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Ureaplasma parvum serovar 3 multiple banded antigen size variation after chronic intra-amniotic infection/colonization.
- Source :
-
PloS one [PLoS One] 2013 Apr 26; Vol. 8 (4), pp. e62746. Date of Electronic Publication: 2013 Apr 26 (Print Publication: 2013). - Publication Year :
- 2013
-
Abstract
- Ureaplasma species are the microorganisms most frequently associated with adverse pregnancy outcomes. The multiple banded antigen (MBA), a surface-exposed lipoprotein, is a key virulence factor of ureaplasmas. The MBA demonstrates size variation, which we have shown previously to be correlated with the severity of chorioamnion inflammation. We aimed to investigate U. parvum serovar 3 pathogenesis in vivo, using a sheep model, by investigating: MBA variation after long term (chronic) and short term (acute) durations of in utero ureaplasma infections, and the severity of chorioamnionitis and inflammation in other fetal tissues. Inocula of 2 × 10(7) colony-forming-units (CFU) of U. parvum serovar 3 (Up) or media controls (C) were injected intra-amniotically into pregnant ewes at one of three time points: day 55 (69d Up, n = 8; C69, n = 4); day 117 (7d Up, n = 8; C7, n = 2); and day 121 (3d Up, n = 8; C3, n = 2) of gestation (term = 145-150d). At day 124, preterm fetuses were delivered surgically. Samples of chorioamnion, fetal lung, and umbilical cord were: (i) snap frozen for subsequent ureaplasma culture, and (ii) fixed, embedded, sectioned and stained by haematoxylin and eosin stain for histological analysis. Selected fetal lung clinical ureaplasma isolates were cloned and filtered to obtain cultures from a single CFU. Passage 1 and clone 2 ureaplasma cultures were tested by western blot to demonstrate MBA variation. In acute durations of ureaplasma infection no MBA variants (3d Up) or very few MBA variants (7d Up) were present when compared to the original inoculum. However, numerous MBA size variants were generated in vivo (alike within contiguous tissues, amniotic fluid and fetal lung, but different variants were present within chorioamnion), during chronic, 69d exposure to ureaplasma infection. For the first time we have shown that the degree of ureaplasma MBA variation in vivo increased with the duration of gestation.
- Subjects :
- Amnion pathology
Amniotic Fluid metabolism
Animals
Blotting, Western
Body Fluids metabolism
Chronic Disease
Clone Cells
Colony Count, Microbial
Delivery, Obstetric
Female
Hydrogen-Ion Concentration
Lung pathology
Lung physiopathology
Male
Molecular Weight
Pregnancy
Pressure
Sheep microbiology
Ureaplasma growth & development
Ureaplasma isolation & purification
Ureaplasma physiology
Amnion microbiology
Antigenic Variation immunology
Antigens, Bacterial immunology
Bacterial Proteins metabolism
Ureaplasma immunology
Ureaplasma Infections immunology
Ureaplasma Infections microbiology
Subjects
Details
- Language :
- English
- ISSN :
- 1932-6203
- Volume :
- 8
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- PloS one
- Publication Type :
- Academic Journal
- Accession number :
- 23638142
- Full Text :
- https://doi.org/10.1371/journal.pone.0062746