Detection of bacteraemia and host response in healthy neonatal foals
Summary Reasons for performing the study Neonatal sepsis is a common problem in foals and is a primary cause of death in the post natal period. Transient bacteraemia and subsequent host responses have not been described in the equine neonate. Objectives The primary objective of this study was to det...
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Veröffentlicht in: | Equine veterinary journal 2015-07, Vol.47 (4), p.405-409 |
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Sprache: | eng |
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Zusammenfassung: | Summary
Reasons for performing the study
Neonatal sepsis is a common problem in foals and is a primary cause of death in the post natal period. Transient bacteraemia and subsequent host responses have not been described in the equine neonate.
Objectives
The primary objective of this study was to determine if transient bacteraemia occurs in foals within the first 72 h of life. Additional objectives included description of bacterial organisms associated with transient bacteraemia and concurrent cytokine gene expression in healthy foals.
Study design
Prospective observational study in healthy foals.
Methods
Blood was aseptically collected for bacterial culture from observed spontaneously born foals at birth and 1, 2, 3, 4, 8, 12, 24, 48 and 72 h following birth. Samples taken at birth, 4, 12, 24, 48 and 72 h were analysed for interferon gamma (IFNγ), interleukin (IL)‐1, IL‐2, IL‐6, IL‐8, IL‐10, IL‐18 and monocyte chemotactic protein 1 (MCP1) cytokine gene expression quantified by RT‐PCR.
Results
Bacteria were cultured from 9 of 70 samples submitted for blood culture. The positive samples were from 4 of the 7 foals, all of which remained healthy throughout and subsequent to the study. All positive blood cultures were from blood samples obtained at 12 h of age or earlier and IL‐10 elevation coincided with positive blood cultures in healthy foals. Cytokine gene expression fluctuated with age.
Conclusions
Positive blood cultures suggest transient bacteraemia may occur in healthy foals early in the post natal period. Age corrected normal values may be necessary to interpret cytokine concentration in diseased populations. |
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ISSN: | 0425-1644 2042-3306 |
DOI: | 10.1111/evj.12307 |