Prenatal opioid administration induces shared alterations to the maternal and offspring gut microbiome: A preliminary analysis

被引:19
作者
Grecco, Gregory G. [1 ,2 ]
Gao, Yong [1 ]
Gao, Hongyu [3 ,4 ]
Liu, Yunlong [3 ,4 ]
Atwood, Brady K. [1 ,5 ]
机构
[1] Indiana Univ Sch Med, Dept Pharmacol & Toxicol, Indianapolis, IN 46202 USA
[2] Indiana Univ Sch Med, Med Scientist Training Program, Indianapolis, IN 46202 USA
[3] Indiana Univ Sch Med, Dept Med & Mol Genet, Indianapolis, IN 46202 USA
[4] Indiana Univ Sch Med, Ctr Med Genom, Indianapolis, IN 46202 USA
[5] Indiana Univ Sch Med, Stark Neurosci Res Inst, Indianapolis, IN 46202 USA
关键词
Prenatal; Microbiome; Development; Methadone; Pregnancy; Opioid; NEONATAL ABSTINENCE SYNDROME; DYSBIOSIS; US;
D O I
10.1016/j.drugalcdep.2021.108914
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background While many studies have described the impact of prenatal opioid exposure on development, possible mechanisms for how opioids exert developmental impairments remain elusive. Emerging evidence indicates disruptions in the maternal gut microbiome can alter offspring development; however, no studies to date have examined the impact of maternal opioid treatment on maternal-offspring microbiome dysbiosis. Methods A mouse model of prenatal methadone exposure (PME) was employed to assess the impact of maternal opioid treatment on the microbiome of methadone-treated dams (MD) and their offspring. Fecal samples were collected from dams (n = 8 per treatment), one male and one female offspring per dam (n = 8 offspring per sex per treatment) for 16S rRNA sequencing. Results Methadone treatment significantly increased the microbial diversity and led to an expansion in family level bacterial abundance. Correlational analysis revealed significant positive associations between dam and offspring measures of diversity indicating methadone-induced shifts in the microbial communities are shared between dam and offspring. Sixteen features in dams and 10 features in offspring were significantly differentially abundant between treatment groups with many features corresponding to the Lachnospiraceae NK4A136 genus. Of the six features identified as differentially abundant in both MD and PME offspring, all were assigned to the Lachnospiraceae NK4A136 group, and the abundances demonstrated strong positive correlations between dam and offspring. Conclusions These preliminary findings indicate that maternal opioid treatment during pregnancy alters the composition of the maternal microbiome, and this opioid-induced shift is similarly observed in offspring which could contribute to the impaired developmental phenotypes previously described.
引用
收藏
页数:6
相关论文
共 26 条
[1]   Gastrointestinal motility, dysbiosis and opioid-induced tolerance: is there a link? [J].
Akbarali, Hamid I. ;
Dewey, William L. .
NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 2019, 16 (06) :323-324
[2]   Opioid-induced gut microbial disruption and bile dysregulation leads to gut barrier compromise and sustained systemic inflammation [J].
Banerjee, S. ;
Sindberg, G. ;
Wang, F. ;
Meng, J. ;
Sharma, U. ;
Zhang, L. ;
Dauer, P. ;
Chen, C. ;
Dalluge, J. ;
Johnson, T. ;
Roy, S. .
MUCOSAL IMMUNOLOGY, 2016, 9 (06) :1418-1428
[3]  
Callahan BJ, 2016, NAT METHODS, V13, P581, DOI [10.1038/NMETH.3869, 10.1038/nmeth.3869]
[4]   MicrobiomeAnalyst: a web-based tool for comprehensive statistical, visual and meta-analysis of microbiome data [J].
Dhariwal, Achal ;
Chong, Jasmine ;
Habib, Salam ;
King, Irah L. ;
Agellon, Luis B. ;
Xia, Jianguo .
NUCLEIC ACIDS RESEARCH, 2017, 45 (W1) :W180-W188
[5]   Opioid agonist and antagonist use and the gut microbiota: associations among people in addiction treatment [J].
Gicquelais, Rachel E. ;
Bohnert, Amy S. B. ;
Thomas, Laura ;
Foxman, Betsy .
SCIENTIFIC REPORTS, 2020, 10 (01)
[6]   Prenatal methadone exposure disrupts behavioral development and alters motor neuron intrinsic properties and local circuitry [J].
Grecco, Gregory G. ;
Mork, Briana E. ;
Huang, Jui-Yen ;
Metzger, Corinne E. ;
Haggerty, David L. ;
Reeves, Kaitlin C. ;
Gao, Yong ;
Hoffman, Hunter ;
Katner, Simon N. ;
Masters, Andrea R. ;
Morris, Cameron W. ;
Newell, Erin A. ;
Engleman, Eric A. ;
Baucum, Anthony J. ;
Kim, Jiuen ;
Yamamoto, Bryan K. ;
Allen, Matthew R. ;
Wu, Yu-Chien ;
Lu, Hui-Chen ;
Sheets, Patrick L. ;
Atwood, Brady K. .
ELIFE, 2021, 10
[7]   Neonatal Abstinence Syndrome and Maternal Opioid-Related Diagnoses in the US, 2010-2017 [J].
Hirai, Ashley H. ;
Ko, Jean Y. ;
Owens, Pamela L. ;
Stocks, Carol ;
Patrick, Stephen W. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2021, 325 (02) :146-155
[8]   Prenatal and postnatal contributions of the maternal microbiome on offspring programming [J].
Jasarevic, Eldin ;
Bale, Tracy L. .
FRONTIERS IN NEUROENDOCRINOLOGY, 2019, 55
[9]   Maternal gut microbiota in pregnancy influences offspring metabolic phenotype in mice [J].
Kimura, Ikuo ;
Miyamoto, Junki ;
Ohue-Kitano, Ryuji ;
Watanabe, Keita ;
Yamada, Takahiro ;
Onuki, Masayoshi ;
Aoki, Ryo ;
Isobe, Yosuke ;
Kashihara, Daiji ;
Inoue, Daisuke ;
Inaba, Akihiko ;
Takamura, Yuta ;
Taira, Satsuki ;
Kumaki, Shunsuke ;
Watanabe, Masaki ;
Ito, Masato ;
Nakagawa, Fumiyuki ;
Irie, Junichiro ;
Kakuta, Hiroki ;
Shinohara, Masakazu ;
Iwatsuki, Ken ;
Tsujimoto, Gozoh ;
Ohno, Hiroaki ;
Arita, Makoto ;
Itoh, Hiroshi ;
Hase, Koji .
SCIENCE, 2020, 367 (6481) :1002-+
[10]   Alterations of the Host Microbiome Affect Behavioral Responses to Cocaine [J].
Kiraly, Drew D. ;
Walker, Deena M. ;
Calipari, Erin S. ;
Labonte, Benoit ;
Issler, Orna ;
Pena, Catherine J. ;
Ribeiro, Efrain A. ;
Russo, Scott J. ;
Nestler, Eric J. .
SCIENTIFIC REPORTS, 2016, 6