Tissue Microbiome Profiling Identifies an Enrichment of Specific Enteric Bacteria in Opisthorchis viverrini Associated Cholangiocarcinoma
Kern Rei Chng,
Sock Hoai Chan,
Amanda Hui Qi Ng,
Chenhao Li,
Apinya Jusakul,
Denis Bertrand,
Andreas Wilm,
Su Pin Choo,
Damien Meng Yew Tan,
Kiat Hon Lim,
Roy Soetinko,
Choon Kiat Ong,
Dan G. Duda,
Simona Dima,
Irinel Popescu,
Chaisiri Wongkham,
Zhu Feng,
Khay Guan Yeoh,
Bin Tean Teh,
Puangrat Yongvanit,
Sopit Wongkham,
Vajaraphongsa Bhudhisawasdi,
Narong Khuntikeo,
Patrick Tan,
Chawalit Pairojkul,
Joanne Ngeow,
Niranjan Nagarajan
Affiliations
Kern Rei Chng
Genome Institute of Singapore, 138672, Singapore
Sock Hoai Chan
Division of Medical Oncology, National Cancer Centre Singapore, 11 Hospital Drive, 169610, Singapore
Amanda Hui Qi Ng
Genome Institute of Singapore, 138672, Singapore
Chenhao Li
Genome Institute of Singapore, 138672, Singapore
Apinya Jusakul
Laboratory of Cancer Epigenome, National Cancer Centre Singapore, 11 Hospital Drive, 169610, Singapore
Denis Bertrand
Genome Institute of Singapore, 138672, Singapore
Andreas Wilm
Genome Institute of Singapore, 138672, Singapore
Su Pin Choo
Division of Medical Oncology, National Cancer Centre Singapore, 11 Hospital Drive, 169610, Singapore
Damien Meng Yew Tan
Department of Gastroenterology and Hepatology, Singapore General Hospital, Outram Road, 169608, Singapore
Kiat Hon Lim
Department of Pathology, Singapore General Hospital, Outram Road, 169608, Singapore
Roy Soetinko
Department of Gastroenterology and Hepatology, Singapore General Hospital, Outram Road, 169608, Singapore
Choon Kiat Ong
Laboratory of Cancer Epigenome, National Cancer Centre Singapore, 11 Hospital Drive, 169610, Singapore
Dan G. Duda
Edwin L. Steele Laboratories for Tumor Biology, Department of Radiation Oncology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA
Simona Dima
Center of Digestive Diseases and Liver Transplantation, Fundeni Clinical Institute, Bucharest, Romania
Irinel Popescu
Center of Digestive Diseases and Liver Transplantation, Fundeni Clinical Institute, Bucharest, Romania
Chaisiri Wongkham
Liver Fluke and Cholangiocarcinoma Research Center, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand
Zhu Feng
Dept. of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore
Khay Guan Yeoh
Dept. of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore
Bin Tean Teh
Laboratory of Cancer Epigenome, National Cancer Centre Singapore, 11 Hospital Drive, 169610, Singapore
Puangrat Yongvanit
Liver Fluke and Cholangiocarcinoma Research Center, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand
Sopit Wongkham
Liver Fluke and Cholangiocarcinoma Research Center, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand
Vajaraphongsa Bhudhisawasdi
Liver Fluke and Cholangiocarcinoma Research Center, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand
Narong Khuntikeo
Liver Fluke and Cholangiocarcinoma Research Center, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand
Patrick Tan
Genome Institute of Singapore, 138672, Singapore
Chawalit Pairojkul
Liver Fluke and Cholangiocarcinoma Research Center, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand
Joanne Ngeow
Division of Medical Oncology, National Cancer Centre Singapore, 11 Hospital Drive, 169610, Singapore
Cholangiocarcinoma (CCA) is the primary cancer of the bile duct system. The role of bile duct tissue microbiomes in CCA tumorigenesis is unestablished. To address this, sixty primary CCA tumors and matched normals, from both liver fluke (Opisthorchis viverrini) associated (OVa, n = 28) and non-O. viverrini associated (non-OVa, n = 32) cancers, were profiled using high-throughput 16S rRNA sequencing. A distinct, tissue-specific microbiome dominated by the bacterial families Dietziaceae, Pseudomonadaceae and Oxalobacteraceae was observed in bile duct tissues. Systemic perturbation of the microbiome was noted in tumor and paired normal samples (vs non-cancer normals) for several bacterial families with a significant increase in Stenotrophomonas species distinguishing tumors vs paired normals. Comparison of parasite associated (OVa) vs non-associated (non-OVa) groups identified enrichment for specific enteric bacteria (Bifidobacteriaceae, Enterobacteriaceae and Enterococcaceae). One of the enriched families, Bifidobacteriaceae, was found to be dominant in the O. viverrini microbiome, providing a mechanistic link to the parasite. Functional analysis and comparison of CCA microbiomes revealed higher potential for producing bile acids and ammonia in OVa tissues, linking the altered microbiota to carcinogenesis. These results define how the unique microbial communities resident in the bile duct, parasitic infections and the tissue microenvironment can influence each other, and contribute to cancer.