International Leibniz Research School for Microbial and Biomolecular Interactions - ILRS Jena
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International Leibniz Research School

for Microbial and Biomolecular Interactions ILRS Jena

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Amin, Shayista
Behnken, Swantje
Brandes, Susanne
Chen, Qian
Eberhardt, Hannes
Enghardt, Tina
Fischer, Juliane
Funk, Alexander
Graupner, Katharina
Heddergott, Christoph
Horn, Fabian
Jbeily, Nayla
Jetha, Khushboo
Kopka, Isabell
Kroll, Kristin
Machanda, Himanshu
MacNelly, Anita
Mauß, Michaela
Mayer, François
Mingo, Felix
Mohan, Karthik Mohan
Mohebbi, Sara
Müller, Christiane
Müller, Sebastian
Ramachandra, Shruthi
Sarkar, Sarbani
Schwenk, Daniel
Seddigh, Pegah
Senftleben, Dominik
Stippa, Selina
Thywißen, Andreas
Weinhold, Arne
 

Sarbani Sarkar

Personal Data:
Country of Origin: India
Start of PhD: April 2009
Institution: HKI

PhD Project:
Complement evasion strategies of Streptococcus pneumoniae

Supervisor(s): P.F. Zipfel (HKI)

Abstract:
My project aims on complement escape strategies used by the human pathogenic bacteria Streptococcus pneumoniae. Upon infection S.pneumoniae similar to other pathogenic microbes is constantly challenged by the complement defense system of the human host. The complement system as a part of the innate immune system forms a human line of defence that recognizes and damages infectious microbes. Complement is activated by three pathways: the alternative, the classical and the lectin pathway. Pathogenic microbes have developed diverse mechanisms to evade host complement system.

Streptococcus pneumoniae is a facultative human pathogen that can cause pneumonia, acute sinusitis, otitis media, bacteraemia and meningitis. S. pneumoniae binds the human plasma protein Factor H, which is the central inhibitor of the alternative complement pathway. Factor H bound to the bacterial surface protects the pathogen from the damaging effects of the complement cascade. My project deals with identifying complement escape strategies used by S. pneumoniae. Particularly, I want to identify and characterise bacterial proteins that bind host complement inhibitors. I aim to study interactions of streptococcal surface proteins with regulators of the complement and coagulation cascades.
JSMC

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