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Virus and host-specific differences in oral human herpesvirus shedding kinetics among Ugandan women and children


Human herpesviruses (HHV) establish lifelong latent infection and are transmitted primarily via shedding at mucosal surfaces. Each HHV causes a unique spectrum of disease depending on the infected individual’s age and immunity. We collected weekly oral swabs from young children and mothers in 32 Ugandan households for a median of one year. We characterized kinetics of oral shedding during primary and chronic infection for each virus. Cytomegalovirus (CMV), Epstein-Barr virus (EBV), and HHV-6 were shed at high rates following primary infection. The rate of oral herpes simplex virus (HSV) shedding was lower overall, and children and mothers with chronic HSV infection had lower shedding rates than children with primary infection. CMV shedding rate and viral load were higher in children with primary infection compared to children with chronic infection, and even lower in mothers with chronic infection. HHV-6 shedding rate and viral load were similar between children with primary or chronic infection, but lower in mothers. EBV shedding rate and quantity decreased less dramatically in mothers versus children, with HIV-positive mothers shedding at a higher rate than HIV-negative mothers. Each HHV has a distinct pattern of oral shedding which depends partially on the age and immune status of the host.


The human herpesviruses (HHVs) are DNA viruses that establish latency, allowing lifelong infection. Periodic viral reactivation results in mucosal shedding, by which transmission to new hosts can occur. Each HHV causes unique manifestations, which reflect virus-specific differences in cell tropism and patterns of replication during primary infection and reactivation, as well as the immune status of the host. Primary HHV infections frequently occur during early childhood, particularly in the developing world1,2,3,4. While levels of HHV replication and mucosal shedding are generally greater in young children and during primary infection4,5,6,7,8, there are limited data that directly contrast shedding patterns in children versus adults. In this study, we utilized a detailed longitudinal cohort to compare the oral shedding patterns of multiple HHVs – herpes simplex virus (HSV), Epstein-Barr virus (EBV), cytomegalovirus (CMV), and HHV-6 – among young children with primary infection, older children with chronic infection, and their mothers to investigate the natural history of mucosal replication by different HHVs. These results illustrate that the pattern of oral shedding is unique for each HHV and depends on the timing of infection and immune status of the infected individual.


Study participants and infection status

Thirty-two mothers, 32 newborns and 49 secondary children were followed for a median duration of 57 weeks. Two secondary children were excluded because they had fewer than 2 swabs collected. The median age for the remaining 47 secondary children was 3.5 years (range 0.3–6.3 years). Seventeen mothers, four secondary children and no infants were HIV-infected at the time of enrollment; seven secondary children had unknown HIV status.

Postnatal EBV, CMV and HHV-6 acquisition occurred in a majority of infants, whereas HSV acquisition was less common (Table 1). Congenital CMV infections occurred in two infants, who were excluded from the analysis of CMV shedding. Combining serology and shedding data, we identified three primary EBV infections among secondary children (at ages 1.7, 1.8, and 2.9 years). We also identified one secondary child with primary HSV-1 infection at 4.4 years of age, based on seroconversion. No other HHV infection in secondary children was deemed to be primary by our criteria which are described in the Methods. Two secondary children were uninfected with CMV, 13 uninfected with HSV, and 8 uninfected with HHV-6. These children were excluded from shedding analyses for those viruses. All mothers had serologic evidence of past CMV infection. All but two mothers had serological evidence of past HSV-1 infection; one mother was HSV seronegative and excluded from HSV analyses and one mother had insufficient quantity of sample for serologic testing but did have at least two HSV-1 qPCR positive oral swabs and so was retained in HSV analyses. We originally tested oral samples for HHV-8 but observed minimal shedding in infants or secondary children so excluded this virus from the analysis.

Table 1 Study participants and samples.

All primary infections were asymptomatic. We did not assess chronically infected children or mothers for symptoms.

General shedding patterns

Primary infection in children had a notable pattern of persistent shedding over time and in higher quantities when compared to the shedding of the same virus by mothers or children with chronic infection in the same household. The nature of HSV shedding was episodic in infants, children with chronic infecion and mothers, with intermitent negative samples frequently noted, most commonly after only 1–2 consecutive positive samples (Figs 1 and S1). EBV displayed a mixed pattern in all three age groups with instances of episodic shedding lasting only a single week and more continuous shedding persisting for many months; in general, viral loads were only somewhat stable during sustained EBV shedding and often were similar across age cohorts (Figs 1 and S2). As previously described, CMV shedding in infants consisted of occasional brief episodic shedding followed by sustained shedding at high viral loads with notable expansion, stabilization and contraction phases of shedding9,10; instances of prolonged, continuous shedding, as well as brief, episodic CMV shedding were noted in chronically infected children and mothers; within each family, viral loads in chronically infected children and mothers were consistently lower than those observed during primary infection (Figs 1 and S3). HHV-6 shedding was continuous in both infants and chronically infected children, but usually episodic and sometimes at lower viral loads in mothers (Figs 1 and S4).

Figure 1
figure 1

Representative oral human herpesvirus shedding patterns within families. Each panel depicts the oral shedding of one virus in a single household. The weekly viral load of (A) HSV, (B) EBV, (C) CMV, and (D) HHV-6 detected in oral swabs by qPCR is shown for each family member (mother, gray; children with primary infection, red; children with chronic infection, blue). Missing data points are not included as points on the graphs. Complete sets of plots for all the families participating in the study can be found in the Supplementary Figures S1S4.

Due to the high incidence and prolonged shedding of primary HHV infections, many infants demonstrated concurrent shedding of multiple viruses (Figs 2 and S5). During the first 365 days of life at any point in time, one infant shed a single virus, four infants shed two viruses, seventeen infants shed three viruses, and ten infants shed four viruses. All infants who shed 3 or 4 HHVs at any point during the first year of life, also shed these viruses concurrently at contemporaneous timepoints.

Figure 2
figure 2

Representative examples of shedding patterns of children with primary infections with multiple human herpesviruses. Beginning at the time of primary infection, shown is the quantity of viral DNA detected in oral swabs collected weekly from the time of birth (Day 0). Each panel shows data from one representative infant. Missing data points are not included as points on the graphs. Complete sets of primary infections can be found in the Supplementary Figure S5.

We describe unique shedding patterns for each virus below and make comparisons across age cohorts within virus, and between viruses within each age cohort. All shedding rate comparisons are summarized in Supplementary Table 1 while all viral load comparisons are summarized in Supplementary Table 2.

Unique age dependent HSV shedding rates and viral loads

There was a higher HSV shedding rate in primary infected children relative to children with chronic infection (Figs 3 and S6A). HIV-negative and positive mothers in turn shed HSV less frequently than secondary children (Figs 3 and S6A).

Figure 3
figure 3

Proportions of positive swabs according to age group for each human herpes virus. Boxplots represent distributions of individual values. The boxes represent the interquartile range. The stems in the plots represent up to 1.5 times the value of this range.

The median HSV shedding rate during primary HSV was comparatively low relative to other primary HHVs, though HSV was still detected in nearly 50% of samples during primary infection; a similar trend was noted for HSV shedding relative to other HHVs among the secondary children (Figs 3 and S6B),. HIV-negative and positive mothers also shed HSV at lower rates than EBV and HHV-6 (Figs 3 and S6B).

HSV viral loads were higher in children with primary infection relative to chronically infected children and HIV negative and positive mothers with chronic infection who had equivalent mean viral loads; however, these differences did not reach statistical significance (Figs 4 and S7A).

Figure 4
figure 4

Estimated mean viral load for positgive samples according to age group for each human herpesvirus. The bars represent 95% confidence intervals.

Unique age dependent EBV shedding rates and viral loads

EBV shedding rates were extremely high in all age cohorts. Children with chronic EBV infection had statistically significantly lower shedding rates than children with primary EBV infections who shed nearly constantly (Figs 3 and S6A). HIV-negative mothers shed EBV at very high rates (median 65%) that were not statistically lower than rates in secondary children. There was considerable variability in the rate of EBV shedding among children with chronic infection and among mothers relative to primary infections (Fig. 3).

Similar trends were noted for EBV viral loads which were highest during primary infection with lower mean viral load in secondary children and lowest mean viral load in HIV-negative mothers; the only statistically significant difference in mean EBV viral load was between primary infected children and HIV negative mothers (Figs 4 and S7A).

EBV viral loads were notably high in secondary children relative to all other HHVs in this age cohort, and in HIV negative mothers relative to CMV and HHV6 (Figs 4 and S7B).

Unique age dependent CMV shedding rates and viral loads

Children with primary CMV infection shed at extremely high rates (median 100%) and had statistically significantly higher shedding rates than secondary children (Figs 3 and S6A). However, the drop off in shedding rates between secondary children and HIV-negative and positive mothers was more profound for CMV than for other viruses (Figs 3 and S6A). There was also greater variability in the rate of CMV shedding among children with chronic infection and mothers relative to primary infections (Fig. 3). While secondary children shed CMV at similar rates to EBV and HHV-6, maternal CMV shedding rates were statistically lower than maternal EBV and HHV-6 shedding rates (Figs 3 and S6B).

There was a dramatic, strongly significant decrease in viral load (almost 2 log10 DNA copies per swab) between children with primary versus chronic CMV infection, with no differences noted between children with chronic infection and mothers (Figs 4 and S7A). HIV negative mothers shed CMV at lower viral loads than HSV and EBV Figs 4 and S7B).

Unique age dependent HHV-6 shedding rates and viral loads

Unlike, the other HHVs, there was no drop off in shedding rate of HHV-6 between primary infection and secondary children: both groups shed at extremely high rates (Figs 3 and S6A). Maternal HHV-6 shedding rates showed great heterogeneity though median rates were high in both HIV-1 negative and positive cohorts with significantly lower rates in HIV-positive mothers relative to both age cohorts in children (Figs 3 and S6A).

In contrast to the other HHVs, children with primary and chronic infection, and HIV negative mothers, shed HHV-6 at equivalent viral loads (Figs 4 and S7A). HHV-6 viral loads during primary infection were lower than all other HHVs (Figs 4 and S7B).

Different EBV shedding rates and viral loads among HIV-positive and -negative mothers

There were no statistically significant differences according to shedding rate (Figs 3 and S6A) or viral load (Figs 4 and S6A) between HIV negative and positive mothers for HSV,CMV or HHV-6. Only EBV infection had a statistically significant higher oral shedding rate in HIV-positive versus HIV-negative mothers (Figs 3 and S6A). EBV mean viral loads appeared higher in HIV positive mothers relative to HIV negative mothers though this trend did not reach statistical significance (Figs 4 and S7A). HHV-6 shedding rate and viral load did not statistically differ between HIV-negative and positive mothers, but median shedding rate and mean viral load were lower in the HIV-positive mothers relative to children with primary and chronic infection.

Summary of differences in shedding by cohort group and virus

We used frequency histograms to simultaneously display shedding rate and quantity, highlighting general trends of shedding specific for each virus (Fig. 5). In general, HSV was notable for lower shedding rates than the other viruses in children with primary infection with a decrease in shedding rate at all viral loads in children with chronic infection (Fig. 5A). EBV was shed frequently by all cohort groups; changes according to age were subtle though HIV-negative mothers shed less frequently and at lower viral loads than chronically infected children or HIV-positive mothers; HIV-positive mothers shed at the highest viral loads, at rates akin to children with primary infection (Fig. 5B). CMV displayed a highly distinct pattern with a small change in shedding rate between children with primary and chronic infection, but a profound decrease in mean viral load; mothers had a lower shedding rate overall than children with chronic infection (Fig. 5C). HHV-6 shedding rates were generally high but viral loads were lower than all other viruses; HHV-6 was also unique because shedding kinetics were comparable in children with primary or chronic infection, while viral load and shedding rates were lower in mothers (Fig. 5D).

Figure 5
figure 5

Summary of shedding rate and quantity across viruses and cohort groups. Mothers are classified according to their HIV status. Frequency histograms demonstrate unique shedding patterns for (A) HSV, (B) EBV, (C) CMV and (D) HHV-6.


The distinct shedding patterns of different HHVs allow inferences about the balance between viral replication and host immunity as infection progresses from acute to chronic phase. While HHV shedding is generally more common and at higher viral loads following primary infection, a more detailed assessment of individual HHVs has not been performed4,5,6,7,8. Here we demonstrate that in a cohort of Ugandan families sampled weekly for a median of over a year, patterns of shedding kinetics were unique for each of the HHVs studied. In particular, shedding rates and viral loads showed distinctive trends as a function of age. HIV infection appeared to only increase oral EBV shedding in mothers. These results imply that each HHV elicits mucosal immune responses that differ dramatically in terms of intensity and timing.

EBV, CMV and HHV-6 were shed nearly constantly during primary infection in infancy and throughout early childhood, while the HSV shedding rate was approximately 50%. Concurrent primary infection was extremely common. This frequent oral replication of multiple HHVs has little overt impact on health or symptoms4, underscoring how well each virus has co-adapted with its human host; viral replication and immune control are compartmentalized such that mucosal shedding is frequent but systemic viral spread and end-organ damage is prevented11,12,13. CMV, EBV and HSV viral loads were higher than those of HHV-6 during primary infection. We speculate that differences in viral load among HHVs reflect underlying heterogeneity in rates of viral replication and spread, the effectiveness of the local immune response, and perhaps target cell availability10,14,15.

Age-dependent control of viral replication and disease manifestations is well recognized for some HHVs16,17,18. By examining a cohort that ranged from birth to adulthood, we quantified profound differences in the dynamics of oral shedding among these viruses. The HSV shedding rate was markedly lower among children with chronic infection compared with primary infection, though the distribution of viral loads decreased less substantially and shedding was episodic in both groups. The HSV shedding rate and viral load were lower still in mothers versus chronically infected children, suggesting that intensification of immunity continues even after resolution of primary infection.

EBV demonstrated an altogether different shedding structure. Overall, shedding rates were considerably higher than HSV. While the shedding rate decreased in a significant stepwise fashion from infancy to childhood, and viral load continued to decrease into adulthood, marked heterogeneity was seen among children and mothers with shedding rates exceeding 50% in over half of both cohorts. On the other hand, as with HHV-6, age-associated decreases in viral load were less impressive relative to CMV and HSV.

Shedding patterns of CMV contrasted starkly with those of HSV and EBV. The shedding rate of CMV decreased markedly in some children with chronic infection relative to primary infection, but many chronically infected children shed CMV nearly constantly akin to primary infection. Yet, CMV viral loads were dramatically lower in children with chronic versus primary infection. Mothers in our cohort had marginally lower viral loads than children with chronic infection, but had a considerably lower shedding rate and a higher likelihood of episodic shedding. Recent analyses by our group suggest that maternal oral shedding may represent re-infection via the neonate rather than reactivation. Overall, these results demonstrate ongoing fortification of the anti-CMV immune response from childhood into adulthood, perhaps by a different mechanism than occurs with transition from infancy to childhood.

For HHV-6, immune control appeared delayed relative to the other HHVs, as continuous shedding and viral load were equivalent between children with primary and chronic infection but decreased in adult women. Yet, there was a wide range of shedding rates observed among both HIV-positive and -negative mothers in our cohort, and the median shedding rate exceeded 50%. As with the other HHVs, it is unclear if high shedding rates observed in certain mothers were due to re-infection or reactivation19,20,21.

EBV was unique among these viruses in that HIV infection was a clear risk factor for enhanced oral shedding rate and potentially higher viral load in mothers, implying that deficits in cell-associated mucosal immunity allow adults with HIV infection to control EBV as poorly as infants with primary infection. The clinicopathologic correlate of high oral EBV viral loads in people with HIV/AIDS is oral hairy leukoplakia22. Increased EBV shedding in the setting of HIV co-infection has been reported23,24. While CMV is associated with numerous HIV-associated opportunistic infections, HIV-positive and -negative mothers controlled CMV in the oral compartment equally effectively, and had considerably lower shedding rates than children. Similarly, the HSV shedding rate also was similar between HIV-positive and -negative mothers. These findings differ from other reports suggesting increased oral CMV and HSV shedding among adults with HIV infection24, but are consistent with the lack of difference observed in genital HSV-2 shedding due to HIV status in pesrons whose CD4 counts are preserved25. Of note, the HIV-positive women in our cohort had relatively high CD4 T cell counts4, which may influence control of oral shedding of these viruses26. We unfortunately did not collect maternal HIV viral load data in our study.

Our study has several limitations. First, swabs were collected weekly. While this should have no bearing on our determinations of shedding rate and quantity, which depend only on swab sample size, we may miss viral shedding episodes (defined as positive oral swabs followed by viral clearance in the oral mucosa), particularly but not limited to those that are less than a week in length.

Second, our cohorts were heterogeneous with respect to age and other demographic features and this may impact shedding kinetics. Our findings from mothers may or may not be generalizable to other populaions such as men who have sex with men. We nevertheless believe that our summary statistics provide a comprehensive ecologic overview of HHV shedding patterns in a sub-Saharan African setting.

Third, we were not able to perform typing on all swabs to distinguish HSV-1 from 2 or HHV-6A from 6B; however, the majority of oral shedding of these viruses is due to HSV-1 and HHV-6B3,27,28.

Fourth, the categorization of age and timing of infection was not precise for all analyses, and it was not feasible to study all household members (e.g., fathers). It was also not possible to determine at what point an infection changed from acute to chronic, and if all oral shedding was followed by systemic infection and subsequent seroconversion; as such, children with primary infection were categorized throughout follow-up. Some women may not have been infected with viruses that they did not shed, and for which serology was not performed. However, given the near universal rates of infection in sub-Saharan Africa with the HHVs studied1,2,4,29, this effect is likely negligible; indeed, most mothers shed HHV-6 and EBV in this cohort. Similarly, 16% of secondary children did not shed HHV-6 and were not included in the analysis but could theoretically have had chronic infection.

Finally, we can not exclude the possibility of a small number of false negative and positive swabs. Occasional error in swabbing technique may have allowed for false negative values or statistical noise. Based on the very clear patterns of shedding which emerge from our analysis, we believe these effects are minimal. Our previous demonstration of nearly continuous shedding during primry CMV infection with highly reproducible patterns of viral expansion, clearance and re-expansion across infants, clearly indicates that swabs were obtained in a consistent and rigorous fashion in all study participants9,10. Our cutoff of 3 DNA copies per reaction has been optimized for HSV infection but not for other HHVs30. Some low level positive results could theoretically represent environmental contamination rather than true viral replication.

In summary, we demonstrate the first kinetic picture of multiple primary viral infections in a prospective study cohort and compare shedding patterns of these viruses according to age and time of infection. We show that each HHV has its own shedding fingerprint, which in turn may have important implications for transmission dynamics and prevention strategies. Future studies are indicated to better understand the complex interplay between host and pathogen that results in highly specific shedding patterns.


Ethics statement

All methods were carried out in accordance with relevant international research and human subjects guidelines and regulations. All experimental protocols were approved by human subjects protection committees in Kampala, Uganda; Seattle, Washington; and Vancouver, Canada. Informed consent was obtained from all subjects.

Study cohort and data collection

A cohort of pregnant women with at least one other child <7 years old (“secondary children”) in the home were enrolled in Kampala, Uganda as previously described4. Oral swabs were collected from all the children and their mothers weekly starting from the birth of the new infant. Blood was collected from mothers and secondary children at baseline and after one year, and every four months from infants. Human subjects review committees approved all study procedures. HIV serostatus was determined using the documentation in the medical record of the results of standard HIV testing per Ugandan national guidelines31.

Laboratory assays

Swabs and plasma samples were tested by real-time quantitative (q)PCR for HSV-1 or 2, EBV, CMV, and HHV-6A or B using published methods4,32,33,34,35,36,37. The cutoffs for a positive test for swabs were three copies/reaction (~150 copies/mL of swab buffer) and one copy/reaction (50 copies/mL) for plasma. Typing was attempted for every sample with detectable HSV, and HHV-6 typing was performed for >1 sample from each subject with at least two positive results. Serology for CMV (IgM and IgG) and EBV (IgM and IgG against the viral capsid antigen, and IgG against nuclear antigen) was performed using ELISA kits (Wampole (Alere), Boucherville, Quebec), and for HSV-1 and HSV-2 using type-specific Western blot38. These serology tests were performed for most infants, but for only a subset of the secondary children, to supplement qPCR data when distinguishing chronic from primary infection. For the mothers, CMV and HSV but not EBV serology testing was done as above. Antibodies to HHV-6A or 6B were not measured.

Definitions of infection

For each virus, primary infection was defined by the onset of repeated detection of viral DNA detection in oral swabs and/or plasma of infants followed from birth4. Primary infection was defined for each virus in secondary children by seronegative status and no viral DNA detection in oral swabs at enrollment, followed by the onset of repeated detection of oral viral DNA detection in oral swabs and/or plasma [4] and/or seroconversion during the study. Secondary children with minimal evidence of virus by qPCR (<2 positive oral swabs, 0 positive plasma samples) and no positive serology were considered uninfected. All remaining secondary children were considered chronically infected (Fig. 6). For mothers, serology was used to confirm chronic infection with CMV and HSV. All mothers were assumed to have chronic infection with HHV-6 and EBV2,4.

Figure 6
figure 6

Infection classification scheme for secondary children in the study. Primary infection among secondary children was defined as those without viral DNA detected at the beginning of the study who either showed seroconversion or were seronegative and met the PCR-based definition of primary infection31. Children with minimal evidence of virus by PCR (<2 positive oral swabs, 0 positive plasma samples) and no positive serology were considered uninfected and excluded from shedding analysis for that virus. All remaining children were considered chronically infected.

Statistical methods

For each virus, all participants were classified into one of four cohort groups for comparisons: 1) infants or children with primary infection; 2) children with chronic infection; 3) HIV-negative mothers; and 4) HIV-positive mothers. Children who were uninfected for a given HHV were excluded from analyses of that virus and children with 1 or fewer swabs

collected were excluded from all analyses. Mothers who were seronegative for CMV or HSV were excluded from analyses for those viruses, respectively. In the case of congenital infections, the entire family of the infant with congenital infection was excluded from analyses for that virus. Swabs collected prior to primary infection in infants and secondary children were excluded to restrict the analyses to time periods during infection. Given the small number of HIV-infected children (four), this group was not analyzed separately. A minority of oral HSV shedding was HSV-2 (nine primary infections of HSV-1 and one primary infection with HSV-2). However, because not all samples were typeable, HSV-1 and 2 data were analyzed together. Because detection of HHV-6A shedding was rare and was only observed in combination with HHV-6B4, HHV-6A and 6B were not analyzed separately.

Shedding rates were defined as the number of positive samples divided by the total number of samples. We compared oral shedding rates and viral loads in two ways: 1) within a given virus across cohort groups; and 2) within a given cohort group across viruses. Viral loads were only analyzed using positive swabs. Shedding rates and quantities were compared using generalized estimating equations (GEE) to account for correlation within participant, with an additional small-sample empirical correction of the variances39,40. Relative risks comparing shedding rates were estimated using a Poisson family with a log link41. Viral loads were compared using a Gaussian family. P-values were adjusted for multiple comparisons using the Holm step-down Bonferroni method42. Statistical models were programmed in the SAS programming language using the GLIMMIX procedure with the FIRORES empirical estimator43 and the STEPDOWN correction.


  1. 1.

    Biggar, R. J. et al. Primary Epstein-Barr virus infections in African infants. I. Decline of maternal antibodies and time of infection. International journal of cancer 22, 239–243 (1978).

    CAS  Article  PubMed  Google Scholar 

  2. 2.

    Smith, J. S. & Robinson, N. J. Age-specific prevalence of infection with herpes simplex virus types 2 and 1: a global review. J Infect Dis 186(Suppl 1), S3–28, (2002).

    Article  PubMed  Google Scholar 

  3. 3.

    Zerr, D. M. et al. A population-based study of primary human herpesvirus 6 infection. The New England journal of medicine 352, 768–776 (2005).

    CAS  Article  PubMed  Google Scholar 

  4. 4.

    Gantt, S. et al. Prospective characterization of the risk factors for transmission and symptoms of primary human herpesvirus infections among Ugandan infants Journal of Infectious Diseases (2016).

  5. 5.

    Zanghellini, F., Boppana, S. B., Emery, V. C., Griffiths, P. D. & Pass, R. F. Asymptomatic primary cytomegalovirus infection: virologic and immunologic features. J Infect Dis 180, 702–707, (1999).

    CAS  Article  PubMed  Google Scholar 

  6. 6.

    Mbulaiteye, S. M. et al. High levels of Epstein-Barr virus DNA in saliva and peripheral blood from Ugandan mother-child pairs. J Infect Dis 193, 422–426 (2006).

    Article  PubMed  Google Scholar 

  7. 7.

    Cannon, M. J. et al. Repeated measures study of weekly and daily cytomegalovirus shedding patterns in saliva and urine of healthy cytomegalovirus-seropositive children. BMC Infect Dis 14, 569, (2014).

    Article  PubMed  PubMed Central  Google Scholar 

  8. 8.

    Stowell, J. D. et al. Cross-sectional study of cytomegalovirus shedding and immunological markers among seropositive children and their mothers. BMC Infect Dis 14, 568, (2014).

    Article  PubMed  PubMed Central  Google Scholar 

  9. 9.

    Mayer, B. T. et al. Transient Oral Human Cytomegalovirus Infections Indicate Inefficient Viral Spread from Very Few Initially Infected Cells. J Virol 91, (2017).

  10. 10.

    Mayer, B. T. et al. Dynamics of Persistent Oral Cytomegalovirus Shedding During Primary Infection in Ugandan Infants. J Infect Dis 214, 1735–1743, (2016).

    Article  PubMed  Google Scholar 

  11. 11.

    Campbell, A. E., Cavanaugh, V. J. & Slater, J. S. The salivary glands as a privileged site of cytomegalovirus immune evasion and persistence. Medical microbiology and immunology 197, 205–213, (2008).

    Article  PubMed  Google Scholar 

  12. 12.

    Balfour, H. H. Jr. et al. A prospective clinical study of Epstein-Barr virus and host interactions during acute infectious mononucleosis. The Journal of infectious diseases 192, 1505–1512, (2005).

    Article  PubMed  Google Scholar 

  13. 13.

    Asano, Y., Nakashima, T., Yoshikawa, T., Suga, S. & Yazaki, T. Severity of human herpesvirus-6 viremia and clinical findings in infants with exanthem subitum. J Pediatr 118, 891–895 (1991).

    CAS  Article  PubMed  Google Scholar 

  14. 14.

    Schiffer, J. T. et al. Rapid localized spread and immunologic containment define Herpes simplex virus-2 reactivation in the human genital tract. Elife 2, e00288, (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  15. 15.

    Hawkins, J. B., Delgado-Eckert, E., Thorley-Lawson, D. A. & Shapiro, M. The cycle of EBV infection explains persistence, the sizes of the infected cell populations and which come under CTL regulation. PLoS Pathog 9, e1003685, (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  16. 16.

    Prendergast, A. J., Klenerman, P. & Goulder, P. J. The impact of differential antiviral immunity in children and adults. Nat Rev Immunol 12, 636–648, (2012).

    CAS  Article  PubMed  Google Scholar 

  17. 17.

    Piriou, E. et al. Early age at time of primary Epstein-Barr virus infection results in poorly controlled viral infection in infants from Western Kenya: clues to the etiology of endemic Burkitt lymphoma. The Journal of infectious diseases 205, 906–913, (2012).

    Article  PubMed  PubMed Central  Google Scholar 

  18. 18.

    Gantt, S. & Muller, W. J. The immunologic basis for severe neonatal herpes disease and potential strategies for therapeutic intervention. Clin Dev Immunol 2013, 369172, (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  19. 19.

    Walling, D. M., Brown, A. L., Etienne, W., Keitel, W. A. & Ling, P. D. Multiple Epstein-Barr virus infections in healthy individuals. J Virol 77, 6546–6550 (2003).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  20. 20.

    Roest, R. W. et al. Genotypic analysis of sequential genital herpes simplex virus type 1 (HSV-1) isolates of patients with recurrent HSV-1 associated genital herpes. J Med Virol 73, 601–604, (2004).

    CAS  Article  PubMed  Google Scholar 

  21. 21.

    Boppana, S. B., Rivera, L. B., Fowler, K. B., Mach, M. & Britt, W. J. Intrauterine transmission of cytomegalovirus to infants of women with preconceptional immunity. N Engl J Med 344, 1366–1371 (2001).

    CAS  Article  PubMed  Google Scholar 

  22. 22.

    Walling, D. M., Flaitz, C. M. & Nichols, C. M. Epstein-Barr virus replication in oral hairy leukoplakia: response, persistence, and resistance to treatment with valacyclovir. J Infect Dis 188, 883–890, (2003).

    CAS  Article  PubMed  Google Scholar 

  23. 23.

    Lucht, E., Biberfeld, P. & Linde, A. Epstein-Barr virus (EBV) DNA in saliva and EBV serology of HIV-1-infected persons with and without hairy leukoplakia. J Infect 31, 189–194 (1995).

    CAS  Article  PubMed  Google Scholar 

  24. 24.

    Miller, C. S. et al. High prevalence of multiple human herpesviruses in saliva from human immunodeficiency virus-infected persons in the era of highly active antiretroviral therapy. J Clin Microbiol 44, 2409–2415, (2006).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  25. 25.

    Phipps, W. et al. Genital Herpes Simplex Virus Type 2 Shedding Among Adults With and Without HIV Infection in Uganda. J Infect Dis 213, 439–447, (2016).

    Article  PubMed  Google Scholar 

  26. 26.

    Schiffer, J. T. et al. Mathematical Modeling Predicts that Increased HSV-2 Shedding in HIV-1 Infected Persons Is Due to Poor Immunologic Control in Ganglia and Genital Mucosa. PLoS One 11, e0155124, (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  27. 27.

    Tembo, J. et al. Prevalence and risk factors for betaherpesvirus DNAemia in children >3 weeks and <2 years of age admitted to a large referral hospital in sub-Saharan Africa. Clin Infect Dis 60, 423–431, (2015).

    CAS  Article  PubMed  Google Scholar 

  28. 28.

    Wald, A., Ericsson, M., Krantz, E., Selke, S. & Corey, L. Oral shedding of herpes simplex virus type 2. Sex Transm Infect 80, 272–276, (2004).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  29. 29.

    Cleghorn, F. R. et al. Comparison of HHV-6 antibody titers in West Africa and the Caribbean. Ann Epidemiol 5, 497–500 (1995).

    CAS  Article  PubMed  Google Scholar 

  30. 30.

    Magaret, A. S., Wald, A., Huang, M. L., Selke, S. & Corey, L. Optimizing PCR positivity criterion for detection of herpes simplex virus DNA on skin and mucosa. J Clin Microbiol 45, 1618–1620, (2007).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  31. 31.

    Gantt, S. et al. Prospective Characterization of the Risk Factors for Transmission and Symptoms of Primary Human Herpesvirus Infections Among Ugandan Infants. The Journal of infectious diseases 214, 36–44, (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  32. 32.

    Boeckh, M. et al. Optimization of quantitative detection of cytomegalovirus DNA in plasma by real-time PCR. J Clin Microbiol 42, 1142–1148 (2004).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  33. 33.

    Zerr, D. M. et al. Case report: primary human herpesvirus-6 associated with an afebrile seizure in a 3-week-old infant. J Med Virol 66, 384–387 (2002).

    Article  PubMed  Google Scholar 

  34. 34.

    Kimura, H. et al. Quantitative analysis of Epstein-Barr virus load by using a real-time PCR assay. J Clin Microbiol 37, 132–136 (1999).

    CAS  PubMed  PubMed Central  Google Scholar 

  35. 35.

    Jerome, K. R., Huang, M. L., Wald, A., Selke, S. & Corey, L. Quantitative stability of DNA after extended storage of clinical specimens as determined by real-time PCR. J Clin Microbiol 40, 2609–2611 (2002).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  36. 36.

    Corey, L., Huang, M. L., Selke, S. & Wald, A. Differentiation of herpes simplex virus types 1 and 2 in clinical samples by a real-time taqman PCR assay. J Med Virol 76, 350–355, (2005).

    CAS  Article  PubMed  Google Scholar 

  37. 37.

    Casper, C. et al. Frequent and Asymptomatic Oropharyngeal Shedding of Human Herpesvirus 8 among Immunocompetent Men. The Journal of infectious diseases 195, 30–36 (2007).

    Article  PubMed  Google Scholar 

  38. 38.

    Ashley, R. L., Militoni, J., Lee, F., Nahmias, A. & Corey, L. Comparison of Western blot (immunoblot) and glycoprotein G-specific immunodot enzyme assay for detecting antibodies to herpes simplex virus types 1 and 2 in human sera. J Clin Microbiol 26, 662–667 (1988).

    CAS  PubMed  PubMed Central  Google Scholar 

  39. 39.

    Mackinnon, J. G. & White, H. Some Heteroskedasticity-Consistent Covariance-Matrix Estimators with Improved Finite-Sample Properties. J Econometrics 29, 305–325, (1985).

    Article  Google Scholar 

  40. 40.

    Long, J. S. & Ervin, L. H. Using heteroscedasticity consistent standard errors in the linear regression model. Am Stat 54, 217–224, (2000).

    Google Scholar 

  41. 41.

    Yelland, L. N., Salter, A. B. & Ryan, P. Performance of the modified Poisson regression approach for estimating relative risks from clustered prospective data. Am J Epidemiol 174, 984–992, (2011).

    Article  PubMed  Google Scholar 

  42. 42.

    Holm, S. A Simple Sequentially Rejective Multiple Test Procedure. Scand J Stat 6, 65–70 (1979).

    MathSciNet  MATH  Google Scholar 

  43. 43.

    Mancl, L. A. & DeRouen, T. A. A covariance estimator for GEE with improved small-sample properties. Biometrics 57, 126–134 (2001).

    MathSciNet  CAS  Article  PubMed  MATH  Google Scholar 

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The authors sincerely thank all of the study participants and their family members, as well as Annet Nakaganda, Zaam Nalule, Ruth Nakuya, Immaculate Mbarusha, Isma Lubega, Keith R. Jerome, Rhoda Ashley Morrow, Stacy Selke, Amalia Magaret, Anne Cent, Erica Sessle, Warren Phipps, James Ferrenberg, Ari Bitton, and Lisa Bunts. This work was supported by grants from the NIH – Roadmap KL2 Clinical Scholar Training Program KL2-RR025015–01 (SG), University of Washington Center for AIDS Research New Investigator Award P30-AI027757 (SG), P01-AI 030731 (LC, AW, JTS); R01-CA138165 (CC), and P30-CA015704 (CC and LC) – and by a Child & Family Research Institute Salary Award (SG).

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S.G., J.O., A.W., L.C., and C.C. conceived and designed the cohort; S.G., J.T.S., and C.C. conceived the analyses; L.M., B.T.M., E.M.K., and J.T.S. conducted the analyses; L.M., S.G., B.T.M., and J.T.S. drafted the manuscript; all authors edited and approved the final manuscript.

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Correspondence to Soren Gantt.

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Competing Interests

Dr. Gantt reports personal fees from Omeros, and research support from VBI Vaccines Inc. Dr. Wald reports personal fees from Aicuris, Amgen, and support from, Genocea, Gilead, and Vical. Dr. Schiffer reports research support from Genocea. Dr. Casper reports grants, personal fees and non-financial support from Janssen Pharmaceuticals, grants and non-financial support from GSK and TempTime Corporation. Dr. Corey reports personal fees from Immune Design. In addition, Dr. Corey has a patent null licensed. No other conflicts for disclosure.

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Matrajt, L., Gantt, S., Mayer, B.T. et al. Virus and host-specific differences in oral human herpesvirus shedding kinetics among Ugandan women and children. Sci Rep 7, 13105 (2017).

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