Transmission of Respiratory Syncytial Virus Among Children Under 5 Years in Households of Rural Communities, the Philippines

Hirono Otomaru, Taro Kamigaki, Raita Tamaki, Michiko Okamoto, Portia Parian Alday, Alvin Gue Tan, Joanna Ina Manalo, Edelwisa Segubre-Mercado, Marianette Tawat Inobaya, Veronica Tallo, Socorro Lupisan, Hitoshi Oshitani, Hirono Otomaru, Taro Kamigaki, Raita Tamaki, Michiko Okamoto, Portia Parian Alday, Alvin Gue Tan, Joanna Ina Manalo, Edelwisa Segubre-Mercado, Marianette Tawat Inobaya, Veronica Tallo, Socorro Lupisan, Hitoshi Oshitani

Abstract

Background: To develop a more effective vaccination strategy for reducing the impact of respiratory syncytial virus (RSV) infection, especially in young infants (<6 months old), it is necessary to understand the transmission dynamics of RSV.

Methods: We conducted a community-based prospective cohort study from 2014 to 2016 in Biliran Province, the Philippines, on children <5 years old. We collected nasopharyngeal swabs from symptomatic children with acute respiratory infection (ARI) during household visits and at health facilities. In households (n = 181) with RSV-positive ARI cases (RSV-ARI), we also identified ARI episodes among other children <5 years old in the same household. In addition, we determined the serial interval to estimate the basic reproduction number (R 0), the average number of secondary cases generated by a single primary case.

Results: In the 181 households analyzed, we found 212 RSV-ARI in 152 households with a single case and 29 households with multiple cases, which included 29 1st RSV-ARI and 31 2nd RSV-ARI. We also found possible index cases among children <5 years old in the same household for 29.0% (18 of 62) of young infants with RSV-ARI. The estimated mean serial interval was 3.2 days, and R 0 was estimated to be 0.92-1.33 for RSV-A and 1.04-1.76 for RSV-B, which varied between different times (2014 and 2015) and places.

Conclusions: Young infants are likely to acquire RSV infection from older children in the same household. Therefore, vaccination targeting older children might protect infants from RSV infection.

Keywords: basic reproduction number; household transmission; respiratory syncytial virus; serial interval; transmission dynamics.

Figures

Figure 1.
Figure 1.
Flow chart of the household analysis. ARI, acute respiratory infection; RSV, respiratory syncytial virus; RSV-HH1, households with 1 RSV-ARI patient; RSV-HH2, households with two or more RSV-ARI patient.

References

    1. Shi T, McAllister DA, O’Brien KL, et al. . Global, regional, and national disease burden estimates of acute lower respiratory infections due to respiratory syncytial virus in young children in 2015: a systematic review and modelling study. Lancet 2017; 390:946–58.
    1. Higgins D, Trujillo C, Keech C. Advances in RSV vaccine research and development - a global agenda. Vaccine 2016; 34:2870–5.
    1. Modjarrad K, Giersing B, Kaslow DC, et al. . WHO consultation on respiratory syncytial virus vaccine development report from a World Health Organization meeting held on 23-24 March 2015. Vaccine 2016; 34:190–7.
    1. Nokes DJ, Okiro EA, Ngama M, et al. . Respiratory syncytial virus infection and disease in infants and young children observed from birth in Kilifi District, Kenya. Clin Infect Dis 2008; 46:50–7.
    1. Crowe JE Jr, Williams JV. Immunology of viral respiratory tract infection in infancy. Paediatr Respir Rev 2003; 4:112–9.
    1. Sande CJ, Cane PA, Nokes DJ. The association between age and the development of respiratory syncytial virus neutralising antibody responses following natural infection in infants. Vaccine 2014; 32:4726–9.
    1. Brandenburg AH, Groen J, van Steensel-Moll HA, et al. . Respiratory syncytial virus specific serum antibodies in infants under six months of age: limited serological response upon infection. J Med Virol 1997; 52:97–104.
    1. Munoz FM, Piedra PA, Glezen WP. Safety and immunogenicity of respiratory syncytial virus purified fusion protein-2 vaccine in pregnant women. Vaccine 2003; 21:3465–7.
    1. Ochola R, Sande C, Fegan G, et al. . The level and duration of RSV-specific maternal IgG in infants in Kilifi Kenya. PLoS One 2009; 4:e8088.
    1. Graham BS. Protecting the family to protect the child: vaccination strategy guided by RSV transmission dynamics. J Infect Dis 2014; 209:1679–81.
    1. Hall CB, Geiman JM, Biggar R, et al. . Respiratory syncytial virus infections within families. N Engl J Med 1976; 294:414–9.
    1. Crowcroft NS, Zambon M, Harrison TG, et al. . Respiratory syncytial virus infection in infants admitted to paediatric intensive care units in London, and in their families. Eur J Pediatr 2008; 167:395–9.
    1. Munywoki PK, Koech DC, Agoti CN, et al. . The source of respiratory syncytial virus infection in infants: a household cohort study in rural Kenya. J Infect Dis 2014; 209:1685–92.
    1. Anderson RM, May RM.. Infectious Diseases of Humans: Dynamics and Control. Oxford: Oxford University Press; 1992.
    1. Ferguson NM, Cummings DA, Cauchemez S, et al. . Strategies for containing an emerging influenza pandemic in Southeast Asia. Nature 2005; 437:209–14.
    1. Wallinga J, Teunis P. Different epidemic curves for severe acute respiratory syndrome reveal similar impacts of control measures. Am J Epidemiol 2004; 160:509–16.
    1. Froda S, Leduc H. Estimating the basic reproduction number from surveillance data on past epidemics. Math Biosci 2014; 256:89–101.
    1. Weber A, Weber M, Milligan P. Modeling epidemics caused by respiratory syncytial virus (RSV). Math Biosci 2001; 172:95–113.
    1. Hogan AB, Glass K, Moore HC, Anderssen RS. Exploring the dynamics of respiratory syncytial virus (RSV) transmission in children. Theor Popul Biol 2016; 110:78–85.
    1. Malasao R, Okamoto M, Chaimongkol N, et al. . Molecular characterization of human respiratory syncytial virus in the Philippines, 2012-2013. PLoS One 2015; 10:e0142192.
    1. Furuse Y, Tamaki R, Okamoto M, et al. . et al. Association between preceding viral respiratory infection and subsequent respiratory illnesses among children: a prospective cohort study in the Philippines. J Infect Dis 2019; 219:197–205.
    1. Akaike H. Information theory and an extension of the maximum likelihood principle. In: Petrov, BN and Csádki, F. eds. Selected Papers of Hirotugu Akaike. Budapest: Akadémiai Kiadó; 1973: pp 267–281.
    1. Cowling BJ, Fang VJ, Riley S, et al. . Estimation of the serial interval of influenza. Epidemiology 2009; 20:344–7.
    1. Cori A, Ferguson NM, Fraser C, Cauchemez S. A new framework and software to estimate time-varying reproduction numbers during epidemics. Am J Epidemiol 2013; 178:1505–12.
    1. R: A Language and Environment for Statistical Computing [computer program]. Vienna, Austria: R Foundation for Statistical Computing; 2016.
    1. Okamoto M, Dapat CP, Sandagon AMD, et al. . Molecular characterization of respiratory syncytial virus in children with repeated infections with subgroup B in the Philippines. J Infect Dis 2018; 218:1045–53.
    1. Klinkenberg D, Nishiura H. The correlation between infectivity and incubation period of measles, estimated from households with two cases. J Theor Biol 2011; 284:52–60.
    1. Fine PE. The interval between successive cases of an infectious disease. Am J Epidemiol 2003; 158:1039–47.
    1. Leecaster M, Gesteland P, Greene T, et al. . Modeling the variations in pediatric respiratory syncytial virus seasonal epidemics. BMC Infect Dis 2011; 11:105.
    1. Shobugawa Y, Saito R, Sano Y, et al. . Emerging genotypes of human respiratory syncytial virus subgroup A among patients in Japan. J Clin Microbiol 2009; 47:2475–82.
    1. Munywoki PK, Koech DC, Agoti CN, et al. . Frequent asymptomatic respiratory syncytial virus infections during an epidemic in a Rural Kenyan household cohort. J Infect Dis 2015; 212:1711–8.
    1. DIVA-GIS. Available at: . Accessed November 3, 2015.

Source: PubMed

3
Iratkozz fel