Mass drug administration with azithromycin for trachoma elimination and the population structure of Streptococcus pneumoniae in the nasopharynx

Rebecca A Gladstone ORCID logo ; Ebrima Bojang ; John Hart ORCID logo ; Emma M Harding-Esch ORCID logo ; David Mabey ORCID logo ; Ansumana Sillah ; Robin L Bailey ORCID logo ; Sarah E Burr ORCID logo ; Anna Roca ; Stephen D Bentley ORCID logo ; +1 more... Martin J Holland ORCID logo ; (2020) Mass drug administration with azithromycin for trachoma elimination and the population structure of Streptococcus pneumoniae in the nasopharynx. Clinical microbiology and infection. ISSN 1198-743X DOI: 10.1101/2020.04.01.20047266
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ABSTRACT

Background

Mass drug administration (MDA) with azithromycin for trachoma elimination reduces nasopharyngeal carriage ofStreptococcus pneumoniaein the short term. We evaluated S.pneumoniaecarried in the nasopharynx before and after a round of azithromycin MDA to determine whether MDA was associated with changes in pneumococcal population structure.

Methods

We analysed 514 pneumococcal isolates cultured from nasopharyngeal samples collected in Gambian villages that received MDA for trachoma elimination. The samples were collected during three cross-sectional surveys conducted before the third round of MDA (CSS-1) and at one (CSS-2) and six (CSS-3) months after MDA. Whole genome sequencing was conducted on randomly selected isolates. Bayesian Analysis of Population Structure (BAPS) was used to cluster related isolates by capturing variation in the core genome. Serotype and multi-locus sequence type were inferred from the genotype. The Antimicrobial Resistance Identification by Assembly (ARIBA) tool was used to identify macrolide resistance genes.

Results

Twenty-seven BAPS clusters were assigned. These consisted of 81 sequence types (STs), 15 of which were novel additions to pubMLST. Two BAPS clusters, BAPS20 (p-value<=0.016) and BAPS22 (p-value<=0.032) showed an increase in frequency at CSS-3 not associated with antimicrobial resistance. Macrolide resistance within BASP17 increased after treatment (p<0.05) and was carried on a mobile transposable element that also conferred resistance to tetracycline.

Conclusions

Limited changes in pneumococcal population structure were observed after the third round of MDA suggesting treatment had little effect on the circulating lineages. An increase in macrolide resistance within one BAPS highlights the need for antimicrobial resistance surveillance in treated villages.


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