Diversified microbiota of meconium is affected by maternal diabetes status.
Diversified microbiota of meconium is affected by maternal diabetes status.
复制标题
DOI:
10.1371/journal.pone.0078257
复制
发表时间:
2013
期刊:
影响因子:
3.7
通讯作者:
Peter I
中科院分区:
文献类型:
--
作者:
Hu J;Nomura Y;Bashir A;Fernandez-Hernandez H;Itzkowitz S;Pei Z;Stone J;Loudon H;Peter I
This study was aimed to assess the diversity of the meconium microbiome and determine if the bacterial community is affected by maternal diabetes status. The first intestinal discharge (meconium) was collected from 23 newborns stratified by maternal diabetes status: 4 mothers had pre-gestational type 2 diabetes mellitus (DM) including one mother with dizygotic twins, 5 developed gestational diabetes mellitus (GDM) and 13 had no diabetes. The meconium microbiome was profiled using multi-barcode 16S rRNA sequencing followed by taxonomic assignment and diversity analysis. All meconium samples were not sterile and contained diversified microbiota. Compared with adult feces, the meconium showed a lower species diversity, higher sample-to-sample variation, and enrichment of Proteobacteria and reduction of Bacteroidetes. Among the meconium samples, the taxonomy analyses suggested that the overall bacterial content significantly differed by maternal diabetes status, with the microbiome of the DM group showing higher alpha-diversity than that of no-diabetes or GDM groups. No global difference was found between babies delivered vaginally versus via Cesarean-section. Regression analysis showed that the most robust predictor for the meconium microbiota composition was the maternal diabetes status that preceded pregnancy. Specifically, Bacteroidetes (phyla) and Parabacteriodes (genus) were enriched in the meconium in the DM group compared to the no-diabetes group. Our study provides evidence that meconium contains diversified microbiota and is not affected by the mode of delivery. It also suggests that the meconium microbiome of infants born to mothers with DM is enriched for the same bacterial taxa as those reported in the fecal microbiome of adult DM patients.
登录
查看更多内容
影响因子:
16.2
作者:
Jeon CY;Haan MN;Cheng C;Clayton ER;Mayeda ER;Miller JW;Aiello AE
通讯作者:
Aiello AE
DOI:
10.1093/bioinformatics/bts342
发表时间:
2012-08-15
期刊:
Bioinformatics (Oxford, England)
影响因子:
--
作者:
Chen J;Bittinger K;Charlson ES;Hoffmann C;Lewis J;Wu GD;Collman RG;Bushman FD;Li H
通讯作者:
Li H
影响因子:
3.7
作者:
Hong PY;Lee BW;Aw M;Shek LP;Yap GC;Chua KY;Liu WT
通讯作者:
Liu WT
DOI:
10.1073/pnas.1002601107
发表时间:
2010-06-29
影响因子:
11.1
作者:
Dominguez-Bello, Maria G.;Costello, Elizabeth K.;Knight, Rob
通讯作者:
Knight, Rob
影响因子:
3.5
作者:
Dunne, F;Brydon, P;Gee, H
通讯作者:
Gee, H