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Detecting circulating microbial cell-free DNA by next-generation sequencing in patients with Mycobacterium avium complex-lung disease: A pilot study.
Tseng, Yen-Han; Pan, Sheng-Wei; Feng, Jia-Yih; Su, Wei-Juin; Huang, Chi-Ying F; Chen, Yuh-Min.
Affiliation
  • Tseng YH; Department of Chest Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
  • Pan SW; School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
  • Feng JY; Program in Molecular Medicine, School of Life Sciences, National Yang Ming Chiao Tung University, Taipei, Taiwan.
  • Su WJ; Department of Chest Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
  • Huang CF; School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
  • Chen YM; Department of Chest Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Tzu Chi Med J ; 36(1): 67-75, 2024.
Article in En | MEDLINE | ID: mdl-38406566
ABSTRACT

Objectives:

Determining a diagnosis for non-Tuberculous mycobacterium (NTM)-lung disease (LD) remains difficult. The value of circulating cell-free DNA (cfDNA) secreted from microbes has been established in the detection of pathogens in septic patients. However, it is unknown whether NTM-derived cfDNA is detectable in plasma from patients with NTM-LD and whether this is associated with the disease status of NTM-LD, especially in patients with Mycobacterium avium complex (MAC)-LD. Materials and

Methods:

In this pilot study, from 2018 to 2019, we enrolled adult patients with MAC-LD at Taipei Veterans General Hospital in Taiwan for the detection of circulating cfDNA. We performed cfDNA extraction from plasma, next-generation sequencing (NGS) for nonhuman cfDNA, and sequence matching to a microbial database and then assessed the association between pathogen cfDNA and MAC-LD.

Results:

Two (40%) plasma samples from MAC-LD patients had detectable MAC-specific cfDNA, namely one instance of DNA polymerase III alpha subunit and one instance of ATP-binding cassette transporters permease. The plasma samples from the three other MAC-LD cases and the one tuberculosis control were negative for either NTM-derived cfDNA or tuberculosis-related cfDNA. In addition to MAC-specific cfDNA, Ralstonia solanacearum, Staphylococcus aureus, and Pasteurella multocida were the most observed bacteria in our patients. The two patients with MAC-cfDNA positivity yielded higher radiographic scores (P = 0.076) and presented a higher number of nonhuman reads than those without MAC-cfDNA positivity (P = 0.083).

Conclusion:

Using NGS method, we demonstrated MAC-cfDNA was detectable in patients with MAC-LD. Further large-scale research is warranted to assess the clinical value of detecting MAC-specific cfDNA in MAC-LD patients.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Tzu Chi Med J Year: 2024 Document type: Article Affiliation country: Taiwan

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Tzu Chi Med J Year: 2024 Document type: Article Affiliation country: Taiwan