The diagnostic value of metagenomic next-generation sequencing for identifying Streptococcus pneumoniae in paediatric

Xi-Xi Zhang1, Ling-Yun Guo1, Lin-Lin Liu1

  • 1Key Laboratory of Major Diseases in Children, Ministry of Education, Department of Infectious Diseases, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, No. 56 Nan Lishi Road, Beijing, 100045, China.

Abstract

Insights

Metagenomic next-generation sequencing (mNGS) shows high accuracy in identifying Streptococcus pneumoniae in pediatric bacterial meningitis. Pathogen load in CSF correlates with collection time, and mNGS is less impacted by prior antibiotic use than traditional culture.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Genomics

Background:

  • Limited research exists on the diagnostic utility of metagenomic next-generation sequencing (mNGS) for single pathogens in cerebrospinal fluid (CSF).
  • Streptococcus pneumoniae is a significant cause of bacterial meningitis in children.

Purpose of the Study:

  • To evaluate the diagnostic value of mNGS for identifying Streptococcus pneumoniae (S. pneumoniae) in pediatric bacterial meningitis cases.

Main Methods:

  • Retrospective review of bacterial meningitis cases at Beijing Children's Hospital from October 2014 to July 2018.
  • Analysis of clinical features and pathogens, including comparison of mNGS with culture and antigen testing.

Main Results:

  • mNGS identified S. pneumoniae in 23.7% of 135 pediatric bacterial meningitis cases.
  • Compared to culture, mNGS demonstrated a sensitivity of 73.1% and specificity of 88.1%.
  • Higher pathogen load (unique reads) was observed in CSF collected earlier from symptom onset, and mNGS showed less inhibition by pre-collection antibiotics.

Conclusions:

  • mNGS offers high sensitivity and specificity for S. pneumoniae detection in pediatric bacterial meningitis.
  • CSF collection timing influences mNGS pathogen load results.
  • mNGS provides a diagnostic advantage over culture when antibiotics have been administered prior to sample collection.

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