Volume 12, Issue 1 (Jan-Feb 2018)                   mljgoums 2018, 12(1): 6-10 | Back to browse issues page


XML Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Ghane M. Investigation of Frequency of Herpes Simplex Virus in Patients with Type 2 Diabetes and Healthy Individuals by PCR and ELISA. mljgoums 2018; 12 (1) :6-10
URL: http://mlj.goums.ac.ir/article-1-1044-en.html
Department of Microbiology, Islamic Azad University, Tonekabon Branch, Tonekabon, Iran
Abstract:   (18006 Views)
 
ABSTRACT
        Background and Objectives: Previous studies have demonstrated the relationship between viral infections and risk of developing type 1 diabetes. The aim of this study was to investigate the frequency of Herpes simplex virus (HSV) in patients with type 2 diabetes and healthy control individuals using PCR and ELISA.
          Methods: Blood samples were taken from 180 diabetic patients and 187 healthy controls referred to the Pasteur medical laboratory in Tonekabon, in 2016. Human beta-globin gene was used as internal control to ensure extraction accuracy. Specific primers were used for amplification of the UL30 gene. In addition, level of anti-HSV IgG antibody was measured using a commercial ELISA kit (Euroimmun, Germany).
         Results: DNA of HSV was found in the samples of 11 patients (6.1%) and five healthy controls (2.7%). In addition, anti-HSV IgG was found in the samples of 117 patients (65%) and 108 healthy controls (57.75%). There was a statistically significant relationship between frequency of anti-HSV IgG and diabetes.
          Conclusion: Similar to previous studies, the present study demonstrated a relationship between frequency of HSV infection and type 2 diabetes. However, further studies should be performed to eliminate the effect of other risk factors to help clarify the exact role of viral infections in increasing the risk of diabetes.
            Keywords: Diabetes, Herpes Simplex Virus, ELISA, PCR.
 
Full-Text [PDF 345 kb]   (2009 Downloads)    
Research Article: Original Paper |
Received: 2018/02/19 | Accepted: 2018/02/19 | Published: 2018/02/19 | ePublished: 2018/02/19

References
1. Precechtelova J, Borsanyiova M, Sarmirova S, and Bopegamage S. Type I Diabetes Mellitus: Genetic Factors and Presumptive Enteroviral Etiology or Protection. Journal of Pathogens. 2014; 738: 512-521. [DOI:10.1155/2014/738512]
2. Qiu YH, Deng FY, Li MJ, Lei SF. Identification of novel risk genes associated with type 1 diabetes mellitus using a genome-wide gene-based association analysis. Journal of Diabetes Investigation. 2014; 13(2): 435-439. doi: 10.1111/jdi.12228. [DOI:10.1111/jdi.12228]
3. Sadeharju K, Hämäläinen AM, Knip M, Lönnrot M, Koskela P, Virtanen SM, et al. Enterovirus infections as a risk factor for type I diabetes: virus analyses in a dietary intervention trial. Clinical and Experimental Immunology. 2003; 132(2): 271–277. [DOI:10.1046/j.1365-2249.2003.02147.x]
4. Lönnrot M, Salminen K, Knip M, Savola K, Kulmala P, Leinikki P, et al. Enterovirus RNA in serum is a risk factor for beta-cell autoimmunity and clinical type 1 diabetes: a prospective study. Childhood Diabetes in Finland (DiMe) Study Group. Journal of Medical Virology. 2000; 61(2): 214-220. https://doi.org/10.1002/(SICI)1096-9071(200006)61:2<214::AID-JMV7>3.0.CO;2-9 [DOI:10.1002/(SICI)1096-9071(200006)61:23.0.CO;2-9]
5. Oikarinen S, Tauriainen S, Hober D, Lucas B, Vazeou A, Sioofy-Khojine A, et al. Virus antibody survey in different european populations indicates risk association between coxsackievirus B1 and type 1 diabetes. Diabetes. 2014; 63(2): 655-662. [DOI:10.2337/db13-0620]
6. Ginsberg-Fellner F, Witt ME, Fedun B, Taub F, Dobersen MJ, McEvoy RC, et al. Diabetes Mellitus and Autoimmunity in Patients with the Congenital Rubella Syndrome. Reviews of Infectious Diseases. 1995; 7(1): S170-S176.
7. Honeyman MC, Coulson BS, Stone NL, Gellert SA, Goldwater PN, Steele CE, et al. Association between rotavirus infection and pancreatic islet autoimmunity in children at risk of developing type 1 diabetes. Diabetes. 2000; 49(8): 1319-1324. [DOI:10.2337/diabetes.49.8.1319]
8. Hyöty H, Leinikki P, Reunanen A, Ilonen J, Surcel HM, Rilva A, et al. Mumps infections in the etiology of type 1 (insulin-dependent) diabetes. Diabetes Res. 1988; 9(3): 111-116.
9. Aarnisalo J, Veijola R, Vainionpää R, Simell O, Knip M, and Ilonen J. Cytomegalovirus infection in early infancy: risk of induction and progression of autoimmunity associated with type 1 diabetes. Diabetologia. 2008; 51(5): 769-772. doi: 10.1007/s00125-008-0945-8. [DOI:10.1007/s00125-008-0945-8]
10. Nassaji-Zavareh M, Taheri R, Ghorbani R, Aminian M. Undiagnosed Diabetes Mellitus in Patients with Herpes Zoster. Indian J Dermatol. 2008; 53(3): 119-121. [DOI:10.4103/0019-5154.43211]
11. Ryan KJ, Ray CG. Sherris Medical Microbiology. 4thed. McGraw Hill; 2004.
12. Najafi S, Ghane M, Yousefzadeh-Chabok S, Amiri M. The High Prevalence of the Varicella Zoster Virus in Patients with Relapsing-Remitting Multiple Sclerosis: A Case-Control Study in the North of Iran. Jundishapur J Microbiol. 2016; 9(3): 34158. doi: 10.5812/jjm.34158. [DOI:10.5812/jjm.34158]
13. Zaravinos A, Bizakis J, Spandidos A. Prevalence of papilloma virus and Human Herpes virus Type 1-7 in Human Nasal Polyposis. Journal of Medical Virology. 2009; 81(9):1613-1618. [DOI:10.1002/jmv.21534]
14. Azimi-Nezhad M, Ghayour-Mobarhan M, Parizadeh MR, Safarian M, Esmaeili H, Parizadeh SM, et al. Prevalence of type 2 diabetes mellitus in Iran and its relationship with gender, urbanisation, education, marital status and occupation. Singapore Med J. 2008; 49(7): 571-6.
15. Sun Y, Pei A, Wu Y, Yang Y. HSV-1 infection with Type 2 diabetes. Diabetes care. 2005; 13(2): 435-436. [DOI:10.2337/diacare.28.2.435]
16. Pak CY, Mcarthur RG, Eun, HM, Yoon JW. Association of cytomegalovirus infection with autoimmune type 1 diabetes. Lancet. 1988; 12(4): 134-139. [DOI:10.1016/S0140-6736(88)92941-8]
17. Guo T, Jia H. Epidemilogic study of cytomegalo virus infection in patients with diabetes mellitus. Zhonghua Liu Xing Bing Xue Za Zhi. 1998; 19(5): 274-276.
18. Nordal KP, Jenssen T, Hjelmesaeth J, Sagedal S, Hartmann A, et al. Asymptomatic cytomegalovirus infection is associated increased risk of new-onset diabetes mellitus and impaired insulin release after renal. Diabetologica. 2004; 47(9): 1550-1556. [DOI:10.1007/s00125-004-1499-z]
19. Roberts BW, Cech I. Association of type 2 diabetes mellitus and sero prevalence for CMV. South Med J. 2005; 98(7): 686-692. DOI:10.1097/01.SMJ.0000163310.12516.2D [DOI:10.1097/01.SMJ.0000163310.12516.2D]
20. Chen S, Decraen AJ, Raz Y, Derhovanessian E, Vossen AC, westendrop RG, et al. Cytome galovirus seropositivity is associated with glucose regulation in the oldest old. Results from the leiden 85-plus study. Immunity. 2012; 8(9): 18-24 Immun Ageing. 2012; 9(1): 18. doi: 10.1186/1742-4933-9-18. [DOI:10.1186/1742-4933-9-18]

Add your comments about this article : Your username or Email:
CAPTCHA

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2007 All Rights Reserved | Medical Laboratory Journal

Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.