Seroprevalence of Hepatitis A and E Virus Infections Among Healthy Population in Shiraz, Southern Iran

authors:

avatar Sadaf Asaei 1 , avatar Mazyar Ziyaeyan 1 , * , avatar Mahsa Moeini 1 , avatar Marzieh Jamalidoust 1 , 2 , avatar Mohammad Amin Behzadi 1

Department of Virology, Professor Alborzi Clinical Microbiology Research Center, Nemazi Hospital, Shiraz University of Medical Sciences, Shiraz, IR Iran
Department of Medical Virology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, IR Iran

how to cite: Asaei S, Ziyaeyan M, Moeini M, Jamalidoust M, Behzadi M A. Seroprevalence of Hepatitis A and E Virus Infections Among Healthy Population in Shiraz, Southern Iran. Jundishapur J Microbiol. 2015;8(7):e19311. https://doi.org/10.5812/jjm.19311v2.

Abstract

Background:

Enterically-transmitted acute viral hepatitis is caused predominantly by hepatitis A virus (HAV) and hepatitis E virus (HEV). The prevalence of HEV and HAV infections varies in different geographical regions.

Objectives:

This study was conducted to determine the prevalence of HEV and HAV infections among Iranian healthy individuals in southern Iran.

Patients and Methods:

Totally, 1030 samples were collected from healthy subjects in schools, those referred to tertiary outpatient clinics and health centers in Shiraz between November 2011 and May 2012. Their ages ranged between six months and 95 years. The presence of total anti-HAV and anti-HEV immunoglobulin M (IgM) in plasma was assessed by ELISA.

Results:

The results showed that 66.2% and 0.6% of the general population in this area were positive for total anti-HAV and IgM antibodies by ELISA, respectively. As seen, 13.4% and 0.9% were positive for total anti-HEV and IgM antibodies, respectively. The difference in total anti-HAV and anti-HEV antibodies was significant among the age groups (P < 0.001).

Conclusions:

This study showed that the prevalence rates of HAV and HEV antibodies were positively correlated with age. The results demonstrated that the infection with these two viruses in the region was high and some high-risk individuals including females at child-bearing age were more susceptible. HAV vaccination could be recommended for antibody-negative adults.

1. Background

Hepatitis A virus (HAV) is a single-strand RNA virus belonging to Picornaviridae with 7500 b length. Its genome consists of a single open reading frame (ORF) which encodes a polyprotein, divided into three regions (P1-P3). P1 encodes four structural proteins and P2-P3 encode seven nonstructural proteins (1). The incubation period of this acute infection is 2 - 6 weeks (2).

HAV infection is a considerable hygienic problem in developing countries with low socioeconomic conditions, especially among some specific populations such as injection drug abusers and patients with clotting factors disorders. This infection is transmitted person to person through fecal-oral route (3, 4). Seafood can be a common HAV infection source if not cooked well. The pattern and prevalence of HAV infection vary greatly in different geographical regions and different populations. Seroepidemiological studies have shown that the prevalence of HAV is closely associated with economic and cultural status (5). Its incidence rate in the world ranges from as low as 13% in Scandinavian countries to nearly 100% in developing countries such as those in Asia, Africa and South America (3). In European countries, HAV incidence in the north is lower than that in the south (2). Therefore, performing serological test seems to be necessary in our region.

Hepatitis E virus (HEV), a small nonenveloped RNA virus and a member of Caliciviridae, is similar to HAV, whose main route of transmission is fecal-oral and through contaminated water in developing nations. Unlike HAV, HEV may be a zoonotic disease, especially in industrialized nations (6). It has a worldwide distribution and is endemic in Asia, Africa, Middle East and Central America (7), while its outbreak mostly occurs in rainy seasons and in overcrowding (8). HEV infection can be more severe in pregnant women with average of fatality reported to be 25% among them (7). Iran is notably located in the HEV endemic areas (9).

2. Objectives

Considering the facts that HAV and HEV are food and waterborne pathogens with the same routes of transmission and mechanisms of spread, causing similarly severe epidemics, the present seroepidemiological study of HAV and HEV infections aimed to determine the prevalence of such infections among different age groups in Shiraz, southern Iran. By doing so, some ways of controlling the infections and preventing new outbreaks, especially among susceptible age groups and mainly pregnant women, could be found within the age range of 15 - 44 years. To the best of the authors’ knowledge, very few studies have been carried out so far on such a wide age group (six months-95 years), as conducted in this study.

3. Patients and Methods

3.1. Study Population and Sampling

Five milliliters of blood was collected from each of 1100 participants, of whom 70 were excluded on account of an ongoing infectious disease. Of the 1030 participants whose blood samples were analyzed, 674 were referred to tertiary outpatient clinics for routine medical check-ups, while the rest (356 individuals) were either school students or referrals from health centers. This second group aged six months to 15 years. The study was conducted from November 2011 to May 2012 in Shiraz, southern Iran. The age range of the present population was between six months and 95 years (mean ± SD: 6.510 ± 4.502), consisting of 725 females and 305 males. The blood samples were centrifuged at 1000 rpm for 10 minutes at 4°C and the plasmas were separated and stored at 20°C until the examination time. The design of the study was approved by the Research Ethics Committee at Professor Alborzi Clinical Microbiology Research Center, ref No. 91-10, Shiraz University of Medical Sciences, Shiraz, Iran. Informed consents were obtained from the participants or their legal guardians. Total antibodies and immunoglobulin M (IgM) against HAV and HEV were determined using commercial ELISA kits (Dia. Pro Diagnostic Bioprobes, Milan, Italy). The testing procedure was based on the manufacturer’s protocols and sensitivity and specificity of the assays were both 98%. Intermediate test results were checked twice; if in the second round the results were again within the gray zone, the upper limit was considered as positive and lower limit as negative.

3.2. Statistical Analysis

The differences between HAV and HEV total antibodies and HAV and HEV IgM among different age groups and genders were analyzed by SPSS software (version 16, SPSS Inc. Chicago, Illinois). P value of less than 0.05 was considered significant.

4. Results

Among 1030 individuals, 682 (66.2%), 6 (0.6%), 138 (13.4%) and 9 (0.9%) were positive for anti-HAV total antibodies, anti-HAV IgM, anti-HEV total antibodies and anti-HEV IgM, respectively (Figure 2). The results showed that 113 (10.9%) were positive for both HAV and HEV total antibodies. From all the participants, 356 (34.5%) were children (≤ 15 years old) and 674 (65.4%) were adults (≥ 16 years old). In the children group, 65 (18.3%) and 0 (0.0%) were positive for anti-HAV total antibodies and anti-HAV IgM, respectively. In addition, 27 (7.6%) and 2 (0.6%) were positive for anti-HEV total antibodies and anti-HEV IgM, respectively. In the adults group, 617 (95.3%) were positive for anti-HAV total antibodies, 6 (0.9%) for anti-HAV IgM, 111 (17.15%) for anti-HEV total antibodies, and 7 (1.08%) for anti-HEV IgM. Positive rates in different age groups in terms of antibodies are presented in Table 1. The difference in the prevalence of positive anti-HAV total antibodies and anti-HEV total antibodies was statistically significant among the age groups (P < 0.001); however, it was not significant for HAV IgM and HEV IgM (P > 0.05, Figure 1). In addition, the prevalence rates of positive anti-HAV total antibodies, anti-HAV IgM, anti-HEV total antibodies and anti-HEV IgM were not significantly different between genders (Table 2).

Table 1.

The Prevalence of Hepatitis A Virus and Hepatitis E Virus Antibodies in Different Age Groups a,b

6-15 (n = 356)16-29 (n = 170)30-55 (n = 333)≥ 56 (n = 171)Total (n = 1030)P Value
HAV Total Antibodies65 (18.3)135 (79.4)314 (94.3)168 (98.2)682 (66.2)0.001
HAV IgM0 (0.00)1 (0.6)3 (0.9)2 (1.2)6 (0.6)0.297
HEV Total Antibodies27 (7.6)25 (14.7)54 (16.2)32 (18.7)138 (13.4)0.001
HEV IgM2 (0.6)1 (0.6)2 (0.6)4 (2.3)9 (0.9)0.166
The Prevalence of Hepatitis A Virus and Hepatitis E Virus in Different Age Groups
The Prevalence of Hepatitis A Virus and Hepatitis E Virus in Different Age Groups
Table 2.

The Prevalence of Hepatitis A Virus and Hepatitis E Virus Antibodies in Different Gender Groups a,b

Male (n = 305)Female (n = 725)Total
HAV Total Antibodies121 (95.3)361 (95.8)482 (95.6)
HAV IgM1 (0.8)4 (1.1)5 (1)
HEV Total Antibodies20 (15.7)66 (17.5)86 (17.1)
HEV IgM2 (1.6)4 (1.1)6 (1.2)
The Prevalence of Hepatitis A Virus and Hepatitis E Virus Total Antibodies in Different Age Groups
+*: HAV total antibodies (P = 0.001); #: HEV total antibodies (P = 0.001).

5. Discussion

HAV and HEV are among the causative agents of acute hepatitis and global health problems in developed and developing countries (10, 11). In endemic regions, over 80% of the population carry anti-HAV antibodies, whereas the level of anti-HEV antibodies is lower in the same population (12). To the best of knowledge, few studies have been conducted on determining the seroprevalence rates of HAV and HEV infections in southern Iran (13). This study had a unique feature of a wider age range in the studied population. IgM indicates current infections, but there might be IgM-positive individuals who are asymptomatic. These subjects can act as a major source of infection and transmit it to other healthy people, leading to the emergency of HAV and HEV epidemics within the community. In comparison with the present study, other ones have been very limited in terms of number of participants, age groups, and simultaneous detection of both HAV and HEV antibodies.

A previous study in Fars province, southern Iran, indicated that 88.2% of the general population carried anti-HAV antibodies (13). Another study carried out in three other provinces, i.e. Golestan, (northern Iran), Tehran, (central Iran), and Hormozgan, (southern Iran), showed that the seroprevalence rates of HAV were 99%, 85%, and 96%, respectively (14). In the current study, 66.2% were positive for anti-HAV antibodies and as one of the main routes of transmission for HAV and HEV among general the population is food and water hygiene (15), improving the hygiene program in our region can help eradicate HAV. Few studies performed in Iran on the seroprevalence of HEV demonstrated that its range varies in different regions; 9.3% in Tehran (16), 3.8% in Isfahan (17), and 9.6% and 9.3% in Nahavand (18, 19). The present findings indicated that HEV seropositivity was 13.4%.

Some studies have also demonstrated that HAV and HEV infections have been the most important causes of hepatitis during pregnancy (20, 21). HAV infection may lead to preterm delivery (21) and HEV can be associated with increased severity of liver injury in pregnant women (22). The present study revealed that 46.7% of females were in the reproductive age (15-44 years old), of which 30% and 17.9% were positive for anti-HAV and anti-HEV antibodies, respectively. The prevalence of both anti-HAV and HEV IgM was 0.8% in the same group. As the results showed, there was no anti-HAV IgM-positive female among the six-month to 15-year-old age group. It may be concluded that the females population infected with HAV are at the reproductive age or older. Taking into account the findings, vaccination against HAV in the abovementioned age range is highly recommended to reduce gestational complications. In addition, controlling measures against HEV infection should be considered in this population.

According to the results, the prevalence of anti-HAV (IgG and IgM) and anti-HEV (IgG and IgM) increased with age. To reduce the incidence of HAV and HEV infections, HAV vaccination campaign across the nation, intensive controlling measures and surveillance for HEV, and hygienic improvement in food preparation and water sources are suggested. In addition, to reduce the risk of transmission to children, adults with acute HAV and HEV infections who work in child care centers and food outlets must not work at least one week after the onset of illness (23). Clinical manifestations of HAV infections vary and may be entirely asymptomatic, especially in children. In such conditions, HAV can be detected only by viral serological assays or abnormal liver tests (24). Similarly, HEV-infected individuals may not present any clinical signs (25). In the present study, all the patients with IgM against HAV or HEV were asymptomatic.

The results also showed that HAV IgG and IgM were not seen at the childhood age (six months to 15 years old); so, this group is more susceptible to the infections. Furthermore, HAV and HEV infections were positively correlated with age. Therefore, HAV vaccination and controlling the measures for HEV are recommended. Considering the importance of infections in the gestational period, such programs should focus more on girls. Since both HAV and HEV infections are currently epidemic in developing nations, health authorities should pay more attention and take measures against these diseases, which may help reduce and better control the future outbreaks in Iran.

Acknowledgements

References

  • 1.

    Costa-Mattioli M, Di Napoli A, Ferre V, Billaudel S, Perez-Bercoff R, Cristina J. Genetic variability of hepatitis A virus. J Gen Virol. 2003;84(Pt 12):3191-201. [PubMed ID: 14645901].

  • 2.

    Yong HT, Son R. Hepatitis A virus. Int Food Res J. 2009;16:455-67.

  • 3.

    Vilibic-Cavlek T, Kucinar J, Ljubin-Sternak S, Kolaric B. Seroepidemiology of hepatitis a in the croatian population. Hepat Mon. 2011;11(12):997-9. [PubMed ID: 22368685]. https://doi.org/10.5812/kowsar.1735143X.756.

  • 4.

    Vancelik S, Guraksin A, Alp H. Hepatitis A seroepidemiology in Eastern Turkey. East Afr Med J. 2006;83(2):86-90. [PubMed ID: 16708879].

  • 5.

    Lee H, Cho HK, Kim JH, Kim KH. Seroepidemiology of hepatitis A in Korea: changes over the past 30 years. J Korean Med Sci. 2011;26(6):791-6. [PubMed ID: 21655066]. https://doi.org/10.3346/jkms.2011.26.6.791.

  • 6.

    Tei S, Kitajima N, Takahashi K, Mishiro S. Zoonotic transmission of hepatitis E virus from deer to human beings. Lancet. 2003;362(9381):371-3. [PubMed ID: 12907011]. https://doi.org/10.1016/S0140-6736(03)14025-1.

  • 7.

    Chandra V, Taneja S, Kalia M, Jameel S. Molecular biology and pathogenesis of hepatitis E virus. J Biosci. 2008;33(4):451-64. [PubMed ID: 19208971].

  • 8.

    Ghorbani GA, Alavian SM, Esfahani AA, Assari S. Seroepidemiology of Hepatitis E Virus in Iranian Soldiers. Hepat mon. 2007;7(3):123-6.

  • 9.

    Sepanlou S, Rezvan H, Amini-Kafiabad S, Dayhim M, Merat S. A Population-based Seroepidemiological Study on Hepatitis E Virus in Iran. Middle East J Dig Dis. 2010;2(2):97-103. [PubMed ID: 25197520].

  • 10.

    Livni G, Plotkin S, Yuhas Y, Chodik G, Aloni H, Lerman Y, et al. Seroepidemiology of hepatitis A antibodies among children's hospital staff. Pediatr Infect Dis J. 2002;21(7):618-22. [PubMed ID: 12237591]. https://doi.org/10.1097/01.inf.0000019888.14612.82.

  • 11.

    Reyes GR, Purdy MA, Kim JP, Luk KC, Young LM, Fry KE, et al. Isolation of a cDNA from the virus responsible for enterically transmitted non-A, non-B hepatitis. Science. 1990;247(4948):1335-9. [PubMed ID: 2107574].

  • 12.

    Ungan M, Yaman H, Taheri N. The seroprevalence of specific antibodies to hepatitis A virus in a Turkish population. Eur J Gastroenterol Hepatol. 2002;14(9):1033-4. [PubMed ID: 12352227].

  • 13.

    Taghavi SA, Hosseini Asl MK, Talebzadeh M, Eshraghian A. Seroprevalence study of hepatitis A virus in Fars province, southern Iran. Hepat Mon. 2011;11(4):285-8. [PubMed ID: 22706273].

  • 14.

    Merat S, Rezvan H, Nouraie M, Abolghasemi H, Jamali R, Amini-Kafiabad S, et al. Seroprevalence and risk factors of hepatitis A virus infection in Iran: a population based study. Arch Iran Med. 2010;13(2):99-104. [PubMed ID: 20187662].

  • 15.

    Traore KA, Rouamba H, Nebie Y, Sanou M, Traore AS, Barro N, et al. Seroprevalence of fecal-oral transmitted hepatitis A and E virus antibodies in Burkina Faso. PLoS One. 2012;7(10). eee48125. [PubMed ID: 23110187]. https://doi.org/10.1371/journal.pone.0048125.

  • 16.

    Mohebbi SR, Rostami Nejad M, Tahaei SM, Pourhoseingholi MA, Habibi M, Azimzadeh P, et al. Seroepidemiology of hepatitis A and E virus infections in Tehran, Iran: a population based study. Trans R Soc Trop Med Hyg. 2012;106(9):528-31. [PubMed ID: 22835757]. https://doi.org/10.1016/j.trstmh.2012.05.013.

  • 17.

    Ataei B, Nokhodian Z, Javadi AA, Kassaian N, Shoaei P, Farajzadegan Z, et al. Hepatitis E virus in Isfahan Province: a population-based study. Int J Infect Dis. 2009;13(1):67-71. [PubMed ID: 18599335]. https://doi.org/10.1016/j.ijid.2008.03.030.

  • 18.

    Taremi M, Mohammad Alizadeh AH, Ardalan A, Ansari S, Zali MR. Seroprevalence of hepatitis E in Nahavand, Islamic Republic of Iran: a population-based study. East Mediterr Health J. 2008;14(1):157-62. [PubMed ID: 18557463].

  • 19.

    Zali MR, Taremi M, Arantibodiesi S, Ardalan A, Alizadeh AHM, Ansari S. Seroprevalence of hepatitis E in Nahavand, Iran: Apopulation-based study. East Mediterr Health J. 2008;14(1):157-62.

  • 20.

    Hoofnagle JH, Nelson KE, Purcell RH. Hepatitis E. N Engl J Med. 2012;367(13):1237-44. [PubMed ID: 23013075]. https://doi.org/10.1056/NEJMra1204512.

  • 21.

    Elinav E, Ben-Dov IZ, Shapira Y, Daudi N, Adler R, Shouval D, et al. Acute hepatitis A infection in pregnancy is associated with high rates of gestational complications and preterm labor. Gastroenterology. 2006;130(4):1129-34. [PubMed ID: 16618407]. https://doi.org/10.1053/j.gastro.2006.01.007.

  • 22.

    Navaneethan U, Al Mohajer M, Shata MT. Hepatitis E and pregnancy: understanding the pathogenesis. Liver Int. 2008;28(9):1190-9. [PubMed ID: 18662274]. https://doi.org/10.1111/j.1478-3231.2008.01840.x.

  • 23.

    Larry K, Carol JB, David WK, Sarah SL. Red Book. 28 ed. America: American Academy of pediatrics; 2009.

  • 24.

    Tong MJ, el-Farra NS, Grew MI. Clinical manifestations of hepatitis A: recent experience in a community teaching hospital. J Infect Dis. 1995;171 Suppl 1:S15-8. [PubMed ID: 7876641].

  • 25.

    Panda SK, Thakral D, Rehman S. Hepatitis E virus. Rev Med Virol. 2007;17(3):151-80. [PubMed ID: 17051624]. https://doi.org/10.1002/rmv.522.