期刊
BMC INFECTIOUS DISEASES
卷 22, 期 1, 页码 -出版社
BMC
DOI: 10.1186/s12879-022-07080-4
关键词
Sub-Saharan Africa; Azithromycin; Bacterial carriage; Group A streptococcus; Streptococcus dysgalactiae subspecies equisimilis
资金
- MRC UK
- UK Department for International Development (DFID) under the MRC/DFID [MR/J010391/1]
- HEFCE/ODA grant from The University of Sheffield [155123]
- Wellcome Trust [110058/Z/15/Z, 208765/Z/17/Z]
- Wellcome Trust [208765/Z/17/Z, 110058/Z/15/Z] Funding Source: Wellcome Trust
This study examined the impact of intra-partum azithromycin on maternal and neonatal Group A Streptococcus (GAS) carriage and antibiotic resistance. The results showed that azithromycin can reduce GAS carriage in the nasopharynx and breast milk of Gambian mothers and neonates, but it did not affect carriage in the vaginal tract. Azithromycin-resistant GAS was mainly found in Streptococcus dysgalactiae subspecies equisimilis (SDSE(A)).
Background Group A Streptococcus (GAS) is a major human pathogen and an important cause of maternal and neonatal sepsis. Asymptomatic bacterial colonization is considered a necessary step towards sepsis. Intra-partum azithromycin may reduce GAS carriage. Methods A posthoc analysis of a double-blind, placebo-controlled randomized-trial was performed to determine the impact of 2 g oral dose of intra-partum azithromycin on maternal and neonatal GAS carriage and antibiotic resistance. Following screening, 829 mothers were randomized who delivered 843 babies. GAS was determined by obtaining samples from the maternal and newborn nasopharynx, maternal vaginal tract and breastmilk. Whole Genome Sequencing (WGS) of GAS isolates was performed using the Illumina Miseq platform. Results GAS carriage was lower in the nasopharynx of both mothers and babies and breast milk among participants in the azithromycin arm. No differences in GAS carriage were found between groups in the vaginal tract. The occurrence of azithromycin-resistant GAS was similar in both arms, except for a higher prevalence in the vaginal tract among women in the azithromycin arm. WGS revealed all macrolide-resistant vaginal tract isolates from the azithromycin arm were Streptococcus dysgalactiae subspecies equisimilis expressing Lancefield group A carbohydrate (SDSE(A)) harbouring macrolide resistant genes msr(D) and mef(A). Ten of the 45 GAS isolates (22.2%) were SDSE(A). Conclusions Oral intra-partum azithromycin reduced GAS carriage among Gambian mothers and neonates however carriage in the maternal vaginal tract was not affected by the intervention due to azithromycin resistant SDSE(A). SDSE(A) resistance must be closely monitored to fully assess the public health impact of intrapartum azithromycin on GAS. Trial registration ClinicalTrials.gov Identifier NCT01800942
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