Synergistic impact of macrolide resistance and H3N2 infection on M. pneumoniae outbreak in children.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
Microbiology spectrum Pub Date : 2025-04-01 Epub Date: 2025-02-25 DOI:10.1128/spectrum.01844-24
Jiali Chen, Yingdan Wang, Juan Cheng, Yunping Ma, Xin Zhang, Xuezhou Bai, Palizhati Rehati, Huashun Cui, Fan Wu, Qiuhui Pan, Jinghe Huang
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引用次数: 0

Abstract

In November 2023, there was a substantial increase in the incidence of Mycoplasma pneumoniae infections in China following waves of SARS-CoV-2 Omicron variant and influenza outbreaks. This study aimed to elucidate the epidemiological features and clinical implications of M. pneumoniae infections in children and explore the potential influence of SARS-CoV-2 Omicron variants and influenza A infections on the M. pneumoniae outbreak. Among 38,668 children with lower respiratory tract infections from January to December 2023, 11,919 tested positive for M. pneumoniae, predominantly between October and December. The majority of the children with M. pneumoniae were aged 5-10 years, with type 1 strains and macrolide-resistant M. pneumoniae strains having the highest prevalence rates. Statistical analysis revealed elevated C-reactive protein, neutrophil, and monocyte levels and decreased lymphocyte, basophil, and eosinophil counts in M. pneumoniae-positive children. M. pneumoniae-positive children also presented significantly increased neutralizing antibody levels against preceding influenza A (H3N2) but not against SARS-CoV-2 Omicron variants. A parallel trend was observed between M. pneumoniae and H3N2 prevalence from June to December 2023. The emergence of macrolide-resistant strains and prior influenza A (H3N2) epidemics notably contributed to the M. pneumoniae outbreak. These findings suggested that H3N2 infection facilitates M. pneumoniae infection through various mechanisms. This study underscores the complex interactions between respiratory pathogens and highlights the need for comprehensive surveillance and response strategies.IMPORTANCEThis study identified key factors contributing to an outbreak of Mycoplasma pneumoniae that affected 11,919 children. The influencing factors included a high prevalence of macrolide-resistant epidemic strains (94.2%) and significantly higher H3N2 neutralizing antibody levels (P < 0.0001) stimulated by the preceding H3N2 influenza epidemic. These findings highlight the complex relationship between the prevalence of M. pneumoniae and H3N2 infection in children, indicating that it is necessary to consider pathogen interactions in respiratory disease management by continuously monitoring respiratory pathogens. The emergence of macrolide-resistant strains in China and the previous H3N2 influenza epidemic significantly exacerbated the severity of the M. pneumoniae outbreak. H3N2 infection potentially amplifies Mycoplasma transmission. This study elucidates the epidemiological and clinical aspects of M. pneumoniae infections in children, yields insights regarding the cause of the outbreak, and provides guidance for improving respiratory infection management.

大环内酯耐药与H3N2感染对儿童肺炎支原体暴发的协同影响
2023年11月,在SARS-CoV-2 Omicron变体和流感爆发之后,中国肺炎支原体感染的发病率大幅增加。本研究旨在阐明儿童肺炎支原体感染的流行病学特征和临床意义,探讨SARS-CoV-2组克隆变异和甲型流感感染对肺炎支原体暴发的潜在影响。在2023年1月至12月的38668名下呼吸道感染儿童中,11919名肺炎支原体检测呈阳性,主要是在10月至12月期间。肺炎支原体患儿以5 ~ 10岁为主,以1型和耐大环内酯肺炎支原体感染率最高。统计分析显示,肺炎支原体阳性儿童的c反应蛋白、中性粒细胞和单核细胞水平升高,淋巴细胞、嗜碱性粒细胞和嗜酸性粒细胞计数下降。肺炎支原体阳性儿童对先前甲型流感(H3N2)的中和抗体水平也显著升高,但对SARS-CoV-2 Omicron变体的中和抗体水平没有升高。从2023年6月到12月,肺炎支原体和H3N2的流行呈平行趋势。大环内酯耐药菌株的出现和先前的甲型流感(H3N2)流行是导致肺炎支原体爆发的主要原因。这些发现提示H3N2感染通过多种机制促进肺炎支原体感染。这项研究强调了呼吸道病原体之间复杂的相互作用,并强调了综合监测和应对策略的必要性。重要性:本研究确定了影响11,919名儿童的肺炎支原体暴发的关键因素。影响因素包括大环内酯耐药流行株的高流行率(94.2%)和先前H3N2流感流行刺激的H3N2中和抗体水平显著升高(P < 0.0001)。这些发现强调了儿童肺炎支原体患病率与H3N2感染之间的复杂关系,表明有必要通过持续监测呼吸道病原体来考虑呼吸道疾病管理中的病原体相互作用。中国出现的大环内酯耐药菌株和之前的H3N2流感流行显著加剧了肺炎支原体暴发的严重程度。H3N2感染可能放大支原体传播。本研究阐明了儿童肺炎支原体感染的流行病学和临床方面,对暴发的原因产生了见解,并为改善呼吸道感染管理提供了指导。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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