Local infusion of Staphylococcus aureus into the porcine internal carotid artery as a model of sepsis-related brain abscesses - a pilot study
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Local infusion of Staphylococcus aureus into the porcine internal carotid artery as a model of sepsis-related brain abscesses - a pilot study. / Astrup, Lærke Boye; Iburg, Tine Moesgaard; Agerholm, Jørgen Steen; Aalbæk, Bent; Jensen, Henrik Elvang; Nielsen, Ole Lerberg; Leifsson, Páll Skúli.
In: Scandinavian Journal of Laboratory Animal Science, Vol. 43, 7, 2017.Research output: Contribution to journal › Journal article › Research › peer-review
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T1 - Local infusion of Staphylococcus aureus into the porcine internal carotid artery as a model of sepsis-related brain abscesses - a pilot study
AU - Astrup, Lærke Boye
AU - Iburg, Tine Moesgaard
AU - Agerholm, Jørgen Steen
AU - Aalbæk, Bent
AU - Jensen, Henrik Elvang
AU - Nielsen, Ole Lerberg
AU - Leifsson, Páll Skúli
PY - 2017
Y1 - 2017
N2 - Brain pathology is an important aspect of human sepsis but is difficult to study in human patients. Therefore, animal models of sepsis-related brain pathology are needed. As pigs mirror multiple aspects of sepsis-related brain pathology in humans, this makes the pig a potentially suitable model. Unfortunately, models of sepsis in pigs are difficult to manage due to the accompanying massive systemic inflammatory response. To overcome these difficulties we designed a model in pigs of brain bacteremia established by local brain infusion in order to evaluate if this approach could reduce the systemic responses but still reflect the brain pathology of sepsis in humans. As a pilot study to obtain basic knowledge, we evaluated two methods of local infusion: long term infusion (60 minutes) of Staphylococcus aureus suspended in saline and, short-term infusion (10 minutes) of S. aureus embedded in autologous microthrombi. The study revealed: 1) bacteria suspended in saline as well as embedded in microthrombi can pass through the rete mirabile and thereby cause local brain bacteremia; 2) despite the high dose of S. aureus used for infusion, only mild clinical signs developed; and 3) despite the mild clinical signs, one pig had developed a brain microabscess by 48 h after infusion. The brain pathology present in this pig thereby reflected human cases of S. aureus-sepsis with microabscess formation as the predominant lesion. In addition, the abscess morphology mirrored previously observed microabscesses in experimental porcine S. aureus sepsis models.
AB - Brain pathology is an important aspect of human sepsis but is difficult to study in human patients. Therefore, animal models of sepsis-related brain pathology are needed. As pigs mirror multiple aspects of sepsis-related brain pathology in humans, this makes the pig a potentially suitable model. Unfortunately, models of sepsis in pigs are difficult to manage due to the accompanying massive systemic inflammatory response. To overcome these difficulties we designed a model in pigs of brain bacteremia established by local brain infusion in order to evaluate if this approach could reduce the systemic responses but still reflect the brain pathology of sepsis in humans. As a pilot study to obtain basic knowledge, we evaluated two methods of local infusion: long term infusion (60 minutes) of Staphylococcus aureus suspended in saline and, short-term infusion (10 minutes) of S. aureus embedded in autologous microthrombi. The study revealed: 1) bacteria suspended in saline as well as embedded in microthrombi can pass through the rete mirabile and thereby cause local brain bacteremia; 2) despite the high dose of S. aureus used for infusion, only mild clinical signs developed; and 3) despite the mild clinical signs, one pig had developed a brain microabscess by 48 h after infusion. The brain pathology present in this pig thereby reflected human cases of S. aureus-sepsis with microabscess formation as the predominant lesion. In addition, the abscess morphology mirrored previously observed microabscesses in experimental porcine S. aureus sepsis models.
U2 - 10.23675/sjlas.v43i0.492
DO - 10.23675/sjlas.v43i0.492
M3 - Journal article
VL - 43
JO - Scandinavian Journal of Laboratory Animal Science
JF - Scandinavian Journal of Laboratory Animal Science
SN - 0901-3393
M1 - 7
ER -
ID: 185681816