Effects of exposure to bisphenol A and ethinyl estradiol on the gut microbiota of parents and their offspring in a rodent model

被引:126
作者
Javurek, Angela B. [1 ,2 ]
Spollen, William G. [1 ,3 ]
Johnson, Sarah A. [1 ,2 ,4 ]
Bivens, Nathan J. [5 ]
Bromert, Karen H. [5 ]
Givan, Scott A. [1 ,3 ,6 ,8 ]
Rosenfeld, Cheryl S. [1 ,2 ,6 ,7 ,8 ]
机构
[1] Univ Missouri, Bond Life Sci Ctr, Columbia, MO USA
[2] Univ Missouri, Biomed Sci, Columbia, MO USA
[3] Univ Missouri, Informat Res Core Facil, Columbia, MO USA
[4] Univ Missouri, Anim Sci, Columbia, MO USA
[5] Univ Missouri, DNA Core Facil, Columbia, MO USA
[6] Univ Missouri, Mol Microbiol & Immunol, Columbia, MO USA
[7] Univ Missouri, Genet Area Program, Columbia, MO USA
[8] Univ Missouri, Thompson Ctr Autism & Neurobehav Disorders, Columbia, MO USA
关键词
bacteria; california mice; DOHaD; endocrine disrupting chemicals; estrogens; metabolic pathway; Peromyscus;
D O I
10.1080/19490976.2016.1234657
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Gut dysbiosis may result in various diseases, such as metabolic and neurobehavioral disorders. Exposure to endocrine disrupting chemicals (EDCs), including bisphenol A (BPA) and ethinyl estradiol (EE), especially during development, may also increase the risk for such disorders. An unexplored possibility is that EDC-exposure might alter the gut microbial composition. Gut flora and their products may thus be mediating factors for the disease-causing effects of these chemicals. To examine the effects of EDCs on the gut microbiome, female and male monogamous and biparental California mice (Peromyscus californicus) were exposed to BPA (50 mg/kg feed weight) or EE (0.1 ppb) or control diet from periconception through weaning. 16s rRNA sequencing was performed on bacterial DNA isolated from fecal samples, and analyses performed for P-0 and F-l males and females. Both BPA and EE induced generational and sex-dependent gut microbiome changes. Many of the bacteria, e.g. Bacteroides, Mollicutes, Prevotellaceae, Erysipelotrichaceae, Akkermansia, Methanobrevibacter, Sutterella, whose proportions increase with exposure to BPA or EE in the P-0 or F-1 generation are associated with different disorders, such as inflammatory bowel disease (IBD), metabolic disorders, and colorectal cancer. However, the proportion of the beneficial bacterium, Bifidobacterium, was also elevated in fecal samples of BPA- and EE-exposed F-1 females. Intestinal flora alterations were also linked to changes in various metabolic and other pathways. Thus, BPA and EE exposure may disrupt the normal gut flora, which may in turn result in systemic effects. Probiotic supplementation might be an effective means to mitigate disease-promoting effects of these chemicals.
引用
收藏
页码:471 / 485
页数:15
相关论文
共 78 条
[1]   Prevention of gut leakiness by a probiotic treatment leads to attenuated HPA response to an acute psychological stress in rats [J].
Ait-Belgnaoui, Afifa ;
Durand, Henri ;
Cartier, Christel ;
Chaumaz, Gilles ;
Eutamene, Helene ;
Ferrier, Laurent ;
Houdeau, Eric ;
Fioramonti, Jean ;
Bueno, Lionel ;
Theodorou, Vassilia .
PSYCHONEUROENDOCRINOLOGY, 2012, 37 (11) :1885-1895
[2]   The Gut Microbiota and Developmental Programming of the Testis in Mice [J].
Al-Asmakh, Maha ;
Stukenborg, Jan-Bernd ;
Reda, Ahmed ;
Anuar, Farhana ;
Strand, Mona-Lisa ;
Hedin, Lars ;
Pettersson, Sven ;
Soeder, Oiie .
PLOS ONE, 2014, 9 (08)
[3]   Intestinal Barrier Function and the Brain-Gut Axis [J].
Alonso, Carmen ;
Vicario, Maria ;
Pigrau, Marc ;
Lobo, Beatriz ;
Santos, Javier .
MICROBIAL ENDOCRINOLOGY: THE MICROBIOTA-GUT-BRAIN AXIS IN HEALTH AND DISEASE, 2014, 817 :73-113
[4]   Epigenetic responses following maternal dietary exposure to physiologically relevant levels of bisphenol A [J].
Anderson, Olivia S. ;
Nahar, Muna S. ;
Faulk, Christopher ;
Jones, Tamara R. ;
Liao, Chunyang ;
Kannan, Kurunthachalam ;
Weinhouse, Caren ;
Rozek, Laura S. ;
Dolinoy, Dana C. .
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 2012, 53 (05) :334-342
[5]  
[Anonymous], 2008, Set back distance guidelines for prairie plant species at risk, P1
[6]   Structure of the gut microbiome following colonization with human feces determines colonic tumor burden [J].
Baxter, Nielson T. ;
Zackular, Joseph P. ;
Chen, Grace Y. ;
Schloss, Patrick D. .
MICROBIOME, 2014, 2
[7]   Impact of oral bisphenol A at reference doses on intestinal barrier function and sex differences after perinatal exposure in rats [J].
Braniste, Viorica ;
Jouault, Aurore ;
Gaultier, Eric ;
Polizzi, Arnaud ;
Buisson-Brenac, Claire ;
Leveque, Mathilde ;
Martin, Pascal G. ;
Theodorou, Vassilia ;
Fioramonti, Jean ;
Houdeau, Eric .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (01) :448-453
[8]   Exposure of the US population to bisphenol A and 4-tertiary-octylphenol:: 2003-2004 [J].
Calafat, Antonia M. ;
Ye, Xiaoyun ;
Wong, Lee-Yang ;
Reidy, John A. ;
Needham, Larry L. .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2008, 116 (01) :39-44
[9]   Global patterns of 16S rRNA diversity at a depth of millions of sequences per sample [J].
Caporaso, J. Gregory ;
Lauber, Christian L. ;
Walters, William A. ;
Berg-Lyons, Donna ;
Lozupone, Catherine A. ;
Turnbaugh, Peter J. ;
Fierer, Noah ;
Knight, Rob .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 :4516-4522
[10]   QIIME allows analysis of high-throughput community sequencing data [J].
Caporaso, J. Gregory ;
Kuczynski, Justin ;
Stombaugh, Jesse ;
Bittinger, Kyle ;
Bushman, Frederic D. ;
Costello, Elizabeth K. ;
Fierer, Noah ;
Pena, Antonio Gonzalez ;
Goodrich, Julia K. ;
Gordon, Jeffrey I. ;
Huttley, Gavin A. ;
Kelley, Scott T. ;
Knights, Dan ;
Koenig, Jeremy E. ;
Ley, Ruth E. ;
Lozupone, Catherine A. ;
McDonald, Daniel ;
Muegge, Brian D. ;
Pirrung, Meg ;
Reeder, Jens ;
Sevinsky, Joel R. ;
Tumbaugh, Peter J. ;
Walters, William A. ;
Widmann, Jeremy ;
Yatsunenko, Tanya ;
Zaneveld, Jesse ;
Knight, Rob .
NATURE METHODS, 2010, 7 (05) :335-336