Microbiology Department, Laboratori Clinic Metropolitana Nord, Hospital Universitari Germans Trias i Pujol, Department of Genetics and Microbiology, Universitat Autònoma de Barcelona, Barcelona, Spain.
Paediatric Department, Hospital Universitari Germans Trias i Pujol, Badalona, Spain.
J Antimicrob Chemother. 2020 Oct 1;75(10):2752-2759. doi: 10.1093/jac/dkaa256.
Mycoplasma pneumoniae (MP) causes community-acquired pneumonia affecting mainly children, and tends to produce cyclic outbreaks. The widespread use of macrolides is increasing resistance rates to these antibiotics. Molecular tools can help in diagnosis, typing and resistance detection, leading to better patient management.
To assess the MP genotypes and resistance pattern circulating in our area while comparing serological and molecular diagnosis of MP.
Molecular and serological diagnosis of MP was performed in 821 samples collected in Badalona (Barcelona, Spain) from 2013 to 2017. Multiple locus variable number tandem repeat analysis (MLVA) and macrolide resistance detection by pyrosequencing were performed in those cases positive by PCR. Presence of respiratory viruses and relevant clinical data were also recorded.
MP was detected in 16.8% of cases by PCR, with an overall agreement with serology of 76%. Eleven different MLVA types were identified, with 4-5-7-2 (50.1%) and 3-5-6-2 (29.2%) being the most abundant, with the latter showing a seasonal increase during the study. A total of 8% of the strains harboured a point substitution associated with macrolide resistance, corresponding mainly to an A2063G 23S rRNA mutation and directly related to previous macrolide therapy. Analysis of respiratory viruses showed viral coinfections in most cases.
Serological and molecular tools combined could improve MP diagnosis and the analysis of its infection patterns. Macrolide resistance is associated with previous therapy. Given that MP pneumonia usually resolves spontaneously, it should be reconsidered whether antibiotic treatment is suitable for all cases.
肺炎支原体(MP)引起社区获得性肺炎,主要影响儿童,且倾向于周期性爆发。大环内酯类抗生素的广泛使用导致这些抗生素的耐药率上升。分子工具可帮助诊断、分型和耐药检测,从而更好地管理患者。
评估本地区流行的 MP 基因型和耐药模式,并比较 MP 的血清学和分子诊断。
2013 年至 2017 年,在西班牙巴塞罗那的巴达洛纳采集了 821 份样本,进行 MP 的分子和血清学诊断。对 PCR 阳性的样本进行多位点可变数目串联重复分析(MLVA)和焦磷酸测序法检测大环内酯类耐药。还记录了呼吸道病毒的存在和相关临床数据。
PCR 检测到 16.8%的病例为 MP,与血清学的总符合率为 76%。共鉴定出 11 种不同的 MLVA 类型,其中 4-5-7-2(50.1%)和 3-5-6-2(29.2%)最为丰富,后者在研究期间呈季节性增加。共有 8%的菌株携带与大环内酯类耐药相关的点突变,主要为 23S rRNA 上的 A2063G 突变,与之前的大环内酯类治疗直接相关。对呼吸道病毒的分析表明,大多数情况下存在病毒合并感染。
联合使用血清学和分子工具可以提高 MP 的诊断水平,并分析其感染模式。大环内酯类耐药与之前的治疗有关。鉴于 MP 肺炎通常会自行消退,应重新考虑是否所有病例都适合抗生素治疗。