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Tytuł pozycji:

Identification and characterization of bacterial vaginosis-associated pathogens using a comprehensive cervical-vaginal epithelial coculture assay.

Tytuł:
Identification and characterization of bacterial vaginosis-associated pathogens using a comprehensive cervical-vaginal epithelial coculture assay.
Autorzy:
Eade CR; Department of Molecular Biology and Microbiology, Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, Florida, United States of America.
Diaz C
Wood MP
Anastos K
Patterson BK
Gupta P
Cole AL
Cole AM
Źródło:
PloS one [PLoS One] 2012; Vol. 7 (11), pp. e50106. Date of Electronic Publication: 2012 Nov 15.
Typ publikacji:
Comparative Study; Journal Article; Research Support, N.I.H., Extramural
Język:
English
Imprint Name(s):
Original Publication: San Francisco, CA : Public Library of Science
MeSH Terms:
Host-Pathogen Interactions*
Coculture Techniques/*methods
Epithelial Cells/*microbiology
Genitalia, Female/*cytology
Vaginosis, Bacterial/*microbiology
Actinobacteria/metabolism ; Analysis of Variance ; Cytokines/metabolism ; Enzyme-Linked Immunosorbent Assay ; Female ; Genitalia, Female/microbiology ; Humans ; Lactobacillus/metabolism ; Lymphocytes/immunology ; Real-Time Polymerase Chain Reaction ; beta-Defensins/metabolism
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Grant Information:
R56 AI052017 United States AI NIAID NIH HHS; AI052017 United States AI NIAID NIH HHS; AI082693 United States AI NIAID NIH HHS; AI35004 United States AI NIAID NIH HHS; R21 AI082693 United States AI NIAID NIH HHS; U19 AI082623 United States AI NIAID NIH HHS; R01 AI052017 United States AI NIAID NIH HHS; AI082623 United States AI NIAID NIH HHS; R33 AI082693 United States AI NIAID NIH HHS; U01 AI035004 United States AI NIAID NIH HHS
Substance Nomenclature:
0 (Cytokines)
0 (DEFB4A protein, human)
0 (beta-Defensins)
Entry Date(s):
Date Created: 20121121 Date Completed: 20130429 Latest Revision: 20211021
Update Code:
20240104
PubMed Central ID:
PMC3499514
DOI:
10.1371/journal.pone.0050106
PMID:
23166828
Czasopismo naukowe
Bacterial vaginosis (BV) is the most commonly treated female reproductive tract affliction, characterized by the displacement of healthy lactobacilli by an overgrowth of pathogenic bacteria. BV can contribute to pathogenic inflammation, preterm birth, and susceptibility to sexually transmitted infections. As the bacteria responsible for BV pathogenicity and their interactions with host immunity are not understood, we sought to evaluate the effects of BV-associated bacteria on reproductive epithelia. Here we have characterized the interaction between BV-associated bacteria and the female reproductive tract by measuring cytokine and defensin induction in three types of FRT epithelial cells following bacterial inoculation. Four BV-associated bacteria were evaluated alongside six lactobacilli for a comparative assessment. While responses differed between epithelial cell types, our model showed good agreement with clinical BV trends. We observed a distinct cytokine and human β-defensin 2 response to BV-associated bacteria, especially Atopobium vaginae, compared to most lactobacilli. One lactobacillus species, Lactobacillus vaginalis, induced an immune response similar to that elicited by BV-associated bacteria, stimulating significantly higher levels of cytokines and human β-defensin 2 than other lactobacilli. These data provide an important prioritization of BV-associated bacteria and support further characterization of reproductive bacteria and their interactions with host epithelia. Additionally, they demonstrate the distinct immune response potentials of epithelial cells from different locations along the female reproductive tract.

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