The 1B vaccine strain of Chlamydia abortus produces placental pathology indistinguishable from a wild type infection.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 28 08 2020
accepted: 28 10 2020
entrez: 16 11 2020
pubmed: 17 11 2020
medline: 5 1 2021
Statut: epublish

Résumé

Chlamydia abortus is one of the most commonly diagnosed causes of infectious abortion in small ruminants worldwide. Control of the disease (Enzootic Abortion of Ewes or EAE) is achieved using the commercial live, attenuated C. abortus 1B vaccine strain, which can be distinguished from virulent wild-type (wt) strains by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis. Published studies applying this typing method and whole-genome sequence analyses to cases of EAE in vaccinated and non-vaccinated animals have provided strong evidence that the 1B strain is not attenuated and can infect the placenta causing disease in some ewes. Therefore, the objective of this study was to characterise the lesions found in the placentas of ewes vaccinated with the 1B strain and to compare these to those resulting from a wt infection. A C. abortus-free flock of multiparous adult ewes was vaccinated twice, over three breeding seasons, each before mating, with the commercial C. abortus 1B vaccine strain (Cevac® Chlamydia, Ceva Animal Health Ltd.). In the second lambing season following vaccination, placentas (n = 117) were collected at parturition and analysed by C. abortus-specific real-time quantitative PCR (qPCR). Two placentas, from a single ewe, which gave birth to live twin lambs, were found to be positive by qPCR and viable organisms were recovered and identified as vaccine type (vt) by PCR-RFLP, with no evidence of any wt strain being present. All cotyledons from the vt-infected placentas were analysed by histopathology and immunohistochemistry and compared to those from wt-infected placentas. Both vt-infected placentas showed lesions typical of those found in a wt infection in terms of their severity, distribution, and associated intensity of antigen labelling. These results conclusively demonstrate that the 1B strain can infect the placenta, producing typical EAE placental lesions that are indistinguishable from those found in wt infected animals.

Identifiants

pubmed: 33196660
doi: 10.1371/journal.pone.0242526
pii: PONE-D-20-27056
pmc: PMC7668586
doi:

Substances chimiques

Bacterial Vaccines 0
Vaccines, Attenuated 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0242526

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Références

J Comp Pathol. 2003 May;128(4):217-44
pubmed: 12834606
Vet Microbiol. 2009 Mar 16;135(1-2):2-21
pubmed: 18986778
Vet Microbiol. 2015 Dec 14;181(1-2):107-18
pubmed: 26255554
Vet Rec. 1983 Dec 3;113(23):535-6
pubmed: 6364542
Vet Microbiol. 2009 Mar 16;135(1-2):90-7
pubmed: 18980813
Front Immunol. 2019 Jan 09;9:3025
pubmed: 30687304
PLoS One. 2013;8(2):e57950
pubmed: 23469113
PLoS One. 2017 May 11;12(5):e0177653
pubmed: 28494018
N Z Vet J. 2015 Sep;63(5):284-7
pubmed: 25695509
J Comp Pathol. 1996 Apr;114(3):221-30
pubmed: 8762580
Vaccine. 2010 Aug 9;28(35):5653-6
pubmed: 20600479
Vet Rec. 1997 Jul 19;141(3):63-7
pubmed: 9257434
Vet Microbiol. 2018 Nov;225:31-33
pubmed: 30322529
Vet Microbiol. 2009 Mar 16;135(1-2):134-41
pubmed: 18930611
Vaccine. 2010 Aug 9;28(35):5657-63
pubmed: 20554095
Infect Immun. 1983 Nov;42(2):525-30
pubmed: 6642642
Vaccine. 2018 Jun 14;36(25):3593-3598
pubmed: 29759381
J Comp Pathol. 2002 Aug-Oct;127(2-3):133-41
pubmed: 12354524
Vet Rec. 1950 Apr 29;62(17):251-4
pubmed: 15418751
Ann Rech Vet. 1983;14(2):155-61
pubmed: 6614792
Res Vet Sci. 2005 Feb;78(1):1-7
pubmed: 15500832
Am J Reprod Immunol. 2010 Oct;64(4):287-94
pubmed: 20712809
J Comp Pathol. 1990 Feb;102(2):221-37
pubmed: 2324344

Auteurs

Sergio Gaston Caspe (SG)

Moredun Research Institute, Penicuik, Midlothian, United Kingdom.
Royal (Dick) School of Veterinary Studies, University of Edinburgh, Edinburgh, United Kingdom.
Estación Experimental Mercedes, Instituto Nacional de Tecnología Agropecuaria (INTA), Mercedes, Corrientes, Argentina.

Morag Livingstone (M)

Moredun Research Institute, Penicuik, Midlothian, United Kingdom.

David Frew (D)

Moredun Research Institute, Penicuik, Midlothian, United Kingdom.

Kevin Aitchison (K)

Moredun Research Institute, Penicuik, Midlothian, United Kingdom.

Sean Ranjan Wattegedera (SR)

Moredun Research Institute, Penicuik, Midlothian, United Kingdom.

Gary Entrican (G)

Moredun Research Institute, Penicuik, Midlothian, United Kingdom.

Javier Palarea-Albaladejo (J)

Biomathematics and Statistics Scotland, Edinburgh, United Kingdom.

Tom Nathan McNeilly (TN)

Moredun Research Institute, Penicuik, Midlothian, United Kingdom.

Elspeth Milne (E)

Royal (Dick) School of Veterinary Studies, University of Edinburgh, Edinburgh, United Kingdom.

Neil Donald Sargison (ND)

Royal (Dick) School of Veterinary Studies, University of Edinburgh, Edinburgh, United Kingdom.

Francesca Chianini (F)

Moredun Research Institute, Penicuik, Midlothian, United Kingdom.

David Longbottom (D)

Moredun Research Institute, Penicuik, Midlothian, United Kingdom.

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Classifications MeSH