Ureaplasma parvum serovar 3 multiple banded antigen size variation after chronic intra-amniotic infection/colonization


Autoria(s): Robinson, James W.; Dando, Samantha J.; Nitsos, Ilias; Newnham, John; Polglase, Graeme R.; Kallapur, Suhas G.; Pillow, J. Jane; Kramer, Boris W.; Jobe, Alan H.; Payton, Diane; Knox, Christine L.
Data(s)

2013

Resumo

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 2x107 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.

Formato

application/pdf

Identificador

http://eprints.qut.edu.au/59260/

Publicador

Public Library of Science

Relação

http://eprints.qut.edu.au/59260/1/59260.pdf

http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0062746;jsessionid=DAA8F1099FAACF98A05573CB204C5B4E

DOI:10.1371/journal.pone.0062746

Robinson, James W., Dando, Samantha J., Nitsos, Ilias, Newnham, John, Polglase, Graeme R., Kallapur, Suhas G., Pillow, J. Jane, Kramer, Boris W., Jobe, Alan H., Payton, Diane, & Knox, Christine L. (2013) Ureaplasma parvum serovar 3 multiple banded antigen size variation after chronic intra-amniotic infection/colonization. PLoS One, 8(4), e62746.

http://purl.org/au-research/grants/NHMRC/303261, 458577

Direitos

Copyright 2013 The Authors

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Fonte

School of Biomedical Sciences; Faculty of Health; Institute of Health and Biomedical Innovation

Palavras-Chave #060500 MICROBIOLOGY #110309 Infectious Diseases #111400 PAEDIATRICS AND REPRODUCTIVE MEDICINE #Ureaplasma species #Intra-amniotic infection #chorioamnionitis #fetal lung infection #broncho-pulmonary dysplasia #multiple banded antigen #MBA size variants #animal model
Tipo

Journal Article