Title |
Disruption of maternal gut microbiota during gestation alters offspring microbiota and immunity
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Published in |
Microbiome, July 2018
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DOI | 10.1186/s40168-018-0511-7 |
Pubmed ID | |
Authors |
Donald D. Nyangahu, Katie S. Lennard, Bryan P. Brown, Matthew G. Darby, Jerome M. Wendoh, Enock Havyarimana, Peter Smith, James Butcher, Alain Stintzi, Nicola Mulder, William Horsnell, Heather B. Jaspan |
Abstract |
Early life microbiota is an important determinant of immune and metabolic development and may have lasting consequences. The maternal gut microbiota during pregnancy or breastfeeding is important for defining infant gut microbiota. We hypothesized that maternal gut microbiota during pregnancy and breastfeeding is a critical determinant of infant immunity. To test this, pregnant BALB/c dams were fed vancomycin for 5 days prior to delivery (gestation; Mg), 14 days postpartum during nursing (Mn), or during gestation and nursing (Mgn), or no vancomycin (Mc). We analyzed adaptive immunity and gut microbiota in dams and pups at various times after delivery. In addition to direct alterations to maternal gut microbial composition, pup gut microbiota displayed lower α-diversity and distinct community clusters according to timing of maternal vancomycin. Vancomycin was undetectable in maternal and offspring sera, therefore the observed changes in the microbiota of stomach contents (as a proxy for breastmilk) and pup gut signify an indirect mechanism through which maternal intestinal microbiota influences extra-intestinal and neonatal commensal colonization. These effects on microbiota influenced both maternal and offspring immunity. Maternal immunity was altered, as demonstrated by significantly higher levels of both total IgG and IgM in Mgn and Mn breastmilk when compared to Mc. In pups, lymphocyte numbers in the spleens of Pg and Pn were significantly increased compared to Pc. This increase in cellularity was in part attributable to elevated numbers of both CD4+ T cells and B cells, most notable Follicular B cells. Our results indicate that perturbations to maternal gut microbiota dictate neonatal adaptive immunity. |
X Demographics
Geographical breakdown
Country | Count | As % |
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United Kingdom | 14 | 24% |
Australia | 5 | 8% |
United States | 4 | 7% |
Spain | 4 | 7% |
South Africa | 2 | 3% |
Canada | 2 | 3% |
Luxembourg | 1 | 2% |
France | 1 | 2% |
Ireland | 1 | 2% |
Other | 7 | 12% |
Unknown | 18 | 31% |
Demographic breakdown
Type | Count | As % |
---|---|---|
Members of the public | 33 | 56% |
Scientists | 21 | 36% |
Practitioners (doctors, other healthcare professionals) | 3 | 5% |
Science communicators (journalists, bloggers, editors) | 2 | 3% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
---|---|---|
Unknown | 225 | 100% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Ph. D. Student | 41 | 18% |
Student > Master | 32 | 14% |
Researcher | 22 | 10% |
Student > Doctoral Student | 20 | 9% |
Student > Bachelor | 14 | 6% |
Other | 33 | 15% |
Unknown | 63 | 28% |
Readers by discipline | Count | As % |
---|---|---|
Immunology and Microbiology | 29 | 13% |
Agricultural and Biological Sciences | 29 | 13% |
Medicine and Dentistry | 26 | 12% |
Biochemistry, Genetics and Molecular Biology | 24 | 11% |
Nursing and Health Professions | 15 | 7% |
Other | 32 | 14% |
Unknown | 70 | 31% |