Grant: Master's Award: Canada Graduate Scholarships
University of Victoria (British Columbia)
$17,500.00
Understanding the Molecular Basis of Treponema pallidum Dissemination
FY 2011-12
Summary
Syphilis is a global public health concern with 25 million cases worldwide. It is caused by the bacterium Treponema pallidum, transmitted by sexual contact, direct contact with lesions or from an infected mother to the fetus. T. pallidum, one of the most invasive pathogens known, spreads throughout the body and establishes chronic infection causing serious clinical symptoms and even death unless treated. Although the disease is easily cured by penicillin, globally there are 12 million new infections per year. Over the last decade a startling increase in new cases has been observed in developed countries, especially in Canada. In addition to the public health concern of syphilis itself, it also significantly increases the risk for HIV infection. A better understanding of the molecular mechanism of syphilis infection is needed to find suitable vaccine targets. The Cameron lab is the only place worldwide studying the critical bacterial ability to spread throughout the human host. We identified two syphilis proteins and showed a role in attaching to and digesting host components. We think they are essential for T. pallidum spread. My project will first determine the proteins` capacity to attach to a wide variety of host components. Then, I will use an otherwise non-infectious model bacterium armored with one of the proteins to show that the protein enables the model to digest its way through an artificial tissue layer to prove its role in the spread of the bacterium. Finally, cell death caused by either protein or the model bacterium will be evaluated. This line of research fits with the general lab research aim to understand the molecular basis of syphilis infection. It will provide invaluable insight for vaccine development to prevent infection through understanding the attachment and spread of the bacterium. Development of a syphilis vaccine will decrease the incidence of this globally prevalent disease and also eliminate a significant risk factor for HIV infection.
Department
Program
Master's Award: Canada Graduate Scholarships
Location
British Columbia, Canada
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
251997
Name
Denchev Yavor P
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Canada Graduate Scholarships Master's Awards A
Projecttitle
Understanding the Molecular Basis of Treponema pallidum Dissemination
Programtype2
Studentship Programs
Orgnameinp2
University of Victoria (British Columbia)
Cihramount2
$17,500
Cihrequipment2
$0
Programname2
Master's Award: Canada Graduate Scholarships
Keyworddelim
Attachment Assay; Co-Factor For Hiv; Darkfield Microscopy; Dissemination; Rt-Qpcr; Syphilis; Treponema Pallidum; Treponema Phagedenis
Abstract
Syphilis is a global public health concern with 25 million cases worldwide. It is caused by the bacterium Treponema pallidum, transmitted by sexual contact, direct contact with lesions or from an infected mother to the fetus. T. pallidum, one of the most invasive pathogens known, spreads throughout the body and establishes chronic infection causing serious clinical symptoms and even death unless treated. Although the disease is easily cured by penicillin, globally there are 12 million new infections per year. Over the last decade a startling increase in new cases has been observed in developed countries, especially in Canada. In addition to the public health concern of syphilis itself, it also significantly increases the risk for HIV infection. A better understanding of the molecular mechanism of syphilis infection is needed to find suitable vaccine targets. The Cameron lab is the only place worldwide studying the critical bacterial ability to spread throughout the human host. We identified two syphilis proteins and showed a role in attaching to and digesting host components. We think they are essential for T. pallidum spread. My project will first determine the proteins` capacity to attach to a wide variety of host components. Then, I will use an otherwise non-infectious model bacterium armored with one of the proteins to show that the protein enables the model to digest its way through an artificial tissue layer to prove its role in the spread of the bacterium. Finally, cell death caused by either protein or the model bacterium will be evaluated. This line of research fits with the general lab research aim to understand the molecular basis of syphilis infection. It will provide invaluable insight for vaccine development to prevent infection through understanding the attachment and spread of the bacterium. Development of a syphilis vaccine will decrease the incidence of this globally prevalent disease and also eliminate a significant risk factor for HIV infection.
Competitiondate
201202
Approvedterm2
1 yr 0 mth
Pinamesdelim
Denchev, Yavor P
Approvedterm
1 an 0 mois
Cihrcontribution2
~ $17,500~ $0~