Brain infection following experimental Staphylococcus aureus sepsis in pigs

Publikation: Bidrag til tidsskriftKonferenceabstrakt i tidsskriftForskning

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Brain infection following experimental Staphylococcus aureus sepsis in pigs. / Astrup, Lærke Boye; Iburg, Tine Moesgaard; Nielsen, Ole Lerberg; Jensen, Henrik Elvang; Leifsson, Páll S.; Agerholm, Jørgen Steen.

I: Journal of Comparative Pathology, Bind 143, Nr. 4, O3, 2010, s. 320.

Publikation: Bidrag til tidsskriftKonferenceabstrakt i tidsskriftForskning

Harvard

Astrup, LB, Iburg, TM, Nielsen, OL, Jensen, HE, Leifsson, PS & Agerholm, JS 2010, 'Brain infection following experimental Staphylococcus aureus sepsis in pigs', Journal of Comparative Pathology, bind 143, nr. 4, O3, s. 320. https://doi.org/10.1016/j.jcpa.2010.09.027

APA

Astrup, L. B., Iburg, T. M., Nielsen, O. L., Jensen, H. E., Leifsson, P. S., & Agerholm, J. S. (2010). Brain infection following experimental Staphylococcus aureus sepsis in pigs. Journal of Comparative Pathology, 143(4), 320. [O3]. https://doi.org/10.1016/j.jcpa.2010.09.027

Vancouver

Astrup LB, Iburg TM, Nielsen OL, Jensen HE, Leifsson PS, Agerholm JS. Brain infection following experimental Staphylococcus aureus sepsis in pigs. Journal of Comparative Pathology. 2010;143(4):320. O3. https://doi.org/10.1016/j.jcpa.2010.09.027

Author

Astrup, Lærke Boye ; Iburg, Tine Moesgaard ; Nielsen, Ole Lerberg ; Jensen, Henrik Elvang ; Leifsson, Páll S. ; Agerholm, Jørgen Steen. / Brain infection following experimental Staphylococcus aureus sepsis in pigs. I: Journal of Comparative Pathology. 2010 ; Bind 143, Nr. 4. s. 320.

Bibtex

@article{9c6d436294bc440398311fd8b86d0329,
title = "Brain infection following experimental Staphylococcus aureus sepsis in pigs",
abstract = "Introduction: Sepsis is a major problem in humans and both the incidence and mortality is increasing. Multiple microabcesses can be found in the brain of septic patients. Staphylococcus aureus is one of the most common causes of sepsis and brain abscesses. S. aureus is also a frequent cause of spontaneous porcine pyemia including endocarditis and associated brain lesions. We present a porcine model of haematogenous S. aureus induced brain infection. Materials and Methods: Twelve pigs received an intravenous injection of S. aureus of 108 CFU/kg body weight once at 0h or twice at 0h and 12h. Four pigs were kept as controls. The pigs were euthanized in groups of four at either 6, 12, 24 or 48 h post infection. The brain was collected from all the animals and examined histologically. Results: All the inoculated pigs developed sepsis and 7 out of 12 animals had microabscesses in the prosencephalon. The brain lesions showed a temporal progression. Conclusion: The brain lesions in the experimental infected pigs were similar to the brain lesions observed in pigs with spontaneous endocarditis and those observed in humans with septic encephalopathy respectively. This proves the porcine model as valid.",
author = "Astrup, {L{\ae}rke Boye} and Iburg, {Tine Moesgaard} and Nielsen, {Ole Lerberg} and Jensen, {Henrik Elvang} and Leifsson, {P{\'a}ll S.} and Agerholm, {J{\o}rgen Steen}",
year = "2010",
doi = "10.1016/j.jcpa.2010.09.027",
language = "English",
volume = "143",
pages = "320",
journal = "Journal of Comparative Pathology",
issn = "0021-9975",
publisher = "Elsevier",
number = "4",

}

RIS

TY - ABST

T1 - Brain infection following experimental Staphylococcus aureus sepsis in pigs

AU - Astrup, Lærke Boye

AU - Iburg, Tine Moesgaard

AU - Nielsen, Ole Lerberg

AU - Jensen, Henrik Elvang

AU - Leifsson, Páll S.

AU - Agerholm, Jørgen Steen

PY - 2010

Y1 - 2010

N2 - Introduction: Sepsis is a major problem in humans and both the incidence and mortality is increasing. Multiple microabcesses can be found in the brain of septic patients. Staphylococcus aureus is one of the most common causes of sepsis and brain abscesses. S. aureus is also a frequent cause of spontaneous porcine pyemia including endocarditis and associated brain lesions. We present a porcine model of haematogenous S. aureus induced brain infection. Materials and Methods: Twelve pigs received an intravenous injection of S. aureus of 108 CFU/kg body weight once at 0h or twice at 0h and 12h. Four pigs were kept as controls. The pigs were euthanized in groups of four at either 6, 12, 24 or 48 h post infection. The brain was collected from all the animals and examined histologically. Results: All the inoculated pigs developed sepsis and 7 out of 12 animals had microabscesses in the prosencephalon. The brain lesions showed a temporal progression. Conclusion: The brain lesions in the experimental infected pigs were similar to the brain lesions observed in pigs with spontaneous endocarditis and those observed in humans with septic encephalopathy respectively. This proves the porcine model as valid.

AB - Introduction: Sepsis is a major problem in humans and both the incidence and mortality is increasing. Multiple microabcesses can be found in the brain of septic patients. Staphylococcus aureus is one of the most common causes of sepsis and brain abscesses. S. aureus is also a frequent cause of spontaneous porcine pyemia including endocarditis and associated brain lesions. We present a porcine model of haematogenous S. aureus induced brain infection. Materials and Methods: Twelve pigs received an intravenous injection of S. aureus of 108 CFU/kg body weight once at 0h or twice at 0h and 12h. Four pigs were kept as controls. The pigs were euthanized in groups of four at either 6, 12, 24 or 48 h post infection. The brain was collected from all the animals and examined histologically. Results: All the inoculated pigs developed sepsis and 7 out of 12 animals had microabscesses in the prosencephalon. The brain lesions showed a temporal progression. Conclusion: The brain lesions in the experimental infected pigs were similar to the brain lesions observed in pigs with spontaneous endocarditis and those observed in humans with septic encephalopathy respectively. This proves the porcine model as valid.

U2 - 10.1016/j.jcpa.2010.09.027

DO - 10.1016/j.jcpa.2010.09.027

M3 - Conference abstract in journal

VL - 143

SP - 320

JO - Journal of Comparative Pathology

JF - Journal of Comparative Pathology

SN - 0021-9975

IS - 4

M1 - O3

ER -

ID: 173388940