Quantitative Profiling of Colorectal Cancer-Associated Bacteria Reveals Associations between Fusobacterium spp., Enterotoxigenic Bacteroides fragilis (ETBF) and Clinicopathological Features of Colorectal Cancer

被引:197
作者
Viljoen, Katie S. [1 ]
Dakshinamurthy, Amirtha [1 ]
Goldberg, Paul [2 ]
Blackburn, Jonathan M. [1 ]
机构
[1] Univ Cape Town, Fac Hlth Sci, Div Med Biochem, Inst Infect Dis & Mol Med, ZA-7925 Cape Town, South Africa
[2] Groote Schuur Hosp, Surg Gastroenterol Unit, Dept Surg, ZA-7925 Cape Town, South Africa
关键词
INFLAMMATORY-BOWEL-DISEASE; ESCHERICHIA-COLI; ENTEROCOCCUS-FAECALIS; MLH1; METHYLATION; DNA METHYLATION; IN-VIVO; CARCINOGENESIS; QUANTIFICATION; TUMORIGENESIS; COLONIZATION;
D O I
10.1371/journal.pone.0119462
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Various studies have presented clinical or in vitro evidence linking bacteria to colorectal cancer, but these bacteria have not previously been concurrently quantified by qPCR in a single cohort. We quantify these bacteria (Fusobacterium spp., Streptococcus gallolyticus, Enterococcus faecalis, Enterotoxigenic Bacteroides fragilis (ETBF), Enteropathogenic Escherichia coli (EPEC), and afaC- or pks-positive E. coli) in paired tumour and normal tissue samples from 55 colorectal cancer patients. We further investigate the relationship between a) the presence and b) the level of colonisation of each bacterial species with site and stage of disease, age, gender, ethnicity and MSI-status. With the exception of S. gallolyticus, we detected all bacteria profiled here in both tumour and normal samples at varying frequencies. ETBF (FDR = 0.001 and 0.002 for normal and tumour samples) and afaC-positive E. coli (FDR = 0.03, normal samples) were significantly enriched in the colon compared to the rectum. ETBF (FDR = 0.04 and 0.002 for normal and tumour samples, respectively) and Fusobacterium spp. (FDR = 0.03 tumour samples) levels were significantly higher in late stage (III/IV) colorectal cancers. Fusobacterium was by far the most common bacteria detected, occurring in 82% and 81% of paired tumour and normal samples. Fusobacterium was also the only bacterium that was significantly higher in tumour compared to normal samples (p = 6e-5). We also identified significant associations between high-level colonisation by Fusobacterium and MSI-H (FDR = 0.05), age (FDR = 0.03) or pks-positive E. coli (FDR = 0.01). Furthermore, we exclusively identified atypical EPEC in our cohort, which has not been previously reported in association with colorectal cancer. By quantifying colorectal cancer-associated bacteria across a single cohort, we uncovered inter-and intra-individual patterns of colonization not previously recognized, as well as important associations with clinicopathological features, especially in the case of Fusobacterium and ETBF.
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共 72 条
[1]  
Abdulamir AS, 2010, MOL CANCER, V9, P1, DOI [10.1186/1476-4598-9-1, DOI 10.1186/1476-4598-9-1]
[2]   Intestinal Inflammation Targets Cancer-Inducing Activity of the Microbiota [J].
Arthur, Janelle C. ;
Perez-Chanona, Ernesto ;
Muehlbauer, Marcus ;
Tomkovich, Sarah ;
Uronis, Joshua M. ;
Fan, Ting-Jia ;
Campbell, Barry J. ;
Abujamel, Turki ;
Dogan, Belgin ;
Rogers, Arlin B. ;
Rhodes, Jonathan M. ;
Stintzi, Alain ;
Simpson, Kenneth W. ;
Hansen, Jonathan J. ;
Keku, Temitope O. ;
Fodor, Anthony A. ;
Jobin, Christian .
SCIENCE, 2012, 338 (6103) :120-123
[3]   Real-time polymerase chain reaction quantification of specific butyrate-producing bacteria, Desulfovibrio and Enterococcus faecalis in the feces of patients with colorectal cancer [J].
Balamurugan, Ramadass ;
Rajendiran, Ethendhar ;
George, Sarah ;
Samuel, G. Vijay ;
Ramakrishna, Balakrishnan S. .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2008, 23 (08) :1298-1303
[4]   Enterococcus faecalis induces inflammatory bowel disease in interleukin-10 knockout mice [J].
Balish, E ;
Warner, T .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 160 (06) :2253-2257
[5]   Distinction of hereditary nonpolyposis colorectal cancer and sporadic microsatellite-unstable colorectal cancer through quantification of MLH1 methylation by real-time PCR [J].
Bettstetter, Marcus ;
Dechant, Stephan ;
Ruemmele, Petra ;
Grabowski, Monika ;
Keller, Gisela ;
Holinski-Feder, Elke ;
Hartmann, Arndt ;
Hofstaedter, Ferdinand ;
Dietmaier, Wolfgang .
CLINICAL CANCER RESEARCH, 2007, 13 (11) :3221-3228
[6]   Carcinogenic properties of proteins with pro-inflammatory activity from Streptococcus infantarius (formerly S.bovis) [J].
Biarc, J ;
Nguyen, IS ;
Pini, A ;
Gossé, F ;
Richert, S ;
Thiersé, D ;
Van Dorsselaer, A ;
Leize-Wagner, E ;
Raul, F ;
Klein, JP ;
Schöller-Guinard, M .
CARCINOGENESIS, 2004, 25 (08) :1477-1484
[7]   Clinical Importance of Streptococcus gallolyticus Infection Among Colorectal Cancer Patients: Systematic Review and Meta-analysis [J].
Boleij, Annemarie ;
van Gelder, Marleen M. H. J. ;
Swinkels, Dorine W. ;
Tjalsma, Harold .
CLINICAL INFECTIOUS DISEASES, 2011, 53 (09) :870-878
[8]   Colonization of the Human Gut by E. coli and Colorectal Cancer Risk [J].
Bonnet, Mathilde ;
Buc, Emmanuel ;
Sauvanet, Pierre ;
Darcha, Claude ;
Dubois, Damien ;
Pereira, Bruno ;
Dechelotte, Pierre ;
Bonnet, Richard ;
Pezet, Denis ;
Darfeuille-Michaud, Arlette .
CLINICAL CANCER RESEARCH, 2014, 20 (04) :859-867
[9]  
BREMNER CG, 1970, CANCER, V26, P991, DOI 10.1002/1097-0142(197011)26:5<991::AID-CNCR2820260505>3.0.CO
[10]  
2-J