In a separate study, we applied these molecular methods and established diversity and composition parameters to the analysis of microbial phylogeny in the oral, vaginal, and check details rectal microbiomes in gestational diabetes prior to onset of active labor.23 Microbial 16S rRNA was amplified by PCR using conserved regions. Samples were pooled into a single pyrosequencing Inhibitors,research,lifescience,medical run. QIIME pipeline was used to validate microbial 16S rRNA sequencing quality and assign sequences to the original specimens as above. Then, a basic local alignment search tool (BLAST) was used to identify OTU sequence homology in the bacterial

databases of the National Center for Biotechnology Information, to name specific genera and form a phylogenetic tree. Data indicate skewed prevalence

for multiple Inhibitors,research,lifescience,medical genera in either gestational diabetes or the healthy state, suggesting changes in microbial composition for the oral, vaginal, and rectal compartments in women with gestational diabetes when compared with healthy pregnancies (Table 1 and Figure 3). Table 1 Skewed microbial composition in oral, Inhibitors,research,lifescience,medical vaginal, and rectal compartments in normal versus gestational diabetes pregnancies. Figure 3 Oral, vaginal, and rectal phylogeny in normal pregnancies (NL) and gestational diabetes melitus (GDM). In conclusion, the microbiome of the urogenital tract plays an important role in health and disease,24,25 prompting more comprehensive study. In particular, relationships between obstetrical pathologies and the vaginal microbiome should be defined and causality differentiated from secondary ecosystem perturbations.23 Acknowledgments We are grateful to our clinical team for facilitating specimen procurement, Rob Knight Inhibitors,research,lifescience,medical for the use of the QIIME pipeline and help with data analysis,

Bruce Paster for advising oral microbiome analysis, and Siegfried Rotmesch for the use of the clinical facility and helpful discussions. Work was supported by a CCFA Senior Research Award #1832 (Offer Cohavy and Bruce Paster), and the Cedars-Sinai Research Institute. Abbreviations: OTU operational Inhibitors,research,lifescience,medical taxonomic units; PCR polymerase chain reaction; SPS sequences Dichloromethane dehalogenase per specimen. Footnotes Conflict of interest: No potential conflict of interest relevant to this article was reported.
Ninety years after its introduction as an anti-epileptic treatment,1,2 and after periods of ups and downs in its use, the ketogenic diet (KD) has found its proper place in clinical practice. The idea of manipulating diets for therapeutic purposes has been around for centuries. For instance, fasting was used in the treatment of epilepsy since Biblical times (Matthew 17:5–21). The first modern reports of its use in the medical literature were by Guelpha in 1911 and Conklin in 1921.3 KD has been used to treat epilepsy in children since 1921 with little variation until recent years.