Identifying transmission routes of Streptococcus pneumoniae and sources of acquisitions in high transmission communities

B M Althouse, L L Hammitt, L Grant, B G Wagner, R Reid, F Larzelere-Hinton, R Weatherholtz, K P Klugman, G L Rodgers, K L O'Brien, H Hu, B M Althouse, L L Hammitt, L Grant, B G Wagner, R Reid, F Larzelere-Hinton, R Weatherholtz, K P Klugman, G L Rodgers, K L O'Brien, H Hu

Abstract

Identifying the transmission sources and reservoirs of Streptococcus pneumoniae (SP) is a long-standing question for pneumococcal epidemiology, transmission dynamics, and vaccine policy. Here we use serotype to identify SP transmission and examine acquisitions (in the same household, local community, and county, or of unidentified origin) in a longitudinal cohort of children and adults from the Navajo Nation and the White Mountain Apache American Indian Tribes. We found that adults acquire SP relatively more in the household than other age groups, and children 2-8 years old typically acquire in their own or surrounding communities. Age-specific transmission probability matrices show that transmissions within household were mostly seen from older to younger siblings. Outside the household, children most often transmit to other children in the same age group, showing age-assortative mixing behavior. We find toddlers and older children to be most involved in SP transmission and acquisition, indicating their role as key drivers of SP epidemiology. Although infants have high carriage prevalence, they do not play a central role in transmission of SP compared with toddlers and older children. Our results are relevant to inform alternative pneumococcal conjugate vaccine dosing strategies and analytic efforts to inform optimization of vaccine programs, as well as assessing the transmission dynamics of pathogens transmitted by close contact in general.

Keywords: Streptococcus pneumoniae (pneumococcus); Infectious disease epidemiology; modelling; spread of disease; vaccine policy development.

Conflict of interest statement

No conflicts of interest.

Figures

Fig. 1.
Fig. 1.
Percentage of subjects with positive NP carriage of SP by age in all seven visits, with 95% confidence intervals.
Fig. 2.
Fig. 2.
Acquisition sources by age group. Figure shows the percentage of SP acquired within an individual's household, their community, their service unit (SU), another SU, or with no discernible source. Binomial confidence intervals are plotted as whiskers.
Fig. 3.
Fig. 3.
Number of contacts across age groups. Figure shows the number of potential contacts between age groups within the household, community, and service unit.
Fig. 4.
Fig. 4.
Proportion of contacts that result in SP transmission between ages. Figure shows the transmission probabilities of SP by age groups from individuals on the Y-axis to individuals on the X-axis within the household, community, or service unit (multiple communities). Transmission probabilities are calculated as the proportion of potential contacts in an age pair (i.e. 3–4 to 2–3 year olds) that resulted in transmission. Transmission events that were not statistically significant are plotted in small italics.

References

    1. Flasche S, et al. The potential for reducing the number of pneumococcal conjugate vaccine doses while sustaining herd immunity in high-income countries. PLoS Medicine 2015; 12(6): e1001839.
    1. Sá-Leão R, et al. High rates of transmission of and colonization by Streptococcus pneumoniae and haemophilus influenzae within a day care center revealed in a longitudinal study. Journal of Clinical Microbiology 2008; 46(1): 225–234.
    1. Bogaert D, de Groot R, Hermans P. Streptococcus pneumoniae colonisation: the key to pneumococcal disease. The Lancet Infectious Diseases 2004; 4(3): 144–154.
    1. Lipsitch M, et al. Estimating rates of carriage acquisition and clearance and competitive ability for pneumococcal serotypes in Kenya with a Markov transition model. Epidemiology 2012; 23(4): 510.
    1. Scott JR, et al. Impact of more than a decade of pneumococcal conjugate vaccine use on carriage and invasive potential in Native American communities. Journal of Infectious Diseases 2012; 205(2): 280–288.
    1. Mosser JF, et al. Nasopharyngeal carriage and transmission of Streptococcus pneumoniae in American Indian households after a decade of pneumococcal conjugate vaccine use. PLoS ONE 2014; 9(1): e79578.
    1. Millar EV, et al. Nasopharyngeal carriage of Streptococcus pneumoniae in Navajo and White Mountain Apache children before the introduction of pneumococcal conjugate vaccine. The Pediatric Infectious Disease Journal 2009; 28(8): 711–716.
    1. Millar EV, et al. Pre-and post-conjugate vaccine epidemiology of pneumococcal serotype 6c invasive disease and carriage within Navajo and White Mountain Apache communities. Clinical Infectious Diseases 2010; 51(11): 1258–1265.
    1. Melnick N, Thompson TA, Beall BW. Serotype-specific typing antisera for pneumococcal serogroup 6 serotypes 6a, 6b, and 6c. Journal of Clinical Microbiology 2010; 48(6): 2311–2312.
    1. Hill PC, et al. Nasopharyngeal carriage of Streptococcus pneumoniae in Gambian infants: a longitudinal study. Clinical Infectious Diseases 2008; 46(6): 807–814.
    1. Turner P, et al. A longitudinal study of Streptococcus pneumoniae carriage in a cohort of infants and their mothers on the Thailand-Myanmar border. PLoS ONE 2012; 7(5): e38271.
    1. Ben-Shimol S, et al. Pneumococcal nasopharyngeal carriage in children! 5 years of age visiting the pediatric emergency room in relation to pcv7 and pcv13 introduction in southern Israel. Human Vaccines & Immunotherapeutics 2016; 12(2): 268–276.
    1. O'Brien KL, et al. Predictors of pneumococcal conjugate vaccine immunogenicity among infants and toddlers in an American Indian pncrm7 efficacy trial. Journal of Infectious Diseases 2007; 196(1): 104–114.
    1. Mossong J, et al. Social contacts and mixing patterns relevant to the spread of infectious diseases. PLoS Medicine 2008; 5(3): e74.
    1. Darboe MK, et al. The dynamics of nasopharyngeal Streptococcus pneumoniae carriage among rural Gambian mother-infant pairs. BMC Infectious Diseases 2010; 10(1): 1.
    1. Gratten M, et al. Colonisation of haemophilus influenzae and Streptococcus pneumoniae in the upper respiratory tract of neonates in Papua New Guinea: primary acquisition, duration of carriage, and relationship to carriage in mothers. Neonatology 1986; 50(2): 114–120.
    1. Shiri T, et al. Dynamics of pneumococcal transmission in vaccine-naive children and their HIV-infected or HIV-uninfected mothers during the first 2 years of life. American Journal of Epidemiology 2013; 178(11): 1629–1637.
    1. Weinberger DM, et al. Association between respiratory syncytial virus activity and pneumococcal disease in infants: a time series analysis of us hospitalization data. PLoS Medicine 2015; 12(1), e1001776.
    1. Hébert-Dufresne L, Althouse BM. Complex dynamics of synergistic coinfections on realistically clustered networks. Proceedings of the National Academy of Sciences 2015; 112(33): 10551–10556.
    1. Black FL. Measles endemicity in insular populations: critical community size and its evolutionary implication. Journal of Theoretical Biology 1966; 11(2): 207–211.
    1. Althouse BM, Scarpino SV. Asymptomatic transmission and the resurgence of Bordetella pertussis. BMC Medicine 2015; 13(1): 146.
    1. Kiti MC, et al. Quantifying age-related rates of social contact using diaries in a rural coastal population of Kenya. PLoS ONE 2014; 9(8): e104786.
    1. Grijalva CG, et al. A household-based study of contact networks relevant for the spread of infectious diseases in the highlands of Peru. PLoS ONE 2015; 10(3): e0118457.
    1. Béraud G, et al. The French connection: the first large population-based contact survey in France relevant for the spread of infectious diseases. PLoS ONE 2015; 10(7): e0133203.
    1. Abdullahi O, et al. Rates of acquisition and clearance of pneumococcal serotypes in the nasopharynges of children in Kilifi district, Kenya. Journal of Infectious Diseases 2012; 206(7): 1020–1029.
    1. Tigoi CC, et al. Rates of acquisition of pneumococcal colonization and transmission probabilities, by serotype, among newborn infants in Kilifi district, Kenya. Clinical Infectious Diseases 2012; 55(2): 180–188.

Source: PubMed

3
Iratkozz fel