Pregnant women who develop preeclampsia have lower abundance of the butyrate-producer Coprococcus in their gut microbiota

被引:64
作者
Altemani, Faisal [1 ,7 ]
Barrett, Helen L. [2 ,3 ]
Gomez-Arango, Luisa [1 ]
Josh, Peter [1 ]
McIntyre, H. David [2 ,3 ]
Callaway, Leonie K. [4 ,5 ]
Morrison, Mark [6 ]
Tyson, Gene W. [1 ]
Nitert, Marloes Dekker [1 ]
机构
[1] Univ Queensland, Sch Chem & Mol Biosci, Bldg 76-452,Cooper Rd, St Lucia, Qld 4072, Australia
[2] Mater Grp, Dept Endocrinol, South Brisbane, Qld 4101, Australia
[3] Univ Queensland, Mater Res, South Brisbane, Qld 4101, Australia
[4] Royal Brisbane & Womens Hosp, Dept Obstetr Med, Herston, Qld 4059, Australia
[5] Univ Queensland, Clin Res Ctr, Herston, Qld 4059, Australia
[6] Translat Res Inst, Woolloongabba, Qld 4102, Australia
[7] Univ Tabuk, Fac Appl Med Sci, Dept Med Lab Technol, Tabuk 71491, Saudi Arabia
基金
英国医学研究理事会;
关键词
Preeclampsia; Pregnancy; Blood pressure; Gut microbiota; Butyrate; CHAIN FATTY-ACIDS; BLOOD-PRESSURE; HYPERTENSIVE DISORDERS; METABOLITE BUTYRATE; SEQUENCE; RECEPTOR;
D O I
10.1016/j.preghy.2021.01.002
中图分类号
R71 [妇产科学];
学科分类号
100211 [妇产科学];
摘要
Preeclampsia is a pregnancy-specific disorder characterized by hypertension and dysfunction of several organs, that is associated with maternal and fetal complications. The human gut microbiota is related to health and disease including hypertension. Alterations in gut microbiota composition can change the short-chain fatty acid profile released by the bacteria and contribute to hypertension and metabolic syndrome. It is unclear if the composition of the gut microbiota is altered in women who develop late-onset preeclampsia. In this study, we investigated the composition of the gut microbiota at 28 weeks gestation in women who developed late-onset (>34 weeks gestation) preeclampsia (DPE) by 16S rRNA gene amplicon sequencing of fecal samples obtained from 213 pregnant women in the SPRING cohort (Study of Probiotics IN Gestational diabetes). Quantitative realtime PCR was used to assess the density of butyrate-producing genes. Gut microbiota composition was compared between women with and without DPE. The abundance of the butyrate-producing Coprococcus genus significantly decreased in DPE. Abundance of Coprococcus is significantly and positively correlated with the abundance of genes encoding the terminal step in bacterial butyrate formation (but and buk). Women with DPE also had significantly reduced levels of serum butyrate prior to the development of symptoms than controls. This study suggests that a reduction in the abundance of butyrate-producing bacteria, and Coprococcus spp. in particular, may contribute to an increased risk of developing preeclampsia in pregnant women.
引用
收藏
页码:211 / 219
页数:9
相关论文
共 42 条
[1]
Andrews S., 2010, FastQC, DOI DOI 10.1186/1472-6963-10-122
[2]
[Anonymous], 2020, Obstet Gynecol, V135, P1492, DOI [10.1097/AOG.0000000000003018, 10.1097/AOG.0000000000003892]
[3]
Hypertensive disorders in pregnancy [J].
Aronow, Wilbert S. .
ANNALS OF TRANSLATIONAL MEDICINE, 2017, 5 (12)
[4]
Trimmomatic: a flexible trimmer for Illumina sequence data [J].
Bolger, Anthony M. ;
Lohse, Marc ;
Usadel, Bjoern .
BIOINFORMATICS, 2014, 30 (15) :2114-2120
[5]
Reproducible, interactive, scalable and extensible microbiome data science using QIIME 2 [J].
Bolyen, Evan ;
Rideout, Jai Ram ;
Dillon, Matthew R. ;
Bokulich, NicholasA. ;
Abnet, Christian C. ;
Al-Ghalith, Gabriel A. ;
Alexander, Harriet ;
Alm, Eric J. ;
Arumugam, Manimozhiyan ;
Asnicar, Francesco ;
Bai, Yang ;
Bisanz, Jordan E. ;
Bittinger, Kyle ;
Brejnrod, Asker ;
Brislawn, Colin J. ;
Brown, C. Titus ;
Callahan, Benjamin J. ;
Caraballo-Rodriguez, Andres Mauricio ;
Chase, John ;
Cope, Emily K. ;
Da Silva, Ricardo ;
Diener, Christian ;
Dorrestein, Pieter C. ;
Douglas, Gavin M. ;
Durall, Daniel M. ;
Duvallet, Claire ;
Edwardson, Christian F. ;
Ernst, Madeleine ;
Estaki, Mehrbod ;
Fouquier, Jennifer ;
Gauglitz, Julia M. ;
Gibbons, Sean M. ;
Gibson, Deanna L. ;
Gonzalez, Antonio ;
Gorlick, Kestrel ;
Guo, Jiarong ;
Hillmann, Benjamin ;
Holmes, Susan ;
Holste, Hannes ;
Huttenhower, Curtis ;
Huttley, Gavin A. ;
Janssen, Stefan ;
Jarmusch, Alan K. ;
Jiang, Lingjing ;
Kaehler, Benjamin D. ;
Bin Kang, Kyo ;
Keefe, Christopher R. ;
Keim, Paul ;
Kelley, Scott T. ;
Knights, Dan .
NATURE BIOTECHNOLOGY, 2019, 37 (08) :852-857
[6]
Callahan BJ, 2016, NAT METHODS, V13, P581, DOI [10.1038/NMETH.3869, 10.1038/nmeth.3869]
[7]
Probiotics for the Prevention of Gestational Diabetes Mellitus in Overweight and Obese Women: Findings From the SPRING Double-Blind Randomized Controlled Trial [J].
Callaway, Leonie K. ;
McIntyre, H. David ;
Barrett, Helen L. ;
Foxcroft, Katie ;
Tremellen, Anne ;
Lingwood, Barbara E. ;
Tobin, Jacinta M. ;
Wilkinson, Shelley ;
Kothari, Alka ;
Morrison, Mark ;
O'Rourke, Peter ;
Pelecanos, Anita ;
Nitert, Marloes Dekker .
DIABETES CARE, 2019, 42 (03) :364-371
[8]
BLAST plus : architecture and applications [J].
Camacho, Christiam ;
Coulouris, George ;
Avagyan, Vahram ;
Ma, Ning ;
Papadopoulos, Jason ;
Bealer, Kevin ;
Madden, Thomas L. .
BMC BIOINFORMATICS, 2009, 10
[9]
The microbial metabolite butyrate regulates intestinal macrophage function via histone deacetylase inhibition [J].
Chang, Pamela V. ;
Hao, Liming ;
Offermanns, Stefan ;
Medzhitov, Ruslan .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2014, 111 (06) :2247-2252
[10]
The role of short-chain fatty acids in the interplay between diet, gut microbiota, and host energy metabolism [J].
den Besten, Gijs ;
van Eunen, Karen ;
Groen, Albert K. ;
Venema, Koen ;
Reijngoud, Dirk-Jan ;
Bakker, Barbara M. .
JOURNAL OF LIPID RESEARCH, 2013, 54 (09) :2325-2340