Characteristics of lower respiratory microbiota in children's refractory Mycoplasma pneumoniae pneumonia pre- and post-COVID-19 era.

IF 4.8 2区 医学 Q2 IMMUNOLOGY Frontiers in Cellular and Infection Microbiology Pub Date : 2025-01-21 eCollection Date: 2024-01-01 DOI:10.3389/fcimb.2024.1438777
Zhimin Xi, Jinglong Chen, Libo Wang, Aizhen Lu
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Abstract

Introduction: Little was known about the characteristics of low respiratory tract (LRT) microbiota of refractory M. pneumoniae pneumonia (RMPP) in children before and after the COVID-19 pandemic.

Methods: Forty-two children diagnosed with RMPP in 2019 (Y2019 group) and 33 children diagnosed with RMPP in 2023 (Y2023 group), entered into the study. The characteristics of the clinical findings were examined, and the LRT microbiota was analyzed by metagenomic next generation sequencing.

Results: The ratio of consolidate, atelectasis, lung necrosis, and erythema multiforme in Y2023 group was significantly higher than that in Y2019 (P<0.05). Mycoplasmoides pneumoniae was the top species of the LRT microbiota in both groups. The rate of macrolide resistance MP in Y2023 was significantly higher than that in Y2019 (P<0.05), and the mutant site was all 23S rRNA A2063G. There were no significant differences in α-diversity and β-diversity of LRT microbiota between Y2019 and Y2023 group. Trichoderma citrinoviride, Canine mastadenovirus A, Ralstonia pickettii, Lactococcus lactis, Pseudomonas aeruginosa were the biomarkers of LRT microbiota in children with RMPP of Y2023. The abundance of Mycoplasmoides pneumoniae positively correlated with the levels of D-dimer and LDH, negatively correlated with the counts of CD3+ T cells, CD8+ T cells, CD19+ B cells and CD16+CD56+ NK cells.

Discussion: Our study showed that high abundance of MP was correlated with the severity of RMPP and decrease of immune cells. Trichoderma citrinoviride, Canine mastadenovirus A, Ralstonia pickettii, Lactococcus lactis, Pseudomonas aeruginosa were the biomarkers in microbiota of LRT in children with RMPP post COVID-19 era.

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儿童难治性肺炎支原体肺炎前后下呼吸道微生物群特征
简介:COVID-19大流行前后,人们对儿童难治性肺炎双球菌肺炎(RMPP)低呼吸道(LRT)微生物群的特征知之甚少:42名在2019年(Y2019组)和33名在2023年(Y2023组)被诊断为难治性肺炎霉菌性肺炎(RMPP)的儿童参与研究。研究人员考察了临床结果的特征,并通过元基因组新一代测序分析了LRT微生物群:结果:Y2023 组合并症、肺不张、肺坏死和多形红斑的比例明显高于 Y2019 组(肺炎原虫是两组 LRT 微生物群中的最高物种)。Y2023组的大环内酯耐药率MP明显高于Y2019组(PTrichoderma citrinoviride、Canine mastadenovirus A、Ralstonia pickettii、Lactococcus lactis、Pseudomonas aeruginosa是Y2023组RMPP患儿LRT微生物群的生物标志物。肺炎支原体的丰度与D-二聚体和LDH的水平呈正相关,与CD3+ T细胞、CD8+ T细胞、CD19+ B细胞和CD16+CD56+ NK细胞的数量呈负相关:我们的研究表明,MP的高丰度与RMPP的严重程度和免疫细胞的减少有关。枸橼酸毛霉、犬乳突病毒 A、Ralstonia pickettii、乳酸乳球菌、铜绿假单胞菌是 COVID-19 时代后 RMPP 患儿 LRT 微生物群中的生物标志物。
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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