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Approaches to increase recovery of bacterial and fungal abortion agents in domestic ruminants

Abortions in domestic ruminants cause significant economic losses to farmers. Determining the cause of an abortion is important for control efforts, but it can be challenging. All available diagnostic methods in the bacteriology laboratory should be employed in every case due to the many limiting fa...

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Autores principales: Jonker, Annelize, Thompson, Peter N., Michel, Anita L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AOSIS 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9900296/
https://www.ncbi.nlm.nih.gov/pubmed/36744493
http://dx.doi.org/10.4102/ojvr.v90i1.2010
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author Jonker, Annelize
Thompson, Peter N.
Michel, Anita L.
author_facet Jonker, Annelize
Thompson, Peter N.
Michel, Anita L.
author_sort Jonker, Annelize
collection PubMed
description Abortions in domestic ruminants cause significant economic losses to farmers. Determining the cause of an abortion is important for control efforts, but it can be challenging. All available diagnostic methods in the bacteriology laboratory should be employed in every case due to the many limiting factors (autolysis, lack of history, range of samples) that complicate the investigation process. The purpose of this study was to determine whether the recovery of diagnostically significant isolates from domestic ruminant abortion cases could be increased through the use of a combination of the existing aerobic culture and Brucella selective method with methods that are commonly recommended in the literature reporting abortion investigations. These methods are examination of wet preparations and impression smears stained by the modified Ziehl–Neelsen method, anaerobic, microaerophilic, Leptospira, Mycoplasma and fungal culture. Samples of placenta and aborted foetuses from 135 routine clinical abortion cases of cattle (n = 88), sheep (n = 25) and goats (n = 22) were analysed by the new combination of methods. In 46 cases, bacteria were identified as aetiological agents and in one case a fungus. Isolation of Brucella species increased to 7.4% over two years compared with the previous 10 years (7.3%), as well as Campylobacter jejuni (n = 2) and Rhizopus species (n = 1). Salmonella species (5.9%) and Trueperella pyogenes (4.4%) were also isolated more often. In conclusion, the approach was effective in removing test selection bias in the bacteriology laboratory. The importance of performing an in-depth study on the products of abortion by means of an extensive, combination of conventional culture methods was emphasised by increased isolation of Brucella abortus and isolation of C. jejuni. The combination of methods that yielded the most clinically relevant isolates was aerobic, microaerophilic, Brucella and fungal cultures.
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spelling pubmed-99002962023-02-07 Approaches to increase recovery of bacterial and fungal abortion agents in domestic ruminants Jonker, Annelize Thompson, Peter N. Michel, Anita L. Onderstepoort J Vet Res Original Research Abortions in domestic ruminants cause significant economic losses to farmers. Determining the cause of an abortion is important for control efforts, but it can be challenging. All available diagnostic methods in the bacteriology laboratory should be employed in every case due to the many limiting factors (autolysis, lack of history, range of samples) that complicate the investigation process. The purpose of this study was to determine whether the recovery of diagnostically significant isolates from domestic ruminant abortion cases could be increased through the use of a combination of the existing aerobic culture and Brucella selective method with methods that are commonly recommended in the literature reporting abortion investigations. These methods are examination of wet preparations and impression smears stained by the modified Ziehl–Neelsen method, anaerobic, microaerophilic, Leptospira, Mycoplasma and fungal culture. Samples of placenta and aborted foetuses from 135 routine clinical abortion cases of cattle (n = 88), sheep (n = 25) and goats (n = 22) were analysed by the new combination of methods. In 46 cases, bacteria were identified as aetiological agents and in one case a fungus. Isolation of Brucella species increased to 7.4% over two years compared with the previous 10 years (7.3%), as well as Campylobacter jejuni (n = 2) and Rhizopus species (n = 1). Salmonella species (5.9%) and Trueperella pyogenes (4.4%) were also isolated more often. In conclusion, the approach was effective in removing test selection bias in the bacteriology laboratory. The importance of performing an in-depth study on the products of abortion by means of an extensive, combination of conventional culture methods was emphasised by increased isolation of Brucella abortus and isolation of C. jejuni. The combination of methods that yielded the most clinically relevant isolates was aerobic, microaerophilic, Brucella and fungal cultures. AOSIS 2023-01-11 /pmc/articles/PMC9900296/ /pubmed/36744493 http://dx.doi.org/10.4102/ojvr.v90i1.2010 Text en © 2023. The Authors https://creativecommons.org/licenses/by/4.0/Licensee: AOSIS. This work is licensed under the Creative Commons Attribution License.
spellingShingle Original Research
Jonker, Annelize
Thompson, Peter N.
Michel, Anita L.
Approaches to increase recovery of bacterial and fungal abortion agents in domestic ruminants
title Approaches to increase recovery of bacterial and fungal abortion agents in domestic ruminants
title_full Approaches to increase recovery of bacterial and fungal abortion agents in domestic ruminants
title_fullStr Approaches to increase recovery of bacterial and fungal abortion agents in domestic ruminants
title_full_unstemmed Approaches to increase recovery of bacterial and fungal abortion agents in domestic ruminants
title_short Approaches to increase recovery of bacterial and fungal abortion agents in domestic ruminants
title_sort approaches to increase recovery of bacterial and fungal abortion agents in domestic ruminants
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9900296/
https://www.ncbi.nlm.nih.gov/pubmed/36744493
http://dx.doi.org/10.4102/ojvr.v90i1.2010
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