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Forney Lab: Mayee Wong

 

Mayee Wong
Mayee Wong
mayeew@uidaho.edu
 

Introduction

Previous investigations of the human vulva microflora showed the presence of diverse microbial communities, but were unable to provide a complete assessment due to limitations inherent to the use of culture-based techniques.  An understanding of genital microbial composition and the relative abundances of various populations in normal healthy adult women is needed to recognize disease conditions.

 

Objectives

Characterize bacterial community structure and composition in two regions of the human vulva: the labia majora and labia minora.  In addition, determine if vulva microflora differ between women and between vulva sites of the same individual.

 

Approach

Total microbial DNA was isolated from scrapes obtained from the labia majora and minora of 5 normal healthy American women from the Cincinnati area.  The 16s rRNA genes of each vulva microbial community were amplified by PCR using bacterial-specific primers, 8 forward and 926 reverse, and clone libraries were constructed.  100 to 200 randomly chosen clones from each plasmid library were sequenced with plasmid primer, T7.  Initial analyses involve an assessment of clone sequence identity by comparison with the National Institute of Health database GenBank via the National Center for Biotechnology Information's BLAST algorithm for standard nucleotide to nucleotide matches.

Findings Thus Far

Preliminary data suggest that the flora of the vulva varies among normal healthy women.  The composition and prevalence of bacterial phylotypes differed between genital sites and amongst the women in this study.  In comparisons of the two vulva regions within the same woman, microorganisms of the labia minora were most similar to the assemblages commonly found in vaginal sites (Xia et al, unpublished data), while the labia majora was found to harbor a composite community of vaginal, fecal, and normal skin origin.  Differences in the microbial communities were also often pronounced between women; identity of the dominant bacterial group varied between women for each genital site, particularly in comparisons of the labia majoras.  These initial results indicate a need for a comparison of more women in order to gain an understanding of what can be considered normal vulva microflora across a larger demography. 

Current efforts are focused on completing another round of sequencing with a second plasmid primer, M13 reverse, and building consensus multiple sequence alignments.  Compilations of consensus clone sequences of a 918 nucleotide region of the 16s rDNA will be used to define differences between phylotype groups in the bacterial community of each vulva site via phylogenetic methods.

 

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Forney Lab
Department of Biological Sciences

Room 282, Life Sciences Building
University of Idaho
P.O. Box 443051
Moscow, ID 83844-3051
Lab Phone: (208) 885-2583
Email: lforney@uidaho.edu


Updated September 2005
Website enhancements were supported by the NSF-Idaho EPSCoR program and by the National Science Foundation under award number EPS-0132626.