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The clinical significance of macrolide resistance in pediatric Mycoplasma pneumoniae infection during COVID-19 pandemic

医学 肺炎支原体 多位点VNTR分析 内科学 临床意义 肺炎 社区获得性肺炎 支原体肺炎 抗药性 阿奇霉素 爆发 胃肠病学 基因型 微生物学 病毒学 可变数串联重复 生物 抗生素 病理 肺结核 生物化学 基因
作者
Tingting Jiang,Lin Sun,Tianyi Wang,Hui Qi,He Tang,Yacui Wang,Qian Han,Xiaoqing Shi,Jing Bi,Weiwei Jiao,Adong Shen
出处
期刊:Frontiers in Cellular and Infection Microbiology [Frontiers Media SA]
卷期号:13 被引量:17
标识
DOI:10.3389/fcimb.2023.1181402
摘要

Background Mycoplasma pneumoniae (MP) is a commonly occurring pathogen causing community-acquired pneumonia (CAP) in children. The global prevalence of macrolide-resistant MP (MRMP) infection, especially in Asian regions, is increasing rapidly. However, the prevalence of MRMP and its clinical significance during the COVID-19 pandemic is not clear. Methods This study enrolled children with molecularly confirmed macrolide-susceptible MP (MSMP) and MRMP CAP from Beijing Children’s Hospital Baoding Hospital, Capital Medical University between August 2021 and July 2022. The clinical characteristics, laboratory findings, chest imaging presentations, and strain genotypes were compared between patients with MSMP and MRMP CAP. Results A total of 520 hospitalized children with MP-CAP were enrolled in the study, with a macrolide resistance rate of 92.7%. Patients with MRMP infection exhibited more severe clinical manifestations (such as dyspnea and pleural effusion) and had a longer hospital stay than the MSMP group. Furthermore, abnormal blood test results (including increased LDH and D-dimer) were more common in the MRMP group (P<0.05). Multilocus variable-number tandem-repeat analysis (MLVA) was performed on 304 samples based on four loci (Mpn13-16), and M3562 and M4572 were the major types, accounting for 74.0% and 16.8% of the strains, respectively. The macrolide resistance rate of M3562 strains was up to 95.1%. Conclusion The prevalence of MRMP strains in hospitalized CAP patients was extremely high in the Baoding area, and patients infected with MRMP strains exhibited more severe clinical features and increased LDH and D-dimer. M3562 was the predominant resistant clone.
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