Seroepidemiology of human enterovirus 71, Singapore. (Dispatches).

Human enterovirus 71 has caused outbreaks in many parts of the world, especially Southeast Asia, with some fatal cases. The epidemiology of this viral infection is not well understood. We conducted a serologic survey in Singapore children, and the results indicate that infection occurs largely in preschool settings.

**********

Human enterovirus 71 (HEV71) is an emerging concern in many parts of the world. It has caused several large outbreaks, occasionally associated with many deaths in children (1-3). In September and October 2000, a large nationwide outbreak of hand, foot, and mouth disease (HFMD) caused by HEV71 occurred in Singapore (4). Most of the cases were in children <6 years of age; four cases were fatal.

The epidemiology of HEV71 infection in Singapore and most parts of the world has not been well studied. A few reports suggest that HEV71 infection is common and mostly subclinical (5,6). Differences in the DNA sequences of the HEV7 i isolates do not appear to play an important role in clinical outcome (7,8). Ho and colleagues (3) cited preliminary evidence indicating that more than half the adult population in Taiwan had been exposed to HEV71 before the 1998 epidemic.

The settings where most HEV71 transmission occurs are, however, uncertain. During the 2000 outbreak of HEV71-associated HFMD in Singapore, a decision was made to close all preschool centers nationwide in an effort to break the chain of transmission of this virus (4). The effectiveness of this control measure is unclear. HFMD was made a legally notifiable disease on October 1, 2000, which coincided with both the middle of the HEV71-associated HFMD outbreak and the closing of the preschool centers in Singapore (4). Although the closure of preschool centers was thus temporally associated with a decline in reported HFMD cases, no comparable data were available before and after the implementation of the preschool closure to allow assessment of the impact of this measure.

To devise appropriate preventive measures, the transmission of this virus in the natural setting needs to be determined. A serologic survey would be useful for this purpose. Such a study in children had not been conducted in this region. We report the findings of an HEV71 serologic survey in Singapore children.

The Study

We surveyed 856 children [less than or equal to] 12 years of age. Serum samples were collected, with informed parental consent, during the 18-month period of July 1996 to December 1997 at a pediatric clinic at the National University Hospital, which serves the entire country. All children who were born at the hospital or who were brought for routine visits and vaccinations during this period were included. The children had no sign of disease at the time of sample collection.

The serum samples, which had been used in a previous study of dengue (9), were divided and stored at -20[degrees]C and inactivated at 56[degrees]C for 30 min before use. Neutralizing antibody against HEV71 (EV71/7423/MS/87), an isolate that had been characterized previously (10), was detected by using a neutralization test by microtechnique as previously described, with modifications (11). Sample dilutions of 1:8 to 1:2,048 were assayed. Twenty-five microliters of 100 tissue culture infective dose (TCI[D.sub.50]) virus was mixed with 25 [micro]L of the appropriate serum dilution and incubated for 2 h at 37[degrees]C in a C[O.sub.2] incubator, followed by the addition of 100 [micro]L of rhabdomyosarcoma cell suspension at a concentration of 2 x [10.sup.4] cells/0.1 mL. Each dilution was tested in duplicate. Readings were taken visually with an inverted microscope after 6 days of incubation at 37[degrees]C in 5% C[O.sub.2]. The antibody titer for the sample is the highest dilution that prevents the development of cytopathic effects in both wells. An antibody titer of [greater than or equal to] 8 was considered positive. The geometric mean titer (GMT) and 95% confidence intervals (95% CI) were also calculated. Statistical analysis was done by Student t test.

The results showed that 44.0% of mothers had antibodies to HEV71 (deduced from antibody prevalence in cord blood), which waned rapidly so that after 1 month, none of the children tested had maternal antibodies to HEV71 (Figure 1). Only 1 (0.8%) of the 124 samples from children ages 1-23 months had anti-HEV71 antibodies. From 2 to 5 years, the seropositive rate increased at an average of 12% per year. In samples from children >5 years old, the age-specific seroprevalence reached a steady state at approximately 50%.

[FIGURE 1 OMITTED]

Figure 2 shows the age-specific GMT in seropositive samples by age group. Formal schooling in Singapore begins at 6 years of age. From 2 to 5 years, however, most children receive preschool education in child-care centers or kindergartens. The GMT of the anti-HEV71 antibodies was higher in preschool children (GMT 46.8; 95% CI 34.7 to 63.1) than in those of formal school age (6-12 years old) (GMT 28.8; 95% CI 25.7 to 32.4). The difference in these two means was statistically significant (t test = 3.07; df = 240; p=0.002). Furthermore, the GMT titer of maternal antibody in neonatal blood (GMT 17.8; 95% C1 13.2 to 24) was also significantly lower than in the preschool children (t test = 4.02; df= 78; p=0.0001).

[FIGURE 2 OMITTED]

Conclusions

This report is the first detailing the seroepidemiology of HEV71 in Singapore children. The results indicate that most infection occurs in preschool-aged children. The concentration of this susceptible group of the population in classrooms, along with the sharing of toys and other teaching tools, are factors contributing to HEV71 transmission.

The differences in GMT in the different age groups indicate that infection outside these preschool years is uncommon. This finding is supported by the following observations: 1) the small proportion of children <2 years old who were seropositive; 2) the proportion of seropositive children reached a steady state after 5 years of age; and 3) the GMT of anti-HEV71 antibody declined with age. If substantial levels of transmission occurred at home, GMT would be expected to increase with age, as reexposure to HEV71 would boost the antibody levels in both children and mothers. Transmission at home would also result in high maternal antibody titers that last for at least 6 months, as observed in our previous study of dengue (9). Furthermore, a fair proportion of children <2 years old would also be expected to be seropositive. Instead, the results of this study indicate that HEV71 is transmitted in preschool centers, where older children and adults are less likely to spend substantial amount of time. The control of HEV71 infection should thus be specifically focused at such places. The cost-effectiveness of implementing preventive measures such as strict observation of handwashing in a preschool setting in Singapore should also be evaluated.

For this study, we used serum samples collected during 1996-1997. In 1997, an outbreak of HEV71 in children occurred in Malaysia that resulted in several deaths (1,2). In Singapore at that time, HFMD was monitored on the basis of volunteer reporting from the operators of preschool centers. This surveillance allowed 12 localized clusters of HFMD to be identified (12). Virus isolation studies were also carried out on samples from the children who attended these centers. Coxsackie virus A16 was isolated in three of these clusters, and HEV71 was isolated in one. No viruses were isolated in the other clusters. No HEV71-related deaths were recorded during this period. These observations indicate that HEV71 was present during or before the time of sample collection, although no nationwide outbreak was observed during that time.

This study is confined in scope to Singapore children. To support the hypothesis that HEV71 transmission occurs largely in the preschool setting, a serologic study of preschool teachers and directors would be very useful. Furthermore, as the mode of transmission of enteroviruses is essentially the same, by the fecal-oral route, the serologic profile for the other enteroviruses may be the same as that observed in this study. No such data are currently available.

In conclusion, HEV71 infection is common in Singapore children and is acquired largely in the preschool years. Transmission of this virus is lower in the other age groups. This finding suggests that HEV71 transmission occurs mainly in places where preschool children congregate, and public health measures to control the spread of this virus should focus on these places.

Acknowledgments

We thank Mark Pallansch for the use of the HEV71 (EV71/7423/ MS/87) isolate and Ling Ai Ee and Chan Kwai Peng for providing the rhabdomyosarcoma cell line.

References

(1.) Lum LCS, Wong KT, Lam SK, Chua KB, Goh AYT, Lim WL, et al. Fatal enterovirus 71 encephalomyelitis. J Pediatr 1998;133:795-8.

(2.) Chan LG, Parashar UD, Lye MS, Ong FGL, Zaki SR, Alexander JP, et al. Deaths of children during an outbreak of hand, foot and mouth disease in Sarawak, Malaysia: clinical and pathological characteristics of the disease. Clin Infect Dis 2000;31:678-3.

(3.) Ho M, Chen ER, Hsu KH, Twu S J, Chen KT, Tsai SF, et al. An epidemic of enterovirus infection in Taiwan. N Engl J Med 1999;341:929-35.

(4.) Anonymous. Surveillance of hand, foot and mouth disease in Singapore. Epidemiol Bull 2001;27:23-7.

(5.) Deibel R, Gross LL, Collins DN. Isolation of a new enterovirus (38506). Proc Soc Exp Biol Med 1975;148:203-7.

(6.) Brown BA, Oberste MS, Alexander JP Jr, Kennett ML, Pallansch MA. Molecular epidemiology and evolution of enterovirus 71 strains isolated from 1970 to 1998. J Virol 1999;73:9969-75.

(7.) AbuBakar S, Chee HY, A1-Kobaisi MF, Sioshan J, Chua KB, Lam SK. Identification of enterovirus 71 isolates from an outbreak of hand, foot and mouth disease (HFMD) with fatal cases of encephalomyelitis in Malaysia. Virus Res 1999;61:1-9.

(8.) Yan JJ, Su IJ, Chen PF, Liu CC, Yu CK, Wang JR. Complete genome analysis of enterovirus 71 isolated from an outbreak in Taiwan and rapid identification of enterovirus 71 and coxsackievirus A16 by RT-PCR. J Med Virol 2001;65:33 I-9.

(9.) Ooi EE, Hart T J, Tan HC, Chan SH. Dengue seroepidemiology in Singapore. Lancet 2001;357:685-6.

(10.) Brown BA, Pallansch MA. Complete nucleotide sequence of enterovirus 71 is distinct from poliovirus. Virus Res 1995;39:195-205.

(11.) Yin-Murphy M, Tan KL, Lim GN, Quek JH, Ishak B, Phoon MC. Poliovirus neutralizing antibody in infants and cord blood. Ann Acad Med Singapore 1993;22:281-5.

(12.) Hand, foot and mouth disease. In: Communicable disease surveillance in Singapore, 1997. Singapore: Quarantine and Epidemiology Department, Ministry of the Environment; 1997. p 5-21.

Address for correspondence: Eng-Eong Ooi, Environmental Health Institute, National Environment Agency, 40 Scotts Road, Singapore 228231; fax: [phone]; e-mail: [e-mail]

Dr. Eng-Eong Ooi is head of the Environmental Health Institute, National Environmental Agencyt, Singapore. His research interest is in the epidemiology and prevention of viral diseases.

Eng-Eong Ooi, * Meng-Chee Phoon, ([dagger]) Baharudin Ishak, ([dagger]) and Soh-Ha Chan ([dagger])

* National Environment Agency, Singapore; and ([dagger]) National University of Singapore, Singapore