4.2 Article

A Preliminary Study of Microbiota Diversity in Saliva and Bronchoalveolar Lavage Fluid from Patients with Primary Bronchogenic Carcinoma

Journal

MEDICAL SCIENCE MONITOR
Volume 25, Issue -, Pages 2819-2834

Publisher

INT SCIENTIFIC INFORMATION, INC
DOI: 10.12659/MSM.915332

Keywords

Bronchoalveolar Lavage Fluid; Carcinoma, Bronchogenic; Microbiota; RNA, Ribosomal, 16S; Saliva

Funding

  1. National Natural Science Foundation of China [81460003, 81760024, 81760419, 81760743]
  2. Innovation Project of Guangxi Graduate Education [201010 LX039]
  3. Guangxi Natural Science Foundation [2016GXNSFAA380297]
  4. Key Research and Development Program of Guangxi [AB16380152]
  5. Basic Ability Improvement Project for Young and Middle-aged Teachers in Colleges of Guangxi [2019KY0125]
  6. Medical Excellence Award - Creative Research Development Grant from the First Affiliated Hospital of Guangxi Medical University

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Background: The present study aimed to evaluate the difference in microbiota diversity in the oral cavity and fluid bron-choalveolar lavage (BALF) of patients with lung cancer. Material/Methods: Buccal (saliva) and lower respiratory tract BALF samples were collected from 51 patients with primary bron-chogenic carcinoma and 15 healthy controls, and bacterial genomic DNA was extracted. High-throughput 16S rDNA amplicon sequencing was performed, and microbial diversity, composition, and functions of microbiota were analyzed by bioinformatics methods. Results: Patients with lung cancer have lower microbial diversity than healthy controls in both saliva and BALF samples. Significant segregation was observed between the different pathological types of lung cancer groups and the control group regardless of the sampling site. Treponema and Filifactor were identified as potential bacterial biomarkers in BALF samples, while Filifactor was ideal to distinguish healthy controls from lung cancer patients. Moreover, the predictive variation analysis of the KEGG (Kyoto Encyclopedia of Genes and Genomes) metabolic pathway showed that the metabolic differences in microbiota varied by sampling site. Conclusions: Lung cancer patients carry a different and less diverse microorganism community than healthy controls. Certain bacterial taxa might be associated with lung cancer, but the exact species depends on the sampling site and the pathological type. This study provides basic data on the microbiota diversity in BALF and saliva samples from lung cancer patients. Further investigation with a larger sample size should help validate the enriched species in different pathological types of lung cancers.

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