Varicella (chicken pox) is caused by varicella zoster virus (VZV). It is one of the most common and contagious childhood infections and characterized by febrile vesicular rash. The disease can lead to serious complications or death especially in adults, infants and immunocompromised individuals. Varicella infection in pregnancy may lead to congenital defects (~1%), if acquired in the first two trimesters of pregnancy [Reference Gershon1]. The defects include scarring on the skin, hypoplastic limbs and some eye and brain abnormalities [Reference Heininger and Seward2]. Following primary infection, VZV can persist in peripheral autonomic ganglia and virus reactivation may result in herpes zoster (shingles) characterized by painful, localized vesicular rash [Reference Kennedy and Gershon3]. Varicella is a vaccine preventable infection; however, the live attenuated vaccine is currently only used in about 25% of World Health Organization (WHO) member states [4]. In Sudan, no varicella vaccine is used, varicella infections are not notifiable and data on disease epidemiology or outbreaks are lacking. Therefore, the aim of this study was to investigate the extent of previous exposure to VZV among children and adults from the general population and among health-care workers (HCWs) in Khartoum, Sudan.
Dried blood spot (DBS) samples collected during a previous cross-sectional study on the seroprevalence of measles, mumps and rubella in Khartoum state, Sudan between 2015 and 2016 and stored at −80 °C were used [Reference Adam5]. Briefly, samples had been collected from 294 children aged 1‒15 years (mean 7.7 years) attending three major paediatric hospitals, 153 adult volunteers between 21 and 60 years (mean 36.2 years) working at the National Centre for Research and 241 HCWs aged 22‒61 years (mean 38.2 years) working at two major paediatric hospitals in Khartoum, Sudan. We used these samples to circumvent the challenges related to collecting, preserving and transporting new samples and because there has been no policy change related to varicella in Sudan since they had been collected. Sample integrity was assessed by re-testing 40 randomly selected sera for measles IgG antibodies using the Euroimmun anti-Measles ELISA (IgG) kit (EI 2610-9601 G, Lübeck, Germany) to verify that the results were qualitatively and quantitatively concordant with our previous findings. After we made sure that there were no issues with sample quality, we performed the extraction of serum from the DBS samples and the detection of VZV IgG antibodies as described in the Euroimmun anti-VZV ELISA (IgG) kit manual (EI 2650-9601 G, Lübeck, Germany). All samples with equivocal results were retested and categorized according to the second test result. Individuals with a second equivocal result were considered as seronegative during data analysis. Using the SPSS software, version 20 (SPSS Inc., Chicago, Illinois, USA), the categorical data were analysed by Pearson's χ 2 test and P-values of <0.05 were considered statistically significant. The protocol of this study was submitted to the National Health Research Ethics Committee, Federal Ministry of Health, Sudan. The committee approved the testing of the stored DBS samples collected in the context of the previous study [Reference Adam5] for IgG antibodies against VZV. Informed consent was obtained from all participants for the initial study [Reference Adam5].
The overall seroprevalence of VZV IgG antibodies in Khartoum state was 50.4%, ranging between 14.3% in children, 74.5% in adult volunteers and 79.3% among HCWs (Table 1). As shown in Figure 1, a significant difference in seropositivity was observed between children and volunteer adults from the general population (P < 0.001). The seropositivity in children increased significantly with age from 6.0% among 1‒5 years old to 24.5% among 11‒15 years old (P = 0.001). Age was also correlated with seropositivity in adults, which ranged from about 65% among both volunteers and HCWs aged 21‒30 years to 78.7% (P = 0.143) and 86.6% (P = 0.009) among those aged ⩾41 years, respectively. In contrast, there was no significant difference between seropositivity of volunteer adults from the general population and HCWs (P = 0.272). Although not significant either, nurses showed a higher seropositivity (82.8%) compared to other occupational groups (P = 0.495). Neither sex nor residence was associated with VZV seropositivity (P > 0.05) in any of the study groups (Table 1). Among the 350 participating women, 317 (90.6%) were of childbearing age (21–49 years) and more than a quarter of them (n = 81/317, 25.6%) were seronegative.
Pos, positive; Neg, negative.
a This age group was not further subdivided because of the limited number of participants and no significant seroprevalence increases.
While data on VZV exposure among African children are limited, our results are comparable to what was previously reported in Congo, where the overall seroprevalence of VZV antibodies was 8.0% among 7195 children and increased with age from 2% in 6 months old to 19% in 59 months old [Reference Doshi6]. Moreover, our findings suggest that a high proportion of Sudanese adults remain susceptible to VZV infection. This agrees with a previous study reporting a seroprevalence of 64% among 2196 adult Sudanese asylum seekers in Germany. In that study, Sudanese had the lowest VZV seroprevalence among all investigated nationalities and among individuals aged <45 years [Reference Toikkanen7]. Our findings also agree with reports from other tropical countries, where varicella is acquired at a higher mean age [8], possibly because of the heat-labile nature of VZV that may influence exposure [Reference Gershon1]. The nearly 21% susceptible HCWs identified in this study pose a risk to vulnerable patients such as severely immunocompromised people, pregnant women and premature infants [8]. In addition, more than 25% seronegative women of childbearing age are susceptible to primary infection during pregnancy with the risk of severe consequences for the child [Reference Gershon1, Reference Heininger and Seward2]. Our findings suggest that both women of reproductive age and HCWs are important target groups for VZV immunity evaluation and vaccination [Reference Shefer9], even though the two sequential vaccinations required pose an additional financial burden.
Although the samples used for this study had been collected in 2015 and 2016, there is no reason to believe that the sero-profiles from later time points look different, since there has been no change in varicella surveillance or prevention policy in Sudan since sample collection took place. Because data on varicella exposure are largely lacking for Africa, our findings on disease epidemiology are not only of local interest, but also to public health authorities and HCWs from similar settings without vaccination and case notification.
A limitation of our study to be addressed by future research is that the results are not necessarily representative of the whole Sudanese population since samples were collected from a limited geographical area and defined population groups, due to logistic and financial reasons. Although we cannot completely exclude cross-reactivity with antibodies against herpes simplex virus [Reference Bernstein10], the manufacturer reported no false positives among sera from 12 herpes simplex virus type 1 patients and an overall assay specificity of 100% in the ELISA kit manual.
In conclusion, the results of this first VZV study in Sudan suggest active virus circulation in different age groups. Especially HCWs at the start of their career would benefit from vaccination, not only to save themselves from herpes zoster and its sequelae, but also to indirectly protect vulnerable patients. Although data from Africa are largely lacking, the high susceptibility rate among women of childbearing age highlights the danger of varicella infection during pregnancy with potential sequelae in infants.
Acknowledgements
We thank all children and their parents, employees at the National Centre for Research, Sudan and HCWs at the paediatric hospitals for accepting to participate in the study. We also wish to thank the administrations of Ahmed Gasim and Mohamed Elamin Hamid Paediatric Hospitals, Ibrahim Malik Teaching Hospital, Khartoum, Sudan for facilitating the sample collection.
Financial support
This work was financially supported by the Luxembourg Ministry of Foreign and European Affairs and the Luxembourg Institute of Health in the context of the ‘Microbiology for Development’ project.
Conflict of interest
None.
Data availability statement
The datasets used in the current study are available upon request from the corresponding author.