulation of ACE2 is important considering the relationship between the expression of ACE2 and the development of coronavirus diseases in individuals with diabetes[45],[46]. The expression of ACE2 is increased in the early phase of DM, however, it is down-regulated in the later phases of this disease[45],[47].
With regard to the fixation and expression of the ACE2 receptor in the endocrine, such as the pancreas, SARS-CoV-1 penetrates islets via ACE2 receptor and devastates islets, which results in acute diabetes[26]. Studies showed that history of diabetes and hyperglycemia were associated with the mortality and morbidity rate of SARS-CoV patients. As a result, metabolic disorders checkup, such as diabetes, is recommended to be listed in the follow-up of SARS-CoV patients[48].
A meta-analysis suggested that diabetes is predominant in roughly 50% of the MERS-CoV patients[48]. Furthermore, diabetes can be related etiologically to the pathogenesis of MERS-CoV[49]. Diabetes, hyperglycemia, and insulinopenia can inhibit the synthesis of interferon-gamma and interleukins[50] and aggravates the MERS-CoV infection[34]. In addition, other studies proposed that the severity condition of MERS-CoV in the lung is associated with diabetes and dysregulation of the immune response[34].
According to surveys, prevalence of diabetes among COVID-19 patients is about 9.7%[51]. Results of studies confirmed that underlying diseases such as diabetes can influence the pathogenesis of COVID-19 due to the weakness in the innate immune response[50].
6. Conclusion | |  |
Diabetes is a common metabolic disease, which can down-regulate the immune system. It has been shown that age, an impaired immune status, and uncontrolled glycemia can affect the susceptibility and severity of coronaviruse infections among patients with diabetes. As mentioned above, coronaviruses such as SARS-CoV, MERS-CoV, and SARS-CoV-2 can cause damage to the pancreas, so coronavirus infections are more dangerous for patients with diabetes. As a consequence, diabetic patients ought to be included in vaccination proposals for flu and SARS-CoV-2.
Conflict of interest statement
The authors report no conflict of interest.
Authors’ contributions
M.Z. designed the study; A.H.N., S.S. and M.M. collected all data; P.H. and S.N. drafted the manuscript; and all authors commented on the drafts of the manuscript and approved the final draft of the paper.
References | |  |
1. | Association AD. Diagnosis and classification of diabetes mellitus. Diabetes Care 2014; 37(Supplement 1): S81-S90. |
2. | Saeedi P, Petersohn I, Salpea P, Malanda B, Karuranga S, Unwin N, et al. Global and regional diabetes prevalence estimates for 2019 and projections for 2030 and 2045: Results from the international diabetes federation diabetes atlas. Diabetes Res Clin Pract 2019; 157: 107843. |
3. | Fowler MJ. Microvascular and macrovascular complications of diabetes. Clin Diabetes 2011; 29(3): 116-122. |
4. | Kirkman MS, Briscoe VJ, Clark N, Florez H, Haas LB, Halter JB, et al. Diabetes in older adults. Diabetes Care 2012; 35(12): 2650-2664. |
5. | Xiu F, Stanojcic M, Diao L, Jeschke MG. Stress hyperglycemia, insulin treatment, and innate immune cells. Int J Endocrinol 2014; 2014: 486403. |
6. | Casqueiro J, Casqueiro J, Alves C. Infections in patients with diabetes mellitus: A review of pathogenesis. Indian J Endocrinol Metab 2012; 16(Suppl1): S27-36. |
7. | Klekotka RB, Mizgala E, Król W. The etiology of lower respiratory tract infections in people with diabetes. Pneumonol Alergol Pol 2015; 83(5): 401-408. |
8. | Fang L, Karakiulakis G, Roth M. Are patients with hypertension and diabetes mellitus at increased risk for COVID-19 infection? Lancet Resp Med 2020; 8(4): e21. |
9. | Ashour HM, Elkhatib WF, Rahman M, Elshabrawy HA. Insights into the recent 2019 novel Coronavirus (SARS-COV-2) in light of past human coronavirus outbreaks. Pathogens 2020; 9(3): 186. |
10. | Fung SY, Yuen KS, Ye ZW, Chan CP, Jin DY. A tug-of-war between severe acute respiratory syndrome coronavirus 2 and host antiviral defence: lessons from other pathogenic viruses. Emerg Microbes Infect 2020; 9(1): 558-570. |
11. | Zumla A, Hui DS, Perlman S. Middle East respiratory syndrome. Lancet 2015; 386(9997): 995-1007. |
12. | Ghinai I, McPherson TD, Hunter JC, Kirking HL, Christiansen D, Joshi K, et al. First known person-to-person transmission of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in the USA. Lancet 2020; 395(10230): 1137-1144. |
13. | Hemida MG. Middle East respiratory syndrome coronavirus and the one health concept. PeerJ 2019; 7: e7556. |
14. | Cheng VC, Lau SK, Woo PC, Yuen KY. Severe acute respiratory syndrome coronavirus as an agent of emerging and reemerging infection. Clin Microbiol Rev 2007; 20(4): 660-694. |
15. | Sanami S, Zandi M, Pourhossein B, Mobini GR, Safaei M, Abed A, et al. Design of a multi-epitope vaccine against SARS-CoV-2 using immunoinformatics approach. Int J Biol Macromol 2020; 164: 871-883. |
16. | Cucinotta D, Vanelli M. WHO declares COVID-19 a pandemic. Acta Biomed 2020; 91(1): 157-160. |
17. | Ye ZW, Yuan S, Yuen KS, Fung SY, Chan CP, Jin DY. Zoonotic origins of human coronaviruses. Int J Biol Sci 2020; 16(10): 1686-1697. |
18. | Cascella M, Rajnik M, Cuomo A, Dulebohn SC, Di Napoli R. Features, evaluation and treatment Coronavirus (COVID-19). [Online] Available from: https://pubmed.ncbi.nlm.nih.gov/32150360/. [Accessed on 01 March 2020]. |
19. | Wang T, Du Z, Zhu F, Cao Z, An Y, Gao Y, et al. Comorbidities and multi-organ injuries in the treatment of COVID-19. Lancet 2020; 395(10228): e52. |
20. | Peiris JS, Yuen KY, Osterhaus AD, Stöhr K. The severe acute respiratory syndrome. New Engl J Med 2003; 349(25): 2431-2441. |
21. | Fani M, Teimoori A, Ghafari S. Comparison of the COVID-2019 (SARS-CoV-2) pathogenesis with SARS-CoV and MERS-CoV infections. Future Virol 2020. 10.2217/fvl-2020-0050. |
22. | Wang H, Yang P, Liu K, Guo F, Zhang Y, Zhang G, et al. SARS coronavirus entry into host cells through a novel clathrin-and caveolae-independent endocytic pathway. Cell Res 2008; 18(2): 290-301. |
23. | Yang JK, Lin SS, Ji XJ, Guo LM. Binding of SARS coronavirus to its receptor damages islets and causes acute diabetes. Acta Diabetolog 2010; 47(3): 193-199. |
24. | Lecube A, Pachón G, Petriz J, Hernández C, Simó R. Phagocytic activity is impaired in type 2 diabetes mellitus and increases after metabolic improvement. PloS One 2011; 6(8): e23366. |
25. | |
26. | Banik G, Khandaker G, Rashid H. Middle East respiratory syndrome coronavirus “MERS-CoV”: current knowledge gaps. Paediatr Respir Rev 2015; 16(3): 197-202. |
27. | Mardani M. Resurgence of Middle East Respiratory Syndrome Coronavirus outbreak in Saudi Arabia. Arch Clin Infect Dis 2015; 10(3): e31466. |
28. | Yeo C, Kaushal S, Yeo D. Enteric involvement of coronaviruses: is faecal-oral transmission of SARS-CoV-2 possible? Lancet Gastroenterol Hepatol 2020; 5(4):335-337. |
29. | Silva Júnior WS, Godoy-Matos AF, Kraemer-Aguiar LG. Dipeptidyl peptidase 4: a new link between diabetes mellitus and atherosclerosis? BioMed Res Int 2015; 2015: 816164. |
30. | Iacobellis G. COVID-19 and diabetes: Can DPP4 inhibition play a role? Diabetes Res Clin Pract 2020; 162: 108125. |
31. | Males VK. Letter to the editor in response to the article “COVID-19 and diabetes: Can DPP4 inhibition play a role?”. Diabetes Res Clin Pract 2020; 163: 108163. |
32. | Raj VS, Mou H, Smits SL, Dekkers DH, Müller MA, Dijkman R, et al. Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMC. Nature 2013; 495(7440): 251-254. |
33. | Du L, Yang Y, Zhou Y, Lu L, Li F, Jiang S. MERS-CoV spike protein: a key target for antivirals. Expert Opin Ther Targets 2017; 21(2): 131-143. |
34. | Kulcsar KA, Coleman CM, Beck SE, Frieman MB. Comorbid diabetes results in immune dysregulation and enhanced disease severity following MERS-CoV infection. JCI Insight 2019; 4(20): e131774. |
35. | Xia C, Rao X, Zhong J. Role of T lymphocytes in type 2 diabetes and diabetes-associated inflammation. J Diabetes Res 2017; 2017: 6494795. |
36. | Poortahmasebi V, Zandi M, Soltani S, Jazayeri SM. Clinical performance of RT-PCR and chest CT scan for COVID-19 diagnosis; a systematic review. Advanced J Emerg Med 2020; 4(2s): e57. |
37. | Zhu N, Zhang D, Wang W, Li X, Yang B, Song J, et al. A novel coronavirus from patients with pneumonia in China, 2019. New Engl J Med 2020; 382(8): 727-733. |
38. | 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(10223): 497-506. |
39. | Walls AC, Park YJ, Tortorici MA, Wall A, McGuire AT, Veesler D. Structure, function, and antigenicity of the SARS-CoV-2 spike glycoprotein. Cell 2020; 181(2): 281-292. |
40. | Chen Y, Guo Y, Pan Y, Zhao ZJ. Structure analysis of the receptor binding of 2019-nCoV. Biochem Biophysical Res Commun 2020; 525(1): 135-140. |
41. | Lai CC, Shih TP, Ko WC, Tang HJ, Hsueh PR. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and corona virus disease-2019 (COVID-19): the epidemic and the challenges. Int J Antimicrob Agents 2020; 55(3): 105924. |
42. | |
43. | Guo W, Li M, Dong Y, Zhou H, Zhang Z, Tian C, et al. Diabetes is a risk factor for the progression and prognosis of COVID-19. Diabetes Metab Res Rev 2020; e3319. doi.org/10.1002/dmrr.3319. |
44. | Pal R, Bhansali A. COVID-19, diabetes mellitus and ACE2: The conundrum. Diabetes Res Clin Pract 2020; 162: 108132. |
45. | Batlle D, Soler MJ, Ye M. ACE2 and diabetes: ACE of ACEs? Diabetes 2010; 59(12): 2994-2996. |
46. | Patel VB, Parajuli N, Oudit GY. Role of angiotensin-converting enzyme 2 (ACE2) in diabetic cardiovascular complications. Clin Sci 2014; 126(7): 471-482. |
47. | Marhl M, Grubelnik V, Magdi M, Markovi R. Diabetes and metabolic syndrome as risk factors for COVID-19. Diabetes Metab Syndr 2020; 14(4): 671-677. |
48. | Yang J, Feng Y, Yuan M, Yuan S, Fu H, Wu B, et al. Plasma glucose levels and diabetes are independent predictors for mortality and morbidity in patients with SARS. Diabet Med 2006; 23(6): 623-628. |
49. | Badawi A, Ryoo SG. Prevalence of comorbidities in the Middle East respiratory syndrome coronavirus (MERS-CoV): a systematic review and meta-analysis. Int J Infect Dis 2016; 49: 129-133. |
50. | Odegaard JI, Chawla A. Connecting type 1 and type 2 diabetes through innate immunity. Cold Spring Harb Perspect Med 2012; 2(3): a007724. |
51. | Yang J, Zheng Y, Gou X, Pu K, Chen Z, Guo Q, et al. Prevalence of comorbidities and its effects in patients infected with SARS-CoV-2: a systematic review and meta-analysis. Int J Infect Dis 2020; 94: 91-95. |
|