Estimation of Seroprevalence of Anti-Herpes Simplex Virus Type-1 IgG Among Healthy Blood Donors in Sakaka City, Aljouf, Saudi Arabia

authors:

avatar Ahmed E. Taha ORCID 1 , * , avatar Amany A. Ghazy ORCID 1 , avatar Abdulrahman Almaeen ORCID 2 , avatar Ibrahim Taher ORCID 1 , avatar Tarek El-Metwally ORCID 3 , avatar Mohammad Ahmad Alayyaf ORCID 4 , avatar Fahad Alrayes 5 , avatar Ahmed Alinad 5 , avatar Saqer Albulayhid 5 , avatar Abdulrahman Aldakhil 5

Microbiology and Immunology Unit, Department of Pathology, College of Medicine, Jouf University, Sakaka 72388, Saudi Arabia
Department of Pathology, Pathology Division, College of Medicine, Jouf University, Sakaka 72388, Saudi Arabia
Department of Pathology, Biochemistry Division, College of Medicine, Jouf University, Sakaka 72388, Saudi Arabia
Consultant Histopathologist and Nephropathologist, Medical Lab Director, Prince Mutaib Bin Abdulaziz Hospital, Sakaka 72388, Saudi Arabia
College of Medicine, Jouf University, Sakaka 72388, Saudi Arabia

How To Cite Taha A E, Ghazy A A, Almaeen A, Taher I, El-Metwally T, et al. Estimation of Seroprevalence of Anti-Herpes Simplex Virus Type-1 IgG Among Healthy Blood Donors in Sakaka City, Aljouf, Saudi Arabia. Jundishapur J Microbiol. 2023;16(7):e136606. https://doi.org/10.5812/jjm-136606.

Abstract

Background:

Herpes simplex virus type-1 (HSV-1) is a highly infectious neurotropic virus. The data on HSV-1 infection in Saudi Arabia, including the seroprevalence of HSV-1 antibodies, are scarce.

Objectives:

This is the first study to evaluate the prevalence of anti-HSV-1 immunoglobulin G (IgG) in donated blood in Sakaka, Aljouf, Saudi Arabia.

Methods:

A total of 300 donated blood samples were collected from the Blood Bank of Prince Mutaib Bin Abdulaziz Hospital in Sakaka. Sensitive and specific enzyme-linked immunosorbent assay (ELISA) was used to detect anti-HSV-1 IgG. A comparison of the age, gender, education, occupation, income, hand hygiene, travel history, and cupping practice of blood donors stratified for the extent of anti-HSV-1 IgG was made.

Results:

There was a low prevalence of anti-HSV-1 IgG (20%; n = 60/300). Moreover, 50.0% of IgG-positive participants were in the age group of 41 - 45 years, and 81.7% of the participants had a household income of < 10000 SAR (statistically highly significant; P < 0.001*). All the participants performed hand washing with soap before handling food and after using the toilet. Furthermore, IgG-positive participants had a bachelor’s degree (50.0%), were governmental employees (60.0%), were international travelers (50.0%), and practiced cupping (50.0%) with statistically significant associations (P < 0.05*).

Conclusions:

The current study’s findings support previous reports about the key importance of improving socioeconomic conditions and hygiene measures in reducing the spread of HSV-1. The present study provides an alarm regarding reaching the age of sexual debut without acquiring protective anti-HSV-1 immunoglobulins, consequently becoming more susceptible to acquiring HSV-1 infection through the genital route. These data support the urgent need to develop an effective anti-HSV-1 vaccine.

1. Background

There are eight members of the Herpesviridae family capable of causing diseases in humans. The human herpes virus family includes three subfamilies (i.e., Alpha-, Beta-, and Gamma-Herpesviridae). The herpes simplex virus type-1 (HSV-1), herpes simplex virus type-2 (HSV-2), and varicellovirus-varicella zoster virus are related to the Alphaherpesvirinae subfamily (1). Herpes simplex virus (mainly HSV-2) is one of the most common causes of genital ulcer disease worldwide and can present in many clinical and psychological manifestations (2).

Herpes simplex virus type-1 is a highly infectious neurotropic dsDNA virus, with most infections occurring among children (3). After the primary infection (mainly non-sexual through oral secretions without clear symptoms) (4), the virus becomes latent in the nerve cells and persists for life (5). Latency of HSV-1 usually occurs in the neuronal nuclei located within the ophthalmic branch of trigeminal ganglion due to an immune mechanism in which the cytotoxic T lymphocytes, specific for the immune dominant gB498-505 HSV-1 epitope, are selectively retained and activated in the infected ganglion to produce interferon-gamma (IFN-γ) necessary for latency (6). Symptomatic infections are often characterized by oral or facial lesions at the site of viral entry (i.e., oral, ocular, and cutaneous) and might lead to central nervous system manifestations (e.g., meningitis and encephalitis), corneal blindness, and death, especially among immunocompromised patients (4). Furthermore, HSV-1 has emerged as a leading cause of primary genital and neonatal disease (7, 8).

Following HSV infection, variable time (from 14 up to 90 days) is required for the development of immunoglobulin G (IgG) antibodies after the onset of symptoms, and the anti-HSV-1 IgG persists indefinitely (9). Most individuals can have anti-HSV-1 IgM detected 9 - 10 days following exposure to the virus. Anti-HSV-1 IgM is usually detectable for 7 - 14 days, although, in a small number of individuals, it can be detectable for up to 6 weeks (10). Socioeconomic and geographic diversities can affect HSV-1 prevalence among different regions and populations (11, 12). Reports from Western countries indicate a major role of HSV-1 as a cause of genital herpes that can be transmitted sexually with major clinical and psychosocial morbidities (8, 13-15). In Western countries, exposure to HSV-1 during childhood was limited due to the improvement in hygienic and socioeconomic conditions; consequently, young individuals might reach the age of sexual activity with no anti-HSV-1 defensive antibodies and become at risk of catching the infection genitally (3, 16, 17). In the United States, HSV-1 seroprevalence (as an indicator for defensive antibodies) has decreased among adolescents aged 14 - 19 years by about 30% over a three-decade period (4).

Public education concerning HSV, its transmission, and its complications is of great value (18). Currently, there are no approved prophylactic or therapeutic vaccines against HSV-1 or HSV-2 due to immune evasion by the virus. The immune responses involved in HSV latency and reactivation are major challenges to the development of anti-HSV vaccines because an effective vaccine must not only prevent or treat the active but also the latent state of the virus. Still, there are several promising trials in the pre-clinical and clinical phases of the study, including live-attenuated (not for immunocompromised patients), subunit, DNA, and replication-defective viral vaccines. The rapid development of anti-severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) messenger ribonucleic acid (mRNA) vaccines has re-energized interest in discovering an effective vaccine against HSV using the same technique; however, there are many concerns regarding the mRNA stability and delivery systems (19).

Although the data are scarce in Saudi Arabia regarding HSV infection and seroprevalence of its antibodies (20-22), HSV-1 is endemic all over the world as indicated by the high seroprevalence of anti-HSV-1 immunoglobulins across different regions (23-25). The virus is typically acquired during childhood (26). In many Western (3, 16, 24, 27-33) and Asian countries (34), the improvement in socioeconomic conditions and hygiene measures appears to have reduced exposure to the virus during childhood. In these countries, many young individuals reach the age of sexual debut without acquiring the protective immunoglobulins against HSV-1 infection; consequently, they become more susceptible to acquiring this infection through the genital route. In Western (13, 15, 30, 35, 36) and Asian countries (34), growing evidence shows that HSV-1 is overwhelming HSV-2 as the leading cause of genital herpes’ first episode of infection. The extent to which such a transition in the epidemiology of HSV-1 is happening in other worldwide areas remains undetermined. From this perspective, the present study aimed to determine the seroprevalence of anti-HSV-1 IgG levels in Sakaka, Aljouf, Saudi Arabia.

2. Objectives

A better understanding of the seroprevalence of HSV-1 antibodies is required in Saudi Arabia to help health policymakers in characterizing the HSV-1 disease burden and exploring its optimal prevention and control strategies, including vaccine development. To the best of our knowledge, this is the first report on the prevalence of anti-HSV-1 IgG in donated blood in Sakaka, Aljouf, Saudi Arabia.

3. Methods

3.1. Study Design, Data, and Samples Collection

Bioethical approval (No. 19-08/42) was obtained from the Local Committee of Bioethics (LCBE) of Jouf University, Kingdom of Saudi Arabia (KSA). The sample size was calculated using an online (Roasoft) sample size calculator (http://www.Raosoft.com/samplesize.html) with a margin of error of 5.66%, response distribution of 50%, and a confidence level of 95% for a total of 250,000 inhabitants of Sakaka, Aljouf, Saudi Arabia. Since HSV-1 is transmitted in the general population mainly by saliva, its seroprevalence among apparently healthy blood donors could reflect that in the total population (11, 12). A cross-sectional study was performed to collect 300 blood samples from the donated blood received in the Blood Bank of Prince Mutaib Bin Abdulaziz Hospital, Sakaka, Aljouf, Saudi Arabia. The participants were randomly selected. Each sample (5 mL) was collected in a sterile tube with anticoagulant ethylenediaminetetraacetic acid (EDTA) (or citrate) and transported in an icebox to the Microbiology and Immunology Laboratory at the College of Medicine, Jouf University, for further processing. Participants' data (i.e., age, gender, education, occupation, income, hand hygiene, travel history, and cupping practice) were collected as shown in Table 1.

3.2. Immunological Detection of Antibodies

On arrival at the Microbiology and Immunology laboratory, the samples were processed using aseptic techniques to avoid contamination. The blood samples were incubated at room temperature for 10 - 20 minutes and then centrifugated at 3,000 rpm for 10 minutes. The plasma supernatant was collected. Plasma aliquots were stored at - 80°C until testing (11). All the samples were tested by indirect enzyme-linked immunosorbent assay (ELISA) (with sensitivity and specificity of 99% and 93%, respectively) for anti-HSV-1 IgG detection according to the manufacturer’s instructions (Catalogue number SL2061Hu, SunLong Biotech Co., LTD, Hangzhou Zhejiang, China). Blank, negative, and positive controls were included with each run. The cut-off value was optical density (OD) ≥ 0.25. The color intensity was directly proportional to the anti-HSV-1 IgG concentration in the samples (12).

3.3. Data Analysis

The data were fed to the computer and analyzed using IBM SPSS software package version 20.0. (Armonk, NY: IBM Corp.). Comparisons between groups for categorical variables were assessed using the chi-square test. The significance of the obtained results was judged at the 5% level.

4. Results

Anti-HSV-1 IgG was detected at a low rate (20%; n = 60/300). There was a highly significant association (P < 0.001*) between anti-HSV-1 IgG-positivity and the age of participants (50.0% of HSV-1 IgG-positive participants in the age group of 41 - 45 years). Another highly significant association with P < 0.001* was observed between having household income less than 10000 SAR and anti-HSV-1 IgG-positivity, where 81.7% of HSV-1 IgG-positive participants had income < 10000 SAR. All the participants performed hand washing with soap before handling food and after using the toilet. Furthermore, there were significant associations (P < 0.05*) between IgG-positivity with education, occupation, travel history, and cupping practice where HSV-1 IgG-positive participants were bachelor’s degree holders, governmental employees, international travelers, and practicing cupping at rates of 50.0% (n = 30/60), 60.0% (n = 36/60), 50.0% (n = 30/60), and 50.0% (n = 30/60), respectively. Moreover, 20.7% (n = 54/261) of the male participants were anti-HSV-1 IgG-positive, compared to the anti-HSV-1 IgG-positive female participants (15.4%; n = 6/39); however, there was no statistically significant association between IgG-positivity and gender (P = 0.440) (Table 1).

Table 1.

Comparison of the Demographics, Lifestyle, and Anthropometrics of Participants Stratified for the Extent of Anti-Herpes Simplex Virus Type-1 Immunoglobulin G in Their Plasma (Total N = 300) a

VariablesTotal participants (N = 300)HSV-1 IgGχ2bP-Value c
Negative (n = 240) (80.0)Positive (n = 60) (20.0)
Age group, (y)39.786 d<0.001 d
≤ 2012 (4.0)12 (5.0)0 (0.0)
21 - 30150 (50.0)132 (55.0)18 (30.0)
31 - 4075 (25.0)63 (26.3)12 (20.0)
41 - 4563 (21.0)33 (13.8)30 (50.0)
Gender0.5970.440
Male261 (87.0)207 (86.3)54 (90.0)
Female39 (13.0)33 (13.8)6 (10.0)
Education7.200.027 d
Student69 (23.0)63 (26.3)6 (10.0)
Bachelor’s degree131 (43.7)101 (42.1)30 (50.0)
Postgraduate100 (33.3)76 (31.7)24 (40.0)
Occupation8.602 d0.035 d
Private sector48 (16.0)36 (15.0)12 (20.0)
Governmental Employee165 (55.0)129 (53.8)36 (60.0)
Student69 (23.0)63 (26.3)6 (10.0)
Not working18 (6.0)12 (5.0)6 (10.0)
Household income34.10.001 d
< 10000 SAR144 (48.0)95 (39.6)49 (81.7)
≥ 10000 SAR156 (52.0)145 (60.4)11 (18.3)
Hand washing with soap before handling food and after using the toilet
No0 (00.0)0 (00.0)0 (00.0)--
Yes300 (100.0)240 (100.0)60 (100.0)
Travel history4.584 d0.032 d
No186 (62.0)156 (65.0)30 (50.0)
Yes114 (38.0)84 (35.0)30 (50.0)
Cupping practice9.803 d0.002 d
No201 (67.0)171 (71.3%)30 (50.0)
Yes99 (33.0)69 (28.8)30 (50.0)

5. Discussion

To the best of our knowledge, this is the first report on the prevalence of anti-HSV-1 IgG in donated blood in Sakaka, Aljouf, Saudi Arabia, that could be valuable for health policymakers in implementing health promotion strategies. In the current study, the anti-HSV-1 IgG was detected at a low prevalence (20%). In contrast, a study was conducted in Qatar to detect the seroprevalence of anti-HSV-1 IgG among blood donors from different nationalities reported that the prevalence among Egyptians, Yemenis, Sudanese, Syrians, Jordanians, Qataris, Iranians, Lebanese, and Palestinians was 97.5%, 92.6%, 90.7%, 88.5%, 86.5%, 82.3%, 81.4%, 81.4%, and 80.5%, respectively (11). Another study was conducted in Iraq to determine the frequency of anti-HSV-1 IgG in healthy blood donors in Baghdad province, and the researchers observed that 94.1% of participants had immunoglobulin in their sera (12). Furthermore, Chaabane et al. reported that the HSV-1 seroprevalence in the Middle East and North Africa was 91.5% and 65.2% among adults and children, respectively (8).

It is well known that the HSV-2-seropositive population can cross-react to many HSV-1 antigens (37). The variation of anti-HSV-1 IgG seroprevalence between different countries and populations might be related to differences in the studied population (38) or diversity in the socioeconomic and hygiene measures (39). The low-income individuals might have a higher level of occupation-related stress and/or weather-related stress (exposure to abnormal levels of cold versus heat), leading to the reactivation of HSV-1 latency. With more improvement in socioeconomic conditions and hygiene measures, there is less exposure to the virus during childhood and less anti-HSV-1 IgG seroprevalence during adulthood (8).

In a national survey conducted in Saudi Arabia and published in September 2015, the overall seroprevalence of HSV-1 was high (88.8%), and most (84%) of the population infected with HSV-2 were also coinfected with HSV-1. According to the Saudi geographic areas, the HSV-1 seroprevalence was 97.14%, 97.00%, 95.28%, 94.72%, 94.44%, 94.41%, 92.35%, 91.07%, 89.61%, 88.97%, 87.68%, 86.07%, and 62.25% in Aljouf, Al-Bahah, Najran, Assir, Northern boarders, Tabuk, Jizan, Riyadh, Madinah, Hail, Makkah, Eastern province, and Al-Qassim province, respectively. The authors observed that rural regions had higher HSV-1 seroprevalence than urban areas and explained this by the fact that rural regions are more tight-knit communities where the transmission of HSV-1 is facilitated, for example, by sharing utensils during community events and food gatherings. It is apparent from the study that the seroprevalence of HSV-1 was high in nearly all studied geographic areas, with the lowest seroprevalence of HSV-1 and HSV-2 detected in Al-Qassim province, which is the most conservative region in Saudi Arabia (22).

In the above-mentioned survey, although the highest (97.14 %) HSV-1 seroprevalence was observed in Aljouf province, this might not reflect the actual HSV-1 seroprevalence due to the very small sample size recruited in the study (only 70 participants from Aljouf). Aljouf is a large province that includes many cities, including Sakaka, which is the largest one and the capital of Aljouf. Although the population in Sakaka was estimated to be 240,866 individuals according to the General Authority for Statistics (GAStat) 2010 (40), the population in the Aljouf region was estimated to be 531,952 individuals according to the GAStat 2019 (41). Education, occupation, and household income are the most used indicators of socioeconomic status (42). The low seroprevalence of anti-HSV-1 IgG detected in the current study can be explained by the conservative nature of the population in Sakaka and their improved socioeconomic conditions and hygienic measures, as shown in Table 1.

Regarding the age and gender of the participants in the conducted study, 50.0% (n = 30/60), 90.0% (n = 54/60), and 10.0% (n = 6/60) of HSV-1 IgG-positive participants were in the age group of 41-45 years (statistically significant; P < 0.05*), male, and female, respectively. There was no statistically significant association between IgG-positivity and gender (P = 0.440). The data of many studies totally agree with the aforementioned data (24, 39). Two Iraqi studies reported the predominance of HSV-1 IgG-seropositivity in a younger age group (21 - 40 years) (12, 43). Several studies reported that there was no major gender-specific difference regarding HSV-1 seroprevalence variation (12, 24, 25, 38, 43-45). In the current study, 81.7% of HSV-1 IgG-positive participants had a household income of less than 10000 SAR (P < 0.001*). In Jordan, a recent study reported a high seroprevalence of HSV-1 (75.3%) with a statistically significant association between the anti-HSV-1 IgG seropositivity and the low household income (P = 0.002*) (46). With the improvement of socioeconomic conditions, the predominance of HSV-1 IgG-seropositivity will be in elderly individuals. It was reported that age and socioeconomic conditions could explain half of the HSV-1 seroprevalence variation, although the other factors, such as gender, type of population, and sampling technique, were not significantly associated with the HSV-1 seroprevalence variation (8). The sample collection bias might be less important for HSV-1 seroprevalence variation because the virus is mostly transmitted through the oral route among the general population (11, 12).

In the present conducted study, 60.0% of the HSV-1 IgG-positive participants were government employees with statistically significant association (P < 0.035*). Conversely, the predominance of HSV-1 IgG-seropositivity was observed among the students (33.4%) (43) and private sector employees (54.6%) (12), respectively, with no statistically significant association. Regarding cupping practice (i.e., a sort of oriental traditional medicine) and travel history, a Korean study reported a rare case of cutaneous herpes infection that was suspected to be caused by direct inoculation or reactivation of the virus by cupping mechanical trauma (47). Furthermore, some reports suggested that the number of different strains of HSV-1 in a person could be an indicator of his/her travel history and viral DNA sequencing might be used as a forensic tool to study the human population and their migration patterns (48, 49). The results of the current study showed significant associations (P < 0.05*) between anti-HSV-1 IgG seropositivity only with cupping practice and international traveling, where 30.3% (n = 30/99) and 26.3% (n = 30/114) of participants with cupping practicing and international traveling were anti-HSV-1 IgG-positive, respectively. Nevertheless, a study by Al-Shuwaikh et al. (12) did not find a statistically significant association between HSV-1 IgG seropositivity on one side and neither the travel history nor the cupping practice on the other side.

However, the world is trying to counteract the bad effect of the coronavirus disease 2019 (COVID-19) pandemic, caused by SARS-CoV-2 (50, 51), on the communities, health systems, and economies (52, 53). Anti-SARS-CoV-2 vaccination constitutes the most promising prevention and control measure (54, 55). Recently, a few cases of herpes keratitis (approved by polymerase chain reaction [PCR]) due to the reactivation of HSV after receiving anti-SARS-CoV-2 mRNA vaccination were detected in Saudi Arabia (56), the United Kingdom (57), and Jordan (58). These cases could be explained by the mRNA vaccine-induced dysregulation of the cytotoxic T lymphocytes specific for the immune dominant gB498-505 HSV-1 epitope in the infected trigeminal ganglion (59), vaccine-induced disruption of humoral immunity, autoimmune response, and/or reduction in the neurotrophin that inhibits HSV replication (60). All the aforementioned studies shed light on the importance of being aware of the potential for the reactivation of herpes eye disease that might lead to blindness following anti-SARS-CoV-2 vaccination to enable prompt, effective prevention, control, and treatment. Likewise, five cases of cutaneous HSV-1 reactivation were reported after receiving anti-SARS-CoV-2 mRNA vaccination (61). Currently, it is worth noting that anti-SARS-CoV-2 vaccination is inevitable, as its benefits overshadow the potential risk of HSV reactivation, and the same is true for discovering and approving anti-HSV-1 vaccines.

5.1. Conclusions

In this study, there was a low prevalence of anti-HSV-1 IgG. The study provides an alarm regarding reaching the age of sexual debut without acquiring the protective anti-HSV-1 immunoglobulins, consequently becoming more susceptible to acquiring the HSV-1 infection through the genital route. Although the current study’s findings support previous reports about the key importance of improving socioeconomic conditions and hygiene measures in reducing the spread of HSV-1, there is an urgent need to develop an effective vaccine against HSV-1.

Acknowledgements

References

  • 1.

    Omarova S, Cannon A, Weiss W, Bruccoleri A, Puccio J. Genital herpes simplex virus-an updated review. Adv Pediatr. 2022;69(1):149-62. [PubMed ID: 35985707]. https://doi.org/10.1016/j.yapd.2022.03.010.

  • 2.

    Gnann JJ, Whitley RJ. Clinical practice. Genital herpes. N Engl J Med. 2016;375(7):666-74. [PubMed ID: 27532832]. https://doi.org/10.1056/NEJMcp1603178.

  • 3.

    Xu F, Lee FK, Morrow RA, Sternberg MR, Luther KE, Dubin G, et al. Seroprevalence of herpes simplex virus type 1 in children in the United States. J Pediatr. 2007;151(4):374-7. [PubMed ID: 17889072]. https://doi.org/10.1016/j.jpeds.2007.04.065.

  • 4.

    Bradley H, Markowitz LE, Gibson T, McQuillan GM. Seroprevalence of herpes simplex virus types 1 and 2--United States, 1999-2010. J Infect Dis. 2014;209(3):325-33. [PubMed ID: 24136792]. https://doi.org/10.1093/infdis/jit458.

  • 5.

    Brady RC, Bernstein DI. Treatment of herpes simplex virus infections. Antiviral Res. 2004;61(2):73-81. [PubMed ID: 14670580]. https://doi.org/10.1016/j.antiviral.2003.09.006.

  • 6.

    Khanna KM, Bonneau RH, Kinchington PR, Hendricks RL. Herpes simplex virus-specific memory CD8+ T cells are selectively activated and retained in latently infected sensory ganglia. Immunity. 2003;18(5):593-603. [PubMed ID: 12753737]. [PubMed Central ID: PMC2871305]. https://doi.org/10.1016/s1074-7613(03)00112-2.

  • 7.

    Awasthi S, Belshe RB, Friedman HM. Better neutralization of herpes simplex virus type 1 (HSV-1) than HSV-2 by antibody from recipients of GlaxoSmithKline HSV-2 glycoprotein D2 subunit vaccine. J Infect Dis. 2014;210(4):571-5. [PubMed ID: 24652496]. [PubMed Central ID: PMC4172040]. https://doi.org/10.1093/infdis/jiu177.

  • 8.

    Chaabane S, Harfouche M, Chemaitelly H, Schwarzer G, Abu-Raddad LJ. Herpes simplex virus type 1 epidemiology in the Middle East and North Africa: Systematic review, meta-analyses, and meta-regressions. Sci Rep. 2019;9(1):1136. [PubMed ID: 30718696]. [PubMed Central ID: PMC6362060]. https://doi.org/10.1038/s41598-018-37833-8.

  • 9.

    LeGoff J, Pere H, Belec L. Diagnosis of genital herpes simplex virus infection in the clinical laboratory. Virol J. 2014;11:83. [PubMed ID: 24885431]. [PubMed Central ID: PMC4032358]. https://doi.org/10.1186/1743-422X-11-83.

  • 10.

    Ashley RL. Performance and use of HSV type-specific serology test kits. Herpes. 2002;9(2):38-45. [PubMed ID: 12106510].

  • 11.

    Nasrallah GK, Dargham SR, Mohammed LI, Abu-Raddad LJ. Estimating seroprevalence of herpes simplex virus type 1 among different Middle East and North African male populations residing in Qatar. J Med Virol. 2018;90(1):184-90. [PubMed ID: 28817197]. [PubMed Central ID: PMC5724503]. https://doi.org/10.1002/jmv.24916.

  • 12.

    Al-Shuwaikh A, Hanna D, Ali Z. Seroprevalence of herpes simplex virus type-1 igg antibody in healthy blood donor from Baghdad-Iraq. J Pure Appl Microbiol. 2019;13(2):1017-23. https://doi.org/10.22207/jpam.13.2.39.

  • 13.

    Gilbert M, Li X, Petric M, Krajden M, Isaac-Renton JL, Ogilvie G, et al. Using centralized laboratory data to monitor trends in herpes simplex virus type 1 and 2 infection in British Columbia and the changing etiology of genital herpes. Can J Public Health. 2011;102(3):225-9. [PubMed ID: 21714324]. [PubMed Central ID: PMC6974205]. https://doi.org/10.1007/BF03404902.

  • 14.

    Whitley RJ. Changing epidemiology of herpes simplex virus infections. Clin Infect Dis. 2013;56(3):352-3. [PubMed ID: 23087393]. https://doi.org/10.1093/cid/cis894.

  • 15.

    Magdaleno-Tapial J, Hernandez-Bel P, Valenzuela-Onate C, Ortiz-Salvador JM, Garcia-Legaz-Martinez M, Martinez-Domenech A, et al. Genital infection with herpes simplex virus type 1 and type 2 in valencia, spain: A retrospective observational study. Actas Dermosifiliogr (Engl Ed). 2020;111(1):53-8. [PubMed ID: 31744595]. https://doi.org/10.1016/j.ad.2019.06.002.

  • 16.

    Sauerbrei A, Schmitt S, Scheper T, Brandstadt A, Saschenbrecker S, Motz M, et al. Seroprevalence of herpes simplex virus type 1 and type 2 in Thuringia, Germany, 1999 to 2006. Euro Surveill. 2011;16(44). [PubMed ID: 22085620].

  • 17.

    Bernstein DI, Bellamy AR, Hook E3, Levin MJ, Wald A, Ewell MG, et al. Epidemiology, clinical presentation, and antibody response to primary infection with herpes simplex virus type 1 and type 2 in young women. Clin Infect Dis. 2013;56(3):344-51. [PubMed ID: 23087395]. [PubMed Central ID: PMC3540038]. https://doi.org/10.1093/cid/cis891.

  • 18.

    Conde-Glez C, Lazcano-Ponce E, Rojas R, DeAntonio R, Romano-Mazzotti L, Cervantes Y, et al. Seroprevalences of varicella-zoster virus, herpes simplex virus and cytomegalovirus in a cross-sectional study in Mexico. Vaccine. 2013;31(44):5067-74. [PubMed ID: 24021305]. https://doi.org/10.1016/j.vaccine.2013.08.077.

  • 19.

    Krishnan R, Stuart PM. Developments in vaccination for herpes simplex virus. Front Microbiol. 2021;12:798927. [PubMed ID: 34950127]. [PubMed Central ID: PMC8691362]. https://doi.org/10.3389/fmicb.2021.798927.

  • 20.

    Madani TA. Sexually transmitted infections in Saudi Arabia. BMC Infect Dis. 2006;6:3. [PubMed ID: 16403220]. [PubMed Central ID: PMC1368987]. https://doi.org/10.1186/1471-2334-6-3.

  • 21.

    Fageeh WM. Sexually transmitted infections among patients with herpes simplex virus at King Abdulaziz University Hospital. BMC Res Notes. 2013;6:301. [PubMed ID: 23898826]. [PubMed Central ID: PMC3751363]. https://doi.org/10.1186/1756-0500-6-301.

  • 22.

    Memish ZA, Almasri M, Chentoufi AA, Al-Tawfiq JA, Al-Shangiti AM, Al-Kabbani KM, et al. Seroprevalence of Herpes Simplex Virus Type 1 and Type 2 and Coinfection With HIV and Syphilis: The first national seroprevalence Survey in Saudi Arabia. Sex Transm Dis. 2015;42(9):526-32. [PubMed ID: 26267880]. https://doi.org/10.1097/OLQ.0000000000000336.

  • 23.

    Nahmias AJ, Lee FK, Beckman-Nahmias S. Sero-epidemiological and -sociological patterns of herpes simplex virus infection in the world. Scand J Infect Dis Suppl. 1990;69:19-36. [PubMed ID: 2175939].

  • 24.

    Smith JS, Robinson NJ. Age-specific prevalence of infection with herpes simplex virus types 2 and 1: A global review. J Infect Dis. 2002;186 Suppl 1:S3-28. [PubMed ID: 12353183]. https://doi.org/10.1086/343739.

  • 25.

    Looker KJ, Magaret AS, May MT, Turner KM, Vickerman P, Gottlieb SL, et al. Global and regional estimates of prevalent and incident herpes simplex virus type 1 infections in 2012. PLoS One. 2015;10(10). e0140765. [PubMed ID: 26510007]. [PubMed Central ID: PMC4624804]. https://doi.org/10.1371/journal.pone.0140765.

  • 26.

    Fatahzadeh M, Schwartz RA. Human herpes simplex virus infections: Epidemiology, pathogenesis, symptomatology, diagnosis, and management. J Am Acad Dermatol. 2007;57(5):737-63. quiz 764-6. [PubMed ID: 17939933]. https://doi.org/10.1016/j.jaad.2007.06.027.

  • 27.

    Vyse AJ, Gay NJ, Slomka MJ, Gopal R, Gibbs T, Morgan-Capner P, et al. The burden of infection with HSV-1 and HSV-2 in England and Wales: Implications for the changing epidemiology of genital herpes. Sex Transm Infect. 2000;76(3):183-7. [PubMed ID: 10961195]. [PubMed Central ID: PMC1744133]. https://doi.org/10.1136/sti.76.3.183.

  • 28.

    Wutzler P, Doerr HW, Farber I, Eichhorn U, Helbig B, Sauerbrei A, et al. Seroprevalence of herpes simplex virus type 1 and type 2 in selected German populations-relevance for the incidence of genital herpes. J Med Virol. 2000;61(2):201-7. [PubMed ID: 10797375].

  • 29.

    Aarnisalo J, Ilonen J, Vainionpaa R, Volanen I, Kaitosaari T, Simell O. Development of antibodies against cytomegalovirus, varicella-zoster virus and herpes simplex virus in Finland during the first eight years of life: a prospective study. Scand J Infect Dis. 2003;35(10):750-3. [PubMed ID: 14606615]. https://doi.org/10.1080/00365540310015881.

  • 30.

    Roberts CM, Pfister JR, Spear SJ. Increasing proportion of herpes simplex virus type 1 as a cause of genital herpes infection in college students. Sex Transm Dis. 2003;30(10):797-800. [PubMed ID: 14520181]. https://doi.org/10.1097/01.OLQ.0000092387.58746.C7.

  • 31.

    Pebody RG, Andrews N, Brown D, Gopal R, De Melker H, Francois G, et al. The seroepidemiology of herpes simplex virus type 1 and 2 in Europe. Sex Transm Infect. 2004;80(3):185-91. [PubMed ID: 15170000]. [PubMed Central ID: PMC1744847]. https://doi.org/10.1136/sti.2003.005850.

  • 32.

    Xu F, Sternberg MR, Kottiri BJ, McQuillan GM, Lee FK, Nahmias AJ, et al. Trends in herpes simplex virus type 1 and type 2 seroprevalence in the United States. JAMA. 2006;296(8):964-73. [PubMed ID: 16926356]. https://doi.org/10.1001/jama.296.8.964.

  • 33.

    Kramer MA, Uitenbroek DG, Ujcic-Voortman JK, Pfrommer C, Spaargaren J, Coutinho RA, et al. Ethnic differences in HSV1 and HSV2 seroprevalence in Amsterdam, the Netherlands. Euro Surveill. 2008;13(24). [PubMed ID: 18761942].

  • 34.

    Khadr L, Harfouche M, Omori R, Schwarzer G, Chemaitelly H, Abu-Raddad LJ. The epidemiology of herpes simplex virus type 1 in Asia: Systematic review, meta-analyses, and meta-regressions. Clin Infect Dis. 2019;68(5):757-72. [PubMed ID: 30020453]. [PubMed Central ID: PMC6376104]. https://doi.org/10.1093/cid/ciy562.

  • 35.

    Lowhagen GB, Tunback P, Andersson K, Bergstrom T, Johannisson G. First episodes of genital herpes in a Swedish STD population: a study of epidemiology and transmission by the use of herpes simplex virus (HSV) typing and specific serology. Sex Transm Infect. 2000;76(3):179-82. [PubMed ID: 10961194]. [PubMed Central ID: PMC1744160]. https://doi.org/10.1136/sti.76.3.179.

  • 36.

    Nilsen A, Myrmel H. Changing trends in genital herpes simplex virus infection in Bergen, Norway. Acta Obstet Gynecol Scand. 2000;79(8):693-6. [PubMed ID: 10949236].

  • 37.

    Kalantari-Dehaghi M, Chun S, Chentoufi AA, Pablo J, Liang L, Dasgupta G, et al. Discovery of potential diagnostic and vaccine antigens in herpes simplex virus 1 and 2 by proteome-wide antibody profiling. J Virol. 2012;86(8):4328-39. [PubMed ID: 22318154]. [PubMed Central ID: PMC3318641]. https://doi.org/10.1128/JVI.05194-11.

  • 38.

    Clemens SA, Farhat CK. Seroprevalence of herpes simplex 1-2 antibodies in Brazil. Rev Saude Publica. 2010;44(4):726-34. [PubMed ID: 20676563]. https://doi.org/10.1590/s0034-89102010000400017.

  • 39.

    Hossain A. Herpes simplex virus type 1 (HSV-1) and varicella-zoster virus (VZV) infections in Saudi Arabia. J Trop Pediatr. 1989;35(4):171-4. [PubMed ID: 2810461]. https://doi.org/10.1093/tropej/35.4.171.

  • 40.

    The General Authority for Statistics, Saudi Arabia; general population and housing census, administrative: Al-Jouf Census 2010. 2022. Available from: https://www.stats.gov.sa/en/13.

  • 41.

    The General Authority for Statistics, Saudi Arabia; population in Al-Jouf region by gender, age group, and nationality. Report period 2019. 2022. Available from: https://www.stats.gov.sa/en/6143.

  • 42.

    Darin-Mattsson A, Fors S, Kareholt I. Different indicators of socioeconomic status and their relative importance as determinants of health in old age. Int J Equity Health. 2017;16(1):173. [PubMed ID: 28950875]. [PubMed Central ID: PMC5615765]. https://doi.org/10.1186/s12939-017-0670-3.

  • 43.

    Al-Kayalli KKI, Al-Azawy MKK, Al-Azawy ATN. Evaluation of seroprevalence of herpes simplex virus igg antibody in Baquba City by using elisa technique. Diyala Journal For Pure Science. 2015;11(2):99-108.

  • 44.

    Artiran Igde F, Yazici Z, Igde M. Seroepidemiological study of herpes simplex virus types 1 in black sea region of Turkey. Medical Journal of Trakya University. 2009. https://doi.org/10.5174/tutfd.2009.02681.2.

  • 45.

    Malary M, Abedi G, Hamzehgardeshi Z, Afshari M, Moosazadeh M. The prevalence of herpes simplex virus type 1 and 2 infection in Iran: A meta-analysis. Int J Reprod Biomed. 2016;14(10):615-24. [PubMed ID: 27921084]. [PubMed Central ID: PMC5124323].

  • 46.

    Swedan SF, Darabseh A. Seroprevalence of herpes simplex virus types 1 and 2 and correlates of infection in Jordan. Int J STD AIDS. 2022;33(3):304-10. [PubMed ID: 34978219]. https://doi.org/10.1177/09564624211060183.

  • 47.

    Jung YJ, Kim JH, Lee HJ, Bak H, Hong SP, Jeon SY, et al. A herpes simplex virus infection secondary to acupuncture and cupping. Ann Dermatol. 2011;23(1):67-9. [PubMed ID: 21738366]. [PubMed Central ID: PMC3120002]. https://doi.org/10.5021/ad.2011.23.1.67.

  • 48.

    Kolb AW, Ane C, Brandt CR. Using HSV-1 genome phylogenetics to track past human migrations. PLoS One. 2013;8(10). e76267. [PubMed ID: 24146849]. [PubMed Central ID: PMC3797750]. https://doi.org/10.1371/journal.pone.0076267.

  • 49.

    Bowen CD, Renner DW, Shreve JT, Tafuri Y, Payne KM, Dix RD, et al. Viral forensic genomics reveals the relatedness of classic herpes simplex virus strains KOS, KOS63, and KOS79. Virology. 2016;492:179-86. [PubMed ID: 26950505]. [PubMed Central ID: PMC5056906]. https://doi.org/10.1016/j.virol.2016.02.013.

  • 50.

    Taha AE. Can COVID-19 Be Transmitted Sexually by Semen? J Pure and Applied Microbiol. 2020;14(4):2287-93. https://doi.org/10.22207/jpam.14.4.06.

  • 51.

    Hetta HF, Muhammad K, El-Masry EA, Taha AE, Ahmed EA, Phares C, et al. The interplay between vitamin D and COVID-19: Protective or bystander? Eur Rev Med Pharmacol Sci. 2021;25(4):2131-45. [PubMed ID: 33660833]. https://doi.org/10.26355/eurrev_202102_25119.

  • 52.

    Taha AE. The severe acute respiratory syndrome coronavirus-2 Pandemic: an overview to control human-wildlife and human-human interactions. J Pure Appl Microbiol. 2020;14(2):1095-8. https://doi.org/10.22207/jpam.14.2.02.

  • 53.

    El-Masry EA, Mohamed RA, Ali RI, Al Mulhim MF, Taha AE. Novel coronavirus disease-related knowledge, attitudes, and practices among the residents of Al-Jouf region in Saudi Arabia. J Infect Dev Ctries. 2021;15(1):32-9. [PubMed ID: 33571143]. https://doi.org/10.3855/jidc.14243.

  • 54.

    Almaeen AH, Alduraywish AA, Ghazy AA, El-Metwally TH, Alayyaf M, Alrayes FH, et al. The pre-vaccination donated blood is free from severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) but Is Rich with Anti-SARS-CoV-2 Antibodies: A cross-section saudi study. Int J Environ Res Public Health. 2022;19(12). [PubMed ID: 35742368]. [PubMed Central ID: PMC9223027]. https://doi.org/10.3390/ijerph19127119.

  • 55.

    Taha AE, Alduraywish AA, Almaeen AH, El-Metwally TH, Alayyaf M, Mallick A, et al. High Seroprevalence of Anti-SARS-CoV-2 IgM/IgG among Inhabitants of Sakaka City, Aljouf, Saudi Arabia. Vaccines (Basel). 2022;11(1). [PubMed ID: 36679870]. [PubMed Central ID: PMC9862882]. https://doi.org/10.3390/vaccines11010026.

  • 56.

    Alkhalifah MI, Alsobki HE, Alwael HM, Al Fawaz AM, Al-Mezaine HS. Herpes simplex virus keratitis reactivation after SARS-CoV-2 BNT162b2 mRNA vaccination: A report of two cases. Ocul Immunol Inflamm. 2021;29(6):1238-40. [PubMed ID: 34637667]. https://doi.org/10.1080/09273948.2021.1986548.

  • 57.

    Richardson-May J, Rothwell A, Rashid M. Reactivation of herpes simplex keratitis following vaccination for COVID-19. BMJ Case Rep. 2021;14(9). [PubMed ID: 34493563]. [PubMed Central ID: PMC8424829]. https://doi.org/10.1136/bcr-2021-245792.

  • 58.

    Al-Dwairi RA, Aleshawi A, Adi S, Abu-Zreig L. Reactivation of herpes simplex keratitis on a corneal graft following SARS-CoV-2 mRNA vaccination. Med Arch. 2022;76(2):146-8. [PubMed ID: 35774041]. [PubMed Central ID: PMC9233471]. https://doi.org/10.5455/medarh.2022.76.146-148.

  • 59.

    Herbort CJ, Papasavvas I. Effect of SARS-CoV-2 mRNA vaccination on ocular herpes simplex and varicella-zoster virus reactivation: Should preventive antiviral treatment be given in known herpes patients. J Ophthalmic Inflamm Infect. 2021;11(1):33. [PubMed ID: 34533628]. [PubMed Central ID: PMC8446741]. https://doi.org/10.1186/s12348-021-00262-2.

  • 60.

    Hassman LM, DiLoreto DJ. Immunologic factors may play a role in herpes simplex virus 1 reactivation in the brain and retina after influenza vaccination. IDCases. 2016;6:47-51. [PubMed ID: 27699152]. [PubMed Central ID: PMC5045948]. https://doi.org/10.1016/j.idcr.2016.09.012.

  • 61.

    Fathy RA, McMahon DE, Lee C, Chamberlin GC, Rosenbach M, Lipoff JB, et al. Varicella-zoster and herpes simplex virus reactivation post-COVID-19 vaccination: A review of 40 cases in an International Dermatology Registry. J Eur Acad Dermatol Venereol. 2022;36(1):e6-9. [PubMed ID: 34487581]. [PubMed Central ID: PMC8656951]. https://doi.org/10.1111/jdv.17646.