Chlamydia psittaci infection as a cause of respiratory disease in neonatal foals.


Journal

Equine veterinary journal
ISSN: 2042-3306
Titre abrégé: Equine Vet J
Pays: United States
ID NLM: 0173320

Informations de publication

Date de publication:
Mar 2020
Historique:
received: 20 05 2019
accepted: 15 08 2019
pubmed: 23 8 2019
medline: 2 7 2020
entrez: 23 8 2019
Statut: ppublish

Résumé

During 2016-2018, 15 critically ill neonatal foals with acute respiratory distress associated with Chlamydia psittaci infection were presented to three referral hospitals in New South Wales. Chlamydia psittaci has not previously been associated with the development of neonatal respiratory disease. To investigate and describe the clinical features and outcome of C. psittaci infection in neonatal foals. Multicentre retrospective case series. The clinical, clinicopathological, necropsy and histological features of 15 foals with confirmed C. psittaci infection were reviewed and reported. Thirteen foals with C. psittaci infection died or were subjected to euthanasia within 36 h of hospitalisation and two foals survived to discharge. Findings during post-mortem examination of nonsurviving foals included bronchopneumonia, pulmonary congestion, hepatic congestion and hepatic inflammation. Detection of C. psittaci was achieved using polymerase chain reaction (PCR) testing of swabs of nasal secretions (4/6) and rectal mucosa (5/7) from live foals, lung tissues of foals at necropsy (11/14) and foetal membranes (4/5). Small numbers of confirmed cases of neonatal C. psittaci infection and inconsistent sampling methods. Chlamydia psittaci should be considered a differential diagnosis for neonatal foals with signs of severe systemic disease, including equine neonatal acute respiratory distress syndrome (EqNARDS). Chlamydia psittaci is a zoonotic pathogen and a personal protective equipment (PPE) should be worn for the management of foals with suspected or confirmed infection.

Sections du résumé

BACKGROUND BACKGROUND
During 2016-2018, 15 critically ill neonatal foals with acute respiratory distress associated with Chlamydia psittaci infection were presented to three referral hospitals in New South Wales. Chlamydia psittaci has not previously been associated with the development of neonatal respiratory disease.
OBJECTIVES OBJECTIVE
To investigate and describe the clinical features and outcome of C. psittaci infection in neonatal foals.
STUDY DESIGN METHODS
Multicentre retrospective case series.
METHODS METHODS
The clinical, clinicopathological, necropsy and histological features of 15 foals with confirmed C. psittaci infection were reviewed and reported.
RESULTS RESULTS
Thirteen foals with C. psittaci infection died or were subjected to euthanasia within 36 h of hospitalisation and two foals survived to discharge. Findings during post-mortem examination of nonsurviving foals included bronchopneumonia, pulmonary congestion, hepatic congestion and hepatic inflammation. Detection of C. psittaci was achieved using polymerase chain reaction (PCR) testing of swabs of nasal secretions (4/6) and rectal mucosa (5/7) from live foals, lung tissues of foals at necropsy (11/14) and foetal membranes (4/5).
MAIN LIMITATIONS CONCLUSIONS
Small numbers of confirmed cases of neonatal C. psittaci infection and inconsistent sampling methods.
CONCLUSIONS CONCLUSIONS
Chlamydia psittaci should be considered a differential diagnosis for neonatal foals with signs of severe systemic disease, including equine neonatal acute respiratory distress syndrome (EqNARDS). Chlamydia psittaci is a zoonotic pathogen and a personal protective equipment (PPE) should be worn for the management of foals with suspected or confirmed infection.

Identifiants

pubmed: 31436332
doi: 10.1111/evj.13170
doi:

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

244-249

Subventions

Organisme : Charles Sturt University

Informations de copyright

© 2019 EVJ Ltd.

Références

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Auteurs

S L Gough (SL)

Veterinary Clinical Centre, School of Animal and Veterinary Sciences, Charles Sturt University, Wagga Wagga, New South Wales, Australia.

J Carrick (J)

Equine Specialist Consulting, Scone, New South Wales, Australia.

S L Raidal (SL)

Veterinary Clinical Centre, School of Animal and Veterinary Sciences, Charles Sturt University, Wagga Wagga, New South Wales, Australia.

S Keane (S)

Dartbrook Equine Clinic, Scone, New South Wales, Australia.

N Collins (N)

Clovelly Intensive Care Unit, Scone Equine Hospital, Scone, New South Wales, Australia.

L Cudmore (L)

Clovelly Intensive Care Unit, Scone Equine Hospital, Scone, New South Wales, Australia.

C M Russell (CM)

Clovelly Intensive Care Unit, Scone Equine Hospital, Scone, New South Wales, Australia.

S Raidal (S)

Veterinary Diagnostic Laboratory, School of Animal and Veterinary Sciences, Charles Sturt University, Wagga Wagga, New South Wales, Australia.

K J Hughes (KJ)

Veterinary Clinical Centre, School of Animal and Veterinary Sciences, Charles Sturt University, Wagga Wagga, New South Wales, Australia.

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