Metatranscriptomic Analysis of Human Lung Metagenomes from Patients with Lung Cancer

This study was designed to characterize the microbiomes of the lung tissues of lung cancer patients. RNA-sequencing was performed on lung tumor samples from 49 patients with lung cancer. Metatranscriptomics data were analyzed using SAMSA2 and Kraken2 software. 16S rRNA sequencing was also performed....

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Published inGenes Vol. 12; no. 9; p. 1458
Main Authors Chang, Ya-Sian, Hsu, Ming-Hung, Tu, Siang-Jyun, Yen, Ju-Chen, Lee, Ya-Ting, Fang, Hsin-Yuan, Chang, Jan-Gowth
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 21.09.2021
MDPI
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ISSN2073-4425
2073-4425
DOI10.3390/genes12091458

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Abstract This study was designed to characterize the microbiomes of the lung tissues of lung cancer patients. RNA-sequencing was performed on lung tumor samples from 49 patients with lung cancer. Metatranscriptomics data were analyzed using SAMSA2 and Kraken2 software. 16S rRNA sequencing was also performed. The heterogeneous cellular landscape and immune repertoires of the lung samples were examined using xCell and TRUST4, respectively. We found that nine bacteria were significantly enriched in the lung tissues of cancer patients, and associated with reduced overall survival (OS). We also found that subjects with mutations in the epidermal growth factor receptor gene were less likely to experience the presence of Pseudomonas. aeruginosa. We found that the presence of CD8+ T-cells, CD4+ naive T-cells, dendritic cells, and CD4+ central memory T cells were associated with a good prognosis, while the presence of pro B-cells was associated with a poor prognosis. Furthermore, high clone numbers were associated with a high ImmuneScore for all immune receptor repertoires. Clone numbers and diversity were significantly higher in unpresented subjects compared to presented subjects. Our results provide insight into the microbiota of human lung cancer, and how its composition is linked to the tumor immune microenvironment, immune receptor repertoires, and OS.
AbstractList This study was designed to characterize the microbiomes of the lung tissues of lung cancer patients. RNA-sequencing was performed on lung tumor samples from 49 patients with lung cancer. Metatranscriptomics data were analyzed using SAMSA2 and Kraken2 software. 16S rRNA sequencing was also performed. The heterogeneous cellular landscape and immune repertoires of the lung samples were examined using xCell and TRUST4, respectively. We found that nine bacteria were significantly enriched in the lung tissues of cancer patients, and associated with reduced overall survival (OS). We also found that subjects with mutations in the epidermal growth factor receptor gene were less likely to experience the presence of Pseudomonas. aeruginosa. We found that the presence of CD8+ T-cells, CD4+ naive T-cells, dendritic cells, and CD4+ central memory T cells were associated with a good prognosis, while the presence of pro B-cells was associated with a poor prognosis. Furthermore, high clone numbers were associated with a high ImmuneScore for all immune receptor repertoires. Clone numbers and diversity were significantly higher in unpresented subjects compared to presented subjects. Our results provide insight into the microbiota of human lung cancer, and how its composition is linked to the tumor immune microenvironment, immune receptor repertoires, and OS.
This study was designed to characterize the microbiomes of the lung tissues of lung cancer patients. RNA-sequencing was performed on lung tumor samples from 49 patients with lung cancer. Metatranscriptomics data were analyzed using SAMSA2 and Kraken2 software. 16S rRNA sequencing was also performed. The heterogeneous cellular landscape and immune repertoires of the lung samples were examined using xCell and TRUST4, respectively. We found that nine bacteria were significantly enriched in the lung tissues of cancer patients, and associated with reduced overall survival (OS). We also found that subjects with mutations in the epidermal growth factor receptor gene were less likely to experience the presence of . We found that the presence of CD8+ T-cells, CD4+ naive T-cells, dendritic cells, and CD4+ central memory T cells were associated with a good prognosis, while the presence of pro B-cells was associated with a poor prognosis. Furthermore, high clone numbers were associated with a high ImmuneScore for all immune receptor repertoires. Clone numbers and diversity were significantly higher in unpresented subjects compared to presented subjects. Our results provide insight into the microbiota of human lung cancer, and how its composition is linked to the tumor immune microenvironment, immune receptor repertoires, and OS.
This study was designed to characterize the microbiomes of the lung tissues of lung cancer patients. RNA-sequencing was performed on lung tumor samples from 49 patients with lung cancer. Metatranscriptomics data were analyzed using SAMSA2 and Kraken2 software. 16S rRNA sequencing was also performed. The heterogeneous cellular landscape and immune repertoires of the lung samples were examined using xCell and TRUST4, respectively. We found that nine bacteria were significantly enriched in the lung tissues of cancer patients, and associated with reduced overall survival (OS). We also found that subjects with mutations in the epidermal growth factor receptor gene were less likely to experience the presence of Pseudomonas. aeruginosa . We found that the presence of CD8+ T-cells, CD4+ naive T-cells, dendritic cells, and CD4+ central memory T cells were associated with a good prognosis, while the presence of pro B-cells was associated with a poor prognosis. Furthermore, high clone numbers were associated with a high ImmuneScore for all immune receptor repertoires. Clone numbers and diversity were significantly higher in unpresented subjects compared to presented subjects. Our results provide insight into the microbiota of human lung cancer, and how its composition is linked to the tumor immune microenvironment, immune receptor repertoires, and OS.
This study was designed to characterize the microbiomes of the lung tissues of lung cancer patients. RNA-sequencing was performed on lung tumor samples from 49 patients with lung cancer. Metatranscriptomics data were analyzed using SAMSA2 and Kraken2 software. 16S rRNA sequencing was also performed. The heterogeneous cellular landscape and immune repertoires of the lung samples were examined using xCell and TRUST4, respectively. We found that nine bacteria were significantly enriched in the lung tissues of cancer patients, and associated with reduced overall survival (OS). We also found that subjects with mutations in the epidermal growth factor receptor gene were less likely to experience the presence of Pseudomonas. aeruginosa. We found that the presence of CD8+ T-cells, CD4+ naive T-cells, dendritic cells, and CD4+ central memory T cells were associated with a good prognosis, while the presence of pro B-cells was associated with a poor prognosis. Furthermore, high clone numbers were associated with a high ImmuneScore for all immune receptor repertoires. Clone numbers and diversity were significantly higher in unpresented subjects compared to presented subjects. Our results provide insight into the microbiota of human lung cancer, and how its composition is linked to the tumor immune microenvironment, immune receptor repertoires, and OS.This study was designed to characterize the microbiomes of the lung tissues of lung cancer patients. RNA-sequencing was performed on lung tumor samples from 49 patients with lung cancer. Metatranscriptomics data were analyzed using SAMSA2 and Kraken2 software. 16S rRNA sequencing was also performed. The heterogeneous cellular landscape and immune repertoires of the lung samples were examined using xCell and TRUST4, respectively. We found that nine bacteria were significantly enriched in the lung tissues of cancer patients, and associated with reduced overall survival (OS). We also found that subjects with mutations in the epidermal growth factor receptor gene were less likely to experience the presence of Pseudomonas. aeruginosa. We found that the presence of CD8+ T-cells, CD4+ naive T-cells, dendritic cells, and CD4+ central memory T cells were associated with a good prognosis, while the presence of pro B-cells was associated with a poor prognosis. Furthermore, high clone numbers were associated with a high ImmuneScore for all immune receptor repertoires. Clone numbers and diversity were significantly higher in unpresented subjects compared to presented subjects. Our results provide insight into the microbiota of human lung cancer, and how its composition is linked to the tumor immune microenvironment, immune receptor repertoires, and OS.
Author Fang, Hsin-Yuan
Hsu, Ming-Hung
Yen, Ju-Chen
Chang, Ya-Sian
Tu, Siang-Jyun
Lee, Ya-Ting
Chang, Jan-Gowth
AuthorAffiliation 5 Department of Bioinformatics and Medical Engineering, Asia University, Taichung 413, Taiwan
1 Epigenome Research Center, China Medical University Hospital, Taichung 404, Taiwan; t25074@mail.cmuh.org.tw (Y.-S.C.); t24399@mail.cmuh.org.tw (J.-C.Y.); t23701@mail.cmuh.org.tw (Y.-T.L.)
2 Center for Precision Medicine, China Medical University Hospital, Taichung 404, Taiwan; t35492@mail.cmuh.org.tw (M.-H.H.); t34752@mail.cmuh.org.tw (S.-J.T.)
4 Department of Thoracic Surgery, China Medical University Hospital, Taichung 404, Taiwan; d17573@mail.cmuh.org.tw
3 School of Medicine, China Medical University, Taichung 404, Taiwan
AuthorAffiliation_xml – name: 3 School of Medicine, China Medical University, Taichung 404, Taiwan
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– name: 2 Center for Precision Medicine, China Medical University Hospital, Taichung 404, Taiwan; t35492@mail.cmuh.org.tw (M.-H.H.); t34752@mail.cmuh.org.tw (S.-J.T.)
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Keywords lung cancer
T cell receptor repertoires
metatranscriptomic
B cell receptor repertoires
microenvironments
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Snippet This study was designed to characterize the microbiomes of the lung tissues of lung cancer patients. RNA-sequencing was performed on lung tumor samples from 49...
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StartPage 1458
SubjectTerms Adenocarcinoma of Lung - genetics
Adenocarcinoma of Lung - immunology
Adenocarcinoma of Lung - microbiology
Bacterial infections
Carcinoma, Non-Small-Cell Lung - genetics
Carcinoma, Non-Small-Cell Lung - immunology
Carcinoma, Non-Small-Cell Lung - microbiology
Carcinoma, Non-Small-Cell Lung - mortality
Carcinoma, Squamous Cell - genetics
Carcinoma, Squamous Cell - immunology
Carcinoma, Squamous Cell - microbiology
CD4 antigen
CD8 antigen
CD8-positive T-lymphocytes
computer software
Dendritic cells
Disease
Epidermal growth factor
epidermal growth factor receptors
Gene Expression Profiling
genes
Genomes
Humans
immunologic receptors
Immunological memory
landscapes
Lavage
Lung cancer
lung neoplasms
Lung Neoplasms - genetics
Lung Neoplasms - immunology
Lung Neoplasms - microbiology
Lung Neoplasms - mortality
lungs
Lymphocytes B
Lymphocytes T
Medical prognosis
memory
Memory cells
Metagenome
metagenomics
microbiome
Microbiomes
Microbiota
Microenvironments
Microorganisms
Mutation
Pilot Projects
Prognosis
Pseudomonas
Receptors, Antigen, B-Cell - immunology
Receptors, Antigen, T-Cell - immunology
RNA, Ribosomal, 16S
rRNA 16S
sequence analysis
Sequence Analysis, RNA
Software
Survival analysis
T cell receptors
Taxonomy
transcriptomics
Tumor Microenvironment - immunology
Tumors
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Title Metatranscriptomic Analysis of Human Lung Metagenomes from Patients with Lung Cancer
URI https://www.ncbi.nlm.nih.gov/pubmed/34573440
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Volume 12
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