Whole genome sequencing confirmed the de novo development of macrolide resistance in a child with Mycoplasma pneumoniae infection receiving azithromycin treatment

全基因组测序证实,一名接受阿奇霉素治疗的肺炎支原体感染患儿体内新出现了大环内酯类耐药基因。

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Abstract

BACKGROUND: Mycoplasma pneumoniae (MPN) is a major pathogen of community-acquired respiratory tract infections, and macrolides are the drug of choice for treating MPN infections. Macrolide resistance in our patient population has been low; however, an increase in resistance rates was observed during a recent resurgence. CASE SUMMARY: A previously healthy 11-year-old male was diagnosed with MPN infection and received azithromycin treatment. His symptoms continued after two courses of azithromycin, and he tested positive for MPN DNA three times. Sanger sequencing of samples collected after his first course of azithromycin revealed a mutation conferring macrolide resistance, while the sample collected before the initiation of antibiotics did not. Additionally, whole genome sequencing (WGS) and single-nucleotide polymorphism (SNP) analysis demonstrated that samples collected before and after receiving azithromycin differed by one SNP, indicating that the two isolates are the same strain, and the development of macrolide resistance occurred de novo during treatment. CONCLUSION: Our case utilized WGS to confirm that the development of de novo macrolide resistance can occur rapidly following macrolide use. Clinicians should be vigilant for macrolide treatment failure and consider alternative drugs if symptoms persist or there are signs of clinical deterioration.

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