Chen Renke, Xie Mengxiao, Wang Shenlong, Yu Fei, Zhang Dan, Yuan Lingjun, Zheng Jieyuan, Wang Jingchao, Zhou Jieting, Li Binxiao, Zheng Shufa, Fan Yongsheng, Han Dongsheng
The First Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, People's Republic of China.
Department of Laboratory Medicine, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, People's Republic of China.
Infect Drug Resist. 2023 Sep 29;16:6463-6472. doi: 10.2147/IDR.S424061. eCollection 2023.
Metagenomic next-generation sequencing (mNGS) is a promising tool for improving antimicrobial therapy and infection control decision-making in complex infections. Secondary infection surveillance using mNGS in COVID-19 patients has rarely been reported.
Respiratory pathogen and antibiotic resistance prediction were evaluated by BALF mNGS for 192 hospitalized COVID-19 patients between December 2022 and February 2023.
Secondary infection was confirmed in 83.3% (160/192) of the COVID-19 patients, with bacterial infections (45%, 72/160) predominating, followed by mixed bacterial and fungal infections (20%, 32/160), and fungal infections (17.5%, 28/160). The incidence of bacterial or viral secondary infection was significantly higher in patients who were admitted to the ICU, received mechanical ventilation, or developed severe pneumonia (all p<0.05). (n=30, 8.4%) was the most prevalent pathogen associated with secondary infection followed by (n=29, 8.1%), (n=29, 8.1%), (n=27, 7.6%), (n=23, 6.4%), (n=20, 5.6%) and (n=14, 3.9%). The overall concordance between the resistance genes detected by mNGS and the reported phenotypic resistance in 69 samples containing five clinically important pathogens (ie, and ) that caused secondary infection was 85.5% (59/69).
mNGS can detect pathogens causing secondary infection and predict antimicrobial resistance for COVID19 patients. This is crucial for initiating targeted treatment and rapidly detect unsuspected spread of multidrug-resistant pathogens.
宏基因组下一代测序(mNGS)是一种很有前景的工具,可用于改善复杂感染中的抗菌治疗和感染控制决策。在新型冠状病毒肺炎(COVID-19)患者中使用mNGS进行二次感染监测的报道很少。
对2022年12月至2023年2月期间192例住院COVID-19患者的支气管肺泡灌洗(BALF)进行mNGS,评估呼吸道病原体及抗生素耐药性预测情况。
83.3%(160/192)的COVID-19患者确诊发生二次感染,其中细菌感染占主导(45%,72/160),其次是细菌和真菌感染混合(20%,32/160),真菌感染(17.5%,28/160)。入住重症监护病房(ICU)、接受机械通气或发生重症肺炎的患者发生细菌或病毒二次感染的发生率显著更高(均p<0.05)。[具体病原体名称1](n=30,8.4%)是与二次感染相关的最常见病原体,其次是[具体病原体名称2](n=29,8.1%)、[具体病原体名称3](n=29,8.1%)、[具体病原体名称4](n=27,7.6%)、[具体病原体名称5](n=23,6.4%)、[具体病原体名称6](n=20,5.6%)和[具体病原体名称7](n=14,3.9%)。在导致二次感染的69份含有5种临床重要病原体(即[具体病原体名称1]和[具体病原体名称2]等)的样本中,mNGS检测到的耐药基因与报告的表型耐药之间的总体一致性为85.5%(59/69)。
mNGS可以检测导致COVID-19患者二次感染的病原体并预测抗菌药物耐药性。这对于启动针对性治疗以及快速检测多药耐药病原体的意外传播至关重要。