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Introduction <p>Respiratory infections re-emerge unpredictably. Rapid pathogen identification is crucial for effective targeted therapy.</p> Methods <p>From November 15, 2023, to December 15, 2023, 574 respiratory tract samples (nasopharyngeal and oropharyngeal swabs) were collected at Beijing Ditan Hospital and Beijing Haidian Hospital. Targeted next-generation sequencing (tNGS) was further used to examine the respiratory samples identified as unfavorable by quantitative real-time PCR (qPCR).</p> Results <p>Using qPCR testing, 368 out of 574 samples (64.1%) were positive, while 206 samples (35.9%) showed no pathogen. TNGS further found that 167 out of these 206 cases (81.1%) had pathogens detected, with 58 different pathogens identified. The most frequent viruses, bacteria, and fungi were H3N2 (<i>n</i> = 73), <i>Streptococcus pneumoniae</i> (<i>S. pneumoniae</i>) (<i>n</i> = 18), <i>Staphylococcus aureus</i> (<i>S. aureus</i>) (<i>n</i> = 18), and <i>Candida albicans</i> (<i>C. albicans</i>) (<i>n</i> = 17). There were 102 cases of mixed infections, among which H3N2 appeared most frequently (51/102, 50%), and coinfections often involved Human betaherpesvirus 7 and <i>S. aureus</i>. In 20 cases where antibiotic resistance genes (ARGs) were detected, four were infected with H3N2. Among these, <i>TEM</i> and <i>tetB</i> were associated with <i>Acinetobacter baumannii</i>, <i>APH</i> was associated with <i>Stenotrophomonas maltophilia</i>, and the remaining resistance genes were linked to <i>S. pneumoniae</i>.</p> Conclusion <p>TNGS is more sensitive than qPCR for detecting pathogens, which is crucial for identifying prevalent and harmful ones like H3N2, <i>S. pneumoniae</i>, and <i>S. aureus</i>. Its integration into routine clinical testing is recommended, though more research is needed for clear guidelines.</p>

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Enhancing upper respiratory tract infection detection: exploring qPCR negative respiratory samples using targeted next-generation sequencing

  • 期刊论文

  • 发表日期：

    2025年7月1日

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  • Zhixia Gu,
  • Tingting Liu,
  • Jun Li,
  • Chuan Song,
  • Xinlong Wang,
  • Ying Tang,
  • Mo Du,
  • Yuhai Bi,
  • Yuanyuan Zhang,
  • Ronghua Jin,
  • Rui Song

摘要

Introduction

Respiratory infections re-emerge unpredictably. Rapid pathogen identification is crucial for effective targeted therapy.

Methods

From November 15, 2023, to December 15, 2023, 574 respiratory tract samples (nasopharyngeal and oropharyngeal swabs) were collected at Beijing Ditan Hospital and Beijing Haidian Hospital. Targeted next-generation sequencing (tNGS) was further used to examine the respiratory samples identified as unfavorable by quantitative real-time PCR (qPCR).

Results

Using qPCR testing, 368 out of 574 samples (64.1%) were positive, while 206 samples (35.9%) showed no pathogen. TNGS further found that 167 out of these 206 cases (81.1%) had pathogens detected, with 58 different pathogens identified. The most frequent viruses, bacteria, and fungi were H3N2 (n = 73), Streptococcus pneumoniae (S. pneumoniae) (n = 18), Staphylococcus aureus (S. aureus) (n = 18), and Candida albicans (C. albicans) (n = 17). There were 102 cases of mixed infections, among which H3N2 appeared most frequently (51/102, 50%), and coinfections often involved Human betaherpesvirus 7 and S. aureus. In 20 cases where antibiotic resistance genes (ARGs) were detected, four were infected with H3N2. Among these, TEM and tetB were associated with Acinetobacter baumannii, APH was associated with Stenotrophomonas maltophilia, and the remaining resistance genes were linked to S. pneumoniae.

Conclusion

TNGS is more sensitive than qPCR for detecting pathogens, which is crucial for identifying prevalent and harmful ones like H3N2, S. pneumoniae, and S. aureus. Its integration into routine clinical testing is recommended, though more research is needed for clear guidelines.