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Role of Bacterial and Host DNases on Host-Pathogen Interaction during Streptococcus suis Meningitis

is a zoonotic agent causing meningitis in pigs and humans. Neutrophils, as the first line of defense against infections, release neutrophil extracellular traps (NETs) to entrap pathogens. In this study, we investigated the role of the secreted nuclease A of (SsnA) as a NET-evasion factor in vivo and...

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Published in:International journal of molecular sciences 2020-07, Vol.21 (15), p.5289
Main Authors: Meurer, Marita, Öhlmann, Sophie, Bonilla, Marta C, Valentin-Weigand, Peter, Beineke, Andreas, Hennig-Pauka, Isabel, Schwerk, Christian, Schroten, Horst, Baums, Christoph G, Köckritz-Blickwede, Maren von, de Buhr, Nicole
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Language:English
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Summary:is a zoonotic agent causing meningitis in pigs and humans. Neutrophils, as the first line of defense against infections, release neutrophil extracellular traps (NETs) to entrap pathogens. In this study, we investigated the role of the secreted nuclease A of (SsnA) as a NET-evasion factor in vivo and in vitro. Piglets were intranasally infected with strain 10 or an isogenic mutant. DNase and NET-formation were analyzed in cerebrospinal fluid (CSF) and brain tissue. Animals infected with strain 10 or S. suis 10ΔssnA showed the presence of NETs in CSF and developed similar clinical signs. Therefore, SsnA does not seem to be a crucial virulence factor that contributes to the development of meningitis in pigs. Importantly, DNase activity was detectable in the CSF of both infection groups, indicating that host nucleases, in contrast to bacterial nuclease SsnA, may play a major role during the onset of meningitis. The effect of DNase 1 on neutrophil functions was further analyzed in a 3D-cell culture model of the porcine blood-CSF barrier. We found that DNase 1 partially contributes to enhanced killing of by neutrophils, especially when plasma is present. In summary, host nucleases may partially contribute to efficient innate immune response in the CSF.
ISSN:1422-0067
1661-6596
1422-0067
DOI:10.3390/ijms21155289