4.7 Article

Improving Pulmonary Infection Diagnosis with Metagenomic Next Generation Sequencing

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fcimb.2020.567615

关键词

pulmonary infection; metagenomic; next generation sequencing; diagnosis; respiration tract infection

资金

  1. National Science and Technology Major Project of China [2018ZX10305409001-001, 2018ZX10305409-001-003]
  2. National Natural Science Foundation of China [82002141]
  3. Project from Science and Technology of Shanghai [18495810600]
  4. Science and Technology Innovation Project of Shanghai [20Y11900400]
  5. Shanghai Youth Science and Technology Talents Sailing Project [20YF1404300]
  6. Project of Shenkang [SHDC22020214]

向作者/读者索取更多资源

Metagenomic next generation sequencing (mNGS) has shown higher sensitivity and better diagnostic performance in detecting pathogens in pulmonary infections, especially for rare and emerging pathogens. It provides reliable phylogenetic and epidemiological information, with a shorter turnaround time, and can complement traditional methods to improve the identification of respiratory infection agents.
Pulmonary infections are among the most common and important infectious diseases due to their high morbidity and mortality, especially in older and immunocompromised individuals. However, due to the limitations in sensitivity and the long turn-around time (TAT) of conventional diagnostic methods, pathogen detection and identification methods for pulmonary infection with greater diagnostic efficiency are urgently needed. In recent years, unbiased metagenomic next generation sequencing (mNGS) has been widely used to detect different types of infectious pathogens, and is especially useful for the detection of rare and newly emergent pathogens, showing better diagnostic performance than traditional methods. There has been limited research exploring the application of mNGS for the diagnosis of pulmonary infections. In this study we evaluated the diagnostic efficiency and clinical impact of mNGS on pulmonary infections. A total of 100 respiratory samples were collected from patients diagnosed with pulmonary infection in Shanghai, China. Conventional methods, including culture and standard polymerase chain reaction (PCR) panel analysis for respiratory tract viruses, and mNGS were used for the pathogen detection in respiratory samples. The difference in the diagnostic yield between conventional methods and mNGS demonstrated that mNGS had higher sensitivity than traditional culture for the detection of pathogenic bacteria and fungi (95% vs 54%; p<0.001). Although mNGS had lower sensitivity than PCR for diagnosing viral infections, it identified 14 viral species that were not detected using conventional methods, including multiple subtypes of human herpesvirus. mNGS detected viruses with a genome coverage >95% and a sequencing depth >100x and provided reliable phylogenetic and epidemiological information. mNGS offered extra benefits, including a shorter TAT. As a complementary approach to conventional methods, mNGS could help improving the identification of respiratory infection agents. We recommend the timely use of mNGS when infection of mixed or rare pathogens is suspected, especially in immunocompromised individuals and or individuals with severe conditions that require urgent treatment.

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