David Longbottom
Intranasal infection with Chlamydia abortus induces dose-dependent latency and abortion in sheep
Longbottom, David; Livingstone, Morag; Maley, Stephen; van der Zon, Arjan; Rocchi, Mara; Wilson, Kim; Wheelhouse, Nicholas; Dagleish, Mark; Aitchison, Kevin; Wattegedera, Sean; Nath, Mintu; Entrican, Gary; Buxton, David
Authors
Morag Livingstone
Stephen Maley
Arjan van der Zon
Mara Rocchi
Kim Wilson
Prof Nick Wheelhouse N.Wheelhouse@napier.ac.uk
Professor
Mark Dagleish
Kevin Aitchison
Sean Wattegedera
Mintu Nath
Gary Entrican
David Buxton
Abstract
BACKGROUND: Latency is a key feature of the animal pathogen Chlamydia abortus, where infection remains inapparent in the non-pregnant animal and only becomes evident during a subsequent pregnancy. Often the first sign that an animal is infected is abortion occurring late in gestation. Despite this, little is understood of the underlying mechanisms that control latency or the recrudescence of infection that occurs during subsequent pregnancy. The aim of this study was to develop an experimental model of latency by mimicking the natural route of infection through the intranasal inoculation of non-pregnant sheep with C. abortus. METHODOLOGY/PRINCIPAL FINDINGS: Three groups of sheep (groups 1, 2 and 3) were experimentally infected with different doses of C. abortus (5x10(3), 5x10(5) and 5x10(7) inclusion forming units (IFU), respectively) prior to mating and monitored over 2 breeding cycles for clinical, microbiological, pathological, immunological and serological outcomes. Two further groups received either negative control inoculum (group 4a,b) or were inoculated subcutaneously on day 70 of gestation with 2x10(6) IFU C. abortus (group 5). Animals in groups 1, 2 and 5 experienced an abortion rate of 50-67%, while only one animal aborted in group 3 and none in group 4a,b. Pathological, microbiological, immunological and serological analyses support the view that the maternal protective immune response is influenced by initial exposure to the bacterium. CONCLUSIONS/SIGNIFICANCE: The results show that intranasal administration of non-pregnant sheep with a low/medium dose of C. abortus results in a latent infection that leads in a subsequent pregnancy to infection of the placenta and abortion. In contrast a high dose stimulates protective immunity, resulting in a much lower abortion rate. This model will be useful in understanding the mechanisms of infection underlying latency and onset of disease, as well as in the development of novel therapeutics and vaccines for controlling infection.
Citation
Longbottom, D., Livingstone, M., Maley, S., van der Zon, A., Rocchi, M., Wilson, K., Wheelhouse, N., Dagleish, M., Aitchison, K., Wattegedera, S., Nath, M., Entrican, G., & Buxton, D. (2013). Intranasal infection with Chlamydia abortus induces dose-dependent latency and abortion in sheep. PLOS ONE, 8(2), Article e57950. https://doi.org/10.1371/journal.pone.0057950
Journal Article Type | Article |
---|---|
Acceptance Date | Jan 27, 2013 |
Online Publication Date | Feb 28, 2013 |
Publication Date | Feb 28, 2013 |
Deposit Date | Jul 21, 2016 |
Publicly Available Date | Jan 28, 2020 |
Journal | PLoS One |
Print ISSN | 1932-6203 |
Electronic ISSN | 1932-6203 |
Publisher | Public Library of Science |
Peer Reviewed | Peer Reviewed |
Volume | 8 |
Issue | 2 |
Article Number | e57950 |
DOI | https://doi.org/10.1371/journal.pone.0057950 |
Keywords | Chlamydia infection, Ovine abortion, Placenta, Sheep, Enzyme-linked immunoassays, Serology, Immune response, Intranasal inoculation, |
Public URL | http://researchrepository.napier.ac.uk/Output/304728 |
Related Public URLs | http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585262/pdf/pone.0057950.pdf |
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Intranasal Infection with Chlamydia abortus Induces Dose-Dependent Latency and Abortion in Sheep
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Copyright Statement
Copyright: 2013 Longbottom et al. 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
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