Abstract

Introduction: Nasopharyngeal (NP) colonization by Streptococcus pneumoniae (pneumococcus) precedes the development of respiratory tract infection. Colonization by antimicrobial-resistant pneumococci, especially in infants, is a major public health concern. We longitudinally investigated antimicrobial-resistance amongst pneumococci colonizing the nasopharynx of South African infants immunized with the 13-valent pneumococcal conjugate vaccine (PCV13).Methods: NP swabs were collected every second week from birth through the first year of life from 137 infants. Pneumococci were identified and serotyped using conventional microbiological techniques, and their antibiotic susceptibility profiles determined by disk diffusion and E-test.Results: All infants were immunized with 3 doses of PCV13. 1520 pneumococci (760 non-repeat) isolates were recovered from 137 infants; including non-typeable (n = 99), PCV13 (n = 133) and non-PCV13 serotypes (n = 528). The prevalence of penicillin, erythromycin, and cotrimoxazole non-susceptibility was 19% (95% CI 17–22%) (3% fully resistant), 18% (95% CI 15–21%) (14% fully resistant), and 45% (95% CI 42–49%) (36% fully resistant), respectively. The predominant penicillin-non-susceptible serotypes included 19A, 19F, 15B/15C, 15A, and 21, while susceptible serotypes included 23A, 34, and 17A. Multidrug-resistance (MDR) was observed in 9% (95% CI 7–11%) of the isolates. PCV13 serotypes were more likely to be non-susceptible, compared to non-PCV13 serotypes, to penicillin (26% vs. 16%, p = 0.007), erythromycin (23% vs. 15%, p = 0.027) and cotrimoxazole (62% vs. 41%, p < 0.001). Non-susceptibility to penicillin, erythromycin, and cotrimoxazole remained relatively constant through the first year of life (X2 test for trend: p = 0.184, p = 0.171, and p = 0.572, respectively). Overall, penicillin or erythromycin-non-susceptible pneumococci were carried for a shorter duration than susceptible pneumococci [penicillin (mean days, 18 vs. 21, p = 0.013) and erythromycin (mean days, 18 vs. 21, p = 0.035)]. Within individual infants carrying the same serotype longitudinally, changes in antibiotic susceptibility were observed over time in 45% (61/137) of infants and these changes were predominantly for penicillin (76%, 79/104).Conclusion: Prevalence of NP carriage with antibiotic-non-susceptible pneumococci was relatively constant throughout the first year of life. PCV13 serotypes were more commonly non-susceptible to penicillin, erythromycin, and cotrimoxazole. Penicillin or erythromycin-non-susceptible pneumococci were carried for a shorter duration than penicillin or erythromycin-susceptible pneumococci.

Highlights

  • Nasopharyngeal (NP) colonization by Streptococcus pneumoniae precedes the development of respiratory tract infection

  • This study aimed to investigate antimicrobial-resistance patterns in pneumococci colonizing the nasopharynx of PCV13 vaccinated South African infants, from birth through the first year of life

  • Penicillin or erythromycin-non-susceptible pneumococci were carried for a shorter duration than susceptible pneumococci, and the difference in the mean carriage duration was significant: penicillin-non-susceptible (18 days, 95% CI 17–20) vs. penicillin-susceptible (21 days, 95% CI 20–22), p = 0.013 and erythromycin-non-susceptible

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Summary

Introduction

Nasopharyngeal (NP) colonization by Streptococcus pneumoniae (pneumococcus) precedes the development of respiratory tract infection. Colonization by antimicrobial-resistant pneumococci, especially in infants, is a major public health concern. We longitudinally investigated antimicrobial-resistance amongst pneumococci colonizing the nasopharynx of South African infants immunized with the 13-valent pneumococcal conjugate vaccine (PCV13). Nasopharyngeal (NP) colonization by antimicrobial-resistant Streptococcus pneumoniae (pneumococcus) is a global public health concern (Ginsburg and Klugman, 2017). The pneumococcus is an important bacterial cause of childhood pneumonia (O’Brien et al, 2009; Andrade et al, 2018). NP colonization with pneumococci is a prerequisite for development of pneumococcal disease (Bogaert et al, 2004). Vaccination with pneumococcal conjugate vaccine (PCV) is effective in reducing both vaccine type pneumococcal carriage and invasive disease (Flasche et al, 2011). Carriage prevalence has remained unchanged due to an increase in carriage of non-vaccine serotypes (Simell et al, 2012)

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