In the U.S., the annual cost of health care for newborns with complications approaches $26 billion, and worldwide, preterm birth is the leading cause of morbidity and mortality among neonates. Despite improved survival rates, the past few decades have seen no significant decrease in preterm births. It is becoming more clear that the billions of bacteria that colonize the human body play important roles in the health of the individual. However, the role of the millions of bacteria and other microbes that colonize the human female urogenital tract in prenatal health and birth of a healthy baby remains obscure. Previous to the recent development of 'omics'technologies;i.e., genomics, transcriptomics, proteomics, metabolomics, interactomics, etc., it was not possible to study these microbial populations in any in depth or highly efficient way. Many of these organisms have never been characterized and a fairly large fraction have not been successfully cultured. Herein, we propose to use these 'omic'technologies to dissect the bacterial populations that inhabit and colonize the female urogenital tract of pregnant women to assess the role(s) of these organisms in maintenance of health or in the cause of disease in these women and their babies. An understanding of the roles these organisms play in the health of the female urogenital tract will lead to better, more efficient prenatal and postnatal care, likely leading to diminished levels of preterm birth and infant morbidity and mortality.

Public Health Relevance

Preterm birth is the leading cause of infant morbidity and mortality worldwide. We are applying revolutionary 'omics'technologies to study the populations of bacteria that live in the female urogenital tract to identify their roles in vaginal health and disease, and to the outcome of the pregnancy. These studies will likely lead to improved outcomes of pregnancy and birth.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
1U54DE023786-01
Application #
8617339
Study Section
Special Emphasis Panel (ZDE1-JH (15))
Program Officer
Lunsford, Dwayne
Project Start
2013-09-06
Project End
2016-08-31
Budget Start
2013-09-06
Budget End
2014-08-31
Support Year
1
Fiscal Year
2013
Total Cost
$2,500,000
Indirect Cost
$778,893
Name
Virginia Commonwealth University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
105300446
City
Richmond
State
VA
Country
United States
Zip Code
23298
Brooks, J Paul; Edwards, David J; Blithe, Diana L et al. (2017) Effects of combined oral contraceptives, depot medroxyprogesterone acetate and the levonorgestrel-releasing intrauterine system on the vaginal microbiome. Contraception 95:405-413
Mariano, Rachelle; Wuchty, Stefan; Vizoso-Pinto, Maria G et al. (2016) The interactome of Streptococcus pneumoniae and its bacteriophages show highly specific patterns of interactions among bacteria and their phages. Sci Rep 6:24597
Abdelmaksoud, Abdallah A; Koparde, Vishal N; Sheth, Nihar U et al. (2016) Comparison of Lactobacillus crispatus isolates from Lactobacillus-dominated vaginal microbiomes with isolates from microbiomes containing bacterial vaginosis-associated bacteria. Microbiology 162:466-475
Allen-Daniels, Matthew Josiah; Serrano, Myrna G; Pflugner, Lindsey P et al. (2015) Identification of a gene in Mycoplasma hominis associated with preterm birth and microbial burden in intraamniotic infection. Am J Obstet Gynecol 212:779.e1-779.e13
Fettweis, Jennifer M; Brooks, J Paul; Serrano, Myrna G et al. (2014) Differences in vaginal microbiome in African American women versus women of European ancestry. Microbiology 160:2272-2282
Fettweis, Jennifer M; Serrano, Myrna G; Huang, Bernice et al. (2014) An emerging mycoplasma associated with trichomoniasis, vaginal infection and disease. PLoS One 9:e110943