Literature DB >> 34751603

Naturalizing laboratory mice by housing in a farmyard-type habitat confers protection against colorectal carcinogenesis.

Henriette Arnesen1,2, Thomas C A Hitch3, Christina Steppeler4, Mette Helen Bjørge Müller4, Linn Emilie Knutsen1, Gjermund Gunnes1, Inga Leena Angell2, Ida Ormaasen2, Knut Rudi2, Jan Erik Paulsen4, Thomas Clavel3, Harald Carlsen2, Preben Boysen1.   

Abstract

Living in a farm environment in proximity to animals is associated with reduced risk of developing allergies and asthma, and has been suggested to protect against other diseases, such as inflammatory bowel disease and cancer. Despite epidemiological evidence, experimental disease models that recapitulate such environments are needed to understand the underlying mechanisms. In this study, we show that feralizing conventional inbred mice by continuous exposure to a livestock farmyard-type environment conferred protection toward colorectal carcinogenesis. Two independent experimental approaches for colorectal cancer induction were used; spontaneous (Apc Min/+ mice on an A/J background) or chemical (AOM/DSS). In contrast to conventionally reared laboratory mice, the feralized mouse gut microbiota structure remained stable and resistant to mutagen- and colitis-induced neoplasia. Moreover, the feralized mice exhibited signs of a more mature immunophenotype, indicated by increased expression of NK and T-cell maturation markers, and a more potent IFN-γ response to stimuli. In our study, hygienically born and raised mice subsequently feralized post-weaning were protected to a similar level as life-long exposed mice, although the greatest effect was seen upon neonatal exposure. Collectively, we show protective implications of a farmyard-type environment on colorectal cancer development and demonstrate the utility of a novel animal modeling approach that recapitulates realistic disease responses in a naturalized mammal.

Entities:  

Keywords:  Gut microbiota; animal model; colorectal cancer; farmyard-like habitat; feralized mice; immunity; naturalized mice; short-chain fatty acids

Mesh:

Year:  2021        PMID: 34751603      PMCID: PMC8583187          DOI: 10.1080/19490976.2021.1993581

Source DB:  PubMed          Journal:  Gut Microbes        ISSN: 1949-0976


  76 in total

1.  Sequential Infection with Common Pathogens Promotes Human-like Immune Gene Expression and Altered Vaccine Response.

Authors:  Tiffany A Reese; Kevin Bi; Amal Kambal; Ali Filali-Mouhim; Lalit K Beura; Matheus C Bürger; Bali Pulendran; Rafick-Pierre Sekaly; Stephen C Jameson; David Masopust; W Nicholas Haining; Herbert W Virgin
Journal:  Cell Host Microbe       Date:  2016-04-20       Impact factor: 21.023

Review 2.  Colorectal cancer.

Authors:  Evelien Dekker; Pieter J Tanis; Jasper L A Vleugels; Pashtoon M Kasi; Michael B Wallace
Journal:  Lancet       Date:  2019-10-19       Impact factor: 79.321

3.  Microbial Exposure Enhances Immunity to Pathogens Recognized by TLR2 but Increases Susceptibility to Cytokine Storm through TLR4 Sensitization.

Authors:  Matthew A Huggins; Frances V Sjaastad; Mark Pierson; Tamara A Kucaba; Whitney Swanson; Christopher Staley; Alexa R Weingarden; Isaac J Jensen; Derek B Danahy; Vladimir P Badovinac; Stephen C Jameson; Vaiva Vezys; David Masopust; Alexander Khoruts; Thomas S Griffith; Sara E Hamilton
Journal:  Cell Rep       Date:  2019-08-13       Impact factor: 9.423

4.  Gut microbial metabolism drives transformation of MSH2-deficient colon epithelial cells.

Authors:  Antoaneta Belcheva; Thergiory Irrazabal; Susan J Robertson; Catherine Streutker; Heather Maughan; Stephen Rubino; Eduardo H Moriyama; Julia K Copeland; Anu Surendra; Sachin Kumar; Blerta Green; Kaoru Geddes; Rossanna C Pezo; William W Navarre; Michael Milosevic; Brian C Wilson; Stephen E Girardin; Thomas M S Wolever; Winfried Edelmann; David S Guttman; Dana J Philpott; Alberto Martin
Journal:  Cell       Date:  2014-07-17       Impact factor: 41.582

Review 5.  Gut microbiome stability and resilience: elucidating the response to perturbations in order to modulate gut health.

Authors:  Marina Fassarella; Ellen E Blaak; John Penders; Arjen Nauta; Hauke Smidt; Erwin G Zoetendal
Journal:  Gut       Date:  2020-10-13       Impact factor: 23.059

6.  Exercise effects on polyp burden and immune markers in the ApcMin/+ mouse model of intestinal tumorigenesis.

Authors:  Jamie L McClellan; Jennifer L Steiner; Stani D Day; Reilly T Enos; Mark J Davis; Udai P Singh; E Angela Murphy
Journal:  Int J Oncol       Date:  2014-05-22       Impact factor: 5.650

7.  Introducing EzBioCloud: a taxonomically united database of 16S rRNA gene sequences and whole-genome assemblies.

Authors:  Seok-Hwan Yoon; Sung-Min Ha; Soonjae Kwon; Jeongmin Lim; Yeseul Kim; Hyungseok Seo; Jongsik Chun
Journal:  Int J Syst Evol Microbiol       Date:  2017-05-30       Impact factor: 2.747

8.  Colorectal Carcinogenesis in the A/J Min/+ Mouse Model is Inhibited by Hemin, Independently of Dietary Fat Content and Fecal Lipid Peroxidation Rate.

Authors:  Christina Steppeler; Marianne Sødring; Jan Erik Paulsen
Journal:  BMC Cancer       Date:  2016-11-02       Impact factor: 4.430

9.  Structure of the gut microbiome following colonization with human feces determines colonic tumor burden.

Authors:  Nielson T Baxter; Joseph P Zackular; Grace Y Chen; Patrick D Schloss
Journal:  Microbiome       Date:  2014-06-17       Impact factor: 14.650

10.  IMNGS: A comprehensive open resource of processed 16S rRNA microbial profiles for ecology and diversity studies.

Authors:  Ilias Lagkouvardos; Divya Joseph; Martin Kapfhammer; Sabahattin Giritli; Matthias Horn; Dirk Haller; Thomas Clavel
Journal:  Sci Rep       Date:  2016-09-23       Impact factor: 4.379

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