Human colon mucosal biofilms from healthy or colon cancer hosts are carcinogenic

被引:151
作者
Tomkovich, Sarah [1 ]
Dejea, Christine M. [2 ,3 ,4 ,10 ]
Winglee, Kathryn [5 ]
Drewes, Julia L. [2 ,3 ,4 ]
Chung, Liam [2 ,3 ,4 ]
Housseau, Franck [2 ,3 ,4 ]
Pope, Jillian L. [1 ]
Gauthier, Josee [1 ]
Sun, Xiaolun [1 ]
Muhlbauer, Marcus [1 ]
Liu, Xiuli [6 ]
Fathi, Payam [2 ,3 ,4 ,11 ]
Anders, Robert A. [7 ]
Besharati, Sepideh [7 ]
Perez-Chanona, Ernesto [1 ]
Yang, Ye [1 ]
Ding, Hua [2 ,3 ,4 ]
Wu, Xinqun [2 ,3 ,4 ]
Wu, Shaoguang [2 ,3 ,4 ]
White, James R. [8 ]
Gharaibeh, Raad Z. [1 ]
Fodor, Anthony A. [5 ]
Wang, Hao [2 ,3 ,4 ]
Pardoll, Drew M. [2 ,3 ,4 ]
Jobin, Christian [1 ,9 ]
Sears, Cynthia L. [2 ,3 ,4 ]
机构
[1] Univ Florida, Dept Med, Gainesville, FL USA
[2] Johns Hopkins Med Inst, Johns Hopkins Sch Med, Dept Oncol, Bloomberg Kimmel Inst Immunotherapy, Baltimore, MD 21205 USA
[3] Johns Hopkins Med Inst, Johns Hopkins Sch Med, Dept Med, Bloomberg Kimmel Inst Immunotherapy, Baltimore, MD 21205 USA
[4] Johns Hopkins Med Inst, Johns Hopkins Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21205 USA
[5] Univ North Carolina Charlotte, Dept Bioinformat & Genom, Charlotte, NC USA
[6] Univ Florida, Dept Pathol Immunol & Lab Med, Gainesville, FL USA
[7] Johns Hopkins Univ, Dept Pathol, Baltimore, MD USA
[8] Resphera Biosci, Baltimore, MD USA
[9] Univ Florida, Dept Infect Dis & Immunol, Gainesville, FL USA
[10] US FDA, Silver Spring, MD USA
[11] Vanderbilt Univ, Sch Med, Nashville, TN 37212 USA
关键词
COLORECTAL-CANCER; SPATIAL-ORGANIZATION; MUCUS LAYERS; MICROBIOTA; MODEL; MUCIN; FLORA;
D O I
10.1172/JCI124196
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Mucus-invasive bacterial biofilms are identified on the colon mucosa of approximately 50% of colorectal cancer (CRC) patients and approximately 13% of healthy subjects. Here, we test the hypothesis that human colon biofilms comprise microbial communities that are carcinogenic in CRC mouse models. Homogenates of human biofilm-positive colon mucosa were prepared from tumor patients (tumor and paired normal tissues from surgical resections) or biofilm-positive biopsies from healthy individuals undergoing screening colonoscopy; homogenates of biofilm-negative colon biopsies from healthy individuals undergoing screening colonoscopy served as controls. After 12 weeks, biofilm-positive, but not biofilm-negative, human colon mucosal homogenates induced colon tumor formation in 3 mouse colon tumor models (germ-free Apc(Min)(Delta 850/+);Il10(-/-)or Apc(Min)(Delta 850/+) and specific pathogen-free Apc(Min)(Delta 716/+) mice). Remarkably, biofilm-positive communities from healthy colonoscopy biopsies induced colon inflammation and tumors similarly to biofilm-positive tumor tissues. By 1 week, biofilm-positive human tumor homogenates, but not healthy biopsies, displayed consistent bacterial mucus invasion and biofilm formation in mouse colons. 165 rRNA gene sequencing and RNA-Seq analyses identified compositional and functional microbiota differences between mice colonized with biofilm-positive and biofilm-negative communities. These results suggest human colon mucosal biofilms, whether from tumor hosts or healthy individuals undergoing screening colonoscopy, are carcinogenic in murine models of CRC.
引用
收藏
页码:1699 / 1712
页数:14
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