Lower respiratory tract microbiota in patients with clinically suspected nontuberculous mycobacterial pulmonary disease according to the presence of gastroesophageal reflux

PLoS One. 2024 Aug 28;19(8):e0309446. doi: 10.1371/journal.pone.0309446. eCollection 2024.

Abstract

Although gastroesophageal reflux has been recognized as one of the risk factors of nontuberculous mycobacterial pulmonary disease (NTM-PD) progression, the effect of reflux on the lower respiratory tract microbiota has not been studied in detail. We investigated the composition of the lower respiratory tract microbiota in patients with clinically suspected NTM-PD, comparing them based on the presence of reflux. Forty-seven patients suspected of having NTM-PD were enrolled and assigned according to presence of reflux (n = 22) and non- reflux (n = 25). We performed a pepsin ELISA assay to identify the presence of reflux and 16S ribosomal RNA gene amplicon sequencing to evaluate the microbiota in bronchoalveolar lavage fluid. There were no significant differences in the diversity or composition of the lower respiratory microbiota between the NTM-PD and non-NTM-PD groups. Bacterial richness was observed in the non-reflux group than in the reflux group [P = 0.03] and a cluster in the reflux group was observed. The reflux group showed a predominance for Pseudomonas aeruginosa or Staphylococcus aureus among the NTM-PD group and for P. aeruginosa, Haemophilus influenzae, Klebsiella pneumoniae, or Eikenella species among the non-NTM-PD group. The non-reflux groups presented diverse patterns. A linear discriminant analysis and volcano plot demonstrated that P. aeruginosa, H. haemolyticus, Selenomonas artemidis, and Dolosigranulum pigrum were specifically associated with the NTM-PD reflux group, while P. aeruginosa was specifically associated with the non-NTM-PD reflux group. These observations confirm that the lower respiratory microbiota is consistently altered by reflux but not in NTM-PD.

MeSH terms

  • Aged
  • Bronchoalveolar Lavage Fluid / microbiology
  • Female
  • Gastroesophageal Reflux* / microbiology
  • Humans
  • Lung Diseases / microbiology
  • Male
  • Microbiota*
  • Middle Aged
  • Mycobacterium Infections, Nontuberculous* / complications
  • Mycobacterium Infections, Nontuberculous* / microbiology
  • Nontuberculous Mycobacteria / isolation & purification
  • RNA, Ribosomal, 16S* / genetics
  • Respiratory System / microbiology

Substances

  • RNA, Ribosomal, 16S

Grants and funding

This study was supported by grants from the National Research Foundation of Korea (NRF) Grant funded by the Ministry of Education, Science, and Technology (grant no. NRF- 2022R1C1C1002741 (Eun Jeong Won) and 2020R1F1A1076570 (Yong-Soo Kwon)). The funding body played no role in the design of the study and collection, analysis, interpretation of data, and in writing the manuscript.