Display options
Share it on

Jundishapur J Microbiol. 2016 Jul 03;9(7):e37329. doi: 10.5812/jjm.37329. eCollection 2016 Jul.

The Prevalence of SEN Virus and Occult Hepatitis B (OBI) Virus Infection Among Blood Donors in Ahvaz City.

Jundishapur journal of microbiology

Samaneh Abbasi, Manoochehr Makvandi, Gharib Karimi, Niloofar Neisi

Affiliations

  1. Health Research Institute, Infectious and Tropical Disease Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, IR Iran; Department of Virology, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, IR Iran.
  2. Iranian Blood Transfusion Organization (IBTO), Tehran, IR Iran.
  3. Department of Virology, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, IR Iran.

PMID: 27679708 PMCID: PMC5035438 DOI: 10.5812/jjm.37329

Abstract

BACKGROUND: The SEN virus (SENV) is a prevalent blood borne pathogen that has a worldwide incidence. SENV is comprised of eight genotypes; genotypes H and D are frequently associated with the pathogenesis of non-A - E hepatitis and post-transfusion hepatitis in blood donors and hepatitis patients. So far, no SENV pathogenesis has been reported in the liver biopsies of SENV carriers, but the frequency of SENV and its related genotypes requires further molecular epidemiology studies in different regions of the world. Occult hepatitis B infection (OBI) is another global public health problem that is primarily transmitted via blood transfusions. Therefore, the identification of OBI among blood donors is key to preventing the spread of this disease. The relationship between SENV and OBI requires further evaluation.

OBJECTIVES: The aim of this study was to determine the prevalence of SENV-D and SENV-H in blood donors in Ahvaz city with a particular focus on co-infection with OBI.

PATIENTS AND METHODS: This study had a cross-sectional design and included 184 healthy consecutive blood donors who visited a blood transfusion center in Ahvaz city from October-November 2013. The sera of all blood donors negative for HBsAg, anti-HCV antibody, and anti-HIV antibody were tested for SENV-D and SENV-H using nested polymerase chain reaction (PCR). In addition, tests for HBV DNA (PCR), HBcIgG (ELISA), liver function (aspartate transaminase and alanine transaminase), and alkaline phosphatase were carried out.

RESULTS: Liver function tests in the healthy blood donors were within the normal range. The incidence rates of SENV-D and SENV-H in the 184 total blood donors were 10 (5.4%) (95% confidence interval (CI): 2.1% - 9.0%) and 32 (17.4%) cases (95% CI: 12.0% - 23.0%), respectively. SENV-H/D co-infection occurred in 2 (1.1%) patients. The sera of 8/184 (4.3%) were positive for anti-HBc antibody but negative for HBV DNA.

CONCLUSIONS: Regardless of the presence of nonpathogenic SENV, 44/184 (24%) blood donors tested positive for both SENV-D and SENV-H. Although 4.3% of blood donors were positive for HBcIgG but negative for HBV DNA, the presence of OBI cannot be ruled out unless their liver biopsies show negative for HBV DNA.

Keywords: Blood Donor; Chronic Hepatitis B Infection; Polymerase Chain Reaction; SEN Virus; Transfusion Transmitted Virus

References

  1. J Med Virol. 2002 Sep;68(1):18-23 - PubMed
  2. Transfusion. 2010 Jan;50(1):221-30 - PubMed
  3. Transfusion. 2005 Jul;45(7):1084-8 - PubMed
  4. Transfusion. 2009 Oct;49(10):2214-20 - PubMed
  5. Turk J Gastroenterol. 2008 Jun;19(2):104-8 - PubMed
  6. Curr Opin Hematol. 2011 Nov;18(6):461-6 - PubMed
  7. J Infect Dis. 1991 Feb;163(2):397-9 - PubMed
  8. Virus Res. 2004 Mar 15;100(2):223-8 - PubMed
  9. World J Gastroenterol. 2004 Aug 15;10(16):2402-5 - PubMed
  10. J Infect Dis. 1999 May;179(5):1070-6 - PubMed
  11. J Gastroenterol. 2003;38(2):142-8 - PubMed
  12. Arch Virol Suppl. 1992;4:116-8 - PubMed
  13. J Infect Dis. 1999 Nov;180(5):1748-50 - PubMed
  14. Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi. 2000 Mar;14(1):77-9 - PubMed
  15. J Hepatol. 2009 Oct;51(4):798-809 - PubMed
  16. World J Gastroenterol. 2008 Jul 14;14(26):4204-8 - PubMed
  17. J Infect Dis. 2003 Nov 15;188(10):1545-52 - PubMed
  18. J Clin Microbiol. 2002 Sep;40(9):3140-5 - PubMed
  19. Pathog Glob Health. 2014 Jul;108(5):223-8 - PubMed
  20. Medscape J Med. 2008;10(12):290 - PubMed
  21. J Clin Virol. 2003 May;27(1):69-73 - PubMed
  22. Hepatology. 2001 May;33(5):1303-11 - PubMed
  23. Lancet Infect Dis. 2002 Aug;2(8):479-86 - PubMed
  24. Ann Hepatol. 2011 Apr-Jun;10(2):133-41 - PubMed
  25. Antiviral Res. 2003 Sep;60(1):27-33 - PubMed
  26. J Viral Hepat. 2002 Jul;9(4):243-57 - PubMed
  27. J Gastroenterol Hepatol. 2009 Apr;24(4):588-98 - PubMed
  28. Arch Iran Med. 2008 Jul;11(4):423-6 - PubMed
  29. Nephrol Dial Transplant. 2003 Feb;18(2):348-52 - PubMed
  30. World J Gastroenterol. 2014 May 28;20(20):5951-61 - PubMed
  31. J Infect Dis. 2001 Aug 15;184(4):400-4 - PubMed
  32. Virol J. 2010 Jan 02;7:1 - PubMed
  33. Virol J. 2010 Aug 27;7:204 - PubMed
  34. J Infect Dis. 2002 Feb 1;185(3):389-92 - PubMed

Publication Types